| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs35452716 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130173094 | TTAATCAGTTAAAAC[-/A]AAAATTAAAGAGTCA | 50807 |
| rs35463619 | in-del | -/T/TT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130205591 | TATAAAATACACGGC[-/T/TT]TTTTTTTTTTTTTTT | 50807 |
| rs35468248 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130074818 | CTGCTGGGCAGCCCC[-/C]AGATGACCATGTGAG | 50807 |
| rs35470764 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130103140 | TCTTCTTGGTTCAAT[-/A]CTTGGTGGTTGTTTC | 50807 |
| rs35491318 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130262100 | GTTTCCAGTGCTATT[-/A]AAAAAGGGAGTACCG | 50807 |
| rs35496476 | in-del | -/TC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130097767 | ATCTCCTGAGACTCT[-/TC]CCCAGGAACTGACAT | 50807 |
| rs35505474 | in-del | -/CT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130276729 | ACACACACACACACA[-/CT]CTCTCTCTCTCTCTC | 50807 |
| rs35542094 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130439692 | ACACAGGTGCTTTTT[-/T]AAAGATGAGTAGCAA | 50807 |
| rs35548518 | in-del | -/A | 0.182614 | 0.240747 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320644 | GAAGGAGGAAGAGTT[-/A]AAAATGAAAATTATA | 50807 |
| rs35550432 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130126993 | TCTTGCTCACAGGGG[-/G]TTCTGCAAGGATTCA | 50807 |
| rs35570986 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130346037 | GAGAGGTAGACTTAA[-/C]CCGTATTTGGAAAAC | 50807 |
| rs35592532 | snp | C/G | 0.408359 | 0.193449 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403477 | CTGAACATGTTCTGA[C/G]TCTTGTTCACCTCTC | 50807 |
| rs35597833 | in-del | -/AC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130372960 | AATACACAGGCATAT[-/AC]ACACACAGACATACA | 50807 |
| rs35606745 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130126512 | GGTCATGGCCTCCCC[-/C]ATGAGCACTTCTTAG | 50807 |
| rs35606959 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130323871 | AGATTACCAGGCATT[-/A]AAAAAAACCACTTAT | 50807 |
| rs35618724 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130198438 | GGAGCTCCAAAATTT[-/C]CCTTTTTATTGCACC | 50807 |
| rs35658546 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327164 | TGAATAATTCTCCCT[G/T]CACTCCAGTTCCTCT | 50807 |
| rs35662981 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130279959 | ATCAACTATGTGCCA[-/G]GTTAGAAACCTGAGT | 50807 |
| rs35673359 | multinucleotide-polymorphism | AT/GG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130437906 | CGCCACTGGAGGGAC[AT/GG]ACTTACTTTTGTTTT | 50807 |
| rs35675281 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130381291 | CCTTGGCCTCCCAAA[-/G]GGCTGGGATTACAGC | 50807 |
| rs35712105 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130170659 | AGTTTTTCAGCAACA[-/G]GGGATGAGAGATAAA | 50807 |
| rs35713491 | snp | C/T | 0.348794 | 0.229651 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091503 | TAGGAGATAAGAGCC[C/T]GATCATGCAGGGCCC | 50807 |
| rs35717171 | in-del | -/AT | 0.230603 | 0.249246 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381444 | AAAGTCTTTGAAAAC[-/AT]ATATTTTAGACTTAT | 50807 |
| rs35718811 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130324211 | AGCATCATGACTCAA[-/C]CCCCACTTCTCTGGC | 50807 |
| rs35746850 | in-del | -/T | 0.186446 | 0.241787 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395674 | GAGACAATACATTTC[-/T]TTTTTTTTTTGAGAC | 50807 |
| rs35752871 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130211528 | GAAACTGATAAACAC[-/A]AATACACCTGCAATA | 50807 |
| rs35755042 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130165816 | AATAAAGAAAACCTT[-/C]CAGGGTTGCTTTAAA | 50807 |
| rs35758549 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130182933 | TGGGGAAAAAACACT[-/G]GAAAAAATAACCTAA | 50807 |
| rs35762160 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130372103 | ATTATAGAATCACTG[-/A]AAAGACTGGTCTCAA | 50807 |
| rs35765185 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130126974 | TAAAATGAGAACATT[-/T]GGGATCTTGCTCACA | 50807 |
| rs35768414 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130390103 | TGATTTTTAACAGCT[-/C]CCCCAGGTGACCCAC | 50807 |
| rs35780831 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130223095 | TGTCATAATTAATAT[-/A]AAAGCTCTTTTGGAA | 50807 |
| rs35785222 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130284032 | TATGTGATGAGGACA[-/G]GCTTTTTGTTAGACT | 50807 |
| rs35800266 | in-del | -/T | 0.430111 | 0.173378 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395674 | GAGACAATACATTTC[-/T]TTTTTTTTTTTGAGA | 50807 |
| rs35805935 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130188690 | AGTGAGCCGAGATCA[-/C]CACACTGCATTCCAG | 50807 |
| rs35812201 | in-del | -/ACG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130342755 | GCCAACTCTCAGAAA[-/ACG]CAAGTTAAAGTTGCT | 50807 |
| rs35813100 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130080015 | TGTCTTTAGATGGGG[-/G]AAATGCAATGAGAAT | 50807 |
| rs35815989 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130234343 | CACCAGAGGCTACTC[-/T]TAATAGTACAAACCT | 50807 |
| rs35822005 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130290554 | TAGCCTAGTCGACAT[-/G]GGGGATGTGTGCCTG | 50807 |
| rs35822290 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130370631 | TCATTCTTAACATTC[-/A]AAAAAATGGAAACAG | 50807 |
| rs35826450 | in-del | -/A | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158365 | AAAAAAAAAAAAAAA[-/A]GTATCCAGGCATGGT | 50807 |
| rs35841555 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130206686 | TGACCTAGAATACTT[-/C]CCGGGTGACTCCCAC | 50807 |
| rs35855151 | in-del | -/T | 0.375 | 0.216506 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143425 | TGTTTTTTTTTTTTT[-/T]GACATATGTTGGTTC | 50807 |
| rs35865490 | snp | C/G | 0.110519 | 0.207473 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392787 | TGCAGAGATCAGATG[C/G]TGAGAGAAGGAGGTG | 50807 |
| rs35871836 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130192278 | CTCCAAAGGGCCACA[-/G]GTATATAACTGATAT | 50807 |
| rs35872777 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130331332 | GCCAAGCCCAGAGCA[-/C]AGAATTCCATGGAAG | 50807 |
| rs35874860 | in-del | -/TG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130099700 | TTTTTTTTTTTTTTT[-/TG]GAGACAGAGTCTTGC | 50807 |
| rs35889961 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130212860 | TGGTCCAGGAACCTT[-/G]GGAGGTGATGACTCT | 50807 |
| rs35895109 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130188860 | ATCATTTTAGCACTT[-/C]CCATTAACACCTCTG | 50807 |
| rs35914521 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130338081 | TCACATATTTGGGCA[-/C]TGGGGGATAAGACGA | 50807 |
| rs35915232 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387658 | GAGACTCCATCTCAG[-/AA]AAAAAAAAAAAAAAA | 50807 |
| rs35918155 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130128164 | TTTTTTTTTTTTTTT[-/T]GCCACTGCAAAAAAA | 50807 |
| rs35923959 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130089277 | AGGCTCAGATCTGAG[-/C]AGAAAAAAATAGAAC | 50807 |
| rs35929308 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130209359 | AGTATGGCGCCTAGG[-/C]CCCTAGAGGTTCCCA | 50807 |
| rs35945499 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130425153 | CCTGGCCAACATGGC[-/C]AAATCCCATCTCTAC | 50807 |
| rs35950038 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130248036 | AAAAACACCACTGAG[-/C]AGTGACTGATTGGTA | 50807 |
| rs35959837 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130287095 | GCCAGAAGGAACACA[-/G]GGGAAATTGACTGTT | 50807 |
| rs35977498 | snp | A/T | 0.372391 | 0.217992 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437910 | ACTGGAGGGACATAC[A/T]TACTTTTGTTTTCCT | 50807 |
| rs35980474 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130192560 | CCTATCCTATGGGCC[-/T]TTAGAAGTTTGGATG | 50807 |
| rs35992202 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130119681 | GAATCCACCCCTTGA[-/A]TTTCCCAGTTACATG | 50807 |
| rs36004574 | snp | A/G | 0.328382 | 0.237395 | intron-variant | ASAP1 | GRCh38.p7 | 8:130190946 | TACATAACCTCGATG[A/G]GGACAGGGACTTTGA | 50807 |
| rs36004599 | snp | A/G | 0.262985 | 0.249663 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269333 | GATTTCTGTGATACA[A/G]TTTCCAAGTAAAATA | 50807 |
| rs36006774 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130136168 | GAGGAGTCCTCTCAG[-/T]CTACAGTGTGGGTCG | 50807 |
| rs36017481 | in-del | -/G | | | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052536 | TCACCAAAGGTATTT[-/G]CTACTGAGTTTTCCT | 50807 |
| rs36024310 | in-del | -/A | 0.49934 | 0.0181589 | intron-variant | ASAP1 | GRCh38.p7 | 8:130282070 | CAAGACTCTGCCTCG[-/A]AAAAAAAAAAAAAAG | 50807 |
| rs36024399 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130176586 | TTGCAATCTGGTAAC[-/A]AAAATCCTAGCTATC | 50807 |
| rs36029388 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130299315 | ATGTTTCTAATGTTT[-/G]GGAGATGTTGGCAAC | 50807 |
| rs36041620 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130401755 | TTCTCCAATAACAAT[-/G]CGTGCACACAGTCTC | 50807 |
| rs36050520 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130247527 | AGATGGAGGACCCTT[-/A]AAAAAAAAACAACAA | 50807 |
| rs36061299 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130396291 | CAAGAAGGCTTTGCC[-/A]ATGAGTCTTATTCAT | 50807 |
| rs36065517 | snp | C/G | 0.35809 | 0.225425 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128980 | TCCCCATAATCCCCA[C/G]GTGTCTGGGGAGAGA | 50807 |
| rs36069299 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130109967 | ATTATGGGCTTTTTT[-/T]GGGGGAAGTGGGGAA | 50807 |
| rs36070317 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130064772 | AGCCCAGGCCTCTGG[-/A]AATTTCTGACCAGTT | 50807 |
| rs36074051 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130206432 | GATATTCTTATTTGA[-/G]GGGGAAAGAAAAGAA | 50807 |
| rs36074954 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130176062 | CATGTCTGAAATTGA[-/C]GCAGTAATTAGTGAG | 50807 |
| rs36092795 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130157124 | CAGGGAAGAACAAGG[-/G]AGCTGAGCCTGAGGC | 50807 |
| rs36094124 | in-del | -/TTA | 0.0592355 | 0.161582 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397144 | TTTATGAGAATTTTG[-/TTA]TTGTTGTTGTTGTTA | 50807 |
| rs36111603 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130288419 | TGAGAATATAAACCT[-/C]CCCTGCAAATGCTTA | 50807 |
| rs36114209 | snp | G/T | 0.0298908 | 0.118541 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092324 | GGTTTCAAAAATTTG[G/T]TTAAAAAAAAAATAA | 50807 |
| rs36115515 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130255064 | TGTCTCGAAAGTCAT[-/C]CTCCCAAATCAAAAT | 50807 |
| rs41400845 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204922 | ATTCTGATAACAGGA[A/G]CTTGTCTTTATACTG | 50807 |
| rs55637017 | snp | C/G | 0.0448719 | 0.142907 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295036 | TGGGAGGCTGAGGTG[C/G]GAGGATTGCTTGAGG | 50807 |
| rs55642195 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | ASAP1 | GRCh38.p7 | 8:130386662 | AGAAACAGTTAGAAG[C/T]GGACTCACCTCTGCC | 50807 |
| rs55676740 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130314974 | AGCTGGGTGACCTTT[C/T]TGAATTTCGGTTACC | 50807 |
| rs55686856 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370210 | AGGAGGCTGAGGCAG[A/G]AGAATAGCTTGAACC | 50807 |
| rs55692599 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245236 | AATTGAAAGTTGGTA[C/T]GTTATCTGCAAATAA | 50807 |
| rs55705977 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148210 | GACCTAACAACAATC[C/T]GGCAGCTGAGGAAAA | 50807 |
| rs55724400 | snp | A/C | 0.0377204 | 0.132699 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114557 | GGTTTATACCAGCAT[A/C]CCACAACCATTTGAG | 50807 |
| rs55756220 | snp | A/G | 0.139903 | 0.224452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088452 | CACGTACACTTATGA[A/G]AGAGAGGCAAAGGCA | 50807 |
| rs55758693 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264608 | ACTATAACTGTATTC[G/T]TGAAATGTTACCAGA | 50807 |
| rs55759245 | snp | G/T | 0.35574 | 0.226537 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114433 | AAAATGGTACATCTA[G/T]GTAGGACACTTTCCA | 50807 |
| rs55759431 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ASAP1 | GRCh38.p7 | 8:130357099 | TATCGTGGCCCCAGA[A/G]GCTTCTGCTGCTCCT | 50807 |
| rs55796310 | snp | C/T | 0.340784 | 0.232934 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059949 | CCAGGCGTAGTGATA[C/T]GTACCTTGGTCCCAG | 50807 |
| rs55807402 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309261 | CACAGAGAGACAGGT[A/G]AGCAATTAATTTCAA | 50807 |
| rs55815182 | snp | C/G | 0.163236 | 0.234461 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170077 | ACTATCTGTTTTGCT[C/G]TCTCCCTACAAACAA | 50807 |
| rs55821463 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121093 | GATCAGCAAATCCTG[C/T]TGGCTCTCCCTTCAA | 50807 |
| rs55823176 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122094 | GGGTGCCTTCATGCC[C/T]CTCAATTCTGCACTT | 50807 |
| rs55848037 | snp | A/C | 0.0337553 | 0.125452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122551 | AAGCACTTTTTATTC[A/C]AGCCCCTTAATTGTC | 50807 |
| rs55867508 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162088 | TACAGGTGTGAGCAC[C/T]ATGCTCGACCTAAAT | 50807 |
| rs55871312 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206319 | CTACCAATTTTACCA[C/T]TAGGCACATCCATGC | 50807 |
| rs55875346 | in-del | -/AAAAAAAAAAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130060095 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAA]TAGAGAGAGAGAGAA | 50807 |
| rs55878237 | snp | C/T | 0.170408 | 0.236992 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377771 | AGGCTCCAGCCCTCC[C/T]GGCTGTGTCTCAGGG | 50807 |
| rs55879798 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130161044 | AGAACAGAAACATGG[C/T]TAAATAGAAGAATGT | 50807 |
| rs55891945 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360192 | TAAAGTGGAGTAAAT[A/G]TAAAGTAAGAAAGTG | 50807 |
| rs55921193 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130314893 | ATTCATTTGCTTACT[C/T]TGAACTTCTGAACTT | 50807 |
| rs55937708 | in-del | -/A | 0.000207447 | 0.0101824 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167628 | TCTGTTTTATCTATG[-/A]AAAAAAAATTACTTC | 50807 |
| rs55961633 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130329710 | AAGAGCTCTGAAATA[C/G]GGACTAAACAGAAAA | 50807 |
| rs55968438 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206461 | AAGAAAAATAAAAAA[A/C]AAAACAACTTTAACA | 50807 |
| rs55979731 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175950 | GTTTATAAATGCTGT[C/T]AACTCTGCAGGTCAT | 50807 |
| rs55993168 | snp | A/C | 0.35574 | 0.226537 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114441 | ACATCTATGTAGGAC[A/C]CTTTCCATAAATGGA | 50807 |
| rs56027659 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130161102 | AAATGGTTGACAAAC[C/T]TCAAATGTGTATGTA | 50807 |
| rs56035628 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130256121 | GGATGAGGTACCAAC[C/T]TTTGCCCTGAAGCAC | 50807 |
| rs56038473 | in-del | -/CAT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130285930 | TACTGGAACAGATAT[-/CAT]AAATAATTTGCTACC | 50807 |
| rs56058876 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130121843 | TTAGAAAATAACTCA[A/G]ATCACGCCACTCCTG | 50807 |
| rs56060465 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317802 | TTGTGGCTGAAGTGA[C/T]GAACATGGCATGGCA | 50807 |
| rs56086422 | snp | A/G | 0.162253 | 0.234095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319316 | AAAATAAAATAAAAT[A/G]AAAAAAGGAATAAAA | 50807 |
| rs56103517 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130163057 | TACTGGAGTTGGCAA[A/G]GGCCTGTGACAATGA | 50807 |
| rs56129204 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130436999 | AATCCCAGCTACTCA[C/G]GAGGCTAAGGCAGGA | 50807 |
| rs56133915 | snp | C/T | 0.0256215 | 0.110247 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054410 | GGTTGCTGGAGACCA[C/T]TTCTATTTGCAAAGC | 50807 |
| rs56150012 | snp | C/T | 0.229136 | 0.249128 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276760 | CTCTCTCTCTCTCTC[C/T]CCTCTAACAAAAAAG | 50807 |
| rs56162445 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425728 | TTAAAATGCCTACAA[A/G]TTATGTCAGGCACTG | 50807 |
| rs56182202 | snp | C/G | 0.326506 | 0.238006 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066441 | GTCTTGAACTCCTGG[C/G]CTCAAGTGATCCTCC | 50807 |
| rs56184034 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130273202 | CATTTACCAAACAAA[C/T]CAACAGATTTTTTTA | 50807 |
| rs56194038 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359914 | AGGCGTGAGCCACCG[C/T]GCCCGGCCCATCTTG | 50807 |
| rs56207589 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130437123 | AAAAAAAAAAAAAAA[-/A]TTAAAAATTAAAACT | 50807 |
| rs56221838 | in-del | -/TGTGCTGGGCAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130437239 | TCATTTGCTGGGCAC[-/TGTGCTGGGCAC]AAAGGGCCAAGAGGA | 50807 |
| rs56241132 | snp | A/T | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332851 | TTCATTTTATTTTTG[A/T]AAAAAAAATTTTAGA | 50807 |
| rs56256466 | snp | A/G | 0.343477 | 0.231866 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070822 | CTTGAGGGGAGAGAG[A/G]GAGAGAGGGAGAGAG | 50807 |
| rs56262640 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130315017 | AGTAACAACTACTGT[C/T]TGCTCCCGTCACAAT | 50807 |
| rs56265751 | in-del | -/CACA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130420277 | ACACACACACACACA[-/CACA]ATAGCAATAACAAGT | 50807 |
| rs56285703 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246149 | AAAGGAAGCCATTTG[C/T]GGTGAAGGGCCTGCC | 50807 |
| rs56287696 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130426425 | GGAAAAAAAAAAAAA[-/A]GGGTAAGCCAAGCTC | 50807 |
| rs56297697 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263351 | AACTAGAGAAGAGAA[C/T]TTGACAGAGAAGAGA | 50807 |
| rs56308942 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390453 | CAGTCAAGATTTCCC[A/G]GAATCTTCAACTGTA | 50807 |
| rs56312218 | in-del | -/AA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130312293 | AAAAAAAAAAAAAAA[-/AA]GTACCATGCCTAAAA | 50807 |
| rs56313701 | snp | A/G | 0.0569829 | 0.158885 | intron-variant, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130386817 | AAACCTCCACTTTTA[A/G]GTTCATGGCTCAGCC | 50807 |
| rs56318716 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130314901 | GCTTACTCTGAACTT[C/T]TGAACTTTAAGAGAG | 50807 |
| rs56323699 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | ASAP1 | GRCh38.p7 | 8:130398143 | TTTATTGACATATAA[A/G]ATACATACACAAAAT | 50807 |
| rs56336751 | snp | A/T | 0.0744748 | 0.178019 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397753 | GAAGCACATCTGTGT[A/T]ATTTCAGCAGATGAG | 50807 |
| rs56347021 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120365 | TCAAGTCTGAGACCA[C/T]GTGCTAACTATGTGA | 50807 |
| rs56349521 | snp | A/C | 0.276534 | 0.248588 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096672 | TTTACATGTTAGTTT[A/C]GCATCAGCTGTCACA | 50807 |
| rs56349599 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311941 | AATGATTTATTAATT[A/G]TACTCCTTCTAAATG | 50807 |
| rs56350423 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437207 | ATACCTGACTCAGCC[C/T]CCTTGTTCAGTGCCT | 50807 |
| rs56355445 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130106364 | AAATATTTCCCATGC[A/G]AGTCTGAATCATGCA | 50807 |
| rs56382712 | snp | C/G | 0.408163 | 0.193609 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074486 | ACACACACACACACA[C/G]AGAGAGAACGAGAGT | 50807 |
| rs56385215 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390408 | TGCCTGAATGATGTA[C/T]TCATGTGTTTTATAC | 50807 |
| rs56386549 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130273723 | GTCACACTTCGAGGA[A/G]AACAAAGTAGTAGT | 50807 |
| rs56405390 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334293 | AAGCACATCAAATAT[C/G]TTCCTTGGGTAACGG | 50807 |
| rs56406931 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094341 | TCAGCCTCCTGAGTA[A/G]CTGGGACTACAGGCA | 50807 |
| rs56677646 | snp | C/T | 0.408359 | 0.193449 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403224 | ATTCCTTGATATCAT[C/T]AAATATTCACACAGT | 50807 |
| rs56705405 | in-del | -/GT/GTGT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130064934 | TGTGTGTGTGTGTGT[-/GT/GTGT]AAGAATCACAGCTCA | 50807 |
| rs56821632 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130242283 | AAAAAAAAAAAAAAA[-/A]CAACTTTTTTTTTTT | 50807 |
| rs56916572 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066588 | TTTTCTTTCTTTCTT[C/G]TCTCTCTCTCCTTCC | 50807 |
| rs56928931 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223935 | TTATTACACTCCAGT[C/T]ATAAAACCTATCCAA | 50807 |
| rs56996962 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130121812 | AAAAAAAAAAAAAAA[-/A]GAACATACGATCAAT | 50807 |
| rs57005471 | in-del | -/CACA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130074484 | ACACACACACACACA[-/CACA]GAGAGAACGAGAGTA | 50807 |
| rs57047177 | snp | A/G | 0.17654 | 0.238964 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059549 | CAGCCCTGAACTCCT[A/G]GCCTCAAGCGATCCA | 50807 |
| rs57123447 | in-del | -/AA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130174115 | AAAAAAAAAAAAAAA[-/AA]GGCTTAGGAGTCAAA | 50807 |
| rs57129132 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241847 | GCCACTATTCATTAA[A/G]ACTTTCTATTTTAGA | 50807 |
| rs57198371 | snp | A/G | 0.341909 | 0.232492 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273264 | CTTATCTTAAATCTA[A/G]TATGAAGAAAGCCCA | 50807 |
| rs57199666 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387161 | AAGGCTGCTGTTTTT[C/T]TTAAGAGAATCTCAG | 50807 |
| rs57213366 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237821 | GGGGCATAGTCAATA[C/T]ACTTGGCACACTGGA | 50807 |
| rs57275592 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130237181 | GTTATATTTTCCGGA[G/T]AAGTGCAGTCATTCC | 50807 |
| rs57315235 | snp | G/T | 0.0592355 | 0.161582 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397975 | GCACATAAGTAATAA[G/T]CAGTTATCAATACAA | 50807 |
| rs57346252 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | ASAP1 | GRCh38.p7 | 8:130361004 | GCACTGACAACACAC[A/G]GCACTTAGGCTTCAC | 50807 |
| rs57409791 | in-del | -/ACAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130284880 | CACACACACACACAC[-/ACAC]CATACTGAGAGAGAG | 50807 |
| rs57422633 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130124347 | ATAGATGCTCATAGT[C/T]TAGTGGGGCCATTGA | 50807 |
| rs57588294 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130256759 | TATATATATATATAT[A/C]TATATATATATATAT | 50807 |
| rs57616884 | in-del | -/GTATGTCTTTATCAGCAGCGTGAAAACGGACTAATACAG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130072554 | ATTACCCAGTCTCAG[lengthTooLong]CACCCCTTCCCCCAT | 50807 |
| rs57854216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130338941 | GCTGCTGGGCAGACA[A/G]TCAAAATCACAAGAT | 50807 |
| rs57950334 | in-del | -/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099700 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 50807 |
| rs57950877 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130056178 | ATGTCCTATTTTTCA[A/G]AGGAAAGTGAGGCTT | 50807 |
| rs57964550 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130151498 | GGATTTCTGATATCA[A/G]ATGGGTAGCTGGACA | 50807 |
| rs58012382 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133799 | CAGTGAAAGGCACAT[A/G]GCAGTTTCCTTCCTT | 50807 |
| rs58012966 | snp | C/G | 0.227074 | 0.248947 | intron-variant | ASAP1 | GRCh38.p7 | 8:130367553 | TGCCAGGGAGGTAGG[C/G]TCCTTTTCCTCAGCC | 50807 |
| rs58070656 | in-del | -/ATAT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130153358 | TATATATATATATAT[-/ATAT]GTATATATATATATA | 50807 |
| rs58143591 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130279832 | AAAATAGTTAGGGGC[A/G]TCCATAACTAAAGCG | 50807 |
| rs58156082 | in-del | -/AG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070856 | GAGAGAGGGAGAGAG[-/AG]GGAGAGAGGGAGAGA | 50807 |
| rs58245112 | in-del | -/ATATATATATATAT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130256769 | TATATATATATATAT[-/ATATATATATATAT]CCTTATATATATATA | 50807 |
| rs58256601 | in-del | -/AT | 0.478768 | 0.100824 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218848 | TATATATATATATAT[-/AT]GCATATGTATGTATG | 50807 |
| rs58262391 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396688 | AGGGACACGTTTCCC[A/G]TCCATGTGCAGCATG | 50807 |
| rs58327713 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130077564 | TTTTTTTTTTTTTTT[-/T]GAGACACAGTCTTGC | 50807 |
| rs58337166 | in-del | -/AA | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121812 | AAAAAAAAAAAAAAA[-/AA]GAACATACGATCAAT | 50807 |
| rs58367856 | in-del | -/AAAAAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130151406 | AAAAAAAAAAAAAAA[-/AAAAAA]GATTGCTGAAGAAAT | 50807 |
| rs58479009 | in-del | -/CATT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130413917 | ATTCATTCATTCATT[-/CATT]TATGTAACACTCCAA | 50807 |
| rs58498075 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352269 | AATTAATGGGCTCCT[C/T]AAGTTTAGCACCTGC | 50807 |
| rs58664881 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383964 | CTCCTTTCCAGAACT[A/G]GCCACCTGCCCTTCC | 50807 |
| rs58682635 | snp | G/T | 0.0655868 | 0.168795 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258494 | GAGTGTATCCTTCAT[G/T]ACTTTCCAGTTGTTT | 50807 |
| rs58862052 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360831 | TAGTTGACAGAACAT[A/G]GTCTTTTGAAGTATG | 50807 |
| rs58904969 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130194394 | AGCAAAAAAAAAAAA[-/A]TCCTTTCTTGGAGAT | 50807 |
| rs58907739 | in-del | -/C/CGCGC/CGCGCGCGCGC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130072831 | GTGTGTGTGCGCGCG[-/C/CGCGC/CGCGCGCGCGC]GGGGGGGGCAGTTTT | 50807 |
| rs59012190 | snp | A/G | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407742 | TGCCATGCAGGAATC[A/G]GGGACATAAATCATT | 50807 |
| rs59076943 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130072838 | TGCGCGCGGGGGGGG[-/A]GCAGTTTTGGGGACT | 50807 |
| rs59180420 | in-del | -/A | 0.344592 | 0.231414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288323 | CTCACTCCTTAGGGT[-/A]AATTCCATTCTTTTA | 50807 |
| rs59297824 | snp | C/G | 0.322721 | 0.23919 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097009 | CATGCACCTGTAATC[C/G]CAGCTACTTGGGAGG | 50807 |
| rs59375266 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130097172 | AAAAGTCCTTGAAAA[-/A]CTGTATTGTGGACAC | 50807 |
| rs59409193 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130380740 | AATTAATTTAATTTT[A/T]TTAGAGACAGGGTCT | 50807 |
| rs59411017 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325278 | TTCCTTTCTTTCAAC[A/G]TATTCAAAAGCAAAG | 50807 |
| rs59481410 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095817 | AGAGATGGGGTTTCA[C/T]CATGTTGGCCAGGCT | 50807 |
| rs59496740 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258461 | CACCCTTAAGTCCCA[C/T]GGATGTTTTAAAACA | 50807 |
| rs59571800 | in-del | -/T | 0.332106 | 0.236133 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211766 | TCGAACATAATAGAC[-/T]TTTGGTACTTGCTGG | 50807 |
| rs59636682 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130312461 | AGGAGGGGAAAAAAA[C/T]CCCATTAGGAATTCT | 50807 |
| rs59704449 | in-del | -/A | 0.347473 | 0.230215 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139922 | TTAAAAAAAAAAAAA[-/A]CAACAAAAAAACACC | 50807 |
| rs59770171 | in-del | -/AAAAAAAAAAAAAA | 0.224116 | 0.248656 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060076 | GAGCGAGCCCTTCTC[-/AAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 50807 |
| rs59779700 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130097768 | TCTCCTGAGACTCTC[-/T]CCCAGGAACTGACAT | 50807 |
| rs59797913 | in-del | -/A | 0.498734 | 0.0251279 | intron-variant | ASAP1 | GRCh38.p7 | 8:130182832 | AAACTATAAAAAGGC[-/A]AAAAAAAAAAAAAAA | 50807 |
| rs59928989 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130153332 | CAGCACTGCTTTTTA[A/T]ATATATATATATATA | 50807 |
| rs59974738 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436753 | CTGCAGTGTGCTATA[C/T]TTGTGCCACTGCACT | 50807 |
| rs60001112 | snp | A/G | 0.0158469 | 0.0875917 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052782 | ATTTTGAGATCAGTG[A/G]AAAGAGTCTAGGCCA | 50807 |
| rs60097873 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130153329 | GGCCAGCACTGCTTT[A/T]TAAATATATATATAT | 50807 |
| rs60197165 | snp | A/C | 0.359152 | 0.224913 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390091 | GGGCCTGAGAATCTG[A/C]TTTTTAACAGCTCCC | 50807 |
| rs60210673 | in-del | -/AGTA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130270903 | GAAATCTTTCCTGTA[-/AGTA]TTACCTGAGAAGTAG | 50807 |
| rs60211358 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130153359 | TATATATATATATAT[A/G]TATATATATATATAT | 50807 |
| rs60232226 | in-del | -/TGCGTGTGCGCGCGCGCGCGCA/TGTGTGTGTGTGCG/TGTGTGTGTGTGTGTGTGCGCGCGCGCG | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072825 | GTGTGTGTGTGTGTG[lengthTooLong]CGCGCGGGGGGGGGC | 50807 |
| rs60276681 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ASAP1 | GRCh38.p7 | 8:130242810 | ATTGACAATGAAGAA[C/T]TGTCACTGTCTCCTC | 50807 |
| rs60433249 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130114789 | TTTTTTTTTTTTTTT[-/T]AAGATATAGGGTCTT | 50807 |
| rs60441663 | in-del | -/TAAAA/TTAAAA/TTTAAA/TTTTAA | 0.414905 | 0.271442 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403301 | CAAGTGTTTTTTTTT[-/TAAAA/TTAAAA/TTTAAA/TTTTAA]AAAAAACCCAGATCC | 50807 |
| rs60744896 | snp | A/G | 0.162253 | 0.234095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389765 | GAGTGCAGTGGCACA[A/G]TCACGGCTCACTGCG | 50807 |
| rs60755991 | in-del | -/AAAAAAAAAAAAAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130151398 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAA]GATTGCTGAAGAAAT | 50807 |
| rs60763799 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160763 | GTAGGACAATATATT[A/C/T]TCATAAAAAGTATTG | 50807 |
| rs60897674 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153017 | CTCATTACAGCACTG[C/T]TTTTTAATTTTTTTT | 50807 |
| rs60941391 | in-del | -/AT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130256782 | TATATATATATATAT[-/AT]CCTTATATATATATA | 50807 |
| rs61019864 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130055170 | TCTAGAGTCCTTGCT[C/T]TGAACCAGGGCGCCT | 50807 |
| rs61047760 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130099030 | TTTTTTTTTTTTTTT[-/T]GAGACAGTCTCACTC | 50807 |
| rs61123306 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093257 | TTATTCAAAGTGACA[C/T]TGAAGTGGCTGGTGT | 50807 |
| rs61154763 | in-del | -/CT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130161194 | CAAATTGTAGCAGGA[-/CT]TTTTTTTTTTATTTT | 50807 |
| rs61183792 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076744 | CAAGCTGGTCTTGTA[C/T]TCCTGAGCTCGTGGA | 50807 |
| rs61191438 | snp | A/T | 0.00667788 | 0.0573964 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237036 | TATTAGAAGATTTGG[A/T]AAATTAAAAAAATAA | 50807 |
| rs61329743 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ASAP1 | GRCh38.p7 | 8:130182310 | CTCCCAAAGAAAGAA[C/T]TGAAGACAAAAAAGG | 50807 |
| rs61358542 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130185818 | AAGTACAAGGAAGAG[C/T]ACCTGTACCATCTTA | 50807 |
| rs61360310 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236139 | TATAGTCTGCTGCCT[C/T]CCCTTCCAGGTTTTC | 50807 |
| rs61367827 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130256760 | ATATATATATATATA[C/T]ATATATATATATATA | 50807 |
| rs61436058 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130298053 | CCCATGTCTTCATTG[C/G/T]TAAACATGGGTGTTG | 50807 |
| rs61558949 | snp | C/T | 0.259913 | 0.249803 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179387 | TGCGTTGATTAATTC[C/T]AGATGGGGCTCTTCA | 50807 |
| rs61578845 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381134 | CAAGTGATCCACCTG[A/C]CTCAGCCTCCCAAAG | 50807 |
| rs61591724 | in-del | -/AA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130097160 | AAAAAAAAAAAAAAA[-/AA]GTCCTTGAAAACTGT | 50807 |
| rs61632449 | snp | A/T | 0.0700422 | 0.173537 | intron-variant | ASAP1 | GRCh38.p7 | 8:130442493 | GGTTGCAATACAGAT[A/T]ACCCTGGCCTAAAAA | 50807 |
| rs61648269 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130311903 | ACAACTCAAAAAAAA[-/A]TAGTAATTTGAATAC | 50807 |
| rs61663506 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130072832 | TGTGTGTGCGCGCGG[-/C]GGGGGGGCAGTTTTG | 50807 |
| rs61705958 | in-del | -/T/TTT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130143425 | GTTTTTTTTTTTTTT[-/T/TTT]GACATATGTTGGTTC | 50807 |
| rs62517682 | snp | C/G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347155 | CATCCTGGATATCTA[C/G/T]GGAAAGATTATTCAA | 50807 |
| rs62517703 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370849 | AGACTAGGCAAATCT[A/G]TAGAGACAGAAAGCA | 50807 |
| rs62517706 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388666 | AGAAATCCAAGCCGG[C/T]TTGGTGTCATAGAAG | 50807 |
| rs62517707 | snp | A/G | 0.298144 | 0.245321 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395956 | TAGGTGTGAGCCACC[A/G]CGCCTGGCCATATTT | 50807 |
| rs62517732 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405934 | ATACCTGAAGATAAA[C/T]ACTGTTCCTATACTA | 50807 |
| rs62517737 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130413052 | TAACAAACCTAGGCA[A/G]CAGGTATTGCTGTTT | 50807 |
| rs62517738 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417185 | ACAGAAAACAACCCA[C/T]GTACAACTGCACACA | 50807 |
| rs62517739 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417616 | CAAGTCCTGGCTTCA[A/G]GGGAAAAAAAAAAAA | 50807 |
| rs62517740 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418791 | GTTTTTTTTTTTTTA[A/T]TTATTCTTTCTTTTG | 50807 |
| rs62517741 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130426320 | GTACAGCCTGCAGAA[A/C]CATGTGCTGATTAAA | 50807 |
| rs62517742 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130426411 | CTAATACACTGGTTA[A/G]GAAAAAAAAAAAAAG | 50807 |
| rs62517743 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428472 | CCATCATCATCACCA[C/T]CACCACCACCATCTT | 50807 |
| rs62517744 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432136 | GAGGAAAGGAGGAAG[A/T]TGGGGGAACAGAGGC | 50807 |
| rs62517745 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | ASAP1 | GRCh38.p7 | 8:130433782 | ACGTGCCAGGCACTC[A/G]CTTAGCCACTTTCCT | 50807 |
| rs62524622 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130055288 | GGCTTGTGTGATACA[A/T]TTAAAAAAGAAAAAA | 50807 |
| rs62524624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130067329 | CCACAAGGCCTCCTA[A/C]AGCTTTCCTTGTCTC | 50807 |
| rs62524625 | snp | C/T | 0.474634 | 0.109726 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072482 | CTTCTGCCATGATTG[C/T]GAGGCCTCCCCTGCC | 50807 |
| rs62524627 | snp | C/G | 0.341685 | 0.232581 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078899 | GTACATAAGATAGTG[C/G]TATTAAAAAAAAGGC | 50807 |
| rs62524628 | snp | C/G | 0.338523 | 0.233803 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088601 | CCCACAGGGCCTCTG[C/G]AGGGAGCAAAACCCT | 50807 |
| rs62524629 | snp | C/G | 0.340559 | 0.233022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093572 | CTCGGGAGGCTGAGG[C/G]TGGAGAATCGCTTGA | 50807 |
| rs62524632 | snp | C/T | 0.331411 | 0.236373 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100995 | GTCTTTAATTCATCT[C/T]GAGTTGAGAGATACC | 50807 |
| rs62524633 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130108075 | TAGCATCTGGTTCAA[A/T]TTTCTCTGTGGCACC | 50807 |
| rs62524634 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130111017 | GCAACACTTTAATGG[C/T]AGCCTGAGGCGCCAG | 50807 |
| rs62524635 | snp | A/G | 0.330482 | 0.236691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111117 | GTGGCTCAAGCCTGT[A/G]GTCCCAGCACCTTGA | 50807 |
| rs62524639 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130214 | AACCTGTAGAATCTT[A/C]TCACATGCCTCTAAG | 50807 |
| rs62524640 | snp | A/C | 0.489434 | 0.0719116 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132500 | CCTTCCCCTACGTTC[A/C]TGAGCCAGCTCAGCC | 50807 |
| rs62524641 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130133533 | CGGTGGCGGGCGCCT[A/G]TAGTCCCAGCTACTC | 50807 |
| rs62524642 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130133580 | AGAATGGCGTGAACC[C/T]GGGAAGCGGAGCTTG | 50807 |
| rs62524643 | snp | C/G | 0.32885 | 0.23724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130142986 | GAGCTACGTACGGTA[C/G]TGGTGCTGGTGGCCA | 50807 |
| rs62524644 | snp | C/G | 0.323197 | 0.239044 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146985 | AATCCCAGAACTTTG[C/G]GAAGCCGAGGTGGGT | 50807 |
| rs62524645 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152586 | ACCACAGGACAAGAT[A/T]AAACTTTTTTTTTTT | 50807 |
| rs62524646 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130152609 | TTTTTTTTTTTTTTG[G/T]TAAAGGAATATCTAA | 50807 |
| rs62524647 | snp | C/T | 0.318896 | 0.240319 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157454 | ATCATCAGCTCCCAT[C/T]TAGGTTTCTGATGCA | 50807 |
| rs62524648 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130158346 | GGGACCCTGCTTATA[A/T]TTAAAAAAAAAAAAA | 50807 |
| rs62524649 | snp | A/C | 0.330947 | 0.236533 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159425 | CAGAAGATCGAGACC[A/C]ACCTGGCTAACATGG | 50807 |
| rs62524650 | snp | C/G | 0.480064 | 0.0978296 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160933 | GTAAAGATAATACCA[C/G]AAAACACATACACCT | 50807 |
| rs62524651 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130161289 | CGAGGTAAGCTGAAC[A/C]AACCACTGGCTATTT | 50807 |
| rs62525876 | snp | C/T | 0.433963 | 0.169285 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179859 | TGTACTTGTACTGTG[C/T]ACTGGTCAAGATTTT | 50807 |
| rs62525877 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130180053 | AAGGAAGGAAGGGAG[C/G]GAGGGAGGAGAAGGG | 50807 |
| rs62525878 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183168 | GTAAAACCTTTTACA[A/G]AGACAAGACCTTACA | 50807 |
| rs62525879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187996 | AAGAGCATTTTTAAC[A/G]CTGAAAATGTTCAAA | 50807 |
| rs62525880 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130191064 | GTTTTTTTTTTTTTT[C/T]CCACTGCTCTGCGGC | 50807 |
| rs62525881 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191132 | GAGGAATCTACAAAG[G/T]AGAAGGAAATGGAGA | 50807 |
| rs62525882 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130202970 | TAAGGGGTTACCATA[A/C]AGTATAATCTAAAAT | 50807 |
| rs62525883 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203403 | CTCCCCTCACTAACC[A/C]GTGTTTCCCGGTGCT | 50807 |
| rs62525884 | snp | A/G | 0.352504 | 0.228019 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204833 | TCATGTATTACTGCA[A/G]TATATCCTAGCCTAT | 50807 |
| rs62525885 | snp | C/G | 0.333491 | 0.235646 | intron-variant | ASAP1 | GRCh38.p7 | 8:130210335 | AAATAGATTTTTAAA[C/G]TGGGTTTATTTTAAA | 50807 |
| rs62525886 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213952 | GTCTGCCTCCCGGGG[A/C]CAGCACCTCTAGTGT | 50807 |
| rs62525887 | snp | A/C | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218745 | GGTAGATGAAACATG[A/C]AATGTGACGTGAGTG | 50807 |
| rs62525888 | snp | C/T | 0.349233 | 0.229462 | intron-variant | ASAP1 | GRCh38.p7 | 8:130243562 | CCTTCTGCCCTCTCC[C/T]CTCTGTTCCCACACC | 50807 |
| rs62525889 | snp | A/T | 0.349233 | 0.229462 | intron-variant | ASAP1 | GRCh38.p7 | 8:130243679 | ACCTCTCTCCTGAAA[A/T]CTTTTTCTTAAAACT | 50807 |
| rs62525890 | snp | C/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251609 | AAAACCAAGACAAAA[C/G]AACTAAGAGGGAAAA | 50807 |
| rs62525919 | snp | A/G | 0.484209 | 0.0874434 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253413 | TTTGCAGATGCATAC[A/G]CTTTGATTTTTTTCC | 50807 |
| rs62525921 | snp | C/T | 0.341235 | 0.232758 | intron-variant | ASAP1 | GRCh38.p7 | 8:130260502 | AAGCAAAACCTGAAA[C/T]CCTGAGAGGTTCAAT | 50807 |
| rs62525922 | snp | G/T | 0.340108 | 0.233197 | intron-variant | ASAP1 | GRCh38.p7 | 8:130268965 | GGGAGGAGGAGGGAG[G/T]GTGGAGAAGGAACAG | 50807 |
| rs62525923 | snp | C/T | 0.482757 | 0.0912364 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272386 | GGTAACTCTACACAT[C/T]GTTGGTAGGAATCTA | 50807 |
| rs62525925 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130276203 | AAACTCCTAGAGCTT[A/C]GTTCCTCATTTGTTT | 50807 |
| rs62525926 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130276433 | ATTCAAAATTTAGGC[C/T]TTTCTTCTACTGTAG | 50807 |
| rs62525927 | snp | A/G | 0.34146 | 0.23267 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286073 | GGTGTTATCTCCCTC[A/G]ATCCTCACAACAAAT | 50807 |
| rs62525928 | snp | A/T | 0.342358 | 0.232314 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286121 | TTGCTATTTTCTAAA[A/T]GAAGAAAAGAAGGCT | 50807 |
| rs62525929 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296528 | TTTTTTTTTTTTTCC[C/T]ATTTGCTAAGCCCAT | 50807 |
| rs62525930 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301457 | GACTTCTGTAGCATG[C/T]TGTGTTCTCTGCCTT | 50807 |
| rs62525931 | snp | C/G | 0.483563 | 0.0891524 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324529 | GCAAACTGACTTGGG[C/G]AAGTACTTAGAAAAA | 50807 |
| rs66488832 | snp | C/T | 0.26271 | 0.249677 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332778 | ACCTGGAAGAAGCCA[C/T]TAATATGTCAATGAC | 50807 |
| rs66489219 | in-del | -/CT | 0.4021 | 0.198407 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097763 | AGCGATCTCCTGAGA[-/CT]CTCTCCCAGGAACTG | 50807 |
| rs66513387 | snp | A/T | 0.125528 | 0.21681 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133151 | ACTCATTAGAAATAA[A/T]AAAAAAAAAAGTGAA | 50807 |
| rs66587581 | in-del | -/T | 0.47885 | 0.100637 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399815 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTTTCGC | 50807 |
| rs66741015 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130257789 | GACTCAAGAGCACCC[-/G]CCCCCCCATTATTTT | 50807 |
| rs66918676 | in-del | CTGGTGTGTGTGTGTGTGTGTGTG/TTGATA | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072788 | GGCCTGGACTTGCAA[lengthTooLong]TGTGTGTGTGTGTGT | 50807 |
| rs67034951 | in-del | -/GTAA | 0.260227 | 0.249791 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270900 | ACAGAAATCTTTCCT[-/GTAA]GTATTACCTGAGAAG | 50807 |
| rs67062847 | in-del | -/A/AA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130092938 | CTGACGCTTTTCTTA[-/A/AA]AAAAAAAAAAAAAAA | 50807 |
| rs67428925 | in-del | -/TAAC | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119089 | TTTGGTCGTCTGATA[-/TAAC]TCTCTATTTTTTATT | 50807 |
| rs67434056 | snp | A/G | 0.10237 | 0.201756 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105934 | AAAGTACCAGGATTC[A/G]AGAGACTTAGGGCTG | 50807 |
| rs67529812 | in-del | -/CATTCAT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130406263 | TATTCATTCATTCAT[-/CATTCAT]TCATTATTCTTAAAT | 50807 |
| rs67550425 | in-del | -/GTA | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399871 | GCCCAGGCTGGAGTA[-/GTA]CAATGGCGCAATCTT | 50807 |
| rs67554567 | in-del | -/AT/TA | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153333 | GCACTGCTTTTTAAA[-/AT/TA]TATATATATATATAT | 50807 |
| rs71302391 | in-del | -/AAAG | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093694 | AAAAAAAAAAGAAAG[-/AAAG]CTAAGAACACTGCCA | 50807 |
| rs71302392 | in-del | -/TT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130095317 | TTTTTTTTTTTTTTT[-/TT]GAGACGCAGTTTCAC | 50807 |
| rs71302393 | in-del | -/GTATGTATGTATGTATGTAT | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107542 | TATGTATGTATGTAT[-/GTATGTATGTATGTATGTAT]TTTTGAGATAGAGTC | 50807 |
| rs71302395 | in-del | -/TCTG | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119639 | GTCCACGTGATGCTG[-/TCTG]ACAGCCTGGATCCAG | 50807 |
| rs71302398 | in-del | -/AAAAA | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151407 | AAAAAAAAAAAAAAA[-/AAAAA]GATTGCTGAAGAAAT | 50807 |
| rs71302399 | in-del | -/AAT | 0.101658 | 0.201233 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171440 | GGCGGCAGGAGAGAG[-/AAT]AATGCCAGCAGGAGA | 50807 |
| rs71302400 | in-del | -/AC | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188691 | AGCCGAGATCACCAC[-/AC]TGCATTCCAGCCTGA | 50807 |
| rs71302401 | in-del | -/AAAGG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216062 | AAGAAAGAAAAGGAA[-/AAAGG]AAAGGAAAGGGAAAA | 50807 |
| rs71302402 | in-del | -/CACACACA | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217560 | ACACACACACACACA[-/CACACACA]GATCTTTTCCTACCA | 50807 |
| rs71303498 | in-del | -/GCGCGCGCGC/GCGCGCGCGCGCGCGCGCGC | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072824 | TGTGTGTGTGTGTGT[lengthTooLong]GCGCGCGGGGGGGGG | 50807 |
| rs71304303 | in-del | -/AA | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283614 | AAAAAAAAAAAAAAA[-/AA]GAAGGCAGGATGCAG | 50807 |
| rs71304304 | in-del | -/AC | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284879 | CACACACACACACAC[-/AC]CATACTGAGAGAGAG | 50807 |
| rs71304305 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130328627 | TTTTTTTTTTTTTTT[-/T]AAGAGACAAGGTCTC | 50807 |
| rs71304308 | in-del | -/TACACACACACACA | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373111 | ACACAGAAATACATA[-/TACACACACACACA]CACACACACACACAC | 50807 |
| rs71304311 | in-del | -/CACACACA | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130420273 | ACACACACACACACA[-/CACACACA]ATAGCAATAACAAGT | 50807 |
| rs71513089 | in-del | AAA/GAGAG | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262417 | AAAAAAAAAAAAAAA[AAA/GAGAG]AGAGAGAGAGAGAGA | 50807 |
| rs71517932 | in-del | -/AAAAA/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085738 | AGACGTTGTCTTTAA[-/AAAAA/G]AAAAAAAAAAAAAAA | 50807 |
| rs71522563 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055235 | CTTGCTAAGCCTTTT[C/T]TCTGTTAAGTGGGGC | 50807 |
| rs71522564 | snp | G/T | 0.5 | 0 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082667 | ACCCACCATGCCTGG[G/T]TAATTTTAATTTTTA | 50807 |
| rs71522565 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098786 | CATTTCTTTGTGTTG[G/T]GAACATTCAAAATCC | 50807 |
| rs71522566 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098839 | TACACCAAATTACTG[G/T]TAACCACAGTCACTC | 50807 |
| rs71522567 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157921 | ATTGAGTATTTTTTG[G/T]CTCTTTCCTTCCTTA | 50807 |
| rs71522568 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233000 | TATGCAACACCACTG[G/T]TTTACTCATTTAGTC | 50807 |
| rs71522569 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283580 | GAACAAGACTCCATC[A/C]CAGAAAAAAAAAAAA | 50807 |
| rs71522570 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313004 | TTGGCAAATGAAAGC[A/C]ATCATAGCATGCACA | 50807 |
| rs71522571 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376836 | TGAAGCCGGGAGGCA[A/G]AGGTTGCGGTGAGAT | 50807 |
| rs71522572 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382246 | AGCCGAGATTGCGCC[A/C]CTGCACTCCAGCATG | 50807 |
| rs71522573 | snp | A/T | 0.408359 | 0.193449 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402933 | GGGTTTTTTTTTTTT[A/T]AATCTTTTATTACAG | 50807 |
| rs71522574 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424444 | GCACCGCTGATTCAA[A/C]CAGTAACAGCTCTCT | 50807 |
| rs71522575 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424513 | TGTAGGCTCAGCGTT[G/T]GTTTTTGTTTTTTTT | 50807 |
| rs71572314 | in-del | -/T | 0.5 | 0 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082714 | AGGTCTCATTACTAA[-/T]TTTTTTTTTTTTTTT | 50807 |
| rs71572317 | in-del | -/A | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093666 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 50807 |
| rs71572318 | in-del | -/T/TT | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099012 | TCTACTAATATAAGC[-/T/TT]TTTTTTTTTTTTTTT | 50807 |
| rs71572319 | in-del | -/TTTTTT/TTTTTTTT | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101732 | ACCACACCTGGTTAA[-/TTTTTT/TTTTTTTT]TTTTTTTTTTTTTTT | 50807 |
| rs71572320 | in-del | -/CTGT | 0.472429 | 0.114129 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102994 | CCACATCCAGCCTAG[-/CTGT]CTGTTTTTTAAAGAT | 50807 |
| rs71572322 | in-del | -/CTGT | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119636 | AGGGTCCACGTGATG[-/CTGT]CTGACAGCCTGGATC | 50807 |
| rs71572324 | multinucleotide-polymorphism | AA/TT | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123800 | GCCCGGCTAATTTTT[AA/TT]AAAATTTTTAATAGA | 50807 |
| rs71572325 | in-del | -/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131649 | TGAAAATTAGCTGGG[-/C]CGTGGTGATGCGTGC | 50807 |
| rs71572327 | in-del | -/A | 0.181978 | 0.240568 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139759 | AAACAAACAAAAAAC[-/A]AAAAAAAAAAAGAAA | 50807 |
| rs71572329 | in-del | -/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151369 | AGCGAGACTCAGTCT[-/C]CAAAAAAAAAAAAAA | 50807 |
| rs71572330 | in-del | -/A | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155488 | CTCCCACCTCGGCCT[-/A]CCTGAGTAGCTGGGC | 50807 |
| rs71572331 | in-del | -/A | 0.338976 | 0.23363 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158348 | ACCCTGCTTATATTT[-/A]AAAAAAAAAAAAAAA | 50807 |
| rs71572332 | in-del | -/A | 0.0848544 | 0.187688 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180907 | TTTAAAAAAAAAAAA[-/A]TACACTCATGTACAA | 50807 |
| rs71572333 | in-del | -/ACAC/ACACAC/ACACACAC/ACACACACACACACACAC | 0.506173 | 0.262225 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217537 | TGTGTGTATATATGT[lengthTooLong]ACACACACACACACA | 50807 |
| rs71572335 | in-del | -/TAAA | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418543 | ACCTCTGTCTCAAAA[-/TAAA]TAAATAAATAAATAA | 50807 |
| rs71812723 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130400502 | TAGGAAAAAAAAAAA[-/A]GGCCAGGTGGGCACG | 50807 |
| rs71893560 | in-del | -/AAACAAAC | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130230090 | GAGATCCTGTCTCCA[-/AAACAAAC]AAACAAACAAACAAA | 50807 |
| rs71983233 | in-del | -/C | 0.158962 | 0.232835 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437621 | ATTTAGATAGATAGA[-/C]TAACTACAATGAAAT | 50807 |
| rs72267792 | in-del | -/ATTC | 0.434447 | 0.168759 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413886 | CTTCTATTTTGCCAG[-/ATTC]ATTCATTCATTCATT | 50807 |
| rs72722303 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066041 | TATCATAAAGCTTAT[C/T]TACATGAGGAAGCTG | 50807 |
| rs72722310 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | ASAP1 | GRCh38.p7 | 8:130071965 | TATAGTCATCTGTTA[C/T]TATGTTAGGTGTGTC | 50807 |
| rs72722312 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072689 | GTTTCCCTGAGTTCT[C/G]TGAGCTGCTACAGCA | 50807 |
| rs72722314 | snp | C/G | 0.235854 | 0.249599 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074484 | ACACACACACACACA[C/G]ACAGAGAGAACGAGA | 50807 |
| rs72722316 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074815 | GGGACTGCTGGGCAG[C/T]CCCAGATGACCATGT | 50807 |
| rs72722318 | snp | G/T | 0.0648419 | 0.167978 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084911 | AAGCAGTAAACCAAT[G/T]TTTGGTATAGTTTTT | 50807 |
| rs72722323 | snp | A/C | 0.0637235 | 0.166737 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096834 | ATCCATGATCAGAAA[A/C]AGTCCTTGAGGCCGG | 50807 |
| rs72722325 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097689 | CCACGGGCAGTTTTC[A/G]GGCCAAAGCTCTTGT | 50807 |
| rs72722330 | snp | C/T | 0.33875 | 0.233717 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100203 | CTTTTTGATGATAGC[C/T]ATTTTAACTGGAAAT | 50807 |
| rs72722339 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111565 | AGATGATTACAAAAG[A/G]AGTACTAGGCGTAGA | 50807 |
| rs72722340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112380 | CCCTTCATGTGTACA[A/G]AGGGCCTCCGCAGGG | 50807 |
| rs72722344 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120336 | CAGCAGACTTAAAAA[C/T]TAAATCGCTCGATTC | 50807 |
| rs72722347 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123411 | TCTCTTACTCATCAC[A/G]ATATGCCATGTTTTT | 50807 |
| rs72722349 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124779 | TATTGCATGGCAAAC[A/G]TTTAGGATTTGGACT | 50807 |
| rs72722353 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132812 | TTTCCTTTGTCTTTC[C/T]ACCTTCTCTCTCAGT | 50807 |
| rs72722355 | snp | A/T | 0.0629771 | 0.165899 | intron-variant | ASAP1 | GRCh38.p7 | 8:130147687 | GCACATACAATAAGA[A/T]CCTGAATGGGCATTT | 50807 |
| rs72722357 | snp | C/T | 0.164546 | 0.234942 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149593 | TTTGATAAGAACAAT[C/T]TGCAAAGGTGACACT | 50807 |
| rs72722358 | snp | A/T | 0.00217434 | 0.0329005 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169104 | ATTTACCACCAGTAT[A/T]AAAAAAAAAGAGTAT | 50807 |
| rs72722360 | snp | G/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170892 | CCTGGCTCATTTTTA[G/T]TTTTGTAAAGATAAG | 50807 |
| rs72722361 | snp | G/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130172285 | GTATTTCATTTTCAC[G/T]TTTAACATAAAGGGA | 50807 |
| rs72722363 | snp | A/T | 0.0479149 | 0.147179 | intron-variant | ASAP1 | GRCh38.p7 | 8:130174269 | AGCATCAGATGAGCT[A/T]CTACAGATAAAAGTG | 50807 |
| rs72722365 | snp | A/G | 0.460589 | 0.13473 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178668 | GCCAAGGTGGATCGC[A/G]AGGTCAGGAGATCAA | 50807 |
| rs72722366 | snp | A/G | 0.34101 | 0.232846 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178702 | CATCCTGGCCAACAC[A/G]GTGAGACCCAGTCTC | 50807 |
| rs72722367 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180977 | ATGGATTTGGGGTGA[C/T]GATGTGTCTATGTAG | 50807 |
| rs72722368 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130184436 | AAGAGGGGCAGGCAG[A/G]AGGCCACTGTGTTTC | 50807 |
| rs72722370 | snp | C/G | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130186601 | CCTAATCCCTAACAA[C/G]AACTCCACGAGGTTG | 50807 |
| rs72722371 | snp | G/T | 0.34101 | 0.232846 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187170 | AGTTAAGTTTTTTTT[G/T]TTGTTGTCCAAAATT | 50807 |
| rs72722372 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130192520 | GTCCTCAATTTCATT[C/G]TTGGAGTACAATTCC | 50807 |
| rs72722374 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130192747 | TGTCTCCCCAGCCTG[A/G]TTGCCAGTTTGAGAG | 50807 |
| rs72722375 | snp | C/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130194455 | TATTTTAGGTGATTA[C/T]TGTGCCACGAAGATG | 50807 |
| rs72722379 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130202746 | GAATCTGCCTCAGGT[A/G]ACCTAGCTTGGGAGG | 50807 |
| rs72722380 | snp | A/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130207064 | CCACTTAGAAACAGC[A/T]AAAACTCAAGAGCAT | 50807 |
| rs72722381 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208022 | ATGTAACAATGTATA[C/T]TAAACACTTTCCCCT | 50807 |
| rs72722384 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215920 | TAGAATGAGACCCTA[C/T]CTCCAAAAAAAAAGA | 50807 |
| rs72722386 | snp | G/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218355 | TTCAAGTGAAAAATA[G/T]AATTAGTTAATCGAA | 50807 |
| rs72722388 | snp | A/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223827 | TTCTCCTTCTGTGTC[A/T]AGAGTCCAGAGGAAC | 50807 |
| rs72722389 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224098 | CATACTTTGTTATAC[C/G]CCCAGTTCCCAGTGC | 50807 |
| rs72722392 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130225216 | CAAATATTTCTTCCA[C/T]TTGTCTTGTAACTTG | 50807 |
| rs72722393 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226076 | AGAGATGGGGCCCTA[C/T]TATGCTGCCCAGGCT | 50807 |
| rs72722394 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229056 | ACAGACAAACTAGCC[A/G]AGCAAAGTCATCCTC | 50807 |
| rs72722396 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130231777 | CATGCTTCCATTTCT[A/G]AAAGTGCAGTATGTC | 50807 |
| rs72722397 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130231799 | CAGTATGTCTCACTG[C/T]GTTTTTTAAACAATA | 50807 |
| rs72722399 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233677 | AGCTTTCTTTTATAG[C/T]GCTTCCTAGTTTCTA | 50807 |
| rs72724403 | snp | C/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246245 | GAGATGAGTGAAGTA[C/T]GGGCCTCCTATCATA | 50807 |
| rs72724407 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130250620 | GATCTGGTCATTGTG[C/G]GTTTTGTTTTGTTTT | 50807 |
| rs72724409 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130254523 | CAAAGAAAAAGTACT[C/G]ATAAAAAAGTTTTAC | 50807 |
| rs72724410 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130254534 | TACTGATAAAAAAGT[C/T]TTACCCCAAAATTGC | 50807 |
| rs72724412 | snp | C/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257816 | TTTTTTAGAAGTGCC[C/T]ACTAATCTCAGAAGT | 50807 |
| rs72724414 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258824 | AAATAGATAACATAC[A/G]TGGTGGTTGACTGAT | 50807 |
| rs72724419 | snp | A/G | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130266357 | ACATTCAGGGATGAG[A/G]GGAATCATATCAGTG | 50807 |
| rs72724420 | snp | C/G | 0.335788 | 0.23482 | intron-variant | ASAP1 | GRCh38.p7 | 8:130267050 | CCCCTCAAAAAAAAA[C/G]TAGTCATTAAGAGGA | 50807 |
| rs72724421 | snp | C/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130271432 | AATTATATATACCTT[C/T]TACATAGTTTTGATA | 50807 |
| rs72724423 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275134 | ACAAGAATGAAATGA[A/G]AGCATATACAAAGCT | 50807 |
| rs72724426 | snp | C/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285271 | GAACTTTCAGAAACA[C/T]ACACAAATAAAAATG | 50807 |
| rs72724429 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286294 | CCTGCTGCAAAATGA[A/G]CTTACAAAGTTATTC | 50807 |
| rs72724432 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316049 | GGCTAGGAGAGAAAA[G/T]CACTTCCGTCTTTTC | 50807 |
| rs72724433 | snp | C/T | 0.333491 | 0.235646 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318474 | AGCACTACTATGTGC[C/T]AGATACCATACCAGA | 50807 |
| rs72724437 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323540 | GTGACCACATTTCCA[G/T]TGCCATCTGCAGAAG | 50807 |
| rs72724440 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ASAP1 | GRCh38.p7 | 8:130326396 | TAAAACATCAGTGCT[A/G]CAATAGGATCCCCAA | 50807 |
| rs72724446 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | ASAP1 | GRCh38.p7 | 8:130329042 | AATGGTTCCACTGAA[A/G]CCTTTGTTCCCCAGA | 50807 |
| rs72724447 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333053 | TTCATATGGAAATTC[G/T]GTTTGGAGGCGAAAC | 50807 |
| rs72724449 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333069 | GTTTGGAGGCGAAAC[C/T]GTGTCATGCTCTATT | 50807 |
| rs72724450 | snp | A/C | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333179 | TTTCCTAAGCACCCC[A/C]AACCCTAGTCCAAAT | 50807 |
| rs72724451 | snp | A/C | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130345090 | TTTTAACTTTTTGAG[A/C]CCGTTTCCTCATCTG | 50807 |
| rs72724452 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130346000 | CTGCTCTATGCAATT[A/G]GTAGGCATATATATA | 50807 |
| rs72724453 | snp | A/C | 0.0456336 | 0.143994 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348501 | CTGACCACAAACAGC[A/C]CCATGACAGAGGGCT | 50807 |
| rs72724454 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349599 | TACAATTAACCTTGG[C/G]AAGAGAATTTCACCC | 50807 |
| rs72724455 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350404 | ATGAGGACTAAACTA[C/G]ATCTGGTGGGTCCCA | 50807 |
| rs72724457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353159 | AAAGAGTTTTAGCCT[C/T]ATTTCTTTATTTCTT | 50807 |
| rs72724460 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366624 | GGGCTAAGAGTGTGC[G/T]ATCTGGATTCAGATT | 50807 |
| rs72724461 | snp | A/C | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130371421 | ACCTGCTATGTAGTC[A/C]CCGTTTCTTCACTAA | 50807 |
| rs72724466 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384417 | TCTTACTCAGAGAAC[C/T]CCACTGCTGGGCAGG | 50807 |
| rs72724470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389103 | TTAAATGCTCTGTGA[A/G]CATTAGCTATTAGTA | 50807 |
| rs72724472 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389121 | TTAGCTATTAGTATT[A/G]TTGTTGCTGCTGTTG | 50807 |
| rs72724473 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389253 | TGCCTAGCACCACCC[A/C]GTAAGCTCTAGGGTG | 50807 |
| rs72724475 | snp | C/T | 0.110872 | 0.20771 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390342 | TCATAGAAAGTTCTA[C/T]TGGAAAGTCTACAAG | 50807 |
| rs72724476 | snp | A/T | 0.110519 | 0.207473 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390541 | ATTACCTGTTAGATA[A/T]CTATTTCCCCTGACA | 50807 |
| rs72724478 | snp | C/T | 0.160938 | 0.233598 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391051 | TTCATCCACGGATGA[C/T]TGGATAAACAAAATA | 50807 |
| rs72724483 | snp | C/T | 0.110519 | 0.207473 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391778 | TATTCTTAGATAGCA[C/T]ATTATACCTTTTTAG | 50807 |
| rs72724485 | snp | C/G | 0.162253 | 0.234095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392989 | TGGCACCGAGGCACA[C/G]AGAAATTAAGTCACT | 50807 |
| rs72724487 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393287 | TGTTCTGATGGTGAA[C/T]AGTGCTAAACAGTGA | 50807 |
| rs72724488 | snp | A/G | 0.117188 | 0.211804 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393288 | GTTCTGATGGTGAAC[A/G]GTGCTAAACAGTGAG | 50807 |
| rs72724490 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395143 | CCTGGCAAGAAATCT[A/G]GAAGCACTCACTCAG | 50807 |
| rs72724491 | snp | C/T | 0.128976 | 0.218754 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395277 | GTGGGCGCTTTCTAA[C/T]ATTACATACGTTTGA | 50807 |
| rs72724494 | snp | A/G | 0.324855 | 0.23853 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395296 | ACATACGTTTGACAC[A/G]TCCTCTTGCAAAAAG | 50807 |
| rs72724496 | snp | C/T | 0.128976 | 0.218754 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397477 | AGGTCCCTGTATACA[C/T]GTCTTCATAAGTGAA | 50807 |
| rs72724497 | snp | C/T | 0.128976 | 0.218754 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397506 | AAGTCTCTGCTCCTG[C/T]GATTCCCTTGTCTTC | 50807 |
| rs72724502 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405301 | ATAACTCACAAGATA[C/T]GAAATAACGTGTCCA | 50807 |
| rs72726203 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408517 | TGGTTTTTAGACCTT[C/T]GGGCTAGGACTGAAT | 50807 |
| rs72726204 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130412070 | GCCCCTTTCAATCAC[A/G]CTGAGTCTTCACCCA | 50807 |
| rs72726205 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414770 | AACTCTTTTTTTTTT[C/T]TTTTTGAGACAGGGT | 50807 |
| rs72726213 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130419955 | CACCACCTTCTTCTT[C/T]TTTTTTTTTTTTTTA | 50807 |
| rs72726214 | snp | C/T | 0.211212 | 0.246973 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421044 | GCAGGCAGGCTCTGT[C/T]ACCAGCTTGTTGGAC | 50807 |
| rs72726216 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422091 | GCTGGTCAGGAACGG[C/T]CTCCTGGAAGAGGGG | 50807 |
| rs72726217 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422899 | GATAAAGATGGATCC[A/G]GAAACAACCTCAAAT | 50807 |
| rs72726218 | snp | A/T | 0.303187 | 0.244277 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424341 | ATTGGTCTGACGGCC[A/T]AGCCCCCACTCTCCT | 50807 |
| rs72726219 | snp | C/G | 0.132066 | 0.220435 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424509 | ACCTTGTAGGCTCAG[C/G]GTTTGTTTTTGTTTT | 50807 |
| rs72726220 | snp | A/C | 0.0744748 | 0.178019 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428128 | GGGATTCCCTTTTCC[A/C]ACACAGTCATGCAGT | 50807 |
| rs72726221 | snp | C/T | 0.127599 | 0.217986 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130429605 | GTTTCTGGTGTATGA[C/T]TACCCTCTGTAGACT | 50807 |
| rs72726223 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430815 | GTGACAGGCGTGAAG[A/G]GAGTCTTCTCTCTTC | 50807 |
| rs72726224 | snp | C/T | 0.404035 | 0.196909 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432421 | TTTTGGAAGAGAATT[C/T]AAACAGGGTGGTTGG | 50807 |
| rs72726225 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434185 | ACTGTGCCTGGTGGC[A/G]CACACCTGTGGCCCC | 50807 |
| rs72726226 | snp | G/T | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435784 | AGAAATGGCAAGAAA[G/T]CAGGATCTGAGTAAG | 50807 |
| rs72726227 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437389 | CATCTACGAGACCCT[C/T]GTGCTGGCTGCTTTT | 50807 |
| rs72726229 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438395 | CTGACCTCTCCTGGG[A/G]CCAATGGCCTGCTCT | 50807 |
| rs72726230 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438744 | CTCAACTCCAACTCT[C/T]CACGGAGGCCTGGCA | 50807 |
| rs72726231 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439749 | CCCCGCAGGGGGAAG[A/G]ACGTAAGCAGACACT | 50807 |
| rs72726232 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130441192 | ACTGGCACCTCCCAC[A/T]GGGAAGCCACTTAGC | 50807 |
| rs72726233 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ASAP1 | GRCh38.p7 | 8:130442983 | TGCTTTAGGCAAGTG[A/G]CCTGGGGCCTGCCAA | 50807 |
| rs72726234 | snp | A/T | 0.0444908 | 0.142359 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444823 | AGGTCGGGCAGCCAA[A/T]GAGTGATTCATTGTG | 50807 |
| rs73405551 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058612 | GTCTATGCAGTTCCT[A/G]AAACAGTTTTAATTT | 50807 |
| rs73405557 | snp | A/C/T | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063640 | TTCCTAAGAGCCCCG[A/C/T]GATGTGGATATCACC | 50807 |
| rs73405561 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066093 | ATTACACCATATTGT[A/G]ATACAATCGTGGTAC | 50807 |
| rs73405562 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068103 | TCAGTTACTAAAGGT[A/G]AAAGTTACCAGTGGA | 50807 |
| rs73405563 | snp | C/G | 0.191147 | 0.242974 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068541 | ATTTAGGGGCAGTAT[C/G]TTTGGTTTTAAACAC | 50807 |
| rs73405564 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068607 | CCACAGCTCACTATT[A/G]AACAACTGCATATGG | 50807 |
| rs73405567 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076880 | TTTGCCTGGCTGAGG[A/C]GGCACAGTAAAAGGA | 50807 |
| rs73405575 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084150 | AATAGTCCCTGCTAG[A/C/T]GAAAGACAGGACTGA | 50807 |
| rs73405584 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102347 | TTTTCTGCATCCATT[C/T]AGGTCATCATATGGC | 50807 |
| rs73405594 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117178 | ACAGGCAGTATTTAT[C/T]TAGAGTGCCAGGTCC | 50807 |
| rs73409308 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262801 | TTACTTCAGCAGAAG[C/T]ATAAACACAAAAGCC | 50807 |
| rs73409310 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264341 | TATAGGATCCTGTGG[G/T]CACCAGCACTCTGTC | 50807 |
| rs73409312 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130265443 | CAGGGTGTGGTGGTA[C/T]ACACCTACAGTCCCA | 50807 |
| rs73409315 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274830 | ACCACCAGTACAGGA[C/T]TGGATTGGCTCTTAG | 50807 |
| rs73409327 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ASAP1 | GRCh38.p7 | 8:130291045 | ATACCATTTCAGGAA[C/T]CCAGTTATCTTGACT | 50807 |
| rs73409328 | snp | C/T | 0.0678174 | 0.1712 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295896 | ATAGGAGCTGCGCTA[C/T]ATTAAAAAGGAAACA | 50807 |
| rs73409330 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130302156 | CATACATTCTCTCAT[A/T]TGCACAAATATTTGA | 50807 |
| rs73409341 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311072 | GCCATTCTATGAGAA[C/T]GCAGTCCAGGGCAGG | 50807 |
| rs73409344 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130312758 | GTTCAACCACTGTAG[C/T]AACAAAGCCTAGCAC | 50807 |
| rs73409347 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314183 | TCCCCCCACTTACAC[C/T]CCACATATTAATTCT | 50807 |
| rs73409350 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130315614 | TGCTTCCCAGCTGTG[C/T]TCCCATGAGGTGTCT | 50807 |
| rs73409351 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316423 | CTGATGTGCTGCCCC[A/G]ACATCCATTCTCCCC | 50807 |
| rs73409355 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317062 | TTGAGACTCATTCCT[A/G]TTTTGCTTTTAGTTT | 50807 |
| rs73409364 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322113 | TGTTAAGAAAAATCA[C/G]CTGGGGAGAAGACAA | 50807 |
| rs73409369 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330029 | GAGACAGTTGTAATC[G/T]AATTCCTCAATTTGT | 50807 |
| rs73416002 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130331066 | AAAAAGGGAATAAGA[C/T]TACTTCCCAAGCAGA | 50807 |
| rs73417906 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130331474 | TGTTAAGTAAAGCAA[A/G]TCACACAGTTGCTTA | 50807 |
| rs73417909 | snp | C/T | 0.413416 | 0.189196 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332643 | CTGGATTTTTTCCCT[C/T]TTCTGAATGGCTGAA | 50807 |
| rs73417927 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341374 | ATCAGTTGTGGGATC[C/T]TGGGTAAGAACTGCA | 50807 |
| rs73417932 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342045 | CCTTTGAGTGAAACA[C/T]GGGAGAGATTTCCTT | 50807 |
| rs73417935 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130345267 | ATAAAGAAAAATCTG[A/C]GAGGTCAATACTTTT | 50807 |
| rs73417936 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130346318 | AAGAAAAAAATCCTA[C/T]TTCCATGGCCATCCG | 50807 |
| rs73417940 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350483 | CAATCACCTCAATGA[C/G]GTAACACTTTGCTTT | 50807 |
| rs73417948 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355570 | TAAAGTTTCCAAATA[C/T]CTCAGTTGTGAAGCA | 50807 |
| rs73417951 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356140 | CAACAGCAACTGCAT[A/G]TAATTTAACATTAAC | 50807 |
| rs73423598 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364385 | CAACCTCACTTAATA[C/T]TTGCAGCAACAATAT | 50807 |
| rs73425361 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122672 | GAAGTGGCAGAGCTA[C/T]GATATGAACTCCAGC | 50807 |
| rs73425364 | snp | G/T | 0.159951 | 0.233219 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128483 | GGATGAGAAAGAAAT[G/T]ATGAGAAATGGAGAG | 50807 |
| rs73425373 | snp | A/G | 0.349671 | 0.229272 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130782 | ACCACCATAGTGCAC[A/G]TATGTAGTCCCAGCT | 50807 |
| rs73425381 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133905 | AAAAACTGAGCAAAG[A/G]CCCCTCCTGAGGGCA | 50807 |
| rs73425387 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ASAP1 | GRCh38.p7 | 8:130142690 | GGAATATGGACAAAC[C/T]GGGAAGTGTGATAAG | 50807 |
| rs73425394 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158589 | TGTGAAGCAGAATCA[C/T]TTGTTTAAGCAACAG | 50807 |
| rs73425514 | snp | A/C/G | 0.0134912 | 0.0810629 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379762 | GCTGAGACACTCCCC[A/C/G]GGCCCTACTGCCACA | 50807 |
| rs73425525 | snp | C/T | 0.162909 | 0.23434 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384072 | GAAGCCAGAGTCCTG[C/T]AGGATTAAATGTGCT | 50807 |
| rs73425534 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389441 | GTGCCTGTTGGTCTG[C/T]AATTGGTTCTGGCAT | 50807 |
| rs73425588 | snp | C/G | 0.0410537 | 0.137264 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404794 | TGGATCACTGACTTG[C/G]TGTAGCCAATGGAAT | 50807 |
| rs73425591 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404926 | CCTTTTAGTCTGAAC[C/T]CAGATCAAAGACATG | 50807 |
| rs73425601 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408252 | ACAGCATTTCTGGTT[G/T]TGTCTGTGAGGGTGT | 50807 |
| rs73427307 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197476 | AGAAAAGAACTGACA[A/C/G]CAATGAAGCTCCACT | 50807 |
| rs73427311 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208255 | TAGGCCACAGACTTT[A/C]CTAGAATTCCCCCCA | 50807 |
| rs73427312 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130210807 | CTATCTCTAAAATGG[A/G]ATATGACTGATAGCT | 50807 |
| rs73427313 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211838 | AGCACCTTCTCTTTA[A/G]TTTCTACTGTATCAG | 50807 |
| rs73427316 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211932 | AGTATGGGTTCCCAC[A/G]GGGGTACTCCTGAGC | 50807 |
| rs73427318 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213414 | TAATGGAGTGTAGAA[A/G]GGTAGTTTTCATTTT | 50807 |
| rs73427320 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219624 | GTGCTAGAAGACTTT[C/T]GGGCACATAGTACAG | 50807 |
| rs73427321 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ASAP1 | GRCh38.p7 | 8:130221158 | AGGCTTGCTGGAGCC[C/T]GGGAAGTTGAGGCTG | 50807 |
| rs73427323 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224703 | AATTATTTTAACTGG[G/T]ATATGTTCCATAATA | 50807 |
| rs73427327 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227822 | CAGATAACGTGTGTC[A/G]TCGTTCTGAGGCTTA | 50807 |
| rs73427331 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228941 | GTGTTCCAGTCCCCC[C/T]AGCACCCATACAGCT | 50807 |
| rs73427332 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130230744 | AAAGATTTTTTAAAA[A/G]ATCTGGCTATCCACA | 50807 |
| rs73427335 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240116 | AAAGATTTCAGCCAT[A/C]ACATTTTTTGAGACC | 50807 |
| rs73427346 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245008 | AATCATCCTGTGTAA[C/G]AACACCCACAGTTAG | 50807 |
| rs73427351 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247854 | TGGACTTCACAAATT[A/G]AAAACTAGTCTTGAC | 50807 |
| rs73427356 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251914 | AGAAATGGCCACAAA[C/T]CATACAGAAGACAAA | 50807 |
| rs73427358 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252628 | TGTCTGGGGCCCAAA[A/C]GAAAACTGTAATCAC | 50807 |
| rs73427361 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130255607 | ACTGATTATAAAAGC[C/T]TAATTTTCAGGATGA | 50807 |
| rs73427362 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130255650 | AAAAAGTTGCTTTTA[C/T]GAAAAATAATTTTAA | 50807 |
| rs73427414 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130412131 | TGTCATCCCACTTTA[C/T]AGAGGAAACAACAGC | 50807 |
| rs73427418 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130416979 | AAATAAAGGCCATAG[A/C]TCCCAGTACACACAT | 50807 |
| rs73427421 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419038 | GGCCTGAGCCGAACA[C/T]GGCACATCAGGCCCT | 50807 |
| rs73427426 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424508 | TACCTTGTAGGCTCA[A/G]CGTTTGTTTTTGTTT | 50807 |
| rs73427428 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130429143 | TTTCCTTTATAAGGA[C/G]ACCAGTCATTTTGGA | 50807 |
| rs73427429 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130429591 | ACAGAAGCAGCGTTG[C/T]TTCTGGTGTATGATT | 50807 |
| rs73427430 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430747 | GCAGACACTGGGAAG[A/G]TGTATTCAGAATTGG | 50807 |
| rs73427432 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431337 | AGCCTTCAGTGGTTC[C/T]TCAGCGGCTTCAAGA | 50807 |
| rs73427436 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436120 | TTTAAAATGAAGATA[G/T]AAAACACAAAACAGA | 50807 |
| rs73427438 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438694 | GAAAGTGAACAATCG[A/G]GCCGACAGCTGAAGA | 50807 |
| rs73711126 | snp | A/G | 0.00953873 | 0.0683987 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445495 | AGACCATCGATAAAC[A/G]CGTGTTGAATAAATG | 50807 |
| rs73711203 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307452 | CTAAGCCACGCCAAG[C/T]AGACTAGGGATGGTT | 50807 |
| rs73711204 | snp | G/T | 0.0482946 | 0.147699 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313739 | TTATGAATTTTTATC[G/T]CAGACATGATCCACA | 50807 |
| rs73711223 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343275 | AGTCACTACTAAGGC[A/G]GATACGGGCTGATAA | 50807 |
| rs73711686 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372668 | CCACAGTTTTTTTCT[A/G]TAGCTTGATATATCT | 50807 |
| rs73711687 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381636 | GAAAAGAATCACTAC[A/G]GTGGCTTCTCAAGGC | 50807 |
| rs73711692 | snp | C/T | 0.140919 | 0.224948 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400251 | CCAACAGGTCAACCC[C/T]GTGCCAGTCAGTCTG | 50807 |
| rs73711697 | snp | C/T | 0.142609 | 0.225759 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410121 | TCTTCTGGGAAAATG[C/T]ATCTATTCATCCACT | 50807 |
| rs73711700 | snp | C/G | 0.095934 | 0.196885 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417977 | TCACTGGACTAGCCA[C/G]GTATTGCTTATGTGC | 50807 |
| rs73711702 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130427606 | AGGCTCAGAAAAAAG[C/G]TGCCGAAGGTCACCA | 50807 |
| rs73712869 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064409 | AAGGCCTGAACACCT[A/G]GAAGAATGACACTGC | 50807 |
| rs73712873 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104094 | GCATGATCTGTACTG[A/T]CTCCACAGCTCTCCT | 50807 |
| rs73712874 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110458 | GAGAATCTCTGCTCT[C/T]TGTCAGACTGCTACC | 50807 |
| rs73712879 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119308 | TCACTGAAGCAACTC[C/T]CCCAGGCCAGGCATT | 50807 |
| rs73712881 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148293 | GTCCAGCTATTTACA[A/G]ACTTCATGACCCTGA | 50807 |
| rs73712882 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165577 | TGGAAATTCTTGTAA[A/G]TCACAGTCAGAGGCC | 50807 |
| rs73712888 | snp | A/C | 0.384401 | 0.210799 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205401 | AAAAAAAAAAAAAAA[A/C]AAAAACCATATTCAA | 50807 |
| rs73712892 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240722 | TAAAGTTGTGCCATA[C/T]GGCATTATTACATTC | 50807 |
| rs73712895 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261834 | AAGGGATCTCCCTCC[C/T]TCCCTATGTTAGTTT | 50807 |
| rs73712897 | snp | C/T | 0.089084 | 0.191327 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292055 | ACTGAGAACTGAACT[C/T]GAAACTGAAGAATTT | 50807 |
| rs73713903 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431294 | TCACCTTTCCAACAG[A/G]CAAGTATCACATGAC | 50807 |
| rs73713904 | snp | G/T | 0.0966517 | 0.197444 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431333 | CTTAAGCCTTCAGTG[G/T]TTCCTCAGCGGCTTC | 50807 |
| rs73713905 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431370 | AAGTTCAAGCTCCAG[A/G]ATATGGCTCCTGCCT | 50807 |
| rs73713907 | snp | C/T | 0.404907 | 0.196224 | intron-variant | ASAP1 | GRCh38.p7 | 8:130433804 | CACTTTCCTTATATA[C/T]TGCTTTATTTGACAC | 50807 |
| rs74275833 | in-del | -/CCCTTCTCCCTGGAAG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130393348 | AATGGGCCAGGGAAG[-/CCCTTCTCCCTGGAAG]GTATTAAAAGTCTTG | 50807 |
| rs74305974 | snp | C/T | 0.244776 | 0.249945 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132877 | TCTTTTCTACCCATG[C/T]TCTCTTCTCTTTCTG | 50807 |
| rs74313933 | in-del | -/T | 0.241053 | 0.24984 | intron-variant | ASAP1 | GRCh38.p7 | 8:130210285 | GCCACCCTTCTAATG[-/T]TTTTTGGTTTGAGAA | 50807 |
| rs74318043 | snp | C/T | 0.283947 | 0.247685 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397432 | AGGCATGAGCCACCA[C/T]GCCCAGCCCGTATAT | 50807 |
| rs74333529 | snp | A/G | 0.257176 | 0.249897 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424973 | ACTCCAGCCTGGGTG[A/G]CAGAGCGAGATTCCG | 50807 |
| rs74333994 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077068 | AAATGGAAGGGAATG[A/G]GGGTGTTGGCGGCTG | 50807 |
| rs74348737 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444280 | ATATGGCCTTTTTTC[C/T]ACTCATGTTACCTTG | 50807 |
| rs74370122 | snp | C/T | 0.0688196 | 0.17226 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130152754 | GGCATGTGAGATGGT[C/T]AGAATCCCATTCTTG | 50807 |
| rs74388018 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130361565 | CCCCCATCTCCTTTG[A/G]CCAAGAAAGGAATAT | 50807 |
| rs74393271 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408112 | GAAGCTCTCTCAAAC[C/T]TTCCCAGCCCAGTAA | 50807 |
| rs74394409 | snp | C/T | 0.236144 | 0.249616 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205257 | CACGTACACATATCG[C/T]GTGCATACACCCTTT | 50807 |
| rs74403851 | snp | C/T | 0.244205 | 0.249933 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208077 | TGATAGGTTATACTT[C/T]TATTTAAACTTATTT | 50807 |
| rs74410977 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130282084 | GAAAAAAAAAAAAAA[A/G]GGAATGGCATGGCAA | 50807 |
| rs74415308 | snp | A/C | 0.0138852 | 0.0822049 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340073 | TAAACAGATGAATAA[A/C]TAAGTCCTGTCCTCA | 50807 |
| rs74415666 | snp | A/C | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130182831 | GAAACTATAAAAAGG[A/C]AAAAAAAAAAAAAAA | 50807 |
| rs74450783 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223905 | ATCTTCCAGAGGATA[A/G]CTGGGATACACGCAT | 50807 |
| rs74458069 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377328 | ACAAATCACCACTAA[A/G]TACCTTATTCAAGTA | 50807 |
| rs74484327 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117307 | GATAAAAAACCCTGA[A/G]GCGCAGAGAGGCTGA | 50807 |
| rs74488461 | snp | C/G | 0.0637235 | 0.166737 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149282 | CACAATATTACTACT[C/G]TTATAGCAAATTCAG | 50807 |
| rs74494628 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356432 | TGTATCAACATGTTT[C/G]AATTTATTACAATTA | 50807 |
| rs74495335 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380501 | AGGGGACCCAGGGGG[A/T]GCACCAATGTGGTGC | 50807 |
| rs74499527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070804 | CTCAAGGAGGAGATA[C/T]TCCTTGAGGGGAGAG | 50807 |
| rs74514929 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130061781 | CTATGTTTAGGAAAG[A/C]TCCAAATCAGTTCTT | 50807 |
| rs74519642 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130347241 | CATACCCTATGTGGA[A/G]TGTTGATTTTTCCTG | 50807 |
| rs74523877 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | ASAP1 | GRCh38.p7 | 8:130135725 | TGTAACAGATGCTCT[A/G]TAACTGCCAACTATT | 50807 |
| rs74531144 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080106 | AAGCCAAAACGGCAT[A/G]CATTTCTGGCCTAAG | 50807 |
| rs74532806 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ASAP1 | GRCh38.p7 | 8:130357323 | GCACCGGCCTCCGAT[C/T]TCCTTGTCCAGCCTC | 50807 |
| rs74533138 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074642 | TCTGTCCCCGAGGGG[A/G]TGGGAGGGTACAAGG | 50807 |
| rs74535866 | in-del | -/CAAAAGAAAAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130197445 | CAGAACAGACTGTCT[-/CAAAAGAAAAA]AGAAAAGAAAAGAAC | 50807 |
| rs74547880 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158945 | ACTGTGTTAGCCAGG[A/C]TGGTCTCGATCTCCT | 50807 |
| rs74577711 | snp | A/G | 0.0287284 | 0.116357 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086095 | CATGCTAAGTTGATC[A/G]CCTTCTCCACACTTC | 50807 |
| rs74581925 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130369081 | GTCAAAGGATTGTTA[C/T]ACAGAATCAATTAGA | 50807 |
| rs74586550 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130125256 | ATGGGGCATTTGTCC[A/G]GTAGGCATCCTACTT | 50807 |
| rs74612957 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137468 | ACCCATAACTAAGCA[C/T]CAACAGTTGGCACTT | 50807 |
| rs74613124 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152327 | GAGTTTTCTGTTGGT[C/T]TAAAAAGGGCAAAAC | 50807 |
| rs74630706 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062745 | GATGTCTGTGCTAGA[A/G]TGTTTGGCACAGTAC | 50807 |
| rs74636257 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238992 | ATCTTCCTTTAAATA[C/G]TCTTGTATCTTTTTA | 50807 |
| rs74637469 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164101 | TCATTTTTCTAAATA[C/T]TTGAATAGTTTTCTG | 50807 |
| rs74639250 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353280 | CAAAAATGTGTTGAA[A/C]AAATGCTGTTCACGG | 50807 |
| rs74641545 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323770 | CACAATGCTAGGCAC[A/T]CAGCAGATCTTTGAT | 50807 |
| rs74645556 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130106947 | CAGTGCCCAGAATGT[A/T]TGTTAAACTGAAAAC | 50807 |
| rs74656989 | in-del | -/AACA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130123588 | ACAAACAAACAAACA[-/AACA]CTGTAAAAAACTAAA | 50807 |
| rs74666986 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097433 | CCCTGGCTATGCCTG[A/G]GTCCCTTCCCACATC | 50807 |
| rs74684720 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380786 | GCTGACGTGCAGTCA[G/T]GAGCTTATTGCAGCC | 50807 |
| rs74698568 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130113790 | TTTTTTTTTTTTTTC[C/T]TCTGAGACAGGGTCT | 50807 |
| rs74699605 | snp | C/G | 0.0539704 | 0.155153 | intron-variant | ASAP1 | GRCh38.p7 | 8:130386636 | CTTCTGACAACTGTA[C/G]CTCACTCTGCAGAAA | 50807 |
| rs74724856 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130427559 | ACTCTGCAGGGGGTA[C/T]TGGCAGCGCAAGTGG | 50807 |
| rs74727316 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341180 | CCAGAGTGAAACACA[C/T]CTACCACCCACAGCT | 50807 |
| rs74739166 | snp | A/T | 0.247621 | 0.249989 | intron-variant | ASAP1 | GRCh38.p7 | 8:130346572 | AGGGCTGTTGGGAGG[A/T]TTATATGAGACGATA | 50807 |
| rs74740043 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062780 | TATAACGAAAAAAAT[A/G]CCACCCATCTGAATG | 50807 |
| rs74786617 | snp | A/G | 0.0535932 | 0.154675 | downstream-variant-500B | ASAP1 | GRCh38.p7 | 8:130051722 | AGGATTCAGGGGTTA[A/G]TGCAGGCAGAGTGCC | 50807 |
| rs74793716 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249963 | ATTTTCAAATCCTAG[C/G]AACATTATTCTTCTC | 50807 |
| rs74800458 | snp | A/T | 0.0562307 | 0.157967 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270274 | CCCCCTCCAATAAGA[A/T]GAAACTTTTTCTTTT | 50807 |
| rs74803753 | snp | A/G | 0.040671 | 0.13668 | intron-variant | ASAP1 | GRCh38.p7 | 8:130357067 | GATGCTGAGTTCCTG[A/G]GCAAATATCCTATTT | 50807 |
| rs74821538 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130345502 | TAAATGCTAACCAGA[C/T]TCTCTTCCGTTTACT | 50807 |
| rs74823608 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213947 | CCTGGGTCTGCCTCC[C/T]GGGGCCAGCACCTCT | 50807 |
| rs74824523 | snp | A/G | 0.0498117 | 0.149749 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130298072 | ACATGGGTGTTGGAT[A/G]GGATAAAACTTAAGG | 50807 |
| rs74860601 | snp | A/C | 0.0494327 | 0.149241 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320002 | CATTTTAACATATTC[A/C]TGTCTAGTTAATGCT | 50807 |
| rs74875451 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241586 | CTTGCTTTGAAAATG[A/G]TTGACAAAATAGTTC | 50807 |
| rs74888036 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437790 | TCCTGTTGTGCCCAC[A/G]GCTGATCCTCCCCAG | 50807 |
| rs74895026 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099344 | CCACCACGCCTGGCT[A/T]ATTTTTTTTGTATTT | 50807 |
| rs74895852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168832 | CATTTGACCATCGAT[A/G]ACTTCTCTGACTTAA | 50807 |
| rs74896277 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118902 | AGTTACAAAGTAAAC[A/G]GGCACATAAATCACA | 50807 |
| rs74898150 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106680 | TCTGACGAGTACTGA[C/T]GAGCATCCTACTCTC | 50807 |
| rs74900844 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110438 | TCCTCTGTAGGGTGC[A/G]GAAAGAGAATCTCTG | 50807 |
| rs74907210 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397932 | CAGCATGGACCTTTG[C/T]ATCCCAGGCATCCTA | 50807 |
| rs74910572 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391322 | GGGTACAGAATTTCA[A/G]TTTTGCAAGATGAAA | 50807 |
| rs74918507 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098015 | AATCTCTTCCTCCTC[G/T]TCTTGCATTTTCTGG | 50807 |
| rs74919440 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175164 | AGGTTTTGATTTGTA[C/T]TTAACACCGACTAAT | 50807 |
| rs74945279 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ASAP1 | GRCh38.p7 | 8:130361086 | CTTGCATTTATTTTG[C/T]TCTCCCATCTATTCC | 50807 |
| rs74966037 | snp | A/C | 0.231775 | 0.249335 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112649 | GGACTTTTTCAGCAA[A/C]ATTTGAATAGTATTT | 50807 |
| rs74975482 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130412851 | GGTTTCACATGTTGG[C/T]CAGGCTGGCCTCGAA | 50807 |
| rs74984564 | snp | A/C | 0.0509478 | 0.151255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098910 | GCTGTTATTTTGTAT[A/C]CATTAATCAGCCTCA | 50807 |
| rs74985814 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165211 | TTAAGTCTCCATGCA[A/G]AACAAAAAGGGGTTG | 50807 |
| rs75030312 | snp | A/G | 0.222035 | 0.248431 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287014 | GGAAGACTTCTTGGT[A/G]GCCAAGGAGGGAGAC | 50807 |
| rs75041667 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130202802 | TATATCCAACTTCAA[A/G]GTCAAGCTATTTCTG | 50807 |
| rs75057693 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126437 | ACTGCTCACAGGGGA[A/G]TGGATTCTATAGCCA | 50807 |
| rs75064243 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130166172 | CCACCATGCGTGGCT[A/G]ATTTTTCAAAATTTT | 50807 |
| rs75074124 | in-del | -/TT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130067563 | CCACATCTGGCTAAG[-/TT]TTTATTTTTTGTAGA | 50807 |
| rs75082629 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274373 | GGAAGTTTTGTTTTG[A/G]AGGAGGTGCAGAAAT | 50807 |
| rs75084003 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115114 | GGTGTTTGGTCAAAT[A/G]CTAGTCTAGATGTTG | 50807 |
| rs75097708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238719 | GGAAATGTAGTAGAC[C/T]TTCAATAAATATTTA | 50807 |
| rs75098496 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343148 | TAACCATTTCCCCTT[C/T]TCATAGTGAATGCTA | 50807 |
| rs75098669 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130096714 | TGAATCATCTAGGAG[C/T]ATGTGTTTTCCACGA | 50807 |
| rs75103912 | snp | C/T | 0.226779 | 0.248919 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388089 | GACTTCAGGATGTGA[C/T]GACCATGGAGTGGGG | 50807 |
| rs75110270 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130113476 | TTTTTCCATACTCTT[A/T]TAATGATTATCACAT | 50807 |
| rs75124512 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362016 | GCTGACTGAGGTTTC[C/T]AACACCATGATTATG | 50807 |
| rs75134632 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164065 | AGGTATCAATGGAGT[A/G]GGCAAAAGATTCCTT | 50807 |
| rs75143892 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123471 | TTCACAGAGCAGGTG[C/T]GCAGCTGCAACAACC | 50807 |
| rs75152332 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385143 | AGAAGGCACGTTGCT[A/G]GCTGGTGGTCGCTTG | 50807 |
| rs75155444 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081819 | ACCCATCAAGACGCC[C/T]TGATAGTAACATTAT | 50807 |
| rs75175056 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402346 | GCAGCTGGGTGCCCA[A/C]GAGAAAGCAAAAGTG | 50807 |
| rs75186484 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124305 | AGTGCTGGAAATACA[A/G]AGATGGGTAAACTAT | 50807 |
| rs75188202 | snp | A/C | 0.0429648 | 0.14013 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245088 | GAGGGACCTGGCAGC[A/C]GCAGCTTATATGAAA | 50807 |
| rs75191282 | snp | C/T | 0.0322114 | 0.122752 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130427841 | GAGGTGAAGGAGGTA[C/T]AGCTGAGCCCCAACA | 50807 |
| rs75202091 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130300192 | GAGAGAGAGAGCGAG[A/C]GAGCGAGCAGTCAAT | 50807 |
| rs75206357 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211558 | AGTGATTTCTTACAT[C/T]GAACAAATAACAAAT | 50807 |
| rs75213421 | snp | C/T | 0.236434 | 0.249632 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154173 | AACTCATACACCACC[C/T]CTTTAGGGGTCTTCC | 50807 |
| rs75256218 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330430 | ACAGCTCTGACCGGT[A/C]TATGCTATATTGCAG | 50807 |
| rs75301843 | snp | C/G | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257827 | TGCCTACTAATCTCA[C/G]AAGTAGTTCTCCATG | 50807 |
| rs75303739 | snp | C/T | 0.030665 | 0.119967 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354560 | CTACTGTCTGGGTCA[C/T]AGCAGTCCTAAAATG | 50807 |
| rs75305704 | snp | A/C | 0.031825 | 0.122064 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431898 | AGGGGGAAGATAAGG[A/C]GGGGGAAATGGCGAG | 50807 |
| rs75308188 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130186710 | TAACTAGCTTTCTAG[C/G]CTTTCATGAGCCCCT | 50807 |
| rs75341478 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215766 | CAACAACAACAACAA[A/C]AAAAAACAATTAGCT | 50807 |
| rs75351814 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130315559 | TCTAAGGAGAAGAGG[A/C]GAGTCTGAATTAGGC | 50807 |
| rs75371577 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223217 | GAGCATTCCAAACCA[C/T]AACCAAGCACAACCT | 50807 |
| rs75375911 | snp | A/G | 0.0358986 | 0.129076 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130127934 | ACAAAAACCTGATGA[A/G]CCACAATCGCAGCAA | 50807 |
| rs75378314 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177069 | GATCTGACTTACTTC[C/T]TATACCTGGACAATT | 50807 |
| rs75378647 | snp | C/G | 0.0168055 | 0.0901129 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342934 | TGGGAAGCAACCAAA[C/G]TAATTCACAACCATG | 50807 |
| rs75382864 | snp | A/T | 0.5 | 0 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082713 | CAAGGTCTCATTACT[A/T]ATTTTTTTTTTTTTT | 50807 |
| rs75399461 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074742 | GAGGAACAGAAACAA[A/G]GTGCTCCTAAGGAGA | 50807 |
| rs75401969 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | ASAP1 | GRCh38.p7 | 8:130416558 | AATAGGTTATCCTGA[C/T]TGTCATCTTCTGGGG | 50807 |
| rs75411646 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ASAP1 | GRCh38.p7 | 8:130182171 | GAGAAGAAATATGGA[A/G]GGACAGGCATAACTT | 50807 |
| rs75414498 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263114 | TTGACTTGGCATATA[C/G]TGTCTGATTACGTGT | 50807 |
| rs75423833 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280103 | TATTTTGCTGACAAG[C/G]AAACCATGGTTCAGA | 50807 |
| rs75432166 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | ASAP1 | GRCh38.p7 | 8:130221913 | ACCTCACAGAGATGT[C/T]ATTAAATTTAAGCAA | 50807 |
| rs75442352 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140893 | AGGGGAGTGGTATGT[C/T]CCACAGAAGTCCAAA | 50807 |
| rs75459265 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234984 | CACCTACTATGTGGC[A/G]GGCAGTGTATTAGGG | 50807 |
| rs75476026 | snp | A/T | 0.0528381 | 0.153711 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143563 | TATTCAAGTTTTTGA[A/T]TTTTGAAAATGTTTC | 50807 |
| rs75476259 | snp | C/T | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428852 | TTCTAGGGCTGTCAT[C/T]AAAAAGTACCAAAAT | 50807 |
| rs75481121 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106301 | ATGAGATAAAAAACC[A/G]CAGGAAACTGTAAAG | 50807 |
| rs75496368 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404862 | TCCTCTTGCCCTCTT[A/C]TGATGCACCACAAAA | 50807 |
| rs75505403 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188811 | CTTAAACACTATACT[A/C]CAGTACACGTATATG | 50807 |
| rs75505738 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130120127 | GAGACCAACTGATTC[A/T]ACTAAGTAACCAAAA | 50807 |
| rs75526651 | snp | C/T | 0.232651 | 0.249397 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306760 | AATTCTTCAGCTATA[C/T]TCACAATGCTCGGAC | 50807 |
| rs75532353 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188314 | CCATGCATTATTTCA[C/T]TGAACCTACATGACA | 50807 |
| rs75532894 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | ASAP1 | GRCh38.p7 | 8:130198633 | AGATATTGCTCACAA[C/T]ACCTCTGTAAGATGG | 50807 |
| rs75552144 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ASAP1 | GRCh38.p7 | 8:130328420 | TTTCAGGATGAGGGA[A/G]GAAAAATAAAGTAAT | 50807 |
| rs75584172 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341904 | GCATTGTTTTCTAAG[A/G]GTTCACTGGACCGAG | 50807 |
| rs75588039 | snp | A/C | 0.0486741 | 0.148216 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116299 | GGAGAACAGTGTGTT[A/C]ACATTTTGAAGACCA | 50807 |
| rs75589792 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141599 | TGCTTGGCACACATC[A/G]GGTACTAGCAAGATC | 50807 |
| rs75616073 | snp | G/T | 0.0513262 | 0.151752 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130429268 | GTACTTCAAGATATC[G/T]TTTGAAGGGACACAA | 50807 |
| rs75623002 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418789 | GAGTTTTTTTTTTTT[A/T]AATTATTCTTTCTTT | 50807 |
| rs75634651 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370820 | CCACATACTGTATGA[C/T]ACCTTAAAGGTCCAG | 50807 |
| rs75636474 | snp | A/G | 0.234692 | 0.249531 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160899 | AGCATTTTATATAAT[A/G]TACACAGAAAATATC | 50807 |
| rs75660267 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343061 | GAGGTTAAAATGTTC[A/G]GGCAAGGAAGAATGG | 50807 |
| rs75671545 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130140111 | GATCATAGATCACTG[A/C]AGTCTCAACCTCCTA | 50807 |
| rs75678251 | snp | G/T | 0.0539704 | 0.155153 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393307 | CTAAACAGTGAGCAT[G/T]AGTCTTTACTGAGGG | 50807 |
| rs75686460 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176514 | CTACAAGGTTTTTAC[C/T]GTGTAGGGTTTTCTT | 50807 |
| rs75688885 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274498 | TTGCACCAGACCACT[C/T]GATCTACCTTAAATC | 50807 |
| rs75718099 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173933 | AAAGAAAAAAAAAAT[A/T]AGCTTGGCGTGGCAG | 50807 |
| rs75718167 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251961 | AAAACCACCCTTACA[C/T]TTGACATAGTAAATC | 50807 |
| rs75720039 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107060 | AAGCAAGGTAGACAC[C/T]TAATCCTTATTTTTC | 50807 |
| rs75729193 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066852 | TGAGGGCCACTGCCC[C/T]CCATTTCAGCCTCTA | 50807 |
| rs75729277 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281587 | AAAGTGTAAAAAATA[A/G]TTTTTTTGGGGGGGT | 50807 |
| rs75732755 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422633 | TCTCCCATGGATCAG[A/C]CTCTTGGAGGGGATT | 50807 |
| rs75746302 | snp | A/C | 0.030665 | 0.119967 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322599 | GACCTTCTAACAATT[A/C]CTTTGTACTTAATGA | 50807 |
| rs75767105 | in-del | -/A | 0.34437 | 0.231505 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307355 | ATCTGATCCTGTGGC[-/A]AAAAAATAAAGAGGG | 50807 |
| rs75770394 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272393 | CTACACATCGTTGGT[A/G]GGAATCTAAATTAGT | 50807 |
| rs75776340 | snp | G/T | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082893 | CACTGTGCTCAATGA[G/T]GAGTCTTCAGGGCTA | 50807 |
| rs75781994 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130274788 | TCTCTGGCATAGAAT[A/C]TTGATCCACATAAAG | 50807 |
| rs75805779 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227294 | ATCTCACTCTGTTGC[A/G]CAGGTTGGAGCACAC | 50807 |
| rs75814285 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130429565 | CCAAACTCTTACCAG[A/C]CATCCATACCACAGA | 50807 |
| rs75814921 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143745 | CTGTGTTTCCTAAAA[C/G]AAAATAAACACCGCA | 50807 |
| rs75818274 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104028 | GGATATTCTCTACCA[C/T]ACATTACAGCTACAA | 50807 |
| rs75822358 | snp | C/T | 0.253544 | 0.249975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415936 | ACATCTTTCTGAAAA[C/T]CCATCTCCATTTCTT | 50807 |
| rs75822653 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111233 | AAAAAAAAAAAAAAA[A/G]AAAGCTGGGCATGGT | 50807 |
| rs75822812 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437877 | TATCCCAAACCAGGC[G/T]CCAACCAGGATCCCG | 50807 |
| rs75829698 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ASAP1 | GRCh38.p7 | 8:130433966 | TCTGTAGAGGCAATA[C/T]TGTATCGTGGTCAAG | 50807 |
| rs75834455 | snp | A/G | 0.24134 | 0.24985 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292736 | TGAAAAGGAAAAAAA[A/G]AGCAAGCTCCCAACT | 50807 |
| rs75846219 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130265861 | GTCTCAAGCCTGGGC[A/G]AAAGTGAAACTGTCT | 50807 |
| rs75849899 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352232 | TTTTTTTTTTTTTTA[A/G]GACTACAATCTCCTT | 50807 |
| rs75850563 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301397 | CCTTCTGTTACCTAG[C/T]AGCATTTTAATGTAA | 50807 |
| rs75863990 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281314 | TTATAGCTTTCTCCA[C/T]TGCTTTTAAGTTTTT | 50807 |
| rs75867003 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234241 | CCCACTAGTCATATA[C/T]GGCTGTTAAGTTCTT | 50807 |
| rs75895100 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245885 | TAAGGTAAATATTGC[A/G]ACACATATTTTTTGT | 50807 |
| rs75911352 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | ASAP1 | GRCh38.p7 | 8:130065242 | ACAGACACACAGGGC[A/G]GGGTCTGGAAGGGTC | 50807 |
| rs75919890 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240000 | GGAGAATAACCTATC[A/G]GTTATCTTTGGGGGA | 50807 |
| rs75925342 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | ASAP1 | GRCh38.p7 | 8:130181506 | GGTCTTTGTGGGTAT[A/G]CACAAAATTTAGTCA | 50807 |
| rs75927318 | snp | A/C/T | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133452 | ATGAGGTCAGGAGAT[A/C/T]GAGACCATCCTGGCT | 50807 |
| rs75935546 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | ASAP1 | GRCh38.p7 | 8:130147603 | ATCTTATTTAATTCT[C/T]GTAACATGGAAGACA | 50807 |
| rs75940749 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136561 | CAATCACCTAGTGGC[C/T]TTTTTTTTTTTTTTA | 50807 |
| rs75967395 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327926 | TTTTTTAAATGATGG[C/T]TTGGTAGACTAATGA | 50807 |
| rs75972641 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418073 | TGCCCCAAGGCCACA[A/G]GGACAGAAGAGAGAG | 50807 |
| rs75977351 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353413 | TCTGAAATATAAACA[C/T]GAAGAAACACTAAGC | 50807 |
| rs75988506 | snp | C/T | 0.0146672 | 0.084371 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296525 | TTTTTTTTTTTTTTT[C/T]CCCATTTGCTAAGCC | 50807 |
| rs75997605 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320900 | ACATGCCCAGTCTTC[A/G]GTTAAAGACATCAGG | 50807 |
| rs76001632 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238086 | AGCCGAAAGGGATAA[A/G]TGCAATGGTAGCAGG | 50807 |
| rs76011355 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130416473 | TCAGTTCCCAGCTGC[C/G]GACCAGTCAACAACA | 50807 |
| rs76016344 | snp | C/G | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276071 | ATGAGAAAGATTCAG[C/G]CCAGTTCCATGAATG | 50807 |
| rs76018370 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130142706 | GGGAAGTGTGATAAG[C/G]AGGTCCAAAGGCCTG | 50807 |
| rs76020108 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322668 | TCGATTCAACAAATA[C/T]TCATTTAGTGCTTAT | 50807 |
| rs76031100 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254905 | TATTACCATTATTCA[A/G]AAACAAAATAATACC | 50807 |
| rs76033184 | snp | C/G | 0.0517044 | 0.152246 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368778 | TGGCAAGAGATGCGG[C/G]AGAGTCGTGGTGACC | 50807 |
| rs76036656 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347888 | TCCCATGAATCCTTC[C/T]AATAAGTCCCCATTT | 50807 |
| rs76038214 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247722 | CGTGAGCTGCACATC[A/G]GCCATTTCACATAGG | 50807 |
| rs76040391 | in-del | -/GCACAG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130389760 | GGCTGGAGTGCAGTG[-/GCACAG]TCACGGCTCACTGCG | 50807 |
| rs76040531 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128165 | TTTTTTTTTTTTTTT[G/T]CCACTGCAAAAAAAA | 50807 |
| rs76047412 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130212260 | CCAGGAATGCCACCA[C/T]CACTTTCAAAGGCAA | 50807 |
| rs76048380 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269816 | TACCTGCATTAGATA[A/G]ATGTGCTAAGTGTGT | 50807 |
| rs76054574 | snp | G/T | 0.0520825 | 0.152737 | intron-variant | ASAP1 | GRCh38.p7 | 8:130345523 | TCCGTTTACTTGCAC[G/T]TTGCAGCTAAATCAC | 50807 |
| rs76055712 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334070 | GATGAGTAGGTGTTC[A/C]TCTGGTACAGGAGGA | 50807 |
| rs76060755 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091837 | GGTAGAATCATGTCA[G/T]ATATACCCGAGTCAG | 50807 |
| rs76069473 | in-del | -/CA | 0.338296 | 0.233889 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286387 | CATTCTACTTCCATT[-/CA]CAGTTTAAGTCCATC | 50807 |
| rs76076007 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206504 | CCCTACAGTCAGAGA[C/T]TGCAAACAGGAAATG | 50807 |
| rs76079340 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130125827 | CATTTTAAACGTCTA[C/T]GCAAACTCACAAAAT | 50807 |
| rs76084354 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238891 | TTTCCAGACTGCAAG[A/T]CTAACACGATTTCCA | 50807 |
| rs76084854 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130097768 | TCTCCTGAGACTCTC[C/T]CCCAGGAACTGACAT | 50807 |
| rs76106903 | snp | A/G | 0.0490535 | 0.14873 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359187 | GGGCTTTTAAAAAAA[A/G]TAATTTTCTAATCTT | 50807 |
| rs76112002 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130171441 | TCCTGCTTGCACGCA[C/T]TCTCTCTCCTGCCTC | 50807 |
| rs76115478 | snp | C/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229860 | AGCCTGGGCAACATG[C/G]TGAAGCCCCATCTCT | 50807 |
| rs76120785 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133886 | GCTGATATGTTTGGC[C/T]ACCAAAAACTGAGCA | 50807 |
| rs76132026 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | ASAP1 | GRCh38.p7 | 8:130194737 | TCACAACAGGGTTTG[C/T]GCTGCTTTGAGAATC | 50807 |
| rs76136560 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289505 | ACCCCAAATCCTTAG[C/G]GAGGCAGCTACCTTG | 50807 |
| rs76176561 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391207 | GTATGATTCCACTTA[C/T]AAAAGATACCTAGAG | 50807 |
| rs76176620 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130426413 | AATACACTGGTTAGG[A/G]AAAAAAAAAAAAGGG | 50807 |
| rs76180135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335615 | CTAGTGGAAAAAGAG[A/G]TGGAAAAAAAGAGTT | 50807 |
| rs76182273 | snp | C/T | 0.132409 | 0.220618 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062926 | TACAGTGAACTATGA[C/T]GGTGCCATTGCACTC | 50807 |
| rs76185688 | snp | C/G/T | 0.127599 | 0.217986 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078370 | TGCGATCATGACTCA[C/G/T]TGCAGCCTCAATTTC | 50807 |
| rs76195661 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223814 | GTCTTTATGCAAGTT[C/T]TCCTTCTGTGTCAAG | 50807 |
| rs76216356 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130276128 | ACAAAAAGAACCCTG[C/T]GGGCCTGACCTCTAG | 50807 |
| rs76225285 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130188746 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAT | 50807 |
| rs76228546 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130250501 | TGAGAACAGAAGTTT[A/G]AAGGGAATACAAGTG | 50807 |
| rs76239957 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128701 | ATATACAGTATGACT[A/T]CTGTATGTCCCAAAC | 50807 |
| rs76250125 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154292 | GTTAGTAACAAGTGA[C/T]AGACATTTTGAAAAA | 50807 |
| rs76253548 | snp | A/C/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415783 | GAAACTCCATCTCAA[A/C/G]AAAAAAAAAAAAAAC | 50807 |
| rs76273377 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130440506 | ACCTAGACTCTGTCA[A/C]AAAAAAAAAAAAAAG | 50807 |
| rs76278922 | snp | C/T | 0.0396925 | 0.135169 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058102 | GAAACTGGGTTTTAA[C/T]TGAAAGAATGGACTG | 50807 |
| rs76280774 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385731 | ACAGAGGCTCTTCAA[C/T]AGCCCGCTAAGGAAG | 50807 |
| rs76325249 | snp | A/C | 0.232651 | 0.249397 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145072 | TGAGGTTACTGCACC[A/C]AATGAATGTGCTAGA | 50807 |
| rs76329708 | snp | A/T | 0.0498117 | 0.149749 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288106 | AGGAGCTCCAGCTAC[A/T]CGCATCAAGCAATCA | 50807 |
| rs76344737 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130320648 | GAGGAAGAGTTAAAA[A/T]TGAAAATTATAACCA | 50807 |
| rs76348049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350322 | CCCTGGGTTGGGCAG[C/T]CCTGAATTCAAATCC | 50807 |
| rs76365541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343816 | ATTTAATACAATGAC[A/G]TGCCTTTTTAAATAT | 50807 |
| rs76367770 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313878 | CTGCAGTCAATGCCA[A/C]TGCACTCGACACCAC | 50807 |
| rs76377766 | snp | C/G | 0.378568 | 0.214407 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130443910 | CCGGGGTCGGGCGTC[C/G]TTCGCCTTCCGCCCC | 50807 |
| rs76382860 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130371872 | TTTTTGTTTGTACAG[A/C]GTTGAAATCTAATCC | 50807 |
| rs76383895 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130230272 | AACCAGCAAAACGGA[-/G]GAAGTGCATACACAG | 50807 |
| rs76385518 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344500 | TGAAAAAAAGATTGG[C/T]CAAAAGCAGACAATT | 50807 |
| rs76395106 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313164 | TGGAAGGAGGTGGTG[C/G]ATGGGCTGAACAATG | 50807 |
| rs76398111 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209442 | GTGTTGACATTTGCA[C/T]TGACAGTGTAAAAGC | 50807 |
| rs76399697 | snp | C/T | 0.406296 | 0.19512 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400966 | GCCCACTGCAACCTC[C/T]GCTTCCGGGGTTCAA | 50807 |
| rs76404401 | snp | G/T | 0.0539704 | 0.155153 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379603 | CAGTTGTTGAACATG[G/T]AGTTCGGGTAGGAAA | 50807 |
| rs76407571 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166815 | CAATATCCAAGGACC[A/C]ACTCACCTCAAATTT | 50807 |
| rs76407966 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130113287 | TTCTCTCCATTCCTC[C/T]GACATCCAGACTCTA | 50807 |
| rs76409721 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253752 | GTACAAAAGTTTGGG[C/T]ACCACTGCTATTAAG | 50807 |
| rs76414506 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064639 | CCCACCACCAAGCAG[C/T]GGATACCAGCCAGGT | 50807 |
| rs76416294 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373228 | CAGACACATTCATTA[A/T]GAATGGCTTTTTTTT | 50807 |
| rs76428972 | snp | A/G | 0.040671 | 0.13668 | intron-variant | ASAP1 | GRCh38.p7 | 8:130212541 | TAACACATACTAATA[A/G]GGTAAATGAACAAGT | 50807 |
| rs76443485 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069031 | AGAGAACAGGGAAAG[G/T]CAAAAGTGAGAGCCA | 50807 |
| rs76446802 | snp | A/T | 0.0429648 | 0.14013 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093993 | GCTATATAATTTACA[A/T]CTTTGTCCCATTGCG | 50807 |
| rs76455951 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309816 | ACAAGCTGTACTGCC[A/C]GGTGAACTCCCAACC | 50807 |
| rs76468129 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109290 | ACTGAGCTCCTCTGA[A/G]ACTCTGGGGCACTGC | 50807 |
| rs76476483 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417632 | GGGAAAAAAAAAAAA[A/G]AAGGAGAGGCAAATG | 50807 |
| rs76481566 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337081 | AGCTAACCCAGTCAG[A/G]ACTCACATCAGAGTT | 50807 |
| rs76489239 | snp | C/G | 0.242201 | 0.249878 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178471 | AGGCAAACAAAAATG[C/G]TGCCAGTGTAGAACA | 50807 |
| rs76504415 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362379 | TGGCTAAAGTGGGAA[A/G]GGAACACACTTTTTA | 50807 |
| rs76514441 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428420 | ATCACCACCACCATC[A/C]CCATCATCATCATCA | 50807 |
| rs76523664 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130291451 | AAAGTCATCTCCTGC[C/T]ACTTCCCTCTGAGAT | 50807 |
| rs76525058 | snp | C/T | 0.245631 | 0.249962 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158154 | TGTACATGTCTCAGA[C/T]TAAGCCAAGGAGTAC | 50807 |
| rs76527033 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | ASAP1 | GRCh38.p7 | 8:130420128 | GATTCCTTTATGTGG[C/T]CAAAAAGCAGGTGAG | 50807 |
| rs76531876 | snp | A/T | 0.123798 | 0.215808 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139246 | GACCATCTTCAAGTA[A/T]ATGAAGGTTGTTATT | 50807 |
| rs76542615 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428454 | CCACCACCATCATTA[C/T]CACCATCATCATCAC | 50807 |
| rs76566901 | in-del | -/A | 0.232943 | 0.249417 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132824 | TCTACCTTCTCTCTC[-/A]AGTTTTCTTTCCCCA | 50807 |
| rs76574347 | snp | C/T | 0.000675692 | 0.0183682 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130180781 | CTGAAAGAGGCGCCT[C/T]TCCTTCTCCATTTCT | 50807 |
| rs76585631 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233859 | ACAAACAAATTACAT[C/T]GACAAATGCATAAAC | 50807 |
| rs76586794 | snp | A/T | 0.0349115 | 0.127424 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444784 | AGTTTGGGAAAACCA[A/T]AATCAATCTCTGACT | 50807 |
| rs76597775 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156526 | GAGTATTTCATCTAT[C/G]TGTGTGGAATGAGTA | 50807 |
| rs76613631 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130061746 | ATACATAGTCTGAAA[C/G]TTTGCTTTTCTCCCA | 50807 |
| rs76629215 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170160 | CACAAAGCAGACTGA[A/C]TGAAGCAATATCAAG | 50807 |
| rs76637511 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317433 | AGGAACAGGGTCTAC[C/G]ACTCACTTAGCTGCT | 50807 |
| rs76646885 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417973 | ACACTCACTGGACTA[C/G]CCAGGTATTGCTTAT | 50807 |
| rs76650366 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101261 | TTACTTTGGCTATTT[A/G]AAGTCTTTTGTGTTT | 50807 |
| rs76652473 | snp | A/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356089 | TCTCATAAAAAAAAA[A/T]ATTTGCTTTTAAATT | 50807 |
| rs76660211 | snp | A/T | 0.0452528 | 0.143452 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295273 | AGGCAACAGAGCAAG[A/T]CTGTCTCACAAAGAA | 50807 |
| rs76663828 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085203 | TGTCAGTCTTAAGGC[G/T]ACCATGAACCTAACA | 50807 |
| rs76688779 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056014 | CTAGGAATGATGCTA[A/G]GGACACCAATGACAG | 50807 |
| rs76701071 | snp | A/G | 0.235564 | 0.249583 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244963 | ACTCCAATTACAGCA[A/G]TTTGAGGAGTTGAGG | 50807 |
| rs76702694 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130221950 | GCATGCCAAGTGCCT[C/T]GTACACGATGAGCTC | 50807 |
| rs76705286 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366245 | GCACAATTGCCTACT[A/G/T]TTTAAAAATTGTAAC | 50807 |
| rs76705648 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203099 | TGAATTAAAAAAAAA[A/C]CACACACAACAACAA | 50807 |
| rs76705697 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130147671 | AGTAGCTTAATAAAA[A/G]GCACATACAATAAGA | 50807 |
| rs76728646 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165645 | ACATGGATGCAGAAA[C/G]TGCCTTAGTGTACAC | 50807 |
| rs76740318 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130135959 | TGGGTCAGGACTATT[C/T]ACACAACTGCATCAG | 50807 |
| rs76745841 | in-del | -/AAAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130420906 | CTCAAAAAAAAAAAA[-/AAAA]GTTACTTCATTCATT | 50807 |
| rs76746423 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141692 | ACTGGCACTATATGC[A/G]CACGCTACCACACGA | 50807 |
| rs76748867 | snp | A/T | 0.5 | 0 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082716 | GGTCTCATTACTAAT[A/T]TTTTTTTTTTTTTTT | 50807 |
| rs76749418 | snp | A/C | 0.0517044 | 0.152246 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169149 | GGAAATAAAAAAAGG[A/C]ACTATAATAACCTAC | 50807 |
| rs76764040 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277385 | ATCCAGTGAATTTAA[A/G]ACAACAAAAGATGAA | 50807 |
| rs76769954 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130336061 | ACTCAACTCCAAACT[C/G]TGTCTCATCAGCCTA | 50807 |
| rs76783810 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352249 | ACTACAATCTCCTTG[C/G]GGGTAATTAATGGGC | 50807 |
| rs76786135 | in-del | -/AA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130313319 | TTTAAAAAAAAAAAA[-/AA]CTTTTAAAAGGTCCA | 50807 |
| rs76809440 | snp | A/G | 0.245631 | 0.249962 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158153 | ATGTACATGTCTCAG[A/G]TTAAGCCAAGGAGTA | 50807 |
| rs76822377 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289563 | AAAGACTGGGGAGGC[A/G]AAGACTGGAAGGCTT | 50807 |
| rs76822650 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130357604 | GGGGTGCGTTCACTG[C/T]CCATCTCCTAGTCCC | 50807 |
| rs76825705 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390489 | GGCATAATATGCTAT[C/T]AGGAATATATGATTA | 50807 |
| rs76828023 | snp | C/T | 0.031825 | 0.122064 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362552 | TCCCTTTGAACTCCC[C/T]TTTTCTGTGAAAGAT | 50807 |
| rs76830015 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136826 | CTAGAGCAGCACATG[C/G]AGGAATAACTGTTCC | 50807 |
| rs76831266 | snp | G/T | 0.178785 | 0.239642 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316847 | TTTCCCCCTGTAATA[G/T]GCAGCTCAATGTAAA | 50807 |
| rs76832712 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391360 | TGGAGATGGATTTCG[C/T]GGCAATGGTTGCACA | 50807 |
| rs76833135 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435124 | GCGCTGTAACCTGGC[A/G]GGGAGGGTGACTCAG | 50807 |
| rs76839420 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130429587 | TACCACAGAAGCAGC[A/G]TTGTTTCTGGTGTAT | 50807 |
| rs76859055 | snp | A/G | 0.464841 | 0.127841 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072791 | CTGGACTTGCAATTG[A/G]TATGTGTGTGTGTGT | 50807 |
| rs76881333 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124927 | CCTGAAGTGAACTAG[G/T]GAGCCGAGTATCAGC | 50807 |
| rs76887152 | snp | G/T | 0.254944 | 0.249951 | intron-variant | ASAP1 | GRCh38.p7 | 8:130416799 | GTGGTAAAACAGAAA[G/T]CATAATGACCACATG | 50807 |
| rs76887420 | snp | A/T | 0.0379877 | 0.132479 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378170 | TGAAATATGCGGTTA[A/T]TAGTAGTGCCTACTT | 50807 |
| rs76890518 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430830 | GGAGTCTTCTCTCTT[C/T]TCAAGCTCAGACCTA | 50807 |
| rs76891167 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428467 | TATCACCATCATCAT[C/T]ACCACCACCACCACC | 50807 |
| rs76892261 | snp | A/G | 0.234982 | 0.249549 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152393 | TACATCTACTGTTAC[A/G]TTTCCTACATTATTT | 50807 |
| rs76911196 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234513 | ACCTCTTTACATCCA[C/T]ACAGGAACAATCTCT | 50807 |
| rs76920052 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101586 | ATTTTTCTTTTTTTT[C/T]CTGAGACAGGGTCTT | 50807 |
| rs76925231 | snp | G/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238225 | CAACGTCATTCCTCG[G/T]ATTTCTGGGCTTGGA | 50807 |
| rs76938681 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374661 | TGGCATCATCATCAC[C/T]TGCTTCCCGATGGGG | 50807 |
| rs76944665 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258933 | CTCCCCAATTTTGGG[A/G]CAAGTGGTAGGAAGG | 50807 |
| rs76947404 | snp | G/T | 0.0543475 | 0.155628 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115163 | GATGCAATTACCATT[G/T]AAATGAGTAGATTTC | 50807 |
| rs76953076 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288638 | AAATGTGAAGGAGAC[C/T]CTGTCCTCCAAGAAT | 50807 |
| rs76954392 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366229 | ATCAAGGAATGCCTA[C/T]GCACAATTGCCTACT | 50807 |
| rs76959780 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158746 | CATATGCTTTATGAT[A/T]TTTTTTTTTTTGTCT | 50807 |
| rs76966418 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322739 | GAACACAGTCCTTAC[C/T]TAAGTGAGTTTACAA | 50807 |
| rs76978774 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133451 | CATGAGGTCAGGAGA[C/T]CGAGACCATCCTGGC | 50807 |
| rs76989195 | snp | C/G | 0.121022 | 0.21416 | intron-variant | ASAP1 | GRCh38.p7 | 8:130442939 | AAGTAGGACTCCCCC[C/G]ACCCCCTTCCCTTTC | 50807 |
| rs76999541 | snp | A/G | 0.2462 | 0.249971 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074126 | TTCTTAAAAAAAAAA[A/G]GGGGGCAATTGTGAG | 50807 |
| rs77005580 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097514 | TCAAGTGGTTGCCGC[C/T]GAACCTACCTGATGT | 50807 |
| rs77006899 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439503 | AATAATAGCTAACAT[C/T]TGTCGAATTTACCCT | 50807 |
| rs77014186 | snp | A/G | 0.102014 | 0.201495 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437470 | GGTGGTGACTACAGT[A/G]GACCCCAGAATCTTC | 50807 |
| rs77022084 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130331601 | CTCATTTGTAAAAAA[A/T]TAGGACGTCCACCCA | 50807 |
| rs77039269 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248453 | ATCAGATGCCTGAAA[C/T]AAGTGGCCACAGGAG | 50807 |
| rs77041194 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368596 | GTACTAGAACAGGCA[A/T]TTAACTCAAGCATGG | 50807 |
| rs77041575 | snp | C/T | 0.23031 | 0.249223 | intron-variant | ASAP1 | GRCh38.p7 | 8:130138414 | GATTTAGGAATGGAA[C/T]CAGAAGTCAAGTACA | 50807 |
| rs77072400 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | ASAP1 | GRCh38.p7 | 8:130147629 | AGACAGGTACTGTTA[C/T]TCTGTTTCACAGATT | 50807 |
| rs77094825 | snp | C/G | 0.0539704 | 0.155153 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378202 | ATAGGGTGGCCATGA[C/G]GATTAAACGAGAGTG | 50807 |
| rs77095555 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292271 | CAATGGTGAAGAAGA[C/T]TCTTTCTAGATCCTC | 50807 |
| rs77099181 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ASAP1 | GRCh38.p7 | 8:130441969 | TGGGAGTTTCTATTT[C/T]GCACAAAAGAATGGG | 50807 |
| rs77107245 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384788 | TCACACTTCACATCC[C/T]TCAATGACTCCCCAT | 50807 |
| rs77118745 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218616 | GGCAGAGACAGGCCA[C/T]AGGAAGAAGGTGTTG | 50807 |
| rs77133113 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176158 | GTGTAGTAGCTTCAT[C/T]CACACGGAAGTGTCG | 50807 |
| rs77135874 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130442279 | GGGACTGAGCCTGAA[A/G]AAGTGGAAACTACTC | 50807 |
| rs77137017 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347073 | TCTGTTATTTAACAC[C/T]GAGGAAAAACCAATT | 50807 |
| rs77137166 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374128 | CCTTGCCCTACTATT[C/T]ACAGATTGCATGACA | 50807 |
| rs77151344 | snp | A/T | 0.000238877 | 0.0109262 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169105 | TTTACCACCAGTATA[A/T]AAAAAAAAGAGTATT | 50807 |
| rs77152054 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209220 | ATAAAGTATGCAGAA[A/C]AAGTACTTTCCCCAT | 50807 |
| rs77157739 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158932 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 50807 |
| rs77159330 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063418 | GACCCTGTTCCACAT[C/G]CTCTCTCCGCACTCC | 50807 |
| rs77159538 | snp | G/T | 0.0539704 | 0.155153 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392729 | TCTGTGAGGGCCTCA[G/T]GTTGCTTCAACTCGT | 50807 |
| rs77162821 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292140 | TTAAAAATCTATAAA[C/G]AGCAGACTATAGGGA | 50807 |
| rs77164811 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374350 | CTAATACTAAAAATA[C/T]TATTTCTCTGATGAT | 50807 |
| rs77165934 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419736 | GAGGCTGAGGCATCC[A/G]ATCTCTTCCCTGGGG | 50807 |
| rs77172770 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383592 | GGATCTAATATTATT[C/T]CCAGATGAGGAAACG | 50807 |
| rs77174445 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229662 | ATATTTATTTTTACC[A/T]AAATAAATCATTAAA | 50807 |
| rs77180742 | snp | C/T | 0.0818113 | 0.184966 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252923 | GACAGTAAGAACTTA[C/T]AGGATCCTACTTCAA | 50807 |
| rs77194086 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325247 | AGGAGGAGAGCTGAA[C/T]AAATTGGAGAAAGAA | 50807 |
| rs77195801 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413488 | TCTCTCCCAACACTG[C/T]TATGATATCAATAAT | 50807 |
| rs77196359 | snp | A/C/G | 0.0391387 | 0.134304 | intron-variant | ASAP1 | GRCh38.p7 | 8:130089340 | ACATGTTCAGCTTTG[A/C/G]GGGTGGAGAGGTAAG | 50807 |
| rs77207625 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111361 | CAAGGGAAAAAAAAA[A/T]TTCCTCTCCAAGTAC | 50807 |
| rs77207909 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438010 | GACAAGCTTAGTTTG[C/T]GGCATTTCCAAGAGA | 50807 |
| rs77218014 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228546 | TCCCTACAAAAACCA[C/T]AAAAATTAGCCAGGC | 50807 |
| rs77225402 | snp | C/G | 0.0535932 | 0.154675 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360723 | TAAAAGCTTGGTTTG[C/G]GACACACCAAGTTTG | 50807 |
| rs77227093 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110197 | GATAAAATTACAGAA[G/T]GGGGTGGAGGGAAAT | 50807 |
| rs77240384 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205384 | TGAATCCTTATAAGA[A/G]AAAAAAAAAAAAAAA | 50807 |
| rs77243482 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093666 | AGCGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 50807 |
| rs77255300 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131494 | GCAGGCTGGGCACTA[C/T]AGCTCACGCCTGTAA | 50807 |
| rs77269502 | snp | A/G | 0.00835572 | 0.0641442 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347150 | CCATCCATCCTGGAT[A/G]TCTACGGAAAGATTA | 50807 |
| rs77272999 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244778 | AGTGTCCCCTGTGGG[C/T]CAGGTGCTGTCCTAG | 50807 |
| rs77288605 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | ASAP1 | GRCh38.p7 | 8:130182755 | AAGGAAGCAGATAAA[A/G]CATTTTACAAAATGT | 50807 |
| rs77295518 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102006 | TTTGGTGACGTCTTT[A/C]GGTTTTTCTATATAG | 50807 |
| rs77301427 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130274036 | GGCTTTGAGATCTTG[A/C]TTCTCAGTTTCCCCA | 50807 |
| rs77303890 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380093 | TGTTGGGCACCCCAG[A/G]TCTCAGGTTGGGTTC | 50807 |
| rs77309140 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120403 | TAAATCAAGTTCTCA[C/T]TGAATCTCAGTTTCT | 50807 |
| rs77319332 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178052 | ACCCAAGCTTTGTGC[A/T]TTTGACATAATATTA | 50807 |
| rs77327630 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350905 | CTGGGCAGCTCATAG[C/G]CAAATCAGGTTGGGT | 50807 |
| rs77354712 | snp | C/T | 0.0879971 | 0.190408 | intron-variant | ASAP1 | GRCh38.p7 | 8:130426952 | TCATGTTTGCTACTG[C/T]TGTCCCGCCCCTAGA | 50807 |
| rs77356925 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375455 | ATCCCAGCAATTGGA[A/G]AGGCTGAGGCTGAAG | 50807 |
| rs77358178 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224633 | TACATACGACCACCA[C/T]GGCTTGCTTTTTTCC | 50807 |
| rs77364323 | snp | G/T | 0.232067 | 0.249356 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278755 | ATGGGTGAAACAGAA[G/T]AGAGGGGGAGCTGTT | 50807 |
| rs77365522 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158955 | CCAGGATGGTCTCGA[A/T]CTCCTGACCTCGTGA | 50807 |
| rs77369735 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438646 | ATTTAATTTTTTTCA[A/G]GAGGCTGGGTGAGAA | 50807 |
| rs77370740 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323763 | CCCATAACACAATGC[A/T]AGGCACTCAGCAGAT | 50807 |
| rs77374850 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130113788 | ACTTTTTTTTTTTTT[C/T]CCTCTGAGACAGGGT | 50807 |
| rs77375297 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295352 | CTCTTTTTTTTTTTT[C/T]TTCAAAGACTATCAC | 50807 |
| rs77378246 | snp | C/T | 0.237303 | 0.249677 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355477 | AATTAATTCCTATTC[C/T]GGAGTTTCCATATCA | 50807 |
| rs77380857 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344754 | AAAAAAACAAACAAA[C/T]AAACAAACAAAAAAC | 50807 |
| rs77388067 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435527 | TGTCTCATTACTAAT[A/G]TTCTGTTACAGATTT | 50807 |
| rs77396950 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064319 | GATGTGGAAGGGGGA[A/G]GAAACAGTATTTGTA | 50807 |
| rs77402262 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130142671 | CAGAGAGGACTTGGA[A/G]GAGGGAATATGGACA | 50807 |
| rs77404791 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253430 | TTTGATTTTTTTCCC[C/T]AAAGTTCCCAACAGA | 50807 |
| rs77420209 | in-del | -/A | 0.429238 | 0.174281 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081589 | AAGAGGGCAGGGCTG[-/A]AAAAAAAACTAACTG | 50807 |
| rs77444039 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248105 | CATCAGGAAAGAAAA[C/T]AGGAGCTTACTTATC | 50807 |
| rs77449536 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | ASAP1 | GRCh38.p7 | 8:130398871 | CTATCCTGTCAGCAC[A/G]ATCTTTCAAGAATGA | 50807 |
| rs77456064 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177966 | AGTATACTGAGGTTT[A/G]GTGAAGTACCTGATT | 50807 |
| rs77460659 | snp | A/G | 0.0558977 | 0.157557 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278667 | CGAGAGACATTGGAC[A/G]AAAAAAACTCTAATT | 50807 |
| rs77462555 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | ASAP1 | GRCh38.p7 | 8:130075043 | GTTGCGGTAAAGCCC[C/T]ATGGGCACTGGGAAG | 50807 |
| rs77467207 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384228 | AGCAGGGAAGGGCCT[C/T]GCTGATTAAAATAAA | 50807 |
| rs77474228 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374058 | AAAAAAAAAAAAAAG[A/C]AGCCATGTCCAAGCT | 50807 |
| rs77522937 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275505 | TCCTGGCTAGCCTAG[A/G]AAGGAGAAAACACCT | 50807 |
| rs77526966 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129460 | AATGAACTTGTATTA[C/T]TTTCATGAATGAGAA | 50807 |
| rs77535355 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130282249 | AGGGATCTAATAATC[C/T]ATATCTGGGAAACCA | 50807 |
| rs77537976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134162 | AGCAACATGTGATGG[C/T]CCACAGGCGGGAAAG | 50807 |
| rs77538337 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395098 | AAGAATGTCCCTGCC[A/G]CAGCACAAGAAAAAC | 50807 |
| rs77539292 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130400213 | ACACTTTCCACTACG[C/T]GGACTTCTTAGAAAC | 50807 |
| rs77540118 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428481 | TCACCACCACCACCA[C/T]CATCTTCATCACCAT | 50807 |
| rs77541703 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099346 | ACCACGCCTGGCTAA[A/T]TTTTTTTGTATTTTT | 50807 |
| rs77550398 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130161318 | TTACTGACTTGTGTA[C/T]GAAATACCTTTAACG | 50807 |
| rs77569195 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253460 | ATACATAGTTAGCAA[A/G]AACAAATTTTATGTG | 50807 |
| rs77580775 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327887 | GATGAAGTATGCTAC[C/G]TGAATTAAGCACCAA | 50807 |
| rs77582042 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390982 | GAGCTATTTGTATAC[C/T]CATATTCATAGCAGC | 50807 |
| rs77582488 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130426867 | TCTCACACACCATCC[G/T]TTTCATGTTTGTTTG | 50807 |
| rs77583556 | snp | C/G | 0.245631 | 0.249962 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253205 | CGCCTGTGGTCAAAT[C/G]CTAGCTCCACTACTT | 50807 |
| rs77586864 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169790 | CATTTGTAAAACTGA[C/G]GTACAGAGTATGTAT | 50807 |
| rs77587525 | snp | A/G | 0.234401 | 0.249513 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108717 | ATTAATCTTAATCAA[A/G]GGTTAAAAAGAAACT | 50807 |
| rs77591193 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130310488 | TAGATGTGTCATGAA[G/T]TGAATTAAACCACAA | 50807 |
| rs77619464 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248120 | TAGGAGCTTACTTAT[C/G]AAAGAGGAATAGTTT | 50807 |
| rs77623550 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100337 | CTTTCTTTCTTTCTT[C/T]CTTTTTTTTGAGACG | 50807 |
| rs77702475 | snp | A/T | 0.0498117 | 0.149749 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112978 | TTCCCCTTGGAAATA[A/T]CCCTTGAAGCCCCTC | 50807 |
| rs77706239 | snp | A/T | 0.241627 | 0.24986 | intron-variant | ASAP1 | GRCh38.p7 | 8:130201000 | TTCTCAAAAGTGTGG[A/T]CCTCAAATCAGTAGT | 50807 |
| rs77710315 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | ASAP1 | GRCh38.p7 | 8:130212464 | ATGAGGTGACAGAGG[C/T]AGGATATTGTAGAAG | 50807 |
| rs77714015 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292362 | ATCAGCTTTGTTAAC[A/C]GAAGTATGAATAAAA | 50807 |
| rs77731931 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130160547 | AGCAGTGAAAAGTGT[A/T]ATGATGTCGTGGAGG | 50807 |
| rs77734038 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130267139 | AAAAAAAAAACAAAA[-/C]AAAAAACAAAACAAA | 50807 |
| rs77738585 | snp | A/G | 0.251859 | 0.249993 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396989 | ACTTCCATGTGCTGC[A/G]CTCCTGTCTCCCTTA | 50807 |
| rs77745572 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130361033 | ACTCCAAGAAGGCCT[G/T]CCTTCCTCTAGGCTG | 50807 |
| rs77754549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164913 | AGTACCATGGTCAGA[A/G]CTCTCTGTGGATGGT | 50807 |
| rs77764044 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130279534 | GTGAAAATAAATTTG[C/T]TTTTGAAACAAGCGC | 50807 |
| rs77773260 | snp | A/G | 0.237882 | 0.249706 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378704 | ATGCTGAGAAGGTTC[A/G]GTCTGGCTGCAATGT | 50807 |
| rs77773581 | snp | G/T | 0.230896 | 0.249269 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220316 | AATAGCTAGTTTGTT[G/T]GGTATTGACTAAATG | 50807 |
| rs77773914 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130347242 | ATACCCTATGTGGAA[A/T]GTTGATTTTTCCTGA | 50807 |
| rs77783234 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421178 | TAGTGTTCTGCATAC[A/G]CTGGGTGCATAACAA | 50807 |
| rs77791167 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281585 | CCAAAGTGTAAAAAA[A/T]AGTTTTTTTGGGGGG | 50807 |
| rs77801024 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428445 | TCATCACCACCACCA[C/T]CATCATTATCACCAT | 50807 |
| rs77810224 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183053 | GAATAAAAGAAAAAA[C/T]AGGAAGAATTACAAG | 50807 |
| rs77813330 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272431 | CTGTGAAAAAGAGTA[C/T]GGAGATCTCTCAAAA | 50807 |
| rs77819268 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374207 | GGCTAATGACAGCAA[C/T]TTCAGAGGCTGTTAT | 50807 |
| rs77825006 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342529 | GGCCCCCTAGGGAAG[C/T]AGAGGCCCAATATAC | 50807 |
| rs77828191 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411254 | CATTACAGGCCAGGT[G/T]CATCTTACTGCAAGC | 50807 |
| rs77847984 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130331705 | GGTGCCAAGCCCTCA[A/G]AATCATGTAGCTAGT | 50807 |
| rs77860237 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188804 | TTGTGTTCTTAAACA[C/T]TATACTACAGTACAC | 50807 |
| rs77879274 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079372 | AGATCTCCTCAAGTA[C/T]ACAATTTCAGTGAAA | 50807 |
| rs77883396 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428486 | ACCACCACCACCATC[A/T]TCATCACCATCACCA | 50807 |
| rs77896596 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237903 | GGTCTGCTTGGGAAC[C/T]CCTAGATGATATGTC | 50807 |
| rs77896823 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158870 | CCAAGTAGCTGGGAC[C/T]ACAGGTGCCTGCCAC | 50807 |
| rs77897932 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139680 | GCTGCTGTAAGCCAA[A/C]GTCACGCCATTGCAC | 50807 |
| rs77900607 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074790 | GAGTGGGCTGAAAGG[C/T]TGCGGTGCTGGGACT | 50807 |
| rs77909735 | snp | A/T | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130290983 | CCTCTTCTAAAACCA[A/T]ATAATGCTTTACAGG | 50807 |
| rs77926193 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400296 | TTCTCAGACTCTACA[A/C]GTTTTCCCGGCCTAG | 50807 |
| rs77958736 | snp | G/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403572 | TTTTTTTTTTTTTTT[G/T]TGAGACAGTTTCACT | 50807 |
| rs77959101 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217920 | TGTCACAGCAGTCCA[A/G]TGAAACGAAATGAGG | 50807 |
| rs77961937 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130298630 | TTTCCAAGATAAGCC[C/T]CCCATCTTTCCAGGC | 50807 |
| rs77969337 | snp | G/T | 0.375 | 0.216506 | intron-variant | ASAP1 | GRCh38.p7 | 8:130304813 | TAAGTGTAAATATGG[G/T]AATTCAGTGCTGCTT | 50807 |
| rs77980514 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069236 | TTGATACAGTTAAAA[C/T]AAAGGTCTTTGTTTT | 50807 |
| rs78002607 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219196 | ACAGGTCTCACATGT[C/T]TTTTTTTTTTTTAAC | 50807 |
| rs78005882 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | ASAP1 | GRCh38.p7 | 8:130267896 | GAGCAGCTGAAAAAG[C/T]AGTCTTTCCTAAAAC | 50807 |
| rs78010453 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098070 | TGCTTGAGCTAAAAC[A/G]CAGTATTTAAAATTT | 50807 |
| rs78015187 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378557 | AACACGTGCAGGGAG[G/T]GATTGGAGCTGAGGT | 50807 |
| rs78015686 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151872 | ATGTCAGACAGACAC[C/T]CGAGTTTGAACTTCC | 50807 |
| rs78030960 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390432 | TTTATACTAAGGCAC[C/T]AAACTCAGTCAAGAT | 50807 |
| rs78040877 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055551 | AAAAAAAAAAAAAAA[A/G]GGCTGCTATGTACTA | 50807 |
| rs78044875 | in-del | -/A | 0.471863 | 0.115225 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148222 | ATCTGGCAGCTGAGG[-/A]AAAAAAAACCCTATG | 50807 |
| rs78052643 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314287 | TGCTCTCAAAACATA[C/T]TGAAATGATGAGGAG | 50807 |
| rs78053364 | snp | A/T | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150997 | GGAATTAAATATAAG[A/T]AAATAAAAATTATCT | 50807 |
| rs78056764 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108356 | CATATCAGGTGTTCA[C/T]CTTTCTAAACGCTTA | 50807 |
| rs78076145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119337 | TTGAGCTCCAAAGGG[A/G]TGAAGATGAGCTGTC | 50807 |
| rs78083315 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347762 | ATCAGGCAGACACCA[A/G]TGTGGTGTAGGGCAC | 50807 |
| rs78096171 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130174822 | TGTAACATGTATCAA[C/T]ATTTCATTCACATTC | 50807 |
| rs78115855 | snp | G/T | 0.0581099 | 0.160244 | intron-variant | ASAP1 | GRCh38.p7 | 8:130212330 | AATTTCCTTTAGATT[G/T]TTCTTAGACTTCTAC | 50807 |
| rs78128672 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144633 | TCTTCCCTCCAGATG[A/C]ACGTTCCAAATTCCA | 50807 |
| rs78138228 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072842 | GCGCGGGGGGGGGCA[C/G]TTTTGGGGACTGAGC | 50807 |
| rs78149066 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130326104 | GTCTATAGTTCTAAG[C/T]AGTAGAGGGTTGCTG | 50807 |
| rs78149993 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | ASAP1 | GRCh38.p7 | 8:130256088 | CCTAACGATTCAATA[C/T]TAACTTGAGGAAGAC | 50807 |
| rs78153356 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383336 | ATCCCAGACTTTTTG[A/T]CGAAAATAAATTCTT | 50807 |
| rs78156447 | in-del | -/AA | 0.488241 | 0.0757703 | intron-variant | ASAP1 | GRCh38.p7 | 8:130135529 | AAAACAAAACAAAAC[-/AA]AAAAAAGAACATGCC | 50807 |
| rs78186817 | in-del | -/AAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130348219 | TAATAGAGCTAAGAA[-/AAA]GAGCTTACATTTTCC | 50807 |
| rs78206452 | snp | C/T | 0.238171 | 0.24972 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332975 | AGGAAATTCTATTCA[C/T]ATTACAGAAAGAACT | 50807 |
| rs78221526 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264938 | AAGGAAAAGAAAAAC[A/G]TCTTAAGAAAGAGGG | 50807 |
| rs78232389 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249688 | GACAAAGAACAGTTA[C/T]TAATCTTTTAAGATA | 50807 |
| rs78237624 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284659 | CAGACTGTGATGTAG[A/G]ATGCAGCCACTGGGA | 50807 |
| rs78240509 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239930 | AAGTCCAAGTTTCCC[C/T]TGAATCAACATTTCT | 50807 |
| rs78248338 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130198705 | GGTTAAGTAACTCGC[C/T]CAAGGTCAAACAGTG | 50807 |
| rs78255946 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199170 | TGCACTTTACAATTA[C/T]CCGTGTGTTCCTTTA | 50807 |
| rs78264967 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372643 | ACATTTGCAGGAAGA[A/G]AAGATTTTTCCACAG | 50807 |
| rs78271179 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066190 | CCCCTTGCCCATATA[C/T]CAAATGTTATTAAGG | 50807 |
| rs78317276 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166705 | ACTGTGCCTGGCACA[A/C]AGCAGGTGTTAATGA | 50807 |
| rs78319713 | snp | A/C | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262395 | GAGACTCCATCTCAA[A/C]AAAAAAAAAAAAAAA | 50807 |
| rs78322376 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076092 | GAGAAAGAATGGTTC[C/T]TGGGGATTATAATAA | 50807 |
| rs78342696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413349 | ATTAACATCAGCCCA[C/T]TTGACCACACTCTTT | 50807 |
| rs78357121 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130156850 | GAACACTTTAGGGTT[C/T]GAACTATGCAACACT | 50807 |
| rs78363913 | in-del | -/A | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167315 | AAGTAAAGAAAAAAG[-/A]AAAAAAAAAAATCCA | 50807 |
| rs78376109 | snp | A/G | 0.444444 | 0.157135 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333530 | AGTAGCTTGAACCTA[A/G]GAGGCGGAGGTTGTG | 50807 |
| rs78393342 | snp | A/C | 0.0494327 | 0.149241 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314171 | AGGTAAGCTTCCTCC[A/C]CCCACTTACACCCCA | 50807 |
| rs78409005 | snp | C/T | 0.234692 | 0.249531 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143084 | GTGAATTATTCAGTG[C/T]AGAAATTTGAATGGT | 50807 |
| rs78419042 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364194 | ACTACTCTGGTTCTA[C/T]CTCCCTGTTCCTCTG | 50807 |
| rs78438157 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063026 | AATTATACTGTTGTA[C/T]AATTAATAGCATGAA | 50807 |
| rs78439789 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130345374 | TCTAGATTTAAATGC[C/T]TCCCCGTCAACTCGA | 50807 |
| rs78443800 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405740 | GACTCTGAACTAATT[C/G]GAAGTAGGTTAGCAG | 50807 |
| rs78448633 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166354 | ACGTTTTTAATTTCT[C/T]CCAGAAAACAAATGG | 50807 |
| rs78454054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240698 | CAAATAAATGAATAC[A/G]GGAGAATGTAAAGTT | 50807 |
| rs78492421 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130305705 | TATCCATCACTTAAC[C/T]ATCTCCATTTTATAA | 50807 |
| rs78493260 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251868 | CTGTAAGAAATAGAA[A/T]AAAGAAATTTGGTGA | 50807 |
| rs78498421 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280220 | TTGCTCATATTCCTC[A/G]CTGTCCCTTTTCTAC | 50807 |
| rs78498858 | snp | C/T | 0.288906 | 0.246954 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130823 | CTGAAGCGGGAAGAT[C/T]GCTCTAGCCTAGGAG | 50807 |
| rs78509390 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344681 | AGAACCTGCAGTAAG[C/T]AAGCATGATTATGTC | 50807 |
| rs78522672 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124271 | ACTGAGCATCTACTA[C/T]GTGCCAAGCACCAAA | 50807 |
| rs78536246 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101587 | TTTTTCTTTTTTTTT[C/T]TGAGACAGGGTCTTT | 50807 |
| rs78543586 | snp | C/T | 0.121022 | 0.21416 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438307 | ATGGGGCCACCAGTG[C/T]GCCAGGCCCTCCAGT | 50807 |
| rs78544780 | in-del | -/TT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130099193 | TAATTTTTTTTTTTT[-/TT]GGTGGACTGAGTCTC | 50807 |
| rs78555250 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133820 | TTCCTTCCTTCAGGG[C/G]CTGGCTCACCTGCTC | 50807 |
| rs78557212 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178605 | CAAAACAAAACTGAA[C/G]ACTCCAGGTGGAAAT | 50807 |
| rs78563125 | snp | A/G | 0.0685596 | 0.171987 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445625 | GATTCAAAAGGGAAC[A/G]CCCAGTGCGGTGGAA | 50807 |
| rs78604170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157738 | ACTACTTCCTCTTCT[C/T]CCAGGTATCTGCATA | 50807 |
| rs78606256 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130152591 | AGGACAAGATAAAAC[-/T]TTTTTTTTTTTTTTT | 50807 |
| rs78608177 | snp | G/T | 0.232359 | 0.249377 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380185 | CAACTAGATGAATGG[G/T]GAAATAAAACAGCGG | 50807 |
| rs78619392 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405945 | TAAATACTGTTCCTA[C/T]ACTAGTCAAGAAAGT | 50807 |
| rs78629627 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137976 | AGAAGCCTGGAGAAA[C/T]AAGCAATGAAACTCT | 50807 |
| rs78633501 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343274 | AAGTCACTACTAAGG[C/T]GGATACGGGCTGATA | 50807 |
| rs78641086 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286519 | CTGAAGGCCAGAATT[C/T]CTGAGTTTCTAATCC | 50807 |
| rs78641170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156088 | AAAGCAATTGCTCCT[C/T]TGTCTCTCAATAATT | 50807 |
| rs78645972 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130426067 | TGTAATTCCCAGTGT[A/C]GGAGGAGGGGCCTTG | 50807 |
| rs78651123 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319718 | ACGTATTAAAATAGC[A/G]GAGGGATGGAAAAAC | 50807 |
| rs78654382 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339623 | TAGGGCTCAAACACA[A/G]AAAAATCAATTACTT | 50807 |
| rs78657811 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130226810 | CTCTTCTGGCTTCAT[C/T]ATACAGCCTTCCTAC | 50807 |
| rs78676282 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130426433 | AAAAAAAAGGGTAAG[A/C]CAAGCTCATATCATT | 50807 |
| rs78677132 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149445 | TTTTTCAGGTGTACA[C/T]AGAAATGTATTTCTC | 50807 |
| rs78693697 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228441 | GGAGCAGTGGCTTAC[A/G]CTGGTAATCAGAGCT | 50807 |
| rs78697778 | snp | A/C | 0.0418186 | 0.138422 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316647 | CAGCTGGAGCTCTGG[A/C]AGCAATCTTAAGCTG | 50807 |
| rs78698203 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227047 | CACAAACTTTCATCA[A/G]GCACCTACAATGGGA | 50807 |
| rs78725295 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432368 | GGGCATTTTGGATGA[C/T]GGGAACAGCAAGACT | 50807 |
| rs78736220 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109435 | TCTTTCTCCTCTTCG[C/T]TTTTGTGGGGACTTT | 50807 |
| rs78805487 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428421 | TCACCACCACCATCA[C/T]CATCATCATCATCAC | 50807 |
| rs78814423 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352821 | GATACTGAATCTACA[C/T]TCTGTATCTTCATTC | 50807 |
| rs78834430 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117723 | AACAATGAAAACTCA[C/T]AAATATGGTTGACCT | 50807 |
| rs78835655 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121368 | TTTAGCACCATCCCT[A/G]ACCTCTACCCACTGG | 50807 |
| rs78838731 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169339 | TGGAAATTACAGTTG[C/T]AGTCCCAAAACAGTG | 50807 |
| rs78873912 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393028 | AATAAACCTTTTTTT[A/T]AACATGACAGTTATA | 50807 |
| rs78874739 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292312 | CAGCCTTGTCTGCGC[A/G]TGTGGGTAATAAGAT | 50807 |
| rs78875356 | snp | G/T | 0.040671 | 0.13668 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356993 | CCAATGGTGCCATTT[G/T]CAGTTGAAATACGTT | 50807 |
| rs78884089 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130185210 | AAAATTGTTGACAGG[A/G]ATTTACTAAGCAAAC | 50807 |
| rs78904133 | snp | C/G | 0.0520825 | 0.152737 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239701 | GACTGAATCCAATGG[C/G]TTTATTCTTAGATGA | 50807 |
| rs78921004 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375041 | TGGCTGCCTCACCTC[A/G]TCCACTTGCACATTT | 50807 |
| rs78926849 | snp | A/C/G | 0.100156 | 0.204873 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064696 | CTACCTGGAGACAGC[A/C/G]TTAGATCCCACAGCT | 50807 |
| rs78928123 | snp | A/T | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130260123 | TTCTTTCCATTCAGT[A/T]GTTATTCCCAATGTT | 50807 |
| rs78949756 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130140112 | ATCATAGATCACTGC[A/T]GTCTCAACCTCCTAG | 50807 |
| rs78950687 | snp | A/C | 0.0528381 | 0.153711 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281019 | TTTTTCCAAATAACA[A/C]ATAGGTTTAGAGTAC | 50807 |
| rs78955596 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077791 | CTTGATCTTCACTGC[C/T]CTTTCCTCAGCTCAC | 50807 |
| rs78960866 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130363121 | CTCAGTGTTCTGAGA[A/G]TTCAACGAGCTAAGG | 50807 |
| rs78967757 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120774 | TCTGTGGCCATAGGA[A/G]GTATCTGGCCTCTTA | 50807 |
| rs78997077 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301317 | ATTCCACCCACAAAC[A/G]AAACAGTGTGTTCTG | 50807 |
| rs78999189 | snp | A/T | 0.040671 | 0.13668 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094514 | CGCCTAGTCTAAATT[A/T]AAAAAAAAAAAATGT | 50807 |
| rs79014478 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439081 | GGTGGCCCAGTGGAA[C/T]CACTTTAAGGGTCCT | 50807 |
| rs79034127 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130194071 | ATTAAGAATTTCTCC[A/G]TGGTTATCTACACAC | 50807 |
| rs79054068 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274471 | AACAGCTGTGGTTTA[C/T]GGTCTGAACCCTTGC | 50807 |
| rs79056048 | snp | C/G | 0.000313079 | 0.0125077 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159835 | TAGGTTAATCACACA[C/G]TGAGACACTGGGCTG | 50807 |
| rs79091711 | snp | G/T | 0.00199192 | 0.0314959 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130115703 | TTCTACGTGGACGTG[G/T]GGATTGAACTTTCCA | 50807 |
| rs79096708 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155174 | AGTTTTACTTACACA[C/T]GTATATTATGGAAAC | 50807 |
| rs79100062 | in-del | -/AAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130282082 | TCGAAAAAAAAAAAA[-/AAA]GGAATGGCATGGCAA | 50807 |
| rs79129799 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204239 | ACTTATGAGAATCTA[A/C]TGATAAATGTAATGT | 50807 |
| rs79137548 | snp | C/T | 0.031825 | 0.122064 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078627 | AGTGTCAGATATTCT[C/T]CTCACTCTGGAAAAA | 50807 |
| rs79140028 | snp | C/G | 0.0505692 | 0.150756 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364835 | AGGGCTTGGCTCTGA[C/G]TCATCTCTCACTTGG | 50807 |
| rs79146269 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258831 | TAACATACGTGGTGG[C/T]TGACTGATTTGCTGA | 50807 |
| rs79154264 | snp | C/G | 0.0482946 | 0.147699 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116218 | ACTAATGTGAAGGCC[C/G]TGACTTGCTAAGCAA | 50807 |
| rs79162713 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130290804 | TCCTCATGCCTGGTA[C/T]TACAGGATCAATTTT | 50807 |
| rs79168379 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425892 | AGCTTAGCCATGGTT[C/T]GGATGAGTTGAGGGA | 50807 |
| rs79183864 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128494 | AAATGATGAGAAATG[G/T]AGAGGAGCCAGGAAA | 50807 |
| rs79190708 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | ASAP1 | GRCh38.p7 | 8:130225774 | TAAAGTACTCAGCAA[C/T]AAGGAAGTCAGTGTT | 50807 |
| rs79200683 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390983 | AGCTATTTGTATACC[C/G]ATATTCATAGCAGCA | 50807 |
| rs79205769 | snp | C/G | 0.242488 | 0.249887 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137168 | TACATTTTCAGCAAA[C/G]AAGAAACAGACATCT | 50807 |
| rs79211092 | snp | G/T | 0.0322114 | 0.122752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422060 | CAAGAAGGTGGTCAA[G/T]TCTACCCAGAATCAG | 50807 |
| rs79213223 | snp | C/G | 0.0501905 | 0.150254 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362365 | TGGAATGACGACAAT[C/G]GCTAAAGTGGGAAGG | 50807 |
| rs79216291 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438590 | GAGAGGACTTGGGGT[A/G]CGAGGCGGGGAGCTG | 50807 |
| rs79225486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374606 | AGCTTACATACTTGT[C/T]GACTTTAATAAAATG | 50807 |
| rs79226896 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130386061 | CAGAGATTTTGCAAA[A/C]TCTTCTGGGAAGAAG | 50807 |
| rs79233826 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081216 | TGAAGAACTTTCTAG[C/T]GGGTGAGCAGCAAAA | 50807 |
| rs79241369 | snp | A/C | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272287 | AAACCATAATGACAT[A/C]TCATCTTATCCCAGT | 50807 |
| rs79247144 | in-del | -/AAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130265590 | AAAAAAAAAAAAAAA[-/AAA]GGTCAGGTTTGGCAG | 50807 |
| rs79254150 | snp | C/T | 0.030665 | 0.119967 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289822 | TTGTTTATTATACAA[C/T]ATACCCCACAGGGAC | 50807 |
| rs79259153 | snp | C/G | 0.040671 | 0.13668 | intron-variant | ASAP1 | GRCh38.p7 | 8:130433832 | CACCCTTAAAAAACT[C/G]TGAGAGTTTTCACAA | 50807 |
| rs79260427 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399760 | AAATCTGAAACATAA[A/G]TATTACCCCTTTTTC | 50807 |
| rs79272541 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121995 | CGCCACATCTTCCTT[C/T]ATGACATAGCTCAAA | 50807 |
| rs79288449 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286241 | TTCTTATAAAACACT[A/G]GAAATAGGCTTTGGC | 50807 |
| rs79290073 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314983 | ACCTTTCTGAATTTC[A/G]GTTACCGATTTGTAA | 50807 |
| rs79291630 | snp | C/T | 0.0452528 | 0.143452 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295364 | TTTCTTCAAAGACTA[C/T]CACATTGATTAGCCA | 50807 |
| rs79315592 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077832 | CCTGTCTCTGGGCAA[C/T]GGGGGAATATTGCTG | 50807 |
| rs79318230 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062322 | GAAGAAACAGATAAA[A/C]CTCATGTTGTAAATG | 50807 |
| rs79334861 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352004 | CCTTTGCTGGTTTCA[C/T]CCAGACAAAACCTCA | 50807 |
| rs79345439 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277856 | GCCCATCACATGGAC[A/G]TAGCAGGACAGTTTT | 50807 |
| rs79347343 | snp | A/C/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323645 | TCCCATTTCCAGCCA[A/C/G]AATGCAGCCTCCACT | 50807 |
| rs79357581 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066491 | GCTAGGATTAAAGGC[C/T]TGAGCCACAATACCT | 50807 |
| rs79374717 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130121925 | CTACACGATCTGGCT[A/C]CACCTCTATCTTGCC | 50807 |
| rs79376657 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355856 | TTAAAATATGCCGAC[C/T]GGAGACAATGTTTTC | 50807 |
| rs79377815 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393030 | TAAACCTTTTTTTTA[A/C]CATGACAGTTATATT | 50807 |
| rs79381620 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110570 | ATTTAAAAACATACA[A/T]TTTAGTACAATGTAT | 50807 |
| rs79384410 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157999 | TTCTCAGGACCTAGA[A/T]GAGTGAGTCCTAGAC | 50807 |
| rs79391119 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423121 | TTTATACTTTTTTTT[G/T]GAGACAGAGTCTCGC | 50807 |
| rs79426037 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130300184 | GAGAGAGAGAGAGAG[A/C]GAGCGAGCGAGCGAG | 50807 |
| rs79443922 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130120117 | CAGTTGAGAAGAGAC[A/C]AACTGATTCTACTAA | 50807 |
| rs79451192 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | ASAP1 | GRCh38.p7 | 8:130433258 | AAGAGTTTCACCTTT[C/T]TCCTTGAACACATTT | 50807 |
| rs79456029 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314662 | CAGTGGCACCTGCAA[A/G]GTGGGGACCTGCAAA | 50807 |
| rs79457215 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334927 | TCCAAATACATATCA[C/G]ACCTCCAACCCTCCT | 50807 |
| rs79458779 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370794 | CTAAGTCAAAAGTCA[A/G]ATACAAAAGACCACA | 50807 |
| rs79459063 | snp | C/G | 0.264358 | 0.249587 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159148 | ATACTCCAGGAGAGA[C/G]AGCAGCAGCTCACCC | 50807 |
| rs79473162 | snp | A/G | 0.232359 | 0.249377 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112775 | CCTGCAAAGTAAACG[A/G]ATTCACACCCACTGC | 50807 |
| rs79473243 | snp | C/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062781 | ATAACGAAAAAAATG[C/G]CACCCATCTGAATGC | 50807 |
| rs79480760 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073431 | TGTGGAGCTTTCCAG[A/G]TGGGTGTAAAGCTGT | 50807 |
| rs79497307 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352977 | TTTTTTGAGGGCAGG[G/T]TTCTTCTTCATTGTA | 50807 |
| rs79502257 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428958 | GGGCCACACCCTCTC[C/T]GGTTCTTCTCAGAGA | 50807 |
| rs79510747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130420310 | TCTTGGCGAGGATGT[A/G]GAGAAACTGGAACCC | 50807 |
| rs79511348 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173931 | AAAAAGAAAAAAAAA[A/T]TTAGCTTGGCGTGGC | 50807 |
| rs79519224 | snp | A/C | 0.325799 | 0.238232 | intron-variant | ASAP1 | GRCh38.p7 | 8:130267134 | CAAACAAAAAAAAAA[A/C]AAAACAAAAAACAAA | 50807 |
| rs79521734 | snp | A/G | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432139 | GAAAGGAGGAAGATG[A/G]GGGAACAGAGGCAGG | 50807 |
| rs79523818 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144938 | TGTTTTTTATTGCAG[C/T]AAGGAATCGGTTACC | 50807 |
| rs79530975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280105 | TTTTGCTGACAAGGA[A/C]ACCATGGTTCAGAGG | 50807 |
| rs79559002 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123110 | TGTGTGGCTCTACCA[C/T]AGAGTATTTCATCAG | 50807 |
| rs79573614 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158938 | GGGTTTCACTGTGTT[A/G]GCCAGGATGGTCTCG | 50807 |
| rs79588759 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360920 | TCTGGAAAATTCTGT[A/G]ACTTGGAACAAATAT | 50807 |
| rs79600047 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428458 | CACCATCATTATCAC[C/T]ATCATCATCACCACC | 50807 |
| rs79601215 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360523 | ATGCTCATCAATGTC[C/T]TCTAAGAGGCCATGC | 50807 |
| rs79605028 | snp | C/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105498 | ACATTTAAAATCTAT[C/T]CTCTTAGCAATTTTC | 50807 |
| rs79608568 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278257 | TTTCAAGGTATTGAG[C/T]CCAGATCTTTAGGAT | 50807 |
| rs79608680 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164059 | AATGCAAGGTATCAA[G/T]GGAGTGGGCAAAAGA | 50807 |
| rs79616166 | snp | A/C | 0.0475351 | 0.146656 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233785 | GAGACTTTGATGTGC[A/C]AAACACCTAACACCC | 50807 |
| rs79628150 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | ASAP1 | GRCh38.p7 | 8:130442190 | CACTAAAGTGGTGAA[C/G]GCTGTGACGCAAAGA | 50807 |
| rs79652644 | snp | G/T | 0.039522 | 0.134904 | intron-variant | ASAP1 | GRCh38.p7 | 8:130442668 | TAAAGTTGAGGTCAA[G/T]TTAACGATGATGGTC | 50807 |
| rs79654892 | snp | C/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344706 | TATGTCACTGCATTC[C/G]AGCCTGGGCAGCAGG | 50807 |
| rs79659033 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176562 | ACCTAGGGGACATTC[A/G]TCTACCAGATTGCAA | 50807 |
| rs79681067 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132778 | AATAATGAATAGCTA[A/T]TTAGACCTTTCTCAT | 50807 |
| rs79701243 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130221639 | TGGGGTTTTTCATTT[C/G]TTTTCCGTGAGGCCC | 50807 |
| rs79704611 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333212 | GTTGGATTTAAAAGG[C/T]TATTTTATAAAGAAT | 50807 |
| rs79707915 | snp | C/T | 0.235854 | 0.249599 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154877 | GAGCTAAATCACATA[C/T]TTTCTTCTAGAAGTA | 50807 |
| rs79726229 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332217 | TGCTCTGCATCTTTC[C/T]GGTGCTTTTCAATGA | 50807 |
| rs79726935 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130136561 | CAATCACCTAGTGGC[-/T]TTTTTTTTTTTTTTA | 50807 |
| rs79731452 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237604 | CTGGTAATGCTTTTA[A/C]ATGATTTCTTGGATG | 50807 |
| rs79746402 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130326389 | ACTTTTATAAAACAT[A/C]AGTGCTGCAATAGGA | 50807 |
| rs79748298 | snp | A/G | 0.120674 | 0.21395 | downstream-variant-500B | ASAP1 | GRCh38.p7 | 8:130051739 | GCAGGCAGAGTGCCT[A/G]GGCCAGGTCTGCTCC | 50807 |
| rs79759689 | snp | A/G | 0.134802 | 0.221877 | intron-variant | ASAP1 | GRCh38.p7 | 8:130331941 | TCTGTGTGAAGTCTC[A/G]GCCCAAGGTCTAGGT | 50807 |
| rs79770926 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435111 | CATACTCATTATCGC[A/G]CTGTAACCTGGCGGG | 50807 |
| rs79790211 | snp | G/T | 0.0696718 | 0.173152 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295876 | TTCAAAGTTAAATCT[G/T]AAGTATAGGAGCTGC | 50807 |
| rs79814615 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428442 | TCATCATCACCACCA[C/T]CACCATCATTATCAC | 50807 |
| rs79826968 | snp | G/T | 0.250168 | 0.25 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432386 | GAACAGCAAGACTGT[G/T]AAAGTATAAAGGTTC | 50807 |
| rs79829215 | snp | A/C | 0.0839998 | 0.186933 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421971 | GCTCTCAGAAAGCCA[A/C]AAAATAGTGGGGGAG | 50807 |
| rs79830692 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130320292 | CAGGAACAGTGGCTG[G/T]CGCCTGTAATCCCAG | 50807 |
| rs79846962 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130188751 | AAAAAAAAAAGAAAA[A/G]AAAAGAAAATTGAAT | 50807 |
| rs79871821 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | ASAP1 | GRCh38.p7 | 8:130440662 | TCACCTTGCGCCATT[C/T]CCCCCATCTCTCCCT | 50807 |
| rs79876138 | snp | A/T | 0.0505692 | 0.150756 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115544 | AACCACAATCAATCA[A/T]TCTCACCAAAAATGG | 50807 |
| rs79887288 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141608 | CACATCGGGTACTAG[C/G]AAGATCATGGCTCAT | 50807 |
| rs79889256 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364067 | GTAATAATAATAATT[A/T]AAAAAAGCCAATTCT | 50807 |
| rs79894749 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335262 | ATTGGATGCCGATCA[C/T]GCAACAGACCCTCAG | 50807 |
| rs79899966 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208380 | AGTTATCAAACTGTT[C/T]CATCAATACAAAGCA | 50807 |
| rs79903422 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130334412 | CCAAAAGTTCTACTT[A/G]TGTTTCACATAGATT | 50807 |
| rs79909153 | snp | A/C | 0.0337553 | 0.125452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130266562 | ACATCAGGCCATATA[A/C]ATTTCCCACAGAGAA | 50807 |
| rs79915287 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130167923 | TTGCTTCTGGTTTTT[C/T]AAAGGGTGGTAATGA | 50807 |
| rs79918848 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295351 | ACTCTTTTTTTTTTT[C/T]CTTCAAAGACTATCA | 50807 |
| rs79920663 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133829 | TCAGGGCCTGGCTCA[C/T]CTGCTCCTCTTACAA | 50807 |
| rs79924231 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401735 | TGTACAAATGCTAGA[A/G]ATCTGTTCTCCAATA | 50807 |
| rs79928066 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336785 | TTGTCTCTAAAAGAC[C/G]GTAAGCCAGATAGAT | 50807 |
| rs79931018 | snp | C/G | 0.0532157 | 0.154195 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408500 | TACACCATCAGTTCC[C/G]CTGGTTTTTAGACCT | 50807 |
| rs79952265 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407605 | TTAAAGCACCTGCCT[A/G]CTAAAGTGAACCAGA | 50807 |
| rs79953081 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330426 | TATCACAGCTCTGAC[A/C]GGTCTATGCTATATT | 50807 |
| rs79992204 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | ASAP1 | GRCh38.p7 | 8:130398903 | TAGTGTGGAGGAAAA[G/T]ATTTGTCCTCCAATA | 50807 |
| rs80015622 | snp | A/C | 0.0422008 | 0.138995 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350855 | ACAGCCCTGAAGAAA[A/C]TGCAACTGAGAGTAG | 50807 |
| rs80016886 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342318 | CAGTTTTCTCATCTG[C/T]AAAATGAAGTTAATA | 50807 |
| rs80020748 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ASAP1 | GRCh38.p7 | 8:130235073 | TAAATTTATGGTAAG[A/G]AAATGTAAGACTCCT | 50807 |
| rs80028384 | snp | A/G | 0.0696718 | 0.173152 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444475 | AGACATCAGAGAAAG[A/G]AGGATTTTAATTTGT | 50807 |
| rs80032286 | snp | C/T | 0.255782 | 0.249933 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411512 | CTCTGTCTCCCTTCC[C/T]CATTCCTCCACCTGT | 50807 |
| rs80037978 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317089 | GTTTCACATCATGCT[C/T]TTTTTTTTTTTTTAA | 50807 |
| rs80038485 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ASAP1 | GRCh38.p7 | 8:130186545 | TGGTATGATACACAC[A/G]GTATCGAGATGGGCC | 50807 |
| rs80041919 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241386 | TATTTTTCTCTCTAC[G/T]AGAAGAATGGAAGTT | 50807 |
| rs80046180 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110339 | GATAGGTCCCCACTG[C/T]TATGTTGGTAACCAC | 50807 |
| rs80053904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280789 | TGTTAGAATTTAACA[C/T]TTCAGTTTTTATTGA | 50807 |
| rs80056438 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309646 | GAGTGCTATGCAGAG[A/G]GTAGCACAAAGAAGA | 50807 |
| rs80058714 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396120 | ACAGACCCTGGCACT[C/T]AGTAGGTCGTCAGAA | 50807 |
| rs80059364 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439208 | AACCACAAGCCAAGA[C/T]ATGCAAGTGGCCTCC | 50807 |
| rs80068567 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348504 | ACCACAAACAGCACC[A/G]TGACAGAGGGCTGTT | 50807 |
| rs80074414 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233104 | CCCTATCAGGCCTCA[A/G]TAGTCTGTGAGGAAC | 50807 |
| rs80075568 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222958 | AGAAACCTGAAAATC[C/T]AGGTCTTAGCTCCAG | 50807 |
| rs80098648 | in-del | -/TT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130242300 | AACTTTTTTTTTTTT[-/TT]AACTCACTTGGAAAA | 50807 |
| rs80105663 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087923 | CAATGGCCAAGACAG[C/G]GGTTTGAGACTTTTG | 50807 |
| rs80108060 | snp | G/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152607 | TTTTTTTTTTTTTTT[G/T]GGTAAAGGAATATCT | 50807 |
| rs80117223 | snp | A/G | 0.21695 | 0.247806 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179053 | CTTCTTGTAAGGAAG[A/G]CAATATTTTTAAGCC | 50807 |
| rs80121461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130268869 | CCTTGAAGCATTCCC[C/T]CATCAATTTTGCCAA | 50807 |
| rs80134793 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, missense | ASAP1 | GRCh38.p7 | 8:130357708 | CAGGAGGGTCACGAA[A/G]ATGTGGAAGCGCCGA | 50807 |
| rs80144607 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319341 | ATAAAAGTATGTTGA[C/G]AAAAATTCCTGGCAC | 50807 |
| rs80150151 | snp | C/T | 0.0456336 | 0.143994 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130358941 | GTACGTGTTCTTTTT[C/T]AGTCGCGTGTGGGTG | 50807 |
| rs80153538 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | ASAP1 | GRCh38.p7 | 8:130194969 | GACATAATACAATAA[C/T]AGTATCAGTAAACTT | 50807 |
| rs80165712 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114443 | ATCTATGTAGGACAC[G/T]TTCCATAAATGGAGC | 50807 |
| rs80176141 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356506 | TGTTTAATCCCAGAC[A/G]AGTATAACAGACTGG | 50807 |
| rs80215014 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396857 | CACAGAGGTTTCTCA[A/T]GGGCTTGGTTGAGGA | 50807 |
| rs80222364 | snp | A/T | 0.231775 | 0.249335 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418666 | CCCATAAGCAGTCAC[A/T]CCCCGTTCCACCCTC | 50807 |
| rs80223438 | snp | C/T | 0.244776 | 0.249945 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128745 | GCTACTAAAATAACC[C/T]AGAAACCCAACAACA | 50807 |
| rs80230739 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132967 | GTGTGTGAGCAATAA[C/T]AAAAGTAAGCGAGTG | 50807 |
| rs80237624 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245547 | CTAAGGATTTAGTCC[A/G]TCCAAGAAAACACCA | 50807 |
| rs80251169 | snp | A/C | 0.0513262 | 0.151752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390763 | GCTACTATCACAAAA[A/C]CAGAAAATAACAAGT | 50807 |
| rs80255221 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130098504 | GCCTGCCACCACGCC[C/T]GGCTAATTTTTGTAT | 50807 |
| rs80310832 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330661 | AAAGGCAATTTGTCT[C/T]ACGGGTAAGCTTTAC | 50807 |
| rs80327240 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205194 | TTCCTTCCTCTCACA[G/T]AGAACCAAAACTCTA | 50807 |
| rs80327396 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380270 | CCTTCGGGAGATGCT[A/G]GAGAACACACCTCAG | 50807 |
| rs80335278 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432403 | AAGTATAAAGGTTCT[C/T]CATTTTGGAAGAGAA | 50807 |
| rs80353678 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122535 | GACCAAATGCTGCTC[C/T]AAGCACTTTTTATTC | 50807 |
| rs111228099 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332974 | AAGGAAATTCTATTC[A/G]CATTACAGAAAGAAC | 50807 |
| rs111250035 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403604 | GTTGCCCAGACTGGA[A/G]TGCAGTGGCGCGATC | 50807 |
| rs111255077 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130323734 | TTAAAATTAGGCATA[C/T]TATGTATGTAAGGCC | 50807 |
| rs111269010 | snp | C/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069711 | AACCCCTCCGCTCTC[C/G]CAACATTAAACGGCC | 50807 |
| rs111274605 | in-del | -/AAAAGAAAAAAG | 0.353587 | 0.22753 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197446 | AGAACAGACTGTCTC[-/AAAAGAAAAAAG]AAAAGAAAAGAACTG | 50807 |
| rs111275430 | snp | A/T | 0.0509478 | 0.151255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098367 | ACTTTTTTGAGATGA[A/T]GTTTTGCTCTTTGTT | 50807 |
| rs111294529 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222764 | TCCTGCATTATCTCG[C/T]TCAGTGTTCACAATT | 50807 |
| rs111297268 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355696 | CCACCTAAGATATTT[A/T]TAATAATGCACTACT | 50807 |
| rs111301342 | in-del | -/ATAC | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373110 | CACACAGAAATACAT[-/ATAC]ACACACACACACACA | 50807 |
| rs111306091 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425956 | GTCCCCACCACTGCC[A/G]CTGCTTCCACTCTCA | 50807 |
| rs111307562 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419604 | GGTCCTCCCTTTTCC[A/G]TCTGACTCTGCACCC | 50807 |
| rs111336952 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130099347 | CCACGCCTGGCTAAT[A/T]TTTTTTGTATTTTTA | 50807 |
| rs111359109 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133943 | TGATTAAAAGATGCA[G/T]AAGGCACGGTCCTTG | 50807 |
| rs111366958 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124181 | CCTATTATTTGTTTT[C/T]GAGATTTATGAATAT | 50807 |
| rs111373607 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245702 | GTTAGGCCCAGAGTA[A/G]GGCTCAATAAATATC | 50807 |
| rs111389154 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286675 | TACCCAATAAGGGTT[A/G]CCCATCATCATCTTC | 50807 |
| rs111406677 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376965 | CATCCAAGTTGAAAT[A/G]GGGCAAGAGATGTGA | 50807 |
| rs111435544 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428708 | CACCATCATCATCAC[C/T]ACCACCATCATCATC | 50807 |
| rs111442735 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130363006 | AAAAAGATAGGCTCC[C/T]GTCTCTGCCATGAAG | 50807 |
| rs111465023 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327629 | CCAACAGCAGTGGAA[C/T]AGCTGCTAAAGTAAG | 50807 |
| rs111466250 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400190 | CAACCACCCCTTCTA[A/G]CACCCACACACTTTC | 50807 |
| rs111489250 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054103 | TAAATCCACTTGTCT[A/G]AACTTGCATGAGGCT | 50807 |
| rs111498219 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309502 | CATAAGATGAGGCAC[A/G]GTATGCAACTGCTGC | 50807 |
| rs111515982 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087349 | ACATGGTGAAACCCC[A/G]TCTCTATTAAAAATA | 50807 |
| rs111517999 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417070 | TACACACATACACAC[A/G]TGCAAAGTGCAACCC | 50807 |
| rs111540991 | in-del | -/A | 0.335101 | 0.23507 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245407 | GGAATTTGACCAAAG[-/A]ACAGGAAAGATCTGT | 50807 |
| rs111541525 | snp | A/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100099 | TCCATACTGTTTTTC[A/T]TTAGTACCTGTACTA | 50807 |
| rs111544957 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283737 | GTTGAGACTGGATAC[A/G]TGAGGAAGGGTCAGA | 50807 |
| rs111550458 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382481 | AGGAGAAGCAGAACA[A/G]GGAGGAAGGACCAAA | 50807 |
| rs111562881 | snp | C/G | 0.0509478 | 0.151255 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085588 | AAAATTAAAAAATCA[C/G]CTGGGTGTGGTGTGA | 50807 |
| rs111563482 | snp | C/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130103411 | ATATATTTCTGCTCT[C/G]ATCTTTTTTCTTTCC | 50807 |
| rs111565075 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074485 | CACACACACACACAC[A/T]CAGAGAGAACGAGAG | 50807 |
| rs111566674 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118427 | TATAATGTTAAAATA[A/C/G]GTCACCTTTTAAACT | 50807 |
| rs111568270 | snp | C/T | 0.0349115 | 0.127424 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445207 | CCTTGTATGGCTGTT[C/T]TTGGCACGCAGCTCA | 50807 |
| rs111582380 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167719 | CAAAATTCTATTATA[C/T]ATTTGGTTTTCTTAC | 50807 |
| rs111583154 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154409 | ACAGACGAGACTGCA[C/T]GTGTGGTAGATCTGC | 50807 |
| rs111583310 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234969 | CTACCATTTGTTAGG[C/T]ACCTACTATGTGGCA | 50807 |
| rs111586043 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ASAP1 | GRCh38.p7 | 8:130089039 | GAGAGAAGCAGCACA[C/T]GCCCTCAGAAGGAGT | 50807 |
| rs111586129 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124233 | AGAATACAAACCACC[A/G]TCCATCTGGTCTACA | 50807 |
| rs111595456 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126733 | CATTTCCTGACACTA[C/T]GTGTGTCACTATCAT | 50807 |
| rs111604364 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153172 | TTACAGGCTCCTGCC[A/G]CTGCGCCCGGCTAAT | 50807 |
| rs111604423 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130130463 | TTCTAGAGAAAATAA[A/T]TCAAATTTGGTGGAA | 50807 |
| rs111611604 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130429042 | TTCCCTGAATTGTAG[C/T]TGCATCACTGCAGTC | 50807 |
| rs111619487 | in-del | -/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333918 | TGAAGCCTCATGGGT[-/G]TTGGGCCACAGTGTG | 50807 |
| rs111624831 | in-del | -/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323629 | GTCTGTTCCCCCTAA[-/T]TCCCATTTCCAGCCA | 50807 |
| rs111630821 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227276 | GTTTTTTTTTGAGAC[A/C]GGATCTCACTCTGTT | 50807 |
| rs111643224 | snp | A/G | 0.00268513 | 0.0365425 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130116920 | GAGCAAAAGCTTCAA[A/G]CACTCAGGTTTACTG | 50807 |
| rs111684170 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307511 | TAGCAATCCAGAGCA[A/G]AGTGGTAAAATTTTA | 50807 |
| rs111685612 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253850 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 50807 |
| rs111690101 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104735 | CAACGACTATAAAGA[G/T]AATTCATGATGTAAG | 50807 |
| rs111698638 | in-del | -/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399397 | TAATTAATATCACCT[-/G]AAAAGATACCTGCAA | 50807 |
| rs111710402 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327483 | TGTAAGACCACAGGT[A/G]AAGATTTTATGTTAC | 50807 |
| rs111740791 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288265 | CCTTTCTGGTTCCAG[C/T]ATTTGACTTCGAGGG | 50807 |
| rs111754194 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404084 | GACTGATTAATATCT[A/G]CTAATTTTCTTCAAT | 50807 |
| rs111756598 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377396 | AAAAAGAATTCCTGA[C/G]ACCATGTGTGATCGA | 50807 |
| rs111765853 | snp | C/T | 0.114036 | 0.209795 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397203 | TGGAGTGCAATGGCA[C/T]GATCTCAGCTCACTG | 50807 |
| rs111808729 | snp | C/T | 5.45539e-05 | 0.00522245 | intron-variant | ASAP1 | GRCh38.p7 | 8:130061079 | GTGCCACTGTGGAAG[C/T]AATCAAAAACAAGGA | 50807 |
| rs111814988 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406330 | ACTGGATGATGATGA[A/T]GATAATGATGATGAC | 50807 |
| rs111821974 | snp | C/T | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409287 | ACAAAAAACCTCCTC[C/T]CCTGTGGTGATTCTT | 50807 |
| rs111828206 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149606 | ATTTGCAAAGGTGAC[A/G]CTGATGAGGGCCTTC | 50807 |
| rs111831017 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374509 | CGCCTGTAATCCCAG[C/G]ACTTTGGGAGGCCGA | 50807 |
| rs111841025 | in-del | -/G | 0.0640965 | 0.167152 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078774 | AACAAGTAGGCTGGA[-/G]AGCTGGCTCTGACAT | 50807 |
| rs111853071 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187637 | TTGCCCAGGCTGGTC[G/T]TGAACTCCTGGGCTC | 50807 |
| rs111859390 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076200 | CCTTTCGTCATTTAA[C/T]GTGTATTTACTAGGC | 50807 |
| rs111859588 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127550 | TTTTTTAGGATAAGT[A/G]AACTACGAATCAGAA | 50807 |
| rs111884491 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063217 | GGTCTCCCTCTGTTA[C/T]TGAGGCTGGAGTGCA | 50807 |
| rs111885661 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130142711 | GTGTGATAAGCAGGT[C/T]CAAAGGCCTGGGGCA | 50807 |
| rs111888778 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117955 | TGCTTGTTTACACAT[G/T]GTCAGTGGCTGCTTT | 50807 |
| rs111888875 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126909 | ACTCCTACTAGCTGT[G/T]TGACCTTATGCAAGT | 50807 |
| rs111893011 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251409 | GGCGATAGAGTGAGA[C/T]TCTGTCTTAAAATAA | 50807 |
| rs111897232 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130242635 | TCTCATGCAGCCTCA[C/T]AGCCAAATCAGTAAA | 50807 |
| rs111903310 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189821 | TTGCTAGCATCCATT[A/T]CTGTTTTTTTTATAA | 50807 |
| rs111916627 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254333 | ATTCACGGCACTTAA[A/G]ACAAGAATGTGACTA | 50807 |
| rs111932352 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145098 | CTAGATAGTCATCCA[C/T]GCAGGCATTTCTGCA | 50807 |
| rs111944242 | in-del | -/AC | 0.174932 | 0.238463 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373014 | GACACAGACACACAT[-/AC]ACACAGACACACACA | 50807 |
| rs111983301 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394492 | ACTTTATTAGCAATT[C/T]TAATGTCGTCCCGGT | 50807 |
| rs111986064 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220221 | GATTTCAACTGCCAG[C/T]ATTTCTGTGGGGAAA | 50807 |
| rs112012963 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375037 | TCACTGGCTGCCTCA[C/T]CTCGTCCACTTGCAC | 50807 |
| rs112024871 | snp | C/T | 0.0520825 | 0.152737 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295153 | CCAGGTGTGGTGGCA[C/T]GCACCTGGAGTCCTA | 50807 |
| rs112031137 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343009 | ACTAAGCCAAAAAGG[C/T]TTTCAGCTGGAGAAA | 50807 |
| rs112031709 | snp | C/T | 3.29919e-05 | 0.00406138 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057924 | TGCTGTATGAATGTA[C/T]GGATGAAGTGGATGG | 50807 |
| rs112056666 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144688 | TAAAGCTCTCACATC[A/C]CCTGTGTGATCCTTC | 50807 |
| rs112063030 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258417 | GTGAAGCTGTCACAG[A/G]CCACCCTGATAATTC | 50807 |
| rs112067529 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321478 | TGGGACCTCAATTTC[C/T]ACATTTACAAAAAAG | 50807 |
| rs112085116 | in-del | -/TTTC | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100314 | ATTTATATGTCGTGT[-/TTTC]TTTCTTTCTTTCTTT | 50807 |
| rs112096914 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153022 | TACAGCACTGCTTTT[C/T]AATTTTTTTTTTGAG | 50807 |
| rs112101235 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151340 | TGCACCACTGCACTC[C/T]AGCCTGGGTGAAAGA | 50807 |
| rs112162058 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432099 | GAAGGGGGAGGAAAG[A/G]GAAGAGGGGGAGAGG | 50807 |
| rs112205590 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406114 | TGTTGTTGTTAAGGG[C/T]AAAACAAAGAATACA | 50807 |
| rs112213294 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | ASAP1 | GRCh38.p7 | 8:130200081 | GGCTACTGGCAGTTT[C/T]CCCCCACTTCTTGAC | 50807 |
| rs112245496 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209352 | TTCTCAAAGTATGGC[A/G]CCTAGGCCCCTAGAG | 50807 |
| rs112246255 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130268523 | CACACACACACACAC[A/G]CACACACACACAACT | 50807 |
| rs112272528 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229433 | CATTTAAGAATGAGG[A/C]AAATGCATTTTGAAA | 50807 |
| rs112274083 | snp | C/T | 0.0658359 | 0.169067 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209795 | TTTTTAGTGGAACAC[C/T]TTTTTTTTTGAAAGA | 50807 |
| rs112276383 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323241 | ATGGACTGCTATGCC[A/G]TTCTATTCAAGCCTG | 50807 |
| rs112288308 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253412 | ATTTGCAGATGCATA[C/T]GCTTTGATTTTTTTC | 50807 |
| rs112291639 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126851 | AACCGCAAAAAAGGT[A/G]TATCACAGTGCTTAA | 50807 |
| rs112310636 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226043 | CACTACCATGCTTGG[C/T]TTTTTTTTTTTTTTT | 50807 |
| rs112341251 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381112 | GCTGGTCTTGAACTC[C/T]GGACCTCAAGTGATC | 50807 |
| rs112367370 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272645 | AAGATGTAGTATATA[C/T]ACAAATGGAATACTA | 50807 |
| rs112400967 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115324 | CAACATTAACTCCTG[A/C]TGGGATTTCCAGCCT | 50807 |
| rs112402958 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335349 | TTTATGACCCCTATT[C/T]TACAGAGGAGAAACC | 50807 |
| rs112403112 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159089 | GGTGAACTGCAGAAA[A/G]AGAAGAATGAGCGAT | 50807 |
| rs112416877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368322 | AAACTACTTTTCTCC[C/T]GATGTTTGGGTTTAA | 50807 |
| rs112418949 | in-del | -/AT | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105075 | ATTGATAACATATAT[-/AT]TTATTATGTATAACA | 50807 |
| rs112428781 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417603 | ACAGAAAACCCCACA[A/T]GTCCTGGCTTCAGGG | 50807 |
| rs112436360 | in-del | -/T | 0.0676201 | 0.17099 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078306 | GTGCCCTGCCAAAAC[-/T]TTTTTTTTGAGACAG | 50807 |
| rs112450761 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413230 | CAGGAGAGGTCTCTG[C/T]TGCATGTATTTCCCT | 50807 |
| rs112457990 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060416 | CTAAAGCCTGGGTTT[A/G]TAACCCACAGGCTCT | 50807 |
| rs112459794 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130365836 | AATGAACAAACATTT[A/T]TAGGGGGAAGGGTAT | 50807 |
| rs112465952 | snp | G/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109664 | TGAAAAAAAACATAG[G/T]GGCCAAAAAAACAGA | 50807 |
| rs112491354 | in-del | -/A | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130426413 | AATACACTGGTTAGG[-/A]AAAAAAAAAAAAGGG | 50807 |
| rs112497046 | snp | C/G | 0.0803491 | 0.183626 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417040 | ACACAGAAGTGCAAC[C/G]CATGTACAACTGCAT | 50807 |
| rs112499847 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115752 | TGGAAGGAACAGCAA[A/G]TGTGCACCATTTTAA | 50807 |
| rs112511606 | snp | C/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130181071 | ATGTGTGGGGGGAGG[C/G]AGCATATGGGAACTC | 50807 |
| rs112512874 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069405 | CACGCCTGGCTAATT[C/T]TGTGTATTTTATGTA | 50807 |
| rs112517433 | in-del | -/GAGA | 0.337614 | 0.234145 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284887 | CACACACACCATACT[-/GAGA]GAGAGAGAGAAAGAG | 50807 |
| rs112523898 | snp | C/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130142693 | ATATGGACAAACTGG[C/G]AAGTGTGATAAGCAG | 50807 |
| rs112599237 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335962 | CTTAATGGTTATGAA[A/G]TATGATTACTGGGAA | 50807 |
| rs112633823 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130308325 | TCAAAATAAGAAACC[C/T]GAATACAGGCAGACA | 50807 |
| rs112654137 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072838 | GTGCGCGCGGGGGGG[A/G]GCAGTTTTGGGGACT | 50807 |
| rs112660745 | in-del | -/T | 0.344054 | 0.231633 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209795 | AACACCTTTTTTTTT[-/T]GAAAGAAAGACTAGC | 50807 |
| rs112664319 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176701 | CTGTTTTTTTTTTTT[C/T]TCTTTTGAGACAGAG | 50807 |
| rs112685450 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350373 | CTTTGGGCCTCAGTC[C/T]CCACCTCTCAAAGCA | 50807 |
| rs112692461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057682 | CTCGAACTCCCGACC[G/T]CGAGATCCATCCGCC | 50807 |
| rs112695620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130067776 | ATCCACAAAAGGAAC[A/G]GTGATAAAAGTGTAC | 50807 |
| rs112703571 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401874 | GACAGGATGGGCTAG[A/G]GATCACTCACCGATT | 50807 |
| rs112720411 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130125894 | AAAAAAAATCCAAAA[C/T]AATATATTAAAATTA | 50807 |
| rs112726349 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145280 | AATATTTGTATAAAA[C/T]GCATTAATTTGATAG | 50807 |
| rs112743882 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180437 | CATACACCAATAAAA[C/T]TTAATATTCACCAGT | 50807 |
| rs112753204 | in-del | -/A/AA/TAA | 0.307176 | 0.243374 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400790 | GCCAGACTCCGTCTC[-/A/AA/TAA]AAAAAAAAAAAAAAA | 50807 |
| rs112753615 | in-del | -/T | 0.0663309 | 0.169604 | intron-variant | ASAP1 | GRCh38.p7 | 8:130103512 | ATTTTTATTTTTTTA[-/T]TTTTTTTTGAGATGG | 50807 |
| rs112765450 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424403 | GACAAGCCTCGGAGA[A/G]CACTCCACTTCCCAA | 50807 |
| rs112775740 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316014 | TTCTCTGCAGAGGAC[C/T]AACTCATCATCTATT | 50807 |
| rs112805869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152859 | ATTCACTCTGGGACA[C/T]GCGACGATACAGTAT | 50807 |
| rs112807694 | snp | A/T | 0.0429648 | 0.14013 | intron-variant | ASAP1 | GRCh38.p7 | 8:130304357 | AGTCATCTTTGAAAG[A/T]CTGACACATTCACCC | 50807 |
| rs112840994 | in-del | -/A | 0.323671 | 0.238899 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092326 | TGGTTAAAAAAAAAA[-/A]TAAAATTGGCCAGGT | 50807 |
| rs112843238 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272304 | CATCTTATCCCAGTT[A/T]GAATGGCCATTAAAA | 50807 |
| rs112854327 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102207 | GCTTTCAGCTTTCCC[C/T]CATTCAGGATGATTT | 50807 |
| rs112858803 | in-del | -/CA | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060564 | TCCTAAGGGCCTGAA[-/CA]TTGTCCCACCCACCG | 50807 |
| rs112860256 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068655 | ACACAGGAGGCTATT[C/T]CTGCGGTAACTGGCA | 50807 |
| rs112868582 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359987 | CTACAAGGGAGTGCC[A/C]CAAAGCAGGGATCTT | 50807 |
| rs112889216 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270060 | CTGTAATCCCAGCTA[C/T]TCTGGAGGCCGAGGC | 50807 |
| rs112905405 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130266574 | ATAAATTTCCCACAG[A/G]GAAAGCCCTCCTGAT | 50807 |
| rs112914275 | snp | A/T | 0.0383715 | 0.133092 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381877 | TGTTCCTTGTCACTC[A/T]CCAGGTCTTATTCCA | 50807 |
| rs112933323 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434785 | ACGGCTCGGCCCATA[C/T]TGATGAGGTCCTGAG | 50807 |
| rs112953422 | in-del | -/C | 0.342134 | 0.232404 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246181 | CCCCTTCGCCCCCCC[-/C]ATGGGAAAAGCAGAC | 50807 |
| rs112955678 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384749 | GTCTTTTATTATCTG[A/G]GGAATGTTGGGCAAG | 50807 |
| rs112959173 | snp | C/G | 0.0517044 | 0.152246 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224945 | AATTCACATTCCCAA[C/G]AGCAATGCACATATA | 50807 |
| rs112986506 | in-del | -/TCATTCA | 0.409212 | 0.192748 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406255 | AGGACTAATATTCAT[-/TCATTCA]TCATTCATTCATTAT | 50807 |
| rs112994301 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ASAP1 | GRCh38.p7 | 8:130433480 | CCTATACAGCTATGA[C/T]TGTTCCTTGGTAACT | 50807 |
| rs112996168 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130268534 | ACACACACACACACA[A/C]AACTGTGTAACTATA | 50807 |
| rs113004783 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130200407 | AAACCCTGCACAAAC[A/G]AGCCTTGATTTAAGA | 50807 |
| rs113018120 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324685 | AATATGAGGCCTCCA[A/G]GTCTATGGATACAAG | 50807 |
| rs113019049 | snp | C/T | 0.5 | 0 | missense | ASAP1 | GRCh38.p7 | 8:130112193 | GGTTGGTGAAGGCTC[C/T]ATAGGAGAGCCGCTG | 50807 |
| rs113019953 | snp | G/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130312837 | GTCATACCCTAGCAT[G/T]CTGGATTTGGTTTTG | 50807 |
| rs113035970 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348771 | GCTTCAAACTGTAAT[C/T]AGTAAAGCACCTAAC | 50807 |
| rs113046492 | snp | A/C | 0.0633504 | 0.166319 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133690 | ACAAACAAACAAACA[A/C]AAAAAAAAACAAAAA | 50807 |
| rs113047853 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111154 | AAGGTGGGAGGATCA[C/G]TTGAGTACAGGAATT | 50807 |
| rs113080201 | in-del | -/AGT | 0.45645 | 0.140991 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399867 | TGTTGCCCAGGCTGG[-/AGT]AGTACAATGGCGCAA | 50807 |
| rs113088303 | in-del | -/A | 0.0652144 | 0.168387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076897 | CACAGTAAAAGGATG[-/A]AAAAAAAAGTCCCTC | 50807 |
| rs113102810 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | ASAP1 | GRCh38.p7 | 8:130440140 | TTCTCTCTACCTCCA[C/T]TGCTGCTGTCCAGTT | 50807 |
| rs113108395 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130425437 | TATGAGAATCCTTTG[A/G]ACCCGTGAGGCAGAG | 50807 |
| rs113123320 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130174534 | ATACACAATTCATGG[A/G]ATCTCTTTTTAGTCT | 50807 |
| rs113129396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157668 | TCCTGGCTTGCTCAC[C/T]ACTCTAGCTACATTG | 50807 |
| rs113140140 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241096 | ATGTTCTCAGAGACG[C/T]GTATGAATCTGACCA | 50807 |
| rs113141272 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175608 | TTCTCCTATTCTGTG[G/T]GTTGTCTTTTACTTT | 50807 |
| rs113163415 | snp | C/G/T | 0.0107558 | 0.0725421 | synonymous-codon, missense | ASAP1 | GRCh38.p7 | 8:130169025 | CAGTTTTTCAATGTA[C/G/T]TGTTTCAACTTATCA | 50807 |
| rs113175475 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060424 | TGGGTTTGTAACCCA[C/T]AGGCTCTAATCCACC | 50807 |
| rs113185605 | in-del | -/T | 0.375399 | 0.216275 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140038 | TCTTTCTCCTTTTTG[-/T]TTTTTTTTTTTTGAG | 50807 |
| rs113187171 | in-del | -/A | 0.458084 | 0.138567 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400623 | AAACCCGTCTCTACT[-/A]AAAAAAAATACAAAA | 50807 |
| rs113203984 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130310281 | ACAGAATTATGAAGT[A/G]GAAAATTATGAGGAA | 50807 |
| rs113211386 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130425452 | AACCCGTGAGGCAGA[G/T]GTTGCAGTGAGCCGA | 50807 |
| rs113240646 | snp | A/C | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132215 | GGACAAAAGTCCCTA[A/C]TTTCTGGGGTTGTGA | 50807 |
| rs113256437 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352268 | TAATTAATGGGCTCC[C/G/T]TAAGTTTAGCACCTG | 50807 |
| rs113293903 | in-del | -/A | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188052 | AGAGGAAAAAAAAAA[-/A]TTAATCCTTTCAAGT | 50807 |
| rs113336038 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217643 | AATGGACACTGCTGT[A/G]GTTCTTTCAGTGAGC | 50807 |
| rs113359937 | snp | A/G/T | 0.0441272 | 0.141924 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258294 | CTGCACGTGACCCAG[A/G/T]ATGGTTTGTCAAGGA | 50807 |
| rs113361743 | snp | A/C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130089836 | TCTAAAATCAAAATT[A/C/T]AAAAAAAAATTTAAA | 50807 |
| rs113375342 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217675 | GGACTTTCAAAGCTG[C/T]GGCTTGGTTAATATT | 50807 |
| rs113388843 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073671 | GCCAAGAGCTGCAGA[C/T]GGCCAAGGAAGACAG | 50807 |
| rs113400841 | in-del | -/T | 0.0629771 | 0.165899 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111661 | AGTGGCATTTTAATG[-/T]AGAGAAAAGTAACTT | 50807 |
| rs113411475 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179173 | TATTTAGTCACGAGA[C/T]GAAGAAAAGATATGA | 50807 |
| rs113416940 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411073 | GCCATGTTGGCCCAG[A/G]CTGGTCTCGAACTCC | 50807 |
| rs113431009 | snp | G/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359653 | ACGGAGTCTCGCTCT[G/T]TCGCCCAGGCCGGAC | 50807 |
| rs113433705 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100476 | CTGGGATTACAGGTG[C/T]ATGCTACCACACCCA | 50807 |
| rs113434267 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437935 | TTTCCTAACTCTGTG[C/T]ACCTTCGCACTTCCT | 50807 |
| rs113435769 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | ASAP1 | GRCh38.p7 | 8:130440611 | GCATGGCTTAGAATC[A/G]GCTGTGTGATCTCGT | 50807 |
| rs113442745 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171214 | TTTTTCAATCCATCC[A/T]TCCCCACTTCAGCCT | 50807 |
| rs113458272 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177358 | TTAACGTGAAAATAG[A/T]TTTCTAAAGTCAGGT | 50807 |
| rs113489287 | snp | C/T | 0.128976 | 0.218754 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394812 | CAGGGGCAGGTTCCC[C/T]GATAACTCTGTCTCA | 50807 |
| rs113493720 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130309541 | AGGCAAGATAAGCAG[C/T]GAGGCAAGACAGAGG | 50807 |
| rs113497138 | snp | A/C | 0.0520825 | 0.152737 | intron-variant | ASAP1 | GRCh38.p7 | 8:130338802 | AAATTCTGACTTCCT[A/C]CTGCTGCTCTGGCTG | 50807 |
| rs113509020 | snp | A/G/T | 0.00428118 | 0.0460686 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118120 | TGTGTTAATTTATAA[A/G/T]GCATATTCAGGTAAT | 50807 |
| rs113520618 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330132 | ATAAAAGGCATTTAA[C/T]AGAGAAAGACACACA | 50807 |
| rs113538133 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130235701 | GGCACCAGGGTGCAA[A/T]ATGTGTTAACAATTA | 50807 |
| rs113545402 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170335 | AATTTTTGTATTTTC[A/G]GTAGAGACAGGGTTT | 50807 |
| rs113555674 | snp | G/T | 0.0244538 | 0.107838 | utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130443524 | CGCTCGCGGCTCTCG[G/T]GTGGGAAAGCGAACT | 50807 |
| rs113571605 | snp | C/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130256038 | CAGAATATCTTATTA[C/G]GAAGAGAGTGAGAGA | 50807 |
| rs113593640 | in-del | -/AAAACAAAAC | 0.499121 | 0.020948 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376430 | ATACTTGCTTCCTTA[-/AAAACAAAAC]AAAAACAAAACAAAA | 50807 |
| rs113622058 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264480 | CTGCTTAGATACCAA[C/T]AGTGCTTGGAAGGAA | 50807 |
| rs113628778 | snp | A/C/G | 0.00518141 | 0.0506816 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383631 | AGGGATTCGTGGCTT[A/C/G]TCCAAGGCCACACAG | 50807 |
| rs113637799 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269683 | CACTATTAGATGAGG[C/T]ACTGTCCTGGGAAAG | 50807 |
| rs113649953 | snp | G/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168566 | CTGTACTCCAGCCTG[G/T]GCGACAGAGTGAGAC | 50807 |
| rs113653569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130266978 | GATAAGAGACATAGA[A/G]GATAGAATGAGAAAG | 50807 |
| rs113701574 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422687 | AGATTAACAATCATC[C/T]TGACAAATCTTGGTT | 50807 |
| rs113708683 | in-del | -/GGGGGG | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072831 | TGTGTGTGTGCGCGC[-/GGGGGG]GGGCAGTTTTGGGGA | 50807 |
| rs113714700 | in-del | -/ACAC | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130268491 | AGATCCCGTCTTAAA[-/ACAC]ACACACACACACACA | 50807 |
| rs113718080 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158266 | CGTAATCCCAATACT[G/T]TGGGGGACCAAGGTG | 50807 |
| rs113733776 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270146 | CTGCACTCCAGCCTG[A/C]GTGACAGAGCGAGAA | 50807 |
| rs113739507 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076641 | ATTCCCTGCCTCAGC[C/T]TCCTGAGTAGCTGGG | 50807 |
| rs113741882 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130198934 | ACCTGTTTTGAGTCC[C/T]TCTACCCATTCTCAC | 50807 |
| rs113777600 | snp | G/T | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273778 | GACATTAGCCCACAT[G/T]TAACACTCCCCAGGT | 50807 |
| rs113790805 | in-del | -/AGAGT | 0.0626037 | 0.165477 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153493 | CCCACCTCAACCTCC[-/AGAGT]AGAGTAGCTGGGACC | 50807 |
| rs113796470 | snp | A/G | 0.5 | 0 | missense | ASAP1 | GRCh38.p7 | 8:130152801 | TCTGCCATACTTTCC[A/G]GATCCTAAGGAGGAA | 50807 |
| rs113829894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062517 | TCTGAAATTGGCTAA[G/T]AAACAATCTGAGCCA | 50807 |
| rs113840584 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070615 | CTTTGGAATAGAGAA[C/T]TTCCACTTAAGGGAC | 50807 |
| rs113861525 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394378 | AGCCCCAGACTCCCA[C/T]AGCGCTCCCAGGCTT | 50807 |
| rs113882152 | snp | A/G | 0.0520825 | 0.152737 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085473 | GGTGAAGAGGCTCAC[A/G]CCTGTAATCCCAGCA | 50807 |
| rs113890391 | snp | A/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169648 | TGGTTGCATGACTTC[A/T]CCTGAAAAATAACAA | 50807 |
| rs113905124 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134033 | GTTATGAAGAGGCCG[C/T]GGGCAAGGAGTAGTG | 50807 |
| rs113912757 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104909 | ATTATCTTGACAGTT[C/T]CTGAAAAAGTTGTCT | 50807 |
| rs113923836 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206159 | AAATGTCCCACAGTA[C/T]TAATTGGTAGTGAGG | 50807 |
| rs113923973 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236695 | ATTAAGCACTTAAGT[A/G]TACAGTAAAATCCAC | 50807 |
| rs113929962 | snp | C/G | 0.0501905 | 0.150254 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110278 | CATTTTCAGGACTCT[C/G]AATGACCTAGAGGCT | 50807 |
| rs113934865 | snp | A/T | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130184795 | AGAAACTATTTATTG[A/T]GTGACTTCCCTATGC | 50807 |
| rs113955646 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166266 | CTCCCACCTTGGCCT[C/T]CCAAAATGTTTGGAT | 50807 |
| rs113962157 | snp | A/G | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327941 | TTTGGTAGACTAATG[A/G]CATGGAGAAATGCTC | 50807 |
| rs113976186 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285933 | TGGAACAGATATCAT[A/G]AATAATTTGCTACCT | 50807 |
| rs113982777 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130151377 | CTCAGTCTCAAAAAA[A/G]AAAAAAAAAAAAAAA | 50807 |
| rs113984494 | snp | C/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403628 | CGCGATCTTGGCTCA[C/T]TGCAACCTCCACCTC | 50807 |
| rs113998796 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073792 | TGAACTTCACACACA[C/G]AGACAATGCGATGGT | 50807 |
| rs114006441 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105491 | AGCGAGAACATTTAA[A/C]ATCTATTCTCTTAGC | 50807 |
| rs114009555 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130174900 | TAACCTTTTATCAAC[C/T]GATGGATATCTGGGT | 50807 |
| rs114011535 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374700 | CAGATGTTAAAGTTG[C/T]GCTGAGCAAGTGTGT | 50807 |
| rs114016997 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130147371 | CTCATTTAATCTTTA[C/T]AATCACTTATGAATT | 50807 |
| rs114020636 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438820 | GGCTGACTCCCACAA[A/G]TGCATCACTACAGCC | 50807 |
| rs114020810 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424398 | ATGTAGACAAGCCTC[A/G]GAGAGCACTCCACTT | 50807 |
| rs114026683 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407770 | ATTTGGTACATAAAC[C/T]CTTCTTTATTGCCAT | 50807 |
| rs114032035 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060446 | TAATCCACCATCATG[C/G]TTGAACCAGAGCACA | 50807 |
| rs114040947 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234524 | TCCATACAGGAACAA[C/T]CTCTCCCTTCTGTCA | 50807 |
| rs114043073 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130255496 | GGCTACTTCAGCAGT[C/T]GCATAGCATTGTATC | 50807 |
| rs114058069 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130250121 | AGATAGGCCATAGTG[C/T]CAGGCTCAGATTCTA | 50807 |
| rs114066037 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400867 | GCAAGTTCTTTACCC[A/G]TAAAATGAATGTAGA | 50807 |
| rs114091904 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389282 | TGGAGACTGCCTTCC[C/T]GCCAGGTCAGACAGC | 50807 |
| rs114101662 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168382 | AGGCGTGGTGGCTCA[C/T]GCTTGTAATCCCAGC | 50807 |
| rs114104989 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130315024 | ACTACTGTCTGCTCC[C/T]GTCACAATTTTACTA | 50807 |
| rs114130051 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252022 | TTGCCATTTCCTCAA[C/T]AATAAAGGATGTGTA | 50807 |
| rs114131859 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277635 | AGGGCACCAAGAAGT[C/T]TAAAGAGTGGGAATA | 50807 |
| rs114139321 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366833 | TAAGTGATCAATAAA[C/T]ATTAGCTACTAATAC | 50807 |
| rs114156474 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078014 | TTTTTTTTTTTGAGA[C/T]GAAGTCTCGCTGTCA | 50807 |
| rs114170037 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122518 | ATACAGCACTAACTA[C/T]AGACCAAATGCTGCT | 50807 |
| rs114179506 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130386839 | GGCTCAGCCAAAAAC[C/T]GTCACTCCACACTTC | 50807 |
| rs114185991 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129581 | TCTCAACAGACAATA[C/G]AGAGGTTCAGAACTG | 50807 |
| rs114186910 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435034 | GGCTGCTGGAAGGCA[C/T]GCTGTCCCATCGGCC | 50807 |
| rs114195377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128329 | TGAGAGAGAGGAGAG[A/G]AGCAGATGAGAAAAG | 50807 |
| rs114200154 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390183 | CTTTACCTCTCTGTC[C/T]CACACAGTAGCCACT | 50807 |
| rs114211041 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150578 | AGGCAAAGAGAGTTA[A/G]GGTATGCATGGTAAC | 50807 |
| rs114213715 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379916 | GCCTGGCACACTCAT[A/G]TCACTGCTCCTTGTC | 50807 |
| rs114214771 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317418 | GTTTGTTGAAACTGT[A/T]GGAACAGGGTCTACG | 50807 |
| rs114249917 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130290764 | CAAATCCTTAACAGG[A/G]TAATGATGATACTCC | 50807 |
| rs114250775 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134727 | AAACAGTGAGGAGAG[C/G]GGAAGGTCCTATTTG | 50807 |
| rs114252520 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263965 | TCTTCTTGCCACAGA[A/C]CTCTGTGGTGCACAC | 50807 |
| rs114257691 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368575 | TCCTGATAACAGCAA[C/T]GATGGGTACTAGAAC | 50807 |
| rs114261973 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092719 | ACAATGGGAAAAACA[A/C]ACACACACACACATC | 50807 |
| rs114262113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220036 | TCATGTGTTCCTCCC[A/G]CATTGGCCACCCAAA | 50807 |
| rs114266713 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104911 | TATCTTGACAGTTTC[C/T]GAAAAAGTTGTCTGT | 50807 |
| rs114298461 | snp | C/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130271882 | CTCCCATTTTGTTAT[C/T]TTTATAATGTATAAA | 50807 |
| rs114302452 | snp | G/T | 0.0584853 | 0.160693 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392596 | ATAGATAAGGAAGCT[G/T]AGTGTCTCAGTCCAT | 50807 |
| rs114318625 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336696 | GGTAAAGCCAACCAG[A/G]GGGAAAAATACTTTT | 50807 |
| rs114323904 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337087 | CCCAGTCAGGACTCA[C/T]ATCAGAGTTTGTATG | 50807 |
| rs114359132 | snp | G/T | 0.0551013 | 0.156571 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418588 | AAATAAAGTGTACAA[G/T]TCAATGGTTTTTAGC | 50807 |
| rs114367915 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247120 | CCTGGTCAAGTTAGT[C/T]ACTCTCTCTGATACT | 50807 |
| rs114376157 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ASAP1 | GRCh38.p7 | 8:130225937 | AGGCTGTAATGCCGC[A/G]GCATGGTCATAGCTT | 50807 |
| rs114381967 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316168 | GTGACCACTATTATG[C/G]CATCTTCATACCAGT | 50807 |
| rs114386024 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395287 | TCTAATATTACATAC[A/G]TTTGACACGTCCTCT | 50807 |
| rs114388564 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111891 | CAAATAATGCACAAA[C/G]AGAGCCCACAGCACT | 50807 |
| rs114389314 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130161256 | AGTTCATAAACAACA[C/T]CTGAAATGTGATAGT | 50807 |
| rs114389582 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130182318 | GAAAGAATTGAAGAC[A/C]AAAAAGGATGACGGA | 50807 |
| rs114399318 | snp | G/T | 0.372391 | 0.217992 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437907 | GCCACTGGAGGGACA[G/T]ACTTACTTTTGTTTT | 50807 |
| rs114403086 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068602 | GGGACCCACAGCTCA[C/T]TATTGAACAACTGCA | 50807 |
| rs114408491 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058457 | CTAAAAATGTTTTTA[A/G]GAAACATGATGTAAA | 50807 |
| rs114417241 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402431 | CATATTTCAGGACAG[C/T]CCCTCTGAACCTGGG | 50807 |
| rs114424235 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238975 | CTGTACTTCTGTTCA[A/G]TATCTTCCTTTAAAT | 50807 |
| rs114431779 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278776 | GGGAGCTGTTGTTTC[C/T]GGGCCACCCAACATC | 50807 |
| rs114432514 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389057 | TGAGTTAATAAACAG[C/T]AAGTGCTTAGAAGAA | 50807 |
| rs114433631 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130365456 | TGGTGTTTTATGGGA[A/G]TCCTAAAAACTTGCG | 50807 |
| rs114446079 | snp | A/C | 0.0333238 | 0.124705 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205630 | AAACTCACTTAATAG[A/C]AAAACCTGTTCTGAC | 50807 |
| rs114447297 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111081 | AACCCTCCTATGAGC[A/G]GGATTCCTCGTCTGG | 50807 |
| rs114453362 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419188 | TCCCCAAGGACACGG[C/T]GCTATGGGTTTTCTG | 50807 |
| rs114456807 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332878 | TAGAAAATATTTCTA[C/T]ATAAAAATCTAAGAA | 50807 |
| rs114498578 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130184503 | CCTGTCATGATTTGT[A/G]AAGAACCCTGTACCA | 50807 |
| rs114503506 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154606 | TTTAAAACAGTATCA[C/T]CTTATGTTTTTCTTT | 50807 |
| rs114506899 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132160 | ACTAGGACTGTTACC[A/G]TGGGCACATTGTGCC | 50807 |
| rs114511713 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335469 | TTAAAACTTGGTTGG[C/T]CACACTAACTTCTAC | 50807 |
| rs114527486 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109077 | ACCGCACCCGGTCCA[A/G]GAACCAGTGTTAATA | 50807 |
| rs114531838 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130291752 | GATTCACTCTTGCTT[A/G]TATTTCCAGGCATGA | 50807 |
| rs114538213 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | ASAP1 | GRCh38.p7 | 8:130242329 | AAAAAAAAGGGCTTC[C/T]ATTGTATTGCTTTAT | 50807 |
| rs114562592 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149689 | AGCTCTTCTCCCCAC[C/T]TTTTCAAAGAAGCCC | 50807 |
| rs114575981 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233935 | GGCCAGTGCAACAGT[C/T]CTTAATTTTGGCTGC | 50807 |
| rs114582185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402458 | TGGGAGAGGATTTTA[A/G]TTAATTCATGCATAC | 50807 |
| rs114585222 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322918 | AGGAAGTCCATGTGT[C/T]GGATGGAACTTTCTA | 50807 |
| rs114586472 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063932 | CAGAGGGTGAGGGCA[G/T]GTAAGCAGGGGAAGG | 50807 |
| rs114591187 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130338198 | TTCAGAAAAAGGTAT[A/T]TATTTATAGGTGATG | 50807 |
| rs114591750 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189762 | GGTTGTACTAATTTA[C/T]ATTACCACCAACAGC | 50807 |
| rs114598087 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097365 | CTGATCTGTTCTTCA[C/T]CGTCCTCCCTTGTTA | 50807 |
| rs114600593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130429718 | CTGAACTTAACTTAC[C/T]CCAACCAACTTTCAA | 50807 |
| rs114632815 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389200 | GTATTGTCTCAGGTA[G/T]AAGCTACTGTTATAC | 50807 |
| rs114650645 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100311 | AGCCATTTATATGTC[C/G]TGTTTTCTTTCTTTC | 50807 |
| rs114664442 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157010 | TTGCTTCAATAGATA[G/T]GTAATAGTACATTGT | 50807 |
| rs114673223 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151484 | CAAGTCTGTAGACAG[A/G]ATTTCTGATATCAGA | 50807 |
| rs114675957 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349568 | CTTGCCCAACACACG[C/T]TAGAAGTAATAGGGA | 50807 |
| rs114677504 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407833 | TGACTCCACGAATGT[C/T]GGGATTTGTATCCTT | 50807 |
| rs114688933 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130142847 | TGGAGAAAGCAGAGT[G/T]GCCAGTTAGATCTCT | 50807 |
| rs114691001 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208464 | CTGCTCTCCATCTTT[C/G]TAATTTTGGATGACT | 50807 |
| rs114704550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321574 | GGGTGCATCCTAAAG[C/T]ACTCACTACTCTAAC | 50807 |
| rs114712811 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306779 | CAATGCTCGGACCAT[G/T]TAACTTAACATGTAT | 50807 |
| rs114778949 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205138 | TTTGCTCCAATAAGC[C/G]ATGGTTTTTCTTCTC | 50807 |
| rs114787719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322919 | GGAAGTCCATGTGTC[A/G]GATGGAACTTTCTAA | 50807 |
| rs114790992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378492 | CACGGAGGCTTGACA[C/T]GCACATAGATGTGGA | 50807 |
| rs114797082 | snp | C/G | 0.247621 | 0.249989 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353891 | GAGAGAAGGGAGTGA[C/G]ATTTTTTTTTTTTGA | 50807 |
| rs114802199 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133964 | ACGGTCCTTGCCCTC[A/G]AAAAGCTCTTGGTCT | 50807 |
| rs114803047 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330270 | TTGCATTTTCTCACC[C/T]TGGGTCTTTGCTCAA | 50807 |
| rs114813292 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157615 | TTCCCCACCTCACGG[A/T]GTGGTTCCCTGTCCC | 50807 |
| rs114819157 | snp | A/G | 0.0228947 | 0.104514 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409761 | TTTCCTCTCCAAAGA[A/G]GAGGTCACTGTGAAG | 50807 |
| rs114835180 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301121 | GACCCAGCATAAGCA[C/G]AGGACATGAGAAATA | 50807 |
| rs114850076 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374110 | AAAGACCTGCAATCA[A/T]ATCCTTGCCCTACTA | 50807 |
| rs114859794 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146455 | GCTCCAAAGTTCGCC[C/T]TCTTACAACTGACAG | 50807 |
| rs114874120 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175720 | TGTCTGCTTTGACAC[A/G]TTTACTAAGCGTTTA | 50807 |
| rs114907639 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130202561 | CAAGTATATCAACCA[C/T]TGCTTAATATTATTT | 50807 |
| rs114916460 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139260 | ATATGAAGGTTGTTA[C/T]TGGGAAGGTTGGGCA | 50807 |
| rs114927099 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313582 | GGGGAGCTGCAGTTT[C/G]AAAATGAGAAACTTC | 50807 |
| rs114957403 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407109 | GGTTGGCTCCCCGTA[A/G]CTGATGAATGCATGG | 50807 |
| rs114983816 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068445 | CTAGAGGGTATAGTG[C/G]GAAAGAACTGTTTCA | 50807 |
| rs114987548 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261244 | GTACACATGACATCA[C/T]AGCCCCTAAACACAG | 50807 |
| rs115009328 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283872 | AATGAAGGGTAAGGG[C/T]CTAAAAAAATGGTGC | 50807 |
| rs115038584 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189623 | ATGAACATGAGAGTA[C/T]GGGTTATCTTGTTGA | 50807 |
| rs115062893 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130202846 | TTTTCAGTTGCTTAA[C/G]ATATCTGTGGCAATA | 50807 |
| rs115064191 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330474 | CCACAACCACCACCC[C/G]ATTCACCTGTGAACA | 50807 |
| rs115075135 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136241 | CCTAAAGGAACATCT[C/T]CCCCCAACTCTTTAC | 50807 |
| rs115087174 | snp | C/T | 0.00148644 | 0.0272215 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340875 | GCTCCTGCATGCTTC[C/T]TGAGGCTGACCAATC | 50807 |
| rs115088902 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164592 | ACTCCGTCTCAAAAA[A/C]ACCAAAACAAAAACC | 50807 |
| rs115097327 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262502 | AAGGTTTATTCACTA[C/T]TCTCTCCTCAAGTGA | 50807 |
| rs115109585 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | ASAP1 | GRCh38.p7 | 8:130216935 | CCAGCAGTCTGGTAC[A/C]AACACAGCATCCAAT | 50807 |
| rs115112553 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389994 | CTCAAACTACGTCTG[C/G]ATCAGAATCACCTGT | 50807 |
| rs115132827 | snp | A/C | 0.0486741 | 0.148216 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445516 | TGAATAAATGAAAGA[A/C]GCAAACAAACTAGAG | 50807 |
| rs115152094 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100088 | TGTGAGAAACCTCCA[C/T]ACTGTTTTTCATTAG | 50807 |
| rs115156862 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292469 | TGAGTTGGGCTTTAC[A/C]GAAGAGGAAGTGAAT | 50807 |
| rs115160110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073515 | CATGACCACGGCCTG[C/T]GGTGCTCAACATGCT | 50807 |
| rs115160413 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106287 | ATGACTGTCTTCCCA[G/T]GAGATAAAAAACCGC | 50807 |
| rs115170877 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379214 | AAGGTGGCACGTCCC[A/G]AGAGGGCATGGAGAC | 50807 |
| rs115174843 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347251 | GTGGAATGTTGATTT[C/T]TCCTGACCACATCAG | 50807 |
| rs115203563 | snp | A/C | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252435 | TTTTTAATCCTCTTA[A/C]CAGTGTCTTATAATA | 50807 |
| rs115205436 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219312 | AGGGTTTACCCAGCA[C/G]ACTTTCAACAGGCAC | 50807 |
| rs115207497 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130302913 | TCTTCTCCTTCTTTG[C/T]TGTTTCTACAACATT | 50807 |
| rs115209128 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ASAP1 | GRCh38.p7 | 8:130365476 | AAAAACTTGCGATCT[A/G]TAGGAACGAGGGATT | 50807 |
| rs115210538 | snp | A/G | 0.0482946 | 0.147699 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052973 | TGCTCTGTTTGGTGT[A/G]GAAATTCACATGTGC | 50807 |
| rs115214408 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330884 | TGAACCCAATTCTAC[A/G]ATTCTCTGGGATGCT | 50807 |
| rs115244976 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394789 | CAGAAAAGAACCTAC[A/G]TGACTATCAGGGGCA | 50807 |
| rs115247857 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362129 | CCCACTTGCCATCAG[C/G]GAATTGGCTCTCAGT | 50807 |
| rs115248554 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093365 | AACTGCTTCTGTAAA[C/T]GTTAAGAAAAAAAAG | 50807 |
| rs115252867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130398139 | TGTTTTTATTGACAT[A/G]TAAGATACATACACA | 50807 |
| rs115254112 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327238 | GCTGGTGATACTATG[A/G]CCCTGTCTGTCTTCC | 50807 |
| rs115277472 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327236 | CAGCTGGTGATACTA[C/T]GGCCCTGTCTGTCTT | 50807 |
| rs115284631 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224372 | ATCACACTTATAAAA[C/T]ATTTAATTCTATTTG | 50807 |
| rs115288410 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227555 | GAGCCACACTGCACC[C/T]GGACTCTCCAAACTA | 50807 |
| rs115290032 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177022 | TGCTCCATGGTACCC[A/G]TCACTGTCCAGCCCC | 50807 |
| rs115290185 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247290 | AATGACAATGTGACA[C/T]TGCCATTAATCTTAT | 50807 |
| rs115293634 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090971 | TTTATTCAGCAAAGC[A/T]TCTGTGAGTGTCTGT | 50807 |
| rs115293831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074623 | GGAGGGACACCTGCT[A/G]GAGTCTGTCCCCGAG | 50807 |
| rs115295936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166882 | TCAAAATATTTCCCT[A/G]GCAAATGAGACATGC | 50807 |
| rs115300792 | snp | C/G | 0.040671 | 0.13668 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383000 | AAGTCCCAGCAGAGA[C/G]AACAGCATGTGCAAA | 50807 |
| rs115301374 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102889 | AGAGACAGGGTCTCA[C/T]CATGTTGCCCAGATT | 50807 |
| rs115319968 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233076 | ATACTATACTTGTTC[A/G]TGACTGCAGAAACCC | 50807 |
| rs115340246 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380832 | CAAGTGATCTTTCGC[C/T]TCAGATTCCTGAGTA | 50807 |
| rs115349015 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096637 | AGAGGAAGTAGAGTA[C/T]ACCTCATTCTTCCTG | 50807 |
| rs115374313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159161 | GACAGCAGCAGCTCA[C/T]CCTAGAGCAGGGGCT | 50807 |
| rs115376712 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237526 | ATTAGTTATGACATA[C/T]GGCAGTTGAATTTTG | 50807 |
| rs115389454 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392261 | CTCCTAAAGGGAGAC[C/T]TGCTGCCTTAGAGAC | 50807 |
| rs115404904 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189885 | CTGAAGTTTTGATTC[A/G]CATTCCTCTGATGAT | 50807 |
| rs115405003 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163541 | CAATCCTAAATTAAC[C/T]ATGAATGAGTTTCAT | 50807 |
| rs115409963 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112882 | TATCTCTGGTATTTG[A/C/T]GCTTGTGGTGATGGC | 50807 |
| rs115434239 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392810 | AGGAGGTGGGGGAGG[A/G]GCTGGGATCTTTTAA | 50807 |
| rs115442121 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064150 | GATTGAATGTGGAAG[C/G]CTCCAGTGTTCTGTT | 50807 |
| rs115479139 | snp | A/T | 0.0482946 | 0.147699 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107711 | GGCCACCAAGCCTGG[A/T]TAATTCTGTGTATTT | 50807 |
| rs115481717 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058868 | TTCCGAGCTCCCTTC[C/T]GGGCCGTGCGGGTGG | 50807 |
| rs115489384 | snp | A/C/T | 0.0205511 | 0.0992634 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205802 | AGGGGGTGTGCTGCA[A/C/T]AATATAAGGCATGTA | 50807 |
| rs115490992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155133 | TAAAGCCTCAGTTTA[G/T]CCATTTTATTAAGTC | 50807 |
| rs115520997 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253248 | CCAGAAACTTAACCC[A/G]GCTGTGCCTCAGTTT | 50807 |
| rs115532472 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264411 | TCAGCAAAGGCAGTC[A/G]TGCGTGCCAGGCAGC | 50807 |
| rs115533239 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436762 | GCTATATTTGTGCCA[C/G]TGCACTCCAGCTGGG | 50807 |
| rs115540783 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078447 | ATGTACCACCATACC[C/T]GGCTGATTTTTTTTA | 50807 |
| rs115545559 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293006 | GAAGCCACTGCTCAA[A/G]ATACTTGGCAAGTAT | 50807 |
| rs115548424 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356168 | AACCCTCTACTACAG[G/T]GTTGCTGGAAAATAT | 50807 |
| rs115577417 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130304981 | ACCTTTCCAACCTCT[A/T]CTTCCTCACACGCTC | 50807 |
| rs115581522 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130369921 | TTGAAATCCTAACCC[A/C]ATGTGATGGTATTAC | 50807 |
| rs115583146 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130351576 | TCTGCGGATGCCTCA[A/G]GGAGTGTTTAGTCAT | 50807 |
| rs115589423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081032 | TCTCACAGAGCTTAT[A/G]CTCTGGCCTGTGAGA | 50807 |
| rs115592734 | snp | A/T | 0.0509478 | 0.151255 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445607 | CTTCCTCTTTGGTGG[A/T]GAGATTCAAAAGGGA | 50807 |
| rs115621139 | snp | C/G | 0.0524604 | 0.153226 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385434 | GGGCGGGCCTTGTGA[C/G]GCCCAAAGCCTCCTC | 50807 |
| rs115624700 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159181 | GAGCAGGGGCTGAGG[A/G]GATGGCAAGAGTATA | 50807 |
| rs115645642 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146300 | TAGTAAAAGTAAAAA[A/G]AACCTTTTTACCCCT | 50807 |
| rs115654326 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430685 | AGAAACCACCCAGAA[C/T]ACTGACCCGAGGCAG | 50807 |
| rs115670436 | snp | A/G/T | 0.013097 | 0.0799021 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254324 | ATTGTTAAAATTCAC[A/G/T]GCACTTAAAACAAGA | 50807 |
| rs115673049 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385149 | CACGTTGCTAGCTGG[C/T]GGTCGCTTGAGGTTC | 50807 |
| rs115691216 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307307 | ATAATTAAGTATTCA[A/G]GAAATAATATTTAAC | 50807 |
| rs115706723 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286476 | GAACTCCTTCATGTA[C/G]TGATGGAGTTGTAGT | 50807 |
| rs115711448 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428815 | CACCACCACCACCAC[C/T]ATCATTATCATTGCA | 50807 |
| rs115713907 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130416200 | CAACTCCGGAGGACA[A/C]GCCGCTGATTTCAGG | 50807 |
| rs115727085 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130198703 | GAGGTTAAGTAACTC[A/G]CCCAAGGTCAAACAG | 50807 |
| rs115728470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434990 | GTGAAGGAAGTTCCC[A/G]AGGCAAGATGGCTGC | 50807 |
| rs115737726 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091762 | TTAGGAAGTGCTCAG[A/C]ACCTTTTAGTTTTTA | 50807 |
| rs115742708 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130267470 | ACCCAATGAGATGGG[A/T]ATAAGAATATGATGA | 50807 |
| rs115772870 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211919 | GAATCTTCTGAGAAG[C/T]ATGGGTTCCCACGGG | 50807 |
| rs115776939 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132600 | TATTCCTCCAGCACA[C/T]GGCCTCCTCTGTCCT | 50807 |
| rs115789400 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285451 | ATCACTAGAAAAAAT[G/T]TTATGGTCTAAATAA | 50807 |
| rs115808592 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130107180 | AGTCTCTCTCTTCTT[C/T]TTCTTTTTTTTTTTT | 50807 |
| rs115826384 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402196 | GCAAGTAAGTGCTCA[C/G]GAATCCTTCTGGCAT | 50807 |
| rs115844175 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080393 | GTGGAATGTGCATGT[A/G]AACACCATTAGCAGG | 50807 |
| rs115854423 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321368 | GGTCTGGTTCAGCAC[C/T]AAAGATTCCAAAGGG | 50807 |
| rs115888475 | snp | A/C/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278311 | TGTAGTCACATCCCA[A/C/T]AATCTAGACATATTT | 50807 |
| rs115891499 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374274 | TAGCCCATAAATGTT[A/C]TTTCAATCCAAAGAA | 50807 |
| rs115892236 | snp | C/T | 0.0441095 | 0.141807 | intron-variant, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130290028 | GGTCATTTATCTAAG[C/T]GCTCTTCCTGGTACT | 50807 |
| rs115892893 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130232349 | TATTAGCAAAAGGGC[A/G]AAGGAGGGAGAAAAT | 50807 |
| rs115899687 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337967 | TAAGATGCCTAATCC[A/C]TTACTTCATTTTTGC | 50807 |
| rs115908456 | snp | A/G | 0.00660308 | 0.0570784 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079862 | CTGTCCATTGCATCA[A/G]TGGATCCAACAGGGG | 50807 |
| rs115918257 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239532 | TCTAATGATATCCGC[C/G]ATAGGCTGAAACTAA | 50807 |
| rs115925038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299782 | AAAGGCAATTCAGAG[A/G]AGAAAAATAAATTCC | 50807 |
| rs115949878 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109694 | AGAAGAATTATCTCT[C/G]CACACAGAGTATCAG | 50807 |
| rs115952772 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151478 | CAGATCCAAGTCTGT[A/G]GACAGGATTTCTGAT | 50807 |
| rs115965694 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097657 | TTGCAGAAGTGACTA[C/T]GCTCACCCTGGCAGG | 50807 |
| rs115999015 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311073 | CCATTCTATGAGAAC[A/G]CAGTCCAGGGCAGGT | 50807 |
| rs116003249 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356655 | CCAATACTGACTCCA[C/G]AGAGAACTCTGGAAG | 50807 |
| rs116003731 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130305216 | TGACACCTAACATAC[C/T]GTTTATTTCTTGACT | 50807 |
| rs116007817 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378456 | AGGATGGTCCAGGCA[C/T]GAGTACAGCAGGTGC | 50807 |
| rs116010526 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411986 | AGGAGTTTACTCCCT[C/T]GCAGGAAGCCCCCAT | 50807 |
| rs116012654 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330058 | GTCAAACAGGACATT[G/T]TCATTACAGCTGGAC | 50807 |
| rs116016913 | snp | A/G | 0.372391 | 0.217992 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437906 | CGCCACTGGAGGGAC[A/G]TACTTACTTTTGTTT | 50807 |
| rs116018422 | snp | A/C | 0.110167 | 0.207236 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391184 | GCAGTAACAAAAAGA[A/C]AAATATTGTATGATT | 50807 |
| rs116021490 | snp | A/C | 0.0566069 | 0.158427 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119652 | TGTCTGACAGCCTGG[A/C]TCCAGCTGTACCTGA | 50807 |
| rs116040208 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126441 | CTCACAGGGGAGTGG[A/G]TTCTATAGCCATCAT | 50807 |
| rs116041112 | snp | C/T | 0.031825 | 0.122064 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150695 | ACCAGCTGGGCAACA[C/T]AGCGAAACCCCTACC | 50807 |
| rs116044599 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405777 | CTATGTCCGTACCTC[A/T]CCCACGGCACTTGGA | 50807 |
| rs116048927 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434174 | TACAAAAATTAACTG[C/T]GCCTGGTGGCGCACA | 50807 |
| rs116077358 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306275 | TTCACTACAAGTATT[A/T]TCATTTAGCAAGTCA | 50807 |
| rs116078557 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144643 | AGATGCACGTTCCAA[A/T]TTCCAAACTTATTAC | 50807 |
| rs116079200 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281642 | TTCTGTTTTGCAACA[C/T]ATCTATATGGTGATA | 50807 |
| rs116079328 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334096 | GAGGAGGCAAGGAGA[C/T]GTGAAAATGCAAGAG | 50807 |
| rs116092606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090668 | TAATGACTTACCCAC[A/G]TGTGTCCTGCATTAG | 50807 |
| rs116102165 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | ASAP1 | GRCh38.p7 | 8:130082096 | CCTGGTCTGACTGCA[C/T]CTACTGAAGAGGGAG | 50807 |
| rs116138894 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130345350 | GCCCCAGATGCATGA[C/T]GTAAATTATCTAGAT | 50807 |
| rs116151742 | snp | A/C | 0.0513262 | 0.151752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130196346 | AAACTCCATCTCAAA[A/C]AAAAAAAAAAAAGTT | 50807 |
| rs116154840 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203044 | AATTACATACTGAAA[C/T]ATAAATTAGAAATAA | 50807 |
| rs116156811 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130298883 | AAACTCCTGTTTATT[A/C]ATATGTCTGCCCGAC | 50807 |
| rs116169408 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146452 | CTGGCTCCAAAGTTC[A/G]CCCTCTTACAACTGA | 50807 |
| rs116172898 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355250 | AAAAGCATCAACATC[A/T]GCACAACACACCACA | 50807 |
| rs116185540 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166839 | CAAATTTCCTAATTG[G/T]GGGGCAAAGCTTCTG | 50807 |
| rs116188177 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074329 | GTATAAACTGTTAAG[C/T]GCTGGAATGGGTGAT | 50807 |
| rs116208133 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108338 | GGAATGAACTGTAAT[C/T]AGCATATCAGGTGTT | 50807 |
| rs116223951 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096544 | TGAAATAATGTCTAT[A/G]TCTTCTTAAAAACAT | 50807 |
| rs116244779 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057744 | TGAGCCACTGTGCCC[A/G]GCCAGCTCCACGGCT | 50807 |
| rs116249658 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252549 | CATACTCTCAGTAAT[C/T]TCCATGTTGCCTTGT | 50807 |
| rs116265001 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228070 | ATTTTAGAGGCTACA[A/G]AAGTATCTTCATCTC | 50807 |
| rs116295620 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183106 | CAAACTTGTAAACAG[A/G]AAGATTGCAAACAGA | 50807 |
| rs116298145 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237484 | TGCTTTTAAGTTTTG[A/C]GATTTCTTTTAGTGT | 50807 |
| rs116303067 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327114 | CAATTTGCAAAGGTG[G/T]TGGTAGGGCACTCTA | 50807 |
| rs116316461 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063552 | ACTCTGGGCAGGAGA[C/G]AGATGGGACTACAGG | 50807 |
| rs116318722 | snp | C/G | 0.0509478 | 0.151255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143498 | AATATACACAGATGT[C/G]TTCATTTTACACACC | 50807 |
| rs116352300 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258966 | TTTTCCCTATTTGCC[C/T]CATCGATTCCAAAAA | 50807 |
| rs116352898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229315 | GACTGCTTGTTAGAG[A/G]TTGTCATGGCATGGT | 50807 |
| rs116354007 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130266144 | TACAATCTCAATGAA[A/G]GGTGAACTAGGGAAG | 50807 |
| rs116360544 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275748 | TTATCCAAATAAACA[C/T]AAAAATGCTTTTAAA | 50807 |
| rs116368959 | snp | C/T | 0.000332613 | 0.0128917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127920 | GTTCAAATATGGGGA[C/T]AAAAACCTGATGAGC | 50807 |
| rs116408528 | snp | A/C/G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218091 | AAAAGAAAGGCCACA[A/C/G/T]GAGCTCAACCGAGAA | 50807 |
| rs116409020 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257386 | GTCACAATCCAACTA[C/T]ATTTATTTACATAGT | 50807 |
| rs116409777 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153886 | ACTTTTGTTATTAAT[A/G]ATTGATTTTTAAAAA | 50807 |
| rs116410358 | snp | C/T | 0.000395726 | 0.0140608 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130112098 | AAAGCCCATACCTTT[C/T]CCGGCGTTCCTAGGA | 50807 |
| rs116413620 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354949 | GGTGTGCAGTGGTGC[A/G]ATCTTGGCTCATTGT | 50807 |
| rs116415437 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350010 | GAGGCTCCCTGGACA[A/G]ACAGACAATGAAGGC | 50807 |
| rs116430668 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366850 | TTAGCTACTAATACC[A/G]CTATTTGCATTCTAA | 50807 |
| rs116442554 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227087 | TATTTAGTGTTTAGA[A/G]TTATGGCCTTGGGTA | 50807 |
| rs116446817 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130232126 | AACAGAAGGACGAGG[A/T]TGAAGCTATCTTGTC | 50807 |
| rs116449226 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320334 | GCCGAGGTGGGAGGA[C/T]TGCCTGAGCTCACGG | 50807 |
| rs116451011 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130225298 | ATATCAATCTGTATG[A/C]AAAAGACTTTTTTGG | 50807 |
| rs116501070 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119464 | GCCTTCTTTACTTCC[A/G]TTCAAGTGTTTCTGG | 50807 |
| rs116501836 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258921 | CCTACTCCTCTCCTC[A/C]CCAATTTTGGGGCAA | 50807 |
| rs116505936 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160638 | ACTGACATTTAACCA[G/T]AGTTTCTAAGGACTA | 50807 |
| rs116525101 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404740 | TACTTCCCACTAGAG[C/T]GAATGGTGTTTACTT | 50807 |
| rs116525582 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370253 | GTTGCAGTCAGCTGA[A/G]ATCACACCGTTGCAT | 50807 |
| rs116528660 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444464 | TTACCATTAAAAGAC[A/G]TCAGAGAAAGGAGGA | 50807 |
| rs116535775 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137565 | GGTAATCAATCATCC[C/G]CAAATTGATCTCCCA | 50807 |
| rs116538159 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130089634 | AATGTCAGCAGGAGG[C/T]GGGGAAGGGATAAAA | 50807 |
| rs116569585 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104166 | AAAAGTACAGTAGAG[A/G]TTCCTCTTCAAAGAC | 50807 |
| rs116572469 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056472 | ATCCCTGGCCACTAA[A/G]CTTCCATCTACTAGT | 50807 |
| rs116573506 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430273 | GTGGATATGAAGGAC[C/T]CACCAAGATGAATAA | 50807 |
| rs116576335 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360306 | TCACCCAGATAATCC[A/T]GTTGTCTATGGCATC | 50807 |
| rs116576494 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215336 | GGTATGGTGGCTCAC[A/G]CCTGTAATCCTAGAA | 50807 |
| rs116578766 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261787 | CAAGGGACCTGGGGC[A/G]GAGAGATTCTGAAGG | 50807 |
| rs116581317 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392841 | ACAAACAGTTGTCAC[A/G]GGAACTAACAGAGTG | 50807 |
| rs116583710 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434289 | GCAGTGAGCTGCCAT[A/G]GCGCCACTGCACTAC | 50807 |
| rs116611891 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233854 | TTCAAACAAACAAAT[C/T]ACATTGACAAATGCA | 50807 |
| rs116613409 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211094 | TGGGACCAAAACCCA[G/T]GATCCTCCAACCACC | 50807 |
| rs116625646 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092560 | TGAAGTCAGGAGTTC[A/G]AGGATACACTGAGCT | 50807 |
| rs116642919 | snp | C/G | 0.0486741 | 0.148216 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146743 | GGCAAGAAAACAACA[C/G]ACCTTAGACCCAAAG | 50807 |
| rs116646547 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | ASAP1 | GRCh38.p7 | 8:130250418 | AAAACATGTTTTATT[C/T]TACTTTTTGTCACGT | 50807 |
| rs116647253 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385983 | GAATAGTCCATGGCC[A/T]TGTCCACAGTGACTG | 50807 |
| rs116649527 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204594 | TCTCCTGCAGCTAGG[C/T]AGGTGGGGCCAAGAT | 50807 |
| rs116673072 | snp | G/T | 0.0640965 | 0.167152 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322320 | AAAAAAAAAAAAAAT[G/T]AAAATGCTGTAACTA | 50807 |
| rs116698365 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137346 | TAAATGTCTTTAAAC[A/T]GTGCATAAATATCCT | 50807 |
| rs116704407 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189751 | TTCTCCATAGTGGTT[C/G]TACTAATTTATATTA | 50807 |
| rs116722160 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349539 | GGAAAGTAGGACACA[A/G]TAAGGCTCAGTAACT | 50807 |
| rs116722640 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252707 | GAGTTAGCACACCCA[C/T]CCACAAGCACCATGG | 50807 |
| rs116731387 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063112 | AGAGAAAAAAAAGAT[A/G]AAAGATATACACTAA | 50807 |
| rs116732836 | snp | C/T | 0.00511027 | 0.0502893 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054724 | AATCTTAAGGTTCTG[C/T]GTTTTGCTAGTCAGA | 50807 |
| rs116739542 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391784 | TAGATAGCACATTAT[A/G]CCTTTTTAGAGAGAG | 50807 |
| rs116741075 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436472 | GGCTAATTTTTGTTA[C/T]TTGTTTTTTGTTATT | 50807 |
| rs116756386 | snp | A/G | 0.00666906 | 0.057359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340927 | TTTCCAAAGTCTTCA[A/G]GGGAATAAAATACTA | 50807 |
| rs116756429 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077239 | TTGGAGGACAGGTAA[A/C]TGAGGGTGACAAAGG | 50807 |
| rs116762312 | snp | C/G | 0.0528381 | 0.153711 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233608 | GGTACTCCCTTAGCA[C/G]CTTCCTCACGCTACC | 50807 |
| rs116778205 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244637 | ATAAAGATACAGAAG[C/T]GAGTGAAACATAGCC | 50807 |
| rs116809934 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164700 | TCATAGAACATTTAT[C/T]TGCTAAGACAATAAA | 50807 |
| rs116812706 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313302 | ATAAAATAACATAAC[C/T]GTTTAAAAAAAAAAA | 50807 |
| rs116816532 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254890 | GATGGCATCAAATGA[C/T]ATTACCATTATTCAA | 50807 |
| rs116824299 | snp | A/C/G | 0.111442 | 0.213545 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072836 | GTGTGCGCGCGGGGG[A/C/G]GGGCAGTTTTGGGGA | 50807 |
| rs116845513 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229407 | CAATCCTACTTTGAT[A/G]AGACATAAACCATTT | 50807 |
| rs116847066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130351870 | ATATCAGGACCAAAA[C/G]CATTAGCATGGAATA | 50807 |
| rs116849444 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083604 | CCTACTACCCTAGAT[A/G]GGCATGAGTATTAAA | 50807 |
| rs116855829 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140164 | CAGCCTCCCAAGTAG[C/T]TGGGACTATGGATGC | 50807 |
| rs116877677 | snp | A/C | 0.0539704 | 0.155153 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387733 | AAAATTGTCTAGTCC[A/C]TGAAAGGATTCTACA | 50807 |
| rs116888250 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390570 | CATACTCTGAGTGCC[A/G]TGAAGGCAGGTACCA | 50807 |
| rs116924122 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110254 | CTGGTGTCATTTTCT[C/T]CTATAAACCATTTTC | 50807 |
| rs116927205 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319246 | CATTGGATCACATAG[C/T]CAGAACCAGCCCCCA | 50807 |
| rs116928023 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229695 | AGAGAAATACATTTT[A/T]ATATTCACCTTTAAC | 50807 |
| rs116930820 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | ASAP1 | GRCh38.p7 | 8:130266362 | CAGGGATGAGGGGAA[C/T]CATATCAGTGACTTA | 50807 |
| rs116971212 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238310 | GTGGTTCTGTTTCTT[C/G]ATGTGAGGAAAAATC | 50807 |
| rs116972294 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130113939 | GGCGCACACCACCAC[A/G]GCCAGCTAATTTTTG | 50807 |
| rs116982990 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244929 | AGTTGAGGCAGAGAG[A/G]AGCAGAACAGAAATA | 50807 |
| rs116984404 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124790 | AAACGTTTAGGATTT[G/T]GACTTTCCTCTTTCT | 50807 |
| rs116993648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352691 | TGCTGTAATCCTGAA[C/T]TTCTTCATCTATAAA | 50807 |
| rs116994893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130326551 | CTGTTGCAACAACTT[G/T]CATTTTTATTTCCCC | 50807 |
| rs117013269 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126837 | AGTTTCACAAGTAAA[A/T]CCGCAAAAAAGGTAT | 50807 |
| rs117015017 | snp | A/T | 0.0295035 | 0.117819 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219504 | TGCCACAGGAATGAG[A/T]GTTTCTGAAGGAGAC | 50807 |
| rs117019764 | snp | C/T | 0.00639718 | 0.0561931 | missense | ASAP1 | GRCh38.p7 | 8:130060583 | GTCCCACCCACCGTA[C/T]TGATTTTTCTGGGCA | 50807 |
| rs117025318 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130190858 | TGCTGGTTTGATTAC[C/T]ACAGCTTAGTAGTAT | 50807 |
| rs117035642 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418671 | AAGCAGTCACTCCCC[A/G]TTCCACCCTCTACAC | 50807 |
| rs117051800 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106714 | GCCAGGGATGCAAAG[C/G]CAGCTCATTCACAGC | 50807 |
| rs117072341 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213516 | CCACAGAAGCCTATG[A/T]GATACATGAATAACT | 50807 |
| rs117090079 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ASAP1 | GRCh38.p7 | 8:130089508 | AGCGTTGGAAAGGTG[C/T]GTCCACAGACGAAAG | 50807 |
| rs117097409 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274158 | ATACTAATGTATACC[A/T]CCCTGCCTGCATTGC | 50807 |
| rs117123722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436311 | GGAGTTTGGTTTCTT[C/T]TGAGACATGGTCTTG | 50807 |
| rs117129430 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323601 | GTTTTGACTCCTCCT[A/G]CCTCCCTCTACTGTC | 50807 |
| rs117134073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083154 | CACACAGACGAGTCA[C/T]CATGTCAGGGGCTGC | 50807 |
| rs117151718 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413263 | TAGTTTTAGAACTAA[A/G]AAAAGATCTTTAACA | 50807 |
| rs117161072 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405254 | CAATCCTGCAAGGGA[A/G]ACACTGGGCCAGATT | 50807 |
| rs117166325 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165312 | CAAAGGTAGGGAGTG[A/G]TTAAGTACATACAGT | 50807 |
| rs117169547 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288083 | GCGTGGAACTCTTCT[C/T]CCCTGGCAGGAGCTC | 50807 |
| rs117175622 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280382 | AACTGGGCATTTTGT[A/G]GATAAAGTCTACTTG | 50807 |
| rs117203453 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415395 | ATCACTTGAGCCCTG[A/G]AGATTGAGGCTGCAA | 50807 |
| rs117206514 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130441161 | TTGAGAACAGGGTCC[C/T]ATTCATCTTTGCAGG | 50807 |
| rs117233491 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204665 | TGAAAAGTATGCATA[C/T]GCTTCTCTAGTCTCT | 50807 |
| rs117236857 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130425950 | TCAGCCGTCCCCACC[A/C]CTGCCGCTGCTTCCA | 50807 |
| rs117248197 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130235947 | ACCCTTTACAGATAT[A/G]AGATCATTAAATCCC | 50807 |
| rs117257404 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141304 | CCCTTCTCGCACTCA[C/G]CTCCTGTCACTCTGA | 50807 |
| rs117282230 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263220 | CTTTTCTCCTAGCTA[C/T]AGCTAACTGAACCAG | 50807 |
| rs117288804 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059914 | AAAACCCCATCTCTA[C/T]CAAAAATATTAAAAA | 50807 |
| rs117307218 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130412348 | CTGTCCTTGCCATAG[C/T]GAGTGAGTGACTTTC | 50807 |
| rs117318988 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073626 | AACACAAGTACATAG[C/T]GTTCCAGGCAGGGGA | 50807 |
| rs117327577 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406054 | TTCCTATACTAAGGC[A/G]ATTTCATTTCTGGGA | 50807 |
| rs117353045 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253936 | TGAGCCATGAGAATC[A/G]CTTGAACCCAGGAGG | 50807 |
| rs117407554 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343817 | TTTAATACAATGACA[C/T]GCCTTTTTAAATATT | 50807 |
| rs117414932 | snp | C/G | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395158 | GGAAGCACTCACTCA[C/G]AGTAACACAGAGTTC | 50807 |
| rs117416177 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334322 | GGAAAAAGAAAAGCA[C/T]ATGATGAAATATTAT | 50807 |
| rs117447475 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373184 | AAAACAAGAGCCAGA[A/G]AAAAAAAAAAACCAT | 50807 |
| rs117453441 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115468 | CAACCTTAATATAGC[C/T]GTTAAATGGTGCCCA | 50807 |
| rs117471115 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130369418 | TTGGCATTCAAAAAG[C/T]TTTGGATTTGGGAGA | 50807 |
| rs117495337 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130179986 | GAAAGAGAAAGAGAA[A/T]GAGAGAGAGAGAGGT | 50807 |
| rs117519109 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336412 | AAACCTACCAAATTA[C/G]AATCAGCACATAATA | 50807 |
| rs117522059 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274245 | ATGACAAATGACTGA[C/T]ACTATGAAGATGGAA | 50807 |
| rs117546058 | snp | A/G | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387365 | ACATGGCAAAACCTC[A/G]TCCCTACTCAAAATA | 50807 |
| rs117580791 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130369712 | TGTAATAAAAAAGAT[A/G]GAAATTGACAAGTAT | 50807 |
| rs117581915 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162880 | TGCTCACTCATAACC[C/T]TCTTCCTTGGAACCC | 50807 |
| rs117589381 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130294457 | ATGAGCTGGACAGAC[C/T]TGGGTTTGAATCCCA | 50807 |
| rs117593476 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188562 | AACATGGGGAGACAC[C/T]GTCTCTGCTAAAAAT | 50807 |
| rs117595320 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154411 | AGACGAGACTGCATG[G/T]GTGGTAGATCTGCGT | 50807 |
| rs117603272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214862 | AGGAGTACACTAAAT[A/G]TTCTAACTCACTCTA | 50807 |
| rs117606691 | snp | A/G | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397442 | CACCATGCCCAGCCC[A/G]TATATTTATTTTAAA | 50807 |
| rs117614048 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130073406 | AAAAAAAAAAAAAAA[A/C]AAATACAAATGTGGA | 50807 |
| rs117615438 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379788 | CCACAGTGACACAAG[A/G]GGCCAGTGCTCATCA | 50807 |
| rs117629136 | snp | A/T | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146091 | TCCTGGACTTAAGCC[A/T]CAAACTCCCAAAGTG | 50807 |
| rs117638352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094383 | ATCCAGCTAATTTTT[A/G]AAAATTTTTAAATTT | 50807 |
| rs117640657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130433087 | GAAGTAACTGTCCTA[C/T]GAGAGGAAACTTGCT | 50807 |
| rs117661117 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130225248 | TAGTGGTGTCCTTTG[C/T]CATGGAGAAATTTAA | 50807 |
| rs117664229 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ASAP1 | GRCh38.p7 | 8:130190422 | ATATTCTTTCCCCAA[C/T]GTATGTTCTTGGTGC | 50807 |
| rs117676994 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245014 | CCTGTGTAACAACAC[C/T]CACAGTTAGTGGGGT | 50807 |
| rs117686316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237383 | CCAGGCAACAGGACA[C/T]ACTTTATCACCTAAA | 50807 |
| rs117697847 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252554 | TCTCAGTAATCTCCA[C/T]GTTGCCTTGTGAACT | 50807 |
| rs117699719 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226436 | CCCACCACTAACTGT[A/G]TTAGTCTATTGTTAA | 50807 |
| rs117714848 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333762 | TACAGATAAAATTAT[A/C]AGACTATTAGATGCA | 50807 |
| rs117718759 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175160 | ATTGAGGTTTTGATT[C/T]GTACTTAACACCGAC | 50807 |
| rs117728292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347291 | AACTAGGCAGCACAG[C/T]GCTCTGACCACAGTC | 50807 |
| rs117728812 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339991 | GCCTAAATTCTTCAA[A/G]GCTTCCGTGTGTGTA | 50807 |
| rs117729869 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378594 | GGTAGGCAAGGGTGG[C/T]CGAGGAAGACCTTGG | 50807 |
| rs117746065 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099957 | CTTGGCTACTGTAAA[C/T]AGCACTGCAGTAAAC | 50807 |
| rs117757229 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ASAP1 | GRCh38.p7 | 8:130369535 | CCAACAATAAAGAGA[C/T]AAATAACTAATTTAA | 50807 |
| rs117765643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130212884 | TGACTCTTGACTTAA[C/G]CCAATACATTTGGTC | 50807 |
| rs117782567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240442 | AGAAATAATACAAGT[C/T]TAAGTGTGCTACAAA | 50807 |
| rs117804839 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081008 | CAAAAACAAATAAAA[A/C]TTCACTGCTCTCACA | 50807 |
| rs117805846 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151455 | ACAGCCTCAATCATA[A/G]TTACAAACAGATCCA | 50807 |
| rs117828165 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283248 | TAGCCTTAAAAGAAG[A/G]CAGGATGCCAGGAAA | 50807 |
| rs117830957 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362427 | TAAAACTCTACTTTC[C/T]TGTTTATTCACCTTC | 50807 |
| rs117857698 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163410 | TCGGAGTGAATGTGC[C/T]TGCTTTACATCAAAC | 50807 |
| rs117858659 | snp | C/T | 0.0471967 | 0.146188 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116875 | GACACTAGACACACT[C/T]TTACCTATATCCACA | 50807 |
| rs117879295 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428350 | AAGCCACAGGACTAT[C/T]TACAGTCAGACACAT | 50807 |
| rs117882043 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356490 | CAATGCCTGGCAATT[C/G]TGTTTAATCCCAGAC | 50807 |
| rs117882606 | snp | A/C/T | 0.00478364 | 0.0487146 | intron-variant | ASAP1 | GRCh38.p7 | 8:130294635 | ACACAAATCTAAGTT[A/C/T]TCTTCTCCCTTACTG | 50807 |
| rs117883303 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248386 | GAGAACAACCACGTG[C/T]ATGCCAACATTCTGA | 50807 |
| rs117884292 | snp | C/G | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195649 | AGTACATACATCAAG[C/G]CTAACCAGAAATTTG | 50807 |
| rs117887269 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280327 | ACAAGTTTTTAAAAG[C/T]GGTGTGTGATATATT | 50807 |
| rs117888261 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234770 | CCCTTTTGCAGCTCA[C/T]AAGCATAGAGCCTCA | 50807 |
| rs117894128 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339562 | GTGCTCTATCTGCTT[C/G]GTTTGTAGATGTTTA | 50807 |
| rs117909822 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313871 | AGCCTGTCTGCAGTC[A/G]ATGCCACTGCACTCG | 50807 |
| rs117910830 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155580 | CCAGGCTGGTGGGCT[C/T]ACGTGATCTGCCGGC | 50807 |
| rs117911060 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159638 | AGTAGCTGCCTTCCT[A/G]TAATTGCACGTTACA | 50807 |
| rs117944071 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | ASAP1 | GRCh38.p7 | 8:130185698 | TGAGCCACTGAACTC[C/T]AGCCTGGGCAACAAG | 50807 |
| rs117946724 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162382 | GGATTGGGTTGCAGG[G/T]AACTGAGGCATGAGA | 50807 |
| rs117947507 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109761 | AAACATTATCAGTTT[C/T]CCAAATGTAAGCGCA | 50807 |
| rs117974474 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379691 | CAGAAAGAAGACATT[A/G]CACCTGGAAACACTC | 50807 |
| rs118007854 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396347 | ACCTGGCACACAGTC[A/G]CTGCTTAATAAATTT | 50807 |
| rs118013681 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130075091 | AGAGAAAGCAGGCTG[A/G]AGAGGTAGGGTGATA | 50807 |
| rs118017556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409919 | GTTGAGTAACACAAG[A/G]TCATTGCCCATAGAG | 50807 |
| rs118024100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112740 | GTTCTTTCTTTGCCT[C/T]TTTTCTCATTTTATA | 50807 |
| rs118054603 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206688 | GACCTAGAATACTTC[C/T]GGGTGACTCCCACTA | 50807 |
| rs118060034 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418722 | TATAACCTCTGTTTA[C/T]ATAGCTTTGCCTATT | 50807 |
| rs118096112 | snp | C/T | 0.0562307 | 0.157967 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083552 | TATTCTGCTAAGCCT[C/T]GATTCCGTCATATAT | 50807 |
| rs118102653 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229055 | AACAGACAAACTAGC[C/T]GAGCAAAGTCATCCT | 50807 |
| rs118113813 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276548 | CATTTGTGTCCTGTA[A/G]GCTGATCCCAGGGTC | 50807 |
| rs118114593 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272528 | GAAAGGAAATCAGTA[C/T]ATAAAAGGGATGCCT | 50807 |
| rs118123858 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400016 | GTACAGACAGAGTTT[C/G]TCCATGTTGCTTAGG | 50807 |
| rs118127353 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130367386 | AGTAATTTGATGTAA[C/T]GCTCTCTCTCTGATT | 50807 |
| rs118128625 | snp | G/T | 0.0345262 | 0.126772 | intron-variant | ASAP1 | GRCh38.p7 | 8:130310638 | ATCTAGTTAAAAATG[G/T]GTCACACTATTTATA | 50807 |
| rs118138898 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118307 | CCAAGGGAGGCTTCA[C/T]ATATATCAGTTGCCC | 50807 |
| rs118139710 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124689 | AAGGGCCTCTAATCA[C/T]TTTATGTAATTTTGG | 50807 |
| rs118150669 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171046 | TAGCATTTGGGTTTT[C/T]GGCACTGCCTATAGC | 50807 |
| rs118163904 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130433973 | AGGCAATATTGTATC[A/G]TGGTCAAGAGTATGG | 50807 |
| rs118184990 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274152 | CTTCTCATACTAATG[C/T]ATACCTCCCTGCCTG | 50807 |
| rs137891870 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165347 | AAAACAACAATAAAC[A/C]AAAAAACCCCAAAAA | 50807 |
| rs137893981 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102414 | TTATTGATTAGCGTA[A/T]GTTGAAACATCCTTG | 50807 |
| rs137904807 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130075978 | GATGAGGAATCTCAG[G/T]TTTAGTGAAGCTACT | 50807 |
| rs137913887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199639 | ACTTTTTGTTTCTGG[C/T]ATCAATAAAGTGTGA | 50807 |
| rs137939866 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352179 | CATTAAGCAAAAGTA[C/T]AAATCTTGATTTTAG | 50807 |
| rs137945437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130271532 | GTACCGCTCAGATGC[A/G]TGGGCTATTCAGCTA | 50807 |
| rs137956969 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208917 | TCATTTCATCTATTT[G/T]CCATCCCCCTAAAAA | 50807 |
| rs137967973 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129519 | AATAAAAAACATTTC[C/T]AAACCAGTGTTAATT | 50807 |
| rs137982406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301417 | TTTTAATGTAAATTG[C/T]GTTCTAGAATGCTCT | 50807 |
| rs137988487 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341751 | CAAGGTTCAGTCACC[A/G]ATGGTTCACGAACAG | 50807 |
| rs137988854 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376621 | GTCCCAGCTACTCGG[C/G]AGGCTGAGGCAAGAG | 50807 |
| rs137993453 | snp | A/C/G | 0.00637415 | 0.0561569 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244153 | CCCAACAGGTAGCAT[A/C/G]GTATCAGACCTATTA | 50807 |
| rs137994853 | in-del | -/CA | 0.221439 | 0.248363 | intron-variant | ASAP1 | GRCh38.p7 | 8:130331779 | ATACACCCCAAAATT[-/CA]CAGACATATCTAGAA | 50807 |
| rs137997203 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130442754 | CTGCTTTAGAAGTGC[C/T]CAAGATGAACCTCTT | 50807 |
| rs137997327 | in-del | -/TGAGGACATTATGTTAAGTAAGGCAG | 0.110167 | 0.207236 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391147 | AATAAGGATGAACCT[-/TGAGGACATTATGTTAAGTAAGGCAG]TAACAAAAAGACAAA | 50807 |
| rs138004460 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130412194 | AAATAACAACAGGTC[C/T]GATAGAGTTTGGATC | 50807 |
| rs138010215 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160126 | GAGGAGGAAACAGGG[C/G]AGCTAAACACTTGCC | 50807 |
| rs138016236 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057266 | TCTGGGGTCAGGGCC[A/G]ATCTGGAATCTTGAC | 50807 |
| rs138023747 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237631 | GATGATGAATCAACA[C/G]ATTAATCTACCTGTG | 50807 |
| rs138028066 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130093858 | CCTATTTCCCATTGT[C/T]AATTACTAGTCCCTA | 50807 |
| rs138039220 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130065603 | ACCAGGAACTGTGGA[C/T]GGATACCAATACATA | 50807 |
| rs138039304 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105110 | TGTTTTAAAATATGT[A/T]TACAGTTGGACCTTT | 50807 |
| rs138069314 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130193661 | TGCATCAATGCCTCA[A/C]ATCCTTTGTGAAATG | 50807 |
| rs138070387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124320 | GAGATGGGTAAACTA[C/T]GTTCCCTTTCCATAG | 50807 |
| rs138073812 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156857 | TTAGGGTTTGAACTA[A/T]GCAACACTTAAGAAA | 50807 |
| rs138076308 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130371096 | TGAAGATGGAAGGCA[C/T]ACCTTACCTGTTAAT | 50807 |
| rs138077188 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380568 | CAAGGAGGAGCACAG[A/G]CAAGTCAAGAGGTGA | 50807 |
| rs138079031 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | ASAP1 | GRCh38.p7 | 8:130331807 | AGAAACACATACACA[A/C/T]ACACATGCAAACACA | 50807 |
| rs138082032 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295777 | GAAGCTGTGGCACAA[A/G]ATTTTTTTTTTCCTA | 50807 |
| rs138109345 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408150 | ACTTGTGAACTCTAA[C/T]AGCACTGCTAATAAC | 50807 |
| rs138116753 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436959 | AAAATACAAAAATTA[C/G]CCAGGCGTGGTGGAA | 50807 |
| rs138127827 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068954 | AGCCTTATTAAATTT[A/G]CTGTCTCAGCTTCCC | 50807 |
| rs138152266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130061829 | GCTGCACAGTATGCA[C/T]AGCTTAGGAAATGTA | 50807 |
| rs138154604 | in-del | -/ATCTGTTTAG | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130230630 | TGAAGGCCCAAAGAA[-/ATCTGTTTAG]ATTTTGCTCAATCCC | 50807 |
| rs138159747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224225 | CAGCAGCCATGTGCC[A/G]GCCATATAAAATACA | 50807 |
| rs138169540 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258839 | GTGGTGGTTGACTGA[A/T]TTGCTGATTTCTTCC | 50807 |
| rs138169797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130433015 | TGCTGCTCAACAGAG[C/T]GTAGACTGCAAATAT | 50807 |
| rs138169820 | in-del | -/A | 0.0182019 | 0.0936463 | intron-variant | ASAP1 | GRCh38.p7 | 8:130363360 | GCGAGACTGCATCTC[-/A]TTTTTTTTAATAAAA | 50807 |
| rs138175891 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150748 | AGCTGGGCGTGGTGA[A/G]GTGTGCCTGCATTCC | 50807 |
| rs138185563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327017 | ATAACTGGATGAATG[C/T]CCCCAGGAGGCAGCA | 50807 |
| rs138191200 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400870 | AGTTCTTTACCCGTA[A/C]AATGAATGTAGAAAT | 50807 |
| rs138199665 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431756 | CAGGATAGCAGAGTA[C/T]GCAGCACAACAGCTG | 50807 |
| rs138204941 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336510 | CAAGGCAATAAACCA[A/G]AGGAACTAATATGTG | 50807 |
| rs138212009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364796 | CTGAGAACTTCCTCA[A/G]CAACAAATAGCTCTG | 50807 |
| rs138247343 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421993 | GTGGGGGAGACAGAG[C/G]TATGAACAAAACAGA | 50807 |
| rs138263684 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137993 | AGCAATGAAACTCTT[C/T]AATTGGACCTATATC | 50807 |
| rs138272369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150116 | CTGAATCCTCATATA[A/C]TCTTTATGTGTTAAA | 50807 |
| rs138277000 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220057 | GCCACCCAAAGTGCT[A/G]GGATTTACAGGTGTA | 50807 |
| rs138285979 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117283 | ATACTAATAATAACC[A/G]CTTTTACAGATAAAA | 50807 |
| rs138290159 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254344 | TTAAAACAAGAATGT[C/G]ACTAGTATAAAACAA | 50807 |
| rs138291073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321037 | TCAAGAATGCTGGCT[G/T]AGGAAACCTAAGGAT | 50807 |
| rs138299592 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153666 | AGCCACTGTGACTGG[A/C]CGTGGCACTGCTTTG | 50807 |
| rs138310140 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292500 | GATTAGTAAACCAAG[A/G]GTAGGAGGAGGGAAA | 50807 |
| rs138312315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130103077 | TGGGAGGCTTTTTAT[C/T]ACTGATTCAATGTTG | 50807 |
| rs138325311 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289058 | GGGCGTGGTGGCACA[C/T]GCCTGTAGTCCCAGG | 50807 |
| rs138325363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330250 | ATGGGAGTCTCCATT[C/G]CACTTTGCATTTTCT | 50807 |
| rs138325537 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403640 | TCATTGCAACCTCCA[C/T]CTCCTGGGTTCAATT | 50807 |
| rs138341844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214496 | ATTGAAATGTTCTCT[A/G]TATGACGTAATATTT | 50807 |
| rs138351225 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ASAP1 | GRCh38.p7 | 8:130386255 | TAGGAATCCAGTCAT[G/T]TCTGGGGCCAGGTTT | 50807 |
| rs138353658 | snp | A/G | 0.000148245 | 0.00860815 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130060701 | TTGGGGATAGATCCA[A/G]TGGGTGTGACTTCAG | 50807 |
| rs138368056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119777 | GTGTGACCATAGTAA[A/C]CTGCTTAATCGTCAT | 50807 |
| rs138369687 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203351 | GGCTCAAAGCACCCA[C/G]CTGGCTTGTACAAGG | 50807 |
| rs138402553 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176888 | AGAAACGGGGTTTTG[A/C]CATGTTGGTCAGGCT | 50807 |
| rs138407410 | snp | A/G | 3.29571e-05 | 0.00405924 | missense | ASAP1 | GRCh38.p7 | 8:130112111 | TTCCCGGCGTTCCTA[A/G]GAGGCAGAGGGGGAG | 50807 |
| rs138426316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160673 | ACTAGAAACAGCCAT[C/T]ACATTACGAAAATGT | 50807 |
| rs138429030 | in-del | -/GCTGTGATG | 0.0138799 | 0.0821421 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082326 | CATAAAATCCTCAGA[-/GCTGTGATG]TTCTTCAAGGTAGGG | 50807 |
| rs138447561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336844 | TACTAAACTCCCAAT[A/G]AAACCACCAGAGAAC | 50807 |
| rs138447838 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349759 | AGACCTTGACACCCA[C/T]AGGGACATACTTTAC | 50807 |
| rs138449279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396426 | ATCATCACTTCCCAT[C/T]TCTCAGTTTAGCCAT | 50807 |
| rs138451877 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130172959 | TGTAGCATAATCCCA[C/T]TTTTGTAAACAAAAC | 50807 |
| rs138466840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381090 | GGGATTTTGCCATGT[C/T]GTCCAGGCTGGTCTT | 50807 |
| rs138473977 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278295 | ACCAACCACAGAAAG[C/T]TGTAGTCACATCCCA | 50807 |
| rs138494380 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076185 | TTGAGTTTATAAATA[C/T]CTTTCGTCATTTAAT | 50807 |
| rs138495590 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130133688 | AACAAACAAACAAAC[-/A]CAAAAAAAAAAACAA | 50807 |
| rs138502536 | snp | C/T | 0.162909 | 0.23434 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393877 | TTATAATTTCTTACA[C/T]CTGTCTTTACTGTAA | 50807 |
| rs138513116 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244477 | TCTATCTCCTCATCT[G/T]AAAGGGTAAGTGGAG | 50807 |
| rs138515156 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287199 | CATTTTTGTATATTG[C/G]CTGTCCAAAGCACAG | 50807 |
| rs138541549 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353826 | CAGTGAGCTGAGATC[A/G]CACCACTGCACTGCA | 50807 |
| rs138558156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130282782 | GTGGGGGTAGACAAC[C/T]AAATGAACAAGAACC | 50807 |
| rs138593403 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306613 | AGATGTTAATAACCT[C/T]AGGGCACAAGCGGAA | 50807 |
| rs138593654 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349245 | CCTAGTCCTCTCCTT[A/G]GTCCCATCTGTGCCT | 50807 |
| rs138597426 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130420819 | AATCACTTGAACTCG[C/G]GAGGCAGAGGTTGCA | 50807 |
| rs138601216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233733 | ATCTGATTAACATTT[A/C]TCTCTCCCCTACTGG | 50807 |
| rs138624136 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130232734 | TTCACAATGTTTAGC[C/T]ATTTTTCAAATCACT | 50807 |
| rs138626196 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156698 | GACCCAGGTTCAAAT[C/T]TGAGTGTTCATACTT | 50807 |
| rs138642426 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132580 | GAGGGTGTGTGCCCC[A/G]AGTCTATTCCTCCAG | 50807 |
| rs138642967 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330546 | TCCCTCAGTCATCTA[C/G]CAAAAACCAGGCACA | 50807 |
| rs138651777 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199027 | ACTCTGTCTGGAACA[C/T]TCTTCCTCTGTCTCC | 50807 |
| rs138655104 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069212 | GAAATGGAATGAATA[A/G]AATGGAAATTGATAC | 50807 |
| rs138659614 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090385 | TTATTTGGGGGAAAG[A/G/T]CCTTTTTGATGAAAT | 50807 |
| rs138661622 | snp | C/G/T | 0.00875412 | 0.0656548 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129240 | TTCCTTTATAAATTA[C/G/T]CCAGTCTACAGTATT | 50807 |
| rs138663615 | in-del | -/TCTTT | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324277 | TGTTAGGCTCACTTC[-/TCTTT]TTAACAAAATGAAAT | 50807 |
| rs138671276 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130441582 | TTCTTTCCTCTAGAC[G/T]TCAGTCACCTAGGTG | 50807 |
| rs138671793 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124490 | GGTTAAACTTTTAAT[A/G]AACAGCAATAGCTTA | 50807 |
| rs138691251 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248470 | AGTGGCCACAGGAGG[C/G]ATGAAGAGATACACT | 50807 |
| rs138692965 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168637 | ACCCCAAAAAACTCT[A/T]TAAACCTGCCTATTC | 50807 |
| rs138705649 | snp | C/G | 0.000115511 | 0.00759881 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136929 | CCACAATAACCAACT[C/G]AGAGAGAGAAAAAGG | 50807 |
| rs138724277 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120343 | CTTAAAAATTAAATC[A/G]CTCGATTCAAGTCTG | 50807 |
| rs138729565 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056224 | TTTATCCAAGGCCCA[C/T]AGAGCTAGTAACTGA | 50807 |
| rs138729709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130429868 | ATGTGGCCCTGCTTA[C/T]GCAAACTCCTCAATT | 50807 |
| rs138741550 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293182 | AATATCTGGGGATCT[C/G]TTTAAAATACAGATT | 50807 |
| rs138745562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404093 | ATATCTGCTAATTTT[C/T]TTCAATTGTAAGCCA | 50807 |
| rs138748576 | in-del | -/TATG | 0.0460142 | 0.144533 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206055 | AATTTTTATAATAAA[-/TATG]TATGATTTTTTAAAT | 50807 |
| rs138757769 | snp | A/C | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072491 | TGATTGCGAGGCCTC[A/C]CCTGCCACATGGAAC | 50807 |
| rs138773752 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093316 | CACTACTATTGCTTT[A/C]TTTAAGGTATATGGT | 50807 |
| rs138792864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130365990 | ATTTTAAGGATAACA[C/T]GCTTTCCAAACTTTT | 50807 |
| rs138799729 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411783 | TCAGCGGCTTCCCAG[C/G]AAGGCCAGCACCATA | 50807 |
| rs138841378 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258241 | AAAAGTCAATCGTCA[A/T]CCAGCCCATCCCCTG | 50807 |
| rs138858386 | in-del | -/A | 0.0513262 | 0.151752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278378 | CTCCTGTGCTAAATG[-/A]AAAAAAAAAAGAAAA | 50807 |
| rs138859919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130326224 | CTTACTGCTGGAGAC[C/T]GACAAATGAGAGAAG | 50807 |
| rs138867462 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370324 | ACAAACAAACAAACA[A/C]AAAAAACAGAGAGCA | 50807 |
| rs138876260 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391099 | GGAATGTTATTTAGC[C/T]TCAAAAATGAAGGAA | 50807 |
| rs138876660 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254865 | TAACAACTTTAAACT[C/T]AGAACACAGGATGGC | 50807 |
| rs138882878 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130107534 | TATGTATGTATGTAT[A/G]TATGTATGTATGTAT | 50807 |
| rs138883395 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263126 | ATAGTGTCTGATTAC[G/T]TGTGTTGATCACAAA | 50807 |
| rs138889354 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130184050 | TGCTAGAGCAGATAA[A/G]AATTCACAGAAGATT | 50807 |
| rs138890127 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081642 | GCTCAATAGCACCAC[C/T]GATTGCCCACATGCT | 50807 |
| rs138896132 | snp | A/G | 8.23988e-05 | 0.00641815 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116662 | TAATAAATCTCCCAC[A/G]TCCATTTTTGCTTAC | 50807 |
| rs138900968 | snp | A/T | 8.23662e-05 | 0.00641688 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130079958 | ACTTGAAGAGGATGG[A/T]CCCCCATCGTTACCT | 50807 |
| rs138905412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288108 | GAGCTCCAGCTACAC[A/G]CATCAAGCAATCAGT | 50807 |
| rs138916310 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | ASAP1 | GRCh38.p7 | 8:130182590 | TTTCTTGGAGAAAGC[A/G]GATCTCTAATGATGC | 50807 |
| rs138924643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133063 | ATAAGAGAGGAACAT[A/G]GCATGTATTCTGTGC | 50807 |
| rs138941571 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375676 | AGAAGGGAGTTCCCA[G/T]GACTGCCCACCTGCC | 50807 |
| rs138949142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301010 | AAACCTAGGCTGACA[A/G]AGCCATAATGGGGCT | 50807 |
| rs138950345 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145243 | CAACAAGGGTACATA[A/C]AACTAAAACCTTCAG | 50807 |
| rs138952232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105821 | TGCCCGGGCATGATA[G/T]GTGCCACATTGCTCT | 50807 |
| rs138965267 | snp | G/T | 0.000153988 | 0.00877328 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130126070 | CAAAATACCCAAGTT[G/T]GTTGAAAGCCAGGTG | 50807 |
| rs138970857 | in-del | -/CA | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274107 | TAAAAGTCTATGACT[-/CA]CACAATACCTTATAT | 50807 |
| rs138983718 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214039 | ATCTCAAAACCCTTT[C/T]CTTGGTTGGGGGTTA | 50807 |
| rs138987805 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130142969 | GAGGAGGGCCTGAAT[C/T]AGAGCTACGTACGGT | 50807 |
| rs138997730 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293869 | CAACATTTACTGAAT[A/G]TGCACCATGTGCCTT | 50807 |
| rs139001393 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108536 | GGGTGTGGTGGCTCA[C/T]GCCTGTAATCTTGGC | 50807 |
| rs139002096 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130072826 | GTGTGTGTGTGTGTG[C/T]GCGCGGGGGGGGGCA | 50807 |
| rs139007026 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421569 | GGGTGTGCTTTCTCC[A/G]GGCTCCTTCCCTCTT | 50807 |
| rs139037363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417358 | GGAAAGGATGCTGGG[C/T]GGTTCCCAGATGCCC | 50807 |
| rs139042428 | in-del | -/G | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069018 | GGTTAATTAACAAGA[-/G]GAACAGGGAAAGGCA | 50807 |
| rs139042649 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058552 | AAAACAGCAAGTCAG[G/T]ACATGCTGGTTAAAC | 50807 |
| rs139052464 | in-del | -/GAAAA | 0.198634 | 0.244666 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084808 | AACAAAAAAACAAAG[-/GAAAA]GAAAAGAAAAGAAAA | 50807 |
| rs139064137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122602 | ATATATGTTCTGGAT[A/G]AGGAAACTAAGGCAC | 50807 |
| rs139084992 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401816 | ATTTTGCATTTCAAC[A/T]CCCAAGAAGAATCCC | 50807 |
| rs139089533 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145692 | CATATGTTTTACATA[C/T]ACTTGCTCACTTAAT | 50807 |
| rs139116417 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | ASAP1 | GRCh38.p7 | 8:130112141 | GCCTCCGTGGTTGGT[A/G]ATGTGGGCGAGTCTG | 50807 |
| rs139117249 | in-del | -/AGAA | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180017 | GAGAAAGAGAGAGAG[-/AGAA]AGAAAGGAGAGGGAG | 50807 |
| rs139121819 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354180 | CAGGCCTGAGCCACC[A/G]CGCCCAGCCGGGAGG | 50807 |
| rs139121951 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425397 | TGTCACACAGCTGTA[G/T]TCCCAACTGTTTGGG | 50807 |
| rs139123188 | snp | A/G | 0.238749 | 0.249747 | intron-variant | ASAP1 | GRCh38.p7 | 8:130268396 | GGAGACTGAGGTGGG[A/G]GAATCACTTGAGCCC | 50807 |
| rs139128742 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130191167 | GATGCTACCCAGCTG[C/T]AGAGAAGAATGGCAG | 50807 |
| rs139129244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130290862 | CCTTGCTTTGATATG[C/T]TTTAAAGCCACTGAG | 50807 |
| rs139131170 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130361594 | ATGCTCACAATGAGA[C/T]ATTGTGCTTTGGTAA | 50807 |
| rs139140433 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084072 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 50807 |
| rs139153308 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154858 | ATAAACCATCCTCAA[A/G]TAAGAGCTAAATCAC | 50807 |
| rs139167483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090663 | TGCTCTAATGACTTA[A/C]CCACGTGTGTCCTGC | 50807 |
| rs139170036 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130185135 | CATCAAAGAGACAAA[C/T]GCTTGTTTTCTTTCT | 50807 |
| rs139170075 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373185 | AAACAAGAGCCAGAA[A/G]AAAAAAAAAACCATG | 50807 |
| rs139173009 | snp | A/C | 0.00983566 | 0.0694341 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118273 | AAGAAAAGTATAAGT[A/C]AGTCAATAATATGCT | 50807 |
| rs139173488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088613 | CTGGAGGGAGCAAAA[C/T]CCTGCTGGATTTTGG | 50807 |
| rs139204644 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252991 | CTTTTAGCTTCCCAC[C/G]AGTTCTAAGATCCTA | 50807 |
| rs139207714 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170644 | AATACTACCTTTAGA[A/C]AGTTTTTCAGCAACA | 50807 |
| rs139213997 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130429007 | TCCTGGCTTGTGGTG[A/G]TTGCCAGAAATCCTT | 50807 |
| rs139227789 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425442 | GAATCCTTTGAACCC[A/G/T]TGAGGCAGAGGTTGC | 50807 |
| rs139239319 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355157 | GTGCTGGGATTACAG[C/G]TATGACCCACCACGC | 50807 |
| rs139241324 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144088 | CCATTATGGTCATTT[C/G/T]AAAGTTTTCATTCAA | 50807 |
| rs139248999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077240 | TGGAGGACAGGTAAA[C/T]GAGGGTGACAAAGGC | 50807 |
| rs139282070 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130201855 | ACATCGGATCACATT[G/T]TCCTTGCTTTCACTC | 50807 |
| rs139286089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131049 | GTAGTTCCAGGTACT[C/T]GCGAGGCTGAGGCAG | 50807 |
| rs139308428 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204422 | ATGCTCTGTGACTCA[G/T]TTTGTGAGCTCTTAA | 50807 |
| rs139312153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130315149 | AGCAAAAAATACTAC[A/G]TATCAATTGGGCAGG | 50807 |
| rs139313336 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054054 | TTTTGCATAATGAGG[C/T]AATATATCAGGGGCG | 50807 |
| rs139316011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246128 | GTCCTACATGTAACA[C/T]GGGCAAAAGGAAGCC | 50807 |
| rs139327594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343125 | AGAAGCTGGCCATGT[C/T]TGGTCTTTAACCATT | 50807 |
| rs139328126 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130426568 | TTTTCCTGCACCAAC[G/T]TTCTTGTCACTTACT | 50807 |
| rs139381484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096169 | TGAAAAATACTATAT[A/G]TAAGACCCCAGAAAT | 50807 |
| rs139385441 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130196875 | CTCCTTCATGCCCTA[C/G]AGAGTTATAATACCT | 50807 |
| rs139392800 | in-del | -/C | 0.030665 | 0.119967 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320685 | ATGTAGCTTTCCACA[-/C]AACCAGGAAGAAGTA | 50807 |
| rs139398150 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397384 | GGCCTCAGGTGATCC[A/G]CCAGCCTTCGCCTCC | 50807 |
| rs139399897 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130298280 | GAAGCTAATACACAT[A/C]TTTTCAACATGATGT | 50807 |
| rs139400082 | in-del | -/A | 0.0573587 | 0.15934 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444331 | TGAGCCTCAGTTTCC[-/A]ATTTATGAAATGGAT | 50807 |
| rs139401036 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373574 | ATAAACTTGGCCAGG[A/T]GCAGTGGCTCACGCC | 50807 |
| rs139406314 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323059 | TGCATCTGCTGGAGT[A/G]AAGACAGTGCTCCAG | 50807 |
| rs139406476 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206463 | GAAAAATAAAAAAAA[A/C]AACAACTTTAACACA | 50807 |
| rs139407720 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130369206 | TATTTTTTTTTATTT[C/G]TGGAATGTTTACATA | 50807 |
| rs139409662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434543 | CAATACATAATAGCT[A/G]TCACTATTGATTCCA | 50807 |
| rs139410153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272337 | ACCAAAACAAACAAA[C/T]AAAACCCCTATGTTG | 50807 |
| rs139418294 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319315 | AAAAATAAAATAAAA[C/T]AAAAAAAGGAATAAA | 50807 |
| rs139433264 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409884 | ACTGCAGGCACTGGG[C/G]CTGACAGTGAGGAGG | 50807 |
| rs139447195 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261247 | CACATGACATCATAG[A/C/T]CCCTAAACACAGGCC | 50807 |
| rs139455769 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054494 | AGATGTAAGTGCTAG[A/T]TGCCAAGGATGGCTT | 50807 |
| rs139461398 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098186 | AGTCACAGCAAATGA[A/G]CAGCTACGTCCAGGC | 50807 |
| rs139485506 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155205 | AATACACACACACGC[A/G]CGCACACACCCCTTC | 50807 |
| rs139486329 | in-del | -/AATA | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144101 | TCAAAGTTTTCATTC[-/AATA]AATAAATAGTTTTTT | 50807 |
| rs139488086 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091434 | AGGCAGAGGATGGTG[C/T]ATCCAAGAAGTGAAA | 50807 |
| rs139488682 | in-del | -/C | 0.470424 | 0.117954 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257787 | TTGGACTCAAGAGCA[-/C]CCCCCCCCCATTATT | 50807 |
| rs139493168 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104030 | ATATTCTCTACCATA[C/T]ATTACAGCTACAATT | 50807 |
| rs139502759 | snp | G/T | 0.000153988 | 0.00877328 | missense | ASAP1 | GRCh38.p7 | 8:130167552 | TCTTTCTGATCCAGT[G/T]GAAGAGAGGATTTTA | 50807 |
| rs139507832 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368007 | ATGCTATTTAGTTAA[C/T]GTCCTTTTTCAAGTG | 50807 |
| rs139512656 | in-del | -/AAAAACCC/AAACC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130282931 | ATCATTTAAGTAAAA[-/AAAAACCC/AAACC]CAGCCACTAATTGAA | 50807 |
| rs139537004 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130327674 | CAGAATATTGTGCAG[C/T]CATTAAAAAGCATGG | 50807 |
| rs139546873 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259935 | CATAGGCAGCACCGA[A/C]AATTATTTTAAAATT | 50807 |
| rs139548111 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284385 | TAATTTAGCCACAAA[G/T]TATGAGGTTCAAATG | 50807 |
| rs139552447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130210061 | AGGAAGGACTACTTA[C/T]GAAGTTTTTATGTAG | 50807 |
| rs139555985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323616 | ACCTCCCTCTACTGT[A/C]TGTTCCCCCTAATTC | 50807 |
| rs139557850 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114231 | CATCATAGAGTATAC[C/T]TACACAAACCTAGAT | 50807 |
| rs139565086 | in-del | -/ATC | 0.0441354 | 0.141844 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285928 | TTTACTGGAACAGAT[-/ATC]ATAAATAATTTGCTA | 50807 |
| rs139576124 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434241 | GGATCACTTGAACCT[A/G]GGAGGATTACTTGAA | 50807 |
| rs139582634 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170065 | ATTTCTCAAAACACT[A/G]TCTGTTTTGCTGTCT | 50807 |
| rs139584636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130256282 | TCCTCAGGTTTTTTG[C/T]TTTAGGAGAATGAGT | 50807 |
| rs139586744 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066787 | ACTTCCGTAAATTCA[A/G]AGGGCCATAAGAGTC | 50807 |
| rs139587082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106562 | GCAAGTCAACTATCA[C/T]ACCTGTGGACATCTG | 50807 |
| rs139590648 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151053 | GCCTACACCAGAACA[C/T]GGCAGAATGGAAGCT | 50807 |
| rs139602175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324525 | TGAGGCAAACTGACT[C/T]GGGCAAGTACTTAGA | 50807 |
| rs139605992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438591 | AGAGGACTTGGGGTA[C/T]GAGGCGGGGAGCTGG | 50807 |
| rs139632528 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130210530 | TTCCAATATGCTATA[A/T]CTCACCAATGAGAGA | 50807 |
| rs139636690 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140958 | TAATAATTGTAACTT[C/T]AGATGTTTGTGTAAC | 50807 |
| rs139637211 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166587 | AGTCATCTTCCAATG[C/T]ATCTCTAATAGTATC | 50807 |
| rs139641406 | in-del | -/AAAT | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281223 | AAAGGATGCTGGGAG[-/AAAT]AAATAAACCTACAAC | 50807 |
| rs139643704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146495 | CTAATCTGTTGGAGC[A/G]AAGAAAAATATTCTC | 50807 |
| rs139653939 | snp | C/T | 0.24019 | 0.249807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382146 | AAAAAATTAGCTGGG[C/T]GTGGTGGCAGGCGCC | 50807 |
| rs139673382 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318686 | ACCTCCTTTTACAGT[C/T]AGGTCCCTTTCCCAA | 50807 |
| rs139681445 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173570 | CAGGAGTTTGAGACC[A/G]GCCTGGACAACATGG | 50807 |
| rs139682596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109303 | GAGACTCTGGGGCAC[C/T]GCTCACTTGTAAGCA | 50807 |
| rs139684484 | in-del | -/AGGGGA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130071000 | GAGAGAGAGAGAGAG[-/AGGGGA]GGGGGGGAGAGAGAG | 50807 |
| rs139691451 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263318 | GGGCCAGTCAGATCC[C/T]ACCCTCTCAGGAATT | 50807 |
| rs139691776 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217975 | CCACATTAAAAATTC[A/G]TGGTGCCTGCAGTGG | 50807 |
| rs139702752 | snp | C/T | 0.031825 | 0.122064 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070227 | ATTTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 50807 |
| rs139707749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144778 | GGCTGAATTCCCTTA[A/G]CCCTCCCAACCATTT | 50807 |
| rs139713743 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378856 | CACACATATAACATG[C/T]CATGATCTGGGCAAC | 50807 |
| rs139715361 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444451 | CTTGTCCTTATTATT[A/G]CCATTAAAAGACATC | 50807 |
| rs139715805 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130089083 | AGACAGGCAAGGAAA[-/C]CAGCCACTGTGATAC | 50807 |
| rs139724938 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163195 | AATCAAAAACAAGCA[A/T]CTGTGTATCTCTAAT | 50807 |
| rs139728112 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109953 | GATTTCTATTTTCAA[C/T]TATGGGCTTTTTTTG | 50807 |
| rs139741089 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099679 | ATGAAAGGATTTCAT[C/T]CTTTTTTTTTTTTTT | 50807 |
| rs139744969 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130111088 | CTATGAGCGGGATTC[C/T]TCGTCTGGGCGCAGT | 50807 |
| rs139747669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342123 | GAGCCAGGGCATTCA[C/T]GGTGAGGTGGAAAAG | 50807 |
| rs139757765 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130225475 | TCAATATTTAAATAC[A/G]TAATACATCTGCAAT | 50807 |
| rs139761337 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339671 | GCTATAATCAGGAAG[A/T]GTTTTAACCAATAAA | 50807 |
| rs139781406 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222109 | TTTATATCCCTAGGC[A/G]TTGGCAATAACAAGT | 50807 |
| rs139782270 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130338746 | CTGAGGACAATCCCA[A/T]CTCCCCTGCCACACC | 50807 |
| rs139783202 | snp | A/G | 3.34426e-05 | 0.00408903 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130179275 | TCACTTGCACTGTGC[A/G]TGGTAATACTTTATA | 50807 |
| rs139786299 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130279862 | GACCCTGAGCTATTT[A/G]CAACCTTTTGCCTCT | 50807 |
| rs139790881 | in-del | -/GAGAGAG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130262418 | AAAAAAAAAAAAAAA[-/GAGAGAG]AGAGAGAGAGAGAGA | 50807 |
| rs139791034 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130344350 | GAGGAAGTGTTTTTT[-/T]CAGACGAGAAAACAT | 50807 |
| rs139792238 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205529 | GTTATGGTACAGATA[C/T]ACAATGAAACAGTAT | 50807 |
| rs139795768 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301790 | TTCCATGTCAACAGA[A/T]ATGCATATGCATTGT | 50807 |
| rs139799922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119105 | AACTCTCTATTTTTT[A/G]TTTATTTTGTAAAAT | 50807 |
| rs139818827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387701 | ACCAACTTTTTAACC[A/G]CTTGTATATATATAT | 50807 |
| rs139840064 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130190657 | TGAATAGCTGGGATC[A/C]CAGGCATGCATCACT | 50807 |
| rs139846121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084592 | GGCCAGGTTGCTACA[C/G]GAGTATTCTGGAATA | 50807 |
| rs139875069 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112801 | ACTGCCCGCTACACA[A/G]TAATTACTTACAGAT | 50807 |
| rs139877739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130186120 | TTGTCTCTGGGCAGC[A/G]GCAGTACTTCGCTTA | 50807 |
| rs139892754 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397955 | GCATCCTAGCCAGGT[A/T]ACTGGCACATAAGTA | 50807 |
| rs139898657 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370591 | TGTGCACATAAAACC[-/T]TGTACACCAATGTTC | 50807 |
| rs139928597 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130395643 | GTTGATCTTGAACTT[C/T]TGGCCTCCAAACTGT | 50807 |
| rs139946461 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158039 | GACTCAAAATATCTT[C/T]GTTGAATGCATGAGT | 50807 |
| rs139947354 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167102 | TGAGTCCAGCAGTTC[A/G]AGACCAGCCAGGGCA | 50807 |
| rs139951615 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347709 | CTGACCCAAGTGGAG[C/T]CAATCCAATCCTCCT | 50807 |
| rs139958987 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069678 | TTAATACAACATTAT[C/T]GAAGCTTGGGTGGAC | 50807 |
| rs139959707 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360504 | GCACTGTGCCTCCAG[C/T]GAGATGCTCATCAAT | 50807 |
| rs139962021 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334268 | AGGTAACAACAACAA[A/C]AAAAATATCAAGCAC | 50807 |
| rs139965449 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247046 | ACGGCTACAAACACA[A/C]GCTTTGAGGTCATAG | 50807 |
| rs139967295 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276129 | CAAAAAGAACCCTGC[A/G/T]GGCCTGACCTCTAGG | 50807 |
| rs139971373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289331 | AGAAAAAGCATCAGT[A/G]TGTTCACAGTAAGAA | 50807 |
| rs139977752 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285241 | AATGACTTTAAATAG[C/T]TGACCTTCCTTGCAG | 50807 |
| rs139982854 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130228542 | CACGTCCCTACAAAA[-/A]CCACAAAAATTAGCC | 50807 |
| rs139993772 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275787 | GGAGGCCATATCAGA[G/T]AAAAGATAGATTTAT | 50807 |
| rs140013789 | snp | A/G | 0.0399052 | 0.1355 | upstream-variant-2KB, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130443729 | ACGATCCCGCTCGGC[A/G]GCGGAGGGCGCGGGT | 50807 |
| rs140013896 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134094 | GCAGAATCTTGCAGG[A/G]GGTACCAGAGCTTAT | 50807 |
| rs140021026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391272 | TATTTCCAGGGATGG[A/G]AAGGGAGAGGGAAGA | 50807 |
| rs140038134 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252312 | TGTAAAGTGCAGAGA[A/G]GTACCTACAGATGTT | 50807 |
| rs140112151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234976 | TTGTTAGGCACCTAC[C/T]ATGTGGCAGGCAGTG | 50807 |
| rs140114059 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130279657 | AAATAGACTTGACTA[A/G]ATAATTTCTAGATCT | 50807 |
| rs140123391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223094 | GTGTCATAATTAATA[C/T]AAAAGCTCTTTTGGA | 50807 |
| rs140126815 | snp | G/T | 0.0501905 | 0.150254 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158899 | ACCATGCCTGGCTAA[G/T]TTTTTGTATTTTTAG | 50807 |
| rs140137305 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410473 | TCACTAACTAGCCAC[A/G]CAATCCAATCCTCAT | 50807 |
| rs140146948 | snp | C/G/T | 0.00041551 | 0.0144079 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126099 | TGGGTTCTGTGGAAA[C/G/T]AATGTTGAAGACAAT | 50807 |
| rs140157360 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063128 | AAAGATATACACTAA[C/T]TCATCAGTTATCTTG | 50807 |
| rs140169739 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381697 | GTCTAAAGGCCTTAT[A/G]TGACCAGGCCACTGT | 50807 |
| rs140177011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264415 | CAAAGGCAGTCGTGC[A/G]TGCCAGGCAGCTGAC | 50807 |
| rs140178871 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130243235 | AAACATTCATTATTG[A/C]TAACCTGGGGCTTGC | 50807 |
| rs140179244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130186462 | AGCTTTAAAAATACA[C/T]ATCTCCTCCCACCCC | 50807 |
| rs140179974 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307123 | TAAAAGTTATCAGTA[A/C]CTGAACTTAATTTTA | 50807 |
| rs140186431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130302374 | ACAGACACAGAAAAT[A/G]TGGCACTGTGAACAG | 50807 |
| rs140193157 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164845 | TAAATGATTTGTTGG[A/G]TGCTTTTGATTCCTC | 50807 |
| rs140201782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378577 | GGAGCTGAGGTCAGA[C/T]GGGTAGGCAAGGGTG | 50807 |
| rs140206330 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240161 | TTTTGTGGGGGGGAG[C/T]GGGTACAGTCTCAGA | 50807 |
| rs140211761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349252 | CTCTCCTTAGTCCCA[C/T]CTGTGCCTCCCCAGT | 50807 |
| rs140213894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122813 | AAGCTGACCAGGTGG[C/T]GCTGATGCTGCTTCC | 50807 |
| rs140215068 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175365 | AGCTGGGAAAATAGG[C/T]GTGTGCCACCACACC | 50807 |
| rs140219526 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111562 | TTGAGATGATTACAA[A/G]AGAAGTACTAGGCGT | 50807 |
| rs140222553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385478 | GCTGGGTGCTAGAGA[C/T]TCCTTTCCCAATTTT | 50807 |
| rs140229324 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421012 | CTCCAATGAGGAACA[C/T]ACAGTATAGCCACTA | 50807 |
| rs140242839 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281490 | TCTACCTTCTAAGAA[C/T]AGGGGTTTATATCTC | 50807 |
| rs140252753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148847 | AGGCTAAAACTTTTT[C/T]TTCTTGAGACAGGGC | 50807 |
| rs140254755 | snp | A/G | 0.0584853 | 0.160693 | utr-variant-5-prime, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130443579 | GGGAGGCGCGGGCCC[A/G]GGGCTGCCCAGCGCA | 50807 |
| rs140255866 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392635 | CTCTAATGGAATAAC[C/T]GAAGCTGGGTAATTA | 50807 |
| rs140256710 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402119 | GCTGTCCAGAAATAT[A/G]AAGGAAACTACTATT | 50807 |
| rs140258532 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085457 | AGAAAGAGGAGGACC[C/G]GGTGAAGAGGCTCAC | 50807 |
| rs140266609 | snp | A/C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130328261 | TATGTAGTGCCACAA[A/C/T]AGAGTTTCAAAACCA | 50807 |
| rs140279378 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313669 | CAGAAAATAAAAAAT[A/T]AAATTAAATTAACTT | 50807 |
| rs140306528 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130065908 | GTGCAGAGCTGTTTC[A/G]CACAGAGATCAGCTG | 50807 |
| rs140313308 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352094 | GAGAGAAACATTATG[C/G]GAAGGTTTGTTTGCC | 50807 |
| rs140320002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439171 | AAGACCAACACTGCC[A/G]GCTTTGGAGGTGGAA | 50807 |
| rs140324863 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199134 | GACCAGTGGCAGAAT[A/G]GGCTCACTTTCACAG | 50807 |
| rs140325070 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316648 | AGCTGGAGCTCTGGC[A/T]GCAATCTTAAGCTGA | 50807 |
| rs140344567 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129986 | TTCAACAGGACTGAT[A/T]ACTGCATTTTATCAG | 50807 |
| rs140353825 | snp | A/C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130135288 | TTAAGCCTAGGAGTT[A/C/T]GAGACCAGCTTCAGC | 50807 |
| rs140363624 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130071435 | GTAAAAATAGCTCAT[A/T]GGTTCTGCATCTATG | 50807 |
| rs140364301 | snp | A/T | 0.495521 | 0.0471118 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262457 | GAGAGAGAGAGAGAG[A/T]ACCTGTGGAATTTCA | 50807 |
| rs140372501 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096897 | TTGGGAGGCCGAGGC[A/G]TGAGGGTCACTTGAG | 50807 |
| rs140376720 | in-del | -/TCTC | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170731 | ACATGTAAAGCCTCA[-/TCTC]ATCTCTCTCTCTCTC | 50807 |
| rs140397345 | in-del | -/T | 0.0146672 | 0.084371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220989 | GTCCCTCCCCCAACA[-/T]TGTGGGGATTACAAT | 50807 |
| rs140397686 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293458 | ACTTCCTGAAACCAA[A/G]CTGCCTCATGACATA | 50807 |
| rs140397878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222389 | CACTGACTAAGTAGA[A/G]GGATTCAATCACAGT | 50807 |
| rs140398724 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159754 | ACCAGTGTGCTAAAG[A/G]TCTGCAGCTAGTGTA | 50807 |
| rs140409323 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276888 | CACTCACAGTGCCAG[C/G]AGCGGTCTTGGCAGA | 50807 |
| rs140410314 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130291210 | TGTGAATGTCAAATT[A/C]TCCTAGTGTCGAAAA | 50807 |
| rs140411801 | snp | C/T | 0.0130921 | 0.0798413 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445527 | AAGAAGCAAACAAAC[C/T]AGAGTTGCAGATGGG | 50807 |
| rs140411972 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333408 | GGAGTTCGGGACCAG[A/C]CTGACCAACATGGTG | 50807 |
| rs140419646 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348474 | TGGCATTAAAATTCA[G/T]TTCTTACACAACTGA | 50807 |
| rs140424638 | in-del | -/AAAAT | 0.232359 | 0.249377 | intron-variant | ASAP1 | GRCh38.p7 | 8:130363374 | CATTTTTTTTAATAA[-/AAAAT]AAAATAAATTCTGAT | 50807 |
| rs140449543 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405350 | CTAAGATCCTGACCC[A/G]GGTGGTCTAAAAAAC | 50807 |
| rs140454503 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336364 | GCATCACCTGAGAAT[C/T]GAAAAGAAATGCAGA | 50807 |
| rs140456925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407496 | ATAGACGCTCAATAA[A/G]TATCTGTCGAAGGAG | 50807 |
| rs140464891 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123789 | CCTGCCACCACGCCC[A/G]GCTAATTTTTAAAAA | 50807 |
| rs140467036 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370782 | GGAAACATTATGCTA[A/T]GTCAAAAGTCAGATA | 50807 |
| rs140480205 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130071011 | AGAGAGGGGAGGGGG[A/G]GAGAGAGAGAGAGAG | 50807 |
| rs140485977 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130303286 | GCAAAACTATAAGTG[C/T]ATGCCTAAAATACTT | 50807 |
| rs140488459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063912 | ACAAGTAAACATGGA[A/G]TTACCAGAGGGTGAG | 50807 |
| rs140492989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130231614 | AAAGACCTAGTAGCA[A/G]GAATATCCTGAGTTC | 50807 |
| rs140508975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436651 | CCAAATATAAAAAAT[A/G]AATAACCAGGCAAGG | 50807 |
| rs140510516 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088621 | AGCAAAACCCTGCTG[C/G]ATTTTGGACCTCTAG | 50807 |
| rs140528166 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292331 | GGGTAATAAGATGTG[C/G]AGTTAAGATGGTGTG | 50807 |
| rs140530305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364699 | CTCCAGGTGGGATTA[A/G]TCTTCATGTGGGTAT | 50807 |
| rs140538639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086366 | TACGTTAACACATGC[A/G]AAGTGCTCAACACAA | 50807 |
| rs140539959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296467 | GGGATTGGTAAGCAG[A/G]GGTCCCTGTGCTATT | 50807 |
| rs140545041 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163918 | TATAAAATGTATTAT[C/T]AAGAGGTAGAGTCTC | 50807 |
| rs140553461 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100026 | TGCACTGGATAAATA[A/C]CCAGTAGTAGAATTG | 50807 |
| rs140559309 | snp | A/G | 7.22491e-05 | 0.00600994 | missense | ASAP1 | GRCh38.p7 | 8:130061022 | GAAAGATTTCGGGCG[A/G]GATGGTGGCTTTGTC | 50807 |
| rs140563079 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402906 | ATGCTGAAAGCAGAA[C/T]AATCTTTTGTGGGGT | 50807 |
| rs140564009 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187697 | AAAGTGCTCAGATTA[C/T]AGGCATGACCACTGT | 50807 |
| rs140564730 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144392 | GGTACTGTTCCCAAA[C/T]CCATTTCATAAATGA | 50807 |
| rs140576126 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078322 | TTTTTTTTGAGACAG[A/G]GTCTTGCTGTCGCCC | 50807 |
| rs140599301 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262124 | AGTACCGGCTGGGCG[C/T]GGTGGCTCACACCTG | 50807 |
| rs140628200 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130440665 | CCTTGCGCCATTCCC[C/G]CCATCTCTCCCTTAC | 50807 |
| rs140630133 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179727 | TCAAAGAATATACCA[C/T]AGGATATTGAAACTT | 50807 |
| rs140640506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334858 | AATGTGACTAAAAAT[C/G]ATCATCCCACTAACA | 50807 |
| rs140647454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254298 | TCAGGAAAGAGCATT[A/G]TAAAAAGTGCATTGT | 50807 |
| rs140649809 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264801 | AAACCACAATGTCAA[A/C/T]ACACGATGATCACTA | 50807 |
| rs140655372 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356483 | TGGGGTTCAATGCCT[C/G]GCAATTCTGTTTAAT | 50807 |
| rs140673010 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418300 | CACACCTGTAATCCC[A/G]GCACTTTGGGAGGGC | 50807 |
| rs140674108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130329588 | GATACTGCTCTCCTC[C/T]AGAGCTCCTGTGCAA | 50807 |
| rs140674458 | snp | C/T | 0.0037786 | 0.043302 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130060609 | GGGCAGTGGTACGGG[C/T]GTCTCTGGCAGAGTA | 50807 |
| rs140683079 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348234 | AGAGCTTACATTTTC[A/C]TCCACCCAAAACGCA | 50807 |
| rs140685922 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080539 | AGAGTGCAGTGGTGC[A/C]ATCATGGCTCACTGT | 50807 |
| rs140693681 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111803 | GGTCAGTGTATCTCA[C/T]TGAGCCTTAGTTTCC | 50807 |
| rs140698505 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428060 | GGCCACAAAGCACCC[A/G]CCCCACCATTGTCTA | 50807 |
| rs140699732 | in-del | -/AAAT | 0.139903 | 0.224452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090264 | ACTTCAAACCTTAAG[-/AAAT]AAAGCCACTTAAACA | 50807 |
| rs140722479 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223291 | GACACAGAGACTTGG[C/G]TCTGAATCCCCACTC | 50807 |
| rs140725209 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149441 | CCAATTTTTCAGGTG[C/T]ACACAGAAATGTATT | 50807 |
| rs140741900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130181446 | TCCTTGAATATCGAC[A/G]GCTTGCAAGACTTCA | 50807 |
| rs140774732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132194 | GTTTCCTCATTTGCA[A/G]ACTAGGGACAAAAGT | 50807 |
| rs140779383 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248013 | CTTTAAAATACTGGT[A/G]ACTTACTGAAAAACA | 50807 |
| rs140789609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145070 | GCTGAGGTTACTGCA[C/T]CCAATGAATGTGCTA | 50807 |
| rs140790609 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389569 | ATACTCCAAGAAACC[C/T]CAGTTCCTTCCCCAG | 50807 |
| rs140794060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417014 | GTACATTTGCATACA[C/T]GCATATGGACACACA | 50807 |
| rs140794718 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428452 | CACCACCACCATCAT[C/T]ATCACCATCATCATC | 50807 |
| rs140795718 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311671 | GAGGCTGAGGCAAGA[C/G]AATCGCTTGAACCCG | 50807 |
| rs140796919 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317006 | ACAGGCTATGCTGTT[C/G]AATGTTCCAGGCCCT | 50807 |
| rs140813721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240511 | CATCCTCTGAAATGT[C/T]ATATATGTAAAATTA | 50807 |
| rs140824983 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130308118 | AGAAATATTTTAAAT[A/G]CACATAACTATCCAT | 50807 |
| rs140832148 | in-del | -/T | 0.238749 | 0.249747 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057458 | CCATGGCTGTTTTTC[-/T]TTTTTTTTCAGATGG | 50807 |
| rs140845811 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115550 | AATCAATCAATCTCA[C/T]CAAAAATGGATCTTG | 50807 |
| rs140862706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104163 | TGAAAAAGTACAGTA[A/G]AGGTTCCTCTTCAAA | 50807 |
| rs140874350 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273072 | CCTGACCTCATAATT[A/G]CACATCCTATGCATG | 50807 |
| rs140890547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277440 | CCAGAAAGTTCAGTA[A/G]AAAAAATACAAATTC | 50807 |
| rs140895461 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130648 | AAAAATAACTTGGCA[C/T]TGTGCTAAGGGCTTT | 50807 |
| rs140899818 | in-del | -/A | 0.030665 | 0.119967 | intron-variant | ASAP1 | GRCh38.p7 | 8:130192231 | AAAAAATAAAAAACC[-/A]AAAAATCTTAGCTGT | 50807 |
| rs140905311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130312829 | ACCATTTAGTCATAC[C/T]CTAGCATTCTGGATT | 50807 |
| rs140907672 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388197 | TGAGTGTGAGGAACA[C/G]AACGGAGGCCAATGT | 50807 |
| rs140915819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330252 | GGGAGTCTCCATTCC[A/G]CTTTGCATTTTCTCA | 50807 |
| rs140922965 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055891 | GTGGTCTTAGTTGGC[A/T]TCATGCATGTGTGAG | 50807 |
| rs140937915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393188 | AGCGGTTTACCATTT[C/T]AAATGATGCTCCAAT | 50807 |
| rs140938739 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130441427 | TAGAAAAGACCTTCC[A/G]GAGCCCATGCCAGAT | 50807 |
| rs140948751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375154 | TGGGGATCAGCAGGC[A/G]CAAAGAACCTAGGCC | 50807 |
| rs140951716 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156192 | GTCAAAAATTACCAA[C/T]GCAAATAATACTTCA | 50807 |
| rs140957711 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092837 | AGAGTACAGGCTAAG[A/C]CTTCACTGGGCCACA | 50807 |
| rs140958424 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245762 | GCATCAAGAATTAAA[C/G]CTGTACAGAAGAAAA | 50807 |
| rs140958518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197490 | ACCAATGAAGCTCCA[C/T]TTTATTCCAGGCCAC | 50807 |
| rs140960440 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127785 | GCTCAGCGGTAGGAA[A/G]AATCACGTTGGGAAT | 50807 |
| rs140961379 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130351565 | TCTGCTTGGCTTCTG[C/T]GGATGCCTCAGGGAG | 50807 |
| rs140969702 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280490 | GTCTGCCACAGTAGA[C/G]AGCAGTCAACCATGT | 50807 |
| rs140981827 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238630 | TATAAGATATATACA[C/T]TTTCAAATATTTTAT | 50807 |
| rs140986607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269700 | CTGTCCTGGGAAAGT[C/T]GAAAGGTACGTAAAG | 50807 |
| rs140991136 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095710 | TGCAACTTCTGCCTC[C/G]CAGATTCAAGGGATT | 50807 |
| rs141017948 | snp | C/T | 0.000314 | 0.012526 | missense | ASAP1 | GRCh38.p7 | 8:130118216 | GATCTGCAGTTCGGA[C/T]GGCAAGGTGAAGGGC | 50807 |
| rs141018655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325642 | AGTGAGACACTAATA[C/T]GTAAACAACTAGTTA | 50807 |
| rs141027227 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348909 | ATGTAACAGAGAAAA[C/T]AGCTCATTACCCCAA | 50807 |
| rs141027922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226762 | AAACAGCACCTGAAC[A/G]TCACTCTCCTATAGC | 50807 |
| rs141041843 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160210 | GTTCAAAACCCACCT[C/G]TACTCTGAACTGAAT | 50807 |
| rs141044744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130201045 | GAAACTTGTTGGTTA[C/T]GAAATCCCAGACCTA | 50807 |
| rs141045282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063526 | CAGGGTACACTGGCC[A/C]AGGTGACTCAACTCT | 50807 |
| rs141046195 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436093 | AGCAATGTGAAAGAG[A/G]ACATTAGTATATTTA | 50807 |
| rs141063755 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152137 | TTCATTGAGCAGTGC[C/T]CCAAGGACATCACTT | 50807 |
| rs141068606 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128586 | GAAAATGAAGGGATA[C/T]TTCATTAGCAGCCAT | 50807 |
| rs141075059 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064106 | TTGCGAGAAGAACCA[C/T]CAGATGGTTCAGGAC | 50807 |
| rs141077836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320180 | TAATGCAAAACCAAA[C/T]TTATCATGCCTATCA | 50807 |
| rs141099231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213723 | TTTCTCTGGGGACTT[A/G]GGAGGATTAAATTAT | 50807 |
| rs141108243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116332 | ACTCTCTGAGCTTTA[C/T]TTGCCCAATTTTTGG | 50807 |
| rs141114977 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241721 | ATGACTATACAGTCA[A/T]GAGAATAATGTCTTA | 50807 |
| rs141118648 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287377 | ATGCAGTATAGATGA[C/T]GGCACCATGCACTTA | 50807 |
| rs141123730 | snp | G/T | 1.6473e-05 | 0.00286988 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130058029 | CTCGTCATCGTTGTC[G/T]GCCTGGCAGTCATAA | 50807 |
| rs141129995 | snp | A/C | 0.115788 | 0.21092 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394697 | ATGTGATGTCTCCCC[A/C]GGACACCCAGCTTTA | 50807 |
| rs141145979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130363509 | CAACTTTATAAAGTA[A/G]GTATATTTATCCCAA | 50807 |
| rs141151882 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378254 | GCAGGGATTCCTATA[G/T]AGTTAATGGTGCAAT | 50807 |
| rs141160705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275260 | TATTCCTGGCCCTAA[A/C]AGAAAGAAGTTACAA | 50807 |
| rs141166789 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095112 | CTTATATACTTCTGA[A/C]TTCCTTCATATTGCT | 50807 |
| rs141171188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069306 | AGTGGCGTGATCTTA[A/G]CTCATTGCAATCTCT | 50807 |
| rs141171296 | snp | A/G | 0.0581099 | 0.160244 | utr-variant-5-prime, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130443581 | GAGGCGCGGGCCCGG[A/G]GCTGCCCAGCGCACA | 50807 |
| rs141183778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101776 | AGGGTTTCACCATGT[C/T]GCCCAGGCTGGTCTC | 50807 |
| rs141183907 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141195 | GAGAAACTCTGGAAA[C/T]GTCTATGTATCTATT | 50807 |
| rs141192426 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130271092 | AGAGCCTGCTGCCGG[C/G]CTGCTCTGATTTGGT | 50807 |
| rs141227840 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130210818 | ATGGGATATGACTGA[G/T]AGCTGTCTTTACACT | 50807 |
| rs141237061 | in-del | -/T | 0.0588605 | 0.161139 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379515 | ATCTGAAGTGGGAGC[-/T]GTTCTATGGGACTGA | 50807 |
| rs141240129 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228372 | GAGAACACAGATGTG[A/C]TGGGTGCTCCAAAAG | 50807 |
| rs141241501 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208339 | TCTGTCACATGTATA[C/G]ATAACTACAACAATC | 50807 |
| rs141241638 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257388 | CACAATCCAACTACA[C/T]TTATTTACATAGTTT | 50807 |
| rs141241729 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137108 | AGGTTCAGTGCCCTG[C/T]AGGGCAGGTATGCTG | 50807 |
| rs141242122 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154350 | AAAAGCCAAAGAGAA[C/T]GAATTAAAACTTGGA | 50807 |
| rs141254175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327294 | CATCCTCTCCCACCA[A/C]ACTGTTGTACCAAAA | 50807 |
| rs141255492 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401680 | TTATAAATAAAGGCA[A/G]TGGATAATGTGACAG | 50807 |
| rs141260131 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131543 | TCGAGGTGGGAGGAT[A/G]GCTTGAGCTCAGGAG | 50807 |
| rs141262579 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437951 | ACCTTCGCACTTCCT[C/G]ACTTAGGGCAGTGAA | 50807 |
| rs141265741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341443 | GTCAGACAGATCTTT[A/G]TATAAACCTCGGTTC | 50807 |
| rs141268203 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130067775 | CATCCACAAAAGGAA[C/T]GGTGATAAAAGTGTA | 50807 |
| rs141280260 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129384 | TGAGTGATTTTCTAT[A/G]GAAAACAACTGATAG | 50807 |
| rs141282868 | in-del | -/CT | 0.234109 | 0.249494 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205822 | TAAGGCATGTACACC[-/CT]GTCACCCTTCTGAAA | 50807 |
| rs141286735 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064538 | GAAAACTTGCTCCTC[C/T]AACCGTGCTTTTCCC | 50807 |
| rs141291002 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130294945 | ATGTGGACAGGGTTG[C/T]TGGATTAACAGCGAG | 50807 |
| rs141311704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406765 | TGGGGTTACAGGAAT[A/G]AGCCACTGTGCCTGC | 50807 |
| rs141311731 | in-del | -/A | 0.0528381 | 0.153711 | intron-variant | ASAP1 | GRCh38.p7 | 8:130089915 | ATGTGGCGAACTGTC[-/A]ACTGTGGCCGAGGAC | 50807 |
| rs141325303 | snp | A/G/T | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374485 | GACTAGGCCGGGCGC[A/G/T]GTGGCGCACGCCTGT | 50807 |
| rs141326030 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415696 | GGGAGGCTTAGGCAG[A/G]AGAATTGCTTGAACC | 50807 |
| rs141331330 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258188 | TGGCCCCAGCTCCAT[A/T]ATGGAAGACGTTAGG | 50807 |
| rs141335517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130298588 | CATGCCAATCCTTTG[C/T]TTCAAACCCTAAAGG | 50807 |
| rs141356636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370170 | ACCCAAGCATGGTGG[C/T]GCACACATATAATCC | 50807 |
| rs141359226 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118094 | GATCTAGGCCACTGA[C/T]AGGACTGGTTTGTGT | 50807 |
| rs141365520 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176981 | AGGCGTGAGCCACCG[C/T]GCCCAGCCGTCTCTC | 50807 |
| rs141369098 | snp | C/T | 0.0154538 | 0.0865337 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130053900 | CATACTATTCCTTTA[C/T]AAAAGGCAGATTTCA | 50807 |
| rs141371930 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130242284 | AAAAAAAAAAAAAAA[A/C]AACTTTTTTTTTTTT | 50807 |
| rs141382136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081261 | GTGGAGGTAAGTGTG[A/C]TATGTCCAGGAGAGG | 50807 |
| rs141389879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295447 | TTCAAGTCAGTTCTG[A/G]CACTTACTGGCTGTA | 50807 |
| rs141392919 | snp | A/C/T | 0.000151131 | 0.00869162 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130060903 | TTCTCCTGGCTTAGG[A/C/T]GGCAAATCTCCAATT | 50807 |
| rs141413325 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397077 | TTTTCCCAGGGATGA[A/C]AACCGCATTGCTGTG | 50807 |
| rs141413545 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130265708 | GCATCATGGCAAAAC[C/T]CTGTCTCGCTAAACA | 50807 |
| rs141423112 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145199 | CACATTTCCTATTAA[C/T]TTCAGTAGCCACTTT | 50807 |
| rs141424058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130308957 | AGTCTACAACTATCA[C/T]GGGCAGTTGAGGGAA | 50807 |
| rs141431018 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261486 | GGGTGGTGGGAGGCT[C/T]GGAAAATACGGGAAT | 50807 |
| rs141458607 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130246050 | ATTTATGAGGGCTTA[C/T]GACCTGGATGAAGCA | 50807 |
| rs141466230 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419509 | TACCAGTCTTGGGGA[A/G]ATGCCAACATAGGAA | 50807 |
| rs141468019 | in-del | -/GA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070867 | AGAGAGGGAGAGAGG[-/GA]GAGAGAGGGAGAGAG | 50807 |
| rs141469782 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178131 | TATAACTATTGAAAA[G/T]AATAAGAAAGATCAA | 50807 |
| rs141470400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380288 | GAACACACCTCAGAG[C/T]TGTGCACCTGAGAAG | 50807 |
| rs141476049 | snp | C/G/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112652 | CTTTTTCAGCAACAT[C/G/T]TGAATAGTATTTCCA | 50807 |
| rs141486599 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233950 | TCTTAATTTTGGCTG[C/T]AAGTTAGAATCAGCT | 50807 |
| rs141488395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354739 | ACGCCAGGATGAAAC[C/T]TTGGCAGAACACCAG | 50807 |
| rs141488729 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306789 | ACCATGTAACTTAAC[A/G]TGTATTTGTATTCCC | 50807 |
| rs141491274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284304 | TGAAAACTGGACAAA[C/T]AACCATTCTAGACAG | 50807 |
| rs141491954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130305423 | GCGATCTCGGCTCAC[A/C]GCAAGCTTCAGCTCA | 50807 |
| rs141506288 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270019 | TACTAAAAATAGAAA[A/C]ATTAGCCAGGCGTGG | 50807 |
| rs141551079 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073684 | GACGGCCAAGGAAGA[C/G]AGGGCTGAAGCTTAA | 50807 |
| rs141558062 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383858 | TGATACAGAAGAGCA[C/T]CAGCCCATTTCTCCC | 50807 |
| rs141561036 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130095622 | AGTGATTCTTTTGTC[-/T]CTTTTTTTTTTTTTT | 50807 |
| rs141564350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239531 | TTCTAATGATATCCG[C/T]GATAGGCTGAAACTA | 50807 |
| rs141564802 | snp | A/G | 0.000345904 | 0.0131466 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130167584 | TAAGTCTCGGAGTGC[A/G]GTTAGCTGTTTCTTT | 50807 |
| rs141575556 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137680 | GAGGCAATGCTTAAT[A/G]AACCCCAATATCTGG | 50807 |
| rs141582722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130172404 | CATGTAACCAAAAAC[C/T]ACCTGTACTCCAGAA | 50807 |
| rs141588043 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366936 | TTCTCTGTCACCCCA[A/G]GCTGGAGTGCAGTGG | 50807 |
| rs141588153 | in-del | -/T | 0.0799831 | 0.183287 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227261 | TTGTGGTTTTTTTTT[-/T]GAGACAGGATCTCAC | 50807 |
| rs141591049 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349571 | GCCCAACACACGCTA[G/T]AAGTAATAGGGATAC | 50807 |
| rs141600724 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155910 | GTCTCGTATAAATAG[A/G]TAATTCCAACTTTGA | 50807 |
| rs141609637 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130196528 | GACAGTCAGTCAGCA[C/G]GGCCTCGTTTTTTCT | 50807 |
| rs141612975 | in-del | -/CC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130126375 | AGAGATGTTCCCTCA[-/CC]CTGCCACTATCACCT | 50807 |
| rs141618395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195938 | AAAGAAATGATCTCA[C/T]TTATTGTTTACTGAT | 50807 |
| rs141635819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409603 | GGAGACCTTGCAGAA[A/G]CCCACCCCAAGAAGA | 50807 |
| rs141636210 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130310396 | CATAAAACCACCTAT[A/C]AACCTCTCCTTGACC | 50807 |
| rs141648357 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272648 | ATGTAGTATATATAC[A/G]AATGGAATACTATTT | 50807 |
| rs141650174 | in-del | -/AA | 0.0197687 | 0.0974348 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327180 | CACTCCAGTTCCTCT[-/AA]GAGTTGTCCTTGGAT | 50807 |
| rs141664594 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130152410 | TTCCTACATTATTTT[C/T]ACATGCAAAGAACAG | 50807 |
| rs141685322 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239113 | ATGTACCTCTACCTA[C/T]ACAAAATGCTCCTCC | 50807 |
| rs141687374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130190843 | TTTATGCCAGCATCA[C/T]GCTGGTTTGATTACT | 50807 |
| rs141688975 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309363 | CCTGACTAACAGAGA[A/G]GTGATGGGTGGCAAG | 50807 |
| rs141713791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293434 | CCATCGCTCATGCCC[C/G]AGCAAACCACTTCCT | 50807 |
| rs141721054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189367 | CTATTCTCTATCTCT[A/G]TGAGATCAATTTCCT | 50807 |
| rs141729390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130367854 | TCAAAAATATGATTT[C/T]GCCTGCAATGTATTT | 50807 |
| rs141732142 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059303 | CAAGTAGCTGGGATC[A/G]CAGGCATGTACCACC | 50807 |
| rs141736515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405187 | TATGATGACCACTGA[C/T]AGCTGTTCTTGCAGA | 50807 |
| rs141740273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431622 | GACCCTCCCTGCAAG[A/G]TGGAGTCAGGCACCT | 50807 |
| rs141743852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306258 | CTTAGAAGGTGTTAC[C/T]TTTCACTACAAGTAT | 50807 |
| rs141753373 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097517 | AGTGGTTGCCGCTGA[A/G]CCTACCTGATGTGCT | 50807 |
| rs141781924 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090446 | CTCTGAAAATGTCAC[A/G]GACATCCTTAGTCTT | 50807 |
| rs141792329 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150967 | TCACTCTGGCATACA[C/T]AGATGACTGTGTATG | 50807 |
| rs141793109 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119485 | GTGTTTCTGGTGGGA[C/T]TGAGCTCACCTCCCA | 50807 |
| rs141796531 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087244 | TGACAGGTGGGCCAA[G/T]TTCGGTGGCTCATGA | 50807 |
| rs141799609 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055460 | TGGCAAGACCCACTG[C/T]GGGGTACCATACTCA | 50807 |
| rs141823552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262768 | TTTTCAGATGCATTA[C/T]TAAATGCTTCACATT | 50807 |
| rs141834751 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360235 | TAGTATAAAGAATCT[A/G]CAGAGAAGGCTTTGC | 50807 |
| rs141838140 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130429757 | AGAAGGAGAACACCC[C/G]CACTCCCCCGCAACA | 50807 |
| rs141874614 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093532 | ATTAGCCAGGTGTGG[C/T]GGTGCACGCCTGTAG | 50807 |
| rs141887130 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360674 | AAATTAGTAAATAAA[C/T]AAACAGGCACCCACT | 50807 |
| rs141887883 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435036 | CTGCTGGAAGGCACG[C/T]TGTCCCATCGGCCTT | 50807 |
| rs141887955 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396026 | AGCAGCCCTAGGAAA[C/G]TAATGGAACATTTTC | 50807 |
| rs141890109 | in-del | -/AGGCCA | 0.0539704 | 0.155153 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178645 | AAATGGTGCAATAAT[-/AGGCCA]AGGCCAAGGTGGATC | 50807 |
| rs141892366 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109017 | CGACGTCAGGTGATC[C/T]GGCCACCTCGGTCTC | 50807 |
| rs141893785 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130205382 | TGTGAATCCTTATAA[-/G]AAAAAAAAAAAAAAA | 50807 |
| rs141895149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220296 | ATTCCAGTAATAATC[A/G]TTACAATAGCTAGTT | 50807 |
| rs141895226 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145508 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 50807 |
| rs141906386 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318136 | GGTCTCACTGTAACA[C/T]AGTGATGCAGTCACA | 50807 |
| rs141912441 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251722 | TATAAAGACCCAGAA[A/G]AACAGAGGGACAAAA | 50807 |
| rs141913119 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130321535 | ATCTCCAGCTTTTCC[A/G]CAAAGTATCCCTTAG | 50807 |
| rs141915064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130255346 | CTATTTTCTTTTTTG[C/T]TGGCTTCCTAACTTG | 50807 |
| rs141929606 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211634 | ACCTGGCCCGCAAAT[C/T]TATCCTTTCCTTTTT | 50807 |
| rs141932747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286658 | GCCTGGTGCACAGGA[A/C]GTACCCAATAAGGGT | 50807 |
| rs141944971 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425085 | CCTGTAATCCCAACA[C/T]TTTGAGAGGCCGAAG | 50807 |
| rs141966900 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432863 | AATCACTGCCAAGGG[C/G]AATAGGACCCAGTGA | 50807 |
| rs141974142 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105661 | AAAAAGTAATTAACC[A/C/G]TATAATTATACAAAG | 50807 |
| rs141975632 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399565 | TCTCGATCATATCAA[A/G]AGCCTCTCAGGTTGG | 50807 |
| rs141978847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366113 | TATCCTGGTTCCCAA[A/G]GGTTTCCCACTCCAC | 50807 |
| rs142002077 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130200865 | ATGTAAATCAGATGT[A/C]ATGTATAAAAGTAAA | 50807 |
| rs142002841 | snp | A/C | 8.5376e-05 | 0.00653305 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168941 | TTTCAAATTTACTGA[A/C]ACTTATCCATGAAAG | 50807 |
| rs142019789 | snp | A/G | 0.241627 | 0.24986 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107751 | ATAGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTC | 50807 |
| rs142024614 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314639 | AAACCACAGCATGCT[G/T]CGCTTCCCAGTGGCA | 50807 |
| rs142026769 | snp | A/G/T | 0.00954224 | 0.0684493 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214048 | CCCTTTTCTTGGTTG[A/G/T]GGGTTAAAAGGATGT | 50807 |
| rs142027661 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390553 | ATATCTATTTCCCCT[A/G]ACATACTCTGAGTGC | 50807 |
| rs142031026 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143595 | ATCAGGGAAGCTCTG[A/G]GTACATTTCATGAAG | 50807 |
| rs142036462 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264117 | ACAACACACATGTCT[C/T]TCTTGAGTGCTACCT | 50807 |
| rs142043427 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130138910 | TCCAAAATCAGAATC[C/T]GTAGCCACGAAGCAG | 50807 |
| rs142054237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430693 | CCCAGAACACTGACC[C/T]GAGGCAGGAACTGTG | 50807 |
| rs142055025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333739 | AAGATTAATATTTTC[A/G]CCAATCATACAGATA | 50807 |
| rs142060566 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171150 | CTTACCATTTTCCCT[A/T]AAAAACTCCAAGGTC | 50807 |
| rs142071958 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218824 | TTGCTAATTCCACAG[C/T]TGAATAACCATGTAG | 50807 |
| rs142073818 | in-del | -/CT | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130061671 | CTGTCTCGGGTTAAC[-/CT]CTGTTACATTTTGGT | 50807 |
| rs142074216 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130168370 | CTTATAAATCAAAGG[C/T]GTGGTGGCTCACGCT | 50807 |
| rs142085338 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130351356 | CTTTATGTATTCATA[C/T]GTAAAGCAATAATAA | 50807 |
| rs142087192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130326320 | TACTCATGCACCGAC[C/T]TGCAAAGCCTGTGAA | 50807 |
| rs142087405 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209699 | AAAGCCCTTTTTAGG[A/C]ATACCAAAATATGAT | 50807 |
| rs142089351 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258381 | GCCTTCTTTTGAAGA[A/C]GTTAAATGTACACTC | 50807 |
| rs142097961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319786 | GCAGTAAGACAGGTA[C/T]ACCCACACAACAGAA | 50807 |
| rs142106279 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111080 | CAACCCTCCTATGAG[C/T]GGGATTCCTCGTCTG | 50807 |
| rs142116281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148315 | TGACCCTGAGCATGG[C/G]ATTTAACCTCTCTGA | 50807 |
| rs142123697 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057847 | GCTGACAGGGTCCTT[C/G]TGCTCAAGAGCCCTC | 50807 |
| rs142134737 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130222554 | TCAGGAAAGACTATC[A/G]TGGATACTAGAATAT | 50807 |
| rs142146203 | in-del | -/AA | 0.0205511 | 0.0992634 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094934 | GAAACAAAAATTGTC[-/AA]AGACAAAATGCTAAT | 50807 |
| rs142153502 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074917 | AACCCAGCACAGGAG[A/G]GGCAGGAGCTGAGGG | 50807 |
| rs142175293 | snp | A/C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105830 | ATGATATGTGCCACA[A/C/T]TGCTCTGTCAACTGA | 50807 |
| rs142206185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392223 | GTTTTTTAAAAAGCC[C/T]CCAAAAGGGACTCTC | 50807 |
| rs142213160 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381816 | GGGCCTTTGCACGTG[C/T]TGTTCCCCTCAGCTG | 50807 |
| rs142213247 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170460 | GCGCCCAGCTTAAGG[C/T]ATATCTTAAGAGACA | 50807 |
| rs142214307 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107444 | CCCGCCTCAGCCTCC[C/G]AAAGTGCTGGGATTA | 50807 |
| rs142216039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072455 | TGCTGCCATGTAAGA[C/T]GTGCCTTTCGCCTTC | 50807 |
| rs142235915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289732 | TCTTACTTGTATCCA[C/T]AATCCTTTAGCTGGG | 50807 |
| rs142246160 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217096 | GTAAGGCAGGAAATA[C/T]GGCATGCACCATCCA | 50807 |
| rs142255017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343935 | AAGTGACAGTAGCGG[C/T]TACCTCTGGTTAGTG | 50807 |
| rs142279950 | in-del | -/CAGGTATGTCTTTATCAGCAGCGTGAAAACGGACTAATA | 0.455621 | 0.142197 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072551 | TAAATTACCCAGTCT[lengthTooLong]CAGCACCCCTTCCCC | 50807 |
| rs142281320 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276390 | ACTGTAAACAAGTGC[G/T]AACAAGGACTGTAAC | 50807 |
| rs142287060 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130071261 | ATAGGTATGAGCCAC[C/T]GCGCCCAACACTTCA | 50807 |
| rs142299085 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444974 | GCTCATGAGCGAAAA[C/T]AGAAGCCTGAAATGA | 50807 |
| rs142302798 | in-del | -/ACAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130284843 | TTCCTTTTACACTCT[-/ACAC]ACACACACACACACA | 50807 |
| rs142308074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130411033 | GTCCAGCTAATTTTC[A/G]TATTTTGAGTAGAGA | 50807 |
| rs142311540 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130271983 | TGAATGATGAAGAAA[C/T]AAAAAATAAAAATAA | 50807 |
| rs142312893 | snp | C/T | 0.00148726 | 0.027229 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340867 | TTATGATGGCTCCTG[C/T]ATGCTTCTTGAGGCT | 50807 |
| rs142318272 | snp | C/T | 0.000598537 | 0.017289 | missense, utr-variant-5-prime, upstream-variant-2KB, intron-variant | ASAP1 | GRCh38.p7 | 8:130358039 | AGCAGCGTGACGGTG[C/T]TCCTGCAGTTGTGCA | 50807 |
| rs142326136 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130303859 | AGGATACATATCATC[A/G]CACATTTGTCAAATC | 50807 |
| rs142326412 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166413 | GAAGTCTACGTCCCT[C/T]AGTACAACACCCAAG | 50807 |
| rs142327057 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130232028 | CTTGCATGGCTAGTA[A/G]GTGAGTGGTAGTTCT | 50807 |
| rs142345704 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341817 | GGAAAAGCATTTATT[C/T]ATATAATTATTTATT | 50807 |
| rs142356017 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385814 | GGGGTGGGCATTTGC[A/G]GTTTTACTTCCCGAG | 50807 |
| rs142377166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229795 | CTGTAAATCCCAACG[C/T]TTTAGTAGGCAGAGG | 50807 |
| rs142385544 | snp | A/C | 0.0554779 | 0.157039 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123318 | CAGAATGTCAGTTTC[A/C]CCACAGTCTTGCTGA | 50807 |
| rs142387302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130745 | GAAGCCAGATGATCT[A/G]CCTAAGGTTAAAAAG | 50807 |
| rs142389280 | snp | A/G | 0.000167328 | 0.00914526 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130187283 | AAATGGCTTCTTGAG[A/G]TCCTTAGAAACGAGA | 50807 |
| rs142397269 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402671 | CATCCAGGGCGAAAA[A/G]CCGAGAGACATCTCA | 50807 |
| rs142401497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130329202 | CTCTGAGTGACACAG[C/T]GGTTCACTAAGCCAC | 50807 |
| rs142405444 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130342396 | CTTCTGTAAAATACC[A/G]TGGGTAAAGTACTCA | 50807 |
| rs142419831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066517 | TACCTGGCCTATTTC[C/T]TTCTTTTCTTTCTTC | 50807 |
| rs142430049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130440157 | GCTGCTGTCCAGTTC[C/T]AAGCCACCATCCTCT | 50807 |
| rs142432527 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130192579 | GAAGTTTGGATGGAT[A/G]GTGGGTAAGTAAGGT | 50807 |
| rs142442934 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233361 | CCCTTGTTGAGCCCC[C/T]ACCATGTGTTAGGTA | 50807 |
| rs142443173 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157277 | CTTTTCTCCTTTTAC[G/T]TTCACAGCAGGATTA | 50807 |
| rs142445780 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130236113 | AACTTCACGGCCTGC[A/G]CTCTTTCTATTATAG | 50807 |
| rs142451959 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120263 | CTGGCTTCTGAGGCC[C/T]CTGCTGCATGTGTCT | 50807 |
| rs142457110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154863 | CCATCCTCAAATAAG[A/C]GCTAAATCACATACT | 50807 |
| rs142457992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119399 | GACCACATGGATAAC[A/G]TGCCCAAAGTCTGAA | 50807 |
| rs142486031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344977 | AAAACATCTCCAGCA[C/T]AGGTCTGTCTCTTTC | 50807 |
| rs142499107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399098 | ATCCTTAAAGGATGG[C/G]ACGTGCCTTTCTCTG | 50807 |
| rs142507246 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297251 | ATTAGTTCGTCTCCC[C/T]CCATGCATCAAAATC | 50807 |
| rs142507659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274610 | CTATCGCATTCATTG[C/T]TGAGGATGTATCTTT | 50807 |
| rs142513366 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130338120 | GCCTGTGATGCTTTA[C/T]ATGCATTCGTTCACC | 50807 |
| rs142539968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130433026 | AGAGTGTAGACTGCA[A/G]ATATCCCACATCTCC | 50807 |
| rs142549700 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070961 | AGAGGGGTAGAGAGA[C/G]GGGGAGAGAGAGGGG | 50807 |
| rs142570789 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130090794 | AAATGCACACACATG[C/T]TTGCACACACATAAC | 50807 |
| rs142579097 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088556 | CACCTGGAGTCACCA[C/G]AAGCTGAGAGAGGCA | 50807 |
| rs142582272 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286191 | TGGCAGAGTAGGTTT[C/T]AGACACCAGGACCAC | 50807 |
| rs142589794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130181042 | GGGGTCAGTGATAAC[A/G]GGGGAGGCTGTGCAT | 50807 |
| rs142594747 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130292177 | AAAGAAAAGAAAGGC[-/A]AAAAAACAAAGTCTG | 50807 |
| rs142595156 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130121384 | ACCTCTACCCACTGG[A/G]TGACAGTAGCACCTG | 50807 |
| rs142603947 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130415663 | CATGGTGGCAGGTGC[A/C]TGTAATCCCACCTAC | 50807 |
| rs142631739 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397554 | CGAGCACTTGCCTAC[C/T]CCATGGAACATCAGG | 50807 |
| rs142633680 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130437151 | ACTCGATGAAAAAAG[C/T]TCAACAAATGTGGTA | 50807 |
| rs142656511 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350853 | AGACAGCCCTGAAGA[A/G]ACTGCAACTGAGAGT | 50807 |
| rs142659886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130357129 | TTGGCTTTCAGGTTC[C/T]TCTTTGCCCATACCA | 50807 |
| rs142660570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423501 | AAGTAAGTATTTGGA[C/G]AAGTATGTACATGCA | 50807 |
| rs142674198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140828 | AAGTACGCATAAGTT[C/T]TGACTGTCTAAGCAG | 50807 |
| rs142676425 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124380 | AGGAAATCAATCATG[G/T]CTACAAATATGTGAT | 50807 |
| rs142683440 | in-del | -/TTG | 0.0659589 | 0.169201 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397141 | ATATTTATGAGAATT[-/TTG]TTTGTTGTTGTTGTT | 50807 |
| rs142685548 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130061894 | CAGCTCTTGGTACTT[A/T]GAAAACTATGGACAT | 50807 |
| rs142686949 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405484 | AGTGGGTCTTCATGA[A/G]AGGCTGCTGGGGTCG | 50807 |
| rs142693215 | in-del | -/TTTG | 0.135825 | 0.222405 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223855 | AACACATGATAAACA[-/TTTG]TTTATCATCTTATCT | 50807 |
| rs142699541 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323085 | TCCAGTCATTACAGA[A/C]AACTACTGCACAGAA | 50807 |
| rs142712568 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132645 | GCACCATGTCGTACC[A/G]ACAGCCTCCTGCAGT | 50807 |
| rs142730681 | in-del | -/GA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070914 | GGAGGGAGAGAGAGG[-/GA]GGGAGAGAGAGGGGG | 50807 |
| rs142733923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130255788 | TGCTTAAGTTTTTGA[C/T]TTCTAAAAAGATGGT | 50807 |
| rs142739996 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173910 | AAACCTTGTCTCTAC[C/T]AAAAAAAAAAGAAAA | 50807 |
| rs142761214 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098047 | GCTACCATTTACTGA[G/T]TATTATGTGCTTGAG | 50807 |
| rs142763239 | in-del | -/AA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130228701 | GTGAGACCCTGTCTT[-/AA]AAAAAAAAAAAAAAG | 50807 |
| rs142764996 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401166 | GGATTACAGGCATGA[A/G]CCACTGCACCCAACT | 50807 |
| rs142779067 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301033 | ATGGGGCTTCTTGGT[A/G]GAGAAATTCATTCCC | 50807 |
| rs142785252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259412 | TTAAAATTCACTTTA[A/C]ACCCTTGCCAGGCCT | 50807 |
| rs142801198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130312401 | GAACACAAACCAGAC[A/G]AGAGCTAAATCTAAC | 50807 |
| rs142801612 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375780 | TGTTCCCCACCTTAT[A/G]CACAAGGAAATTGAG | 50807 |
| rs142807865 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411833 | GAAATCCTGTTGGTG[C/T]CCACTGACCACTGTC | 50807 |
| rs142808658 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372592 | CTCATCAGGGTTCTT[C/T]AGAATTCAAGCCACA | 50807 |
| rs142812094 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296785 | AAAAAAATTAAGCTA[C/T]TTTCCAAGCAGGTAA | 50807 |
| rs142820493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241369 | TTTGTTTGCTTTTAC[A/G]GTATTTTTCTCTCTA | 50807 |
| rs142834654 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254747 | TGTAAAGAGAAGTTA[C/T]CAAACATCAAGTAAC | 50807 |
| rs142842170 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173481 | TCAGTGGACATGCAA[A/G]GGCTACTGCACACAT | 50807 |
| rs142856973 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417815 | CTCACCAAAGGGGCC[A/G]CTGGCTTTCAGGCTT | 50807 |
| rs142858495 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170134 | TCATCTCCCTATCAC[A/T]GTGGGCCCAACACAA | 50807 |
| rs142866492 | in-del | -/GTTT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130402920 | ATAATCTTTTGTGGG[-/GTTT]TTTTTTTTTTAATCT | 50807 |
| rs142885909 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130146155 | CTGAAACATTTTAAA[A/G]AACTCTATTATTTCT | 50807 |
| rs142885934 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188980 | TAGCATGTATCATTA[C/T]CTGAAATTACTGTGT | 50807 |
| rs142898676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130184961 | GGTAATGATTTCTAA[C/G]TCTGTGATCTAAATC | 50807 |
| rs142900202 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269557 | CCACCTACCAAAGTC[C/T]CTCTCCAAGTTTCAT | 50807 |
| rs142901384 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130192213 | GTTCTTGGGGAGTGG[A/G]GCAAAAAATAAAAAA | 50807 |
| rs142903660 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292598 | TGATTATTGCAGAAC[A/G]CCATTCCTGGTCCAG | 50807 |
| rs142911269 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370052 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCTG | 50807 |
| rs142924621 | in-del | -/GTGTGT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130072790 | CTGGACTTGCAATTG[-/GTGTGT]ATATGTGTGTGTGTG | 50807 |
| rs142928119 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382159 | GGCGTGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 50807 |
| rs142933891 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307922 | TTTAGTGTTAAAATA[C/T]ACTTGAGAGAAATAA | 50807 |
| rs142937267 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098970 | AATAACCTCTCTTAT[A/G/T]CTCTCTACTAATATA | 50807 |
| rs142943689 | in-del | -/G/GGG/GGT | 0.0357772 | 0.12942 | intron-variant | ASAP1 | GRCh38.p7 | 8:130256401 | ATCTGCAGAGGATCT[-/G/GGG/GGT]GGGGGGTGGGGGGCG | 50807 |
| rs142946636 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263198 | GGTTCTGGACCAAAG[A/G]GCCACACTTTTCTCC | 50807 |
| rs142973206 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422824 | CTTGGAGCAAGCCAG[G/T]AAGCAGGCTGAAGCC | 50807 |
| rs142977159 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087813 | CAACAACTATTACCC[C/T]CAAATCTCCCCTGTG | 50807 |
| rs142987406 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130138180 | CCTTCAATGACACAC[G/T]GCCACCTCTCCTTCT | 50807 |
| rs142988807 | in-del | -/A | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307582 | CAACACCCAACAGGT[-/A]AACCACCTTTCTATG | 50807 |
| rs142993377 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074235 | GTAGTAATAGAATTG[C/T]GTATGTATGAAATTG | 50807 |
| rs142998703 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151797 | AGTGCCCAAGGGGGC[A/G]CTTACAGTCTAGTAA | 50807 |
| rs143012515 | in-del | -/T | 0.0256215 | 0.110247 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252912 | ATCTTTTCAGGACAG[-/T]TAAGAACTTACAGGA | 50807 |
| rs143025221 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413222 | GCCAGCCTCAGGAGA[A/G]GTCTCTGCTGCATGT | 50807 |
| rs143030945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314536 | CCAGAAATACTAAGT[G/T]CTGTATCAAGGATAA | 50807 |
| rs143031786 | in-del | -/G | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297431 | TTCACACCTGTGGCT[-/G]GTTCAAGGGTCAACT | 50807 |
| rs143032531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150644 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 50807 |
| rs143033015 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244225 | TGGAAGGTGAAAGAA[G/T]GAATATCTCTCTTAT | 50807 |
| rs143034168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211864 | ATCAGTTTGCTTAAC[A/G]TTTCTGGCCTTCACT | 50807 |
| rs143039911 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | ASAP1 | GRCh38.p7 | 8:130086783 | CACTCCAGCCTGGGT[C/G]ACAGAATAAGACCCT | 50807 |
| rs143053690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130420533 | CAAAACCTATCAGCC[A/G]AGGAATGGAATGGAT | 50807 |
| rs143071341 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425434 | AGGTATGAGAATCCT[C/T]TGAACCCGTGAGGCA | 50807 |
| rs143078400 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130142860 | GTGGCCAGTTAGATC[A/T]CTATTTCACGGTGGG | 50807 |
| rs143080840 | snp | C/T | 5.33433e-05 | 0.00516418 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076321 | GACACTTTAATTACA[C/T]GTAAATGTAAAAATG | 50807 |
| rs143091199 | in-del | -/CTTT | 0.110167 | 0.207236 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393019 | TCCTCAAAAATAAAC[-/CTTT]CTTTTTTTTAACATG | 50807 |
| rs143097134 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342189 | CTTAGGGGGTGAGGA[A/G]GATGAAGAAGGCAAA | 50807 |
| rs143106166 | in-del | -/GAACTCTTGTTCAG | 0.238749 | 0.249747 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287173 | AAGAGTTCAAGGACT[-/GAACTCTTGTTCAG]GAACTTTACACATTT | 50807 |
| rs143126904 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270690 | GTTTAATAAAAAACA[A/C]ACAAAATCTATCCTA | 50807 |
| rs143129249 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130194298 | TAATTACCTTTGTCA[A/T]TATAAAGGCACAAAG | 50807 |
| rs143130763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130186234 | CGTTTTTGTTCTCTG[C/T]TGCATTTAGAACTGT | 50807 |
| rs143131859 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119141 | AAAGGATCGGGTCTC[A/G]CTATGTTGCCCAGGC | 50807 |
| rs143136463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309246 | GAGTCAAATGGTGGA[C/T]ACAGAGAGACAGGTG | 50807 |
| rs143143449 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130207694 | CACTTGTAAGTATGC[C/T]ACAAATATAGTAAAA | 50807 |
| rs143152713 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384771 | TTGGGCAAGTTACCC[A/T]GTCACACTTCACATC | 50807 |
| rs143162146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275887 | AGAACTGGAGGAGAA[C/T]GTAAACCGTTACAAC | 50807 |
| rs143170080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317604 | CACTGATGCTTCCAT[A/C]AGAACCTGTAGAGGT | 50807 |
| rs143188354 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064230 | GAGGCTCCAACTGTC[C/T]AGACAAGAGATGATG | 50807 |
| rs143191010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301948 | TGTAATGAGAAGACT[A/G]TAACCTCCACGATGG | 50807 |
| rs143195511 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437743 | CAACATCCCCCAGAA[A/G]CCGCGGGTGGGCGCT | 50807 |
| rs143198111 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393993 | TTTAATCTCTTAATC[C/T]CATCATTTTCATAAG | 50807 |
| rs143203012 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154131 | ACAAGCTTAGCCAGG[C/G]CTCAAGAATGCATCA | 50807 |
| rs143211614 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391250 | TACAGACAGAAAGTA[A/G]AATGGTTATTTCCAG | 50807 |
| rs143226428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336217 | AATGATTCCTGCTTC[A/G]AACTTAATAATCACA | 50807 |
| rs143237498 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130265429 | TTTTAAAAAAGTAAC[A/C]GGGTGTGGTGGTACA | 50807 |
| rs143254652 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130230069 | ATCCTGTCTCCAAAA[A/C]AAACAAACAAACAAA | 50807 |
| rs143261202 | snp | C/G | 6.58892e-05 | 0.00573936 | missense | ASAP1 | GRCh38.p7 | 8:130060803 | GCTGTGGTTTGGGGG[C/G]CAGGTCCTTCATCTG | 50807 |
| rs143262783 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087323 | TCAGGAGTTTGAGAC[C/T]AGCCTGGCCAACATG | 50807 |
| rs143274384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321204 | TTATAGTGAATAAGC[C/T]CCAGTGGCTACAGAG | 50807 |
| rs143276944 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121709 | GAATCACTTGAACCC[A/G]GGAGGTGGAGGTTGC | 50807 |
| rs143277061 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085293 | CCACTTCCAGACACT[A/G]TATGTGACTTTTTGT | 50807 |
| rs143277191 | snp | G/T | 0.00209611 | 0.0323057 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112343 | AGATGAAATAAGAAG[G/T]TGAGATAATAATCAA | 50807 |
| rs143294563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060270 | CACTGTATTTAATCA[C/T]CTGTGAGCTCAAATA | 50807 |
| rs143298362 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208956 | TACAGACAAAAGGAC[C/T]AGAAAGATAAACTCC | 50807 |
| rs143301685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432382 | ATGGGAACAGCAAGA[C/T]TGTGAAAGTATAAAG | 50807 |
| rs143308471 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162513 | CTCTGCCCTATCTGT[A/G]TCTTCCAGAAACATT | 50807 |
| rs143308870 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223915 | GGATAGCTGGGATAC[A/T]CGCATTATTACACTC | 50807 |
| rs143310701 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098245 | AGACTCTCAGCCTTG[A/T]CAACAGCTTGCTTCC | 50807 |
| rs143312293 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150209 | GCCACAGTCCATTAT[C/G]TTAGCCACTAAACAA | 50807 |
| rs143315116 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123658 | TTGAGATGGGGTCTC[A/G]CACTGTTGCCCAGGC | 50807 |
| rs143322680 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204467 | GGTTACTACCTGGTA[G/T]GGCTGCTGTGAGGAG | 50807 |
| rs143356134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130279362 | CATGGCTGTCCCACA[G/T]GGAGTCTTGAATATG | 50807 |
| rs143368840 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393810 | GCCGTGGCAGAAGAA[C/T]ATAAATTGTGAAGAT | 50807 |
| rs143371426 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355579 | CAAATATCTCAGTTG[G/T]GAAGCATATGCCAAC | 50807 |
| rs143383120 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108417 | AGGTTCTTGAGATTG[A/G]AATTATCATTCTTTT | 50807 |
| rs143383817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130351869 | CATATCAGGACCAAA[A/G]GCATTAGCATGGAAT | 50807 |
| rs143388911 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165457 | GAGAAATCATTCAAA[A/G]AGACCACATTTCTCC | 50807 |
| rs143396281 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438631 | TGCATGGGTTGGTAA[A/G]TTTAATTTTTTTCAA | 50807 |
| rs143410177 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130291828 | CCAAACTGTGGAAAC[C/T]TGACAACTCTTCGGC | 50807 |
| rs143410469 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219422 | GAGTACAGTAAGCCA[A/T]CTGAGGGGAATGTCA | 50807 |
| rs143421870 | in-del | -/C | 0.0248432 | 0.108648 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167250 | TGAGCCATAAGTGTG[-/C]CTGCCGCCTCACTCT | 50807 |
| rs143428477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073563 | AAAGCAGTTAAGGGG[A/G]TCGGGAAGGAACTGA | 50807 |
| rs143446191 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278896 | GCCCTCACAATTAGA[C/G]AGTGTTAGGCATGTT | 50807 |
| rs143452534 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102509 | TTGTTAGTATTTGGT[C/T]AGGATTTTTTGCATC | 50807 |
| rs143458278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171979 | CATTTAAATTTAAGA[C/T]GGATGTTGTCAGGAC | 50807 |
| rs143466571 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349270 | GTGCCTCCCCAGTCC[A/G]GGTCCCTGAAGTATA | 50807 |
| rs143478128 | in-del | -/G | 0.0547245 | 0.156101 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402917 | AGAATAATCTTTTGT[-/G]GGGTTTTTTTTTTTT | 50807 |
| rs143478941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068959 | TATTAAATTTGCTGT[C/T]TCAGCTTCCCTTCAT | 50807 |
| rs143487902 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130344487 | AAGGAGGCAGAAATG[-/A]AAAAAAGATTGGCCA | 50807 |
| rs143516443 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247109 | GACTGTGTGACCCTG[C/G]TCAAGTTAGTCACTC | 50807 |
| rs143529243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131943 | GTAAGTTCTAAGAGT[A/G]AATAAAATATTGAAG | 50807 |
| rs143534447 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068817 | CTGGCTTTATGATGA[C/T]AGGGCTATTCACACG | 50807 |
| rs143544540 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130205978 | TTGTTTCAAATACTA[A/C]TCTTAAATATTAACA | 50807 |
| rs143550037 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233335 | CAGCCAACATGTAGC[A/G]ATTCACTCAACCCTT | 50807 |
| rs143558863 | snp | A/T | 0.00244798 | 0.0348998 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134260 | GAGGTGCTTTTTCAA[A/T]CCAAGGCATCGCACC | 50807 |
| rs143566509 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130442273 | GGGCATGGGACTGAG[C/T]CTGAAGAAGTGGAAA | 50807 |
| rs143573394 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344740 | AGATTGCGTCTCTTA[A/C]AAAAACAAACAAACA | 50807 |
| rs143586072 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336575 | GCACTTTACATGGGT[A/T]AAAGAAATAAAGACT | 50807 |
| rs143611261 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252400 | TACAATATTAAAAGA[C/T]TGATTCAGTACTTAA | 50807 |
| rs143611310 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318900 | CTGATGGTCTCATCA[C/G/T]TGCAACACTGCCCTA | 50807 |
| rs143613106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130202758 | GGTGACCTAGCTTGG[A/G]AGGTGGTGGAGCAGA | 50807 |
| rs143620975 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189028 | CAGATTTATCTTTTA[A/G]TTTTTAGTTTTTATG | 50807 |
| rs143626323 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408349 | GGGCATCATCCAATC[C/G]ATTGAAGGCATAATA | 50807 |
| rs143639111 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128273 | ATCAAACTTGAAGGA[A/G]GGTGAGAGTTAAAGA | 50807 |
| rs143648340 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374869 | AAGGATAGTGGTGTC[A/G]CTGTTCACAGAGCCC | 50807 |
| rs143665108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410685 | GCGAGTATGCTGAGC[A/G]CAGAGCCATCTGGGC | 50807 |
| rs143668464 | in-del | -/TCA | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130346519 | CTTTCTAAACCTAGT[-/TCA]TCATCTGTGAAATGA | 50807 |
| rs143681730 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410931 | AGTGACGTAATCTCC[A/G]CTCACTGCAACCTCC | 50807 |
| rs143685558 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359903 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 50807 |
| rs143686981 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130103877 | TAGTATTGTTTTTAC[A/T]GTATCCCACAGGTTT | 50807 |
| rs143700954 | snp | A/T | | | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082681 | GTTAATTTTAATTTT[A/T]ATTTTTTTTGTAGAG | 50807 |
| rs143705290 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099721 | AGAGTCTTGCTGTGT[C/T]GTCCAGGCTGGAGTG | 50807 |
| rs143710179 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092639 | ACAAAGGTAAGAAGA[A/G]TGTGTGCTTTTAGGA | 50807 |
| rs143713549 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179461 | AGTTACCAAGCCTTG[C/G]TGTCCTTTAGACAGT | 50807 |
| rs143713855 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228121 | AAAAAATCATCTCTG[A/T]TTCACTGGTAGAAAA | 50807 |
| rs143725649 | snp | A/G | 0.47726 | 0.104176 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262455 | GAGAGAGAGAGAGAG[A/G]GAACCTGTGGAATTT | 50807 |
| rs143727064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130113608 | CAATCAATTAATGCA[C/T]GAATGAACTTTCAGA | 50807 |
| rs143774605 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145467 | GGATTACAGGCACGC[A/G]CCACCACACCCGGCT | 50807 |
| rs143777301 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295792 | GATTTTTTTTTTCCT[A/G]TCAATCCCTAACTAG | 50807 |
| rs143779201 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224507 | AAGTTAATAATCTGG[A/G]GTGTATCTCAGTGAA | 50807 |
| rs143793043 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378583 | GAGGTCAGACGGGTA[C/G]GCAAGGGTGGCCGAG | 50807 |
| rs143799385 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325445 | TGTTAAGAAAAAGAC[A/G]TCTGTAGCACTTATC | 50807 |
| rs143801261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299007 | TTTCGAAACACAAAT[A/G]AACAAACATCCTTAT | 50807 |
| rs143804206 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183883 | GCCATCCCAGGATGG[C/T]AGCTGTACTGCTGAT | 50807 |
| rs143805993 | in-del | -/CAT | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252255 | TATCATAATTTAGAA[-/CAT]CAAGTTACATGTATT | 50807 |
| rs143807298 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414078 | ACTGGATAGTGAGTG[A/G]CTTCATGGGGGACAT | 50807 |
| rs143807316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374601 | TAACAAGCTTACATA[C/T]TTGTCGACTTTAATA | 50807 |
| rs143832774 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257899 | AAATCTGTTAAAGAA[C/G]AGATTGCAAATGTGG | 50807 |
| rs143846922 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129685 | AGCAATAGTGACAGC[A/G]TAAGAATTAAAAACC | 50807 |
| rs143862178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117468 | TATACAATTTGGCTT[C/G]TGTCTATGTACCATT | 50807 |
| rs143865586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301744 | TTGTTTTATATCATG[C/T]TGTTTTCCAGTTAAT | 50807 |
| rs143867974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077305 | TCTAAATCATCAAAC[A/G]TTAACCTCTGCAACT | 50807 |
| rs143872456 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130200677 | TAAGATTACTGTTGA[G/T]TTTTATTTTAGTCTT | 50807 |
| rs143877463 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149136 | AGCGGATTACAGGCA[C/T]GAGCCACCGCGCCTG | 50807 |
| rs143886120 | in-del | -/AAAC | 0.33303 | 0.235809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123587 | GGGGTTTGCTCTGGA[-/AAAC]AAACAAACAAACAAA | 50807 |
| rs143886785 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130412580 | AAATTACCCAGTCTC[C/T]GATATTTCTTTATAA | 50807 |
| rs143889634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086678 | GCATGGTGGTGCACA[C/T]CTGTAGTCCCAGCTA | 50807 |
| rs143917525 | snp | A/G | 9.88663e-05 | 0.00703018 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130112272 | GGAGATGCTGGAGGA[A/G]TGGCAGAAGCTCTGA | 50807 |
| rs143923068 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083559 | CTAAGCCTCGATTCC[A/G]TCATATATCAACTGG | 50807 |
| rs143925816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263722 | ATCAAGCTCAGCAAT[A/G]TCTTGCTCTACATCC | 50807 |
| rs143930961 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394185 | TGACCACCGGTGAGC[C/T]GGGCGGAACAGAGCC | 50807 |
| rs143941991 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187068 | GTCAGTGTACCCAAC[A/C]TCTTAGCCCTAATAA | 50807 |
| rs143950916 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283349 | ACTTTGGGAGGCTGA[A/G]GCGGGTGGATCACGA | 50807 |
| rs143950972 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240412 | ACTGTCCTTCAATCA[A/G]ACAAGGCTCCCTCTA | 50807 |
| rs143951275 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430502 | CGGTCTGAGCAGTTG[A/T]AACGTCCAGCTGCTT | 50807 |
| rs143959152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376991 | TGTGAAAAGTTTTGC[A/G]AGAACCACAGAAAAG | 50807 |
| rs143961839 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130225288 | GTAGTCATATATATC[A/T]ATCTGTATGCAAAAG | 50807 |
| rs143964506 | in-del | -/ACACAG | 0.225301 | 0.248777 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373016 | CACAGACACACATAC[-/ACACAG]ACACACACACACATA | 50807 |
| rs143967434 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130185915 | GAGATTTAAAAAATA[C/T]AAATAAAGTTGTACT | 50807 |
| rs143967499 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151448 | CTGTTAGACAGCCTC[A/G]ATCATAATTACAAAC | 50807 |
| rs143985131 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353930 | CTTGCTCTGTCGCCC[A/G]GGCTGGAGTGCAGTG | 50807 |
| rs143996408 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396428 | CATCACTTCCCATCT[C/T]TCAGTTTAGCCATAA | 50807 |
| rs144001088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130268449 | GCTGGGATCATGCCA[C/T]TATACTCCAGCCTGG | 50807 |
| rs144011993 | in-del | -/AATA | 0.0130921 | 0.0798413 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295106 | CAGTCTCTACAAAAT[-/AATA]AATAAATGAATAAAC | 50807 |
| rs144012872 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349878 | AACAGAGGCTTAGAC[A/G]TGAAGTGTAGCCCCA | 50807 |
| rs144013348 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105816 | GCTGGTGCCCGGGCA[C/T]GATATGTGCCACATT | 50807 |
| rs144016351 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054111 | CTTGTCTAAACTTGC[A/G]TGAGGCTGTGTGCAT | 50807 |
| rs144016631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130279712 | AATTTCTATACTACA[A/G]ATGAGAAAGAGTTAG | 50807 |
| rs144018166 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130426849 | CATAAGGACTATTTG[C/T]CGTCTCACACACCAT | 50807 |
| rs144033253 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130099681 | GAAAGGATTTCATTC[-/T]TTTTTTTTTTTTTTT | 50807 |
| rs144038616 | snp | A/T | 8.27883e-05 | 0.0064333 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118698 | AGAACAAAATAAAGA[A/T]TTTTTATTTTCCAAG | 50807 |
| rs144044812 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115262 | AGACTGAGGTCCCCC[A/G]AAGGGTAAGGAATGC | 50807 |
| rs144049348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130065945 | AGCTAGATCCAGTTC[C/G]TTCTTGGGCCGTTTT | 50807 |
| rs144056476 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130147300 | TACTAATAGCTGACA[C/T]TTATTGAGCACTAAT | 50807 |
| rs144080008 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249319 | TTCACAGACTCGCCT[G/T]TGCAGCCAACCCACC | 50807 |
| rs144084061 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130088 | TTTGGCTAATATTGG[C/T]CAGTATCTACTATGT | 50807 |
| rs144086934 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395614 | TTTCAGAGGAAGCAC[A/G]ACACTGCCAACACGT | 50807 |
| rs144090904 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319536 | ATTTACAAATCCTGT[A/G]AATGGGGAGTCAGAG | 50807 |
| rs144097978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316805 | GAGAAATAAACTATC[A/G]CATTTAAGCTTCTGT | 50807 |
| rs144114908 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258963 | GCCTTTTCCCTATTT[G/T]CCCCATCGATTCCAA | 50807 |
| rs144119266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392674 | AAGAGGTTTATTTGG[C/T]TCTTGGTTCTGCAGG | 50807 |
| rs144119500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430329 | TGTGTTTGTACGTAC[A/G]TATGTGTTAGGATGG | 50807 |
| rs144126241 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130053123 | CACTTAAGCAGAACT[A/G]AATTAATATTCACTG | 50807 |
| rs144132518 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425594 | CAGACAGACAATGAA[A/C]GATCAGAGTGACAGA | 50807 |
| rs144138729 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130210194 | TTGCAACAAAATGAA[C/T]ACAGAAGTAGACATG | 50807 |
| rs144139031 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163993 | GGGGCTATAAATGTT[G/T]CTGGTATCCAATTTA | 50807 |
| rs144145749 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244726 | ACAAAAAGAAGGTTG[C/G]AAAGTAATTAAGCAG | 50807 |
| rs144160367 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130372042 | TAAGAGGCTTAGGGA[G/T]CCTACTGAATTCTTC | 50807 |
| rs144169358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280168 | CAGTAAGTAGCCCAG[C/G]TGGAACTGAACAAAG | 50807 |
| rs144180585 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362597 | CTGCTTTCATTCCAC[A/G]ACTCAGATATCTCTA | 50807 |
| rs144185950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166731 | AATGAAATGTTTGAA[C/T]AAATGACATTTATAA | 50807 |
| rs144188096 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104122 | CCTGCCAGGGCCCGG[C/T]ATGCTCTGGGTACTC | 50807 |
| rs144189753 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090183 | GTGATGATTTTCAAG[C/T]CAGAAAGCAGAAATT | 50807 |
| rs144190637 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130291218 | TCAAATTCTCCTAGT[G/T]TCGAAAAATCTCAGA | 50807 |
| rs144195415 | in-del | -/AGA | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236001 | CTATCCTCACGTTAC[-/AGA]AAGAAAAATGGAGGC | 50807 |
| rs144202019 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107276 | CAAGCTCCGCTTCCC[A/G]GGTTCACGCCATTCT | 50807 |
| rs144209331 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284984 | CCTGTGAAACAGGAA[C/T]TGGAAAACCTCTCCC | 50807 |
| rs144240976 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144211 | CATGCTGAACACTTA[A/C]CACTGCAGAGAGATC | 50807 |
| rs144244960 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402577 | ATAGAGGGAAACAGA[A/G]GTGGGGATATAAAAA | 50807 |
| rs144245892 | snp | A/G | 0.00835141 | 0.0640778 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444622 | AAACGGCTCTCTGCA[A/G]AGGAAATGGTTAGTG | 50807 |
| rs144248211 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391517 | CTACTACCAACCAGA[A/G]AAAATATATCAGTCC | 50807 |
| rs144249791 | in-del | -/AAGAAG | 0.0433465 | 0.140692 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359436 | ATGAATTTGGTTTAA[-/AAGAAG]AAGAAGAAGAAAAAA | 50807 |
| rs144258688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316155 | CACAAGTTCACCTGT[A/G]ACCACTATTATGCCA | 50807 |
| rs144271212 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368463 | TTGTAGGAACTACTC[C/G]TCCCTGACTCCAGGT | 50807 |
| rs144281576 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130174930 | TGTTTCCGTGTTTTG[C/T]TTATTGTAAATAACG | 50807 |
| rs144304642 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130067135 | TGCACCTATCTCCTA[C/T]AAGGCCCTTTTCTGT | 50807 |
| rs144316767 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130305530 | CACCATGTCTGGCTA[A/C]TTTTTGTATTTTTAG | 50807 |
| rs144317024 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | ASAP1 | GRCh38.p7 | 8:130103627 | TCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 50807 |
| rs144325231 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272361 | TATGTTGGCGAGGAC[A/G]TGGAAAAAAGGTAAC | 50807 |
| rs144333992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293765 | TCTTGTGTGAAGGAC[C/T]CCATGTCCCCTATTG | 50807 |
| rs144334813 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166276 | GGCCTCCCAAAATGT[C/T]TGGATTACAGGCATG | 50807 |
| rs144340531 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283551 | CGTCACTGCACCACT[A/C]CAGCCTGGTGACAGA | 50807 |
| rs144342525 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253622 | AAATACTGTAACTTC[C/T]GTCTGCCATTTTTAT | 50807 |
| rs144348553 | in-del | -/GGGGG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130093601 | AACCCAGGAAGTGGC[-/GGGGG]GGTTGCAATGAGCTG | 50807 |
| rs144353878 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130386730 | CGCTGCTGATGAAAA[G/T]GCAGGAGCGATGAAG | 50807 |
| rs144371825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141027 | TAATTTATAGGTATA[C/T]TGATTGGAGACTGTA | 50807 |
| rs144371956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180255 | ACAGGTTGGTTTCTA[A/G]GTCAAGAAGTGTTCA | 50807 |
| rs144377089 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410007 | CAGTGATATCATCTG[C/G]GTGTGAACACAATGT | 50807 |
| rs144382039 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130075314 | TCAGCAGTCATTTGG[C/G]AGTCCCCTCATCTTA | 50807 |
| rs144397070 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130338900 | GTTGCTGGGCTCTTT[A/C]TGCACACTGGTTGGT | 50807 |
| rs144400388 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342217 | AAATTGGCAAGGGTG[A/G]CACTCATCATGTAAG | 50807 |
| rs144413361 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334936 | ATATCAGACCTCCAA[C/G]CCTCCTTTCAGAATA | 50807 |
| rs144417916 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130161893 | GCGGCCTGAACCTCC[C/G]AAGCTGAAATGAGTC | 50807 |
| rs144432674 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337957 | ATGTGGAGTGTAAGA[C/T]GCCTAATCCATTACT | 50807 |
| rs144435843 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239181 | TGCATGTCATGCTTA[A/G]GGGAATGTTTTATGA | 50807 |
| rs144437374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130256630 | CAAAAATGTATTCAC[C/T]TAGAAGCTAAGTATG | 50807 |
| rs144442258 | snp | C/T | 0.000153988 | 0.00877328 | missense | ASAP1 | GRCh38.p7 | 8:130116993 | TGCTTATCCAGGTTC[C/T]CACTGAAAAATTAGA | 50807 |
| rs144469993 | snp | C/G | 0.0803491 | 0.183626 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415614 | CCAACATGGTGAAAC[C/G]CCATTTCTACGAAAA | 50807 |
| rs144481321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224850 | ATATCTTCACAAAAG[C/G]AGGACTGCTGGGGGA | 50807 |
| rs144484851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130181601 | AGTCAACCACTTGTC[A/C]CTGGAATGTACAAAA | 50807 |
| rs144485087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228870 | ACATTAATATCACTG[C/T]ACTTTCACAATGGGG | 50807 |
| rs144493149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115895 | AGCTGCACTGCTATG[C/T]GACAGGCTCAAGAAG | 50807 |
| rs144496457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434418 | TATTTCAGGTTCGTC[A/G]TATATAAAATGGGAG | 50807 |
| rs144509345 | snp | C/T | 0.000250173 | 0.0111814 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130179314 | CAGCAGATCCACACC[C/T]TTTTTGGTCTTGATT | 50807 |
| rs144515644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130125019 | CAGATCACGATTGCT[C/T]AGTGAACGCTCAGAT | 50807 |
| rs144523149 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070972 | GAGAGGGGGAGAGAG[-/A]AGGGGGAGGGGGGGA | 50807 |
| rs144523376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144423 | GGTAACCAAGGATCA[C/G]GAAGGTGAAGTAAAC | 50807 |
| rs144527068 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130356403 | TAGTACAGAAAGGGG[A/G]TGCAAAATGCTCCTG | 50807 |
| rs144529245 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078333 | ACAGGGTCTTGCTGT[C/T]GCCCCGGATGGAGTG | 50807 |
| rs144545369 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130298299 | TCAACATGATGTACA[A/T]CATAGATGAAGACTC | 50807 |
| rs144555161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226020 | TAGTAGCTGGGACTA[C/T]AGGAATGCACTACCA | 50807 |
| rs144586542 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293196 | TCTTTAAAATACAGA[C/T]TCTGATTCAGCAGGT | 50807 |
| rs144587210 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080975 | TATGTGCAAGGCATA[A/T]ATGTGAAGCAGAAGG | 50807 |
| rs144591485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130086822 | AACAAAGAAAAAGGA[A/G]TTTATGAAGGCATGA | 50807 |
| rs144597071 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393526 | TTTGGGAGGCCAAGG[C/T]GGGCAGATCACTTGA | 50807 |
| rs144600983 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274775 | AAGGAATCTGTGTTC[G/T]CTGGCATAGAATCTT | 50807 |
| rs144617983 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130308211 | CTAAGATTTTCACAG[C/T]TGTCCAATTCAAAAT | 50807 |
| rs144625230 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404897 | TATGTCTCCATAGCC[G/T]CTGTCTGTTGCTGCC | 50807 |
| rs144631201 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389610 | GTGTGATCCCCTAAC[A/G]TGTATAAAGTTCTGG | 50807 |
| rs144641427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277784 | TGTCCCCAGATTACA[C/T]AAATGTCTTTGCCAC | 50807 |
| rs144645491 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348997 | AGTGGGGTGTAGAAG[A/G]AGGCAGAAAGATTAT | 50807 |
| rs144647977 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121082 | ATATTAAAACTGATC[A/C]GCAAATCCTGTTGGC | 50807 |
| rs144662689 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418414 | TTAGTCGGTCATGGT[G/T]GCATGAGCCTGTAAT | 50807 |
| rs144683064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173795 | AAAAATAAAAAGGCC[A/G]GGTGTGGTGGCTCAC | 50807 |
| rs144683832 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387120 | TAAACCGAAATCAAA[C/T]CTGCTTTCATATGAA | 50807 |
| rs144699818 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197590 | CTTGGCCAAACACAC[A/G]CAGTTAGCTGAGACA | 50807 |
| rs144712387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288740 | CACAGGTAATCTGCC[C/G]CAGTAATCTGGTCAA | 50807 |
| rs144714194 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407818 | TTTATTCAACAGAAG[-/T]GACTCCACGAATGTT | 50807 |
| rs144732578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124451 | ATATGAGATTACAGA[A/G]AGCAGGCTCCATATG | 50807 |
| rs144758299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311955 | TGTACTCCTTCTAAA[C/T]GAGAAGATCCGAATT | 50807 |
| rs144771386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130242853 | AAAGATATAGGCAAA[A/C]CACGCAAATGTGTGC | 50807 |
| rs144785651 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238679 | TACAGAAACCTGTTA[A/G]GGATCATCTTCATTT | 50807 |
| rs144789140 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130201197 | AGAAAAACCAAAGTT[C/G]CTTTAGAGAAGGAAA | 50807 |
| rs144790765 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155593 | CTCACGTGATCTGCC[A/G]GCCTCGGCCTCCTAA | 50807 |
| rs144792496 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130250431 | TTCTACTTTTTGTCA[C/T]GTCCAAGTATGGCGC | 50807 |
| rs144797150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092299 | CATCAACCTAATAAC[C/T]CACAAGTAGGGTTTC | 50807 |
| rs144802022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160336 | TGAAGTGGACCAGAA[A/G]ATAAAGTCCATGCAA | 50807 |
| rs144804751 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417500 | GCGGAAAGAGCAGTC[C/T]CTTCTCACAGTTCAG | 50807 |
| rs144811034 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347315 | CACAGTCCTTCCAAG[G/T]ATCCCAAATGAGTAC | 50807 |
| rs144836191 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272524 | AAACGAAAGGAAATC[A/G]GTATATAAAAGGGAT | 50807 |
| rs144864801 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093273 | TGAAGTGGCTGGTGT[A/G]TGCCAGGTATTCCAT | 50807 |
| rs144875964 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431434 | GTTAGGTTCCAACCA[C/T]AACGAACCACTTGTA | 50807 |
| rs144889481 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141297 | CGCAGGCCCCTTCTC[A/G]CACTCAGCTCCTGTC | 50807 |
| rs144893982 | in-del | -/GGAAGCCCTTCTCCCT | 0.241053 | 0.24984 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393343 | TGCTGAATGGGCCAG[-/GGAAGCCCTTCTCCCT]GGAAGGTATTAAAAG | 50807 |
| rs144896560 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175689 | TATATTTTTATTTGG[C/T]TTCCTGTGCTTACTT | 50807 |
| rs144903882 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130087643 | TGGCTAGTGAGACTG[A/G]TGGGTACAACAGAGT | 50807 |
| rs144913055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257757 | TTTCTTTAACACAAT[A/G]TTTTCTAAACTGATT | 50807 |
| rs144917404 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199022 | GCTTTACTCTGTCTG[A/G]AACACTCTTCCTCTG | 50807 |
| rs144924614 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058818 | CTCTCTGTCCCCTGG[C/T]TTCTCCTTTAATCAC | 50807 |
| rs144925354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362223 | GCAAGATGACTGACC[A/G]GAAACCAGAGGTGGG | 50807 |
| rs144930786 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158139 | AATTACAGTAAAAAA[C/T]GTACATGTCTCAGAT | 50807 |
| rs144932053 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128852 | AATTTTTGGGTGACA[C/T]TGGATAAATGCTCAT | 50807 |
| rs144937276 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095779 | GCACGCCGCCACACC[C/G]GGCTAAGTTTTGTAT | 50807 |
| rs144957824 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096469 | GAACTCTGCCAGAGG[C/T]CTGTGGAAGTAACAA | 50807 |
| rs144965931 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293111 | TCTTGTTCCTAAGCT[G/T]AAAGTCTACAGAATT | 50807 |
| rs144969536 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406768 | GGTTACAGGAATGAG[A/C]CACTGTGCCTGCCCT | 50807 |
| rs144971165 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130365442 | GAAGAAAAAAATCAT[C/G]GTGTTTTATGGGAGT | 50807 |
| rs144981279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419910 | AGCCTTGGGGCTTTG[C/T]TATCCCTGGAGCTTC | 50807 |
| rs144982398 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257589 | ATCAGTATTTCTCAA[A/C]ATCTGTGCCCAACTA | 50807 |
| rs144993206 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206636 | TTGTCCAAAGGCCTC[C/T]GGAGAGAAGAAACCA | 50807 |
| rs144995228 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136219 | CAGTACAAGCACAGG[C/T]AGCCAGCCTAAAGGA | 50807 |
| rs145025192 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403784 | GTCTCGAACTCCTGA[C/T]CTCAGGTGATCTGCC | 50807 |
| rs145027318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324844 | TGAAAAGCAAAAGCA[C/T]ACCCTTGCATCCTCA | 50807 |
| rs145027360 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373229 | AGACACATTCATTAT[C/G]AATGGCTTTTTTTTG | 50807 |
| rs145030880 | in-del | -/CGT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130342647 | GTTACAAACACAAAA[-/CGT]AACAAACTCACATGA | 50807 |
| rs145032840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319565 | AGCCTACCTTATCCG[C/T]GAAGATGGGACACAC | 50807 |
| rs145040028 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130369495 | GATAAAGGCCTAGTA[C/T]TCAAAATATATAAAC | 50807 |
| rs145061348 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062846 | AGGTGTGGTGGTACA[C/T]GCCTGCAGTCCTAGC | 50807 |
| rs145069292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434550 | TAATAGCTATCACTA[C/T]TGATTCCAAGTCCAG | 50807 |
| rs145083399 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130182331 | ACAAAAAAGGATGAC[A/G]GAATTCAATAAATAT | 50807 |
| rs145087396 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130142882 | CACGGTGGGGTGGTG[G/T]GGGGGCAGTTGGTGG | 50807 |
| rs145106932 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261783 | GGGGCAAGGGACCTG[A/G]GGCGGAGAGATTCTG | 50807 |
| rs145113898 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258237 | GGAGAAAAGTCAATC[A/G]TCAACCAGCCCATCC | 50807 |
| rs145116300 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309006 | TTAAATTTGCCTGAT[A/G]CTCCACACCACAAAT | 50807 |
| rs145117338 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144946 | ATTGCAGCAAGGAAT[C/T]GGTTACCTTACTTTT | 50807 |
| rs145121183 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177654 | TACTTCAATATATTA[C/T]TTTTATTTTTGAAAG | 50807 |
| rs145122590 | snp | A/G | 0.223225 | 0.248562 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100352 | TCTTTTTTTTGAGAC[A/G]GAGTTTCACTCTTGT | 50807 |
| rs145161578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415491 | TTAAAAAAACAAAAC[A/G]AAACAAAACAAAACA | 50807 |
| rs145162905 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081380 | CCCAGGAGGATTCCC[C/T]GGGACCCTGCATGGG | 50807 |
| rs145164478 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130260728 | GGCCTCTGAAGGGAT[A/C]CCCAGGGTCTGTCTC | 50807 |
| rs145168589 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327787 | TGACAGTTACAGGAC[A/T]TCCTTTTGCATGATA | 50807 |
| rs145179905 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130202644 | ATGAATATCTCTTGA[A/T]AATTTACGGCTCAGA | 50807 |
| rs145184878 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145217 | CAGTAGCCACTTTAC[A/G]TCATGCTATCCAACA | 50807 |
| rs145190511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222110 | TTATATCCCTAGGCG[C/T]TGGCAATAACAAGTA | 50807 |
| rs145207785 | in-del | -/AGAC | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405160 | TAAAGCCATGCACAT[-/AGAC]AGCACAAGTATGATG | 50807 |
| rs145209893 | in-del | -/TAG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130122438 | ACAAGGAAGTAATAA[-/TAG]TAGTAGTAGTAAATA | 50807 |
| rs145216276 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309534 | GCAGATGAGGCAAGA[C/T]AAGCAGTGAGGCAAG | 50807 |
| rs145228307 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187949 | CAATACCATTATGTG[A/C]AGAGGCACATTTTTT | 50807 |
| rs145232555 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159026 | GTGAGCCACCGCGCC[C/T]GGCTGTGCTTTATGA | 50807 |
| rs145249600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379406 | AGTTCTGTGAGTTCT[A/G]GCCAATCATCACACT | 50807 |
| rs145254931 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130303828 | TGCTGCTAAAACTAC[A/T]CTGATACAGTAACAG | 50807 |
| rs145255895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218060 | GTTCACTCAGAGGAG[C/T]GGCTCAGAAAAACAG | 50807 |
| rs145266050 | in-del | -/AT | 0.0648419 | 0.167978 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105069 | TTTTTAATTGATAAC[-/AT]ATATATTTATTATGT | 50807 |
| rs145276196 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421437 | CTCCTGGGTGCATGG[C/T]TAGACTACATTTCCC | 50807 |
| rs145295041 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130074699 | CCAGGCAGGTGGTAG[C/T]AGGGGTGGACTCCTG | 50807 |
| rs145301054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110454 | GAAAGAGAATCTCTG[C/T]TCTCTGTCAGACTGC | 50807 |
| rs145301305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389213 | TAGAAGCTACTGTTA[C/T]ACCCATTTTGCAGAT | 50807 |
| rs145310630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314170 | AAGGTAAGCTTCCTC[C/G]CCCCACTTACACCCC | 50807 |
| rs145347933 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272852 | GAAGAGTATGTAGGT[A/G]GGAGAGAGAGAGAAT | 50807 |
| rs145348143 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343314 | TACTCACCACCCCCT[A/T]ACACTGAGATGACAC | 50807 |
| rs145348763 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391424 | TCTTAAAAACAGTTA[A/G]CAATAGTAATTTTTA | 50807 |
| rs145353997 | snp | A/C | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387951 | GGTGGCAGACATACA[A/C]AAGAGAACAAACAAT | 50807 |
| rs145362835 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059904 | GCAACATGGCAAAAC[C/T]CCATCTCTACCAAAA | 50807 |
| rs145365141 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424588 | ACTGGCTGGAAACAC[C/T]GCCCTTCTCAGCAGG | 50807 |
| rs145384550 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261465 | AAGGACTAGAAGGGA[G/T]ATGTAGGGTGGTGGG | 50807 |
| rs145384721 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130328480 | ATCATCTGCCCCCTG[C/T]GGTAGGCCCTCCACA | 50807 |
| rs145400912 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130202884 | GAAAAGATCCACTCA[C/T]TTTTACTGAAAGATG | 50807 |
| rs145412938 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439990 | TGTCTCCCACAACAA[C/T]GCCACCATACACCCA | 50807 |
| rs145417839 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374287 | TTCTTTCAATCCAAA[G/T]AACTGAGATTTTACT | 50807 |
| rs145423303 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155232 | CTTCTCTTCTGCTGC[A/T]AATAAAGCCAAGGAA | 50807 |
| rs145426637 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159023 | GGCGTGAGCCACCGC[A/G]CCCGGCTGTGCTTTA | 50807 |
| rs145432268 | in-del | -/ACT | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350558 | GATTCGTCCTACACC[-/ACT]GAGCTGATGCATTTC | 50807 |
| rs145443549 | snp | C/T | 0.117188 | 0.211804 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393699 | AGGCAGAGATTGCAG[C/T]GGGCCAAGATCTCAC | 50807 |
| rs145451278 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277323 | GACAACGGCTATAGG[C/T]AACAGGAGAAAAACA | 50807 |
| rs145464086 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273496 | ACATCCAATACACTG[G/T]CTGTGCATCAGAATT | 50807 |
| rs145466251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199162 | CAGAGTACTGCACTT[C/T]ACAATTATCCGTGTG | 50807 |
| rs145481514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347780 | TGGTGTAGGGCACTG[A/G]AGCTGGGAATAATTT | 50807 |
| rs145483634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130231761 | CGCTTATTATGAACC[A/G]CATGCTTCCATTTCT | 50807 |
| rs145484118 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219131 | CCGCTATATATCCAT[A/G]ACTACTTACAATACA | 50807 |
| rs145484434 | in-del | -/A/AA | 0.478603 | 0.101197 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209550 | TAAAAAAAAAAAAAA[-/A/AA]GAAAGGCTATTTTCA | 50807 |
| rs145485209 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276195 | GGCACAGCAAACTCC[C/T]AGAGCTTCGTTCCTC | 50807 |
| rs145506267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130398456 | TAGTCACAACAGTAG[C/T]AGCAGCAGCAGAAGT | 50807 |
| rs145518009 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162894 | CCTCTTCCTTGGAAC[C/G]CTTGTTACGGAACTA | 50807 |
| rs145518205 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123074 | TTTGTGCTTTTTTTT[C/T]CCATCTGCATAGTGT | 50807 |
| rs145541098 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078752 | GTGTGGAATGTGGAG[G/T]TGGGAGAACAAGTAG | 50807 |
| rs145545584 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100034 | ATAAATACCCAGTAG[C/T]AGAATTGCTCAGTGG | 50807 |
| rs145560976 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167233 | TGAGGTCAAGGCTGC[A/G]ATGAGCCATAAGTGT | 50807 |
| rs145564952 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104499 | CTAAGTTACTAGCCA[A/G]TCAGGACAAATACAA | 50807 |
| rs145573516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114511 | CCTAGGACATTACTG[C/T]ACATTTTTATACAAC | 50807 |
| rs145582131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059607 | TGTAACATTTTATAA[C/T]AGAATGTGAGGCAGG | 50807 |
| rs145582530 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388743 | CAGATGATTCGCAGA[A/C]GCTGAGTTGACTTAC | 50807 |
| rs145590638 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285861 | TGAGCGAGTACCAAC[A/T]ATGTTCCAATACTGA | 50807 |
| rs145604838 | in-del | -/GGG | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130360044 | AGTAGCAGAGTGGCT[-/GGG]GTCAAAATACAGCAC | 50807 |
| rs145625657 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130326594 | AAACAGCTCGCTCCA[C/T]GCTAGTCAAAGAATA | 50807 |
| rs145629990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344525 | ACAATTGTTGAAACT[A/G]AATGATAGTTACATG | 50807 |
| rs145631045 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399566 | CTCGATCATATCAAA[A/C]GCCTCTCAGGTTGGC | 50807 |
| rs145648401 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273277 | TAATATGAAGAAAGC[C/T]CATATGCTAAATCTC | 50807 |
| rs145654749 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436800 | AGCAAGATCCTATCA[C/G]TTAAAATAATAATAA | 50807 |
| rs145677252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130329666 | TCTCAAGCTAAAGTT[C/G]AGAGTATTTTACATT | 50807 |
| rs145702499 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240803 | TTCCAACCTTGATAC[A/G]AAGACTTTTTACTTT | 50807 |
| rs145703543 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163742 | GAATGAAATAGGTTC[A/T]GAATCCTTTGATAGT | 50807 |
| rs145705229 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130440887 | CCCTACTTTGGTCCC[A/T]GGTTTGTTTCCTTGA | 50807 |
| rs145708324 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130200033 | TTAATTTGATCAGAG[-/C]CAAGGCACCAACTAT | 50807 |
| rs145717727 | in-del | -/TAAAA | 0.0509478 | 0.151255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362851 | TTAAGACCAACTCAC[-/TAAAA]TAAAATAAAATAAAA | 50807 |
| rs145718319 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168568 | GTACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 50807 |
| rs145740243 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299481 | AACACTATATGGCAC[A/C]GTACCTTTCTCATCC | 50807 |
| rs145743273 | snp | C/T | 0.000115349 | 0.00759349 | missense | ASAP1 | GRCh38.p7 | 8:130118568 | AGTAAATCCCTGGAT[C/T]TGATGGCCTCAAGCA | 50807 |
| rs145750061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130172684 | CATTTCCACCATAGC[A/G]GAAAGTTCTACTGGA | 50807 |
| rs145750167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223466 | AAATTCAGAGCTGAA[A/G]TTCTGATGCTAATGG | 50807 |
| rs145756093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108932 | AGGCAGGCGCCACTA[C/T]GCCCGGCTCATTTTG | 50807 |
| rs145758111 | in-del | -/AG | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411633 | GATGATACTTTTAAC[-/AG]AGTGTTGTTAGGAGG | 50807 |
| rs145769731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286835 | CTTATCATTATGAAA[C/T]GATGAGAAGCAAAAG | 50807 |
| rs145770490 | snp | C/G/T | 0.000280006 | 0.0118294 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130060693 | CTGCACATTTGGGGA[C/G/T]AGATCCAATGGGTGT | 50807 |
| rs145772206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339948 | TCCTTATCCTCACTT[A/C]CACCATACACAGAGC | 50807 |
| rs145774943 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127837 | GAGTGTGTCCATAGG[A/G]GTTAAGGTTTTTCAA | 50807 |
| rs145775766 | snp | A/C/T | 0.0193772 | 0.0965046 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356485 | GGGTTCAATGCCTGG[A/C/T]AATTCTGTTTAATCC | 50807 |
| rs145780216 | snp | C/G | 0.00199481 | 0.0315187 | | | GRCh38.p7 | 8:130063841 | GCACTTGGGACACAG[C/G]TGATGGAAAGAACTA | 50807 |
| rs145814363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220049 | CCACATTGGCCACCC[A/G]AAGTGCTAGGATTTA | 50807 |
| rs145845865 | snp | A/C | 0.0021798 | 0.0329416 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136916 | CAGGTGTCAGAAGCC[A/C]CAATAACCAACTCAG | 50807 |
| rs145846268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130294376 | TCCTCTGTATCCCAT[A/G]AAGCCCAGCCTTCAC | 50807 |
| rs145850169 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191543 | CATATTCTAGGAACA[C/G]AGGCAGTCACTACAC | 50807 |
| rs145860211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072465 | TAAGACGTGCCTTTC[A/G]CCTTCTGCCATGATT | 50807 |
| rs145862311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370038 | GGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 50807 |
| rs145863781 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395957 | AGGTGTGAGCCACCG[C/T]GCCTGGCCATATTTC | 50807 |
| rs145868891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406412 | CCCCTAGAACAAACA[C/T]ATCTGGGTTAGAATC | 50807 |
| rs145883763 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130122671 | GGAAGTGGCAGAGCT[A/G]TGATATGAACTCCAG | 50807 |
| rs145885589 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076167 | CTTTGCTAATCACCA[A/T]ATTTGAGTTTATAAA | 50807 |
| rs145886039 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130179992 | GAAAGAGAATGAGAG[A/T]GAGAGAGGTGAGAAA | 50807 |
| rs145902224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171322 | AAGGAACACCCAAGA[C/T]GGAGTAATTTATAAA | 50807 |
| rs145902473 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132525 | TCAGCCTTACCTTCC[A/T]CTTGGAAGTCATCTC | 50807 |
| rs145917673 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176005 | GGAGCAGGTGAACTG[C/G]AGGATATGTCTGTTT | 50807 |
| rs145921868 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111922 | GCCTGTCCTGCTCTT[C/G]GTACCTGGCAAATGG | 50807 |
| rs145923803 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130107535 | ATGTATGTATGTATG[A/T]ATGTATGTATGTATG | 50807 |
| rs145937658 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228645 | TGGCGAGGCTGAAGT[A/C/G]AGCCAAGATCATGCC | 50807 |
| rs145937832 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154881 | TAAATCACATACTTT[C/T]TTCTAGAAGTACTGG | 50807 |
| rs145941263 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272285 | TAAAACCATAATGAC[A/G]TATCATCTTATCCCA | 50807 |
| rs145954408 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341929 | ACCGAGAGATGGGAA[A/C/G]AGACAGCCAGCTACC | 50807 |
| rs145963150 | snp | C/T | 0.239037 | 0.24976 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057541 | GCAACCTGTGCCTCC[C/T]GGGTTCAAGCGATTC | 50807 |
| rs145978631 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233575 | ATAAATACAAAATGA[A/G]TATCATTTCCTCCAA | 50807 |
| rs145980563 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157350 | GATTTTCTTTCTCTA[C/T]ACCCCATATCAGCAA | 50807 |
| rs145980613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118779 | ATTTTAATTAAGATA[C/T]GCTTCTTTTCACCAT | 50807 |
| rs146014785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408905 | CTAAGCAAGGCACTA[C/T]GGATCATGACCAAAC | 50807 |
| rs146017152 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285060 | ATAAAGATGGTCCTA[C/G]TGGTTCCTTATAATT | 50807 |
| rs146017327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401186 | TGCACCCAACTGAAT[A/G]TAGAAATTCTTACTT | 50807 |
| rs146018775 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355358 | TCAGTTGCGCTCTAT[A/G]TATGTGCATTAGTGA | 50807 |
| rs146038922 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | ASAP1 | GRCh38.p7 | 8:130193420 | CCCCAAAAAACTCTC[G/T]GCTTTAATTATTTCT | 50807 |
| rs146054860 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252083 | TGTTTTATAGAAAGT[C/T]AGAAGTAACCTAAAT | 50807 |
| rs146059410 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170248 | CTGGAGTGCAGCGGC[A/G]TGATCTCAGCTCACT | 50807 |
| rs146063233 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320632 | CTAGGGCTGTATGAA[A/G]GAGGAAGAGTTAAAA | 50807 |
| rs146065260 | snp | A/C | 0.0581099 | 0.160244 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389364 | GTTAAAGTCCAGGAC[A/C]AGGGAAAAAATGGCT | 50807 |
| rs146075346 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360236 | AGTATAAAGAATCTG[A/C]AGAGAAGGCTTTGCT | 50807 |
| rs146076842 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344514 | GCCAAAAGCAGACAA[C/T]TGTTGAAACTGAATG | 50807 |
| rs146076899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130300659 | TCAACAGATAATGAA[A/G]TTGAAAGAACCTGAA | 50807 |
| rs146083074 | snp | C/T | 0.0138852 | 0.0822049 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254844 | CTTAAGTAGCAACAA[C/T]CAATCTAACAACTTT | 50807 |
| rs146102390 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133725 | CAACCCAGGAGTATG[G/T]GATACCAACCTGTTC | 50807 |
| rs146102405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173534 | ACTTTGGGGGGCCAA[A/G]GCAGGACGATTGCTT | 50807 |
| rs146111332 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076512 | ACATAATCATCTAAA[A/G]AATGCTTTCAAAATT | 50807 |
| rs146129606 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130138293 | CAATGAGATTAAACA[A/T]AGAAAACAATGCCCT | 50807 |
| rs146139083 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130302124 | TTAGGTATAATATCT[A/G]CATGCATGCAAAGAC | 50807 |
| rs146141097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417299 | CATACACAAATGCAA[C/T]GGACTATGTGCCGCA | 50807 |
| rs146159598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413341 | TAGGTCCAATTAACA[C/T]CAGCCCACTTGACCA | 50807 |
| rs146178150 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130267944 | GCTAGTGGTGTTACA[A/C]AAAGCAACATGGCAG | 50807 |
| rs146180149 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130190891 | TTTGAAGTCAGGTAA[C/T]GTGATGCCTCCAGCT | 50807 |
| rs146194861 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306899 | TAACAAACTAGAAAC[A/G]TGTTTCCTTCACTCC | 50807 |
| rs146196352 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381691 | GACTTAGTCTAAAGG[A/C]CTTATATGACCAGGC | 50807 |
| rs146197760 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411207 | TGCAGACTATGATGA[C/T]GCCCACACACAATGC | 50807 |
| rs146204991 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130271095 | GCCTGCTGCCGGGCT[G/T]CTCTGATTTGGTCTC | 50807 |
| rs146206329 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090657 | AACATGTGCTCTAAT[A/G]ACTTACCCACGTGTG | 50807 |
| rs146214341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228259 | TGTACAGGTGGCATA[A/G]AACACCCCCCAAAAC | 50807 |
| rs146221885 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130196067 | CAGTTGTAGGTCGGG[C/T]ACAGTGGCTCACGCC | 50807 |
| rs146227431 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130059169 | ACTGCAACATTTAAA[-/T]TTTTTTTTTTTTTTG | 50807 |
| rs146232201 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130053998 | TTGAACTTCATATGT[C/G]TTTTAAACTTTTGTC | 50807 |
| rs146258737 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366623 | GGGGCTAAGAGTGTG[C/T]GATCTGGATTCAGAT | 50807 |
| rs146262244 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252545 | GGTACATACTCTCAG[G/T]AATCTCCATGTTGCC | 50807 |
| rs146270389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432935 | CCAGCAAAAGAGAAG[A/G]GGAAAAGATGTTGGG | 50807 |
| rs146273927 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057093 | TTTTCCTAAAATTAC[A/G]TGGAGAAGGTGTCTT | 50807 |
| rs146274467 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430213 | AATTCATTCATCAAA[C/T]ATGAATTAAGCATCT | 50807 |
| rs146276750 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130361542 | GATTATGTTATGTAT[A/C]TGCTCCTCCCCCATC | 50807 |
| rs146277888 | snp | C/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188682 | GAGGTTGCAGTGAGC[C/T]GAGATCACCACTGCA | 50807 |
| rs146285933 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130351652 | GGGCGAGAGAGAGAG[-/A]AAAGTGGAGACCCAA | 50807 |
| rs146291960 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130188694 | AGCCGAGATCACCAC[A/T]GCATTCCAGCCTGAG | 50807 |
| rs146297773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120281 | GCTGCATGTGTCTTA[C/T]ATAAAGTGTGAAAGG | 50807 |
| rs146298863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209726 | TGATGGTTGTTTTGA[A/G]GAAAAGTACTTATGT | 50807 |
| rs146300645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130138939 | AGGCTTAGCTCACTG[C/T]AAAAAGAACTGTTAG | 50807 |
| rs146302302 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130255393 | CTATGTACCTAATAA[A/G]TGTTTTATGTGCAAC | 50807 |
| rs146313988 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322991 | CACTAGGCATTTGTG[C/G]AATCAAACTGGATGA | 50807 |
| rs146330785 | in-del | -/A/AA/G | 0.0826429 | 0.188692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390942 | ATATATCCCCCGCCC[-/A/AA/G]CCCCAAAATTGAAAG | 50807 |
| rs146341224 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214429 | CTAGGACTAAAAAGC[G/T]TTTTGTTTTTTCTTT | 50807 |
| rs146342754 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130103898 | CCACAGGTTTTGGTT[A/G]CATCTTCATTTTTTT | 50807 |
| rs146350640 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069958 | AAGAAGTTCCTGAAA[C/G]TAGAATATAAAAATG | 50807 |
| rs146357452 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130304360 | CATCTTTGAAAGTCT[G/T]ACACATTCACCCTAA | 50807 |
| rs146369775 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170048 | TGTCCCTACAGCAGA[C/T]TATTTCTCAAAACAC | 50807 |
| rs146371198 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106223 | CCCTAAAACAAAACA[C/T]GAATCAAGGGTGACA | 50807 |
| rs146381804 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130386014 | GTACAGGGCTGACCA[C/T]GTGACCCAAGATAGA | 50807 |
| rs146383016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130338532 | TAGCTTTACTGCCCA[C/G]AGTCATCCCAGCAAA | 50807 |
| rs146397020 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130232144 | AAGCTATCTTGTCTA[C/T]GGACTGGCCTTGGAA | 50807 |
| rs146400118 | snp | A/G | 0.239326 | 0.249772 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382069 | AGGCGGGCAGATCAC[A/G]AGGTCAGGAGATCAA | 50807 |
| rs146407982 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073804 | ACAGAGACAATGCGA[C/T]GGTGTACACCTCGTG | 50807 |
| rs146414712 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424602 | CTGCCCTTCTCAGCA[A/G]GTGATAAAAGGGACC | 50807 |
| rs146423114 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115496 | CCAATAAGGACTGAA[A/C]AACATAAATGGCCCT | 50807 |
| rs146424371 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130225419 | GCACAGGAAAGGGTT[C/T]GTTAAAGTAAGTTAT | 50807 |
| rs146426484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111765 | CTCAACTTTACCTCT[C/T]ACCAGTGGTGTGACC | 50807 |
| rs146453683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392975 | AAATATCCAAACCAT[A/G]GCACCGAGGCACACA | 50807 |
| rs146457128 | in-del | -/AAACAAAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130230066 | GAGATCCTGTCTCCA[-/AAACAAAC]AAACAAACAAACAAA | 50807 |
| rs146457316 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | ASAP1 | GRCh38.p7 | 8:130427428 | ACAAGCACCAATAAG[C/G]CCTTGCCGAGAATCC | 50807 |
| rs146467066 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054493 | GAGATGTAAGTGCTA[G/T]ATGCCAAGGATGGCT | 50807 |
| rs146479273 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273634 | GCATCCTGATGGAGG[C/T]TGTCTACAAACCTCA | 50807 |
| rs146480970 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280274 | GATTTCAGGAGAATC[C/T]AGCAGGATAAAATGG | 50807 |
| rs146497697 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395631 | CACTGCCAACACGTT[C/G]ATCTTGAACTTCTGG | 50807 |
| rs146499219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277429 | AGAGGAAAGAACCAG[A/G]AAGTTCAGTAGAAAA | 50807 |
| rs146508428 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241424 | AGCAGGGGCTTGTAT[A/C]ACCTGTTCATGGCTG | 50807 |
| rs146509862 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164355 | TTTGGGAGGCTGAGG[C/T]GGGCAGATCACTTGA | 50807 |
| rs146525740 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088580 | AGAGGCAAGAAACAG[A/C]TTCTTCCCACAGGGC | 50807 |
| rs146534186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130067272 | CCATACTAGAGTTAG[A/G]TGAGTGGTGGTCACA | 50807 |
| rs146546412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131301 | TCATTCAATTTCATC[A/G]AACACTTTCATATGA | 50807 |
| rs146550332 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128546 | TATTTTCTGCAAGTC[C/T]ATGTCAGTGGGGACA | 50807 |
| rs146550363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166752 | ACATTTATAACTAAG[A/G]ATCTGTACTGCATTC | 50807 |
| rs146551390 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063972 | GTGCTGGCTGGGTGG[G/T]GAGGAGGAGAGTGAC | 50807 |
| rs146560467 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246654 | GAGTCAATTAAACGT[C/T]TTTTCTTTATAAATT | 50807 |
| rs146575040 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335214 | TTCATTTGATGACAC[G/T]GATCATCTTTATCAC | 50807 |
| rs146575529 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406632 | GATTACAGGCATGTG[C/T]CACCATGCCCAGCTA | 50807 |
| rs146580802 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444721 | AATCTGAGAGTCTGG[A/G]TGTAGTGGGGAGTGG | 50807 |
| rs146603317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226245 | ACTTAGTGCCACCTG[C/T]CCTGTGACCCGGAAA | 50807 |
| rs146615049 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339436 | TATCCTTGAGTACAT[C/T]GATGCGGTCAGGGAG | 50807 |
| rs146616020 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410382 | CAGAGAAACAGCCTC[A/G]GGACCCCCAAGAAGA | 50807 |
| rs146620949 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223479 | AAGTTCTGATGCTAA[C/T]GGATGCTAATTTAAA | 50807 |
| rs146628182 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130181777 | TCTGGTAATAATACC[A/T]AAGATTATAGCCTGC | 50807 |
| rs146640259 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130298370 | TTGAAAATCACTCCT[A/G]CCCTGAGACAGAAGG | 50807 |
| rs146643023 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116278 | GCACAGGAAGGGGAG[A/G]GGCTGGGAGAACAGT | 50807 |
| rs146645496 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130192651 | CTTTTCCTCTGTTCA[C/T]GGAGATCCTTGCCTT | 50807 |
| rs146649995 | snp | C/T | 0.0325976 | 0.123435 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085456 | AAGAAAGAGGAGGAC[C/T]GGGTGAAGAGGCTCA | 50807 |
| rs146662581 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148408 | GCAATGTGTTAGGTA[C/T]TGAAAATTCAAAGAT | 50807 |
| rs146666220 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130186257 | AGAACTGTCAATGTA[C/T]GGATATATTCCTAAG | 50807 |
| rs146669461 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081076 | AAATACACTAATAAT[A/G]TGTAATGAGATGAAC | 50807 |
| rs146692087 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130351935 | AGCATGAGTTCCAAC[A/G]TATACAATTTCCTTC | 50807 |
| rs146693929 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424459 | ACAGTAACAGCTCTC[C/T]GACTTTGCTCTTCCC | 50807 |
| rs146715835 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130426542 | AAGCCCTCATCCCCA[A/C]CCCATCAACCTTTTC | 50807 |
| rs146719336 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247376 | TGACAGATAAGAAAA[C/T]TGAACATCAGAATGG | 50807 |
| rs146724326 | in-del | -/TGAGAAAGGGAAA | 0.174288 | 0.23826 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132047 | TTTCACTTAGGGTTT[-/TGAGAAAGGGAAA]TGAGAAAGGGAAATG | 50807 |
| rs146728199 | in-del | -/AC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130268525 | ACACACACACACACA[-/AC]CACACACACAACTGT | 50807 |
| rs146734603 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355760 | TTCAACTATGGTGGC[C/T]ATCCTTCAGTAAAAA | 50807 |
| rs146737386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130243198 | AGGCTTCTGATAAGA[C/T]TGATAAAGTAAGTTG | 50807 |
| rs146738438 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130357362 | CTGCGGGCAGGTCCT[A/G]CTGGCGCAGCAGCCC | 50807 |
| rs146744979 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130202809 | AACTTCAAAGTCAAG[C/G/T]TATTTCTGCCAATTT | 50807 |
| rs146749440 | in-del | -/A | 0.110519 | 0.207473 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393468 | CTCACAAAGACTCCT[-/A]AGGAAGGCCAAGCAC | 50807 |
| rs146760565 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316547 | TAAATACTAGTGTTA[C/T]TTATATGGGTTCTGG | 50807 |
| rs146764926 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131738 | GAGGACTGAGGCTGC[A/C]AGTGAGCTATAATCA | 50807 |
| rs146786195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099825 | ATTACAGATGTGAGT[C/T]ATTGTGCCCAGCCTA | 50807 |
| rs146787948 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206247 | CAATGATTGATGACC[A/T]TTTTTTTAAAAGATA | 50807 |
| rs146791496 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096626 | AAGATCTTCTAAGAG[A/G]AAGTAGAGTACACCT | 50807 |
| rs146791614 | snp | A/C | 0.000909986 | 0.0213111 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134264 | TGCTTTTTCAATCCA[A/C]GGCATCGCACCTTTA | 50807 |
| rs146806029 | in-del | -/AAC | 0.173965 | 0.238157 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132395 | CAACTCTATACCCAT[-/AAC]AACAAGTCATCAATC | 50807 |
| rs146810183 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | ASAP1 | GRCh38.p7 | 8:130440437 | ACCTGAACCCAGGAG[A/G]CAGAGGTTGCAGTGA | 50807 |
| rs146829713 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436380 | GTTCACTGCAGCCTC[A/G]ACCTCCCTGGGCTCA | 50807 |
| rs146835894 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444316 | CTCGCTCAACTTTCC[C/T]GAGCCTCAGTTTCCA | 50807 |
| rs146840771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264630 | GTTACCAGATATTCA[C/T]GCACAACATATTTCA | 50807 |
| rs146857896 | in-del | -/CTTA | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227834 | GTCGTCGTTCTGAGG[-/CTTA]CTAAGGGGTCTATGA | 50807 |
| rs146858392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378774 | CCCTGCAGATGTCTG[C/T]CAAATGCATATTAGC | 50807 |
| rs146859937 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262082 | TTTATACATTGTCTT[C/G]ATGTTTCCAGTGCTA | 50807 |
| rs146866968 | snp | A/G | 0.000133659 | 0.00817383 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130060606 | TCTGGGCAGTGGTAC[A/G]GGCGTCTCTGGCAGA | 50807 |
| rs146869137 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149356 | AATAGTTGGTAAAAG[A/C]ATTTTTTTTGTTTTA | 50807 |
| rs146875773 | in-del | -/CAGTAA | 0.0352966 | 0.128072 | intron-variant | ASAP1 | GRCh38.p7 | 8:130174449 | AAGATCTTCAAAAAC[-/CAGTAA]CAGTAACAGTAATGG | 50807 |
| rs146885841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334631 | TTTTATTTAACAATT[C/G]AGAGGGAAAAAAACA | 50807 |
| rs146886116 | snp | C/G | 0.000230635 | 0.0107361 | missense | ASAP1 | GRCh38.p7 | 8:130116694 | AGATCTTCACACTGG[C/G]TAGCTTTTAGTCTCT | 50807 |
| rs146896554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130363653 | TAACAGTCCTGAGAT[A/G]CAAGTATTACAATAA | 50807 |
| rs146907595 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130054920 | GGCGGTGGAATCCCA[A/G]GCTTACCCTTCTTCC | 50807 |
| rs146912477 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249476 | TTCTGAACAATACTT[A/C]TGCCTCTCACCATTT | 50807 |
| rs146919182 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130208649 | GTCATCTTCGATCAT[C/G]TTCCTGCCCCAGTAG | 50807 |
| rs146921078 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137225 | AAGACAACAGATCTG[C/T]AGGTTTCTGCCCTCA | 50807 |
| rs146933731 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320542 | CAGAGTCAGATCTTG[C/T]CTAAAAAAAAAAGAA | 50807 |
| rs146935777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204133 | GCGAAGCTGAGTTCC[A/G]CCTCCTGTTAGATCA | 50807 |
| rs146935862 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254120 | TTATAAGCATTACAG[C/G]AAAGGTGGAGTAAAA | 50807 |
| rs146952473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105038 | CACTTTCTAATAGTT[C/T]TCTTTTTTCAATTTA | 50807 |
| rs146965959 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211047 | AAAGGCTATAAAGCT[A/G]GTGAGGCGGAAACTA | 50807 |
| rs146968939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101869 | TGAAGCATCACACCC[A/G]GCTTTTTCTTGATTT | 50807 |
| rs146970347 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141292 | CCAATCGCAGGCCCC[C/T]TCTCGCACTCAGCTC | 50807 |
| rs146979132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380391 | CCAGCACTTCTGACC[C/T]GCCCTGCATGCAGCC | 50807 |
| rs146995912 | in-del | -/AC | 0.0142653 | 0.0832415 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060563 | TTCCTAAGGGCCTGA[-/AC]ATTGTCCCACCCACC | 50807 |
| rs146996598 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376510 | AGGTGGGTGGATCAT[C/G]AGGTCAGGAGTGCCA | 50807 |
| rs146996661 | snp | C/T | 0.000153988 | 0.00877328 | missense | ASAP1 | GRCh38.p7 | 8:130127953 | CAATCGCAGCAAATG[C/T]CATTCCCTGGGAGCC | 50807 |
| rs147001991 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384325 | TGCAACATCAAAGCT[A/G]TCATTGCTATGTAAT | 50807 |
| rs147002238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130265903 | AGCAAAGAAGGACTT[C/T]CAGTGTTACAGCATA | 50807 |
| rs147002483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336371 | CTGAGAATTGAAAAG[A/C]AATGCAGATTATTGG | 50807 |
| rs147014256 | snp | G/T | 0.00755907 | 0.0610114 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445634 | GGGAACGCCCAGTGC[G/T]GTGGAAGGAGCACCA | 50807 |
| rs147026002 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152861 | TCACTCTGGGACATG[C/T]GACGATACAGTATGA | 50807 |
| rs147030527 | snp | C/T | 0.000314854 | 0.012543 | missense | ASAP1 | GRCh38.p7 | 8:130124094 | CTATTGTTTCCTACA[C/T]TCTTGGCCAGCTGTA | 50807 |
| rs147035297 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227215 | GGTGGTAGCCTACGA[C/T]AGGACTCAGCCTGAG | 50807 |
| rs147038072 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130224115 | CCAGTTCCCAGTGCT[A/G]AGCCTGGCACATAGT | 50807 |
| rs147038227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270085 | CGAGGCACAAGAATC[A/G]CTTGAACTTGGGAGG | 50807 |
| rs147038667 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340199 | ATAAGTCACTGTTTA[C/T]CAAGGATCCCACACA | 50807 |
| rs147051314 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130429181 | TCGCCCTAATGACTT[C/T]ATTTTAATTTTTGTT | 50807 |
| rs147058183 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119655 | CTGACAGCCTGGATC[C/G]AGCTGTACCTGAATC | 50807 |
| rs147062095 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130217623 | TCACTTCTGCATCCC[C/T]ACCCAATGGACACTG | 50807 |
| rs147063475 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ASAP1 | GRCh38.p7 | 8:130051867 | TTCACATCAACGGGC[G/T]CACAAGTGGACGTGG | 50807 |
| rs147074246 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130117201 | CCAGGTCCTATGGGA[A/C]AGACACTGTTTCTTA | 50807 |
| rs147074610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155999 | GTTATTTGACCTCTT[A/G]GAGACTCATTCTCCT | 50807 |
| rs147082810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320907 | CAGTCTTCGGTTAAA[A/G]ACATCAGGAACAATA | 50807 |
| rs147083865 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396128 | TGGCACTTAGTAGGT[C/T]GTCAGAAAAGTGATC | 50807 |
| rs147100218 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394131 | AAAAGAACAGGATAA[C/T]AGCAATGTTCAGGGA | 50807 |
| rs147100248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431663 | GCCCATTACATGTTA[C/T]GTTCCTGCAGGACCA | 50807 |
| rs147106994 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130282433 | ATTGGTAAAAACAAA[C/T]CAAAATATTTTTGAA | 50807 |
| rs147130410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130065894 | CTTAGGATAAACTTG[C/T]GCAGAGCTGTTTCGC | 50807 |
| rs147143916 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166157 | GACTACAGGCACATG[C/T]CACCATGCGTGGCTA | 50807 |
| rs147149141 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439129 | GCCAGAAGGGAGAAT[C/T]AGAGAGATGGAAGCT | 50807 |
| rs147154115 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333022 | ACAGTGATTCAAGCA[A/C]AAAGCGGTTCAATCT | 50807 |
| rs147167267 | snp | G/T | 0.125528 | 0.21681 | intron-variant | ASAP1 | GRCh38.p7 | 8:130443087 | GGGCGCCCCATCGGC[G/T]GGGTCCGGGCCGCCA | 50807 |
| rs147171955 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402112 | CAGAGTGGCTGTCCA[A/G]AAATATGAAGGAAAC | 50807 |
| rs147189604 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130174503 | GTATTTACTCTGTAC[C/T]AGTCACCGCACTATT | 50807 |
| rs147190164 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224634 | ACATACGACCACCAT[A/G]GCTTGCTTTTTTCCT | 50807 |
| rs147193398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222225 | CACAGCAATTATTAA[A/G]TAGGTCTCTCCCTGA | 50807 |
| rs147202962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293436 | ATCGCTCATGCCCCA[A/G]CAAACCACTTCCTGA | 50807 |
| rs147212884 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077833 | CTGTCTCTGGGCAAC[A/G]GGGGAATATTGCTGA | 50807 |
| rs147223205 | snp | A/G | 0.000145164 | 0.00851828 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130061050 | GTCTAGGGAGAGATG[A/G]TCTGTTTTCCTTAGT | 50807 |
| rs147225620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179530 | ACAAATTGACTAGAG[C/T]GTTAGCATTTTATAA | 50807 |
| rs147226532 | in-del | -/C | 0.0402882 | 0.136092 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432782 | AAAAATCTTTCTTCA[-/C]CCCCACTGCCAGGCA | 50807 |
| rs147229567 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130113906 | CCCACCTCTGCCTCC[C/T]GGGCAGCTGGGACCA | 50807 |
| rs147235003 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083648 | AAAGTACGGGACACA[A/G]TGCTAGACCACAGGA | 50807 |
| rs147249203 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183979 | TATATAATCATGCTA[A/C]TAAAATACATAATGT | 50807 |
| rs147259115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350111 | CAGGGAAAGCTACTG[C/T]GGCCTCGCACAGTGT | 50807 |
| rs147266245 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060036 | TGAGCTGTGATCGCA[C/T]CACTGCACTCCAGCC | 50807 |
| rs147269965 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145340 | TTTCTTTTTTTTAGA[C/T]GGAGTCTCGCTCTGT | 50807 |
| rs147270807 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422407 | TGACTTTCTAATTCC[C/T]TGATAGAAAAGTAAA | 50807 |
| rs147276112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347915 | ATTTTGCTTTAACCA[A/G]TGTATTTCATTTTGC | 50807 |
| rs147277802 | in-del | -/GA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070849 | AGAGAGGGAGAGAGG[-/GA]GAGAGAGGGAGAGAG | 50807 |
| rs147296733 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244955 | AAATAGGAACTCCAA[G/T]TACAGCAGTTTGAGG | 50807 |
| rs147297184 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197170 | TGCAGTGGCACATCT[A/G]TAATTCCAGCACTTT | 50807 |
| rs147312270 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354033 | CTGGGACTACAAGGC[A/G]CCTGACAACACGCCC | 50807 |
| rs147312325 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311513 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCA | 50807 |
| rs147334243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130201038 | TCACCTGGAAACTTG[C/T]TGGTTATGAAATCCC | 50807 |
| rs147334564 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130141 | CATATAGATTGAACA[A/C]CCCAAATTTGAAATC | 50807 |
| rs147357446 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132977 | AATAACAAAAGTAAG[C/T]GAGTGGGAGAGAGAA | 50807 |
| rs147358595 | snp | A/T | 0.0524604 | 0.153226 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095353 | TCGCCCAGGCTGGAG[A/T]GCAGTGGCGTGATCT | 50807 |
| rs147361577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405818 | ATGCTCTGAGAATGA[C/T]TTTTTATTCAAACAG | 50807 |
| rs147384777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409542 | CCTTCTGATAACTCT[A/G]TCTTCCCAGGATAAT | 50807 |
| rs147385098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130369147 | AATCGTATACAGGTT[A/G]AGTATTCCTTATCTG | 50807 |
| rs147400110 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263257 | TAGCATGACCCAAAG[A/G]CTTCCCAGCAACCCA | 50807 |
| rs147401036 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130331448 | ATCAGCTGAAGAAAA[C/T]GGGCCCAGAATGTTA | 50807 |
| rs147401049 | snp | A/G | 0.000543474 | 0.0164755 | missense | ASAP1 | GRCh38.p7 | 8:130112132 | AGAGGGGGAGCCTCC[A/G]TGGTTGGTGATGTGG | 50807 |
| rs147446349 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112758 | TTCTCATTTTATATC[C/T]CCCTGCAAAGTAAAC | 50807 |
| rs147462415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109912 | TGTGAACAGCCATGA[A/G]GAACACTCTTGGTTT | 50807 |
| rs147463291 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150649 | TTTGGGAGGCCGAGG[C/T]GGGTGGATCACTTAA | 50807 |
| rs147465423 | in-del | -/TGTGTGTG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130064894 | TCAGTTTACTAAGAA[-/TGTGTGTG]TGTGTGTGTGTGTGT | 50807 |
| rs147465620 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423054 | TACCAAGTAATAGAA[C/T]TAAATTGCGCCATTG | 50807 |
| rs147471416 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130315074 | TGTGACAAGAGCCTC[C/T]ATTAAACCACAAAAC | 50807 |
| rs147472164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391271 | TTATTTCCAGGGATG[A/G]GAAGGGAGAGGGAAG | 50807 |
| rs147488588 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425441 | AGAATCCTTTGAACC[C/T]GTGAGGCAGAGGTTG | 50807 |
| rs147488641 | snp | C/T | 0.0543475 | 0.155628 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387643 | GCCTGGATGACAGAG[C/T]GAGACTCCATCTCAG | 50807 |
| rs147506147 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130279426 | CGCAGTGGATGTTAA[C/T]GGCAGATGTTAGAAA | 50807 |
| rs147507474 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204508 | TACATACAGATGAGG[C/G]AGAGGATAATGCTCA | 50807 |
| rs147512991 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130201335 | GCAAGACAAATTACA[C/T]CATGTGCTAAAGGCA | 50807 |
| rs147520894 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317801 | TTTGTGGCTGAAGTG[A/T]TGAACATGGCATGGC | 50807 |
| rs147535116 | in-del | -/AC/ATAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130373109 | CACACAGAAATACAT[-/AC/ATAC]ATACACACACACACA | 50807 |
| rs147543305 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162679 | AAAAATTAGCCGGGC[A/G]TGGTGGCGGGCGCCT | 50807 |
| rs147544981 | in-del | -/CT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130357145 | TCTTTGCCCATACCA[-/CT]CTCTCATTAACTCAC | 50807 |
| rs147545982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098256 | CTTGACAACAGCTTG[C/T]TTCCCTTCCTCTAAA | 50807 |
| rs147557666 | snp | G/T | 0.0490535 | 0.14873 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359623 | ATCTTGCACTGTTTT[G/T]TTTTTTTTTTTGAGA | 50807 |
| rs147570080 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324945 | CCGAGCTCTGCAAAA[G/T]CCAAGCAAAGGTGAC | 50807 |
| rs147571451 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399479 | AATAAACATGACTTT[A/G]GGTAATCCTATAATA | 50807 |
| rs147576242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130291104 | CTAAAAATGAATCTG[C/T]TCAGATTCTTGTATA | 50807 |
| rs147579056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218288 | CTCCCAAGGGAAGCA[C/T]CTCAGTAGTAAAAAT | 50807 |
| rs147579359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168243 | TATTTACCCCCAAAT[A/G]ATTTTTGGGCAACAA | 50807 |
| rs147592546 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327971 | CAATATAAAAGGAAA[C/T]GGCAGTTTTTAAGAC | 50807 |
| rs147592851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286217 | ACCACCTGAAGTACA[C/T]TGCACTGTTTCTTAT | 50807 |
| rs147602467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110900 | AAACCTGTGGGAGCA[C/T]GAGCTGAGCACACAG | 50807 |
| rs147602565 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072163 | GACAGGGTTCAGTGA[C/G]CCTCTGGAGAGCTGA | 50807 |
| rs147615748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170976 | TCTCCTTGGTCTCCC[A/G]AAGTGCTGAGATTAA | 50807 |
| rs147638686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388027 | CAAAGAGAATAAAGG[C/T]TAGAGTGGCTAGGAA | 50807 |
| rs147638695 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340627 | TTAAAAAGGCTATAA[C/G/T]GTCTAAGAAAGCAGT | 50807 |
| rs147639752 | in-del | -/TGTATGT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130107517 | TTTTTTTTTAAAAAA[-/TGTATGT]ATGTATGTATGTATG | 50807 |
| rs147641354 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384331 | ATCAAAGCTGTCATT[A/G]CTATGTAATTTACAG | 50807 |
| rs147651715 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074908 | GAGTGGCAGAACCCA[C/G]CACAGGAGGGGCAGG | 50807 |
| rs147661381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130231976 | GGCTGCAGTCACCTG[A/G]AAGTTTGACTGGGGT | 50807 |
| rs147667256 | snp | C/T | 0.00145357 | 0.0269198 | missense | ASAP1 | GRCh38.p7 | 8:130214684 | CTTGTGCATAGTTTT[C/T]TTCATTTTGTACATG | 50807 |
| rs147674121 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343432 | TATAATGCACCAACA[C/T]ACACAAGGGCAACAG | 50807 |
| rs147677845 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273011 | CTAGAAATCTTCCCA[A/T]CACACAGAAATGACA | 50807 |
| rs147680552 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307946 | GAAATAATGTTTGCA[A/C]AGCCTCAGCAAGCAG | 50807 |
| rs147684755 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130235814 | CCAGCTCTGATGAGA[A/C]GGGAAGGCCATAAAG | 50807 |
| rs147710896 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133692 | AAACAAACAAACAAA[A/C]AAAAAAACAAAAAAC | 50807 |
| rs147718282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127247 | TTTTTGAGACAGTCT[C/T]GCTCTGTCGCCCAGG | 50807 |
| rs147718693 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088081 | GTAAATGTGACCTGA[C/G]TAGGAAAAAGGGTCT | 50807 |
| rs147720788 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | ASAP1 | GRCh38.p7 | 8:130192326 | TGTATTAAAATTTCA[C/T]GGGGGGGAGCGATGG | 50807 |
| rs147722149 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123247 | ATTTTGGTAAATATG[A/G]TTAATTTGTTTTTCA | 50807 |
| rs147744579 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402649 | TCCTAGCTCAATGTG[A/G]CATCTCCATCCAGGG | 50807 |
| rs147745045 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356510 | TAATCCCAGACGAGT[A/G]TAACAGACTGGCAGT | 50807 |
| rs147754493 | snp | C/T | 0.00267548 | 0.0364772 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091931 | GAGCCCCACACGCTG[C/T]CTGGCCCCAGCAGCT | 50807 |
| rs147764225 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130131196 | CAAACAAACAAAAAA[A/G]CCACTAGCCAGCAGA | 50807 |
| rs147766325 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253652 | TTTTGTATAATTATA[C/T]GGCATTAGAACAGAA | 50807 |
| rs147766661 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171427 | CACCTCTTCACAGGG[C/T]GGCAGGAGAGAGAAT | 50807 |
| rs147766821 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293847 | AGAAAAGAAATCAAT[C/G]ACTCACCAACATTTA | 50807 |
| rs147781232 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362945 | GGGATGATAGCATGG[A/G]GCATTTCTTTTGCAG | 50807 |
| rs147783396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130291321 | AAGCATATTAATTCC[A/G]GGAAAAATAATTCTG | 50807 |
| rs147789206 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257357 | ACTAAGAACAAACAA[G/T]TAGTTCAAAACCAGT | 50807 |
| rs147789841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175208 | TTTTCACGTGTTTTT[C/G]TGGCCATTTGTGTGT | 50807 |
| rs147823971 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144730 | AAGATAAGTAGTGAT[C/T]ATCTAACTGAAGTAA | 50807 |
| rs147824930 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130165031 | AACAGGCATGTTGTG[A/T]AAGATCAATGTATTA | 50807 |
| rs147825847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141101 | TAAATGATTTACTCT[C/G]GGCTACACCACAGTG | 50807 |
| rs147828617 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130075366 | CCAGTCAGTGCTCTT[C/T]AAAGTGTGTTACTTC | 50807 |
| rs147850093 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380145 | GGAGGATCTGAGTAC[A/G]AGGAGTCTATTTGGG | 50807 |
| rs147857008 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130099180 | ACCAGGCCTAGCTAA[-/T]ATTTTTTTTTTTTTT | 50807 |
| rs147873384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130192965 | GTTTCTAAACAACAG[C/T]CAAAAAAAACGAGAA | 50807 |
| rs147885026 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130308724 | CTCAGTACATATCAA[C/G]TAATAAGAAATGGGC | 50807 |
| rs147885422 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383666 | GAGATGTTAGATGGG[A/G]GATAATAATGTTTAT | 50807 |
| rs147896120 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197683 | TAACTTAAGCACACC[C/G]TTAGAATGACCCTGT | 50807 |
| rs147896501 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152395 | CATCTACTGTTACGT[C/T]TCCTACATTATTTTT | 50807 |
| rs147908174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311990 | CTAGAACATGTAGGT[A/G]CAAATATACTCTTGT | 50807 |
| rs147908510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269870 | AATTTTGAGGCATTC[A/G]TTCCAAGTTAAATAT | 50807 |
| rs147916936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096166 | GGTTGAAAAATACTA[C/T]ATATAAGACCCCAGA | 50807 |
| rs147918109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055148 | TGCTCTCCCACAGGC[A/G]TGGGGCTCTAGAGTC | 50807 |
| rs147933068 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155650 | CTGCGCCCAGCCAGC[A/G]CCTGATCTTTGTGAA | 50807 |
| rs147935110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092559 | TTGAAGTCAGGAGTT[C/T]GAGGATACACTGAGC | 50807 |
| rs147954767 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320628 | AAGTCTAGGGCTGTA[C/T]GAAGGAGGAAGAGTT | 50807 |
| rs147955815 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434899 | ATAGCCCCTTAGCTC[A/G]AACAAGCTTTGAAGA | 50807 |
| rs147958990 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431572 | CGTTATTTAAGATTC[A/G]GCTCAAGGATTACAC | 50807 |
| rs147960074 | in-del | -/AAAT | 0.484975 | 0.0853625 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418540 | GTGACCTCTGTCTCA[-/AAAT]AAATAAATAAATAAA | 50807 |
| rs147967286 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058856 | GTTCCAGCTGCTTTC[A/C]GAGCTCCCTTCTGGG | 50807 |
| rs147982906 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137497 | TTTTAATGCTGTATC[A/T]TACTATGAAATGTAG | 50807 |
| rs147990258 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239401 | CCATTTTATGGATGA[A/G]GAAACAGAGGCTTGG | 50807 |
| rs147993979 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162168 | TCACTAAGTCCTCCC[C/T]AATAGATATTTTCAC | 50807 |
| rs148001021 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130416183 | CGCCCCACTAGTGTC[A/G]CCAACTCCGGAGGAC | 50807 |
| rs148002397 | in-del | -/G | 0.0248432 | 0.108648 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136044 | TTTGGCTGTGGGTCT[-/G]GCCTTGCTGGGCTGT | 50807 |
| rs148007621 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344867 | AGGTGGGGAGGAAGG[A/G]GAATCTAATAATGCA | 50807 |
| rs148026645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405107 | AAAAAACTGCCTAAT[C/T]CACATGGGAATATTA | 50807 |
| rs148028509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189056 | ATGGATACATAATAG[C/T]TGTATTTATGAAGTA | 50807 |
| rs148030695 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130121380 | CCTGACCTCTACCCA[A/C]TGGGTGACAGTAGCA | 50807 |
| rs148031695 | snp | A/G | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097051 | GAATCGCTTGAACCC[A/G]GGAGATGGAGGTTGC | 50807 |
| rs148034794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132027 | CACCCAAATTACTCA[A/C]CTGTGTTTCACTTAG | 50807 |
| rs148035395 | snp | C/G | 3.29511e-05 | 0.00405887 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130136958 | GGACTCACGTGATAT[C/G]AGGTCAAAAGATTTT | 50807 |
| rs148045437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233339 | CAACATGTAGCGATT[C/T]ACTCAACCCTTGTTG | 50807 |
| rs148046010 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203058 | ATATAAATTAGAAAT[A/G]AATTGTTGGAGGGCA | 50807 |
| rs148053558 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130086966 | CAACATCAGCTGCCT[A/T]GCTTATTTCCTCCTG | 50807 |
| rs148077844 | in-del | -/T | 0.0573587 | 0.15934 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437668 | TACACACAGGACAAG[-/T]TTTTTACAGAGGCAG | 50807 |
| rs148078026 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375143 | TGGTGGGCACTTGGG[C/G]ATCAGCAGGCGCAAA | 50807 |
| rs148080473 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183867 | CTAAAGAGAGTCAAA[C/T]GCCATCCCAGGATGG | 50807 |
| rs148085267 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092650 | AAGAGTGTGTGCTTT[C/T]AGGAACAAAATGCCA | 50807 |
| rs148103983 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145504 | CTGTATTTTTAGTAG[A/T]GACGGGGTTTCACCA | 50807 |
| rs148112029 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251568 | CAAAAAGATAAATAA[C/T]TGTAATCAATTTTTA | 50807 |
| rs148116385 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130360182 | CACAAATACATAAAG[G/T]GGAGTAAATATAAAG | 50807 |
| rs148120832 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083235 | CTTTGGCTTCTCAAA[A/G]TGAGTCTCCTTTTTC | 50807 |
| rs148122068 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055695 | AAATTTTCTAATTAC[C/T]TCAATTAGATTAGTA | 50807 |
| rs148125041 | in-del | -/T | 0.0119138 | 0.0762559 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275927 | ATAATACCAGTCACA[-/T]TTTTTTTGCAGAAGT | 50807 |
| rs148156020 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213506 | TCACCTAAGGCCACA[A/G]AAGCCTATGTGATAC | 50807 |
| rs148162193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413003 | TATGTGTATCTGACA[C/T]TAACTACACAAGCAA | 50807 |
| rs148172568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257955 | CATGGGTGTTTTACA[C/T]GGCCTGTATAATATC | 50807 |
| rs148178423 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424980 | CCTGGGTGACAGAGC[A/G]AGATTCCGTCTCAAT | 50807 |
| rs148196048 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105572 | CAGATCTCTTGAACT[G/T]ATTCCTCCTAACTGA | 50807 |
| rs148203617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274897 | GGGTGGAAATGGAGG[A/C]TAAACCTCTCTTCGC | 50807 |
| rs148205079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130200806 | TGATATAATTAACCA[A/G]CAGCCTATTTCTCAT | 50807 |
| rs148219153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385021 | CTTGAGGTCCAAATA[C/T]TGTCTTTGATCTAAC | 50807 |
| rs148233622 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437941 | AACTCTGTGCACCTT[C/T]GCACTTCCTGACTTA | 50807 |
| rs148239166 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372366 | CTGCCCAATCTCTCC[A/T]GAGCAATCATTTAAA | 50807 |
| rs148246369 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064283 | CGGTGGAGATGATGA[G/T]AAGTGACTGGGTTTT | 50807 |
| rs148247563 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164750 | GAGTTTACTGAAATT[C/T]CAGGGATCCTATTCA | 50807 |
| rs148249849 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101577 | GCTTTCTCAATTTTT[A/C]TTTTTTTTTCTGAGA | 50807 |
| rs148255252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341140 | GCAGAAGGTAAAGTC[A/G]ACACAAAACTTCCAA | 50807 |
| rs148255828 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270709 | AAATCTATCCTAAAC[A/G]GAGGTACCTAAAGAA | 50807 |
| rs148264190 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117756 | GCTGTTAAGTCTTCT[C/T]TCTTTTAACCTCTCC | 50807 |
| rs148278942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228284 | CAAAACATGACCTCA[A/G]CTAGGCTTCTCCACT | 50807 |
| rs148287099 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432804 | AGGCAATTTCCCTTC[A/G]TATTTCACTGGCCAG | 50807 |
| rs148303820 | in-del | -/C | 0.031825 | 0.122064 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152527 | TTCATTTTGAGAGAG[-/C]CAAAAAAACAAGTTT | 50807 |
| rs148308310 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336334 | CCTAGTGTGGTCAGT[G/T]AACCAGCAGCAGTGG | 50807 |
| rs148314249 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177724 | TCATCAAATTTATGT[A/G]AACAACAATTTGATC | 50807 |
| rs148317171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112515 | CCACACTTTCATATC[A/G]TTCACCACTATGAAT | 50807 |
| rs148325571 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321458 | GTCAATAGGAATGTG[A/G]ACTCTGGGACCTCAA | 50807 |
| rs148330176 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224085 | GGTCCCAGCTTTACA[C/T]ACTTTGTTATACGCC | 50807 |
| rs148330795 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295042 | GCTGAGGTGGGAGGA[C/T]TGCTTGAGGCCAGGA | 50807 |
| rs148352533 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077059 | CAGACAAGGAAATGG[A/C]AGGGAATGGGGGTGT | 50807 |
| rs148366962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254222 | TAAAGGCCACTGCCA[A/C]GGATTCCAGTGGGTT | 50807 |
| rs148370660 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130345653 | TGTGAGAGTTTGAAA[-/C]CAGCCTATGTAAAGT | 50807 |
| rs148375548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130279232 | TAGCCTAAAAGTACA[C/T]GGGGGAGGCACAGGA | 50807 |
| rs148375785 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349521 | AGGTACTTATCCCCA[C/T]GAGGAAAGTAGGACA | 50807 |
| rs148391331 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409569 | TAATCCAATAGGCTA[C/T]AGTTCAGAGAGATAC | 50807 |
| rs148395936 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130338073 | GCCCTAGATCACATA[C/T]TTGGGCACTGGGGGA | 50807 |
| rs148398867 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130125161 | GAGCCTCCTGTCTGA[A/G]AAGTCATACTTTATT | 50807 |
| rs148417560 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180441 | CACCAATAAAACTTA[A/G]TATTCACCAGTGTTA | 50807 |
| rs148418858 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115222 | GGGTGTGCCTCACCT[A/G]ATCAGCCAAAGAAAG | 50807 |
| rs148425039 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355968 | CATGGGTATCATCAA[C/T]GTACTCTAACATGAC | 50807 |
| rs148432421 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297206 | TTAAAATCTGAAGTC[C/T]AATTGTGGTTGTCCC | 50807 |
| rs148433630 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130225260 | TTGCCATGGAGAAAT[C/T]TAAAAATGTCATGTA | 50807 |
| rs148440900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130398653 | ATAGCTAGAACTTAT[A/G]TAGCACTTACCATGT | 50807 |
| rs148467980 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078993 | GAGCCCAGAAGTTCA[A/C]GACCAGCTTGGGCAA | 50807 |
| rs148469432 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173857 | ATGGGTAGATTGCCT[A/G]AGCTCAGGAGTTCGA | 50807 |
| rs148473893 | in-del | -/CA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130232648 | AAACCAAAAAACCCT[-/CA]TTTTTATAATGTTTA | 50807 |
| rs148477696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350673 | TACAGACCCCCATCA[C/T]AGCTTTCATGAGCCT | 50807 |
| rs148479759 | in-del | -/C | 0.0517044 | 0.152246 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368881 | ATGTGAGCAACTGTA[-/C]TTCTTTTTTAGTGTA | 50807 |
| rs148481120 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130255742 | ATACTAATAATTTAT[A/G]TCCCTAAGTCGCAAC | 50807 |
| rs148482521 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293407 | TTCTGGCTCTTTTCT[A/G]ACTTCCAACATCCAT | 50807 |
| rs148500948 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130312121 | TCTCTCCAAAAAAAA[C/T]ACAAAAATTAGCTGG | 50807 |
| rs148507625 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130248218 | GAGGAATGTGGCGGG[G/T]GCCGGGGGGGTTGGA | 50807 |
| rs148508716 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074638 | GGAGTCTGTCCCCGA[A/G]GGGGTGGGAGGGTAC | 50807 |
| rs148511594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423265 | AACTTTAGCATTAAA[C/T]TTAAAAATGCAAATA | 50807 |
| rs148516132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241094 | AGATGTTCTCAGAGA[A/C]GCGTATGAATCTGAC | 50807 |
| rs148518423 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140803 | ATCCCAAATGTGACT[C/T]TGAGGAGCCAAGTAC | 50807 |
| rs148540620 | in-del | -/A | 0.236724 | 0.249647 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173922 | TACTAAAAAAAAAAG[-/A]AAAAAAAAATTAGCT | 50807 |
| rs148550441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307891 | CCTTTCCTAATATAT[A/G]AAATGGATTTTTAAC | 50807 |
| rs148555503 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098596 | CTCATGATCCGCCCG[C/T]CTCGGCCTCCCAAAG | 50807 |
| rs148568361 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204715 | GGGGAGCTTCCATGC[A/G]TCTAAGTCTCTGAGT | 50807 |
| rs148570138 | in-del | -/AGGA | 0.0584853 | 0.160693 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389359 | GGCTGGTTAAAGTCC[-/AGGA]CAAGGGAAAAAATGG | 50807 |
| rs148588637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269426 | GATGTCCTGAGAATA[C/T]AGATAGTGACAGTTC | 50807 |
| rs148589331 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130192059 | AAACAATCACTTCTT[C/T]CTTATTTCAAAGACA | 50807 |
| rs148603629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378010 | AGCCATGTAAACAGA[C/T]AGTTACAACATAATG | 50807 |
| rs148606807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157492 | CTCTAACTGGTCTCC[C/T]TGTCTCTGTGCTTTC | 50807 |
| rs148607950 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095040 | TGTAACCATAAACCA[A/T]GTAAAATCCAACCTC | 50807 |
| rs148640119 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264034 | AGGAGGAAAAAACCA[C/T]AACTGGAAAAGGCAG | 50807 |
| rs148646148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430505 | TCTGAGCAGTTGAAA[C/T]GTCCAGCTGCTTTCC | 50807 |
| rs148650873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362336 | GCATTCATCACAGGC[C/T]CCCGATGCCCTCATG | 50807 |
| rs148676672 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111076 | ACAACAACCCTCCTA[C/T]GAGCGGGATTCCTCG | 50807 |
| rs148679018 | snp | C/G | 0.240478 | 0.249819 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215061 | GCATGCCACCATGCC[C/G]GGCTAATTTTTTGTA | 50807 |
| rs148684726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316372 | TATCTCTTTTCTACT[A/C]CAAGTATTCCTGATG | 50807 |
| rs148695191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258971 | CCTATTTGCCCCATC[A/G]ATTCCAAAAATAAAT | 50807 |
| rs148698077 | snp | C/T | 0.00914312 | 0.0669923 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130053152 | TGAGCACTGTAACGA[C/T]GGAAGAGGGCTTTTC | 50807 |
| rs148703133 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425976 | TTCCACTCTCACCAG[C/T]ATTAAGCATTTGCAG | 50807 |
| rs148705051 | in-del | -/AC/ACAC | 0.420574 | 0.182769 | intron-variant | ASAP1 | GRCh38.p7 | 8:130268490 | AGATCCCGTCTTAAA[-/AC/ACAC]ACACACACACACACA | 50807 |
| rs148710015 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276261 | CGCTCCAGCTGTAAC[A/G]ATCTCTTCCATTTCC | 50807 |
| rs148730329 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107344 | TCCTCCACCACACCC[A/G]GCTAATTTTTGTTTG | 50807 |
| rs148731134 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209359 | AGTATGGCGCCTAGG[C/T]CCCTAGAGGTTCCCA | 50807 |
| rs148734715 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130373872 | AAAAAAAAAAAAAAA[-/G]ATAAACCTGTGTAAT | 50807 |
| rs148738900 | in-del | -/GA | 0.173643 | 0.238054 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353858 | CCTCGGCGACAGAGT[-/GA]AGAGAGCCTGTTTCA | 50807 |
| rs148740127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130386939 | CCTTTGTAGCTGTTT[A/G]TAAGCACCAAACCCC | 50807 |
| rs148763206 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130342395 | CCTTCTGTAAAATAC[C/T]GTGGGTAAAGTACTC | 50807 |
| rs148774514 | snp | A/G | 4.94295e-05 | 0.00497115 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130180850 | CCCATGTTGTTTTGC[A/G]TGCTCTCTTTTCTCT | 50807 |
| rs148780552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166293 | GGATTACAGGCATGA[A/G]CCACTGCTCTTAAAT | 50807 |
| rs148799293 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229112 | ATGGCACTGATTATC[A/G]ATGAAAACCAGTTCA | 50807 |
| rs148803647 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155351 | TCTCCTGGCACAGTT[G/T]AGAGCAGTATTGCCT | 50807 |
| rs148821216 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130136576 | TTTTTTTTTTTTTTT[A/T]AACTATGTCTGGGCC | 50807 |
| rs148828538 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317405 | TGCCACCATCAGGGT[G/T]TGTTGAAACTGTAGG | 50807 |
| rs148831024 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171526 | GAGAACAGCATGGGG[G/T]AAACTGCCCCCATGA | 50807 |
| rs148845006 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286056 | GGTACTAGAAAATAA[C/G]AGGTGTTATCTCCCT | 50807 |
| rs148853669 | in-del | -/TAAAG | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090062 | TGTCAGGCACTCTTT[-/TAAAG]TAAATTTTGTTTAAT | 50807 |
| rs148866561 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344552 | CATGTCGCTCTGCTA[C/T]TGCATGTGCAAAAAT | 50807 |
| rs148875199 | in-del | -/TGGT | 0.0260105 | 0.111035 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209713 | CATACCAAAATATGA[-/TGGT]TGGTTGTTTTGAGGA | 50807 |
| rs148885845 | in-del | -/G | 0.0146672 | 0.084371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379635 | ATTGGAGAATTGCTT[-/G]GTATAGAGAAAACCC | 50807 |
| rs148886160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167264 | GCCTGCCGCCTCACT[A/C]TAGCCTGGGTGACAG | 50807 |
| rs148903893 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233329 | CACATCCAGCCAACA[C/T]GTAGCGATTCACTCA | 50807 |
| rs148908777 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131847 | CAACTTCAGGGTGGG[C/T]CATGTAATTCTTTTA | 50807 |
| rs148916452 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340160 | AGAAAAGGCTGAAAG[C/G]ACTGGCTGGAGAAAT | 50807 |
| rs148918244 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410900 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 50807 |
| rs148934825 | snp | A/G | 0.00655451 | 0.0568708 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130118584 | TGATGGCCTCAAGCA[A/G]TTCATTTAGTTTAGC | 50807 |
| rs148945117 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092591 | ATGATTATGCCACTG[C/T]GCTCCAGCCTAGGCA | 50807 |
| rs148952623 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183307 | AGAAAACAATGGAAC[A/G]ATGCCTTCAACATTT | 50807 |
| rs148955263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227162 | TATATGTAAAATCGA[A/G]ATAATAAAACCTCAT | 50807 |
| rs148959393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197914 | ATCCTATATAAGCTA[C/T]GTGCTGTTCACTAGT | 50807 |
| rs148960016 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128260 | GAAAAACAAAGAAAT[C/T]AAACTTGAAGGAAGG | 50807 |
| rs148964773 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400553 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 50807 |
| rs148965594 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299485 | CTATATGGCACAGTA[C/T]CTTTCTCATCCTCAT | 50807 |
| rs148994119 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130151610 | CTGAAAAGTGTGCTG[C/T]GAGGGGCAAGGGACA | 50807 |
| rs148996783 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087714 | GGCCTCGAGTCTTGC[C/G]TACTTTACAAGTTTG | 50807 |
| rs149018231 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130294484 | CCCAGATCGACTACA[C/T]GTCCAGCTGCACAGT | 50807 |
| rs149018755 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370039 | GGCACAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 50807 |
| rs149034274 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424776 | AGGTGGGCGGATCAC[A/G]AGGTCAGGAGATCAA | 50807 |
| rs149036533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352647 | GAATACTTACTGGCT[A/G]TACGACCTAGCTGGA | 50807 |
| rs149042495 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141468 | GGCCTGACCACCTCC[A/C]CATGATGTTCCATTT | 50807 |
| rs149044367 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076038 | TAAGTGGTAGAGCTG[A/G]TGTTGGTTCCCAAGT | 50807 |
| rs149057122 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253528 | ATGTAGATACAAAGC[C/T]TTCCATTGAACAAGC | 50807 |
| rs149057640 | in-del | -/AGAGAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130179985 | TGAAACAGAAAAAAG[-/AGAGAA]AGAGAAAGAGAAAGA | 50807 |
| rs149060990 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130282206 | CAAAGCAGAAGTGTC[-/T]TAAAATCCTGCAAGT | 50807 |
| rs149074957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384572 | CAACCTCCCCCTCGC[C/T]GGTTCAAGTGATTCT | 50807 |
| rs149094238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136634 | TCTAAGACAGAAATG[A/G]GAATATACTAAGAAA | 50807 |
| rs149118172 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101188 | GTTACTATAGCTTTG[C/T]AGTATATTTTGAAGT | 50807 |
| rs149124257 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270190 | AATAAAAAATCAAAC[C/G]AAATCAAATAAAAAG | 50807 |
| rs149128454 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130379717 | CACTCTACTTCACCA[C/G]AGATGCTGGACGCTG | 50807 |
| rs149132327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096434 | GATGCAGAGGTGACT[A/G]AGAGGCAATTTTCTC | 50807 |
| rs149136304 | in-del | -/GA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130351641 | GGCGAAAGCAGGGGC[-/GA]GAGAGAGAGAAAAGT | 50807 |
| rs149136447 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444864 | GAAATGCCACATTTC[A/G]GGGGTGTCTACCTGG | 50807 |
| rs149145707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130202739 | AATGAATGAATCTGC[C/T]TCAGGTGACCTAGCT | 50807 |
| rs149161756 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | ASAP1 | GRCh38.p7 | 8:130060800 | CCAGCTGTGGTTTGG[A/G]GGGCAGGTCCTTCAT | 50807 |
| rs149162973 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223735 | TAAGTACCATCCCAC[A/T]CTCCAGAGTCTCACT | 50807 |
| rs149164726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150175 | GCAAAGTTGGCATTC[A/G]GACTCACATCAGACA | 50807 |
| rs149166416 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130265045 | AAAAGATCTTTCAAA[G/T]AATATTGTGAACTGA | 50807 |
| rs149177610 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335857 | AGGTTAATAAAAATG[A/G]TATGGAAACTTATTT | 50807 |
| rs149190381 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130323878 | AGATTACCAGGCATT[-/A]AAAAAAAACCACTTA | 50807 |
| rs149209877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130054858 | CAGGCAGTGGCCCCA[C/T]GACAAACCCAGTGGG | 50807 |
| rs149211997 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130291619 | GGGAAGAGGAGGCTG[A/G]TAAGTTTGACGAGTG | 50807 |
| rs149226098 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402670 | CCATCCAGGGCGAAA[A/T]ACCGAGAGACATCTC | 50807 |
| rs149226885 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428939 | CAAAATCAATATATC[A/G]GCAGGGCCACACCCT | 50807 |
| rs149228601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130328833 | GGTGGTCTCCCTATG[C/T]CGCTCAGGTTGGTCT | 50807 |
| rs149238444 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203646 | CCTGGGATGGAAAAT[A/G]GGAAATCAAGGAATA | 50807 |
| rs149259551 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062372 | TGTTTCTGCTCATGA[C/T]CTGTCTAGTCATATC | 50807 |
| rs149265289 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224781 | AAAACACAATGCTAC[A/G]ATAAATACTCTTATA | 50807 |
| rs149273998 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130161181 | CTAGGAATAGCCACA[A/G]ATTGTAGCAGGACTT | 50807 |
| rs149278017 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337170 | TGGTAAAAGGGTGAG[A/G]TTAATTCAAAAATAT | 50807 |
| rs149297251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130441750 | GTGTAGAGAATTTCA[A/G]TTTCCCTCACCAAAT | 50807 |
| rs149313065 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056670 | ATGTGTGCCCATGCC[A/T]ATGTGTGTGTGCACA | 50807 |
| rs149323703 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120833 | GGCACTCAGCCCATA[C/G]TCCCCTGGCAATTTA | 50807 |
| rs149325921 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156849 | TGAACACTTTAGGGT[C/T]TGAACTATGCAACAC | 50807 |
| rs149332908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404254 | ATGCCAACAGCAATT[C/G]AATCTTCCTGAGCAC | 50807 |
| rs149341088 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173674 | TTGGGAGACTGAGGT[A/G]GGTGGATCGCTTGAA | 50807 |
| rs149353384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394436 | AATTTTGGTCAGACC[A/G]GTTGCTCTCAAACAT | 50807 |
| rs149354896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293190 | GGGATCTCTTTAAAA[C/T]ACAGATTCTGATTCA | 50807 |
| rs149357338 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109368 | GCTTCCTTGAATTTC[A/G]ATGAGGCAGCTGGAG | 50807 |
| rs149372349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288275 | TCCAGTATTTGACTT[C/T]GAGGGCACCATTCCT | 50807 |
| rs149395432 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249829 | GTACAGAAACTGGAA[A/C]CTACCATCTAAATTT | 50807 |
| rs149396878 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170004 | CGTGTTTAGAATTTT[C/T]TCTGCCCTATTGGAA | 50807 |
| rs149398203 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417421 | TGGGTCGGGACATTC[C/T]ATTGTCAGCCCGTTT | 50807 |
| rs149401200 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130345707 | TGGCTCATGCCTATA[A/T]TCCCACCACTTTTGA | 50807 |
| rs149410024 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359512 | TAATTCAAGCCAGGA[A/G]AGCCTTTGATAGCCT | 50807 |
| rs149434197 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133378 | CTCCAACCCAGGGGC[C/T]GGGCGCGGTGGCTCA | 50807 |
| rs149435280 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130069946 | GGTCTGGGGGTGAAG[A/T]AGTTCCTGAAACTAG | 50807 |
| rs149438080 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307194 | CTATGAAGAAGGGAA[C/T]TCTGTCTGTGCTTTT | 50807 |
| rs149444727 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314426 | GTATCATCATGCCCA[C/T]GTTACAGATGAGAGG | 50807 |
| rs149456090 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130412394 | TTAAAACTGTGTTGC[A/G]CCTTGCTCTCTCTCT | 50807 |
| rs149479928 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130185652 | GAGAATCGCTTGAAC[C/T]CAGGAGGCAGAGGCT | 50807 |
| rs149483226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094008 | TCTTTGTCCCATTGC[A/G]TAATTCTATTACACA | 50807 |
| rs149484284 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ASAP1 | GRCh38.p7 | 8:130200578 | TGACTTTAAAAATAC[A/G]AGAAAAAAGATGTTT | 50807 |
| rs149486266 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129620 | ATTTTTTTGTATATC[A/G]TTGAATGAAATGGAT | 50807 |
| rs149491917 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301694 | TCCTACAATATTTCC[C/T]TATAGGTACATAAAA | 50807 |
| rs149492397 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376858 | CGGTGAGATGAGATC[A/G]CACCATTGCACTCCA | 50807 |
| rs149515504 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263659 | CCTATGAAGTGAGTA[G/T]TATTAACCTCTGCAG | 50807 |
| rs149523718 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130089374 | TGGTGAGAGCTAAGG[A/G]GCTGTTCTTTTACTA | 50807 |
| rs149529727 | in-del | -/TC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130170732 | ACATGTAAAGCCTCA[-/TC]TCTCTCTCTCTCTCT | 50807 |
| rs149530165 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247822 | CTTCAGGCACACCCT[A/G]GGAACCACAGCTTTT | 50807 |
| rs149530995 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258896 | CGATTCCCATGTTTC[C/T]TATGCCTTCCCTACT | 50807 |
| rs149535908 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154023 | ACATAGGGAAATCCC[A/G]TATCTACAAAAAATA | 50807 |
| rs149539366 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130193881 | AAAAAGCAGATATGG[G/T]GTCTTCCCTTGTTGG | 50807 |
| rs149545807 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130371850 | ATAATTGCTAATGTT[A/C]TTTGGGTTTTTGTTT | 50807 |
| rs149554589 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144159 | TATATTTTTGGCATA[C/T]AATCAATAACTACAA | 50807 |
| rs149563780 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355177 | ACCCACCACGCCCAG[C/G]CTTCTTACCATATAT | 50807 |
| rs149564841 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425576 | ATGGACCAGCAGAGG[G/T]AACAGACAGACAATG | 50807 |
| rs149595751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130365191 | AGTAACCTAGTGAGG[C/T]AGTGTGTTTTCTGCA | 50807 |
| rs149603402 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311377 | TATGCTGTCTCATAG[A/C]GACAATCTCTACTGG | 50807 |
| rs149604886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209257 | AGTGAGGAAATTTAC[A/G]TCTGTAAGTTAGGCA | 50807 |
| rs149614504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130386533 | GCGCTGCGCTCTCCA[C/G]CCTGTAGATACACAA | 50807 |
| rs149617573 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422211 | GGGGGATGGGCACAT[C/T]TTCAACAACAGCTGC | 50807 |
| rs149618742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321147 | GCAGCTAATTAAATC[C/T]TCCAAAAGGCTGTCA | 50807 |
| rs149622851 | snp | A/G | 0.00209036 | 0.0322616 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112342 | CAGATGAAATAAGAA[A/G]GTGAGATAATAATCA | 50807 |
| rs149644165 | snp | A/T | 0.0471551 | 0.14613 | intron-variant | ASAP1 | GRCh38.p7 | 8:130103610 | CCGGGTTCAAGTGAT[A/T]TTCTGCCTCAGCCTC | 50807 |
| rs149654307 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218988 | ACAGTTTAGTAAGAT[A/G]TATCTTGGGGTAATA | 50807 |
| rs149670451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261335 | TGTAAGCCTCCATCA[C/T]GGAATCTTCCTAAGC | 50807 |
| rs149674644 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054630 | CCCTTCCATGAGTTT[C/T]TTACTCTGTAACAGC | 50807 |
| rs149684540 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434291 | AGTGAGCTGCCATAG[C/T]GCCACTGCACTACAG | 50807 |
| rs149688582 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151098 | TGAAGAAGGGCCAGG[A/C/T]GTGCAGGCTCACGCC | 50807 |
| rs149696327 | in-del | -/CT | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292804 | GATTTTACTGTGTGA[-/CT]CTAGGCATGTCACAT | 50807 |
| rs149712860 | in-del | -/TATTT | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094092 | GCAGTTTTCAGAAAC[-/TATTT]TATTTTTGTAACAAT | 50807 |
| rs149717243 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285829 | TCTGATGTAACTTTA[C/T]CACGTTCTGTTCCTG | 50807 |
| rs149720742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323742 | AGGCATACTATGTAT[A/G]TAAGGCCCATAACAC | 50807 |
| rs149721286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130398413 | TAATAATGGTATAGT[A/G]GTAATAATAGTAGAA | 50807 |
| rs149721970 | in-del | -/A | 0.079617 | 0.182947 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191531 | CTGTGGAGAGCTCAT[-/A]TTCTAGGAACAGAGG | 50807 |
| rs149729656 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423609 | TGATCATGTAAATCT[A/G]TATTTATTCAACATG | 50807 |
| rs149742861 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130336063 | TCAACTCCAAACTCT[C/G]TCTCATCAGCCTACC | 50807 |
| rs149747020 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104308 | TGTACTTTATGTTCT[C/T]AGTTCCCAAAATTTA | 50807 |
| rs149757877 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167182 | GGTGGCATGTGCCTG[A/T]AGTCCCAGCTACCTG | 50807 |
| rs149759865 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280050 | TCCTTATTTTATTTG[A/G]TCATCAAAAAGAGAT | 50807 |
| rs149766557 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382688 | CTCATTTCTATTAAA[A/G]ATACAAAAATTAGCT | 50807 |
| rs149789592 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339789 | ATGATGTGGAAAATG[A/C]GATGGTTGACCTCCA | 50807 |
| rs149793765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127791 | CGGTAGGAAAAATCA[C/T]GTTGGGAATACGTGT | 50807 |
| rs149805124 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269798 | GTCTTATCTGGTCTC[C/T]GGTACCTGCATTAGA | 50807 |
| rs149810196 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163627 | TCAGCTTGCTAAGCA[G/T]GGCACTCTAGACAAA | 50807 |
| rs149814597 | in-del | -/AA/AAAGT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216005 | AAAGGAAAGGAAAGG[-/AA/AAAGT]AAAGGAAAGGAAAAA | 50807 |
| rs149820310 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444004 | ACCCTGGACGCGGAA[G/T]GTGCCTTTCTAAGGC | 50807 |
| rs149844653 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406011 | AATTAAAATCAATTA[C/T]TATCCCAATACCTGA | 50807 |
| rs149845137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191324 | GTGGAACCCAAGACT[C/G]CAGAGACCTGCAGGA | 50807 |
| rs149849016 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122626 | AAGGCACAGACAATT[A/G]AAGTTACTTGTCCAA | 50807 |
| rs149855856 | in-del | -/GGG | 0.0509478 | 0.151255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143495 | ACAATATACACAGAT[-/GGG]GTCTTCATTTTACAC | 50807 |
| rs149860432 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334274 | CAACAACAACAAAAA[C/T]ATCAAGCACATCAAA | 50807 |
| rs149868082 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175648 | ATACTTCCATGAACA[A/G]AAGTTTTTAATTTTG | 50807 |
| rs149883337 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130294033 | CTCACAATAATCTTA[C/T]GTAATAGGTATTATA | 50807 |
| rs149884409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223164 | TACTTAATGGGTATA[A/G]TAAGGCCTTGAGAAC | 50807 |
| rs149885432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087493 | CCACTGCATTCCAGC[C/T]TGGGCAACAGAGTGA | 50807 |
| rs149895377 | snp | A/G | 0.00850907 | 0.0646694 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401849 | TGTATCTCCCACGCC[A/G]AGTTTTCTGGACAGG | 50807 |
| rs149904556 | snp | C/T | 3.29457e-05 | 0.00405854 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130112176 | TGTGGAAACGAAGAT[C/T]TGGTTGGTGAAGGCT | 50807 |
| rs149918906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253337 | AAGTGAAGAAATCCA[C/T]ATAAAGTGCCTTAGA | 50807 |
| rs149920029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170975 | CTCTCCTTGGTCTCC[C/T]GAAGTGCTGAGATTA | 50807 |
| rs149923890 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146989 | CCAGAACTTTGGGAA[A/G]CCGAGGTGGGTGGAT | 50807 |
| rs149926067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348766 | TCAGTGCTTCAAACT[A/G]TAATCAGTAAAGCAC | 50807 |
| rs149926213 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419749 | CCGATCTCTTCCCTG[A/G]GGCTCCCTCTCTAGG | 50807 |
| rs149931228 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362048 | CAGGATGCACTTTGT[C/T]GCCTTGAAAAAAAGG | 50807 |
| rs149938939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084121 | TTTAACAAAATGTCT[A/G]GCACAGAGCAGTCAA | 50807 |
| rs149959140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130071652 | AGAGTCTCAGGGCAA[A/G]AGATGACACTGCCTC | 50807 |
| rs149969317 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130135636 | TCTTGGAGTCTGAGT[C/T]TTTTCTTCTGTAAAA | 50807 |
| rs149970710 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246578 | AGAAGGTGCTTGCTT[C/T]GTCTTTGCCTTCTGC | 50807 |
| rs149981090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130315828 | CACTTCTGCCCATCC[A/G]TCATTCCCATTCTCC | 50807 |
| rs149995760 | in-del | -/AAAC | 0.387263 | 0.208947 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131153 | AGAGCAAGACTCTGA[-/AAAC]AAACAAACAAACAAA | 50807 |
| rs149996383 | in-del | -/TTC | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263949 | AATGACTCACACACA[-/TTC]TTCTTGCCACAGACC | 50807 |
| rs150002002 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130192259 | GTTATAACTGTCTGT[-/G]GGCCCTCCAAAGGGC | 50807 |
| rs150006754 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096371 | GAACACAGCATCAAA[C/G]GCAACACAAAAAAGG | 50807 |
| rs150011057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131263 | TGCTCTTTGTGAACT[C/T]TCCTCAGTGAGAAGA | 50807 |
| rs150012547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107023 | GTGCCAGTCATTTCA[C/T]AGACATTATTTCATG | 50807 |
| rs150018200 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130303750 | AGCAAAAAGATCAGT[A/G]GTTGCCAGGGGTTTA | 50807 |
| rs150020033 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130202479 | AACTGCTGGCAGAGA[A/T]AAGAACACACTTCAT | 50807 |
| rs150049692 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439527 | TTACCCTTACTGTGA[C/G]CACTTATTATCTGGT | 50807 |
| rs150058424 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155206 | ATACACACACACGCG[C/T]GCACACACCCCTTCT | 50807 |
| rs150059594 | snp | C/T | 0.000144878 | 0.00850987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091926 | CAGTGGAGCCCCACA[C/T]GCTGCCTGGCCCCAG | 50807 |
| rs150073020 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272342 | AACAAACAAACAAAA[A/C]CCCTATGTTGGCGAG | 50807 |
| rs150074301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130196996 | TTTCCAAGGTACTGT[A/G]ATACAGAGCAAAGAA | 50807 |
| rs150078818 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145075 | GGTTACTGCACCCAA[C/T]GAATGTGCTAGATAG | 50807 |
| rs150082789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317013 | ATGCTGTTGAATGTT[C/T]CAGGCCCTACTATCA | 50807 |
| rs150101048 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428113 | TCTGAGAGAACTTTG[A/G]GGATTCCCTTTTCCC | 50807 |
| rs150101251 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130380777 | GTCATGCAGGCTGAC[A/G]TGCAGTCATGAGCTT | 50807 |
| rs150108796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097669 | CTATGCTCACCCTGG[C/T]AGGCCCACGGGCAGT | 50807 |
| rs150115032 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107872 | CTCTTTTGTGTGGCA[C/T]GGAAAAGAAGGCTTC | 50807 |
| rs150117797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417053 | ACCCATGTACAACTG[C/T]ATACACACATACACA | 50807 |
| rs150123419 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203269 | TATACTCTTGCTCCC[A/G]GGCAAGAAGATGCCA | 50807 |
| rs150139553 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313009 | AAATGAAAGCAATCA[C/T]AGCATGCACATACCT | 50807 |
| rs150155424 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375342 | GCTGGGAAGAGAGGC[C/T]CAAGGGGTCTGGCTA | 50807 |
| rs150156841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130441506 | AGCAGGATCCAAATA[C/T]GGCTGAGACCTAGGT | 50807 |
| rs150164966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130067908 | ACATAAAAATCAGTC[C/T]GCTGGGAGCCGTACA | 50807 |
| rs150185796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055911 | GCATGTGTGAGGTCT[C/T]TGTGAATTTCACATC | 50807 |
| rs150195168 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393743 | ACTGGGTGACAGAGC[A/G]AGACTCTGTGTTGCG | 50807 |
| rs150196108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262998 | CTTACGTTGAGAATA[C/T]TTCTGCTTTTGTACA | 50807 |
| rs150198442 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156231 | TCACAGGACATATCA[A/G]TGGTCATTGTTTGCA | 50807 |
| rs150203856 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330425 | TTATCACAGCTCTGA[C/G]CGGTCTATGCTATAT | 50807 |
| rs150208851 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436101 | GAAAGAGAACATTAG[C/T]ATATTTAAAATGAAG | 50807 |
| rs150213974 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152224 | TAAACAGCAAGCACA[C/T]TAAAAAAGTCTTGGC | 50807 |
| rs150221582 | snp | G/T | 3.29636e-05 | 0.00405964 | missense | ASAP1 | GRCh38.p7 | 8:130118542 | CTTCTGCATAGACTT[G/T]AATTAGTGCAAGTAA | 50807 |
| rs150235891 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116534 | TACCACTTTTTCTAA[C/T]GTAGCACATTGCTCA | 50807 |
| rs150243927 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287956 | CCTATCTCTTCCCCA[C/G]GCTTGTCCTTTCTAG | 50807 |
| rs150244177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213948 | CTGGGTCTGCCTCCC[A/G]GGGCCAGCACCTCTA | 50807 |
| rs150248920 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226854 | TACACAATACACTTT[C/G]GTTTACTGATGGCTC | 50807 |
| rs150248996 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130200076 | CTTGGGCTACTGGCA[-/G]GTTTTCCCCCACTTC | 50807 |
| rs150257421 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400100 | GCTGGGATTACAGGC[A/G]TGAGCCATCGCGCCT | 50807 |
| rs150279620 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169276 | GATGTACCAACAAAT[A/G]AATTATGGCTGTCAG | 50807 |
| rs150288477 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111635 | ACTATTATTACTAGC[A/G]TCTTCAAAAGAGTGG | 50807 |
| rs150291375 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352108 | GGGAAGGTTTGTTTG[C/T]CTTTTGTTGTATTAT | 50807 |
| rs150294362 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130282150 | TGTTCTACATTTTGC[A/G]GTATCTTTTAATTAG | 50807 |
| rs150311707 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341686 | AGATTAAATAATTCC[C/G]TGTCTTCAACTTGAC | 50807 |
| rs150313587 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130412010 | CCCCCATTACCCAGT[C/G]CTCACCAGGTACCAC | 50807 |
| rs150317926 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129410 | GATAGAGGAATTGCC[C/T]GACTTTGTGCCTTTC | 50807 |
| rs150319021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130065268 | GGGTCCTGAGCACAG[C/G]AGCTTCTGAACCTGA | 50807 |
| rs150324560 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130075683 | CATAACTATCACTTG[A/T]GTTGTAATAAGAAGA | 50807 |
| rs150330931 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130243809 | CTCCCAGTCACTGTC[C/T]ATTCATTACCCTCTC | 50807 |
| rs150363831 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407659 | TTTGTTACCACCCAC[A/G]TTTCTGCTTTTCCAC | 50807 |
| rs150367732 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309000 | GGTATTTTAAATTTG[C/T]CTGATGCTCCACACC | 50807 |
| rs150371249 | snp | A/C/T | 0.0170316 | 0.0907494 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123855 | GGATGGTCTTGATCT[A/C/T]CTGACCTCGTGATCC | 50807 |
| rs150379562 | snp | A/C/G | 3.31539e-05 | 0.00407137 | utr-variant-5-prime, synonymous-codon | ASAP1 | GRCh38.p7 | 8:130401920 | CGACGAAAAACTGGA[A/C/G]AGCCTGGAGGCTGAA | 50807 |
| rs150394199 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088692 | CCAGTTTGCGGTATG[C/T]GTTACAGGAGCCTCA | 50807 |
| rs150400821 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428805 | TCATCACCATCACCA[C/T]CACCACCACCATCAT | 50807 |
| rs150408698 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130193514 | TAGGGTGGGAGAGGA[G/T]ATTTTTGCATTTTAA | 50807 |
| rs150413119 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130371013 | ACACTAAAAACCACT[A/G]AATTGTATATCTTAA | 50807 |
| rs150444385 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149541 | ACAAACCCTGCATCA[C/T]TAATCTAAATGCATA | 50807 |
| rs150448279 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086509 | AGCCATAAACCTGTA[C/T]TAAGAATTTATGGGC | 50807 |
| rs150452801 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254305 | AGAGCATTGTAAAAA[C/G]TGCATTGTTAAAATT | 50807 |
| rs150460873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264821 | GATGATCACTATGTA[C/T]GCAAAGGGGTTCCAG | 50807 |
| rs150467360 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364770 | GATATTGGCACCATT[C/T]AGAGGAGAAACTGAG | 50807 |
| rs150489012 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421984 | CACAAAATAGTGGGG[A/G]AGACAGAGGTATGAA | 50807 |
| rs150511543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130196711 | CTCTCTCTCTCCATA[A/G]CTGAAACAGTTTCTC | 50807 |
| rs150513478 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130344284 | TAAACCATTTTTTTT[-/T]AAAGAGACAACCAGG | 50807 |
| rs150513698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130125461 | TCTCACAATTTCTTC[C/T]CTTACTACCTAAAGA | 50807 |
| rs150516574 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373488 | ATAAATTCTAAATAC[A/G]TGGGCCTGCTAATTA | 50807 |
| rs150522679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297746 | CGGGGAGCAGAGGTA[A/G]AGCTGGAAGACAATG | 50807 |
| rs150529106 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306276 | TCACTACAAGTATTA[C/T]CATTTAGCAAGTCAT | 50807 |
| rs150535813 | in-del | -/G | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354768 | AGCTCATCCATTCCT[-/G]CCTCCCCAAGGTAGC | 50807 |
| rs150550122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151010 | AGAAAATAAAAATTA[C/T]CTAATTTTTCATTCA | 50807 |
| rs150551008 | snp | G/T | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087276 | TATAATCCCAGCACT[G/T]TGAGAGGCCGAGATG | 50807 |
| rs150553300 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062255 | AGTGACTCACATTAG[C/G]AATTTGATCCTAAAA | 50807 |
| rs150558552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130255845 | TAACTAATCCTCTTG[C/T]AAATTACATGTGAGT | 50807 |
| rs150566939 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189509 | TTTATGGCTGAATAA[C/T]ATTCCATTGTGTATA | 50807 |
| rs150570274 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130367984 | CTGCAGAGTTTTCTT[C/G]TTAACATATGCTATT | 50807 |
| rs150572319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434006 | ATTGAACACAGATCG[C/T]CTTGCTTAAAATCTT | 50807 |
| rs150593568 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323338 | AACACTAGTGTAAAG[A/C]AACAAGAGGGAACAT | 50807 |
| rs150602195 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145651 | GTTGATGAGAACACA[C/G/T]CATTTACTCATGCTG | 50807 |
| rs150610879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318293 | CACTATGTTGCCCAG[A/G]CTGGTTTCAAATTCC | 50807 |
| rs150614721 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220643 | GGAGTTTGAGACCAG[C/T]GTGGGCAACATGGTA | 50807 |
| rs150622271 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | ASAP1 | GRCh38.p7 | 8:130429841 | ACGCATGTATACTTC[A/G]CTGACTAATTCATGT | 50807 |
| rs150632325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130279739 | TTAGCAATGTAGTAG[C/T]TGACAGAGAAGGAGA | 50807 |
| rs150633045 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205412 | AAAACAAAAACCATA[C/T]TCAAATTCAGCCTGA | 50807 |
| rs150642404 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418069 | AACTTGCCCCAAGGC[C/G]ACAAGGACAGAAGAG | 50807 |
| rs150644849 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394310 | GGTAGGTCTCTGAAA[C/T]GGCCCCCTTGGGTGT | 50807 |
| rs150652479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109143 | GCTACTGATCACAAA[C/T]GAGAAACTACCACAC | 50807 |
| rs150669279 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163062 | GAGTTGGCAAAGGCC[C/T]GTGACAATGAGATAT | 50807 |
| rs150680446 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130345486 | GTTTCCACCAAGAAA[C/G]TAAATGCTAACCAGA | 50807 |
| rs150681591 | in-del | -/CT | 0.333261 | 0.235728 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321609 | TAAACCTAATAAAGA[-/CT]CTGTTTTATCACCAA | 50807 |
| rs150682211 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378493 | ACGGAGGCTTGACAC[A/G]CACATAGATGTGGAG | 50807 |
| rs150683325 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275319 | GCTTTCCACAGGTCA[A/C]AGAGAGCTAAAGAAA | 50807 |
| rs150687560 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069643 | GCATATGTGCTGCCG[A/C]AGTGAGCACAACAAA | 50807 |
| rs150691716 | snp | A/C | 0.0696718 | 0.173152 | utr-variant-5-prime, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130443641 | GCGAGGCGCGGGAGC[A/C]GAGCGCGGCGCAGGA | 50807 |
| rs150696419 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391088 | GTACATACAATGGAA[A/T]GTTATTTAGCCTCAA | 50807 |
| rs150706151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122575 | AATTGTCACCACAAC[C/T]CTATGAGGTAGATAT | 50807 |
| rs150708834 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058430 | CATCAGCTTGCAGAA[A/T]GACAGCAGAGTCTAA | 50807 |
| rs150718989 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234027 | ACAATTCGAGGGTAA[C/G]GGTCTGAGAGATTCC | 50807 |
| rs150723563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157875 | GCTTGATCTTTCTCC[A/G]TAGCACTAATTACCA | 50807 |
| rs150730350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334071 | ATGAGTAGGTGTTCA[C/T]CTGGTACAGGAGGAG | 50807 |
| rs150742187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438114 | GTGGCCAAGAGAGCT[C/T]ATGTGCCTCTCCAAA | 50807 |
| rs150757676 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130197266 | AACCCTCATCTCTAC[-/A]AAAAAATACAAACAT | 50807 |
| rs150767722 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130290062 | CAGTTGGCAACGGCC[C/T]GAGAGGTGTCATATT | 50807 |
| rs150769688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217847 | GCACTCATGAAACAG[A/C]ACATGAGTCTGGATT | 50807 |
| rs150771514 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130185060 | TCAAAACTAATAAAT[C/G]AACTTTTTTGTGTGG | 50807 |
| rs150774204 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130228408 | GTGTTTGTGATTCAG[A/C]ATATACACAATGGGC | 50807 |
| rs150778857 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401768 | AATCGTGCACACAGT[C/G]TCTGTTAGATTCCAG | 50807 |
| rs150783983 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327559 | TGACTCTACTGAGAC[A/G]GGTAAAGAAGATTAA | 50807 |
| rs150809478 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083950 | GGCATGCGCCACCAC[A/G]TCTGGCTAATTTTTG | 50807 |
| rs150821166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284379 | ATAGTGTAATTTAGC[A/C]ACAAAGTATGAGGTT | 50807 |
| rs150823825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178191 | GTATTTTATCTAGTC[C/T]AAACGACCTTTACAT | 50807 |
| rs150844180 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246091 | AATTAATCACTGCGA[A/G]TTGTAAAGGAAGTCT | 50807 |
| rs150850508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414259 | TCCAAGGCACAATGA[C/T]GATACTTCCAGAATT | 50807 |
| rs150855533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354960 | GTGCGATCTTGGCTC[A/G]TTGTAACCTCGGCCT | 50807 |
| rs150859344 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166424 | CCCTTAGTACAACAC[C/T]CAAGGTCCTCCGTAG | 50807 |
| rs150859990 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143922 | CATCTTACTGAATTG[C/T]TCTGCTTTACAAACA | 50807 |
| rs150872970 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349673 | CCTACCTATCTAACT[A/C]TCCATGAAGGAATGC | 50807 |
| rs150882945 | snp | A/G/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130903 | CGCTCACGCCTGTAA[A/G/T]CCCAGCACTTTGGGA | 50807 |
| rs150896778 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130310887 | ATGATGCCAACATAA[C/T]GTTTAAGTTACACTT | 50807 |
| rs150898274 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102537 | ATCTACGTTCCACAA[A/G]AATATTGGCTGGTAG | 50807 |
| rs150901631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409653 | TATTCTCCCTGACAA[C/T]GCCGAGGCTGCTGGA | 50807 |
| rs150916144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137789 | GTATCTAGATAGTCA[C/T]GCTAACTTAGGAAGT | 50807 |
| rs150925111 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261027 | ACATTTATTCAATTA[C/T]ATATTCTCAAAAAAC | 50807 |
| rs150928949 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130181250 | ATCAAACAGAACACA[A/C]ACACTGTATGGATTT | 50807 |
| rs150929534 | snp | A/G | 0.000329402 | 0.0128294 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130058023 | TGTGAGCTCGTCATC[A/G]TTGTCTGCCTGGCAG | 50807 |
| rs150934941 | in-del | -/A | 0.134119 | 0.221521 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439580 | TTCACATAAGATATT[-/A]AAAAAAAAAGGGTAA | 50807 |
| rs150946081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317005 | TACAGGCTATGCTGT[C/T]GAATGTTCCAGGCCC | 50807 |
| rs150946702 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247927 | CCTGCATACAGAAAA[C/T]AGGCTTAATATAAAT | 50807 |
| rs150962712 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356262 | AATACAGCAACACTA[C/T]CTAAATGTGCAGGAA | 50807 |
| rs150965369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145032 | AAAAAAAGAGCTTAC[C/T]GGGGCTCCTGCTAAG | 50807 |
| rs150967413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080064 | GACAGGCATTGCTCA[A/G]GTTCCAGAACGGCAT | 50807 |
| rs150999475 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130312770 | TAGTAACAAAGCCTA[C/G]CACAGAAATTTTCCC | 50807 |
| rs151002798 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130210498 | GTTTGAGAACTACCA[A/T]CTAACACTCTCACTC | 50807 |
| rs151004377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410978 | CAATTCTCCTGCCTC[A/G]GCCTCCCAAGTAGCT | 50807 |
| rs151010561 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423507 | GTATTTGGACAAGTA[C/T]GTACATGCAAAAACT | 50807 |
| rs151021142 | in-del | -/AAAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130133665 | GAGACTCCGTCTCAA[-/AAAC]AAACAAACAAACAAA | 50807 |
| rs151041295 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104131 | GCCCGGCATGCTCTG[A/G]GTACTCAGTACACAA | 50807 |
| rs151048587 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130198189 | TCCAGGCTGGAGTGC[A/T]GCCTTGCTCACTGCA | 50807 |
| rs151078831 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063366 | ATTTTTTAGTAGAGA[C/T]GTGCAGGGCCATGCT | 50807 |
| rs151082398 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435772 | CCATCAGCCCAGAGA[A/C]ATGGCAAGAAAGCAG | 50807 |
| rs151088013 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151850 | GAGAGAAAGGCCACA[A/T]GGACTAATGTCAGAC | 50807 |
| rs151088808 | snp | C/T | 0.000247834 | 0.011129 | missense | ASAP1 | GRCh38.p7 | 8:130118183 | GTACAAGGAAGTCAA[C/T]CAAATGGAGAGATGT | 50807 |
| rs151095364 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099008 | TACTCTCTACTAATA[C/T]AAGCTTTTTTTTTTT | 50807 |
| rs151098414 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370053 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCTGA | 50807 |
| rs151102929 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269645 | TAACTATGTGTGACT[C/G]TCTCTTTCACCCCTA | 50807 |
| rs151122308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325510 | ATCTGTTCTTAAACT[A/G]TGTGATCTAAAAGTT | 50807 |
| rs151138657 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222671 | TCCTGTCCTGTAATA[A/G]TATTGACAAAGTAAT | 50807 |
| rs151155339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264164 | GAATGAAATTTCAGA[A/G]CATCAGAGATGGGCT | 50807 |
| rs151156622 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281158 | TTATTTCATCTAGAT[A/G]AACTCAATTACCTTA | 50807 |
| rs151161166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208020 | TTATGTAACAATGTA[C/T]ACTAAACACTTTCCC | 50807 |
| rs151175620 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319979 | ACTATATAATGCATA[C/G]AAAAGTACATTTTAA | 50807 |
| rs151214916 | in-del | -/AAAAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130338428 | GTATTCAACAAAGAA[-/AAAAC]CAGCCAGCAACAACA | 50807 |
| rs151216639 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445428 | CTGCATGGGTAAACT[A/G]CATTACAGCAGTACC | 50807 |
| rs151220140 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348457 | AAAATTATACCATAG[C/G]TTGGCATTAAAATTC | 50807 |
| rs151229691 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170587 | AACATTTTTTAAGGC[G/T]GACATCTTTGGCAAA | 50807 |
| rs151230266 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107546 | TATGTATGTATGTAT[G/T]TATGTATGTATGTAT | 50807 |
| rs151246179 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123696 | CAGGGGTGCGATCTC[A/G]GCTCACTGCAAGCTC | 50807 |
| rs151248392 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159692 | CACAGAGCAATTACT[C/G]TTTCTTCTAAAGAGA | 50807 |
| rs151253308 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ASAP1 | GRCh38.p7 | 8:130071327 | TAACCATGTTTTTAA[A/G]TATTATGTCAAAATT | 50807 |
| rs151260492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236192 | TTCCTAGAGAAGTAA[C/T]CTATTGGTAGGTGAG | 50807 |
| rs151263325 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342711 | GCTCAAGGACAAAAT[A/G]TGAAATATAACTTGA | 50807 |
| rs151271864 | in-del | -/A | 0.0444908 | 0.142359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130202377 | GTAGTGCTTTAGGGT[-/A]AACTATTAAAATATT | 50807 |
| rs151281725 | snp | A/T | 1.66366e-05 | 0.0028841 | missense | ASAP1 | GRCh38.p7 | 8:130214561 | AATGTCTTACCAGAT[A/T]TTTCAGCAGTGTGGA | 50807 |
| rs151292146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402747 | ATGTCTACTTTACTT[C/T]CTAAAGATCTCTCCA | 50807 |
| rs151295555 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289061 | CGTGGTGGCACACGC[C/T]TGTAGTCCCAGGTAC | 50807 |
| rs151296260 | snp | A/G | 0.00208127 | 0.0321917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187220 | AAACAAAAACTCTAA[A/G]CAAAAAACCACTTAC | 50807 |
| rs151299240 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119483 | AAGTGTTTCTGGTGG[A/G]ACTGAGCTCACCTCC | 50807 |
| rs151311737 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130230360 | ACTAGGATCCAAAAA[C/G/T]TGAAACTTCCTAAGA | 50807 |
| rs151327085 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364039 | CTTCCCAATTGCACT[C/T]GTGCAATTTCAGGTA | 50807 |
| rs151329374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292200 | TGAATCATGCATACA[C/T]GCATTCATTCACTTA | 50807 |
| rs151334961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086242 | CTGCAGGTGAATCCT[A/G]GCCCCCACGTACTAG | 50807 |
| rs180683802 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168168 | TATATAAAAGGCATT[C/T]TTTGTAATTATAAAA | 50807 |
| rs180699529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247198 | TGTTTGCTTCTTTTC[C/G]TCCTTTCCCCAATGG | 50807 |
| rs180706079 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130209011 | ATTAGGGGGAATATG[A/G]AAGAGAAATTGCAAT | 50807 |
| rs180707803 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228984 | ACAAGTACATGTCTG[A/G/T]TCAATTACCCAAGAC | 50807 |
| rs180731311 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130117389 | GAACACAGGTAATCT[A/G]TCTCTGGAGCCAATG | 50807 |
| rs180734567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124374 | TTGACAAGGAAATCA[A/G]TCATGTCTACAAATA | 50807 |
| rs180752138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150252 | GATGAGACTTGTTAA[C/T]TCAAGCCTTAAGAAT | 50807 |
| rs180754435 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130065822 | GTCACACAAACACTT[C/T]CATAATCGTGTACTA | 50807 |
| rs180757634 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134030 | AAGGTTATGAAGAGG[C/G]CGCGGGCAAGGAGTA | 50807 |
| rs180759327 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107497 | GCCCATAGTCTCTCT[C/T]TTTTTTTTTTTTTAA | 50807 |
| rs180763426 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083741 | ATTTACTCAATGAGT[G/T]GTCACTTCAAAGAAT | 50807 |
| rs180763669 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056064 | ATCTCTGCTGTAGTC[A/G]TCAGTTGCTTAGCAA | 50807 |
| rs180763745 | snp | A/G | 0.0103295 | 0.0711199 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130443937 | CCCCATGCCCCGGCC[A/G]GCCGGCCTCCTCCCC | 50807 |
| rs180763842 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073267 | TGGTGGTACATGCCT[A/G]TAATCCCAGCTACTT | 50807 |
| rs180769718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091755 | GTAAGATTTAGGAAG[C/T]GCTCAGCACCTTTTA | 50807 |
| rs180771814 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140570 | TTTCAAAGTATTTTG[C/G]TGATAAGGAATTTAT | 50807 |
| rs180778584 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159100 | GAAAAAGAAGAATGA[C/G]CGATACAAAGAGACC | 50807 |
| rs180780450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100762 | TGTAAGATGAATAGT[C/T]TGCAGATAGTTTCTG | 50807 |
| rs180804790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384001 | TCATGGTGAAGACTG[C/T]CCTTTGTAACGCAGG | 50807 |
| rs180815452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399373 | TAATGCACTGAGTTA[C/T]TGCAATTATAATTAA | 50807 |
| rs180820525 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421504 | CTTCTAGCTAAGGAA[A/T]GAGATAGAAATGTTG | 50807 |
| rs180824697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130429541 | AGGACCCACACCTAA[C/G]TCCAGGATCCAAACT | 50807 |
| rs180849521 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409219 | GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC | 50807 |
| rs180857615 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104067 | CCTTTCCAGACTGTG[G/T]GCATCCATAGGGCAT | 50807 |
| rs180891676 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130078047 | TAGGCTGGAGTGCAG[C/T]GGCGTGATCTCGGTT | 50807 |
| rs180894540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068589 | TGTTTGGATTGATGG[A/G]ACCCACAGCTCACTA | 50807 |
| rs180898167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097185 | AAACTGTATTGTGGA[C/T]ACCCACTGGTGCCTG | 50807 |
| rs180907317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137813 | AGGAAGTCTCACCAC[A/G]TATTCACACTGGTCA | 50807 |
| rs180912193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120841 | GCCCATAGTCCCCTG[A/G]CAATTTAATGTTTTC | 50807 |
| rs180915279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060508 | CTTGTGTAAGTTGGA[A/G]CACCTGCCCTCCCAC | 50807 |
| rs180939795 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344461 | CTGATATTGCTTCAA[A/G]AAATCAGGGGAAGGA | 50807 |
| rs180939877 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324573 | CCAAGAACTGACAAT[A/G]CATGCAATGGATGAC | 50807 |
| rs180943750 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130087212 | GGGGAACCAAAGAGG[G/T]GTATAGGCTTCACAC | 50807 |
| rs180948363 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130386595 | CATTTCCAGTCTCCT[C/G]TTACCAAACTCACAT | 50807 |
| rs180958481 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130361545 | TATGTTATGTATCTG[A/C]TCCTCCCCCATCTCC | 50807 |
| rs180958737 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130402849 | CTGCCTCCTAACTGA[C/T]CTCCCCTCATCACCA | 50807 |
| rs180959978 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379974 | GAGACTGGCCAGGAT[A/C]CCCCTGCGACCTCAC | 50807 |
| rs180963546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437393 | TACGAGACCCTTGTG[C/G]TGGCTGCTTTTCTTA | 50807 |
| rs180964202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424957 | GAGATCTCACCACTG[C/T]ACTCCAGCCTGGGTG | 50807 |
| rs180999706 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130371494 | AAGACTCATCTTCCA[A/G]CCTCCCTTACAGCTA | 50807 |
| rs181010269 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292651 | TCACGTTCCCTGTTG[C/T]GCACCTACACAAATG | 50807 |
| rs181017986 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273567 | AACCCAGGAGCTTGT[A/G]TTAAGGAGGAGCTCA | 50807 |
| rs181020786 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130310064 | TACATTAACCATACC[A/G]ACCTGGCATACTTGC | 50807 |
| rs181022015 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130416746 | AGGCTGCCACCTAAT[A/G]GAAAGTCCACTGGCT | 50807 |
| rs181027181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280701 | AAATAGTCAGAATTA[C/T]CCAGTTACTTAAAAT | 50807 |
| rs181032564 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395095 | CACAAGAATGTCCCT[C/G]CCGCAGCACAAGAAA | 50807 |
| rs181053128 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317039 | TATCATTTGGTACAT[C/T]ATACACCTTGAGACT | 50807 |
| rs181055314 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262460 | AGAGAGAGAGAGAAC[C/T]TGTGGAATTTCAGAT | 50807 |
| rs181058286 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130300321 | TCAAACCAAACAAGA[C/T]ATCTAAATGAATTCA | 50807 |
| rs181068707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333774 | TATCAGACTATTAGA[C/T]GCATTTATTCATTCA | 50807 |
| rs181070262 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130351520 | ATAAAGAAAGGAAAT[C/T]CTGCAGGCTGTACAA | 50807 |
| rs181083485 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403558 | TTTTTCTTTTTCTTT[C/T]TTTTTTTTTTTTTGT | 50807 |
| rs181101366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425058 | GGGTCAGGCCGGGCG[A/C]AATGGCTTATCCCTG | 50807 |
| rs181134668 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130317518 | GGACCTGTCTGTGAA[C/T]CAGAATGAGCCCACG | 50807 |
| rs181135908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359995 | GAGTGCCCCAAAGCA[A/G]GGATCTTGTCTTAGC | 50807 |
| rs181137667 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130343062 | AGGTTAAAATGTTCA[A/G]GCAAGGAAGAATGGA | 50807 |
| rs181149731 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378744 | CCTGGGCACCGCATG[A/C]ACACACAGTAGGTGC | 50807 |
| rs181152722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334485 | TTTAAACCACAGGAT[A/G]AGTAACCAAATTTGA | 50807 |
| rs181155273 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178016 | TGCAGAGCCAAAATG[C/T]TGACTCATCTAATTT | 50807 |
| rs181157111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130367041 | AGACCACAGGTGTGC[A/G]CCACCACACCCAGCT | 50807 |
| rs181159379 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159722 | AGCTGGTCAAATCTC[A/G]GATTTACTTGAAGAA | 50807 |
| rs181171936 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130352262 | TGGGGGTAATTAATG[A/G]GCTCCTTAAGTTTAG | 50807 |
| rs181173661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130371978 | AAATGAGAAGCATTC[C/T]ACCAGAGTCATTTTC | 50807 |
| rs181174436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141018 | ATTTAGTACTAATTT[A/C]TAGGTATATTGATTG | 50807 |
| rs181178854 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130229441 | AATGAGGAAAATGCA[C/T]TTTGAAATAGGAGGC | 50807 |
| rs181179427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387497 | GCCAAGATTACACCA[C/G]TGCACTCCAGCCTGG | 50807 |
| rs181182592 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247832 | ACCCTGGGAACCACA[G/T]CTTTTGTGGACTTCA | 50807 |
| rs181186287 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209714 | CATACCAAAATATGA[C/T]GGTTGTTTTGAGGAA | 50807 |
| rs181194168 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130273016 | AATCTTCCCAACACA[C/T]AGAAATGACAAATAC | 50807 |
| rs181206371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301338 | GTGTGTTCTGAGAAA[C/T]GATGGAAATCCTGAG | 50807 |
| rs181210258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263066 | TGATTTTTACTAATA[C/T]GAATATGAATTTACT | 50807 |
| rs181211345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281361 | TCAATGACATCATTT[A/C]TTGATTTTGTCCATA | 50807 |
| rs181211481 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323513 | CAGTCCCCTGTCATG[C/T]TGGATAAGAAAGTGA | 50807 |
| rs181214418 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307767 | CCAAAAGCCTGCGGA[A/G]AGTCAAAACACTAGT | 50807 |
| rs181221859 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253862 | CCCGTCTCTACTAAA[A/G]ATATAAAAATTAGCC | 50807 |
| rs181239593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289997 | GACCTATAATTGCAC[A/G]TACCCCATTGTACAT | 50807 |
| rs181264419 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237257 | ATCATGCTAAGCTAT[A/G]CACAAGAAAGACAGT | 50807 |
| rs181264542 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169180 | AAAATCTGAAAATAC[A/T]CTTATCTGTATATAT | 50807 |
| rs181268560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197275 | CTCTACAAAAAAATA[C/T]AAACATTAGCTGGGC | 50807 |
| rs181283423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320027 | AATGCTATTAGTATT[C/T]ACAAAATTAGCACAC | 50807 |
| rs181287199 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130304461 | ATAAAGATAAAAACA[C/G]TTTTAACCTATGAAC | 50807 |
| rs181290037 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130338582 | TGACTCTAGCTAGTC[A/T]TGCATCTGTGTGGAA | 50807 |
| rs181294023 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296267 | GGTTTACCTGGTTGA[A/C]CACCAGAAAAAGTAG | 50807 |
| rs181302397 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130328718 | CTTGAACTCCTGGGC[G/T]CAAGCAATCCTCCCA | 50807 |
| rs181309594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355857 | TAAAATATGCCGACC[A/G]GAGACAATGTTTTCC | 50807 |
| rs181316930 | snp | A/C | 0.00199529 | 0.0315338 | downstream-variant-500B | ASAP1 | GRCh38.p7 | 8:130051616 | TTAGTGATTTACAAG[A/C]CACATGTCTCCTGTG | 50807 |
| rs181317259 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187426 | CGTTACACCATTTTT[G/T]TTTTTTTTTGACAGG | 50807 |
| rs181317456 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219055 | GATAGAAAATTAAAT[A/G]TAAGGTGCTTAAAAT | 50807 |
| rs181319835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233959 | TGGCTGCAAGTTAGA[A/G]TCAGCTGGGGAATAA | 50807 |
| rs181321777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392501 | TGCCAAGTACTATTC[A/G]TGTGTTTTAGAGGTA | 50807 |
| rs181322249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095462 | TGTGCCACCACGTCT[A/G]GCTAATTTTTGTATT | 50807 |
| rs181327053 | snp | C/G/T | 3.30018e-05 | 0.00406202 | synonymous-codon, missense | ASAP1 | GRCh38.p7 | 8:130112302 | AGGTCTGGGTGAGCG[C/G/T]TCTTTCTTGATAGGG | 50807 |
| rs181327222 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068969 | GCTGTCTCAGCTTCC[C/T]TTCATGGGTCTTATA | 50807 |
| rs181349710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249578 | GAAAGTTTCACTGCC[C/G]CCCTTCCCCAATTAA | 50807 |
| rs181350394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258836 | TACGTGGTGGTTGAC[C/T]GATTTGCTGATTTCT | 50807 |
| rs181352915 | snp | C/T | 0.00122499 | 0.0247183 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285927 | CTTTACTGGAACAGA[C/T]ATCATAAATAATTTG | 50807 |
| rs181354225 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224812 | CACAAGCTCTTACAC[A/C/G]CTGTTACTTTATCTC | 50807 |
| rs181355423 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130269120 | TTGAAACCAGAACAG[A/G]CCTTGAATTTCAAAT | 50807 |
| rs181359075 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077099 | GCAGAAGGTCTCACG[A/T]GGGTCAGAGGTAGAA | 50807 |
| rs181362438 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130174135 | TTAGGAGTCAAAACC[A/G]TATCATATTTTATAT | 50807 |
| rs181363932 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151147 | GGAGGCCGAAGCGGG[A/C]AGATCACAAGGTCAG | 50807 |
| rs181366968 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204461 | AACTATGGTTACTAC[C/T]TGGTAGGGCTGCTGT | 50807 |
| rs181368614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223781 | ACTCTTTCCTGGGAG[C/T]CTAGCCTCTCTTCCA | 50807 |
| rs181368685 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130121292 | CAGCTGGGTTTCTCA[A/G]CCTCAGCCCTACTGA | 50807 |
| rs181375220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155487 | TACTCCCACCTCGGC[C/T]TCCTGAGTAGCTGGG | 50807 |
| rs181379557 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139005 | GCTGACTTTCTCATA[A/T]AAATGACAATGGCAT | 50807 |
| rs181382221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130181103 | CTTGTATCTTCTGCT[C/T]AAGAAGGAAGTCTAC | 50807 |
| rs181383127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257981 | ATATCTTTTGTAAAT[C/T]TGTGTATTAGTGTAC | 50807 |
| rs181391205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277033 | TACGGCTTTGACAGC[A/G]TAACCCCACCCTCAC | 50807 |
| rs181395814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276111 | CCCTGACAAAAGATG[C/T]CACAAAAAGAACCCT | 50807 |
| rs181399945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376106 | TCCCAGATGCACATA[C/T]TACAGTAATTCAGGT | 50807 |
| rs181401775 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130313965 | CCTCACACACAATTT[A/G]CTGCAGTCCACCCCT | 50807 |
| rs181404083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240154 | TACTTCCTTTTGTGG[C/G]GGGGAGCGGGTACAG | 50807 |
| rs181406366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191384 | CCCCTCACTCAAGAA[A/G]TGATTTTACTCACAC | 50807 |
| rs181412896 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347232 | TTTTCTGGCCATACC[C/G]TATGTGGAATGTTGA | 50807 |
| rs181416889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106283 | TCTAATGACTGTCTT[C/T]CCATGAGATAAAAAA | 50807 |
| rs181418784 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154922 | GTCTGATTAGAGGTG[G/T]CATCTCTCAACTAAT | 50807 |
| rs181432665 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163705 | TAACATTAACAACAA[C/T]TTAAAAACTGACACA | 50807 |
| rs181435913 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122403 | AGAGGTTCACTTTAT[C/G]CTTCTGGGTCACTGG | 50807 |
| rs181442712 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087758 | TGTTAGGCAAGCGAT[C/G]AGCGTGAACCCATTG | 50807 |
| rs181459895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214428 | CCTAGGACTAAAAAG[A/C]TTTTTGTTTTTTCTT | 50807 |
| rs181461113 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059514 | GTTACCCAGGCTGGA[A/G]TGTAGTGGTGTGATC | 50807 |
| rs181471238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241566 | GAGAAGTAGGCAACA[G/T]AAGACTTGCTTTGAA | 50807 |
| rs181495190 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215008 | CAGGATCAAGTGATT[C/T]TCCTGCCTCAGCCTC | 50807 |
| rs181495476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130138017 | CTATATCCCTGTTTC[A/G]ATTGAGAGCTGTGGT | 50807 |
| rs181527340 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104610 | TCTCGTGGCAAAACT[G/T]CTGGCAAGTATACCC | 50807 |
| rs181532427 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173544 | GCCAAGGCAGGACGA[C/T]TGCTTGAGCCCAGGA | 50807 |
| rs181536049 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077718 | CAACAAAACAAAAAG[C/T]AGTCAAAGAGAGAAG | 50807 |
| rs181557633 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092418 | GATTGCTTGAGGCCA[A/T]GAGTTTGAGACCAGC | 50807 |
| rs181563221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107853 | CACGCCCGACCACCA[C/T]AGTCTCTTTTGTGTG | 50807 |
| rs181563709 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145507 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 50807 |
| rs181570163 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124772 | TTGGGTTTATTGCAT[G/T]GCAAACGTTTAGGAT | 50807 |
| rs181577872 | snp | G/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388814 | GGGGAGGGGATGAAA[G/T]GATCATCTTAACAGG | 50807 |
| rs181581030 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073351 | GCTGAGATCGCACCA[C/T]TGCACTCCAGCCTGG | 50807 |
| rs181581229 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436285 | TGAGACAGGAGGTCC[A/G]CTTGAAACTAGGAGT | 50807 |
| rs181588094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404142 | GTTTGGATTTGTTTA[C/T]TGGTGTATGTTGCAG | 50807 |
| rs181593989 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425495 | GCACTCCAGCCTGGG[C/G/T]GACAGAGCAAGACTC | 50807 |
| rs181629176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234721 | CTCAGCACGGTAAAT[A/G]CAGCAGCACCTCGTG | 50807 |
| rs181641413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130193347 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 50807 |
| rs181665056 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295510 | TGTAAAACAGGGATA[C/T]GGGATAATAATACCT | 50807 |
| rs181680988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356104 | TATTTGCTTTTAAAT[C/T]TATTAACCTTAAACT | 50807 |
| rs181691586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376844 | GGAGGCAGAGGTTGC[A/G]GTGAGATGAGATCGC | 50807 |
| rs181694287 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394777 | GCTTAGGGAAAACAG[A/G]AAAGAACCTACGTGA | 50807 |
| rs181696333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096168 | TTGAAAAATACTATA[C/T]ATAAGACCCCAGAAA | 50807 |
| rs181701406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392844 | AACAGTTGTCACGGG[A/G]ACTAACAGAGTGAGA | 50807 |
| rs181704441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409905 | AGTGAGGAGGGTGAG[C/T]TGAGTAACACAAGGT | 50807 |
| rs181705426 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129169 | CCCTTCCACCATAAT[C/T]GTAAGTCTCCTGAGG | 50807 |
| rs181712350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430734 | AAGGGGCTGGACTGC[A/C]GACACTGGGAAGGTG | 50807 |
| rs181756623 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059779 | GCAGCGAGAAAGTCT[C/G]ACTTAGCAACTCAGG | 50807 |
| rs181757771 | snp | A/C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339333 | CTGGAAACTTTCACA[A/C/T]CTGTTTAAAGACCAT | 50807 |
| rs181762588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320230 | ATATCAATGAGCATA[C/T]ATGTCATGTGCCTCC | 50807 |
| rs181773911 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410547 | ATACATTTTCTTCAG[C/G]GTTCCCCTGGGAAGA | 50807 |
| rs181778294 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130346993 | TATTTCGTATGTAAC[C/T]GGGCAGTGAAGAAGC | 50807 |
| rs181779893 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130367792 | GGGGCCCCCGTTAAA[A/G/T]ATACCCTATATTACA | 50807 |
| rs181781549 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431782 | AGCTGGCAAATGGTA[A/G]GCACTTAATACAGAA | 50807 |
| rs181790484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383461 | ACAGCAGAGCCCAGA[A/G]GATCGACTATGAACC | 50807 |
| rs181813082 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130415155 | TAAAAACAAATAAGG[A/G]AAGCATCAGGAAGAC | 50807 |
| rs181831774 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276519 | TGACAGGTATCCTCA[A/G]ACAAAAAAGCTGGCA | 50807 |
| rs181832936 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313643 | TCACAGAAAAGCAGA[C/T]GTTTCAGCTACAGAA | 50807 |
| rs181835754 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295662 | CTTTGCAGAAAGCTT[G/T]TACCATAAGCTGCAA | 50807 |
| rs181882458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286132 | TAAATGAAGAAAAGA[A/C]GGCTCAGGGCACAGT | 50807 |
| rs181883742 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249946 | ATTTCTGAAAATCAC[A/G]TATTTTCAAATCCTA | 50807 |
| rs181886896 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313298 | CAAAATAAAATAACA[C/T]AACCGTTTAAAAAAA | 50807 |
| rs181890444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189635 | GTACGGGTTATCTTG[C/T]TGATACACTGATTTC | 50807 |
| rs181901668 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130172323 | CTTTATGCTTTAAAA[A/C]AATGTGAGTTTTGCT | 50807 |
| rs181906734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154215 | GGTGCCTCAGAGCCC[C/T]GAGAAAAAACTGTTC | 50807 |
| rs181907134 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114359 | CTGTAACACAATGGT[A/C]ATTACTTGTGTATCT | 50807 |
| rs181916206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220454 | CCCTTGATCATACAA[C/T]TCATAAATAAGGAAA | 50807 |
| rs181916604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213776 | AATAATTTCATCCCC[C/T]AAAACCAACAAAATC | 50807 |
| rs181923739 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130442284 | TGAGCCTGAAGAAGT[G/T]GAAACTACTCCTGGC | 50807 |
| rs181924919 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199065 | TTTCTCAGTGAGGCC[G/T]TGACCATTCTAAATA | 50807 |
| rs181926554 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178363 | TCACACACAGACTCT[A/G]CCAGAAAACCCATGA | 50807 |
| rs181943923 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254531 | AAGTACTGATAAAAA[A/C]GTTTTACCCCAAAAT | 50807 |
| rs181947605 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280510 | GTCAACCATGTCAGC[A/C]TTTTCAGAATCCAGA | 50807 |
| rs181949317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273363 | AGCGGTCCCTCCCAA[A/G]GCAGGGTCACGCCTG | 50807 |
| rs181952465 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237328 | GCATTTACAATCTGG[A/T]AAGGAGAAAAGGCAA | 50807 |
| rs181983521 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160275 | TGTAAGACTGAATCC[A/C]GTTTACACTAGCGGC | 50807 |
| rs181984670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339742 | AGGTCAGTTGGCAGT[A/G]GCTGTAAACTCAGGA | 50807 |
| rs181987530 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130398583 | TATCAGAAGTGGCAG[C/T]AGCAGTAGTAGTAGA | 50807 |
| rs181994570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377230 | CTCAGGGGGAAAGGG[C/T]AGGAAGGGGGTGAGG | 50807 |
| rs182004267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056563 | CCCTGGAGGGCAAAA[C/T]TGCCCCAGTTGAGTC | 50807 |
| rs182004282 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444126 | GATTTCACCAGGCTG[C/T]CCCCTTTCACCACTT | 50807 |
| rs182018589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240549 | GCTAAGAGAAAAATG[A/G]TAGATAATATAGGCT | 50807 |
| rs182022704 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117227 | TCTTAACATTTACAT[A/G]TATTAGTTCATTGAA | 50807 |
| rs182044959 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064952 | GAATCACAGCTCACT[A/G]CAGTCTCGGTCTCCC | 50807 |
| rs182052135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083187 | CCCAATACCCACAGG[C/T]CCAAATGTCCAGAGT | 50807 |
| rs182060419 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100581 | CAATCTACCCACCTC[A/G]GCCTCCCAACGTGCT | 50807 |
| rs182066907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170080 | ATCTGTTTTGCTGTC[C/T]CCCTACAAACAACGA | 50807 |
| rs182069303 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130129606 | GAACTGAGTCTCTCA[A/T]TTTTTTGTATATCGT | 50807 |
| rs182071327 | snp | C/T | 0.0109588 | 0.0732073 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152710 | TTCTGGCCCATGAGG[C/T]AGGGTAAATTAAGAA | 50807 |
| rs182077716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136332 | TCACAAGAGAAAAGC[A/G]AACTCTGAACCATGA | 50807 |
| rs182092751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204771 | CTTCAGTAGACATGT[C/T]ACACGAGAAGAAAAT | 50807 |
| rs182103617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164055 | TTCTAATGCAAGGTA[C/T]CAATGGAGTGGGCAA | 50807 |
| rs182132733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130291184 | GGAAACATTACAGAA[C/T]ACTCTTAGAATGTGA | 50807 |
| rs182133973 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269888 | CCAAGTTAAATATCA[A/G]GCCAGGCATGGTGGC | 50807 |
| rs182134916 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074300 | GGGCAGGGAACTAGA[A/T]GAAAGAAGATCAGGT | 50807 |
| rs182143111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323860 | TACTGCCTAATAGAT[C/T]ACCAGGCATTAAAAA | 50807 |
| rs182145698 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093741 | CAGATTAGTAGATAC[A/C]TAGTAATCCAGAAGG | 50807 |
| rs182151334 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109045 | CTCCCAAAGTGTTGG[G/T]ATTATAGGCGTAAGC | 50807 |
| rs182162064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341081 | CTGTGAGGGTGCTTA[A/C]AGATCAAATTAAGTC | 50807 |
| rs182163170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360308 | ACCCAGATAATCCTG[C/T]TGTCTATGGCATCTT | 50807 |
| rs182168718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130304977 | TGCCACCTTTCCAAC[A/C]TCTTCTTCCTCACAC | 50807 |
| rs182171485 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321650 | ATAGTTTGCACTCCT[C/T]TGTATTTCCATGGTT | 50807 |
| rs182174674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057211 | GCATTCTGATTCCCA[A/G]CCTGGGGACAGTGTG | 50807 |
| rs182177382 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327362 | TCCAACTGGACCTCA[A/G]TGTAGGGTGTTACCA | 50807 |
| rs182180328 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385241 | GAGGCTGAGGTGGGC[A/G]GATCACTTGAGGTCA | 50807 |
| rs182181283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261980 | TATAAAACTTAACTG[C/T]TAGACAATATATAAA | 50807 |
| rs182183354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130357328 | GGCCTCCGATCTCCT[C/T]GTCCAGCCTCGGAGT | 50807 |
| rs182186026 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228674 | CCATCGCACTCCAGC[A/C]TGGGCAACAGAGTGA | 50807 |
| rs182190399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400832 | CTGCAGTAAGGGAAA[A/G]TTGACTTACATCTAG | 50807 |
| rs182193864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422859 | TTTCCTCCACTGCTG[C/T]CTTCTATTATTCTTA | 50807 |
| rs182197245 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392969 | GGGGTCAAATATCCA[A/T]ACCATGGCACCGAGG | 50807 |
| rs182222227 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148718 | TTCTGTTGTAATTTG[C/T]TTTATGATATTTATT | 50807 |
| rs182248033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130185808 | GTTGAGTGAGAAGTA[C/T]AAGGAAGAGCACCTG | 50807 |
| rs182249591 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093015 | CATTACCTAGAAAAA[A/C]GAGAAATCCAAAAAC | 50807 |
| rs182252963 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321180 | CTCCTGCCCCCAAAA[A/C]AACATGGATTATAGT | 50807 |
| rs182270843 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130125215 | AAGACTCTCTCACAG[C/T]GCACCAGGTGTTAAA | 50807 |
| rs182274505 | snp | A/C | 0.00478085 | 0.0486577 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445371 | TTTAATGTAGCCTAC[A/C]TGATTGGTTGCTTAT | 50807 |
| rs182280342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356970 | CCATCTCCCTTCCTA[C/T]TTTCCACCCAATGGT | 50807 |
| rs182283766 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421203 | TAACAACAACAACAA[A/C]AAAATCACAGTGTCT | 50807 |
| rs182301479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224724 | TTCCATAATAAATAC[A/G]CCTGCTGAAAGGATA | 50807 |
| rs182304307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056943 | AAAACCAATAGATGT[A/G]TGGACTGCCCTCGCA | 50807 |
| rs182323751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211815 | TTACAAAGTCTATAA[A/T]GTACCAAAGCACCTT | 50807 |
| rs182333814 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130230510 | TCCCTTTGGGGGAAA[A/C]AAACCCCTTCCTTGA | 50807 |
| rs182345052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130365338 | GCCTAGTTGGGGTCC[C/T]TTGTGGGCCCCCATA | 50807 |
| rs182346263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405039 | CCTTGAGCATGAAGA[C/T]ACATATCTGCTGTCA | 50807 |
| rs182349521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382457 | AGTAACAAGTAACTG[C/T]TCTGATAAAGGAGAA | 50807 |
| rs182354167 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145908 | GTACGGTGGTGTGAT[C/T]TCGGCTCATTGCAAC | 50807 |
| rs182356537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130426034 | GATCTGTGTCCCCAC[C/T]CAAATCTCAGGTAGA | 50807 |
| rs182357736 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130142981 | AATTAGAGCTACGTA[C/T]GGTAGTGGTGCTGGT | 50807 |
| rs182360165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248157 | CTGGTATTTCTAATC[C/T]TAACTCTGGCCCATT | 50807 |
| rs182360757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396534 | ATTATTTTGAAAGGA[C/T]TTTCGCAGCAGAACT | 50807 |
| rs182366544 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337005 | GGAAGGATCCTGGGA[C/T]TTCCCACAGGGAACC | 50807 |
| rs182369559 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362102 | TCTTCTGAACAGCAA[G/T]GGCGCTAACGACCCA | 50807 |
| rs182375133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380595 | GTGACTATAACCCAT[C/G]AAGGTAAAAGCAATG | 50807 |
| rs182379066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085713 | GTACTCCAGCCTAAG[C/T]GACAGAACAAGACGT | 50807 |
| rs182379993 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395667 | AAACTGTGAGACAAT[A/C]CATTTCTTTTTTTTT | 50807 |
| rs182382737 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353979 | GCAAGCTCCGTCTCC[C/T]GGGTTCATGCCATTC | 50807 |
| rs182386801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417337 | GGCTGTTCCCTGTGG[A/G]CCCATGGAAAGGATG | 50807 |
| rs182388116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178600 | TGAAACAAAACAAAA[C/T]TGAAGACTCCAGGTG | 50807 |
| rs182390103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130181885 | CTAACTGATTTATCC[A/G]TCAAGTCTTCTTTAA | 50807 |
| rs182390983 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437960 | CTTCCTGACTTAGGG[C/T]AGTGAAGGAAGAGGA | 50807 |
| rs182401142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119230 | ATTACAGGTGTGAGC[C/T]GGCCTGTACCCGGCC | 50807 |
| rs182405196 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248783 | GGCTTCCTCCAAATC[G/T]TCTCTTCCTCCTCCA | 50807 |
| rs182410607 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130266629 | AAAAACATGAAAGAA[A/T]ACAATCTACCATGGG | 50807 |
| rs182419271 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309184 | TATTTTAAAAAGCAC[A/C]ATGCTTGCTTTGGGG | 50807 |
| rs182420816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344122 | GCAGTCAACACTATC[C/T]ATACTATGGGAAACT | 50807 |
| rs182429214 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130283450 | GCGCATGGTGGCATG[A/C]GCGCCTGTAGTCCCA | 50807 |
| rs182433304 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130318430 | CATGGAGTTAGACAG[A/T]GCTACAAGGAGGAGA | 50807 |
| rs182435915 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130379550 | ACAGAATTGTGGGGG[A/T]TGCCCTAATTCCAGA | 50807 |
| rs182441373 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246579 | GAAGGTGCTTGCTTC[A/G]TCTTTGCCTTCTGCC | 50807 |
| rs182443788 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130302393 | CACTGTGAACAGCTA[A/T]CTCAAAGGCAGAAAG | 50807 |
| rs182471127 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432975 | ACTGTCTGCTACACC[A/T]GGTCGCTCACTCGCC | 50807 |
| rs182515961 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073961 | CGAGGGGATGGAATC[C/T]AGACTGGAGAAATCT | 50807 |
| rs182523693 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208470 | TCCATCTTTGTAATT[G/T]TGGATGACTTTGACT | 50807 |
| rs182525919 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141316 | TCAGCTCCTGTCACT[C/T]TGAGTTGTTCCTTTG | 50807 |
| rs182527478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251112 | TTTGGAACACCAATA[C/T]AGAACACTAAATTTT | 50807 |
| rs182536432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270932 | AGTAGTTCACCCTAC[A/G]GTGTAAGATGAGTCA | 50807 |
| rs182540365 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108218 | GGAAGTCTACATTAT[A/G]GCAAATGTGTATGAA | 50807 |
| rs182541195 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332746 | CAAGTAAAAGGATAA[A/T]CTTTATTAATTTTCC | 50807 |
| rs182549696 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287082 | TTTTTAGTAATGGGG[C/T]CAGAAGGAACACAGG | 50807 |
| rs182555105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393135 | CCCTAATTTGTTAAC[C/T]CACTGCTCATTGTAG | 50807 |
| rs182562613 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130369381 | ATGAAATATCAGAAA[G/T]CAAAAGTGTCAGCAT | 50807 |
| rs182565648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130305668 | CATGAGCTACCACTC[A/C]CAGCCTATTCATTCA | 50807 |
| rs182591808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070220 | TTTTTCTATTTTTTA[A/G]TAGAGACGGGGTTTC | 50807 |
| rs182593441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130200908 | AAAAGTGAATCTGGA[A/G]AGAAAAACAGTTGCA | 50807 |
| rs182605196 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130161543 | GCTCACACTCTCACC[A/C]TATCACTGTCCTGCT | 50807 |
| rs182607998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160818 | GGAAGGGCAAAAGAA[A/T]CAGAGAAAAAAGGCA | 50807 |
| rs182627081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130125397 | AAAGGAAAACAAGTT[C/T]AAGTGTACATAACCC | 50807 |
| rs182631611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110198 | ATAAAATTACAGAAG[C/G]GGGTGGAGGGAAATG | 50807 |
| rs182636415 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199802 | AAACTGCCTCAGAGA[C/T]AGGGCAGCCCTGGTC | 50807 |
| rs182647251 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102517 | ATTTGGTTAGGATTT[C/T]TTGCATCTACGTTCC | 50807 |
| rs182656207 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130418309 | AATCCCAGCACTTTG[C/G]GAGGGCCAGGCGGGC | 50807 |
| rs182663433 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143709 | TGCAGAAACAGAATG[A/C]GTCAATCCCAATTAA | 50807 |
| rs182670072 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126320 | GAAAAAGTGAGAAAG[C/G]CTTTCCTTAAGAGAC | 50807 |
| rs182676425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094080 | GTGTCAGTCACAGCA[C/G]TTTTCAGAAACTATT | 50807 |
| rs182681179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130282895 | GAGTGGGTTTCGCTG[C/T]GGCAAAGTTACAACA | 50807 |
| rs182689042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130067274 | ATACTAGAGTTAGAT[A/G]AGTGGTGGTCACATC | 50807 |
| rs182691081 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318195 | CAAGTAATCCTCCCA[A/C]CTCAGCCCCCCAAGT | 50807 |
| rs182700838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353257 | ACTTGTATATAGCAG[A/G]GCCTCCCCAAAAATG | 50807 |
| rs182726947 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130205255 | ATCACGTACACATAT[C/T]GCGTGCATACACCCT | 50807 |
| rs182727039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130182945 | CACTGAAAAAATAAC[C/T]TAAAATATAATATAA | 50807 |
| rs182732804 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164772 | TCCTATTCACAACTA[A/G]AATTCTTGGAACTTC | 50807 |
| rs182735274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130221062 | CCAGACCATATCACC[A/G]GTCTCTACCAAAAAT | 50807 |
| rs182754048 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088560 | TGGAGTCACCAGAAG[A/C]TGAGAGAGGCAAGAA | 50807 |
| rs182771873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070336 | GCCACCGTGCCCGGC[C/T]GACTGCATCTCTTTT | 50807 |
| rs182771899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114832 | AGGTCAAGAGTGCAG[C/T]AGTACAATCATAGCT | 50807 |
| rs182775752 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130089105 | CTGTGATACCCACTA[C/T]ACCAGTGGGGACAAA | 50807 |
| rs182782156 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130053291 | ATTTAAGCAAATGTA[A/G]TGCCAGAATGACACA | 50807 |
| rs182786185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069800 | AGATTACAATGAAAC[A/G]TATGATATGAAATTG | 50807 |
| rs182790041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146330 | TTAGCATATACCTTC[A/G]TATATGCTAAGACCT | 50807 |
| rs182793321 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373692 | TGTCCCTACAAAAAA[G/T]ACAAAAACAGCCAGG | 50807 |
| rs182799127 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130129942 | AGAAACTAGAAATTG[C/T]TTTGTTAAAAACAAA | 50807 |
| rs182805050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098290 | CATCACATCCTTTCC[A/G]GCTAGAACTTTCAGG | 50807 |
| rs182807036 | snp | A/G | 1.64868e-05 | 0.00287109 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054681 | CAGGGTTACATGAAG[A/G]CAGCAGTCTTGCATG | 50807 |
| rs182811144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407267 | ACTAAGGGACCTTCT[A/G]AGAGACTGTGGAGAG | 50807 |
| rs182817540 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314610 | TTCAGTACCAATGCC[G/T]GGGCAGGCTTTCCAA | 50807 |
| rs182830306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349137 | TACAGAGCCCACTAA[A/G]GGCTGATTATACAGT | 50807 |
| rs182832328 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130310236 | ATTCTCTACAAATAA[C/T]AGAAATAACCATTGT | 50807 |
| rs182837443 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274400 | AAATGGGGAGGTTAC[C/T]ATGTTCTTTGGTAGA | 50807 |
| rs182837854 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130072399 | TCTGATGGTTTTATA[A/G]GGGGTTTCCCCTTTT | 50807 |
| rs182848726 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411100 | CTCCTGACCTCAGGT[A/G]ATCCACCCACCTTGG | 50807 |
| rs182869578 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054093 | TAAGACAGTATAAAT[A/C]CACTTGTCTAAACTT | 50807 |
| rs182870136 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130344951 | ATTGTTTTAGTTACA[A/C]ATTACTTGACAAAAC | 50807 |
| rs182893467 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066167 | CCTTTGCCTTCCCAA[C/T]AAAATCTCCCCTTGC | 50807 |
| rs182914187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238575 | GCACTTACTAGACAT[C/T]AGGTATAAAACTTAT | 50807 |
| rs182936384 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377660 | ACACATCTCAGGGCT[A/C]CTCCACCCTCTGGCT | 50807 |
| rs182943292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393982 | CCTGTCTTTACTTTA[A/G]TCTCTTAATCTCATC | 50807 |
| rs182944094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134592 | AGTGACTTACACAAG[A/G]TCACACGGCAATAAA | 50807 |
| rs182945620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439469 | TATTTATATGTCTAT[C/T]ACCCCCATCAATAAT | 50807 |
| rs182946338 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411731 | GTATTATGACAGCCC[A/G]AAACTAGAAATGACA | 50807 |
| rs182953683 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130301892 | AAGTAAAGCTTGCAT[A/G]CAGGATAATCTTCAA | 50807 |
| rs182954008 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130434445 | GGAGTTAGAAATAGC[A/G]CCTATTTCATAGGGT | 50807 |
| rs182977534 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101312 | CTTTTTTCTGTTTCT[A/G]TGAGGAATGTCATTA | 50807 |
| rs182981232 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335907 | TCAGTCAAAAATAAG[G/T]TTCAGGACACTAAAA | 50807 |
| rs182981395 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074793 | TGGGCTGAAAGGTTG[C/T]GGTGCTGGGACTGCT | 50807 |
| rs182997793 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311067 | GGACAGCCATTCTAT[A/G]AGAACGCAGTCCAGG | 50807 |
| rs182999777 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372936 | TACACAGACACACAC[A/G]CATACACAAATACAC | 50807 |
| rs183004347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352687 | TAACTGCTGTAATCC[G/T]GAATTTCTTCATCTA | 50807 |
| rs183006767 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372659 | AAGATTTTTCCACAG[G/T]TTTTTTCTGTAGCTT | 50807 |
| rs183009066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341468 | CGGTTCTTTCCCTTC[A/G]GCAGTAAAACCTGGG | 50807 |
| rs183011193 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130357812 | CACCTCCAGTCCCCA[A/G]GCCTTTCAACCCGCA | 50807 |
| rs183022113 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237747 | ATTCAGCAAATTGTG[A/C]GTTTAGGCTATGTAC | 50807 |
| rs183022981 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130235282 | CTTCAGTGAACCTCC[C/T]TGTATATAATACTTT | 50807 |
| rs183025998 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130266039 | TAAGGGAGCTTAGGT[G/T]TCAACACTCTTGCAG | 50807 |
| rs183053301 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156368 | AGGAGGTGGAACCAC[C/G]TGACTTCCAACCTCC | 50807 |
| rs183089950 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130194304 | CCTTTGTCATTATAA[A/T]GGCACAAAGAAAGGT | 50807 |
| rs183107865 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389866 | CTACTATGCCCAGCT[A/G]AATTTTTTTTTCGTA | 50807 |
| rs183131222 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130314230 | CTTTCATACTGTGAC[A/T]TCCCTGACTTTATTT | 50807 |
| rs183145964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292950 | ACTATTATTTTCATC[A/G]GCAATCATGCCACCT | 50807 |
| rs183150493 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130325211 | TTTCTTGGGGTCAAA[C/T]ATGGTAGTTTCTTTT | 50807 |
| rs183155758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215481 | GGGAGCGGTGGCTCA[C/T]GCCTATAATCCCAGC | 50807 |
| rs183165812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130193571 | TTATTTAAAAAGTCA[A/G]AAATTTAAAACAAAA | 50807 |
| rs183166265 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130147900 | AAATACTGTTGGTGT[C/T]GGTTGATTGAGAAAA | 50807 |
| rs183166894 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195180 | TTCAAGTCTATAAGA[A/C]GTCGAAGGGTATGTT | 50807 |
| rs183169698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130174922 | TATCTGGGTGTTTCC[A/G]TGTTTTGTTTATTGT | 50807 |
| rs183173752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130242413 | CATAATCGCCACAAG[A/G]CAAATGTTCTTATAT | 50807 |
| rs183178750 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270664 | GAAGGCAATTTGGTT[A/C]TAATATTTGAGTTTA | 50807 |
| rs183180385 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206316 | AAGCTACCAATTTTA[C/T]CATTAGGCACATCCA | 50807 |
| rs183183666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130225714 | AAGTAGACTTGGGGT[A/G]TGGACATTCAAGGCA | 50807 |
| rs183186909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130235006 | GTATTAGGGGCCTTA[A/G]ATGGTCTCTCCTTTT | 50807 |
| rs183188053 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277255 | AGTCTGCCCCATCCA[A/G]TCTGGCCATTCACCT | 50807 |
| rs183191718 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130250525 | ACAAGTGGTAAGCCA[C/T]TGGTGACTTCTCCAC | 50807 |
| rs183196539 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130098865 | CACTCTACAGTGTTA[C/T]AGAACACAGGAACTT | 50807 |
| rs183198643 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297156 | ATCAACTATGGGCCA[A/G]GCGCTGCACTGGTTT | 50807 |
| rs183198886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259351 | CAAGTTATTTCTCAC[A/G]AGTTCCTTCTATGAA | 50807 |
| rs183205087 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130256039 | AGAATATCTTATTAG[C/G]AAGAGAGTGAGAGAA | 50807 |
| rs183207006 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130221735 | TGTCAGCCACTGAAC[C/T]TTACAGGGTACCCTC | 50807 |
| rs183207211 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130115390 | CCTTCAATCATGTGA[A/G]CCAATTCCTTAAAAA | 50807 |
| rs183212983 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130369222 | TGGAATGTTTACATA[G/T]ACATAATGAGACACC | 50807 |
| rs183214533 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131043 | GCGCCTGTAGTTCCA[A/G]GTACTCGCGAGGCTG | 50807 |
| rs183216417 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348062 | TCCAGTTCTACAGAA[C/T]GTGCGTCATAATAAC | 50807 |
| rs183221849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156161 | TTTAAGTAATAAAGA[A/G]CATTCCAAAGCTAGG | 50807 |
| rs183228849 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384994 | CACACCATGGCTCTA[C/T]GGAGGCCGGGGCTTG | 50807 |
| rs183230657 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130139071 | TGAGAACAACTCTTG[C/T]TACGATATTATGTTC | 50807 |
| rs183232337 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080979 | TGCAAGGCATAAATG[C/T]GAAGCAGAAGGCACA | 50807 |
| rs183233187 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130400445 | TCCCAGCTGCAAAAT[A/G]GAATAAATCATATCT | 50807 |
| rs183248667 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183216 | AATGCAACAAACAAC[A/C]ACCACATATCACATA | 50807 |
| rs183255552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114951 | ACTTTGTAGAGACAG[A/G]GTCTCACCATTTTGC | 50807 |
| rs183257988 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058164 | AATGGTTGACCTTGG[A/C]CAGTAACTTAACCTC | 50807 |
| rs183263049 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118042 | CCAAAAATAATTTTT[A/G]TATCTAGCATGACAC | 50807 |
| rs183273772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314425 | GGTATCATCATGCCC[A/G]TGTTACAGATGAGAG | 50807 |
| rs183281027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297900 | GTAAAACTGGCAAAG[C/T]GACATGCTCTTGTAG | 50807 |
| rs183290521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146818 | TGAAATGCCATGGAA[A/G]GTGACAGAGCTGCTG | 50807 |
| rs183301220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079742 | TCACAAGATGTGCAT[A/G]CAAACCAAGAGTGAA | 50807 |
| rs183323519 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139367 | TCCCAAGCTTAAGTT[G/T]ATTATGCATAATAAG | 50807 |
| rs183332528 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151636 | GGACAGAGACAATGC[A/T]ACTGCTCAAGTTCCA | 50807 |
| rs183340765 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438556 | GGACCCAGCTCACAC[A/C]CTGCCCATCCCTTCC | 50807 |
| rs183346668 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130135009 | CTCAATCTCTGCTAT[A/C]CATGTAAGGGAAGGA | 50807 |
| rs183353376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215889 | GTGCTTGTGCCACTG[C/T]ACCCAGCCTGGGTGA | 50807 |
| rs183367909 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130175876 | TCCCAGAAAATAAGC[C/T]CTCGGTAAATGTTAG | 50807 |
| rs183372930 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238898 | ACTGCAAGTCTAACA[C/T]GATTTCCACCATACC | 50807 |
| rs183381210 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130325379 | GAGAAAAGACCAGTG[C/T]TACACTATGCTTGCC | 50807 |
| rs183382741 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130101716 | GACTACAGGCATGTG[C/T]TACCACACCTGGTTA | 50807 |
| rs183386715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130201501 | AATTCAATTTAGTAA[A/G]TGGTGGGTTAGATTT | 50807 |
| rs183388077 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106719 | GGATGCAAAGGCAGC[C/T]CATTCACAGCCCTTA | 50807 |
| rs183389093 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222333 | CTGCCAACCTAACCT[C/T]TGATTCTCAGCGACT | 50807 |
| rs183389889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118824 | TTTTAGACCAAATTA[C/T]TCCAACAGAGACAGA | 50807 |
| rs183397328 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301686 | GAAATATATCCTACA[A/G]TATTTCCTTATAGGT | 50807 |
| rs183406534 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066777 | CCCTCAGAGAACTTC[C/T]GTAAATTCAGAGGGC | 50807 |
| rs183408202 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334897 | TTGTCATAAATAAAC[C/T]CTCCCTTTAGATTAT | 50807 |
| rs183408492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293579 | GGCCAAAAGTAGTAA[C/G]TAAGGATTCCCCCAC | 50807 |
| rs183408666 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078659 | AACACCAGAACTTTA[A/G]TTTTACAGGGTCCCC | 50807 |
| rs183410922 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317713 | GGGCTCTGTTGCTAC[A/G]CGTTTGTTTCACTAG | 50807 |
| rs183411625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364188 | CAAAAAACTACTCTG[C/G]TTCTACCTCCCTGTT | 50807 |
| rs183412416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274664 | ATATTTCATTCAAGT[C/T]CGAGTGATCAACAGA | 50807 |
| rs183413018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084951 | TTTGCTCTATATTAA[A/G]TAAAAGTACAATTCT | 50807 |
| rs183420418 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130427282 | ATCATGGCCTCCCAG[A/G]AGCCACCATGTCTCA | 50807 |
| rs183425995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434878 | ATACTGACCATACAC[C/T]GAACAATAGCCCCTT | 50807 |
| rs183431100 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130395866 | AGATGGGGTTTCACT[A/G]TGTTAGCTAGGCTGA | 50807 |
| rs183458066 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095241 | CGTGTAGAGTAAATA[G/T]TTACTGAATAAATAG | 50807 |
| rs183465434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111970 | GCTGCTCCTGACAAC[A/G]CGATCCGCGCCACTC | 50807 |
| rs183470695 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130888 | TAAAAAAAAAAGCCA[C/G/T]GCTCACGCCTGTAAG | 50807 |
| rs183470914 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179734 | ATATACCATAGGATA[C/T]TGAAACTTTAGGAAA | 50807 |
| rs183480539 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130127707 | AAGGTAGTATTTTGG[C/T]AGTGACACCTAGGAG | 50807 |
| rs183481525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059038 | TGGTGCTTGGGAGTC[A/C]TGGGAGAGTTCCCTT | 50807 |
| rs183488951 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098548 | ACAAGGTTTCACCAT[G/T]TTGGCCACCTAGGCT | 50807 |
| rs183493297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422495 | TCTTACACAGTGTAC[C/T]TTCCCGCCTTCTCCC | 50807 |
| rs183494168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076961 | CATTTATGAAGGCAC[C/T]TGGCACACTCTAAGT | 50807 |
| rs183498436 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165432 | TGGGTCTTTTTAATG[C/T]TCTTACACTGAGAAA | 50807 |
| rs183504093 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425029 | AAATAAAAAAAAGAG[C/T]GGACAAACAGTGTGG | 50807 |
| rs183537140 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130061169 | GAAGGGAACTGACCT[A/C]TAGTGAGCACTTGAA | 50807 |
| rs183559979 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347699 | GGGTGGTCTCCTGAC[A/C]CAAGTGGAGCCAATC | 50807 |
| rs183565109 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287944 | TCCCTACCCCAGCCT[A/C]TCTCTTCCCCAGGCT | 50807 |
| rs183572356 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418012 | ATGGACACGGGGAGC[A/G]GGTCAGCTCCACAAG | 50807 |
| rs183574995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322038 | GAGCTGGGAATGCAA[A/G]TCATAAATGTAATGA | 50807 |
| rs183577810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384858 | GTCCACTACATCCTC[C/T]AAGCTATGCACTGTG | 50807 |
| rs183583819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402994 | GTGTATCATATACCC[C/T]CTGAACCCACCAGCC | 50807 |
| rs183625214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251412 | GATAGAGTGAGACTC[C/T]GTCTTAAAATAAATA | 50807 |
| rs183630219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130216949 | CCAACACAGCATCCA[A/G]TGCAACACTGTTATA | 50807 |
| rs183630500 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428338 | CTCGCTAAATTAAAG[A/C]CACAGGACTATCTAC | 50807 |
| rs183630967 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130345846 | ACAGCCAACTCTGTG[A/C]CTAGTATTACTAGGC | 50807 |
| rs183647897 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130265664 | CAGACTGCTAGAGCC[A/C]AGGAGTTCAAGACCA | 50807 |
| rs183665180 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381488 | TTCAGACTAGCCATA[C/T]TTTAAGTTCTTAGTA | 50807 |
| rs183693228 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130305382 | AACGGACTCTTGCTC[A/T]GTTGCCCAGGCTGGA | 50807 |
| rs183696725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277818 | TATTGTGTCTGTTGA[C/T]GAAGGGCTGTAGGCG | 50807 |
| rs183700100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084606 | AGGAGTATTCTGGAA[C/T]AGTGAATTACTATAC | 50807 |
| rs183704566 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359861 | ATCTCCTGACCTCAT[A/G]ATCCACCCGCCTCGG | 50807 |
| rs183706334 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378480 | CAGGTGCAAGTGCAC[A/G]GAGGCTTGACACGCA | 50807 |
| rs183706501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130243793 | CATTCTGATGGTCCA[A/C]CTCCCAGTCACTGTC | 50807 |
| rs183736967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272858 | TATGTAGGTGGGAGA[C/G]AGAGAGAATAAAGAA | 50807 |
| rs183751138 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289222 | CAAAAAAAAAAACTA[C/T]ACTTACCAAGACTAT | 50807 |
| rs183766798 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307395 | GGGAACTGTTAATCT[A/C]TAATATGTACAACCT | 50807 |
| rs183772332 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342599 | AACTTCTGGAACTGA[A/G]AAAGCACCATCCTAA | 50807 |
| rs183773238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322911 | GAGGAGAAGGAAGTC[A/C]ATGTGTCGGATGGAA | 50807 |
| rs183782125 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130271608 | TTTCTTGGTCTTTTG[C/T]TTTTGCATCTTTTAG | 50807 |
| rs183782521 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306412 | CTCTCCCCACACTGA[C/G]AACCCCTTTAGTCTT | 50807 |
| rs183783990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330958 | TCTCAGTAGCAGATG[A/G]TATGGTGTACCAAAA | 50807 |
| rs183784726 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166097 | CACAAATACAGCTTA[C/T]TACAGCCTCCACTTC | 50807 |
| rs183801593 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368892 | TGTACTTCTTTTTTA[G/T]TGTAAGCTAGTCTGA | 50807 |
| rs183810369 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399855 | GAGTTTCGCTCTTGT[C/T]GCCCAGGCTGGAGTA | 50807 |
| rs183814034 | snp | A/G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130206522 | CAAACAGGAAATGCT[A/G/T]TGCAGATGGAGAAAT | 50807 |
| rs183848212 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130346039 | AGAGGTAGACTTAAC[C/T]GTATTTGGAAAACTT | 50807 |
| rs183854561 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236400 | ACAAAGTCACTAGAC[A/T]GTTAAAACATTTAGT | 50807 |
| rs183855054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223394 | TGGGACAATGCCTAT[A/G]AGGAACATGGAATGA | 50807 |
| rs183857764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130232152 | TTGTCTATGGACTGG[C/G]CTTGGAAATCACATG | 50807 |
| rs183859061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106344 | GAATAACACCACTGA[C/T]AGGAAAATATTTCCC | 50807 |
| rs183863269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203972 | TAAATTTTACATTAT[A/G]TCCAAAACAGGATGT | 50807 |
| rs183864443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180675 | AGTCTGCCTTTAAGC[A/G]TAAAGACTGCTGACT | 50807 |
| rs183887946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275590 | TTATCAACTTATAAA[A/G]CAATTCGTTCAAATT | 50807 |
| rs183887993 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233735 | CTGATTAACATTTAT[A/C]TCTCCCCTACTGGAT | 50807 |
| rs183894082 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249025 | TGCCTCAGCTTCCAG[A/C]GCAGCTGGGACTACA | 50807 |
| rs183894199 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130213823 | GTGGTGTTACCCAGA[A/T]CCTTTCTAAGTGTGC | 50807 |
| rs183894333 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130294234 | CTGTGACTTGGAACT[A/T]GTTCTCGATGTACTC | 50807 |
| rs183896214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422543 | GCAGTTCCTCCTAAG[C/T]TGTCTCTGTCAAGAT | 50807 |
| rs183909965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264646 | GCACAACATATTTCA[C/T]TTTGTTTCAATTCAC | 50807 |
| rs183912271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286363 | ATGTTTATCTCACTG[C/T]GTATATGACATTCTA | 50807 |
| rs183913690 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311828 | AAGCAAAGATTTTAG[G/T]CTAAATAATAATAGT | 50807 |
| rs183920042 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163643 | GGCACTCTAGACAAA[G/T]GCAAAGAGGATTTTC | 50807 |
| rs183921954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145466 | GGGATTACAGGCACG[C/T]GCCACCACACCCGGC | 50807 |
| rs183925552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130268284 | TGAGCCCAGGAGCTC[A/G]AGACCAGCCTGGGAA | 50807 |
| rs183928223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284998 | ACTGGAAAACCTCTC[C/T]CATCCACACCCTATT | 50807 |
| rs183928268 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325837 | CAAAACCAAGGCTCC[A/G]AGAAGAGACCACAAA | 50807 |
| rs183928863 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130260445 | GAGCTGGTAAGACCT[C/T]AGAGGTAACATATTC | 50807 |
| rs183935418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112855 | TGTGTTCCAAACCAA[C/T]GGCCCATGAGGTATC | 50807 |
| rs183942608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128545 | GTATTTTCTGCAAGT[C/G]CATGTCAGTGGGGAC | 50807 |
| rs183956193 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130190316 | CTTTAATCCATTTGG[A/G]TTTGATTTTTGTATA | 50807 |
| rs183959256 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183395 | GCCCAGGCTGGAGTG[A/C]AGTGGTCCGATCTCG | 50807 |
| rs183959983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130172454 | TTTAAAAATAAGAGA[A/G]CACTAATTAAATCTC | 50807 |
| rs183965800 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229756 | TAAAAAACCCCAAAA[C/T]AGGCTGGGCGTGCTG | 50807 |
| rs183967433 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154495 | AGAAGAAATGGGCAG[A/G]GAACAGTGATTCCCT | 50807 |
| rs183969664 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162010 | TCACTGTGTTGCCCA[C/G]GCTGGTCTTGAACTC | 50807 |
| rs183978760 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187908 | CTTCCCAATCTTCTT[C/G]AAAGTGCCTAATCTC | 50807 |
| rs183982118 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227070 | CAATGGGATACAAAG[A/G]TTATTTAGTGTTTAG | 50807 |
| rs183991232 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130207005 | AAAAAAAAGGTTGAA[C/T]GTAATTTTTCAGTAC | 50807 |
| rs183992642 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227656 | ATCAATTATAAATTA[C/T]TATATATATTATACT | 50807 |
| rs184004501 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130184057 | GCAGATAAGAATTCA[C/T]AGAAGATTCACACAG | 50807 |
| rs184006812 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130338601 | ATCTGTGTGGAATTT[C/T]TTCCATTTCTTTTAT | 50807 |
| rs184007251 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123200 | AATTCCCAGGAGTGG[A/G]ACTGCTGAGTCAAAG | 50807 |
| rs184010268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383038 | AGGCACAGAAGAGCA[C/T]GGTATATGTTGCTAA | 50807 |
| rs184024485 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245011 | CATCCTGTGTAACAA[C/T]ACCCACAGTTAGTGG | 50807 |
| rs184032207 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091845 | CATGTCATATATACC[C/T]GAGTCAGCACCCAGC | 50807 |
| rs184032900 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088765 | AATGCTAGGCTGAGA[A/G]TAATGGTAACAGTAG | 50807 |
| rs184043036 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107557 | GTATGTATGTATGTA[G/T]GTATTTTTGAGATAG | 50807 |
| rs184058941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166486 | TTTCTGACTCCTCCA[C/T]CCATCCTGCCCCAAA | 50807 |
| rs184063050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124415 | GCTAGAACAGAATCT[C/G]GTTCTACACACATAT | 50807 |
| rs184065492 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130282044 | ATTACACTCCAGTCC[A/G]GGCGACAGTGCAAGA | 50807 |
| rs184066041 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056247 | GTAACTGATTCACGT[C/G/T]GGGGGGCTTCAGAGC | 50807 |
| rs184067401 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247960 | CCAACCACAACACCA[C/T]GTGGAGATGCACAGG | 50807 |
| rs184069069 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073330 | GGGAGGCGGAGGTTG[C/T]GGGGAGCTGAGATCG | 50807 |
| rs184070294 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148201 | ACTTTCAAAGACCTA[A/G]CAACAATCTGGCAGC | 50807 |
| rs184075997 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116028 | GGCTGAAAGGCAAAA[C/T]GAGTCTTTGAAGTTT | 50807 |
| rs184076245 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132081 | AAGAGAGAATGAAAT[C/T]GGAGAAGGAGAAACA | 50807 |
| rs184101845 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144055 | CTATGCTAGTGTCTG[A/C]AAACAGAGCTGCTCA | 50807 |
| rs184109640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169783 | TCATCTCCATTTGTA[A/G]AACTGAGGTACAGAG | 50807 |
| rs184134593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086293 | CACTTAACCTTTCTG[C/T]GCCCCGAAGTTGAGA | 50807 |
| rs184150495 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130210613 | TTAGTTTAATTATCA[A/C]CAGGACAGGCCCTGG | 50807 |
| rs184240928 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130394321 | GAAATGGCCCCCTTG[G/T]GTGTGGCCATCTTCT | 50807 |
| rs184251557 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374520 | CCAGCACTTTGGGAG[A/G]CCGAGGCATTTAGTT | 50807 |
| rs184255063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327439 | TCTAGGAGCCTGAAG[C/T]TCTTCAGGAACATCT | 50807 |
| rs184265076 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391125 | AGGAAATTTTGATAC[A/G]TGGTATAATAAGGAT | 50807 |
| rs184265993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435079 | GACCCCTTACCCCTC[C/T]GAGGCTCCTACACTT | 50807 |
| rs184267507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408263 | GGTTGTGTCTGTGAG[A/G]GTGTTTCTGCAAGAG | 50807 |
| rs184276371 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130427863 | GCCCCAACAGAGGGA[C/T]GTTTCTAAAGCACAA | 50807 |
| rs184295863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257988 | TTGTAAATTTGTGTA[C/T]TAGTGTACAAACATT | 50807 |
| rs184301726 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130298443 | ATCCCATCTCCTCTT[A/C/T]GAGGCCAGGCCACCA | 50807 |
| rs184309429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240182 | CAGTCTCAGAATTTC[C/T]GTTCAATGTTTACCA | 50807 |
| rs184311251 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295511 | GTAAAACAGGGATAC[A/G]GGATAATAATACCTA | 50807 |
| rs184313680 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337729 | TTTCTTTCCATTTTT[A/G]TAAGTCTTTTACTTT | 50807 |
| rs184315173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397081 | CCCAGGGATGACAAC[C/T]GCATTGCTGTGGACT | 50807 |
| rs184316816 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355950 | TTGCTATATTTTTGA[C/G]AACATGGGTATCATC | 50807 |
| rs184320629 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130276290 | CCTCTAAGTTCACAA[A/G]GTGATTCCATATACA | 50807 |
| rs184320778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419063 | GGCCCTGCAGCCAGG[A/G]CAGGGACCCTTCCTG | 50807 |
| rs184321001 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376371 | GGCCCAGTCATCTCA[A/G]TAATTGTGGCTGTAT | 50807 |
| rs184324400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354978 | GTAACCTCGGCCTCC[C/T]GGGTTCATATGATTC | 50807 |
| rs184325718 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130440675 | TTCCCCCCATCTCTC[C/T]CTTACACTCTAGCCC | 50807 |
| rs184330480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313512 | TGTAGGGTTATCTGC[C/T]GAGTAACAGACTACC | 50807 |
| rs184347041 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107054 | CTCTCTAAGCAAGGT[A/G]GACACCTAATCCTTA | 50807 |
| rs184375565 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139850 | TATTTTTTAATTCTC[C/T]CAAAATCTAGATTTC | 50807 |
| rs184376955 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130071104 | TTTCTCCCCTACCCG[A/T]TGCAGTGATCCTAGG | 50807 |
| rs184381325 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123712 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAT | 50807 |
| rs184382735 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130089907 | GTCCATGCCATGTGG[A/C]GAACTGTCACTGTGG | 50807 |
| rs184384237 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064497 | TTCCAGTTTTAAGTA[C/G/T]AGAAGCCTGTCAGAC | 50807 |
| rs184391089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333178 | ATTTCCTAAGCACCC[C/G]CAACCCTAGTCCAAA | 50807 |
| rs184399233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319581 | GAAGATGGGACACAC[C/T]GGCATCCACTGGTGG | 50807 |
| rs184399788 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414235 | ATGTTTGCTGACCCA[A/C/T]CTGCCATGTCCAAGG | 50807 |
| rs184429129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355364 | GCGCTCTATGTATGT[A/G]CATTAGTGATCTAAA | 50807 |
| rs184430807 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261548 | GGCTTAGGGAAACCC[A/G]GGGCATCTTTGATTG | 50807 |
| rs184437775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253531 | TAGATACAAAGCCTT[C/T]CATTGAACAAGCTCT | 50807 |
| rs184438296 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130392065 | TTGTCCCATCTTCTC[A/C]TCTGGTTTGCAGACT | 50807 |
| rs184441106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228496 | GCTTGAGCCCAGGCG[A/G]TCAAGACCAGCCTGG | 50807 |
| rs184444991 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246034 | AAATCATTTTATAAT[A/C]ATTTATGAGGGCTTA | 50807 |
| rs184447123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299496 | AGTACCTTTCTCATC[C/T]TCATCCCCTTTTTAA | 50807 |
| rs184473133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257060 | ACCCATAATTTTATA[A/G]AAACTAATGTAACTG | 50807 |
| rs184478496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409064 | GTCAGGAGTTCGAGA[C/T]CAGCCTGGCCAACAT | 50807 |
| rs184504641 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180278 | AGTGTTCATGTTCAA[A/C/T]TGGAATTCAGTTTGA | 50807 |
| rs184513778 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120963 | TCTCCTCTGTCCCCT[C/T]AAACCCAGTCCTCTC | 50807 |
| rs184521714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144639 | CTCCAGATGCACGTT[C/T]CAAATTCCAAACTTA | 50807 |
| rs184529146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222980 | TAGCTCCAGACTCTA[C/T]CATGTCAGGAGACTG | 50807 |
| rs184535983 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394500 | AGCAATTTTAATGTC[A/G]TCCCGGTCCTGTGGT | 50807 |
| rs184541617 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333631 | AAAACAAAACAAAAA[A/C]CAAACGGCATGGCTG | 50807 |
| rs184548333 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130338501 | AGAAAAGAACATTAT[C/T]CTGACTACTCCCCAA | 50807 |
| rs184549051 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414961 | CAGGATTTCACCATA[C/T]TGGTCAGGCTAGTCA | 50807 |
| rs184549878 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316803 | GAGAGAAATAAACTA[G/T]CGCATTTAAGCTTCT | 50807 |
| rs184556516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436219 | TAAAAGTAAAATGTA[C/T]AGTCATTAAAATTAT | 50807 |
| rs184561633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130351215 | CAAACTGGCAGACAG[A/G]AAGCATAAAAGACAG | 50807 |
| rs184564862 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374820 | GCTTCTTTTCACACA[A/C]AGAGGATAACAGAGC | 50807 |
| rs184572005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311965 | CTAAATGAGAAGATC[C/T]GAATTCAGCCTAGAA | 50807 |
| rs184585380 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130346230 | CTACTAAAAGTGAAG[A/T]CATACGTGAACATGA | 50807 |
| rs184613484 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130360120 | TTGAGTAATGCCAAG[A/G]CCCCTGCTCTCATGA | 50807 |
| rs184620241 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130304313 | TTCTGTTCCAGTTCT[A/G]AGTAGATATGAACAC | 50807 |
| rs184627103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378911 | GTTTTCTCATCTGAT[C/T]TCATTAATATTATGA | 50807 |
| rs184631771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275793 | CATATCAGAGAAAAG[A/G]TAGATTTATTTTGCT | 50807 |
| rs184635850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239904 | ATGCCATCTAATCTG[C/T]TGTGGAAGGCAAGTC | 50807 |
| rs184639116 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130137936 | GAAATGTTTGAGTGC[C/T]CAGGCTGGGCTGTGC | 50807 |
| rs184641074 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162744 | AATGGCGTGAACCCA[C/G]GAGGCGGGGCTTGCA | 50807 |
| rs184661448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136615 | ACAACTATAATTCAG[C/T]AGATCTAAGACAGAA | 50807 |
| rs184666674 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239451 | CCAGGGTGGCTGAGC[A/T]GGAATTTGAACCCAG | 50807 |
| rs184669961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203475 | GGACCTCCCAACAGT[C/T]CAGATCTGGAGTGGT | 50807 |
| rs184682768 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130212270 | CACCACCACTTTCAA[A/G]GGCAAAATTTGTTTT | 50807 |
| rs184690532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295070 | GGAGTTCAAGACCAG[C/G]CTGGGCAATATAGCG | 50807 |
| rs184692332 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130170592 | TTTTTAAGGCTGACA[C/T]CTTTGGCAAAGAAAC | 50807 |
| rs184697787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176163 | GTAGCTTCATCCACA[C/T]GGAAGTGTCGTGACT | 50807 |
| rs184699517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062327 | AACAGATAAACCTCA[C/T]GTTGTAAATGTCACA | 50807 |
| rs184699922 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157672 | GGCTTGCTCACTACT[C/G]TAGCTACATTGAACT | 50807 |
| rs184701534 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130326628 | ACAGGGTGTCCATCC[A/G]GAGGCCAACAAAGAG | 50807 |
| rs184717933 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102901 | TCACCATGTTGCCCA[A/G]ATTGGTCTCAAACTT | 50807 |
| rs184721694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366271 | GTAACAGTATAAAGT[C/T]TGGCACACCATCACT | 50807 |
| rs184726074 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077395 | GAGGTTTTGGCGATT[C/G]TCAGAGGACACCAGG | 50807 |
| rs184738029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223882 | CTTATCTTCATGAAC[A/G]AAGAAAAATCTTCCA | 50807 |
| rs184764079 | snp | C/T | 2.04109e-05 | 0.00319453 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236874 | ACTAACAAAACTCTG[C/T]AGACATTATTTATAA | 50807 |
| rs184782167 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167720 | AAAATTCTATTATAT[A/G]TTTGGTTTTCTTACT | 50807 |
| rs184784402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217283 | AAATGAATAAATAGA[C/T]ATTTATCAAAGTCAT | 50807 |
| rs184787292 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130159293 | CCAAGGTTGGGTGGC[C/T]TGGTGAGCAACAGGC | 50807 |
| rs184791095 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257506 | TTTATAGGTCTGGTT[A/T]AAAAAAACAGGATTT | 50807 |
| rs184796063 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261066 | GGAGAGGTCAATTAC[C/T]AGTCACAGACCCCAC | 50807 |
| rs184796753 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252185 | TATGGAACAAATTAG[A/T]ATGGACAAAGGTCTA | 50807 |
| rs184799263 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153402 | TGAGACAGGGTCTTG[C/T]TCTGACATCCAGGCT | 50807 |
| rs184805685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288616 | GCAGTGTAGAGGACC[A/C]AGAGACAAATGTGAA | 50807 |
| rs184807643 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237185 | TATTTTCCGGAGAAG[A/T]GCAGTCATTCCACAA | 50807 |
| rs184808736 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130272395 | ACACATCGTTGGTAG[C/G]AATCTAAATTAGTAC | 50807 |
| rs184812619 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119496 | GGGACTGAGCTCACC[C/T]CCCAGCCACAGGGGT | 50807 |
| rs184822398 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130196894 | GTTATAATACCTTGA[A/T]GCTATTTAAAACTGG | 50807 |
| rs184828427 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189015 | ATTTTTTTTTGCTCA[A/C/G]ATTTATCTTTTAATT | 50807 |
| rs184839329 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130371317 | TTCAAACAGAAGTCT[A/G]TCTAATTTCAAAGTT | 50807 |
| rs184841490 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130386399 | GTTCCATTGCCGAGT[C/T]CATAGCTTGAAGCTC | 50807 |
| rs184841995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195887 | AACATACATCTTCTG[C/T]TCTGATTTTTAAAAT | 50807 |
| rs184845123 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130177096 | AATTAACTCCTGAGC[A/G]GAAAAGCCTTGCTTT | 50807 |
| rs184850456 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130059552 | CCCTGAACTCCTGGC[C/T]TCAAGCGATCCACTC | 50807 |
| rs184851788 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402368 | GCAAAAGTGTTCACC[C/T]GGCAAAGGAAACCAG | 50807 |
| rs184857362 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423934 | GGGGGTGACTGCTAA[A/T]GAGTATGGATGGAGT | 50807 |
| rs184864432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100005 | CTTTAATATACTGAT[C/T]TCCTTTGCACTGGAT | 50807 |
| rs184885407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177692 | TATAAGGTACAATTT[A/C]CTTTGAAAAAAAGTT | 50807 |
| rs184891017 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063607 | TTCTTGAGACCTGCT[A/G]CATGACGTAGCTTCA | 50807 |
| rs184908565 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140592 | GGAATTTATATGGTT[A/T]AAGTCATTCCATGAT | 50807 |
| rs184920655 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130278791 | TGGGCCACCCAACAT[C/G]TACTCACCGTACCCA | 50807 |
| rs184927301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171662 | CCTGCCAAACTCTCT[C/T]TTATCAAGACTCAGC | 50807 |
| rs184929102 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218234 | TCTGATTTTGGAGAC[A/C]TATGAAAAAAGAATT | 50807 |
| rs184932232 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380173 | GGGAAGTGATCCCAA[C/T]TAGATGAATGGGGAA | 50807 |
| rs184948645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395283 | GCTTTCTAATATTAC[A/G]TACGTTTGACACGTC | 50807 |
| rs184953935 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409439 | CCTGATTTAGGCATC[C/T]GTAACCTCAGGCCAG | 50807 |
| rs184956371 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130416916 | TATAAACACATCAAA[A/T]CTTGAATGACTATGA | 50807 |
| rs184963899 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081678 | ATTCATCCAGCCTTC[C/T]TTCCTCACAGCATGA | 50807 |
| rs184982135 | snp | C/G | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083057 | TTATTAATGCAGGTT[C/G]CATGTGCTATACATG | 50807 |
| rs184983496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292749 | AAAAGCAAGCTCCCA[A/C]CTTCTTGGAATTTTA | 50807 |
| rs184989137 | snp | A/G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130153620 | CAATCTGCCCGCCTC[A/G/T]CCCTCCCAGAATGCT | 50807 |
| rs184989334 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068470 | GTTTCATTCTGTAGA[C/T]CAGTATCATCAGCTT | 50807 |
| rs184997891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137741 | TAACTTATCAGCAAA[C/T]CTCTTGGTCACACAT | 50807 |
| rs185000213 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086411 | TGAGGCACTTACAAG[A/T]GATGGCCTTATAAAA | 50807 |
| rs185004922 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120304 | GTGAAAGGCAGCTAC[C/T]GTGTTGATGGATGGA | 50807 |
| rs185009043 | snp | A/C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130103334 | CTTGTCAATTTTTTT[A/C/T]ATCTTTTCAAAAAAA | 50807 |
| rs185018370 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324762 | ACCCAGACAGTTAAG[A/G]TTCTTGTAATGAACA | 50807 |
| rs185026602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344650 | GCTGAAGCGAGATCA[C/T]TTGAGCCCAGGAGAT | 50807 |
| rs185027865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130441932 | GTACATTATGTGCTA[A/G]GATACTGCCCTTTTT | 50807 |
| rs185028625 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362044 | ATGGCAGGATGCACT[C/T]TGTCGCCTTGAAAAA | 50807 |
| rs185042522 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055682 | CAGTTACCTGTAAAA[A/G]TTTTCTAATTACCTC | 50807 |
| rs185052214 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392748 | GCTTCAACTCGTGGC[A/G]GAAGGGGAAGGGGAG | 50807 |
| rs185075424 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430332 | GTTTGTACGTACGTA[C/T]GTGTTAGGATGGCAC | 50807 |
| rs185090053 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383571 | TCTTCACTGCAGTGG[C/T]GTGTGGGATCTAATA | 50807 |
| rs185095764 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130367381 | GTAAAAGTAATTTGA[G/T]GTAACGCTCTCTCTC | 50807 |
| rs185096071 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130398686 | CAGGCACTGTTCCAA[A/G]TGCTTTAGCTTAACT | 50807 |
| rs185098734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100200 | TGTCTTTTTGATGAT[A/G]GCCATTTTAACTGGA | 50807 |
| rs185104393 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397872 | GTATTTACCTCTTTC[A/C]TTTTCCTCTAGATAA | 50807 |
| rs185104615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421378 | GAGCCCCATTCACCA[C/T]CTGTGGCAGCACTGC | 50807 |
| rs185132284 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130267483 | GGAATAAGAATATGA[C/T]GATGATTTTACAGAT | 50807 |
| rs185136234 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130303676 | ATCTGAAAAGGCTAC[A/G]TACTTTACTTTATGA | 50807 |
| rs185136835 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270771 | GGAAAAAACAGTCCT[G/T]AGAAAAGAGTTACAG | 50807 |
| rs185140371 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130235008 | ATTAGGGGCCTTAGA[C/T]GGTCTCTCCTTTTGT | 50807 |
| rs185140624 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313682 | ATAAAATTAAATTAA[C/T]TTCACTGCCTAAAAC | 50807 |
| rs185149586 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130250943 | AGATACTGAATGCAC[A/C/G]TCAGGCTATCAAAGA | 50807 |
| rs185154172 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130328207 | AATGACCACGACTGG[C/T]GGACAAAAAAAAAGG | 50807 |
| rs185160878 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286477 | AACTCCTTCATGTAC[C/T]GATGGAGTTGTAGTT | 50807 |
| rs185168878 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130368055 | CTAGGGGCTCTAATT[A/C]AGAAAAAAAAACAAG | 50807 |
| rs185170623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347200 | TCACTTTGGATTTAG[C/T]GGCAATGGGATGTTT | 50807 |
| rs185170952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130305416 | CAGTGGTGCGATCTC[A/G]GCTCACCGCAAGCTT | 50807 |
| rs185187242 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130346357 | TTAATACACTGTCAG[G/T]AAGTTCTTCTGAGTC | 50807 |
| rs185207842 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215502 | TAATCCCAGCACTTT[A/G]GGAGGCCAAGGCGGG | 50807 |
| rs185215113 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383258 | CAGGCTCCAGCCCCT[G/T]GGAGGAGTGCTTCCT | 50807 |
| rs185230918 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130420692 | TGAGGTCAGGAGTTC[A/G]AGACTAGCCTGGCCA | 50807 |
| rs185231466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130290101 | TATCTCCAATACTAG[C/T]ACAGCAATAGCAACA | 50807 |
| rs185232774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323555 | GTGCCATCTGCAGAA[A/G]AGCTGAAAGTTCTAT | 50807 |
| rs185235740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284124 | GGACAAAACCCATCC[C/G]TGAGAAGAGATTAAA | 50807 |
| rs185238596 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350264 | CTCCCAGACTGTGAA[C/T]TGCCAGTCCCCACAA | 50807 |
| rs185246121 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385953 | ATGATCAGGTGACAT[G/T]GGCTTGTCCAATCAG | 50807 |
| rs185266643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319167 | CCTTGGTGAAGAACA[C/T]TAAGATGGCAAGGAA | 50807 |
| rs185267115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423187 | CGGCTCACTGCAACC[C/T]CCAGCTCCCAGGTTC | 50807 |
| rs185272611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247262 | CTTTTCTCCCCAGTA[C/T]TGATGATGATAAAAT | 50807 |
| rs185279139 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209297 | TACTTAACGGTAGGG[C/T]TGGAATCATAACAAA | 50807 |
| rs185285195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229110 | TTATGGCACTGATTA[C/T]CAATGAAAACCAGTT | 50807 |
| rs185303280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262854 | GATTTCCTTGAATGA[C/T]GCGCTAATGAAAAAT | 50807 |
| rs185324231 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148435 | AGATGAGTAAGATGC[A/G]GTCCCTACCTCCTAG | 50807 |
| rs185334735 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130308798 | TGTAATCCCACCACT[A/T]TGGGAGGCCGAGGCA | 50807 |
| rs185357222 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130184695 | CAGAGTAAGTCTTAA[C/T]TAGTAAAAGCACTAT | 50807 |
| rs185357564 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370214 | GGCTGAGGCAGGAGA[A/C]TAGCTTGAACCCAGG | 50807 |
| rs185369983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343705 | ACACAAATATTCACC[C/G]CTCCAAGGTGAACAA | 50807 |
| rs185371118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280606 | CTGTAGCATTATCCA[A/G]ATCAACAAAAGGCAA | 50807 |
| rs185372212 | snp | A/T | 0.00179458 | 0.029901 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401834 | CAAGAAGAATCCCGC[A/T]GTATCTCCCACGCCG | 50807 |
| rs185375438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106026 | CTTCCCTTTCCACAC[C/T]CTGGCAGTCAGGTGA | 50807 |
| rs185376581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306711 | CATTCATATATTTAG[A/G]GTAAACTTTAAGTAA | 50807 |
| rs185389145 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341886 | CAAACTAGGAGACTC[C/T]TGGCATTGTTTTCTA | 50807 |
| rs185396720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377940 | TCTCTTCGGATTACC[C/T]TATTTCCAGTGTGCT | 50807 |
| rs185404888 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ASAP1 | GRCh38.p7 | 8:130051645 | TGTGTGAATGAATGC[C/T]TCTGAGCCTCATTTG | 50807 |
| rs185411909 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069178 | CCCAGCAGGGTAGAA[A/G]TCTTTAGATGGTTAT | 50807 |
| rs185416209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087788 | GATCTAAAAAATAGA[A/G]AGCTGCTGACAACAA | 50807 |
| rs185418039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208648 | GGTCATCTTCGATCA[C/T]CTTCCTGCCCCAGTA | 50807 |
| rs185422758 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417464 | CAGTTTTCTTGGCTC[A/G]CTCTGACACAAGTGA | 50807 |
| rs185431926 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246999 | ACATAGCCTATCACG[C/T]GGCAAGCTACCATCT | 50807 |
| rs185432893 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438461 | CAGCTTTGGAACAAG[A/G]TTTTAGCCATACAAA | 50807 |
| rs185453792 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130132792 | AATTAGACCTTTCTC[A/G]TCCTTTTCCTTTGTC | 50807 |
| rs185458738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140135 | CCTCCTAGGCTCAAG[C/T]GATCCTCCCACCTCA | 50807 |
| rs185462126 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130207655 | GTATTTTAATACAGG[C/T]CTCATTAAAAATCAA | 50807 |
| rs185462623 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114458 | TTTCCATAAATGGAG[C/G]TGGAAGGACTGGAAG | 50807 |
| rs185482393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167012 | TAGGATTGAAAATCT[A/G]TAGTCATGGGGCTGG | 50807 |
| rs185489767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146326 | CCCCTTAGCATATAC[C/T]TTCGTATATGCTAAG | 50807 |
| rs185490491 | snp | A/G | 0.00817203 | 0.0633974 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060544 | TGCAAAGTGCGGAAT[A/G]GGGTTCCTAAGGGCC | 50807 |
| rs185491152 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107328 | GCTGGGACTACAGGC[A/G]TCCTCCACCACACCC | 50807 |
| rs185494139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322407 | AATCAGGTGTCTTGA[A/G]TCCCCGCTGTCTCCT | 50807 |
| rs185496263 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078134 | AGCTGGGACTACAGG[C/T]GCACCCCACTATGCC | 50807 |
| rs185498508 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130129774 | CTCACCTTCAGTATG[C/T]TGGGAGAAACGCATA | 50807 |
| rs185499923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097895 | ATCTCTCCACTTAGC[C/T]CAGAAAAAATGTCCT | 50807 |
| rs185511840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299930 | ACAAATCTTCGTGGT[A/G]GACTGGAAAACCACT | 50807 |
| rs185517704 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359474 | AGCTAGGCCTTTGGG[A/C]AGGGCCACAGGATTG | 50807 |
| rs185520505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249581 | AGTTTCACTGCCCCC[C/T]TTCCCCAATTAAGAA | 50807 |
| rs185522320 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073105 | AATTCGGATTATGGA[C/T]GAATACTTTGGTAGG | 50807 |
| rs185525057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205807 | GTGTGCTGCATAATA[C/T]AAGGCATGTACACCC | 50807 |
| rs185530824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130225325 | TTGGGTTTCCGGCCT[C/T]ATGTTCCTAAGCCTT | 50807 |
| rs185531025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269336 | TTCTGTGATACAGTT[G/T]CCAAGTAAAATAGCC | 50807 |
| rs185534999 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130320034 | TTAGTATTCACAAAA[C/T]TAGCACACAATCTTC | 50807 |
| rs185535767 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394051 | CCCTGTGATGATTGC[A/G]TTAACTGCACAAATT | 50807 |
| rs185539093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130304866 | AAAACAAACAAATGG[A/G]AAACCCAAAACAACA | 50807 |
| rs185545992 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130186147 | CTTACAAGTTGAGTA[C/T]TCATGACCCACTTTT | 50807 |
| rs185557689 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146575 | AGCCAAGGAGAGCTC[C/T]GAAGGCCAGTAACAG | 50807 |
| rs185566012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189471 | GTTGGATCCATTTTG[C/T]GGCAAGTGGCATGAC | 50807 |
| rs185566964 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130620 | TAAACGTCGCTTTGA[A/G]TTTTATAAGATAAAA | 50807 |
| rs185573337 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262032 | GAATACTTTTTTCAC[G/T]TGCTAACAACCAGCA | 50807 |
| rs185577845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421536 | ATGCCATTCTTCAGG[C/T]CAAGGTTTTTAAGAA | 50807 |
| rs185585381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228923 | GAGAAAAATCAGCAC[A/G]GGGTGTTCCAGTCCC | 50807 |
| rs185590684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183010 | GTCTAGGAAGTCAAA[C/T]ATTATATAATGAAAA | 50807 |
| rs185595211 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165015 | AACAGCATGAGAAAG[A/G]AACAGGCATGTTGTG | 50807 |
| rs185602020 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130232382 | GAAAGGGAGAGGGAC[C/T]ACTAAGGCAGACTTC | 50807 |
| rs185613268 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126876 | GCTTAAGAATACCAG[C/G]TTTGCATCCTTGTTC | 50807 |
| rs185628522 | snp | A/C/G | 0.02016 | 0.0983543 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158905 | CCTGGCTAATTTTTT[A/C/G]TATTTTTAGTAGAGA | 50807 |
| rs185638941 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055966 | CATCTTTACATCTGG[C/T]GAGGCACGTAATGGT | 50807 |
| rs185656449 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130443940 | CATGCCCCGGCCGGC[A/C]GGCCTCCTCCCCGCC | 50807 |
| rs185656951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090539 | AACACCAAACTCCAA[C/T]GTCTCCTCTTCTCTA | 50807 |
| rs185662990 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399433 | ATGCCATTTTGTGCT[A/G]GACTCTTGACTTAAA | 50807 |
| rs185663881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058580 | AACACAGCAGGATCG[A/G]CCTGGGGCTCGGAGA | 50807 |
| rs185675358 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094387 | AGCTAATTTTTAAAA[A/T]TTTTTAAATTTTTAG | 50807 |
| rs185716897 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248928 | AGCAGCATTTCTTTT[C/T]TGTTGCTTTCTATTT | 50807 |
| rs185728246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187111 | GGATATACTAAACAG[A/G]TTTTTGTTGAGAAGT | 50807 |
| rs185729312 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213245 | AAATAATTCTATGTT[C/T]GATATTTATTTTCTT | 50807 |
| rs185733389 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143138 | GAAGGCTGTCTTGAG[C/T]AGCATCTCTTTCAAA | 50807 |
| rs185745483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168620 | GAAACAAACAAACAA[A/G]AACCCCAAAAAACTC | 50807 |
| rs185749538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150828 | GAGGTTGCAGTAAGC[C/T]GAGATCGTGCTACTG | 50807 |
| rs185768708 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111098 | GATTCCTCGTCTGGG[C/T]GCAGTGGCTCAAGCC | 50807 |
| rs185775404 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087286 | GCACTTTGAGAGGCC[A/G]AGATGGGTGGATCAC | 50807 |
| rs185837386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437467 | ACAGGTGGTGACTAC[A/G]GTAGACCCCAGAATC | 50807 |
| rs185843121 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130193404 | AAAAGACAAAAAAAA[A/C]CCCCAAAAAACTCTC | 50807 |
| rs185870077 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273973 | GGAGCTGGGGTCCAC[A/G]AGAAAAGTAAAGAGA | 50807 |
| rs185875785 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334229 | TGCTGAGGCACACAT[A/T]TAAAGAGGTACTCTT | 50807 |
| rs185890781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130371873 | TTTTGTTTGTACAGA[A/G]TTGAAATCTAATCCT | 50807 |
| rs185899163 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380730 | GAACACATGAAATTA[A/T]TTTAATTTTTTTAGA | 50807 |
| rs185904983 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199849 | AACAAAAACAAACAA[A/G]CAAACAGTTCTGTGG | 50807 |
| rs185912454 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395711 | TCACTCTGTCACACA[G/T]GCTGGAGTGCAGTGA | 50807 |
| rs185926882 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160988 | GACAGGACAATCAAA[A/T]GTCTGTATTTATCAG | 50807 |
| rs185947272 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130300499 | CACCTGGCAGCTTTA[A/C]AACACTGCTGCCTAG | 50807 |
| rs185949681 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238033 | GAACTTCAGACCAGA[A/G]AACTGAAGCCCACAG | 50807 |
| rs185952163 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392853 | CACGGGAACTAACAG[A/G]GTGAGAACTCATTCA | 50807 |
| rs185953673 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347734 | CCTCCTTCCCAGATA[C/T]CCTCGCCTCAGAATC | 50807 |
| rs185957477 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410129 | GAAAATGCATCTATT[C/T]ATCCACTAATATACT | 50807 |
| rs185962844 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219099 | TGGCATGTGCCCCAA[A/C]ATGTCAGCTACTGTT | 50807 |
| rs185966078 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431137 | CTCTTCCCCATCCCC[C/G]CTCCAAATGATCCCC | 50807 |
| rs185976442 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130357145 | TCTTTGCCCATACCA[C/T]TCTCTCATTAACTCA | 50807 |
| rs185977647 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130198035 | TGGGTCTTTTCTTCG[A/G]CCTCTTGAACCTGGT | 50807 |
| rs185990813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392987 | CATGGCACCGAGGCA[C/G]ACAGAAATTAAGTCA | 50807 |
| rs185993239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317242 | AGCAAGTGAGGGTTC[A/G]TTTTATTTTTCACTC | 50807 |
| rs186001431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130351938 | ATGAGTTCCAACATA[C/T]ACAATTTCCTTCTCC | 50807 |
| rs186005064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431784 | CTGGCAAATGGTAGG[C/T]ACTTAATACAGAAAG | 50807 |
| rs186013713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124893 | TACAGGTAATAGGTC[G/T]GTGTCTTTTCTCTAC | 50807 |
| rs186024554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356791 | ATCCCAGTTCTACGT[A/G]TGTGGAAACATGAGT | 50807 |
| rs186024732 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314285 | GATGCTCTCAAAACA[C/T]ATTGAAATGATGAGG | 50807 |
| rs186027184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130386899 | GTGACGTCCTTGTTG[C/T]CGTGGTTACCAACGC | 50807 |
| rs186027524 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295918 | AAGGAAACAAAAAAA[A/T]TTATGATATCCCATC | 50807 |
| rs186034787 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130377016 | GAAAAGAATCAGATC[A/T]TCTCAGAGTTGAATG | 50807 |
| rs186040556 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092428 | GGCCAAGAGTTTGAG[A/G]CCAGCCTGGGTAACA | 50807 |
| rs186042284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178196 | TTATCTAGTCCAAAC[A/G]ACCTTTACATTATTT | 50807 |
| rs186044812 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130331014 | TAGCTGTCCATTGGC[A/C]AGACCAGCCTTTCCA | 50807 |
| rs186048108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321479 | GGGACCTCAATTTCT[A/G]CATTTACAAAAAAGG | 50807 |
| rs186048707 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159756 | CAGTGTGCTAAAGGT[C/G]TGCAGCTAGTGTATT | 50807 |
| rs186051585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178709 | GCCAACACGGTGAGA[C/T]CCAGTCTCTACTAAC | 50807 |
| rs186052525 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107962 | GCCATGGTCTGGCTT[C/G]ACACAGACTGATCTG | 50807 |
| rs186052723 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141142 | GGAAATGCTTTCATA[C/T]TGTTTAAGTACAGGA | 50807 |
| rs186052882 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066183 | AAAATCTCCCCTTGC[A/C]CATATACCAAATGTT | 50807 |
| rs186056544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084737 | CAGTAACTGGGACAA[C/T]GACAGTCCCACTTCC | 50807 |
| rs186061037 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254615 | AAATAAAAATAATAA[A/C]ATTCAACTCAAAAGG | 50807 |
| rs186068320 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130255685 | TGTGTGTTTAAAAAT[A/C]TGATTATGAATTATC | 50807 |
| rs186071244 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273546 | AACACAGCAGCCAGG[C/G]TTCTGAACCCAGGAG | 50807 |
| rs186071912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130182178 | AATATGGAGGGACAG[A/G]CATAACTTAATAATA | 50807 |
| rs186074810 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130221079 | TCTCTACCAAAAATA[C/T]GAAAATTAGCCAGGC | 50807 |
| rs186077013 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237552 | TTTTGGCAATCTTTT[A/C]ATTTAAAAAAACAGG | 50807 |
| rs186084684 | snp | G/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280868 | GCTTGGTCATTAATA[G/T]CACCATTTCATTTAA | 50807 |
| rs186085902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258477 | GGATGTTTTAAAACA[C/T]TGAGTGTATCCTTCA | 50807 |
| rs186090245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224725 | TCCATAATAAATACG[C/T]CTGCTGAAAGGATAC | 50807 |
| rs186090831 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130291220 | AAATTCTCCTAGTGT[C/T]GAAAAATCTCAGAGA | 50807 |
| rs186096747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340718 | CAATTTGGGCATTTA[C/T]TGATCTTCTCTAAGC | 50807 |
| rs186101992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352439 | CACAGAAAATCACTT[A/G]AGGACCTAACAGTAT | 50807 |
| rs186105196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309484 | TGACATGAATGGACA[C/T]ATCATAAGATGAGGC | 50807 |
| rs186105882 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377237 | GGAAAGGGTAGGAAG[C/G/T]GGGTGAGGAATAAAA | 50807 |
| rs186118715 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130443805 | AGCATTCCCGGCCCC[G/T]AGCCGCTCCGCGCCG | 50807 |
| rs186126952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410793 | AGACACATTCCAACA[C/T]GGGCTCTCCCACCTA | 50807 |
| rs186140619 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199428 | ACCAGAATGGGGGAA[A/G]GGGCTAGATTCAGGA | 50807 |
| rs186140828 | snp | A/C | 0.00993785 | 0.0698258 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220511 | ACAAGCCACTTCGGC[A/C]TAACAATTATTTTGA | 50807 |
| rs186153710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276891 | TCACAGTGCCAGGAG[C/T]GGTCTTGGCAGACAC | 50807 |
| rs186157629 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247872 | AACTAGTCTTGACAA[C/T]GAGCATCATTTTCAC | 50807 |
| rs186163493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281551 | GTACTGGTCCAGATT[C/T]TCAGGCTAAAAAACT | 50807 |
| rs186163745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263951 | TGACTCACACACATT[C/T]TTCTTGCCACAGACC | 50807 |
| rs186169562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317563 | TTTTTATAGCCTCCT[A/C]TCCCAAATGGAAAAG | 50807 |
| rs186178038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301400 | TCTGTTACCTAGTAG[C/T]ATTTTAATGTAAATT | 50807 |
| rs186180116 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334647 | AGAGGGAAAAAAACA[C/T]AAGATGAATGAAAAG | 50807 |
| rs186195844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205037 | TTTATCAAAGAGATA[C/T]TGATTAGCAAAATGT | 50807 |
| rs186200625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277145 | CTCCTAGTTGATTAC[A/G]ATGCATGCTCTAGCT | 50807 |
| rs186203615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164187 | GTCAAACCTGCAAAC[A/G]ATAATGTGATGGGGT | 50807 |
| rs186211774 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241185 | TCTCTGGATGACTGG[C/T]TCTTTCTTCTTACAC | 50807 |
| rs186212144 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173716 | GAAGCTGCAGTGAGC[C/T]AGGATTGTACCACTG | 50807 |
| rs186226759 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130138165 | CATACAATCAAGACA[A/C]CTTCAATGACACACT | 50807 |
| rs186234877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114873 | TCAAACTCCTGGGCT[C/T]AAGCAATCCTCCTGC | 50807 |
| rs186247599 | snp | C/T | 1.65244e-05 | 0.00287436 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130214652 | ACTTAAAAAATTACT[C/T]CCAAACTTATCAAGA | 50807 |
| rs186260500 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122722 | TGACCCTAACCACTA[A/C]ATTAGAGATATTGGA | 50807 |
| rs186261791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104140 | GCTCTGGGTACTCAG[C/T]ACACAACTGAAAAAG | 50807 |
| rs186282237 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204578 | CCCTCCCATTTCCAG[C/G]TCTCCTGCAGCTAGG | 50807 |
| rs186284417 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | ASAP1 | GRCh38.p7 | 8:130174444 | ATAACAAGATCTTCA[A/G]AAACCAGTAACAGTA | 50807 |
| rs186287202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088570 | AGAAGCTGAGAGAGG[C/T]AAGAAACAGATTCTT | 50807 |
| rs186294824 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155490 | TCCCACCTCGGCCTC[C/G]TGAGTAGCTGGGCCT | 50807 |
| rs186295020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106324 | CTGTAAAGTCATCAA[C/T]ATATGAATAACACCA | 50807 |
| rs186306784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139016 | CATATAAATGACAAT[C/G]GCATATGACCACCTG | 50807 |
| rs186340031 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259120 | ATGACCTGAGCTGAT[C/G/T]TGAGAAATAACAATC | 50807 |
| rs186345776 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296589 | TTATCATTCATTACA[A/C/T]GATACTTCCTTCTGG | 50807 |
| rs186354206 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134031 | AGGTTATGAAGAGGC[C/T]GCGGGCAAGGAGTAG | 50807 |
| rs186361262 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117281 | AAATACTAATAATAA[C/T]CGCTTTTACAGATAA | 50807 |
| rs186373553 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155167 | ACTCATTAGTTTTAC[A/T]TACACATGTATATTA | 50807 |
| rs186373979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100804 | TTGTCTCTTTGCTCT[C/G]ATTGTTTCTTTTGCT | 50807 |
| rs186382442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130065479 | AGATGGGAAAAGATT[A/G]GAGTCCTGCCTTGGG | 50807 |
| rs186383680 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149226 | AGCATCTTATACTGT[G/T]TTTAGAACATACTAG | 50807 |
| rs186388808 | snp | A/T | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083383 | CCTTTAGAGTCACTT[A/T]CTGAGAATTCTTCCA | 50807 |
| rs186389756 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133723 | TCCAACCCAGGAGTA[C/T]GTGATACCAACCTGT | 50807 |
| rs186390238 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234212 | TTTCTATTTCTGCAC[C/T]ATCCAATATGGCACC | 50807 |
| rs186394088 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130100592 | CCTCGGCCTCCCAAC[A/G]TGCTGGGATTACAGG | 50807 |
| rs186405187 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066101 | ATATTGTGATACAAT[C/T]GTGGTACAATTTAGC | 50807 |
| rs186411854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191612 | TTAGTGGCAGAGGGA[A/G]AGAGTGGTGTGAGAA | 50807 |
| rs186433503 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098523 | TAATTTTTGTATTTT[C/T]TTAGTAGAGACAAGG | 50807 |
| rs186442930 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130121643 | CAAAAAACTAGTCGG[G/T]CATAGTGGCGCATGC | 50807 |
| rs186512055 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130314035 | AAGTCAATCTGAATA[C/T]AGAAGTACTGCATGT | 50807 |
| rs186512895 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347477 | GTACCATCATTTACA[A/T]TTAACTGTCATGTCA | 50807 |
| rs186513686 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060142 | CAGAACCCCGAGAGG[G/T]AAATTGGTTTCTCGT | 50807 |
| rs186522892 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404239 | TTCCTTCAAACTTAG[A/G]TGCCAACAGCAATTG | 50807 |
| rs186529082 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425615 | GAGTGACAGATGTTT[C/T]GAAAAGGTTAAGCAT | 50807 |
| rs186529621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384223 | TTACCAGCAGGGAAG[A/G]GCCTCGCTGATTAAA | 50807 |
| rs186550138 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056658 | AGTCAAAGGTGAATG[A/T]GTGCCCATGCCTATG | 50807 |
| rs186566412 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335048 | TCACTGGGTATGAGA[C/T]GGATTAACGATCACT | 50807 |
| rs186574989 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130266190 | CCAGCACAGAGAGAT[G/T]CAAGAAAGCTGGTCT | 50807 |
| rs186576679 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353011 | CTGGGCCTAGCACAC[C/T]GCTGGGCACATAGGA | 50807 |
| rs186582805 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130230740 | TCAAAAAGATTTTTT[A/T]AAAAATCTGGCTATC | 50807 |
| rs186590003 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130248214 | TGCTGAGGAATGTGG[C/T]GGGTGCCGGGGGGGT | 50807 |
| rs186590568 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130372803 | AATTCAGATTGAAAT[G/T]TATTACAGTCCTTTC | 50807 |
| rs186593357 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117614 | AAGTCCAAACTTCCT[A/C]TATTCACTCTTATAC | 50807 |
| rs186595386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130388952 | AGCAATGTGGCCTTA[A/C]ATAATTTTCCAAACC | 50807 |
| rs186597523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130369089 | ATTGTTATACAGAAT[C/G]AATTAGATAATACAC | 50807 |
| rs186602263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396786 | TGACAGCCTGTGGCA[C/T]GATAATGACAGGGCG | 50807 |
| rs186605530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130282896 | AGTGGGTTTCGCTGC[A/G]GCAAAGTTACAACAA | 50807 |
| rs186614651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418325 | GAGGGCCAGGCGGGC[A/G]GATCATGAGGTCAGG | 50807 |
| rs186616781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170178 | AAGCAATATCAAGAC[A/G]TTTTAAGGAATATCT | 50807 |
| rs186619577 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399880 | GGAGTAGTACAATGG[C/T]GCAATCTCGGCTCAC | 50807 |
| rs186622512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439480 | CTATCACCCCCATCA[A/G]TAATAATAATAATAG | 50807 |
| rs186623653 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083828 | GATGGAGTTTTGCTC[C/T]TGTTGCCCAGGCTGG | 50807 |
| rs186632297 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211931 | AAGTATGGGTTCCCA[C/T]GGGGGTACTCCTGAG | 50807 |
| rs186642270 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188769 | AAGAAAATTGAATTT[A/G]GGTGGTGTAGCTCCA | 50807 |
| rs186642856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311890 | TAAGTAAACAAAAAC[A/T]ACTCAAAAAAAAATA | 50807 |
| rs186651756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130305068 | CTACCTGAGGACCTT[C/T]GTGCTGTCGGACCCC | 50807 |
| rs186661333 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130326212 | CCAGCGCATATCCTT[A/C]CTGCTGGAGACCGAC | 50807 |
| rs186673731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130365372 | GTGTTTTGAATTGAA[C/T]TGGCTCCCTTTTATG | 50807 |
| rs186674947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130346158 | CATTAAAAACAAAAC[A/G]AGTTTAAAAACCTAG | 50807 |
| rs186682644 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339611 | ACAAAATCATCTTAG[A/G]GCTCAAACACAAAAA | 50807 |
| rs186683515 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382480 | AAGGAGAAGCAGAAC[A/G]GGGAGGAAGGACCAA | 50807 |
| rs186701168 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434113 | TTGAGTCCAGGAGTT[C/T]GAGACCAACTTGGGC | 50807 |
| rs186711806 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130234746 | CTCGTGGCTGTAAAG[C/T]AAGGGTCTCCCTTTT | 50807 |
| rs186718341 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130329537 | AGAAAGTGGCATGGG[C/T]GGGTGGCTATACAAC | 50807 |
| rs186736366 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270013 | CATCTCTACTAAAAA[C/T]AGAAAAATTAGCCAG | 50807 |
| rs186739944 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368476 | TCCTCCCTGACTCCA[C/G]GTAATTTTCTAGACT | 50807 |
| rs186772451 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099368 | TGTATTTTTAGTAGA[C/G]ACGGGGTTTCACCAT | 50807 |
| rs186772732 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166110 | TACTACAGCCTCCAC[C/T]TCCTGGGCTCCTCAG | 50807 |
| rs186777171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115396 | ATCATGTGAGCCAAT[C/T]CCTTAAAAAAAATTT | 50807 |
| rs186777364 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130194041 | GGCATGAGGGGAAGA[C/T]AGAAAACCCCAAGAA | 50807 |
| rs186778795 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388001 | TAGGAAGAAAACATA[C/T]GGGGAGCAACCAAAG | 50807 |
| rs186779285 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148038 | TTCTTAGAACACTTG[C/T]ATTATCTTCATGACA | 50807 |
| rs186779550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175420 | TTGTAGAGACAGAGT[A/C]TCCCTGTGTTGCCCA | 50807 |
| rs186784676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073404 | TCAAAAAAAAAAAAA[A/G]ACAAATACAAATGTG | 50807 |
| rs186784726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131113 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 50807 |
| rs186793400 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425285 | TACAGTGAGGTGAGA[C/T]TGTGCCACTGCACTC | 50807 |
| rs186803162 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062486 | ATTTACATGAATCTC[A/G]TTCCTCTCTTGGAAG | 50807 |
| rs186804950 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080982 | AAGGCATAAATGTGA[A/G]GCAGAAGGCACAAAA | 50807 |
| rs186805862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332142 | ACCAACATCTGAAAT[C/T]TTCCATTCAACTTTG | 50807 |
| rs186819925 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322498 | ACTGGCTGCCAAATC[C/G]TTCAGGCTGCAGATG | 50807 |
| rs186824798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348348 | GGGCTTTACCTCCTT[G/T]GCATATGAGGTTCTG | 50807 |
| rs186824852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306922 | TTCACTCCACCCAGG[C/T]CTGAGTGTCTGTACT | 50807 |
| rs186828886 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130369321 | TGAAGGTAATCTTAT[A/T]CTATATTTTTAATGA | 50807 |
| rs186830563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385099 | CCTCCTTCTACTACA[C/G]AGACATGGCCTGGAG | 50807 |
| rs186839081 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384940 | GAGAGGCAGAGACTG[A/C]ACATAAATAAAAGCG | 50807 |
| rs186849162 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130207636 | CACACAAGTAAGATG[C/T]TGAGTATTTTAATAC | 50807 |
| rs186855243 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422501 | ACAGTGTACTTTCCC[A/G]CCTTCTCCCTTGCCT | 50807 |
| rs186856241 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227927 | CCTTTCTGGGTGCAC[A/C]GTTGGCGAGTCTGAG | 50807 |
| rs186870173 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130184187 | AGCAATGAATGCTTA[C/T]ACCTATAAAAATGTA | 50807 |
| rs186878289 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187517 | AACTCCCAGGCTCAA[C/T]TGATCTTCCCACCTC | 50807 |
| rs186892838 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151427 | GATTGCTGAAGAAAT[A/G]AATAACTGTTAGACA | 50807 |
| rs186904510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229566 | TGAATCTTTATGTAA[A/T]CAGTGAAAATAACTA | 50807 |
| rs186918950 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215119 | GTTGGTGAGGCTGGT[C/T]TCAAACTCCTGACCT | 50807 |
| rs186927479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253887 | TTAGCCAGCCGTGGC[A/G]GTGGGAGCCTGTAAT | 50807 |
| rs186941931 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130118345 | ATTATAAGGAGCACA[C/G]CTCTTCACTCTCATA | 50807 |
| rs186956678 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286159 | CAGTAATCTGCTCAA[C/G]TTCTCACAGTATCAA | 50807 |
| rs186964666 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130250435 | ACTTTTTGTCACGTC[A/C]AAGTATGGCGCATGC | 50807 |
| rs186967211 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373802 | CAGTGAGCCGAGATC[A/G]TGCCACTGCACTCCA | 50807 |
| rs186976126 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372032 | ATTGTATATTTAAGA[C/G]GCTTAGGGATCCTAC | 50807 |
| rs186999568 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403702 | GGATTACAGGTGTCC[A/G]CCACCACGCCCAGCT | 50807 |
| rs187016943 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130282104 | TGGCATGGCAAAAAT[C/T]GCAATTACTCTTGCA | 50807 |
| rs187049391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141752 | AGACAGGATTTCACT[C/G]TGTTGCCCAGGCTGG | 50807 |
| rs187055051 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070551 | TGGAGCAGTTCCTGG[G/T]GCTTATGGCAAAAGT | 50807 |
| rs187064586 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130089167 | CAAAAGGCCTTTTAA[A/G]TAGATCCCAGGACAG | 50807 |
| rs187069479 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123679 | TTGCCCAGGCTGGAG[C/T]GCAGGGGTGCGATCT | 50807 |
| rs187071323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106966 | TAAACTGAAAACATG[A/C]AGGAGGATTGAACAA | 50807 |
| rs187077678 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130169312 | ATTTGATAGAAGATA[C/T]CACAAGGACACTGGA | 50807 |
| rs187087125 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178463 | TGCAATATAGGCAAA[A/C]AAAAATGGTGCCAGT | 50807 |
| rs187091161 | snp | A/G/T | 0.487524 | 0.140996 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055297 | GATACATTTAAAAAA[A/G/T]AAAAAAAAAAAAAAA | 50807 |
| rs187100298 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073983 | GAGAAATCTATAGAA[C/T]GAATAACACAGTTTC | 50807 |
| rs187103062 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377410 | AGACCATGTGTGATC[A/G]ACAAGCAGACATTGC | 50807 |
| rs187104814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273237 | CTAGTTTTAGTGTTG[C/T]AATTATCATTTCTTA | 50807 |
| rs187107900 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393758 | GAGACTCTGTGTTGC[A/G]GGAAGTCAGGGACCC | 50807 |
| rs187115036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108478 | GCCTACCAAGTGCCC[A/G]GTCTCATTATCCAGA | 50807 |
| rs187116749 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130237298 | GAAGAAATCTTAAGG[C/T]TTGGATTCTTTCATG | 50807 |
| rs187128921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101374 | GATTGCTCTTGGTAG[C/T]ATGATCATTTTAACT | 50807 |
| rs187151021 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134816 | TCATTTTCAATTCAA[C/T]TGTTACTGTGTTTTC | 50807 |
| rs187159609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287328 | AGGGTAGGTAAGGTT[A/C]CTTCAGATTAGGAAG | 50807 |
| rs187160523 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261266 | TAAACACAGGCCAGT[C/T]ACTTTGGTGCTCAAA | 50807 |
| rs187163031 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130072408 | TTTATAAGGGGTTTC[C/T]CCTTTTGCTTGGCTC | 50807 |
| rs187165073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278906 | TTAGAGAGTGTTAGG[C/T]ATGTTTACAAAGCCC | 50807 |
| rs187171139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130305994 | CCCTTACTTACAGTT[C/T]CAACATCATCAGGGC | 50807 |
| rs187171268 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245055 | AGCAGCAGTGCAGAA[C/T]ACTTGCCAACAGAGG | 50807 |
| rs187177243 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130341255 | AAAATGGATGTATGG[C/T]TCAAGTGTTACAATG | 50807 |
| rs187180812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321768 | CCAGAAAGATACCAC[A/G]TTTGTCTTTTAACAT | 50807 |
| rs187184218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130357571 | AGCTACGCCTGCCTG[A/G]TCCAGTCGGGCCGCT | 50807 |
| rs187186512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163823 | ACATAAAACATAAAC[A/G]ATGAACTTAAAATCT | 50807 |
| rs187197804 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129425 | CGACTTTGTGCCTTT[C/G]TATAATTTTTCAAAA | 50807 |
| rs187201674 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074716 | GGGGTGGACTCCTGT[C/G]CTGACTCAATGAGGA | 50807 |
| rs187203312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411736 | ATGACAGCCCAAAAC[C/T]AGAAATGACATCTGC | 50807 |
| rs187207507 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130125815 | CCACAAAAGTTACAT[A/T]TTAAACGTCTACGCA | 50807 |
| rs187207789 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093786 | TTATACACTCTTCAT[A/G/T]TTAAAAAAAAAAGTC | 50807 |
| rs187208236 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434585 | TTTCCCACAGCATCA[G/T]GACAAATGCTCCTAC | 50807 |
| rs187211298 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445624 | AGATTCAAAAGGGAA[C/T]GCCCAGTGCGGTGGA | 50807 |
| rs187212096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264758 | CTTCTAGAAACATGC[C/G]GGGTGACAGTGCTGG | 50807 |
| rs187221995 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109125 | GGGTGGGGGCAGGGG[G/T]AAGCTACTGATCACA | 50807 |
| rs187222441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323966 | TGGCTCCCAGAGCTG[A/C]CAGGGCTTCCTAACA | 50807 |
| rs187234577 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160680 | ACAGCCATTACATTA[C/T]GAAAATGTAAGAAAT | 50807 |
| rs187239928 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057388 | CTCACAAGGTTACAT[C/G]ATACCATGGGTAAAG | 50807 |
| rs187250347 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130125301 | AGGCTCCCCTTCTGT[A/T]TTTTGGTATATCTCG | 50807 |
| rs187270554 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096232 | AGCTCAGAAGACTTC[C/G/T]AAAATTAGTAACCAG | 50807 |
| rs187273932 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377666 | CTCAGGGCTCCTCCA[C/T]CCTCTGGCTTCTACC | 50807 |
| rs187276513 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069843 | ATGGGGCAGACTAAT[A/C]AAAATAAAGATTGAC | 50807 |
| rs187276961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394045 | TCAGGACCCTGTGAT[A/G]ATTGCATTAACTGCA | 50807 |
| rs187280897 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093163 | CAGCAGGAATGATAG[G/T]AATATTCCACATACA | 50807 |
| rs187307445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422930 | ATCCATCTGCTTCAC[C/T]TCCAACACTTTAAAG | 50807 |
| rs187328858 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057081 | TTTCATTTAATCTTT[C/T]CCTAAAATTACGTGG | 50807 |
| rs187368012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283453 | CATGGTGGCATGCGC[A/G]CCTGTAGTCCCAGCT | 50807 |
| rs187376068 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344261 | GATCTCATACAGATC[A/C/T]GTTTAAATAAACCAT | 50807 |
| rs187392964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318725 | AACTACTACGTGATA[A/G]AGTTGGGGTTCAGTC | 50807 |
| rs187393789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317965 | TCACTTTTACCAAAA[C/T]AGCTAAAACAAGGAA | 50807 |
| rs187395271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130303279 | TAGCACAGCAAAACT[A/G]TAAGTGTATGCCTAA | 50807 |
| rs187398094 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337127 | GGAAAGGCTTGGGCA[G/T]CAACAGCAAGAAAAT | 50807 |
| rs187406392 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145792 | AAAGGTTAAGTTAAC[G/T]CAGCCTTAAGGTCAC | 50807 |
| rs187410702 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130441789 | TGCGAAAAGTCCTTT[C/G]TCTCCAACATTATCA | 50807 |
| rs187414327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415719 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 50807 |
| rs187421102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354408 | AATGAGCAGAACTTG[C/T]CTCCTTCATTGTCAC | 50807 |
| rs187429824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130181266 | ACACTGTATGGATTT[C/T]CATATGGGAAACCTC | 50807 |
| rs187435852 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277273 | TGGCCATTCACCTAA[A/C]AGATGGTTTCCTGTA | 50807 |
| rs187439526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077883 | AAGAAACAGTAAACA[C/T]GAGAGGGCTTTGTTT | 50807 |
| rs187447123 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297254 | AGTTCGTCTCCCCCC[A/T]TGCATCAAAATCTGT | 50807 |
| rs187448704 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217039 | GTTCCCAATCCTTGC[A/G]GGGTTACAGAAAGGA | 50807 |
| rs187449527 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130267156 | AAAAACAAAACAAAA[A/C]AAAACTAGTACAGCC | 50807 |
| rs187451976 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130259405 | AAAATGCTTAAAATT[C/T]ACTTTAAACCCTTGC | 50807 |
| rs187460345 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130053776 | TCATAACACAATATG[C/T]CAATCCATACTCTTG | 50807 |
| rs187482327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139869 | AATCTAGATTTCTCC[A/G]GTGTTTCTGAACAAT | 50807 |
| rs187484637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336556 | GTACCAGTTTTGGTA[C/T]TAGGCACTTTACATG | 50807 |
| rs187491398 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123860 | GTCTTGATCTCCTGA[C/T]CTCGTGATCCGTTTG | 50807 |
| rs187496607 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373576 | AAACTTGGCCAGGTG[C/T]AGTGGCTCACGCCTG | 50807 |
| rs187498450 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114199 | AAATGTGTTAGGTGA[G/T]TTCGTTCTTGTGCGA | 50807 |
| rs187500137 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195206 | ATGTTTTTTAAAGTG[C/T]ATTTTTTTCATTTTA | 50807 |
| rs187500345 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107234 | GTGGCCCAGGTTGGA[A/G]AGAAGTGGCACAATC | 50807 |
| rs187500590 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226278 | AATTTGTTTTAACTT[C/T]ACAGACACCATATTA | 50807 |
| rs187505650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130243101 | TCTACCTCTCCTTAA[C/T]CAGCTGCAGGCCTCC | 50807 |
| rs187510466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176511 | TCCCTACAAGGTTTT[C/T]ACTGTGTAGGGTTTT | 50807 |
| rs187511003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405633 | TCCCAGCCTGGCCTA[C/T]GTCACTAGACCATCG | 50807 |
| rs187512056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158573 | CTACTTATGCACTTA[C/T]TGTGAAGCAGAATCA | 50807 |
| rs187541964 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275596 | ACTTATAAAGCAATT[C/T]GTTCAAATTTTACTG | 50807 |
| rs187550761 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239499 | GCCTTATCTTCTAAC[C/T]ACTACCTAATTCTGC | 50807 |
| rs187555148 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187973 | ATTTTTTCCAATGAT[A/C]ATTTTCCAAGAGCAT | 50807 |
| rs187571377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136390 | ATCAATTCACAGAGG[C/T]TGAAGGCAGTTCTGC | 50807 |
| rs187576167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436738 | GCCCTGGATTAGAGG[A/C]TGCAGTGTGCTATAT | 50807 |
| rs187581270 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130221812 | CAAGTCTATCATTTA[C/T]TGTCTGTGTGGTACC | 50807 |
| rs187605332 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143781 | GTCTTTAGACAGCTT[A/C]GTGTGCACCATGGTT | 50807 |
| rs187611148 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130126523 | TCCCCATGAGCACTT[C/G]TTAGTAATAAGACAG | 50807 |
| rs187625814 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085489 | CCTGTAATCCCAGCA[A/C]TTTGGGAGGTCAAGG | 50807 |
| rs187626019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169804 | AGGTACAGAGTATGT[A/G]TAAAACTTGGTTAAG | 50807 |
| rs187626503 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130201441 | TAAGAGTACCAGGGA[A/G]TATGAGAATTCCTTA | 50807 |
| rs187626705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179427 | TCAGGTGGCTGAACA[C/T]CACCCCTGAATCTGC | 50807 |
| rs187635485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058605 | CGGAGAAGTCTATGC[A/G]GTTCCTAAAACAGTT | 50807 |
| rs187636685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101839 | CATCCTCCTAAAGTG[A/C]TGGGATTACAGGCAT | 50807 |
| rs187639682 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151937 | CTTTGTGCTTCAGTT[G/T]CTTCATCTGTAAAAT | 50807 |
| rs187640193 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130161730 | TAATCATTTGGGAGA[A/G]ATGAGGCATGGACTT | 50807 |
| rs187640641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301709 | TTATAGGTACATAAA[A/G]TGGGATCATCCTTTC | 50807 |
| rs187643848 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130118947 | CTTGACCAACAGCAT[A/G]AGAAATCAACTATTT | 50807 |
| rs187646966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130135436 | GCTGCAGTGAGCTGC[A/G]ACTGAACCACTGCAC | 50807 |
| rs187647793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360737 | GGGACACACCAAGTT[C/T]GAAGTTCAGAGGAGA | 50807 |
| rs187648814 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227307 | GCGCAGGTTGGAGCA[C/T]ACTGGCGCAATTACA | 50807 |
| rs187655029 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183572 | GTCTCAAACTTTCGA[C/T]CTCAAGCGATTTGCC | 50807 |
| rs187661248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394814 | GGGGCAGGTTCCCTG[A/G]TAACTCTGTCTCAAA | 50807 |
| rs187679983 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130260788 | CAGTACACTACAGTA[A/T]AAACAAAGGAATACC | 50807 |
| rs187682528 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066848 | AGACTGAGGGCCACT[A/G]CCCCCCATTTCAGCC | 50807 |
| rs187686882 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156289 | TTCAATTTTTTACTC[C/T]TCCACAGAAGTCACA | 50807 |
| rs187701796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123383 | AAAAGGAATCTCCCA[C/T]TGTCTTTGAATGTCT | 50807 |
| rs187720672 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239007 | CTCTTGTATCTTTTT[A/T]AAAAAATTTAAATAA | 50807 |
| rs187731000 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130222716 | GCAATCACAAGTTTT[A/G]ATTAATGTGCCAAGA | 50807 |
| rs187734866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353375 | GGGAAAAAATAGTAT[A/G]TTTAAGTATCACTAT | 50807 |
| rs187735191 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088834 | TTTTATGTGTTCTTC[C/T]CATTTAATCTTCATA | 50807 |
| rs187738798 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130294240 | CTTGGAACTAGTTCT[C/T]GATGTACTCATAAGA | 50807 |
| rs187748942 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389375 | GGACAAGGGAAAAAA[C/T]GGCTGACTAATGCAC | 50807 |
| rs187766650 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130426958 | TTGCTACTGTTGTCC[C/T]GCCCCTAGAATACCA | 50807 |
| rs187774182 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054480 | AGAACAGCATAGAGA[C/G]ATGTAAGTGCTAGAT | 50807 |
| rs187787472 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130061229 | AGGCAGTTTTACAAA[C/G]ACAAAGTTTGAAAGC | 50807 |
| rs187792464 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130216034 | AAGGAAAGGAAAGGA[A/C]AAAGGAAAGGAAAAG | 50807 |
| rs187798862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176012 | GTGAACTGGAGGATA[G/T]GTCTGTTTGGAAAGC | 50807 |
| rs187803043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080867 | AAAATTCCTGGCCTC[C/T]GGTGATCCACCTGCC | 50807 |
| rs187808577 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318301 | TGCCCAGGCTGGTTT[C/G]AAATTCCTGGCTTCA | 50807 |
| rs187812735 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428101 | CATGGGCCACCATCT[C/G]AGAGAACTTTGGGGA | 50807 |
| rs187814066 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251220 | GTCAGGAGTTCAAGA[A/C]CAGCCTGGCCAACAT | 50807 |
| rs187821813 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445242 | CCAGAAGTCAGCTCC[A/G]CAGATAGGTTTTCCC | 50807 |
| rs187825110 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152929 | AAAAATCCAACCCCC[C/G/T]CAAAAAAATCCTGGT | 50807 |
| rs187848495 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400559 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACGAGGT | 50807 |
| rs187860428 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422703 | TGACAAATCTTGGTT[C/G]ATTTCCCATAAAGGG | 50807 |
| rs187869237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314557 | TCAAGGATAACAGAG[C/T]TAATACCCACACTAG | 50807 |
| rs187869850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355265 | TGCACAACACACCAC[A/G]ATCTCTACCAAGGAG | 50807 |
| rs187870282 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139595 | TTAGCTAAGCATGAC[A/G]GCGCATGCCTGTAAT | 50807 |
| rs187880197 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374522 | AGCACTTTGGGAGGC[A/C]GAGGCATTTAGTTAG | 50807 |
| rs187897098 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391673 | CTGACCAATGCATGC[A/G]TGGTTCCCGCCTTCA | 50807 |
| rs187897615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079524 | TATCTTTTCATTTCC[A/G]AATCTGCAAAAGGAG | 50807 |
| rs187904830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408518 | GGTTTTTAGACCTTC[A/G]GGCTAGGACTGAATT | 50807 |
| rs187906051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342114 | GTCGGTCCTGAGCCA[A/G]GGCATTCACGGTGAG | 50807 |
| rs187938303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206895 | TCCTTAACTTCTTTG[C/T]TAGGATCACAGGAAT | 50807 |
| rs187938668 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390078 | AACACTAAAGGGAGG[C/G]CCTGAGAATCTGATT | 50807 |
| rs187949158 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278259 | TCAAGGTATTGAGTC[C/G]AGATCTTTAGGATGG | 50807 |
| rs187953614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130328570 | CAGTTTTAAGACAAA[A/C]AGCTGTAAAAACCCA | 50807 |
| rs187955137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244222 | AAATGGAAGGTGAAA[A/G]AATGAATATCTCTCT | 50807 |
| rs187958635 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130427336 | TCCTCTTGATATTGA[C/T]AGTGTGTTTACTCCT | 50807 |
| rs187973693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347213 | AGTGGCAATGGGATG[C/T]TTCTTTTCTGGCCAT | 50807 |
| rs187980417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139074 | GAACAACTCTTGCTA[C/T]GATATTATGTTCCAA | 50807 |
| rs187981605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368193 | GGTTGAGAGGCATTA[C/T]ACAAACAAATTTATA | 50807 |
| rs187992668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399104 | AAAGGATGGGACGTG[C/T]CTTTCTCTGTCTCGT | 50807 |
| rs187995901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102736 | TGTCACCCAGGCTGG[A/C]GTGCAGTGGTGTGAT | 50807 |
| rs188025847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130067543 | TGGGACCACAGGTGC[A/G]GACCACCACACTCTG | 50807 |
| rs188034290 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130106404 | TTTCATGGTGGCAGG[C/T]GCTGTCATATACTGA | 50807 |
| rs188041661 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274672 | TTCAAGTCCGAGTGA[C/T]CAACAGAAGTTCACT | 50807 |
| rs188056882 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293699 | ACAATGGGTCATTTT[A/C]TTTAGATTATTTTCA | 50807 |
| rs188058828 | snp | A/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130256787 | TATATATATATCCTT[A/T]TATATATATAAGCTT | 50807 |
| rs188059989 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070317 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCC | 50807 |
| rs188073194 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311330 | GGTAATTTTGAAAAG[C/T]AGAGAAATTTACGTC | 50807 |
| rs188074154 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130194582 | TTTCTGGCACCAGAG[A/G]CTGGTTTTGTGGAAG | 50807 |
| rs188082085 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349139 | CAGAGCCCACTAAGG[C/G]CTGATTATACAGTTA | 50807 |
| rs188085065 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325500 | AGTAAGAGACATCTG[C/T]TCTTAAACTATGTGA | 50807 |
| rs188098864 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411415 | CTCCTTGCCCCTTGG[G/T]TCTGACAACCTGAGA | 50807 |
| rs188105999 | snp | C/T | 8.24273e-05 | 0.00641926 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130128021 | CAGGCTGTTCTCTCC[C/T]GCACTCTGCTCTCCA | 50807 |
| rs188110382 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385295 | ACATGGTGAAACCCC[A/G]TCTCCACTAAAATAA | 50807 |
| rs188113334 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130235514 | TATCAAACATAAGGG[C/T]CTACCACAGTGTGGG | 50807 |
| rs188131933 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095339 | GCAGTTTCACTCTGT[C/T]GCCCAGGCTGGAGTG | 50807 |
| rs188137339 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162824 | CTCCGTCTCAAAAAA[A/C]AAAAAAAACAAACAA | 50807 |
| rs188143632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111972 | TGCTCCTGACAACAC[A/G]ATCCGCGCCACTCAA | 50807 |
| rs188144094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156471 | ACCGTATCTCATTTA[C/T]GTTTTACCTCCAGCA | 50807 |
| rs188145926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145348 | TTTTAGACGGAGTCT[C/T]GCTCTGTTGCCCAGA | 50807 |
| rs188159749 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285924 | AGGCTTTACTGGAAC[A/T]GATATCATAAATAAT | 50807 |
| rs188165622 | snp | C/G | 1.64849e-05 | 0.00287092 | missense | ASAP1 | GRCh38.p7 | 8:130060640 | GGCGTGAGGTCGTTG[C/G]AGTCTTCAGATGCTT | 50807 |
| rs188172423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130304364 | TTTGAAAGTCTGACA[C/T]ATTCACCCTAAAAAA | 50807 |
| rs188193084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130190939 | TCACTAGTACATAAC[C/T]TCGATGGGGACAGGG | 50807 |
| rs188193579 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402101 | TTCTTGCACCACAGA[A/G]TGGCTGTCCAGAAAT | 50807 |
| rs188218022 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233828 | TATAATAGGTGCTCA[A/G]TAAATATCTTTTCAA | 50807 |
| rs188222051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249559 | GGGTTTTATCACCCA[A/G]TAAGAAAGTTTCACT | 50807 |
| rs188230938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407467 | CATGAGCAGGGGAGC[A/G]GCAGCATCTGTACAT | 50807 |
| rs188236291 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214309 | TCGATAAATCTACTC[C/T]ATCAGCTGGGCCAAA | 50807 |
| rs188246901 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341696 | ATTCCGTGTCTTCAA[A/C]TTGACTGCCCAGCCC | 50807 |
| rs188266516 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085850 | TTTGCTATCAAAAGC[C/T]TGCCTTAGAAGTCTC | 50807 |
| rs188276606 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056061 | GGTATCTCTGCTGTA[C/G]TCATCAGTTGCTTAG | 50807 |
| rs188281621 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236676 | CAAATTTACTCATAA[A/C]TCTATTAAGCACTTA | 50807 |
| rs188286309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119444 | TTTCCTTTTCTTGAG[A/G]AATTGCCTTCTTTAC | 50807 |
| rs188298179 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253314 | AATCTCATAGAGTTA[C/T]AAGGATTAAGTGAAG | 50807 |
| rs188303958 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289087 | GGTACTCGGGAAGCT[A/G]AGGCAGGAGAATCAC | 50807 |
| rs188304633 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421493 | CATGTGTCAGACTTC[C/T]AGCTAAGGAATGAGA | 50807 |
| rs188308668 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272768 | AAGAACAATATCTTA[G/T]GTTCTCACTCATATG | 50807 |
| rs188312289 | snp | C/T | 0.0399052 | 0.1355 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130443850 | GCTTAACCCTTGGCC[C/T]GCCGGCAGCCACGAG | 50807 |
| rs188314051 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306462 | GCCACAAAATCAATT[C/T]AAAGGCAAAGAGAAT | 50807 |
| rs188319821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130271973 | TGTCTCAAGTTGAAT[A/G]ATGAAGAAATAAAAA | 50807 |
| rs188335463 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130150236 | ACAATGTGGATGATG[C/T]GATGAGACTTGTTAA | 50807 |
| rs188337692 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165534 | CATATCTGTGCTTCA[A/G]TCTGAAGTCTACTGG | 50807 |
| rs188345304 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133802 | TGAAAGGCACATGGC[A/C]GTTTCCTTCCTTCAG | 50807 |
| rs188354361 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166565 | TTGTAGGTTTCTGTC[G/T]GGCTGCAGTCATCTT | 50807 |
| rs188354406 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124583 | CAGGATTACTTTATA[A/T]CTGGATACAGATTAA | 50807 |
| rs188360397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148388 | GAGCACTAAGTACAC[A/G]TCAGGCAATGTGTTA | 50807 |
| rs188361342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237072 | AAAATTCATTTGTAA[G/T]TGCATTTGTTTTCCT | 50807 |
| rs188365326 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117282 | AATACTAATAATAAC[C/T]GCTTTTACAGATAAA | 50807 |
| rs188366625 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130206333 | ATTAGGCACATCCAT[A/G]CTCTCCATACTTTTT | 50807 |
| rs188369541 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130186705 | ACACATAACTAGCTT[A/T]CTAGCCTTTCATGAG | 50807 |
| rs188372844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167911 | CATTGAGATTATTTG[C/T]TTCTGGTTTTTCAAA | 50807 |
| rs188375891 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370143 | CCGTCTCTACCAAAA[A/C]TACAAAAAATTACCC | 50807 |
| rs188376823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130196117 | AAGGCCGAGGCAGGC[A/G]GATCACCTGAGGTCA | 50807 |
| rs188377626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325331 | GGTAATACAGATTTC[C/T]AGCACTGAGGCCAAC | 50807 |
| rs188387410 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130107629 | CTTGGCTCACTGCAA[C/T]CTCTGCCTCCTGGGT | 50807 |
| rs188393668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140638 | GTGGTGATGACGTTA[C/T]GATGTTTATTCTCTT | 50807 |
| rs188397129 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083639 | ATAAACTATAAAGTA[C/T]GGGACACAGTGCTAG | 50807 |
| rs188398747 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401001 | TTCTCCCTCCTCAGC[C/T]TCCCGAGTAGCTGGG | 50807 |
| rs188405378 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100742 | TTCCGGATATACAAG[C/T]CCCTTGTAAGATGAA | 50807 |
| rs188406206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362471 | GTTTCAGATTATTGT[A/G]TGAAATAAAATGAGA | 50807 |
| rs188408034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056273 | AGAGCCCACCTCCTC[A/G]TCATGAGATGAAGTG | 50807 |
| rs188422531 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073344 | GCGGGGAGCTGAGAT[C/T]GCACCATTGCACTCC | 50807 |
| rs188428804 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130271059 | CTCCTGGTCCCCAAG[C/G]ATGGCCCACTGATCA | 50807 |
| rs188432021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189077 | TTATGAAGTACATGT[G/T]AAATTTGATACAAGC | 50807 |
| rs188434120 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130256078 | GACCCAGGGACCTAA[C/T]GATTCAATATTAACT | 50807 |
| rs188443630 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130298825 | CATGGTCTCCCAGAA[C/G/T]CTCTGCACTAACTCC | 50807 |
| rs188465946 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130232197 | ACATTCTATTCATTA[C/G]AAGGGAGTTAGTAAC | 50807 |
| rs188472817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293216 | ATTCAGCAGGTCTGA[C/G]GAGGAGGCTCAGATT | 50807 |
| rs188487006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423339 | TAATTGATAATGCCT[G/T]GGGCGGGCAAGAAAT | 50807 |
| rs188506184 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130153535 | CCACCATGCCTGGCT[A/C]ATTTTTACATTTTTT | 50807 |
| rs188530443 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058179 | CCAGTAACTTAACCT[C/T]GCTGAGCCTTGATTT | 50807 |
| rs188532491 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130357857 | CGAGGAGATGGGGAA[A/G]GCGCCGCCCGTCCGA | 50807 |
| rs188544405 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094169 | TAGTTTTCAAAATGT[C/G]TTTATATATGCTATT | 50807 |
| rs188563095 | snp | A/T | 0.0387552 | 0.1337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059169 | ACTGCAACATTTAAA[A/T]TTTTTTTTTTTTTGA | 50807 |
| rs188568901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251838 | TAATAAAATGCATTT[C/T]TTATCCTTCTAAAGC | 50807 |
| rs188569454 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076971 | GGCACCTGGCACACT[C/G]TAAGTGGTGACCCCA | 50807 |
| rs188578926 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179822 | TAACCCACTAATTTA[C/T]TGAGGTAACTAAACA | 50807 |
| rs188580429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130440977 | CTCCTCCAGAGGAAT[G/T]CAAGCTCCAGAAGGG | 50807 |
| rs188586431 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409526 | TGTGTTTGAGATGGG[C/G]CCTTCTGATAACTCT | 50807 |
| rs188597763 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211383 | GGAGTTTTCACATAA[A/C]ATCTCACTTGATCGT | 50807 |
| rs188602055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144231 | GCAGAGAGATCTTAT[C/T]GCCAGAATTTTAGCA | 50807 |
| rs188609107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288070 | CTGCATCCATGCTGC[A/G]TGGAACTCTTCTCCC | 50807 |
| rs188612653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183361 | TGTTATTATTTTTGA[A/G]ACAAAGTCTCGCTTT | 50807 |
| rs188618504 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248126 | CTTACTTATCAAAGA[A/G]GAATAGTTTATCTAC | 50807 |
| rs188630984 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130147463 | GGGTTGAAATTCAAG[C/T]CTAGGCAGTCTGGCT | 50807 |
| rs188635031 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111300 | AGGTGGGAGGATCAG[A/G]ATCACTTGAGCCCCG | 50807 |
| rs188638160 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130304908 | ACTCCCTATTATTTA[C/G]AGTAAAAGCCAAAGT | 50807 |
| rs188646511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339280 | CTCAAGGTAAAATAA[C/T]GTAAAGAAAAATTCT | 50807 |
| rs188648636 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320129 | ATAAAATAAAAAAGG[A/G]AAATTACTTTCATAA | 50807 |
| rs188651365 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355973 | GTATCATCAATGTAC[C/T]CTAACATGACACTGA | 50807 |
| rs188665968 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130076671 | GATTACAGGTGCCCA[C/T]CACCACACCCGGCTA | 50807 |
| rs188669829 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376508 | CGAGGTGGGTGGATC[A/T]TGAGGTCAGGAGTGC | 50807 |
| rs188670190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419485 | AAAAACGGCTGCAGC[C/T]GATCTCACTACCAGT | 50807 |
| rs188670527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130310475 | AACTTCATGGTGATA[A/G]ATGTGTCATGAAGTG | 50807 |
| rs188672173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392754 | ACTCGTGGCAGAAGG[A/G]GAAGGGGAGCCAGCA | 50807 |
| rs188684252 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130345379 | ATTTAAATGCCTCCC[C/T]GTCAACTCGAAAGAA | 50807 |
| rs188716632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130212490 | AGAAGAGCAAAGGCA[A/G]CGGGTTCAGAGACAG | 50807 |
| rs188728110 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359571 | CGACACACACCCACC[A/G]CGCCCTACCCCTCAC | 50807 |
| rs188731166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394396 | CGCTCCCAGGCTTAT[G/T]AGGACAGGAAATTCC | 50807 |
| rs188733887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171104 | ATTTTAAAAGTTTAC[A/G]TTCTGACCCTTGAAT | 50807 |
| rs188735926 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130248839 | CACAAAGATGTTCAC[C/T]CGGACACCAAAGTCA | 50807 |
| rs188737423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414318 | GCCATTAAGTCTGTG[C/T]TTCCATCTAAAACCT | 50807 |
| rs188751076 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394177 | TTAAACTTTGACCAC[A/C]GGTGAGCTGGGCGGA | 50807 |
| rs188754439 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274523 | TAAATCCTAAATGGA[A/T]AACAGGTAAGGGGAT | 50807 |
| rs188762667 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434882 | TGACCATACACCGAA[A/C]AATAGCCCCTTAGCT | 50807 |
| rs188775032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098683 | CAATTGTACATATTT[A/G]TAGGATACATAGTGA | 50807 |
| rs188777498 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307686 | TAACAGCTTGGTGAG[G/T]TAGGAGTAACAGCGA | 50807 |
| rs188781011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130071920 | ATATGTATTAGTTTT[C/T]GTCCACAGTTGCTGG | 50807 |
| rs188787235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110631 | CCTTTGGCTTACATG[C/T]ACTATTACTGTGTGG | 50807 |
| rs188789598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301161 | ATTTTATCCAGACTA[C/T]CCTAAAGATAAGTGG | 50807 |
| rs188797149 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281280 | CCGTGGATCAACATA[A/C]ACAATGTTTCCCTAT | 50807 |
| rs188797306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322951 | AAAACACCCATAGGA[C/T]CAGTTCTATCCAGGC | 50807 |
| rs188797720 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137262 | AGCTGGTAAGTTTAG[G/T]AAAGTTTTATTTATC | 50807 |
| rs188804628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316211 | GGGCTATGCCAACCA[C/T]CTTTCTCTACTGAGC | 50807 |
| rs188806098 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342836 | AACCTGGTTGCCCCC[C/T]ACCCTACACCCCTCC | 50807 |
| rs188806774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130980 | GCTAACACGGTGAAA[C/T]CCCATCTCTACTAAA | 50807 |
| rs188808758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280092 | GTGTTCTTGACTATT[C/T]TGCTGACAAGGAAAC | 50807 |
| rs188810512 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237316 | GGATTCTTTCATGCA[C/T]TTACAATCTGGTAAG | 50807 |
| rs188812535 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378665 | GGAGAGTTTCTAAGA[C/T]GGCAATGGACACGAA | 50807 |
| rs188814059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254131 | ACAGGAAAGGTGGAG[C/T]AAAATGTGACAAAAA | 50807 |
| rs188815993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299548 | TGTCAGCTAGGAAAC[A/G]ATGATATACATGTTT | 50807 |
| rs188817582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074804 | GTTGCGGTGCTGGGA[C/T]TGCTGGGCAGCCCCA | 50807 |
| rs188826844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333315 | TATAGTAAAAAGGCA[C/T]GGCTGGCTGGGCGCG | 50807 |
| rs188837157 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350990 | TCACATCTGCCCAGT[C/G]CAAGGAGGATTGCTT | 50807 |
| rs188837292 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370407 | TGCAAGGGAAGAGGG[A/C]CTCACCAGAATCCAA | 50807 |
| rs188850564 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130159800 | TGTGTTTCCCTATAT[G/T]AGAGACTGGAAACAT | 50807 |
| rs188868286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229960 | CCAGCTGCTACTCGG[A/G]AGGCTGAGGAGGGAG | 50807 |
| rs188874462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162544 | AAAAACATGGCCAGG[C/T]GCAGTGGCTCACGCC | 50807 |
| rs188875792 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130261818 | AGTTAGGATTATAGT[C/T]AAGGGATCTCCCTCC | 50807 |
| rs188876912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219987 | AGAGATGGGGTCTTG[C/T]CATGTTGCCCAGGCT | 50807 |
| rs188884966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178349 | TAGCTGGCACATTTT[C/T]ACACACAGACTCTAC | 50807 |
| rs188894158 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381971 | CCCGTGTTTATTTTC[G/T]TAAGGTACACACCAT | 50807 |
| rs188896058 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203003 | AAAGAAAAGGGGAAG[A/T]GGCAACCAGCTTAAA | 50807 |
| rs188901461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394659 | GGTTTTGCGGCTTGT[A/G]GGGCATCACGGAACC | 50807 |
| rs188908049 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094929 | GCTAGGAAACAAAAA[C/T]TGTCAAAGACAAAAT | 50807 |
| rs188910506 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418023 | GAGCGGGTCAGCTCC[A/T]CAAGACCCACAGACC | 50807 |
| rs188911837 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415004 | CTCAGGTGATCCCCC[C/T]ACCTTGGCCTCCCAA | 50807 |
| rs188922118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436284 | CTGAGACAGGAGGTC[C/T]GCTTGAAACTAGGAG | 50807 |
| rs188938047 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127096 | CTGGTAATATAGTGC[A/T]ATTTGAAAATAAAAG | 50807 |
| rs188940812 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257731 | ATTACATTTCTGTTT[C/T]TTAAAAAATGTTTCT | 50807 |
| rs188951756 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240015 | GGTTATCTTTGGGGG[A/T]ATAATGACTAAAAAA | 50807 |
| rs188965369 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130345952 | ATCTGCAGCACAACC[A/T]TCAAGAAATTTAGTA | 50807 |
| rs188983113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375981 | GTTAATTTACCTCTA[C/T]CCCTGCCTCTTCAGA | 50807 |
| rs188988592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163699 | ATTTAATAACATTAA[C/T]AACAATTTAAAAACT | 50807 |
| rs188999728 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409135 | GGCATGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 50807 |
| rs189001956 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145498 | ACTTTTCTGTATTTT[C/T]AGTAGAGACGGGGTT | 50807 |
| rs189021776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377944 | TTCGGATTACCCTAT[A/T]TCCAGTGTGCTGTCT | 50807 |
| rs189022208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223640 | ATACCTACTTGATGG[A/G]GTTATTAAAGGAAAT | 50807 |
| rs189029657 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204037 | GAGCACGGGTCCCCA[G/T]TCCCCAGGCCACGAA | 50807 |
| rs189033680 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180686 | AAGCATAAAGACTGC[C/T]GACTAGCAGGAAAAG | 50807 |
| rs189035278 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130412809 | GGCACATGCCACTAC[A/G]CCTGGCTAATTTTTT | 50807 |
| rs189055260 | snp | C/G/T | 0.013108 | 0.0800372 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083147 | CTGCTGTCACACAGA[C/G/T]GAGTCATCATGTCAG | 50807 |
| rs189063526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100368 | GAGTTTCACTCTTGT[C/T]GCCCAGGCTGGAGTG | 50807 |
| rs189066238 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115191 | TTCGAGTCAAGGGAA[C/G]TACCCTTCATGATGT | 50807 |
| rs189070950 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130338502 | GAAAAGAACATTATC[C/T]TGACTACTCCCCAAT | 50807 |
| rs189071981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090382 | ATGTTATTTGGGGGA[A/G]AGGCCTTTTTGATGA | 50807 |
| rs189079146 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130173006 | TCTAGTAATCATCTA[A/T]GTGAGGAGATTACAG | 50807 |
| rs189096641 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203828 | AGGCTTCTGGGACAA[A/T]GATCATGCAGACAGA | 50807 |
| rs189114477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286131 | CTAAATGAAGAAAAG[A/G]AGGCTCAGGGCACAG | 50807 |
| rs189126686 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104205 | CCATCTAATTAGGAA[C/T]AAATAGTAACTTCTC | 50807 |
| rs189151412 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130138016 | CCTATATCCCTGTTT[C/T]GATTGAGAGCTGTGG | 50807 |
| rs189155320 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068864 | CCCAAGTCATGGTAA[A/G]TGTGTGGTTAAGAGG | 50807 |
| rs189167958 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130364656 | ATGCAAGCTTGACTG[A/G]TCTAGAGAGCAGCTC | 50807 |
| rs189180273 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396140 | GGTCGTCAGAAAAGT[A/G]ATCAAAAAATAAAGT | 50807 |
| rs189197275 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130394315 | GTCTCTGAAATGGCC[C/T]CCTTGGGTGTGGCCA | 50807 |
| rs189198734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438674 | GAAATTAGTGTCCCT[A/G]GGTTGAAAGTGAACA | 50807 |
| rs189200132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068292 | CAGATGTGGGTCTGC[C/T]TGAGCTTAGTCCACT | 50807 |
| rs189206050 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086295 | CTTAACCTTTCTGCG[C/T]CCCGAAGTTGAGATA | 50807 |
| rs189208848 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262287 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 50807 |
| rs189213662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102934 | GGCCTCAAGTGAGCC[C/T]CCTGACTTGGCCTCC | 50807 |
| rs189215703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119629 | GAGAGCTAGGGTCCA[C/T]GTGATGCTGTCTGAC | 50807 |
| rs189217100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130300216 | AGTCAATACAAAAGG[C/T]TTCTAAGGTCCCAGA | 50807 |
| rs189232427 | snp | A/T | 0.0383715 | 0.133092 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424927 | GAACCCGGGAGGCAG[A/T]GGTTGCAGTGAGCCG | 50807 |
| rs189236133 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130159055 | GATTTTTAAAAGACC[A/G]CTCTAATTGCTGTGT | 50807 |
| rs189266770 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130355438 | GGAAAATGTTTTTTT[A/T]AAATGAGAATTCCAA | 50807 |
| rs189272203 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130065545 | GAGGCCTAACACATC[C/T]AGCATTACAACCAGA | 50807 |
| rs189278690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137812 | TAGGAAGTCTCACCA[C/T]GTATTCACACTGGTC | 50807 |
| rs189279910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392359 | TAAGACATCTAACAG[A/G]GAAAAGGGATGTGCA | 50807 |
| rs189286701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120314 | GCTACTGTGTTGATG[A/G]ATGGAGCAGCAGACT | 50807 |
| rs189287408 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130351453 | TATATATATAAGGTG[A/T]GTTAGGCAGTTCTTG | 50807 |
| rs189295909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130429288 | AAGGGACACAATTCA[A/G]CCTGTAACAGTCATC | 50807 |
| rs189301250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130371456 | GCCCCAGTTTGATTC[A/G]GGGCAGCAATGTGTT | 50807 |
| rs189306616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189547 | TATTTTCTTTATCTA[C/T]TCAACTGTTGATGGA | 50807 |
| rs189307259 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124165 | TACTAGTTAAAAGTC[C/T]CCTATTATTTGTTTT | 50807 |
| rs189307708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130386520 | GACACAGGGCTAAGC[A/G]CTGCGCTCTCCACCC | 50807 |
| rs189310925 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171963 | AGTTTTGAAGGTAGA[A/G]CATTTAAATTTAAGA | 50807 |
| rs189315144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153801 | GGGGACCCAAACCTG[C/T]TGGGGGTGGTGTTAA | 50807 |
| rs189319355 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402791 | ACCTCCACTGGTCCA[A/G]CTCTGGACCAAGCCT | 50807 |
| rs189322450 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090698 | GACCATGAACTCCAC[A/G]AGCATATGGACTGAG | 50807 |
| rs189332766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319585 | ATGGGACACACTGGC[A/G]TCCACTGGTGGAAGC | 50807 |
| rs189342329 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130103448 | TAATTTTGGATTTGG[C/T]TTGTCCTTGCTTTTC | 50807 |
| rs189356959 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223211 | CCTGAGGAGCATTCC[A/C]AACCACAACCAAGCA | 50807 |
| rs189377297 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154563 | GGAAACAAATGACAT[C/T]AGGAGACCACTGTAG | 50807 |
| rs189398357 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177722 | TATCATCAAATTTAT[A/G]TAAACAACAATTTGA | 50807 |
| rs189422185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082581 | TAATCATAGCTCACT[A/G]CAGCCTTAAACTCCT | 50807 |
| rs189423608 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295518 | AGGGATACGGGATAA[C/T]AATACCTAGTTATTG | 50807 |
| rs189435760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276300 | CACAAAGTGATTCCA[C/T]ATACATTCTGCTACT | 50807 |
| rs189435996 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ASAP1 | GRCh38.p7 | 8:130051612 | CACCTTAGTGATTTA[C/T]AAGCCACATGTCTCC | 50807 |
| rs189437957 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180322 | AAGTTTAAGGCAGCA[A/T]GCTTTTTGTTGCATT | 50807 |
| rs189439386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313620 | AGTGGAACACATAAT[C/G]AACGTCCTCACAGAA | 50807 |
| rs189442667 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116126 | GGGATAATTGTCTCA[A/C]AGGATTCTTTTAAGA | 50807 |
| rs189443680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121248 | GCCCCGCCACACTCC[C/T]CGCCAGTCTGTCCTT | 50807 |
| rs189451183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087755 | TAATGTTAGGCAAGC[A/G]ATCAGCGTGAACCCA | 50807 |
| rs189451902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130346476 | TGAGGATGAGTCTGA[A/G]TAGAAAGAGCATAAA | 50807 |
| rs189458013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327541 | TTCATTAAGACTCTC[A/G]GGTGACTCTACTGAG | 50807 |
| rs189461953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247041 | AAGCCACGGCTACAA[A/G]CACAAGCTTTGAGGT | 50807 |
| rs189484977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280670 | CGATTCTATTAGAGA[A/G]TGAAAATTTGTAATA | 50807 |
| rs189486734 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064555 | ACCGTGCTTTTCCCT[C/T]TACTCTCACACCACA | 50807 |
| rs189487702 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430385 | TCATCCCTCAGTAAG[G/T]CAAGTTATCTCCATT | 50807 |
| rs189500297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258264 | ATCCCCTGCAGTCTA[C/T]CTCCTCCAAGAATTC | 50807 |
| rs189515204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240343 | GGCCACTGGCAAAAA[C/T]AAGCTAAATAAAATG | 50807 |
| rs189517843 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177181 | TATTTGTGGAAAGGG[A/C]AAAAGCAAAGAATAA | 50807 |
| rs189527535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286863 | AAGTTCACACCCACA[A/G]GGAACATTTATCTAG | 50807 |
| rs189535367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366387 | TACCCAGAGAAGCTT[C/T]CCAGCACATGCAGAG | 50807 |
| rs189536940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208679 | GTTGGATTGCCATTC[C/T]GCAGATGTCACCGCA | 50807 |
| rs189537815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321483 | CCTCAATTTCTACAT[C/T]TACAAAAAAGGAGAG | 50807 |
| rs189543563 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130305445 | TTCAGCTCACCACAA[A/C]CTCCGCCTCCCGGGT | 50807 |
| rs189552754 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397198 | CAGACTGGAGTGCAA[A/T]GGCACGATCTCAGCT | 50807 |
| rs189564863 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107480 | GTGAGCCACCATGCC[C/T]GGCCCATAGTCTCTC | 50807 |
| rs189578072 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215737 | CAACAGAGTGAGACT[C/T]TGTCTCAAAACAACA | 50807 |
| rs189584085 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130140204 | CACCTGGTTATTACT[A/T]TTTTTTTTTGGTATT | 50807 |
| rs189595494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251080 | TTTTATTTTTGCACA[C/T]CTGCAGAACAATGTT | 50807 |
| rs189598056 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130073192 | GTCAGGAGTTCAAGA[C/T]CAGCCTGACCAACAC | 50807 |
| rs189602665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270927 | TGAGAAGTAGTTCAC[C/T]CTACAGTGTAAGATG | 50807 |
| rs189606632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130235039 | CCATACAATCCCCTG[C/T]ACATTAGATATTATT | 50807 |
| rs189621747 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130213332 | AAAAACTGTCAGGAA[A/G]ACAGACACATACACA | 50807 |
| rs189643738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387302 | GCATTTGGGGAGGCC[A/G]AGGTGGGCAGATCAC | 50807 |
| rs189665203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425053 | AGTGTGGGTCAGGCC[A/G]GGCGCAATGGCTTAT | 50807 |
| rs189673602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132212 | TAGGGACAAAAGTCC[C/G]TACTTTCTGGGGTTG | 50807 |
| rs189685478 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159635 | CTCAGTAGCTGCCTT[C/T]CTATAATTGCACGTT | 50807 |
| rs189706889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100114 | ATTAGTACCTGTACT[A/C]ATTTACATTCCAACC | 50807 |
| rs189714353 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170064 | TATTTCTCAAAACAC[A/T]ATCTGTTTTGCTGTC | 50807 |
| rs189720344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317338 | TCAGCCAAAATTGGG[C/T]AAGAGAGAATGACCC | 50807 |
| rs189722541 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152460 | AAAGACCTAGGTTTT[A/T]CAGAACAATCAATAT | 50807 |
| rs189734189 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130135514 | AAACAAAAAAAACCC[A/G]AAACAAAACAAAACA | 50807 |
| rs189736253 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352238 | TTTTTTTTAAGACTA[C/T]AATCTCCTTGGGGGT | 50807 |
| rs189743413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130255357 | TTTGTTGGCTTCCTA[A/G]CTTGTTCATGTACAT | 50807 |
| rs189743548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211803 | TGGGAATACAATTTA[A/C]AAAGTCTATAAAGTA | 50807 |
| rs189743765 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130230370 | AAAAATTGAAACTTC[C/G]TAAGAAGCCTCGGGT | 50807 |
| rs189743972 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063887 | GGAGCTCACATTCCA[C/T]GAGAGGGTGACAAGT | 50807 |
| rs189749029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218354 | TTTCAAGTGAAAAAT[A/G]TAATTAGTTAATCGA | 50807 |
| rs189750227 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273561 | CTTCTGAACCCAGGA[C/G]CTTGTATTAAGGAGG | 50807 |
| rs189753859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146329 | CTTAGCATATACCTT[C/T]GTATATGCTAAGACC | 50807 |
| rs189759719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129939 | GTTAGAAACTAGAAA[C/T]TGTTTTGTTAAAAAC | 50807 |
| rs189760592 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130237629 | TGGATGATGAATCAA[C/T]ACATTAATCTACCTG | 50807 |
| rs189761812 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188051 | TATGATCTTGAAAGA[C/G]GAAAAAAAAAATTAA | 50807 |
| rs189776271 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130114572 | CCCACAACCATTTGA[A/G]GAATGTGTTGCACTA | 50807 |
| rs189778458 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130182355 | TAAATATTTGGAAGA[C/G]CAAGGCTGAAGAGAG | 50807 |
| rs189781117 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130289721 | CACCTGAAGTATCTT[A/G]CTTGTATCCACAATC | 50807 |
| rs189789083 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253855 | GTGAAACCCCGTCTC[C/T]ACTAAAAATATAAAA | 50807 |
| rs189797169 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164709 | ATTTATTTGCTAAGA[A/C]AATAAAAACTTAATA | 50807 |
| rs189804447 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343917 | ATCTGAGCAAAATAC[C/T]TGAAGTGACAGTAGC | 50807 |
| rs189805501 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130078379 | GACTCACTGCAGCCT[C/T]AATTTCCTGGGCTCA | 50807 |
| rs189810741 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130379484 | ACACACGCAGCCTCT[G/T]GGAATTGTGACTGGC | 50807 |
| rs189815809 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383148 | CCTGGAAATGACATC[C/T]TACCTTCAATCTGGT | 50807 |
| rs189818474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098033 | TTGCATTTTCTGGAG[C/T]TACCATTTACTGAGT | 50807 |
| rs189849176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273300 | TAAATCTCTTTCCTT[G/T]CTGAGGAAGGAGAAA | 50807 |
| rs189888256 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309084 | AGATTTTCAGTACTT[A/C]ACCAAACATGTCCTG | 50807 |
| rs189901328 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130208177 | TTCCCCCAATAGTAA[C/T]ATCTTATATATGTTA | 50807 |
| rs189903269 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130371958 | GGCTTATCTCAGAAG[C/T]GGTCAAATGAGAAGC | 50807 |
| rs189907742 | snp | C/T | 1.6483e-05 | 0.00287076 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167454 | ATCACTGTGCCTGTC[C/T]TGCAGATCAGGAAAC | 50807 |
| rs189914314 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435299 | CAGCATCTTAGTAAG[C/T]CTTTTGCGTCAGCAT | 50807 |
| rs189922580 | snp | A/T | 0.0382454 | 0.132891 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403301 | ACAAGTGTTTTTTTT[A/T]AAAAAACCCAGATCC | 50807 |
| rs189922888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074178 | GGGTATTTGATGATA[C/T]TAAGAAATTTTTGAT | 50807 |
| rs189934639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246417 | CTGTAATCCCCACAT[A/G]TCAGGGAAGGGGCCT | 50807 |
| rs189964609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434427 | TTCGTCGTATATAAA[A/G]TGGGAGTTAGAAATA | 50807 |
| rs189972342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057111 | GAGAAGGTGTCTTGG[C/T]CTATTTGACAAAGAA | 50807 |
| rs189976892 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132978 | ATAACAAAAGTAAGC[G/T]AGTGGGAGAGAGAAA | 50807 |
| rs189989709 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334253 | TACTCTTTGATTTTC[A/C/G]GGTAACAACAACAAC | 50807 |
| rs189999145 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234618 | GAGGAGCCTTTGTAT[G/T]AGCTGCTGAGTGATG | 50807 |
| rs190002006 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237187 | TTTTCCGGAGAAGTG[C/T]AGTCATTCCACAAAG | 50807 |
| rs190013390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269620 | CAAACCTAGGTTTTC[C/T]AGGTTTTGATAACTA | 50807 |
| rs190014133 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341364 | TTAACCAAGCATCAG[C/T]TGTGGGATCTTGGGT | 50807 |
| rs190016766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197169 | GTGCAGTGGCACATC[A/T]GTAATTCCAGCACTT | 50807 |
| rs190019571 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295227 | GTTCAAGGCTACAGT[A/G]AGCCATGATCACACC | 50807 |
| rs190020801 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272962 | ACAGTTAATGACAAT[A/G]TATCGTGTATTTCAA | 50807 |
| rs190021980 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130322013 | TGCAAAATATGCATT[A/G]CAAAGTGCTGAGCTG | 50807 |
| rs190024230 | snp | A/G | | | intron-variant, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130357788 | TCCACAGCTCGCTCA[A/G]TCCTCTCCCACCTCC | 50807 |
| rs190028018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130326924 | TAGCCTTTCAGATTC[C/T]GGCACACCAGACCCA | 50807 |
| rs190032894 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377577 | CAAGGAGCCTATGGT[A/C]AATCAGAGTATGCAG | 50807 |
| rs190037931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422719 | ATTTCCCATAAAGGG[A/G]ACAGGAGCCAGGGAA | 50807 |
| rs190046169 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445247 | AGTCAGCTCCGCAGA[C/T]AGGTTTTCCCCAACC | 50807 |
| rs190048114 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393925 | TGAAGATTTCATGGA[C/T]ACTTATCACTTCCCC | 50807 |
| rs190053733 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130386194 | ACTAGAGAGGAAGGG[G/T]GCGAGAGATTCAGTG | 50807 |
| rs190056143 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411669 | AAAGGAAGTTGTATA[A/T]GTGTAGAAATGCCAG | 50807 |
| rs190058691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074759 | TGCTCCTAAGGAGAG[C/G]AGAGACAGTGTAGGG | 50807 |
| rs190061330 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360243 | AGAATCTGCAGAGAA[A/G]GCTTTGCTGACAAGG | 50807 |
| rs190061904 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130128792 | GGCCTGAAATAACCA[A/C]AAAGTAGAACAGTTA | 50807 |
| rs190062498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093864 | TCCCATTGTCAATTA[C/T]TAGTCCCTACCAATA | 50807 |
| rs190065317 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130443973 | AGGTGGAAGGGGTGG[A/G]ATTTATCCACAGAAA | 50807 |
| rs190098418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095885 | CAGACTCCCAAAGTA[C/T]TGGGATTACAGGCGT | 50807 |
| rs190113710 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130437664 | TTGTTACACACAGGA[C/T]AAGTTTTTACAGAGG | 50807 |
| rs190124888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059732 | CTATTCTATTATATC[A/G]AGAGCTTTATCTCCA | 50807 |
| rs190127392 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130290817 | TACTACAGGATCAAT[C/T]TTAGTACCGTATCAC | 50807 |
| rs190131857 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323619 | TCCCTCTACTGTCTG[C/T]TCCCCCTAATTCCCA | 50807 |
| rs190159711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130185193 | AAGAAGTCTATCTCA[A/G]GAAAATTGTTGACAG | 50807 |
| rs190163257 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324924 | TAGACAGTCTGCCTC[A/G]TAACCCCGAGCTCTG | 50807 |
| rs190173534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362049 | AGGATGCACTTTGTC[A/G]CCTTGAAAAAAAGGC | 50807 |
| rs190175334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344732 | GCAGGGTGAGATTGC[A/G]TCTCTTAAAAAAACA | 50807 |
| rs190180124 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228663 | CCAAGATCATGCCAT[C/T]GCACTCCAGCCTGGG | 50807 |
| rs190188359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380556 | GGTCACTGTCCTCAA[A/G]GAGGAGCACAGACAA | 50807 |
| rs190191826 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117159 | TATAAGCAATACAGT[A/G]ATAACAGGCAGTATT | 50807 |
| rs190192072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395437 | GTCCCGCAATCCAGT[A/G]TGACTGCTGTCCTTG | 50807 |
| rs190202289 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417067 | GCATACACACATACA[C/T]ACATGCAAAGTGCAA | 50807 |
| rs190213273 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259307 | TTTCTACTCCTTTTA[A/C]ATCTGTCCCCTTTTA | 50807 |
| rs190219581 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277188 | CCACGGTAACCTGAG[C/T]GAGACTGGAGAGAAA | 50807 |
| rs190219789 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145812 | CTTAAGGTCACAGCT[A/G]TTAACAACAGAACAT | 50807 |
| rs190224512 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130148701 | ACTATAATTCTTATA[C/T]TTTCTGTTGTAATTT | 50807 |
| rs190236096 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114242 | ATACTTACACAAACC[C/T]AGATGGGAGAGCCTA | 50807 |
| rs190250861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276012 | ACAGAGTGATCAAGG[A/C]AAGAACCAAGTTTCA | 50807 |
| rs190254738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087078 | CATGGGGGACTGGGC[A/G]GGGCTAATCATCAGC | 50807 |
| rs190280825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249778 | CTTGCTGGCCCTGCA[C/T]CCCAGGGTGTAGGAG | 50807 |
| rs190288800 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130312540 | CTCCCTTTTGATAGT[C/G]AATGTCCTCTGCATT | 50807 |
| rs190293614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395067 | AAGAGCATTTCCCAT[C/T]AACCAGGGACCACAC | 50807 |
| rs190314150 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437220 | CCCCCTTGTTCAGTG[C/T]CTGTCATTTGCTGGG | 50807 |
| rs190341048 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077595 | TCTGTCACCAGGCTG[G/T]AGTGCAGTGGCACGA | 50807 |
| rs190341668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333751 | TTCGCCAATCATACA[A/G]ATAAAATTATCAGAC | 50807 |
| rs190356573 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112924 | CTCAACTGCCCAGGT[G/T]AGAAACCTCAGTGTC | 50807 |
| rs190361135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263008 | GAATATTTCTGCTTT[C/T]GTACAACATGGAAAC | 50807 |
| rs190396678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187396 | TATAGGACACTGGGA[A/G]CTTCACTTTATGCAC | 50807 |
| rs190408673 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126207 | TGAAGAAAAGACTTA[A/T]ATGGAAGAAATGGAC | 50807 |
| rs190410630 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168828 | GGAGCATTTGACCAT[C/T]GATGACTTCTCTGAC | 50807 |
| rs190417918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141144 | AAATGCTTTCATATT[G/T]TTTAAGTACAGGAGA | 50807 |
| rs190419275 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109718 | GTATCAGCTGATCTT[C/T]AACAATGTCTTCTAA | 50807 |
| rs190423889 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229330 | GTTGTCATGGCATGG[C/T]TGTTTTCAGAGGGCA | 50807 |
| rs190424718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130125155 | AAGGGTGAGCCTCCT[C/G]TCTGAGAAGTCATAC | 50807 |
| rs190432243 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130101585 | AATTTTTCTTTTTTT[G/T]TCTGAGACAGGGTCT | 50807 |
| rs190433042 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209324 | CAAAGCCTTCAATTT[C/G]TGACACCAGTGGTTC | 50807 |
| rs190437909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130161332 | ACGAAATACCTTTAA[C/T]GCCAGGATGGCTTCT | 50807 |
| rs190440695 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383329 | TGTCCACATCCCAGA[C/T]TTTTTGTCGAAAATA | 50807 |
| rs190444828 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317686 | TACCTCCATTGTGAG[C/T]TTTGAGGCCTGGGGC | 50807 |
| rs190453102 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301509 | TCCATATATAGTGGT[C/T]GAATGAATGAAAAAA | 50807 |
| rs190455180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334672 | GAAAAGGTCTATTAT[A/G]TTTCAAGTGTGTAGT | 50807 |
| rs190458848 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130256180 | GTTTCCGTAAACATA[A/C]ATCTTCCTGTTCGCA | 50807 |
| rs190460552 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421200 | GCATAACAACAACAA[A/C]AAAAAAATCACAGTG | 50807 |
| rs190462161 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164043 | GAAGCCTAAAATTTC[C/T]AATGCAAGGTATCAA | 50807 |
| rs190464663 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274599 | CTCTCTTCTCACTAT[C/T]GCATTCATTGTTGAG | 50807 |
| rs190468322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066451 | CCTGGGCTCAAGTGA[A/T]CCTCCCGCTTCAGCC | 50807 |
| rs190474771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084838 | ATAAGTAAATATGCA[C/T]GTCTCAGACATTTCA | 50807 |
| rs190476079 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352651 | ACTTACTGGCTGTAC[A/G]ACCTAGCTGGACAAA | 50807 |
| rs190478699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129579 | ATTCTCAACAGACAA[C/T]ACAGAGGTTCAGAAC | 50807 |
| rs190483952 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372075 | AAGACATGCAACAGG[A/C]CTATTTTGTGGCATT | 50807 |
| rs190489713 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388395 | ATGAGCTGCAAGAGG[A/G]GTGAGGAGAATAATC | 50807 |
| rs190496526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319436 | TTCAAGGGGTGGTGG[A/G]GATTGCTCCAGGCCC | 50807 |
| rs190497227 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068569 | CACTACAGAGTAGAA[A/G]TACATGTTTGGATTG | 50807 |
| rs190531673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281556 | GGTCCAGATTTTCAG[A/G]CTAAAAAACTTATCC | 50807 |
| rs190544642 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248961 | TAGAAACAGGGGTCT[A/C/G]ACTATGTTAATAGGC | 50807 |
| rs190550217 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130181734 | CATACAGTAGCTGAC[A/G]CTAGTGCTCGGCTCT | 50807 |
| rs190555102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122253 | GTGTTTTCATCTCCT[C/T]AGAATGTAAGCAGGA | 50807 |
| rs190557717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130416693 | AGAATGCATTAGTGC[C/T]CCAAAAGGGGCAGGA | 50807 |
| rs190560405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284382 | GTGTAATTTAGCCAC[A/G]AAGTATGAGGTTCAA | 50807 |
| rs190576613 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088510 | AGTGGGGAGATGACC[A/G]TGAAGGCAGAGGCTG | 50807 |
| rs190580875 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106038 | CACCCTGGCAGTCAG[A/G]TGACTTAGCTAGAGA | 50807 |
| rs190597771 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316996 | TTATGTCAGTACAGG[A/C]TATGCTGTTGAATGT | 50807 |
| rs190597838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130138307 | ATAGAAAACAATGCC[C/T]TTTGTCCCATATCTA | 50807 |
| rs190608051 | snp | C/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130053138 | AAATTAATATTCACT[C/G]AGCACTGTAACGATG | 50807 |
| rs190609417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340847 | AGCTTAATACCTTGT[A/G]ACTCTTATGATGGCT | 50807 |
| rs190610206 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069303 | TGCAGTGGCGTGATC[C/T]TAGCTCATTGCAATC | 50807 |
| rs190629183 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377320 | AAAAGCTCACAAATC[A/T]CCACTAAATACCTTA | 50807 |
| rs190635247 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130241506 | AAATGAAGCGACAAA[C/T]GACTGAATACATAAA | 50807 |
| rs190641200 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055706 | TTACCTCAATTAGAT[G/T]AGTATTGATTGCACT | 50807 |
| rs190648073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183031 | ATAATGAAAATTCCC[A/G]AAAGAGGAATAAAAG | 50807 |
| rs190654396 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165402 | GAAATCTACCACCCC[A/G]TACTCCCTTCTACCT | 50807 |
| rs190657819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175825 | TAAATGAGAAAACAC[A/G]TGTAAGGAACTTAGA | 50807 |
| rs190670551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130242074 | ACCTACCATCTAGGA[A/G]TGCTCTGAGCATTCA | 50807 |
| rs190674115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313683 | TAAAATTAAATTAAC[C/T]TCACTGCCTAAAACC | 50807 |
| rs190677758 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276991 | GGGGTCCCTTGTCCA[C/T]GTGCAGCCTAGCTGA | 50807 |
| rs190678215 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417728 | TCAGAGGATGTGGTC[A/G]GGGAGAGGTTAGTCT | 50807 |
| rs190679082 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205817 | TAATATAAGGCATGT[A/G]CACCCTGTCACCCTT | 50807 |
| rs190681204 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130225642 | TGGATGGAGTGGGTT[A/G]GGTTTCATAAGAGAA | 50807 |
| rs190684574 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438500 | CTGTAGGGATGCGTG[C/T]TGTGCTAGGAAATGG | 50807 |
| rs190700359 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130398078 | GCTTTGGAATCAGGC[A/G]AGTGTAGGTTTCACT | 50807 |
| rs190716084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205095 | CAATCATTCTTAAAG[C/T]TCAATCTTTTCTTAT | 50807 |
| rs190716722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130442206 | GCTGTGACGCAAAGA[A/C]GACGTTTCCAAATCT | 50807 |
| rs190723181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139147 | AGATGAAGAGATGAT[C/T]GAAAGGGTGGAAAAT | 50807 |
| rs190723813 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130122798 | ACTAGATGAGGCACA[A/G]AGCTGACCAGGTGGC | 50807 |
| rs190727372 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130106625 | GGCCACCTATTTCTG[G/T]GACATGCTTTCACTG | 50807 |
| rs190757268 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337947 | CTACATACCAATGTG[A/G]AGTGTAAGATGCCTA | 50807 |
| rs190783812 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130367768 | GTCTGGAGGTCTTCC[A/G]TCTGGGTTGGGGCCC | 50807 |
| rs190786142 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204635 | ACCAATGAACTACAA[C/T]ACCTAGGAAAGCTGT | 50807 |
| rs190790604 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199663 | AGTGTGAGGTCTCTA[A/C]AAAGACCTCTAAGGT | 50807 |
| rs190805432 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130232580 | AGACACAAATTCCTA[C/G/T]AACAATCTTGAAACC | 50807 |
| rs190827795 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130268167 | AACATCTCTATATGA[A/T]GATATTATTATGTGG | 50807 |
| rs190829803 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130303851 | AGTAACAGAGGATAC[A/G]TATCATCGCACATTT | 50807 |
| rs190847858 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130291657 | AAGTAAAGGGACATA[A/T]ATGAGTGGACTGAAT | 50807 |
| rs190861902 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078005 | AACTTTTTTTTTTTT[C/T]TTTTGAGACGAAGTC | 50807 |
| rs190864172 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309579 | AGGACGGCCTTGTGG[A/G]CTGCACCACCACATG | 50807 |
| rs190871706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344314 | GGAAATTTGAACAGC[A/G]ACTGAATATTTAATG | 50807 |
| rs190873111 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130125316 | ATTTTGGTATATCTC[A/G]GGGAGCAATTTGGAC | 50807 |
| rs190873668 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324055 | CCCTCTCCTTCCCTG[A/C]CAGCTCTGTTAGAAA | 50807 |
| rs190873828 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130096840 | GATCAGAAAAAGTCC[A/T]TGAGGCCGGGCATGG | 50807 |
| rs190884474 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130357153 | CATACCACTCTCTCA[A/T]TAACTCACTGAAAAT | 50807 |
| rs190892266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130194139 | ATGTTATTATGAATT[C/T]AGAATGTTCCCAGTG | 50807 |
| rs190897763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258789 | ATACTCCAAATGGAA[C/T]GGTTTTGGGTTCTTA | 50807 |
| rs190900372 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224729 | TAATAAATACGCCTG[A/C]TGAAAGGATACTAGG | 50807 |
| rs190904212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060481 | GGTCAGGTGAGCAAG[C/T]TCTCACTTTTTCTTG | 50807 |
| rs190930124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296101 | CAGCTGCATAGTGAC[A/C]TTTAACTCTCTCTGC | 50807 |
| rs190945423 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410797 | ACATTCCAACACGGG[A/C]TCTCCCACCTAATTT | 50807 |
| rs190947838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372874 | TCTGAGAGAGCACAC[G/T]CATGCATATGGACAC | 50807 |
| rs190959536 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389201 | TATTGTCTCAGGTAG[A/G]AGCTACTGTTATACC | 50807 |
| rs190963464 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156328 | CAGGTTATTAGTGCT[C/G]ATCTTTGCTATCTGT | 50807 |
| rs190969446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130089009 | TGAGTTCACCTTAGA[G/T]CACTTTGCTCTGCTG | 50807 |
| rs190971455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404284 | CTGAATCACAAATTT[A/G]AATTAGATGGGGAAC | 50807 |
| rs190979257 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425762 | TAGGTTTTAAGGACA[C/T]TTAAGAAAGAAGACA | 50807 |
| rs190979647 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123547 | ATTTCTAAATACTTT[C/T]CTTTGTTCTGCTTTC | 50807 |
| rs190986666 | snp | A/C | 0.00565439 | 0.0528699 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060559 | AGGGTTCCTAAGGGC[A/C]TGAACATTGTCCCAC | 50807 |
| rs190989149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117811 | CTGTGCAGCAGATTT[C/T]TGGATACAGACATAA | 50807 |
| rs191003590 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234835 | CATTCTTCCTGAGAC[A/C]AACAATGGTTCTCAT | 50807 |
| rs191021664 | snp | C/G | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084582 | AGCAGCGAATGGCCA[C/G]GTTGCTACAGGAGTA | 50807 |
| rs191035611 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220553 | TTAAGAAACAGCAAG[A/G]TGGCTGGGTGCAGTG | 50807 |
| rs191039943 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130174551 | TCTCTTTTTAGTCTC[A/G]TTACAGAACCAACCA | 50807 |
| rs191048113 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130155524 | AGCATGTGCCACTAC[A/G]CCTGGCTAATTTTTG | 50807 |
| rs191052009 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178502 | ATGGTATTTCTCAAA[A/C]TGTAACACAAATTAT | 50807 |
| rs191052853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139062 | AGTTAATGGTGAGAA[A/C]AACTCTTGCTACGAT | 50807 |
| rs191063227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215418 | GCCTGGGCAACATGG[C/T]GAGACCCCGTCTCTA | 50807 |
| rs191075639 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130193463 | AGAAATCTGTTGATA[A/C]CAATTTCCTCCAGGG | 50807 |
| rs191079627 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368885 | GAGCAACTGTACTTC[C/T]TTTTTAGTGTAAGCT | 50807 |
| rs191088308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314375 | TGAGCTCCTTTTATA[C/T]AGCAGTTTATTTAAT | 50807 |
| rs191094353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297591 | TACAGAAGTGCAGGA[C/T]GACTATCTCCCATCA | 50807 |
| rs191103774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399847 | TTGAGACAGAGTTTC[A/G]CTCTTGTTGCCCAGG | 50807 |
| rs191106467 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130331217 | TCGAGTGGAAAGAGC[A/G]AGTAGGGCCCTATTA | 50807 |
| rs191108503 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392937 | ATTGGGGATCACATT[A/T]CAACATGAGGTTTAG | 50807 |
| rs191113714 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130142605 | GGGACCTGAGCTCAA[C/G]GGTGTGCACCAAAGA | 50807 |
| rs191116023 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130369220 | TCTGGAATGTTTACA[A/T]ATACATAATGAGACA | 50807 |
| rs191116109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347874 | TTCCATAAAATATCT[C/T]CCATGAATCCTTCCA | 50807 |
| rs191121694 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410295 | CCTACCTACTATAAG[C/T]GATTAATAAATCCTC | 50807 |
| rs191124456 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109034 | GCCACCTCGGTCTCC[C/G]AAAGTGTTGGGATTA | 50807 |
| rs191128009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431437 | AGGTTCCAACCATAA[C/T]GAACCACTTGTAATT | 50807 |
| rs191130492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384970 | GAGACAGTGTCCCAC[A/G]TACATACACACACCA | 50807 |
| rs191138043 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166263 | ATCCTCCCACCTTGG[C/T]CTCCCAAAATGTTTG | 50807 |
| rs191146814 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148080 | TTCTCCTCCCTTCCC[A/G]GAATCCCTTACAGCC | 50807 |
| rs191147827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296995 | TTAGAAGGGCAGAGA[C/T]AAAGAATCCCACACT | 50807 |
| rs191154897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131680 | TTATAGCACTAGCTA[C/T]TTGCAAGGCTGCGAC | 50807 |
| rs191163693 | snp | G/T | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277805 | TCTTTGCCACTCATA[G/T]TGTGTCTGTTGACGA | 50807 |
| rs191176673 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130329824 | CACCATTCTAAGTTC[C/T]CCTTGGAGGAAAACC | 50807 |
| rs191176861 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206961 | TGCTTAGCAAGTAAT[G/T]ATTTTATTGGTTTCC | 50807 |
| rs191177061 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183665 | AAAATCAGTATTTTA[A/T]ACTGATTTACCACTT | 50807 |
| rs191178076 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130260079 | ACATTGTCCAGTTAT[A/G]GGAAAAAACCCATTA | 50807 |
| rs191187883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393033 | ACCTTTTTTTTAACA[C/T]GACAGTTATATTATG | 50807 |
| rs191189201 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099420 | CTCCTGACCTCGTGA[A/T]CCGCCCATCGTGGCC | 50807 |
| rs191190981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389671 | CTCTACTCTCTGTTC[C/T]ATACACTGAGCTCTT | 50807 |
| rs191199415 | snp | G/T | 0.000263609 | 0.0114776 | missense | ASAP1 | GRCh38.p7 | 8:130115678 | CCTCCTGTCGAAGAT[G/T]CCACTCATATTCTAC | 50807 |
| rs191201642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432958 | ATGTTGGGTAAGCAA[C/T]CACTGTCTGCTACAC | 50807 |
| rs191208865 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130427250 | GGACTTCATGGTTAT[A/T]CCTGCCAGTAAGAGT | 50807 |
| rs191227996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100821 | TTGTTTCTTTTGCTG[C/T]GCAGAAGCTTTTTAG | 50807 |
| rs191238213 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237080 | TTTGTAATTGCATTT[A/G]TTTTCCTGAGTACCA | 50807 |
| rs191255314 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134584 | AGAGGTTCAGTGACT[C/T]ACACAAGGTCACACG | 50807 |
| rs191257405 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066164 | TTTCCTTTGCCTTCC[C/G]AATAAAATCTCCCCT | 50807 |
| rs191268914 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289140 | GCAGTGAGCCAAGTT[G/T]GTGCCACGGCACTCC | 50807 |
| rs191269169 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253492 | ATGGTGGTGCTACTA[C/T]AGAAGGAAAAGAAAA | 50807 |
| rs191277040 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272803 | AGCTAAAAATGTTGA[A/G]GTAGAAAGTGGAATG | 50807 |
| rs191291426 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130255954 | ACCCACTCCTCCCAC[A/G]CACACAGAACAGCTG | 50807 |
| rs191298963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130221418 | TTGTCACAAGAGATG[A/G]AATGTCAGTACCAAG | 50807 |
| rs191305528 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095195 | CATAAGACTGGGAGA[C/G]TTGTATTAGGGCCAG | 50807 |
| rs191333820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292851 | CAGTTTTATTACCTG[C/T]AAAGCAGAGATGAGA | 50807 |
| rs191338763 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130058645 | GATTAGTTTTGATTT[C/G]AGCATTTATTTGTTG | 50807 |
| rs191342429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384398 | TGTGCCACCCTCCCC[C/G]TCTTCTTACTCAGAG | 50807 |
| rs191345160 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076674 | TACAGGTGCCCACCA[C/T]CACACCCGGCTAATT | 50807 |
| rs191349429 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119081 | GAAAGGATTTTGGTC[A/G]TCTGATATAACTCTC | 50807 |
| rs191352409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150859 | CATTCCAGCCTGGGC[A/G]ACAGAGCCAGACCCT | 50807 |
| rs191355941 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070333 | TGAGCCACCGTGCCC[A/G]GCCGACTGCATCTCT | 50807 |
| rs191356629 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422453 | CACCCACGCTTCCTG[A/G]CTCCTGCTCCCTGGG | 50807 |
| rs191375812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178999 | AATAAGAGCTCCACA[G/T]GCGATCAAATTTAGG | 50807 |
| rs191392399 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054636 | CATGAGTTTCTTACT[C/G]TGTAACAGCAGCTAT | 50807 |
| rs191404703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314039 | CAATCTGAATATAGA[A/C]GTACTGCATGTAAAT | 50807 |
| rs191413169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347567 | TGGGTATAAACGGTG[C/T]GCTTCCCTATCCTCC | 50807 |
| rs191418221 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130310652 | GGGTCACACTATTTA[C/T]AGAGTCAATCACCAA | 50807 |
| rs191419632 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130345640 | TACTAGCAGGGTAAT[G/T]TGAGAGTTTGAAACA | 50807 |
| rs191432718 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406601 | ATTCTCCTGCCTCAG[A/C]CTCCCAAGTAGCTGG | 50807 |
| rs191453937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209928 | TTTATTGCTAATGAT[A/G]AAAACAGAGCTTTCA | 50807 |
| rs191470665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247896 | TTTTCACTAAAACTG[A/G]TCGCTGGCATGTGTA | 50807 |
| rs191483449 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134840 | TGTTTTCTTTTTTTT[A/T]AAAGAAATCTCCTTT | 50807 |
| rs191509377 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130074655 | GGGTGGGAGGGTACA[A/G]GGTCTACCTTAGGAC | 50807 |
| rs191516420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169472 | CATGAGGTTGATCTG[C/G]ACACTATAAAGAGAA | 50807 |
| rs191517006 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373649 | AGTTTGGGAGTTTGA[C/G]ACCAGCCTGGCCAAC | 50807 |
| rs191544427 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238294 | CAGCTTAAGACTGCC[A/C]GTGGTTCTGTTTCTT | 50807 |
| rs191547327 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108127 | TATTGACGCTCTCAG[C/T]ATGCCACACAGCACG | 50807 |
| rs191560783 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130310197 | AGGGATTAAATGGTA[C/G]AACAAATATGAAAGA | 50807 |
| rs191564889 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274285 | TGCATATCAATAAGG[C/T]ATGAAAGATGGAGGT | 50807 |
| rs191574757 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073735 | AGAGGGATGGAAAGA[A/G]AGGATGGATGGATCA | 50807 |
| rs191580623 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130298919 | TACAGGTATTAGGGC[A/G]GCAGAAAACACATCT | 50807 |
| rs191580984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307348 | AGATTTTTATCTGAT[C/T]CTGTGGCAAAAAATA | 50807 |
| rs191589335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130369369 | AGTTTGTATACAATG[A/G]AATATCAGAAAGCAA | 50807 |
| rs191589552 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130342451 | AAGAGTGGACCTTGA[C/T]TTAACAGATGTCCAT | 50807 |
| rs191591003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278912 | AGTGTTAGGCATGTT[C/T]ACAAAGCCCTTCCTC | 50807 |
| rs191592683 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322847 | AAGACCTGCAATGGA[C/G]AGCAGTGGGAAAAGA | 50807 |
| rs191593730 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385240 | GGAGGCTGAGGTGGG[C/T]GGATCACTTGAGGTC | 50807 |
| rs191601522 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130192232 | AAAAATAAAAAACCA[A/G]AAAATCTTAGCTGTT | 50807 |
| rs191602711 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400816 | AAAAAAGGCAAGGGT[C/G]CTGCAGTAAGGGAAA | 50807 |
| rs191609936 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199898 | AAAGTCCATTCATAA[C/T]TCTTATAACAATTCT | 50807 |
| rs191632654 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130207652 | TGAGTATTTTAATAC[A/T]GGCCTCATTAAAAAT | 50807 |
| rs191643547 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130184598 | TACAAAGGGTACCTG[A/G]TCCATCCTAGAATGC | 50807 |
| rs191648312 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130293219 | CAGCAGGTCTGACGA[C/G]GAGGCTCAGATTCAG | 50807 |
| rs191659125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261377 | GCATTTCTGCCTATA[C/T]GCTACTTGCACCTAA | 50807 |
| rs191660083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325364 | CAAACAGTGCACAGT[A/G]AGAAAAGACCAGTGC | 50807 |
| rs191670323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306136 | CATAAATTTTTCATA[C/T]AAAGAATGGTGATAG | 50807 |
| rs191671662 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228495 | AGCTTGAGCCCAGGC[A/G]GTCAAGACCAGCCTG | 50807 |
| rs191672077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130785 | ACCATAGTGCACGTA[C/T]GTAGTCCCAGCTACT | 50807 |
| rs191673771 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245097 | GGCAGCCGCAGCTTA[C/T]ATGAAAGGAAGAGGT | 50807 |
| rs191674894 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130060788 | CTAGCAGGTCTCCCA[A/G]CTGTGGTTTGGGGGG | 50807 |
| rs191676901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155469 | CCTCCCAGGCTCAAG[A/C]GATACTCCCACCTCG | 50807 |
| rs191677387 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394458 | CTCAAACATGTTATC[A/C]ATGACAATGGTGCCC | 50807 |
| rs191680484 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414711 | TTTTTCTTGATATAC[A/G]TGTCTTATTTATGAG | 50807 |
| rs191686231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229610 | AAGCACAATGGACTC[C/T]ACCTGGCACAGAGTA | 50807 |
| rs191688126 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435781 | CAGAGAAATGGCAAG[A/C]AAGCAGGATCTGAGT | 50807 |
| rs191689353 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098537 | TTTTAGTAGAGACAA[C/G]GTTTCACCATGTTGG | 50807 |
| rs191702866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187586 | ACCCCTGGCTAATTC[C/T]TGTACTTCTTCTGTA | 50807 |
| rs191733946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264367 | CTGTCCAGATGGACA[C/T]GACTCTCAGGCCAGC | 50807 |
| rs191742200 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403806 | TGATCTGCCCACCTT[G/T]GCCTCCCAAAGTGCT | 50807 |
| rs191742795 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130282998 | TGCACTATTATTAAA[C/T]GGTCTATGTTCTTCA | 50807 |
| rs191745687 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380913 | TTATTGAGACAGGGT[A/C]TCTCTCTCTTGTCCA | 50807 |
| rs191752270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318308 | GCTGGTTTCAAATTC[C/T]TGGCTTCAAGTGATC | 50807 |
| rs191781344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151611 | TGAAAAGTGTGCTGC[A/G]AGGGGCAAGGGACAG | 50807 |
| rs191789298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130346173 | AAGTTTAAAAACCTA[C/G]GGTTAAAAAGTGAGG | 50807 |
| rs191790374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088713 | AGGAGCCTCAGGAAA[C/T]GAATGCAGGTTTCTC | 50807 |
| rs191796044 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130163230 | ACCTTTGCTAACCTT[C/T]AAAATAAAACACTAA | 50807 |
| rs191796562 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092626 | AGAAAAATTTACAAC[A/G]AAGGTAAGAAGAGTG | 50807 |
| rs191797727 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130212223 | CTACAGTAGAAACTG[A/G]TTCTTCTACTTGGCT | 50807 |
| rs191799283 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130365648 | GAACGTTCCTCTTTT[A/G]TGGCCCTTTTCAATG | 50807 |
| rs191802483 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130382926 | TCACTTTAGCCAGAG[A/G]AAGCTTCATTGAAGA | 50807 |
| rs191806032 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145464 | CTGGGATTACAGGCA[C/T]GCGCCACCACACCCG | 50807 |
| rs191807390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397005 | CTCCTGTCTCCCTTA[C/T]GGTATTTGGGGTGAA | 50807 |
| rs191815682 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130418983 | ACCCTCCCTAAGAGG[A/C]CTGGTAAAAGGCAGA | 50807 |
| rs191818436 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130266604 | TAACGAGATTACCTT[A/C]CAAAAATATAAAAAC | 50807 |
| rs191823825 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130440159 | TGCTGTCCAGTTCTA[A/T]GCCACCATCCTCTTT | 50807 |
| rs191827410 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130053888 | ATTCCACTTATCCAT[A/G]CTATTCCTTTATAAA | 50807 |
| rs191830828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130231454 | AGACCAACAATGTTA[C/T]AGATTCTAAGGGGCA | 50807 |
| rs191833466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180458 | ATTCACCAGTGTTAC[C/T]TCTCACCAATGTTTT | 50807 |
| rs191835971 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130203956 | TAAATTAATTTAAAA[A/G]TAAATTTTACATTAT | 50807 |
| rs191836314 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248589 | GGGTTTTAGAACAAA[C/G]ACGTGATTAGCTCTG | 50807 |
| rs191840583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056701 | CATGTATATACATAT[A/G]TATTTCTGGGTATTC | 50807 |
| rs191858864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128426 | CTGAATAAAGGGAAT[A/G]TTGGAATGGAGAGGA | 50807 |
| rs191888476 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335576 | AGCCAGAAATCAACA[C/G]TGCCTAAAGAGCATA | 50807 |
| rs191891232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214986 | GCTCACTGCACCCTC[C/T]GCCTCCCAGGATCAA | 50807 |
| rs191893960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146665 | TTCCTGTTTCCTGTA[C/T]GTGCTTTCAGTGCTT | 50807 |
| rs191926368 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130303638 | AGGAACCTTAAATGC[A/G]TACTGCTAAGTGAAA | 50807 |
| rs191926418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130265176 | CCTAGAGCAGGCAGA[A/G]TAACAGGAGATGCTC | 50807 |
| rs191933958 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130114925 | ACCACGTTTTATTGA[C/T]TGATCCATTTACTTT | 50807 |
| rs191947210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301886 | AATTCTAAGTAAAGC[C/T]TGCATACAGGATAAT | 50807 |
| rs191954974 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130173813 | TGTGGTGGCTCACGC[A/C]TGTAATCCTAACACT | 50807 |
| rs191955758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360964 | TGAGCTAATTAAGCT[C/T]TCTGAGACTCAGTTA | 50807 |
| rs191967880 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079700 | TTGCTGCTCAGAGAA[C/T]GGTCTGCAGACCTGT | 50807 |
| rs191974947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422508 | ACTTTCCCGCCTTCT[C/T]CCTTGCCTCGGGCTT | 50807 |
| rs192007607 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356966 | AAAACCATCTCCCTT[A/C]CTACTTTCCACCCAA | 50807 |
| rs192012484 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130201464 | ATTCCTTAACTTAAA[A/G]TAATGCAATTATATT | 50807 |
| rs192016566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179521 | GTGTTCAAAACAAAT[G/T]GACTAGAGTGTTAGC | 50807 |
| rs192018948 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137600 | TCCATGGATTCAACA[A/C]ATTTTGGTTGTGATG | 50807 |
| rs192021021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130161926 | TCGCCTCAGCCTTCT[A/G]AGTAGCTGGGACTAC | 50807 |
| rs192025859 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130119944 | CTCAAAAATATGCAT[G/T]CCACCTGTGGAAGCT | 50807 |
| rs192032466 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238815 | TCACATTCTACACTT[A/G]TATCTACCAAATCCC | 50807 |
| rs192036730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362736 | TATTTTCAAAGTATC[C/G]TTTGTTAGGTCAGAT | 50807 |
| rs192047433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226866 | TTTGGTTTACTGATG[A/G]CTCTGTAGGTAATTG | 50807 |
| rs192050836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425490 | CCACTGCACTCCAGC[C/T]TGGGCGACAGAGCAA | 50807 |
| rs192054015 | snp | C/G/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222100 | GCTGAAGAGTTTATA[C/G/T]CCCTAGGCGTTGGCA | 50807 |
| rs192056647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395841 | CCAGCTAATTTTGTA[C/T]TTTTAGTAGAGATGG | 50807 |
| rs192056999 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068300 | GGTCTGCCTGAGCTT[A/C]GTCCACTAGCCTTAA | 50807 |
| rs192057577 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130250453 | GTATGGCGCATGCTA[A/G]GCTTACTATAGTTGC | 50807 |
| rs192072127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286240 | TTTCTTATAAAACAC[C/T]AGAAATAGGCTTTGG | 50807 |
| rs192074839 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086353 | GTTAAGAATGAGGTA[C/T]GTTAACACATGCGAA | 50807 |
| rs192075700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320790 | CTGAAAGTAGAATTT[A/C]CCAATGGAAAAGAGT | 50807 |
| rs192079893 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102979 | TACAGGCACGAGCCA[C/T]CACATCCAGCCTAGC | 50807 |
| rs192083588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143823 | GCTGGAAGTGTAAAG[C/T]TGTTAGCACAGGCAT | 50807 |
| rs192099527 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106331 | GTCATCAATATATGA[A/G]TAACACCACTGATAG | 50807 |
| rs192135440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070020 | ATTTGAACACACTTC[A/G]TGTGAATTGACTGCA | 50807 |
| rs192144235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278731 | TATCCTTTCTAAATA[C/T]AAATACGCATGGGTG | 50807 |
| rs192151529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244793 | CCAGGTGCTGTCCTA[C/G]GTCATCTCCATCTTT | 50807 |
| rs192157067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217960 | GCCTTCTAATCACCA[C/T]CACATTAAAAATTCA | 50807 |
| rs192157788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157177 | AATTTACAATTTATG[C/T]ACACTTTATCTCATG | 50807 |
| rs192161856 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139699 | ACGCCATTGCACTCC[A/T]GCCTGGGCAACAGGG | 50807 |
| rs192172014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123689 | TGGAGTGCAGGGGTG[C/T]GATCTCGGCTCACTG | 50807 |
| rs192181583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314587 | GGAAACACAGATTGC[C/T]AGGCCTGTTCAGTAC | 50807 |
| rs192191888 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379940 | CCTTGTCCTCAGGCT[C/G]AAGGTCTAGAGGCTG | 50807 |
| rs192211588 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177638 | GAAGGTGAAAACTTT[A/C]TACTTCAATATATTA | 50807 |
| rs192220818 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130089612 | CTGCCTTTGGCTTCT[A/G]CAATACAATGTCAGC | 50807 |
| rs192225206 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130081258 | CAGGTGGAGGTAAGT[A/G]TGCTATGTCCAGGAG | 50807 |
| rs192235600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106986 | GGATTGAACAAACTT[A/G]TATTTACTGAATGCT | 50807 |
| rs192253137 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130282622 | TGTGTACATCAACCA[C/T]GGCATTCAAGCCACA | 50807 |
| rs192253777 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337629 | GAGGTTTCTCTCCTT[C/G]CCATGAAAATTGAAG | 50807 |
| rs192256665 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055349 | GGCACCTGGCCAATC[C/G]CAGTACTATTACCTA | 50807 |
| rs192259178 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130319074 | TCAGTCTTCTGAAGC[A/G]TTTTTACAATTTTCA | 50807 |
| rs192262195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248137 | AAGAGGAATAGTTTA[C/T]CTACCTGGTATTTCT | 50807 |
| rs192273360 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354927 | GCCTCACTCTGTCGC[C/T]TAACCTGGTGTGCAG | 50807 |
| rs192285857 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317981 | AGCTAAAACAAGGAA[C/T]AGGAAACTATTAGCA | 50807 |
| rs192286449 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130441303 | CCAAGAAGTTTCCGC[G/T]CCTCCTTAGGACTTC | 50807 |
| rs192292841 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400184 | AGGATTCAACCACCC[C/T]TTCTAGCACCCACAC | 50807 |
| rs192294588 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407578 | TCCCGCTGCCACCAG[C/T]GACAGAAAGATTTAA | 50807 |
| rs192307218 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130061759 | AACTTTGCTTTTCTC[C/T]CACTTACTATGTTTA | 50807 |
| rs192321770 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080924 | AGGCATAAGCCACCA[C/T]ACCCGGCCAAGTATT | 50807 |
| rs192326782 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127373 | AGGTGCCCGCCACCT[C/T]GCCCAGCTAGTTTTT | 50807 |
| rs192355739 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339713 | AAAGAGGTATGTCTG[A/G]TTCTGTGCCCTGAAG | 50807 |
| rs192361193 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391991 | GCAAAGTTGTGCAGG[C/G]GGAGCCAGACCTGGG | 50807 |
| rs192364462 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130162691 | GGCGTGGTGGCGGGC[A/G]CCTGTACTCCCAGCT | 50807 |
| rs192369301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130409001 | ATGTGGTGGCTCATG[C/T]TTGTAATCCCAGCAC | 50807 |
| rs192372634 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377031 | ATCTCAGAGTTGAAT[A/G]GACTTTGCCATCATC | 50807 |
| rs192377356 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445097 | ATTCTCTCTCCGTGG[C/G]CAGAAGCAGTAGGAC | 50807 |
| rs192382290 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428231 | ATTTACTTTGAATCA[C/T]CTGCTCCTAGTATAA | 50807 |
| rs192408953 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270442 | GGAATCAGCTCTGTA[G/T]GTAAAAGTATAAAGA | 50807 |
| rs192413001 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130243537 | GCCTGCAAGGCCCTA[C/G]GTGACCCAGCCTTCT | 50807 |
| rs192420060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066896 | TGTGAAGAGGCCCTG[C/T]TGGGTCTGGGTACAG | 50807 |
| rs192428092 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413562 | TATATCTAAGAAATG[G/T]TCAAATCTCATCAAG | 50807 |
| rs192428238 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130305127 | TTGCTCATGAAGTCT[C/T]CCCTCCTGCTACCAC | 50807 |
| rs192442285 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311685 | AGAATCGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 50807 |
| rs192456512 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130346008 | TGCAATTGGTAGGCA[G/T]ATATATAAAGCCCAG | 50807 |
| rs192457991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325785 | TTCTTATAAACTGCT[A/G]TTGAGATAGATGTTT | 50807 |
| rs192470179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364868 | TCAGGAGTTTGAGGC[G/T]GCCGTGAGCTATGAT | 50807 |
| rs192472192 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348546 | GTGGGCTGGAAAGAG[C/T]CTACTGTGAACTCCT | 50807 |
| rs192495164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333417 | GACCAGCCTGACCAA[C/T]ATGGTGAAACCCTGT | 50807 |
| rs192501978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275423 | CAGATGGATGACCCA[A/G]GTCAATACCCCTCTC | 50807 |
| rs192506389 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248984 | TAATAGGCTAGATTC[A/G]AACCCTTGGGCTCAA | 50807 |
| rs192511272 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293966 | TTTGAGCCTCTATGT[A/G]AGAGCCAAATACTCT | 50807 |
| rs192512672 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130256910 | AATTAAAGGGATATC[A/G]ATGATTTAAGAAGTG | 50807 |
| rs192513316 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378152 | ATCCTCAGTTTGCAC[A/T]TTTGAAATATGCGGT | 50807 |
| rs192515743 | snp | C/G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130232857 | AGCATTGTGAGAAAA[C/G/T]AAGAAAATTATGAAA | 50807 |
| rs192516260 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130260917 | AACCAAATTTGCTTT[C/T]CCCCCCCTCAAGATA | 50807 |
| rs192516795 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370936 | GGTACAGGGTTTCTT[G/T]TGAGGAGTGACAAAA | 50807 |
| rs192519400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130351015 | TTGCTTGCAGCACTG[C/T]CTTTGATCACAAAAG | 50807 |
| rs192523272 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411812 | TAGGCATGTTTTATG[C/T]GGCTGGAAATCCTGT | 50807 |
| rs192532884 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434777 | TCTCTGTGACGGCTC[A/G]GCCCATATTGATGAG | 50807 |
| rs192535071 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130386368 | ACTAAAACTGTGCTG[A/T]CCACGGAGGTAACAC | 50807 |
| rs192537453 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130196690 | CCTCTCCACTGCCCA[C/T]TGGTTCTCTCTCTCT | 50807 |
| rs192538430 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402255 | ATTTACAAGTCATTA[A/C]CTTCTCTAGACCTAG | 50807 |
| rs192552377 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297989 | ACATCTGGGTTCCAG[A/T]CCCAATTCTCTGTGG | 50807 |
| rs192563927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332177 | AACAGTCTGATTTGA[C/T]GGCACTTGTGAAGTT | 50807 |
| rs192585215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401832 | CCCAAGAAGAATCCC[A/G]CTGTATCTCCCACGC | 50807 |
| rs192592687 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316379 | TTTCTACTCCAAGTA[G/T]TCCTGATGTGGCCTT | 50807 |
| rs192601797 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177051 | CCATTATGATTAATA[A/G]TGGATCTGACTTACT | 50807 |
| rs192603503 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299708 | ATCAAGAAGACAAAA[A/G]TCAGCAGAAACTTTC | 50807 |
| rs192613031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158794 | TGGAGTGCAGTGGTG[C/T]GATCTCAGCTCACTG | 50807 |
| rs192616597 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227498 | CCTGGGCTCAAGTGA[G/T]TCGCCTCCCTTGGCC | 50807 |
| rs192617721 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236775 | GGCTGACAGTCGAGA[A/T]AAGAGAAAAAAAGAG | 50807 |
| rs192625586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217106 | AAATATGGCATGCAC[C/T]ATCCAAGGCCATGTG | 50807 |
| rs192653550 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333028 | ATTCAAGCACAAAGC[G/T]GTTCAATCTTTCATA | 50807 |
| rs192665798 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370171 | CCCAAGCATGGTGGC[A/G]CACACATATAATCCT | 50807 |
| rs192666480 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062635 | AGAAACTCTAAGTGC[C/G]AGGCATGGAAAACCT | 50807 |
| rs192680334 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140082 | TTGTCGGCCAGGCTA[C/G]AGTGCACTGGGGTGA | 50807 |
| rs192683935 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236220 | GAGCTGGTACTGCAA[C/T]AGTAACAAAAGATGT | 50807 |
| rs192684879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098790 | TCTTTGTGTTGTGAA[C/T]ATTCAAAATCCTTGC | 50807 |
| rs192691128 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115197 | TCAAGGGAACTACCC[C/T]TCATGATGTGGGTGT | 50807 |
| rs192700549 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130271112 | TCTGATTTGGTCTCA[C/T]TTGCCCTGCAAGCAA | 50807 |
| rs192723603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180231 | CTCTTACTCAACAGC[C/T]GTGTCAGAACAGGTT | 50807 |
| rs192726435 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111383 | TCCAAGTACTGTCTC[C/T]GGAAAAATGTTCCTT | 50807 |
| rs192737944 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144286 | TCCAAACAGATAAAA[C/G]GTAACAATTTTTTGA | 50807 |
| rs192740787 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085492 | GTAATCCCAGCACTT[C/T]GGGAGGTCAAGGCAG | 50807 |
| rs192742231 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257457 | TATTAGGCACAGTAC[A/T]TCATAAAGAATATTT | 50807 |
| rs192747485 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130294589 | ATAATACATCTAAAG[C/T]ATGTTTAAGTGTCCA | 50807 |
| rs192749236 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130326294 | TTACAAGTCTACTAT[A/C]ATGATTACAGTACTC | 50807 |
| rs192752426 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353452 | AACTTAGGCACCTTT[A/T]TTAATCAGACCAAAA | 50807 |
| rs192762619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188812 | TTAAACACTATACTA[C/T]AGTACACGTATATGT | 50807 |
| rs192768030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223372 | GGCCTCAACTTCATA[C/T]GTGAAATGGGACAAT | 50807 |
| rs192773409 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434932 | TGAAATGCTTACAGC[A/C]CATCCCCTGAAAACC | 50807 |
| rs192779285 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119463 | TGCCTTCTTTACTTC[C/T]GTTCAAGTGTTTCTG | 50807 |
| rs192795592 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085874 | AAGTCTCCTGAGACA[G/T]ATGGCTGGATTCATC | 50807 |
| rs192807475 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130248840 | ACAAAGATGTTCACC[C/T]GGACACCAAAGTCAC | 50807 |
| rs192812402 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394189 | CACCGGTGAGCTGGG[C/T]GGAACAGAGCCATAT | 50807 |
| rs192818102 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283869 | TCCAATGAAGGGTAA[C/G]GGCCTAAAAAAATGG | 50807 |
| rs192825548 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130067697 | TGAGCCACCGTGCCC[A/G]GCCCCACTGCTTTAA | 50807 |
| rs192839986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385550 | CAGCTTTTCCGACCC[A/G]TTACATGGGGATGTT | 50807 |
| rs192845020 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213067 | GGCCTCCAGTGAAAG[G/T]GCAGGCAATGCTCAG | 50807 |
| rs192849426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422987 | TAAGCAGCCTGAGGT[C/T]ACAGTTGACGGCAAA | 50807 |
| rs192853072 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171366 | ATTGACTCACAGTTC[C/G]ACATGGCTAGGGAGA | 50807 |
| rs192857079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110656 | GTGTGGCCACTGGTT[A/G]TCTTTGAGGATAGCT | 50807 |
| rs192871838 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130315952 | GTTTCATGGCTCATC[C/T]TCCCACTGGCATTGG | 50807 |
| rs192874669 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130075182 | TTGTTTCAAACTCTT[C/T]TGAGATCAAAACAGC | 50807 |
| rs192878341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349763 | CTTGACACCCATAGG[A/G]ACATACTTTACTGAC | 50807 |
| rs192878677 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423471 | CCTGAAATTCCACCT[A/C]TGGGAATTTGTCAAA | 50807 |
| rs192890380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251235 | CCAGCCTGGCCAACA[C/T]AGCGAAACCGCATTT | 50807 |
| rs192901471 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130287577 | TGATGGGGACATAAA[G/T]CCTAACCCACAAAGC | 50807 |
| rs192917393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166718 | CACAGCAGGTGTTAA[C/T]GAAATGTTTGAACAA | 50807 |
| rs192921418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130194721 | CCCTCACATTCACAG[C/T]TCACAACAGGGTTTG | 50807 |
| rs192923470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100186 | GATTTGTTATTTCTT[A/G]TCTTTTTGATGATAG | 50807 |
| rs192924542 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132704 | TCCATCTAATTTAAT[A/G/T]TTGTATTCTCAAGGC | 50807 |
| rs192939851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064239 | ACTGTCCAGACAAGA[A/G]ATGATGCTCATTTGA | 50807 |
| rs192940672 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275652 | AAAAACTATGTATAT[A/G]AAGATTCTTGCACAA | 50807 |
| rs192946443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239887 | CCTATGCTTTTTCAA[C/T]CATGCCATCTAATCT | 50807 |
| rs192950815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311940 | TAATGATTTATTAAT[C/T]GTACTCCTTCTAAAT | 50807 |
| rs192954415 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383249 | AGGATTCCCCAGGCT[C/G]CAGCCCCTGGGAGGA | 50807 |
| rs192954793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336977 | AAAATAGTTTTGATC[C/T]CTCAGAACCCCTGGA | 50807 |
| rs192962595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130420636 | CGGTGGCTCACACCT[A/G]TAATCCCAGCACTGT | 50807 |
| rs192973068 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170393 | CTCCTGACCTCAAGT[C/G]ATCTGCCCACCTCGG | 50807 |
| rs192990974 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130346347 | CGGTTGGTATTTAAT[A/G]CACTGTCAGGAAGTT | 50807 |
| rs193007160 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102867 | ATTTTTTATTTATAT[C/T]TTTTGTAGAGACAGG | 50807 |
| rs193007225 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136539 | TCTTAACCACAGGTG[A/C]ACATTACAATCACCT | 50807 |
| rs193017297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130267380 | TACTGACAGCTAAGA[C/T]TTACTGAGTACTTAG | 50807 |
| rs193022479 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130232340 | TTAATCATATATTAG[C/T]AAAAGGGCGAAGGAG | 50807 |
| rs193028436 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130396453 | CCATAACCTTCCTTC[A/C]TTTATGTATTTAACT | 50807 |
| rs193033384 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374728 | TGTCTGAATCCTGAC[C/T]TGTACCATGGTTGCA | 50807 |
| rs193036024 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153619 | GCAATCTGCCCGCCT[C/T]GCCCTCCCAGAATGC | 50807 |
| rs193036399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439041 | CTGTTGACCTTAAAA[C/T]AGGGAGAGTAGCCTA | 50807 |
| rs193051948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189122 | GATCGAATCAGGGAA[C/T]TGGGGTTTCCATCAC | 50807 |
| rs193059457 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130304061 | GGTAGCAAAATGAGA[C/T]GGTACATAAGAACTC | 50807 |
| rs193061554 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130268214 | GTATAGGCCTGGCAC[A/G]GTAGCTCATGCCTGT | 50807 |
| rs193073393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058498 | CAGCTTCTGCATAAT[A/G]AATGTGCAGCATAAA | 50807 |
| rs193074134 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130338104 | TAAGACGACCTAAGG[A/C]GCCTGTGATGCTTTA | 50807 |
| rs193077413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126620 | GCCCTAGAACAATGG[A/G]AACTATTACTTCCAT | 50807 |
| rs193080086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239147 | TAGGATCTCAAGTCA[C/T]CTCACATACCTGTCA | 50807 |
| rs193083769 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130094255 | TTGCTTTGTCATCCT[C/G]CTTGGAGTGCAGTGG | 50807 |
| rs193084159 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203360 | CACCCACCTGGCTTG[C/T]ACAAGGGAAGCCTGA | 50807 |
| rs193098330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359424 | CATTCGCTGAGTATG[A/G]ATTTGGTTTAAAAGA | 50807 |
| rs193101207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394049 | GACCCTGTGATGATT[A/G]CATTAACTGCACAAA | 50807 |
| rs193116752 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288274 | TTCCAGTATTTGACT[G/T]CGAGGGCACCATTCC | 50807 |
| rs193117867 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322182 | AAGTCAATAAAACAA[C/G]TTCCAAAAGAAGGCT | 50807 |
| rs193146234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055782 | GCATATTGGCTTCCA[A/G]TGCCAAATCGATAGA | 50807 |
| rs193146875 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183381 | AGTCTCGCTTTCTTG[A/C]CCAGGCTGGAGTGCA | 50807 |
| rs193149578 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123899 | TCCCAAAGTGCTGGG[A/G]TTACAGGCGTGAGCC | 50807 |
| rs193151528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090468 | CTTAGTCTTTATGTA[C/T]ATATGTGCTAGCACA | 50807 |
| rs193151825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130147723 | AGATGGACTCAAAAG[A/G]ATGTGGTCTGACTCT | 50807 |
| rs193161568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082870 | GCCTGGTAGGCATTT[C/T]TTTCTAGCACTGTGC | 50807 |
| rs193163964 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130148424 | TGAAAATTCAAAGAT[A/G]AGTAAGATGCGGTCC | 50807 |
| rs193164321 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176038 | AAAGCAGCATGTTCC[C/T]GACAATGTTCATGTC | 50807 |
| rs193166671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116495 | CTGCATTCCAAAAAC[A/G]TGTGGATGACAAATT | 50807 |
| rs193180599 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130427340 | CTTGATATTGACAGT[A/G]TGTTTACTCCTATGA | 50807 |
| rs193182401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397744 | GTTGGTTGAGAAGCA[A/C]ATCTGTGTTATTTCA | 50807 |
| rs193201524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366464 | TTGACACAGTTCCTC[C/T]TCCCTTGGTCATTTT | 50807 |
| rs193218457 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418273 | ATACAATTCAGGCCC[A/G]GCACGGTCGCACACA | 50807 |
| rs193234807 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130284679 | AGCCACTGGGAGGGA[C/G]GGGTAATTTAGCAAT | 50807 |
| rs193237371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319519 | CACAGAACAGAGCAA[C/G]TATTTACAAATCCTG | 50807 |
| rs193238113 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382243 | GTGAGCCGAGATTGC[A/G/T]CCACTGCACTCCAGC | 50807 |
| rs193239268 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355288 | CCAAGGAGACATAGT[A/G]AAAGAAAGAGTATGG | 50807 |
| rs193242418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222970 | ATCCAGGTCTTAGCT[C/T]CAGACTCTACCATGT | 50807 |
| rs193255522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377769 | CCAGGCTCCAGCCCT[C/T]CCGGCTGTGTCTCAG | 50807 |
| rs193269511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306561 | AGAGCTGGTTCTTTG[C/T]TTCCTCTCAAACTTT | 50807 |
| rs193270534 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272173 | TGTCTCAAAAAACAA[A/C]AACAAAAAATGGGCA | 50807 |
| rs193277462 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341872 | CAAGAAACGAGAGTC[A/C]AACTAGGAGACTCTT | 50807 |
| rs193291532 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107327 | AGCTGGGACTACAGG[C/T]GTCCTCCACCACACC | 50807 |
| rs193291552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130981 | CTAACACGGTGAAAC[C/T]CCATCTCTACTAAAA | 50807 |
| rs193298454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166022 | ATTGCTCTTCATTTT[C/T]TGTTTGTTTGTTTGT | 50807 |
| rs193298760 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073095 | GTTGTTGGTGAATTC[A/G]GATTATGGACGAATA | 50807 |
| rs199518849 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428821 | CACCACCACCATCAT[C/T]ATCATTGCATTAATT | 50807 |
| rs199524839 | in-del | -/GAAAAAGGAAAGGAAAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216032 | AAAAGGAAAGGAAAG[-/GAAAAAGGAAAGGAAAA]GAAAGAAAAGGAAAA | 50807 |
| rs199570899 | in-del | -/GAA | 0.0322114 | 0.122752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130125695 | GAAAAATGTAGTTTT[-/GAA]GAAGACCATCCCAAA | 50807 |
| rs199577556 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130148230 | GCTGAGGAAAAAAAA[A/C]CCCTATGATACAGTA | 50807 |
| rs199580611 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130178893 | ACTCCGTCTCAAAGG[-/A]AAAAAAAAAAAAGGC | 50807 |
| rs199581897 | in-del | -/TT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130277805 | TCTTTGCCACTCATA[-/TT]GTGTCTGTTGACGAA | 50807 |
| rs199603852 | snp | A/T | 0.000181589 | 0.00952687 | missense | ASAP1 | GRCh38.p7 | 8:130214594 | GTTCCTTTGTAAGAG[A/T]AGAAAACTTGACAAA | 50807 |
| rs199611828 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130249724 | CACACATATGTATGT[A/G]TTTATTTATATATTA | 50807 |
| rs199631667 | in-del | -/A | 0.0263992 | 0.111815 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052624 | GAACAAAAAAACTAG[-/A]AAAAAAAGGTGTTAA | 50807 |
| rs199631877 | in-del | -/TCT | 0.467234 | 0.12373 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080477 | GTCATTCATTCTCTC[-/TCT]TTTTTTTTTTTTTTT | 50807 |
| rs199638992 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130249141 | CCCCAGCCAGGTACT[C/T]CCACAGCCTCTAGCA | 50807 |
| rs199685280 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130273527 | CTTGGGAAACTTGCT[-/T]ATAAACACAGCAGCC | 50807 |
| rs199685908 | in-del | -/GGAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130437901 | ATCCCGCCACTGGAG[-/GGAC]GGACATACTTACTTT | 50807 |
| rs199689989 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130160546 | CAGCAGTGAAAAGTG[G/T]TATGATGTCGTGGAG | 50807 |
| rs199692530 | in-del | -/TAAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130200270 | AAACAGGAAGTTGGG[-/TAAA]TAAATTATAGTGCAA | 50807 |
| rs199704701 | snp | A/C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148222 | ATCTGGCAGCTGAGG[A/C/T]AAAAAAAACCCTATG | 50807 |
| rs199708236 | snp | C/T | 0.00299544 | 0.0385843 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116825 | ATAATCAAATTACAA[C/T]GTACCATGCAACACA | 50807 |
| rs199711648 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086492 | TTTTCTTTTGTCTTA[A/C]AAGCCATAAACCTGT | 50807 |
| rs199723795 | in-del | -/ATCAT | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428543 | ACCACTATCATCACC[-/ATCAT]ATAACTACCACCATC | 50807 |
| rs199740640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139566 | CCCCGTTGTCTCTAC[C/T]GAAAATACAAAACTT | 50807 |
| rs199740968 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130281493 | ACCTTCTAAGAACAG[A/G]GGTTTATATCTCCAA | 50807 |
| rs199755918 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130162324 | TTGTTGTTGTTTTTT[A/T]AAGAGAGGCAGCAGT | 50807 |
| rs199759148 | snp | C/T | 0.00199798 | 0.0315436 | missense | ASAP1 | GRCh38.p7 | 8:130124017 | GAAATACTTACATAT[C/T]ACTTGAAGGGGTGGG | 50807 |
| rs199760248 | snp | C/G/T | 0.000300604 | 0.0122562 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124135 | CAAACAACCACAATA[C/G/T]AGCAAACTCTTTGCT | 50807 |
| rs199764504 | in-del | -/GCTCACT | 0.021333 | 0.101051 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101641 | AGTAGCGTAATCACA[-/GCTCACT]GCAGCCTCCTATGCT | 50807 |
| rs199766652 | snp | A/G/T | 4.94176e-05 | 0.00497059 | missense | ASAP1 | GRCh38.p7 | 8:130060730 | AGTGTGACCTCAGAG[A/G/T]GTTGCTGAGCCTTGG | 50807 |
| rs199768413 | in-del | -/TTG | | | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052738 | TTTTTGTTTTTGTTT[-/TTG]TTTTTTTTTTTTTGA | 50807 |
| rs199770520 | in-del | -/A | 0.000809353 | 0.0201003 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134351 | TCTATTATCTAAAAT[-/A]AAAAAAAAAGAAAAA | 50807 |
| rs199771267 | in-del | -/AAG | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169662 | CACCTGAAAAATAAC[-/AAG]AATTAATATCTGTGG | 50807 |
| rs199774290 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130140890 | CAGAGGGGAGTGGTA[C/T]GTTCCACAGAAGTCC | 50807 |
| rs199776069 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130209794 | TTTTTTAGTGGAACA[-/C]CTTTTTTTTTGAAAG | 50807 |
| rs199777096 | in-del | -/TGT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130389132 | TATTGTTGTTGCTGC[-/TGT]TGTTGTTGTTACAAT | 50807 |
| rs199779145 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130256721 | AATTCAAAATCTTCT[C/T]CCTGAATATACACAT | 50807 |
| rs199802181 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130379376 | GGGTGGTATGGCTGT[A/G]GATGTATTTTCCTGA | 50807 |
| rs199808862 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130300180 | GAGAGAGAGAGAGAG[A/C]GAGAGAGCGAGCGAG | 50807 |
| rs199809080 | in-del | -/TCTGTT | 0.0283406 | 0.115616 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109461 | ACTTTATCTCAAGTG[-/TCTGTT]TCTGTCTCACTGGAA | 50807 |
| rs199811164 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148841 | TTTTGAGGCTAAAAC[-/T]TTTTTTTTCTTGAGA | 50807 |
| rs199814916 | in-del | -/A | 0.0197687 | 0.0974348 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309972 | GTAATAGCAGACAAT[-/A]AAAAAACAGAGGCTC | 50807 |
| rs199815534 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130174189 | GTGGTAACCTTGGGC[A/T]GTTATTCACCCTGTC | 50807 |
| rs199823423 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130160545 | ACAGCAGTGAAAAGT[-/G]TTATGATGTCGTGGA | 50807 |
| rs199829889 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130311046 | CAAGGGCTCCCACAG[G/T]GGGGAGGACAGCCAT | 50807 |
| rs199838935 | in-del | -/ATTC | 0.0509478 | 0.151255 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397104 | GTGGACTGTGATTTT[-/ATTC]ATTCATTCATTCATT | 50807 |
| rs199850931 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130357176 | CTGAAAATCCTAAAG[-/A]AAATCGATTTGGCCT | 50807 |
| rs199857305 | in-del | -/GTT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130402920 | ATAATCTTTTGTGGG[-/GTT]TTTTTTTTTTTAATC | 50807 |
| rs199872957 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409270 | GTGTCTCAAAAAAAA[A/C]AACAAAAAACCTCCT | 50807 |
| rs199880805 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130092937 | GCCTGACGCTTTTCT[-/A]TAAAAAAAAAAAAAA | 50807 |
| rs199892460 | in-del | -/GA | 0.233527 | 0.249457 | intron-variant | ASAP1 | GRCh38.p7 | 8:130230273 | ACCAGCAAAACGGAG[-/GA]AGTGCATACACAGGC | 50807 |
| rs199903371 | in-del | -/TGTAGT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130284438 | GAGTCAAATTGTAGT[-/TGTAGT]AACTCAACTTTTCTC | 50807 |
| rs199913617 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130198355 | ATTCTTTACACTTGA[A/G]AAGCTCAGCAGTAGT | 50807 |
| rs199914568 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130257939 | TCCAAATTCAACCTG[C/T]CATGGGTGTTTTACA | 50807 |
| rs199921596 | in-del | -/TTTT | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066571 | CTCATTCTTTCTTTC[-/TTTT]TTCTTTCTTTCTTCT | 50807 |
| rs199922446 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130095459 | ATGTGTGCCACCACG[C/T]CTGGCTAATTTTTGT | 50807 |
| rs199926213 | snp | A/G | 0.00173372 | 0.0293914 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136919 | GTGTCAGAAGCCACA[A/G]TAACCAACTCAGAGA | 50807 |
| rs199956270 | in-del | -/CT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130317042 | ATTTGGTACATTATA[-/CT]CACCTTGAGACTCAT | 50807 |
| rs199961508 | in-del | -/AAAAAAAAAAAAAAAAAAAAAAAAAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130151371 | GCGAGACTCAGTCTC[-/AAAAAAAAAAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 50807 |
| rs199962185 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130245407 | GGAATTTGACCAAAG[A/G]ACAGGAAAGATCTGT | 50807 |
| rs199998244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058203 | TTGATTTCCTCACCC[C/T]TGAAGGGCGGGAAGA | 50807 |
| rs200011464 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130121813 | AAAAAAAAAAAAAAA[A/G]AACATACGATCAATT | 50807 |
| rs200013346 | snp | C/T | 8.23621e-05 | 0.00641672 | missense | ASAP1 | GRCh38.p7 | 8:130058001 | TAATCACTTCTCCCT[C/T]GATGAATGTGAGCTC | 50807 |
| rs200025500 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130219815 | TGATGTTGAGACAAG[A/G]TCTTGCTATTGTAGA | 50807 |
| rs200033813 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130226044 | ACTACCATGCTTGGC[-/T]TTTTTTTTTTTTTTT | 50807 |
| rs200037434 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130097766 | GATCTCCTGAGACTC[-/T]CTCCCAGGAACTGAC | 50807 |
| rs200047056 | snp | A/G | 2.0262e-05 | 0.00318286 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130358149 | GTCCGGCATCCTGCC[A/G]GGAGGGACGAGACAC | 50807 |
| rs200050815 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130342752 | AGATGCCAACTCTCA[A/G]AAACAAGTTAAAGTT | 50807 |
| rs200055386 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130402917 | AGAATAATCTTTTGT[G/T]GGGTTTTTTTTTTTT | 50807 |
| rs200056824 | in-del | -/CTT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130423782 | GATGATGATTATTTG[-/CTT]CTTTATCTTTTCTTG | 50807 |
| rs200064489 | in-del | -/TTGTAG | 0.0524604 | 0.153226 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284431 | AAAACGGGAGTCAAA[-/TTGTAG]TTGTAGTAACTCAAC | 50807 |
| rs200066208 | snp | A/C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130250750 | TTCTCATAAAAAAAA[A/C/G]TGATGGAGTTAAAAA | 50807 |
| rs200078763 | in-del | -/T | 0.000798722 | 0.019968 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114114 | TGATCTGAGATAACG[-/T]TAAGTGCTTAAATCT | 50807 |
| rs200097909 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130236342 | TTTTTAATTTAGTTT[A/C]TTTCCTCTTATTCAC | 50807 |
| rs200115609 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130066599 | TCTTCTCTCTCTCTC[C/T]TTCCTTCCTTGTTTC | 50807 |
| rs200118972 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130250024 | AAGAAATTTTAATTT[A/T]AAAAAAAGTAACACA | 50807 |
| rs200123504 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130102996 | ACATCCAGCCTAGCT[A/G]TCTGTTTTTTAAAGA | 50807 |
| rs200130521 | snp | C/T | 0.000148245 | 0.00860815 | missense | ASAP1 | GRCh38.p7 | 8:130060698 | CATTTGGGGATAGAT[C/T]CAATGGGTGTGACTT | 50807 |
| rs200134485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188074 | AAAATTAATCCTTTC[A/C]AGTTAAAGTGAAAAT | 50807 |
| rs200150977 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428475 | TCATCATCACCACCA[C/T]CACCACCATCTTCAT | 50807 |
| rs200162830 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130119768 | ACCCCAGCTGTGTGA[-/C]CATAGTAAACTGCTT | 50807 |
| rs200162907 | in-del | -/C/CCCCCCC | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373084 | AAGCACACACAGACA[-/C/CCCCCCC]CCCCCCCACACACAC | 50807 |
| rs200170924 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130247232 | TCAGAGTCTGATTTT[G/T]GTTCATTCTTGTCTC | 50807 |
| rs200185585 | snp | A/C/G | 1.64792e-05 | 0.00287042 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079874 | TCAATGGATCCAACA[A/C/G]GGGAAATGAAGCGCT | 50807 |
| rs200208205 | snp | C/G | 0.00199792 | 0.0315431 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116665 | TAAATCTCCCACGTC[C/G]ATTTTTGCTTACCAG | 50807 |
| rs200210080 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130091480 | AGATAGAGTGGCAGG[A/G]GAGGGTCTAGGAGAT | 50807 |
| rs200214004 | in-del | -/CC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130389356 | ATGGCTGGTTAAAGT[-/CC]CCAGGACAAGGGAAA | 50807 |
| rs200221922 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130262178 | AAAGTGGGTGGATCA[C/T]GAGGTCAGGAGTTCA | 50807 |
| rs200228967 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130282629 | ATCAACCATGGCATT[A/C]AAGCCACAATATCAA | 50807 |
| rs200232434 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130307355 | TATCTGATCCTGTGG[A/C]AAAAAATAAAGAGGG | 50807 |
| rs200265381 | in-del | -/C | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414019 | GATTGCTGGTACCTG[-/C]CAAGAACAGAAGTTG | 50807 |
| rs200268356 | snp | C/T | 0.00199792 | 0.0315431 | missense | ASAP1 | GRCh38.p7 | 8:130180776 | TGGAGCTGAAAGAGG[C/T]GCCTTTCCTTCTCCA | 50807 |
| rs200287803 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130145328 | GGCATATGTTTTTTT[C/T]TTTTTTTTAGACGGA | 50807 |
| rs200314915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070322 | GATTACAGGCGTGAG[C/T]CACCGTGCCCGGCCG | 50807 |
| rs200323353 | snp | C/T | 0.000210428 | 0.0102552 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236908 | ATGTTACCTCATTTT[C/T]AGTAAGTGCTTACCT | 50807 |
| rs200323716 | snp | G/T | 1.64751e-05 | 0.00287007 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130112218 | CCGCTGTTTGTCCCT[G/T]GGAGTGCTGAATCCT | 50807 |
| rs200338365 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130394942 | CAGGAGAGGAGCCTG[G/T]TTTAACCACTTTACC | 50807 |
| rs200340421 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130113635 | AGAGGTAGTTAACTG[-/C]CTTATAAGGAAAACT | 50807 |
| rs200344901 | snp | C/T | 1.67351e-05 | 0.00289263 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123997 | TAAAAAAGTTCAATA[C/T]ATCAGAAATACTTAC | 50807 |
| rs200348638 | in-del | -/ATA | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428410 | AAATGCCAAATCACC[-/ATA]ACCACCATCACCATC | 50807 |
| rs200357465 | snp | A/T | 0.158962 | 0.232835 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437622 | TTTAGATAGATAGAC[A/T]AACTACAATGAAATA | 50807 |
| rs200376344 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130198135 | TTTATTTTCATAAGA[-/T]TTTTTTTTTTTTTTT | 50807 |
| rs200383209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413910 | TTCATTCATTCATTC[A/G]TTCATTCATTTATGT | 50807 |
| rs200388609 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130285323 | CACCAAGTTGGAAAG[-/A]AAAAAAAAACAAAAA | 50807 |
| rs200392278 | snp | G/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409132 | CCAGGCATGGTGGCA[G/T]GCGCCTGTAGTCCCA | 50807 |
| rs200393704 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130389134 | TTGTTGTTGCTGCTG[C/T]TGTTGTTGTTACAAT | 50807 |
| rs200395609 | in-del | -/G | | | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052740 | TTTGTTTTTGTTTTT[-/G]TTTTTTTTTTTGAAA | 50807 |
| rs200402833 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130393020 | CCTCAAAAATAAACC[-/T]TTTTTTTTAACATGA | 50807 |
| rs200402852 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130385007 | TATGGAGGCCGGGGC[C/T]TGAGGTCCAAATATT | 50807 |
| rs200412481 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056956 | GTGTGGACTGCCCTC[-/G]CAGGTCACTCACAGC | 50807 |
| rs200416384 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130406476 | TTCATACTTTAGTTC[-/T]TTTTTTTTTTTTTTT | 50807 |
| rs200420720 | in-del | -/GTTTATTTATATATTACTTCCTCCC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130249724 | CACACATATGTATGT[-/GTTTATTTATATATTACTTCCTCCC]AGTTGTAGAGCCATC | 50807 |
| rs200431164 | snp | C/T | 1.80703e-05 | 0.0030058 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091947 | CTGGCCCCAGCAGCT[C/T]TGGCCCTGACTTTAG | 50807 |
| rs200433830 | in-del | -/GG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070900 | GAGAGAGGGAGAGAG[-/GG]AGGGAGAGAGAGGGG | 50807 |
| rs200448508 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130060705 | GGATAGATCCAATGG[A/G]TGTGACTTCAGTGTG | 50807 |
| rs200450021 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130147228 | AAAAAAAAAAAAAAA[C/T]AATTCCAATAAACCA | 50807 |
| rs200482062 | in-del | -/AAC | 0.0232847 | 0.105357 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163697 | ACATTTAATAACATT[-/AAC]AACAATTTAAAAACT | 50807 |
| rs200490215 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130245409 | AATTTGACCAAAGAA[A/C]AGGAAAGATCTGTAA | 50807 |
| rs200495606 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130195403 | AAAAAAAAAAAAAAA[A/G]ATGAGCTGGGCATGA | 50807 |
| rs200504967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214719 | AAAAACAAAAAAGAA[A/G]AAGAAAGGAGTCTGA | 50807 |
| rs200510287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188087 | TCAAGTTAAAGTGAA[A/G]ATCAAATTTCTGAAC | 50807 |
| rs200515876 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130352213 | AATCCTTCCTAAGGG[-/T]TTTTTTTTTTTTTTT | 50807 |
| rs200523896 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130339747 | AGTTGGCAGTGGCTG[A/C]AAACTCAGGACTGAT | 50807 |
| rs200526599 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130137308 | TCTCATTAAAGATGG[-/A]AAAAAAAAATTAGGT | 50807 |
| rs200531646 | in-del | -/AT/CACA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130373108 | ACACACAGAAATACA[-/AT/CACA]TATACACACACACAC | 50807 |
| rs200537060 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130092337 | TGGTTAAAAAAAAAA[A/T]AAAATTGGCCAGGTG | 50807 |
| rs200548543 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285824 | GGTTTCTGATGTAAC[-/T]TTTATCACGTTCTGT | 50807 |
| rs200553664 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130245409 | AATTTGACCAAAGAA[-/C]AGGAAAGATCTGTAA | 50807 |
| rs200556664 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404641 | GCAGCTGAGTTAGTA[C/T]GGTAGACTGCATGAG | 50807 |
| rs200558359 | in-del | -/AAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130267132 | AACAAACAAAAAAAA[-/AAC]AAAACAAAAAACAAA | 50807 |
| rs200561211 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130312454 | CACTAAAAGGAGGGG[A/G]AAAAAAACCCATTAG | 50807 |
| rs200567631 | snp | C/G | 0.286564 | 0.247312 | intron-variant | ASAP1 | GRCh38.p7 | 8:130300149 | ACACACACACACACA[C/G]ACACAGAGAGAGAGA | 50807 |
| rs200574836 | in-del | -/TC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130419954 | GCACCACCTTCTTCT[-/TC]TTTTTTTTTTTTTTA | 50807 |
| rs200593872 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130265129 | ATAGGAACTGTGATG[G/T]GGGAGCTTGTTCCCT | 50807 |
| rs200598241 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130310130 | ATGGGGCTAATACAG[-/T]TTTTTTTTGGGGGGG | 50807 |
| rs200598391 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130183262 | CAGAAAGGTATCAGA[A/T]TTTTTTTTTTATTAG | 50807 |
| rs200612318 | in-del | -/TCC | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428670 | ACCATCCCCCCACCA[-/TCC]TCATCATCACCATCA | 50807 |
| rs200622423 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130230103 | ACAAACAAACAAACA[A/C]ACACCAACCCCAAAC | 50807 |
| rs200643581 | in-del | -/TAAAT | 0.0322114 | 0.122752 | intron-variant | ASAP1 | GRCh38.p7 | 8:130200274 | AGGAAGTTGGGTAAA[-/TAAAT]TATAGTGCAAATATA | 50807 |
| rs200654824 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130136908 | GAAATGTGCAGGTGT[G/T]AGAAGCCACAATAAC | 50807 |
| rs200661367 | snp | A/G | 0.000115402 | 0.00759524 | missense | ASAP1 | GRCh38.p7 | 8:130128022 | AGGCTGTTCTCTCCC[A/G]CACTCTGCTCTCCAC | 50807 |
| rs200667825 | in-del | -/T | 0.0170251 | 0.090679 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066148 | AGAATGACAGAGGTA[-/T]TTTCCTTTGCCTTCC | 50807 |
| rs200670290 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130139999 | AGTTAAACAGCACTA[-/A]TTTACCTCTCATTTC | 50807 |
| rs200673327 | snp | A/G | 0.000567537 | 0.0168359 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126116 | ATGTTGAAGACAATG[A/G]AACAAAAAAGACATC | 50807 |
| rs200674154 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130102528 | ATTTTTTGCATCTAC[A/G]TTCCACAAGAATATT | 50807 |
| rs200675500 | in-del | -/T | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095704 | GCTCACTGCAACTTC[-/T]GCCTCCCAGATTCAA | 50807 |
| rs200677318 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130434341 | CCTTGTCTCAAAAAA[C/T]AAAAAAAAAATCTTG | 50807 |
| rs200682369 | snp | A/C | 0.000117767 | 0.00767265 | missense | ASAP1 | GRCh38.p7 | 8:130060909 | TGGCTTAGGCGGCAA[A/C]TCTCCAATTTGGGGC | 50807 |
| rs200691713 | in-del | -/GATT | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252398 | TATACAATATTAAAA[-/GATT]GATTCAGTACTTAAA | 50807 |
| rs200707448 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257794 | CAAGAGCACCCCCCC[C/G]CCATTATTTTTTAGA | 50807 |
| rs200721948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130113377 | TCCCTGGCAAGCTTC[C/T]ACCTATCCTTAGAAA | 50807 |
| rs200727161 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130074127 | TCTTAAAAAAAAAAA[G/T]GGGGCAATTGTGAGA | 50807 |
| rs200734457 | in-del | -/GTT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130397158 | GTTGTTGTTGTTGTT[-/GTT]AAGAAAGAGTCTAGT | 50807 |
| rs200734607 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130321613 | CCTAATAAAGACTCT[A/C]TTTTATCACCAACAC | 50807 |
| rs200740835 | in-del | -/AAA | 0.0573587 | 0.15934 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444333 | GCCTCAGTTTCCATT[-/AAA]TATGAAATGGATGTT | 50807 |
| rs200747887 | snp | A/G | 3.29457e-05 | 0.00405854 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130060669 | TTGCTTTTGGATGGC[A/G]TCTCTGGACTGCACA | 50807 |
| rs200757073 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130262424 | AAAAAAAAAGAGAGA[A/G]AGAGAGAGAGAGAGA | 50807 |
| rs200760463 | snp | C/G | 8.23608e-05 | 0.00641667 | missense | ASAP1 | GRCh38.p7 | 8:130060762 | TGAGACATCTCCAGT[C/G]TGGGATTTTGCTAGC | 50807 |
| rs200762597 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091504 | AGGAGATAAGAGCCC[C/T]ATCATGCAGGGCCCT | 50807 |
| rs200764058 | snp | A/G | 0.000100757 | 0.00709708 | missense | ASAP1 | GRCh38.p7 | 8:130060904 | TCTCCTGGCTTAGGC[A/G]GCAAATCTCCAATTT | 50807 |
| rs200781794 | in-del | -/ATTCATTC | 0.0505443 | 0.150723 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413886 | CTTCTATTTTGCCAG[-/ATTCATTC]ATTCATTCATTCATT | 50807 |
| rs200783546 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130414265 | GCACAATGACGATAC[C/T]TCCAGAATTTTAAGA | 50807 |
| rs200794839 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130164481 | CTGTAGTCCCAGCTA[C/G]TTGGGAGGCTGAGGC | 50807 |
| rs200797320 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130249725 | ACACATATGTATGTG[G/T]TTATTTATATATTAC | 50807 |
| rs200810772 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130278086 | AAAAAAAAAAAAAAA[-/A]TCAAAGGGCCTTATA | 50807 |
| rs200814119 | in-del | -/T | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354055 | AACACGCCCAGCTAA[-/T]TTTTTTTTGTATTTT | 50807 |
| rs200820429 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130373874 | AAAAAAAAAAAAAGA[A/T]AAACCTGTGTAATAA | 50807 |
| rs200824943 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130143411 | GTGTGTGAGATGTCT[G/T]TTTTTTTTTTTTTTG | 50807 |
| rs200826936 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162735 | AGGCAGAAGAATGGC[A/G]TGAACCCAGGAGGCG | 50807 |
| rs200850326 | in-del | -/C/CTTT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130393023 | CAAAAATAAACCTTT[-/C/CTTT]TTTTTAACATGACAG | 50807 |
| rs200865919 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130307360 | ATCCTGTGGCAAAAA[-/C]ATAAAGAGGGACTCA | 50807 |
| rs200870516 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130219216 | TTTTTTTAACATACT[-/A]GTATTATAAAGTTAG | 50807 |
| rs200882512 | snp | A/C/G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130228722 | AAAAAAAAAGAAAAA[A/C/G/T]AATCTAAATAATGAA | 50807 |
| rs200884106 | in-del | -/TGA | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072993 | AATCTTCTTCTGTGT[-/TGA]TGATTGTTGTGATGT | 50807 |
| rs200907447 | snp | A/G | 0.000247209 | 0.011115 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130126028 | AACCCCCATTTCCCT[A/G]TGGATGCCAGAACAT | 50807 |
| rs200917753 | in-del | -/AAAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130230066 | GAGATCCTGTCTCCA[-/AAAC]AAACAAACAAACAAA | 50807 |
| rs200921562 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116573 | TCTTTAGCAAGTGTT[-/A]AAAAAAAATGAATCT | 50807 |
| rs200922168 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130094512 | CACGCCTAGTCTAAA[-/T]TTAAAAAAAAAAAAT | 50807 |
| rs200929889 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130102997 | CATCCAGCCTAGCTG[G/T]CTGTTTTTTAAAGAT | 50807 |
| rs200987306 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130111351 | GGCCTGTCTCAAGGG[-/A]AAAAAAAAAATTCCT | 50807 |
| rs200994455 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296765 | AAGAAAAAAAAAAAA[-/A]TTAAGCTACTTTCCA | 50807 |
| rs200995849 | snp | A/G | 0.43555 | 0.167544 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167315 | AAGTAAAGAAAAAAG[A/G]AAAAAAAAAAATCCA | 50807 |
| rs201005988 | in-del | -/A | 0.046775 | 0.145601 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199846 | GTAACAAAAACAAAC[-/A]AAACAAACAGTTCTG | 50807 |
| rs201012056 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130408264 | GTTGTGTCTGTGAGG[G/T]TGTTTCTGCAAGAGA | 50807 |
| rs201013455 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130284901 | TGAGAGAGAGAGAGA[A/G]AGAGAGAGAGAGACA | 50807 |
| rs201034114 | in-del | -/TTTC | 0.0232847 | 0.105357 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066574 | ATTCTTTCTTTCTTT[-/TTTC]TTTCTTTCTTCTCTC | 50807 |
| rs201049937 | in-del | -/AA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130123800 | GCCCGGCTAATTTTT[-/AA]AAAATTTTTAATAGA | 50807 |
| rs201052362 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130173774 | AAAGAAAAAAAAAAA[-/A]TAAAAAGGCCGGGTG | 50807 |
| rs201059768 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130227943 | GTTGGCGAGTCTGAG[A/G]GAAGGGCAACAGCAC | 50807 |
| rs201065078 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130055527 | GAGTAAAGTGTTGTT[C/T]TAGCCAGTAAAAAAA | 50807 |
| rs201074693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167506 | CTTACCTACACTGTT[A/G]GCCCTGTTGTAAACA | 50807 |
| rs201094035 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130393566 | TTCAAGAACAGCCTG[A/G]CCAACATGGTGAAAC | 50807 |
| rs201100735 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388292 | TCATGCTAGTCTTTG[C/T]AGGCCACGGTAAGAA | 50807 |
| rs201107687 | in-del | -/TATATATATATATATATATATATG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130153336 | ACTGCTTTTTAAATA[-/TATATATATATATATATATATATG]TATATATATATATAT | 50807 |
| rs201116509 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130114769 | TTTTTTTTTTTTTTT[-/T]AAGATATAGGGTCTT | 50807 |
| rs201122001 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130111361 | CAAGGGAAAAAAAAA[-/A]TTCCTCTCCAAGTAC | 50807 |
| rs201124127 | in-del | -/CACA | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284628 | CCAGTGACAATGAAC[-/CACA]CACAGAGACCACATG | 50807 |
| rs201145957 | in-del | -/G | 0.0221141 | 0.102801 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093409 | CGGTGGCTCTCGCCT[-/G]TAACTCCAGCACTTT | 50807 |
| rs201146023 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130322304 | ATGCCATCTGTGGTT[A/T]AAAAAAAAAAAAAAT | 50807 |
| rs201149061 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130161777 | TGCAAAATTCTCCCT[-/A]AATATTTCCTTTTAA | 50807 |
| rs201149689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411324 | CCAAGGCACAGGCTC[A/G]GAGTGCCAGGAAATG | 50807 |
| rs201159765 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130379375 | AGGGTGGTATGGCTG[G/T]AGATGTATTTTCCTG | 50807 |
| rs201162549 | in-del | -/TAAAAA | 0.0418186 | 0.138422 | intron-variant | ASAP1 | GRCh38.p7 | 8:130147072 | CTCTACTAAAAATAC[-/TAAAAA]TTAGCTGGCTGTGGT | 50807 |
| rs201164317 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130198151 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTAC | 50807 |
| rs201166603 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130337770 | CAACTTGAAATCTCA[C/T]CCATCCACCAAAACA | 50807 |
| rs201169435 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130161144 | TACCTCAGTGAAACC[A/C]AAAATGAATTATTCA | 50807 |
| rs201171912 | in-del | -/A | 0.0463947 | 0.145069 | intron-variant | ASAP1 | GRCh38.p7 | 8:130250741 | AGAATTGCTTCTCAT[-/A]AAAAAAAACTGATGG | 50807 |
| rs201172592 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130176703 | GTTTTTTTTTTTTTT[C/T]TTTTGAGACAGAGTT | 50807 |
| rs201182139 | in-del | -/C | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318200 | ATCCTCCCACCTCAG[-/C]CCCCCCAAGTGGCTG | 50807 |
| rs201186844 | snp | C/T | 1.65026e-05 | 0.00287246 | missense | ASAP1 | GRCh38.p7 | 8:130214624 | ACGCGGTGCCAAGGT[C/T]GGGGTTGTCTCGACT | 50807 |
| rs201191799 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130405091 | GTTTTTGCTACTCAG[-/A]AAAAAACTGCCTAAT | 50807 |
| rs201194645 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130132065 | AGAAAGGGAAATGAG[C/T]AAGAGAGAATGAAAT | 50807 |
| rs201198834 | in-del | -/TTCT | 0.0441095 | 0.141807 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423783 | ATGATGATTATTTGC[-/TTCT]TTATCTTTTCTTGTT | 50807 |
| rs201199592 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130158207 | AAGGAGCTTTCTTTT[-/A]AAAAAAAAACAATGA | 50807 |
| rs201205344 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130417621 | CTGGCTTCAGGGGAA[-/C]AAAAAAAAAAAAAGG | 50807 |
| rs201207695 | in-del | -/TG | | | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052739 | TTTTGTTTTTGTTTT[-/TG]TTTTTTTTTTTTGAA | 50807 |
| rs201240224 | snp | A/G/T | 4.95817e-05 | 0.00497884 | synonymous-codon, stop-gained | ASAP1 | GRCh38.p7 | 8:130118213 | TCTGATCTGCAGTTC[A/G/T]GACGGCAAGGTGAAG | 50807 |
| rs201249850 | in-del | -/AA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130375553 | TTGGACTCTCGAGGG[-/AA]AAAAAAAAAAAGGTC | 50807 |
| rs201257458 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130251650 | AATCATGCATTAGAC[A/G]TATCGAAGTTGACAT | 50807 |
| rs201260599 | snp | A/G | 3.29592e-05 | 0.00405938 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159970 | TCTGAGAATCCTAGG[A/G]AAGAAAAACTACAGA | 50807 |
| rs201264529 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130102652 | TCTTCAATTTTTTTG[A/G]AACAGTTTAAGAATT | 50807 |
| rs201264577 | in-del | -/AAA/AAAAAAAAAAA | 0.335559 | 0.234904 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311761 | CAAAAAAAAAAAAAA[-/AAA/AAAAAAAAAAA]GGCAAAATAAGTGAT | 50807 |
| rs201321739 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130107183 | CTCTCTCTTCTTCTT[-/C]TTTTTTTTTTTTTTT | 50807 |
| rs201344399 | in-del | -/CAG | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428684 | CATCATCATCACCAT[-/CAG]AACTACCACCATCAT | 50807 |
| rs201380090 | snp | A/G | | | missense | ASAP1 | GRCh38.p7 | 8:130060838 | TTGGGAGGTAAGTCT[A/G]AGAGTTGGGGTTTGG | 50807 |
| rs201380435 | snp | A/C | 0.00657239 | 0.0569473 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180885 | CAATTTTTGTACTGT[A/C]ATTAAAGCCAATGTC | 50807 |
| rs201388503 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130403554 | TTTCTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 50807 |
| rs201400242 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130338422 | AGGGGAAGTATTCAA[G/T]AAAGAACAGCCAGCA | 50807 |
| rs201407903 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130315064 | GTGGAGAAAATGTGA[G/T]AAGAGCCTCTATTAA | 50807 |
| rs201415574 | in-del | -/ATAT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130072791 | CTGGACTTGCAATTG[-/ATAT]GTGTGTGTGTGTGTG | 50807 |
| rs201422861 | snp | C/T | 0.000529773 | 0.0162667 | missense, intron-variant | ASAP1 | GRCh38.p7 | 8:130091985 | TACCCCAAGGAACTG[C/T]GCCTTTGTTTGGGGG | 50807 |
| rs201423638 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208927 | ATTTGCCATCCCCCT[-/A]AAAAAAAAAGAGGTA | 50807 |
| rs201435973 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130138855 | AAAAAAAAAAAAAAA[C/T]AAAACAGCTGAAGTG | 50807 |
| rs201436100 | snp | A/C/T | 1.66277e-05 | 0.00288333 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126102 | GTTCTGTGGAAAGAA[A/C/T]GTTGAAGACAATGAA | 50807 |
| rs201437541 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130368881 | ATGTGAGCAACTGTA[C/T]TTCTTTTTTAGTGTA | 50807 |
| rs201451863 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130300151 | ACACACACACACACA[C/G]ACAGAGAGAGAGAGA | 50807 |
| rs201471995 | in-del | -/T | 0.35574 | 0.226537 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119801 | CAGTTTTTTTTTTTT[-/T]AATCTGAAAATGGGG | 50807 |
| rs201473563 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359591 | CTACCCCTCACCCCC[A/G]GGATTGGGCTTCTGC | 50807 |
| rs201476130 | in-del | -/TG | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215339 | ATGGTGGCTCACGCC[-/TG]TAATCCTAGAACTTT | 50807 |
| rs201482465 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130064035 | CTGATATGGCAAGAG[C/T]GCGTCAAAAATGTGC | 50807 |
| rs201488655 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130211766 | TCGAACATAATAGAC[C/T]TTTGGTACTTGCTGG | 50807 |
| rs201490803 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130117861 | AAGAGATGGCAAACT[A/C]CAGCCTGTAGGCCAT | 50807 |
| rs201497148 | in-del | -/TGTC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130109459 | GGACTTTATCTCAAG[-/TGTC]TGTTTCTGTCTCACT | 50807 |
| rs201499638 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130242281 | AAAAAAAAAAAAAAA[A/C]AACAACTTTTTTTTT | 50807 |
| rs201501012 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130373029 | ACACACAGACACACA[C/T]ACACATACACACATA | 50807 |
| rs201528417 | snp | C/T | 0.000230669 | 0.0107369 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116670 | CTCCCACGTCCATTT[C/T]TGCTTACCAGATCTT | 50807 |
| rs201566245 | snp | C/T | 0.00151483 | 0.0274794 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159843 | TCACACACTGAGACA[C/T]TGGGCTGGGCTCATA | 50807 |
| rs201573375 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428725 | CCACCATCATCATCA[C/T]CACTACCAACATCAC | 50807 |
| rs201590380 | snp | C/T | 0.00199809 | 0.0315445 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128094 | ACTGATATCCATCTG[C/T]TGGTAAAAACATAAG | 50807 |
| rs201591935 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130337769 | CAACTTGAAATCTCA[-/G]CCCATCCACCAAAAC | 50807 |
| rs201592152 | in-del | -/CAT | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428493 | CACCATCTTCATCAC[-/CAT]CATCACCATCACCAC | 50807 |
| rs201593257 | in-del | -/AA | | | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082680 | GTTAATTTTAATTTT[-/AA]TATTTTTTTTGTAGA | 50807 |
| rs201598406 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130372339 | AGACTTCTTTGCTTT[A/T]AAATCAATGTTCTGC | 50807 |
| rs201607597 | in-del | -/TTTTTT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130352213 | AATCCTTCCTAAGGG[-/TTTTTT]TTTTTTTTTTTTAAG | 50807 |
| rs201608015 | in-del | -/GAAAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216044 | AAGGAAAAAGGAAAG[-/GAAAA]GAAAGAAAAGGAAAA | 50807 |
| rs201629241 | in-del | -/AC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130097762 | CAGCGATCTCCTGAG[-/AC]TCTCTCCCAGGAACT | 50807 |
| rs201640282 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130312462 | GGAGGGGAAAAAAAA[-/C]CCATTAGGAATTCTG | 50807 |
| rs201645783 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130267102 | AGTGAGACTCTGTCT[A/C]AAAACAAACAAACAA | 50807 |
| rs201649133 | in-del | -/AAAGGAAAGG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130215976 | GAAAAAGAAAAAGAA[-/AAAGGAAAGG]AAAGGAAAGGAAAGG | 50807 |
| rs201665012 | in-del | -/TTCA | 0.0913226 | 0.193188 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066621 | CTTGTTTCTTTTTCT[-/TTCA]TTCATTCATTCATTC | 50807 |
| rs201668313 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130115238 | ATCAGCCAAAGAAAG[C/G]CCTTAAAAAGACTGA | 50807 |
| rs201669726 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130133691 | AAACAAACAAACAAA[-/C]AAAAAAAACAAAAAA | 50807 |
| rs201707613 | in-del | -/TTA | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397147 | ATGAGAATTTTGTTG[-/TTA]TTGTTGTTGTTAAGA | 50807 |
| rs201735455 | snp | A/G | 0.000994636 | 0.0222784 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134366 | TAAAAAAAAAGAAAA[A/G]TAAGTGAAACCTTAG | 50807 |
| rs201760897 | in-del | -/GGCACA | 0.0185938 | 0.0946107 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389759 | AGGCTGGAGTGCAGT[-/GGCACA]GTCACGGCTCACTGC | 50807 |
| rs201773504 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130311775 | TCAAAAAAAAAAAAA[A/C]GGCAAAATAAGTGAT | 50807 |
| rs201814093 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130093788 | ATACACTCTTCATAT[A/T]AAAAAAAAAAGTCTA | 50807 |
| rs201825279 | snp | A/T | 0.000829999 | 0.0203546 | utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130401959 | GTCTCAGCCGTCACA[A/T]CAGAAAACGACCTGG | 50807 |
| rs201844317 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130103000 | CCAGCCTAGCTGTCT[A/C]TTTTTTAAAGATTTG | 50807 |
| rs201844591 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130364173 | TGGTTTGTTTGGAGA[-/C]AAAAAACTACTCTGG | 50807 |
| rs201845060 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130116588 | AAAAAAAAATGAATC[C/T]GCATTTTTAATATTC | 50807 |
| rs201851522 | snp | A/G | 1.64811e-05 | 0.00287059 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057946 | AGTGGATGGATATTC[A/G]TACGTACCCACCACT | 50807 |
| rs201865748 | in-del | -/AT/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130356088 | TCTCATAAAAAAAAA[-/AT/T]TATTTGCTTTTAAAT | 50807 |
| rs201869073 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130092326 | TTTCAAAAATTTGGT[A/T]AAAAAAAAAATAAAA | 50807 |
| rs201887077 | in-del | -/AC | 0.0267878 | 0.112589 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118829 | GACCAAATTACTCCA[-/AC]AGAGACAGAATAAAG | 50807 |
| rs201899512 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130352209 | CTAAATCCTTCCTAA[-/G]GGGTTTTTTTTTTTT | 50807 |
| rs201907440 | in-del | -/C/CTTGTTCAGGAACT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130287178 | TTCAAGGACTGAACT[-/C/CTTGTTCAGGAACT]TTACACATTTTTGTA | 50807 |
| rs201911089 | in-del | -/GAGTA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130399866 | TTGTTGCCCAGGCTG[-/GAGTA]GTACAATGGCGCAAT | 50807 |
| rs201911846 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130183465 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 50807 |
| rs201930107 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130187435 | TTTTTTTTTTTTTTT[-/T]GACAGGGTCTCACTC | 50807 |
| rs201951831 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130189693 | GGGATTCCTGGATCT[C/T]ATGGTAGTTCTCTTT | 50807 |
| rs201962417 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130131189 | AAACAAACAAACAAA[G/T]AAAAAAGCCACTAGC | 50807 |
| rs201965271 | in-del | -/TG | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130338855 | AATCCTTCTGAGGAC[-/TG]TTTCCTGGGCATTTC | 50807 |
| rs201968567 | in-del | -/T | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245687 | AGGGCAGGGCCTATG[-/T]TTAGGCCCAGAGTAG | 50807 |
| rs201976916 | in-del | -/CTT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130419946 | ATCTGCCTGCACCAC[-/CTT]CTTCTTCTTTTTTTT | 50807 |
| rs201991665 | in-del | -/TGGTCTCG | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130420004 | CTATGTTTACCAGGC[-/TGGTCTCG]AACTCCTGGTCTCAA | 50807 |
| rs201992671 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130356079 | AACAGTATTTCTCAT[-/A]AAAAAAAAATATTTG | 50807 |
| rs201996911 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130145118 | GCATTTCTGCAAATA[C/T]GTATTAAGTACCTAC | 50807 |
| rs202007239 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228744 | ATAATGAAAAAAAAC[-/A]AAAAAAACCTTTAAC | 50807 |
| rs202011708 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130135530 | AAACAAAACAAAACA[A/C]AAAAAAGAACATGCC | 50807 |
| rs202023029 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139752 | AAAAAACAAACAAAC[-/A]AAAAAACAAAAAAAA | 50807 |
| rs202024532 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130176690 | TGTCTCTCTTCCTGT[G/T]TTTTTTTTTTTTCTT | 50807 |
| rs202029643 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130245408 | GAATTTGACCAAAGA[A/C]CAGGAAAGATCTGTA | 50807 |
| rs202034226 | snp | A/T | 0.000379016 | 0.013761 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116652 | AGCCAATGTCTAATA[A/T]ATCTCCCACGTCCAT | 50807 |
| rs202048029 | in-del | -/TTTAA | | | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082677 | CTGGTTAATTTTAAT[-/TTTAA]TTTTATTTTTTTTGT | 50807 |
| rs202053207 | snp | C/G | 0.000131783 | 0.00811628 | missense | ASAP1 | GRCh38.p7 | 8:130057974 | ACTCCTGGTCCTCTT[C/G]CCCTGTGACGATAAT | 50807 |
| rs202057940 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130301187 | AGTGGCTGGCATAAC[C/G]CATTAGGCTACCTTC | 50807 |
| rs202105294 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130333731 | AACACCAGAAGATTA[A/G]TATTTTCGCCAATCA | 50807 |
| rs202118706 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428463 | TCATTATCACCATCA[C/T]CATCACCACCACCAC | 50807 |
| rs202126408 | snp | A/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428687 | CATCATCACCATCAG[A/T]ACTACCACCATCATC | 50807 |
| rs202142952 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130376967 | TCCAAGTTGAAATGG[C/G]GCAAGAGATGTGAAA | 50807 |
| rs202147241 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130285304 | ATACTCAAGGAGTTG[G/T]AAACCACCAAGTTGG | 50807 |
| rs202149178 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130260818 | CAGGGCACATCCAGC[C/T]ACGGGATGAACACAG | 50807 |
| rs202161554 | in-del | -/CATT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130066647 | ATTCATTCATTCATT[-/CATT]TGATGGGTGTTTAGA | 50807 |
| rs202165530 | in-del | -/T | 0.0437281 | 0.141251 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418198 | AGTCTTTCTTTAATG[-/T]TTTTTTTCCAACAGG | 50807 |
| rs202167993 | snp | A/G | 0.00164507 | 0.0286327 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179236 | GCAGTAATTGGGCTA[A/G]TAACAATGCTTGCAA | 50807 |
| rs202172988 | in-del | -/TATATATATATATATATATATATATG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130153334 | GCACTGCTTTTTAAA[-/TATATATATATATATATATATATATG]TATATATATATATAT | 50807 |
| rs202186430 | in-del | -/A/AA | 0.475702 | 0.107512 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162817 | AAAAAAAAAAAAAAA[-/A/AA]CAAACAAAATCTAAA | 50807 |
| rs202201444 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130337771 | AACTTGAAATCTCAC[C/G]CATCCACCAAAACAT | 50807 |
| rs202216323 | snp | A/G | 0.000137492 | 0.00829019 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179251 | ATAACAATGCTTGCA[A/G]TATTCTACTCACTTG | 50807 |
| rs202222834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377972 | TCTGTTTCCTCCTGG[A/G]ACCCTGACTGATACA | 50807 |
| rs202223527 | snp | C/T | 0.000791159 | 0.0198734 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116793 | ATCTAGGAAACACCT[C/T]AAGAAGGCAAGGAAC | 50807 |
| rs202245694 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130135535 | AAACAAAACAAAAAA[C/T]AGAACATGCCATGGG | 50807 |
| rs367560619 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130106797 | CCTAATCCTCTCTCT[C/G]AAGCTGTGAACAGCA | 50807 |
| rs367564579 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070161 | CCTGCCTCAGCCTCC[G/T]GAGTAGCTGGGACTA | 50807 |
| rs367574829 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130078178 | TATTTTTCGTACAGA[C/T]GGGGTTTCACCATGT | 50807 |
| rs367587715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334984 | TCTTCATTGCCTTCC[C/T]GTGCTTCCTGTTCTT | 50807 |
| rs367590175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317399 | CTGAAATGCCACCAT[C/T]AGGGTTTGTTGAAAC | 50807 |
| rs367602758 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130343771 | GTACAAAACACACAA[C/T]TGGGAGCAACTTAAG | 50807 |
| rs367605331 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130176777 | CTCACTGCAACCTCT[A/G]CCTCCTGGATTCAAG | 50807 |
| rs367609502 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130275995 | CAAGAACAGATTCTA[C/T]GACAGAGTGATCAAG | 50807 |
| rs367609896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306923 | TCACTCCACCCAGGT[C/T]TGAGTGTCTGTACTA | 50807 |
| rs367615802 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130284543 | TAAAAGGGATGCGCC[C/T]AGTACAGCCAGGATT | 50807 |
| rs367621066 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130268536 | ACACACACACACACA[A/C]CTGTGTAACTATAGA | 50807 |
| rs367623543 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130243245 | TATTGCTAACCTGGG[G/T]CTTGCTTTATCCATA | 50807 |
| rs367628057 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130308914 | GGGCACGGTGGTGTG[C/T]GCCTCAAAAAAAAGA | 50807 |
| rs367640853 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130129027 | TTGGATCAAGGTGGC[A/G]GTTTCCCCCATGCTG | 50807 |
| rs367649193 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130268305 | AGCCTGGGAAACACA[C/G]CAAGACTTTGCCTCT | 50807 |
| rs367650049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349447 | ACAATCATTTATAGA[A/G]CACTTAGCACACCAG | 50807 |
| rs367656057 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130367616 | TTGTGGTTAAAATCA[C/G]CACCTTGGGGCACAG | 50807 |
| rs367656493 | in-del | AAA/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130055307 | AAAAAGAAAAAAAAA[AAA/G]AAAAGCAAATGAAAA | 50807 |
| rs367656661 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130328747 | CACCTCACAGCCTCC[C/T]GAGTAGCTAGGAGTA | 50807 |
| rs367682809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257917 | ATTGCAAATGTGGGG[C/T]CCCAAATCCAAATTC | 50807 |
| rs367695377 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130056659 | GTCAAAGGTGAATGT[A/G]TGCCCATGCCTATGT | 50807 |
| rs367698792 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130235792 | AGTTTCATTTGGCTA[A/G]GGATTCCCAGCTCTG | 50807 |
| rs367709413 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130181423 | AGAAAGTTGGAGACA[C/G/T]GAGGCTTTCCTTGAA | 50807 |
| rs367715699 | in-del | -/ATT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130397149 | GAGAATTTTGTTGTT[-/ATT]GTTGTTGTTAAGAAA | 50807 |
| rs367719682 | in-del | -/AC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130373112 | CACAGAAATACATAT[-/AC]ACACACACACACACA | 50807 |
| rs367722017 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130173922 | TACTAAAAAAAAAAG[A/G]AAAAAAAAATTAGCT | 50807 |
| rs367739420 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130226843 | GCCAGAAGAAATACA[C/T]AATACACTTTGGTTT | 50807 |
| rs367757888 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388384 | AGGGGTGCAGCATGA[C/G]CTGCAAGAGGAGTGA | 50807 |
| rs367757978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077061 | GACAAGGAAATGGAA[A/G]GGAATGGGGGTGTTG | 50807 |
| rs367764035 | snp | A/G | | | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444258 | GCAGGCTCTGTGTCC[A/G]GTTGGAATATGGCCT | 50807 |
| rs367771492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405760 | TAGGTTAGCAGCTAC[A/G]TCTATGTCCGTACCT | 50807 |
| rs367772917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130067471 | TGCAAACATGGCTCA[C/T]TACTACCTCGACCTC | 50807 |
| rs367773783 | snp | C/G | 0.000116683 | 0.00763728 | missense | ASAP1 | GRCh38.p7 | 8:130118244 | GGCTGTCTCCCCAAG[C/G]TCCTAAAAAGGGAAA | 50807 |
| rs367783801 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058092 | CTTAAAGAAAGAAAC[C/T]GGGTTTTAATTGAAA | 50807 |
| rs367788697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156720 | TTCATACTTACTGTC[C/T]GTATGATCTTAGTCA | 50807 |
| rs367791793 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130200250 | GGAAACAATAGAAAT[A/G]TTCAAAACAGGAAGT | 50807 |
| rs367803841 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130422279 | GGAGATGAAGCCGAT[A/G]AGGACTCTGGAGCCA | 50807 |
| rs367807223 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130188016 | AAATGTTCAAAGAGT[C/G]TTTCAAATACAAGTA | 50807 |
| rs367812159 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102606 | TAGGGCAATGCTGGC[A/C]TCATTGGAAGAGTTA | 50807 |
| rs367812411 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130139452 | TTAAGCTGACCAGGC[A/G]TGGTGTCTCATGCCT | 50807 |
| rs367815852 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130072824 | GTGTGTGTGTGTGTG[C/T]GCGCGCGGGGGGGGG | 50807 |
| rs367817608 | in-del | -/C | 0.0193772 | 0.0965046 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356370 | TAATCAATGTCACAT[-/C]CTTAGAAGTATATAC | 50807 |
| rs367842829 | snp | A/C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130073509 | GCAGTCCATGACCAC[A/C/G]GCCTGTGGTGCTCAA | 50807 |
| rs367847861 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130165759 | TCCCCAGTGCATATA[C/T]CTGGATTTGGAGAAC | 50807 |
| rs367855713 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130379208 | TCCGGGAAGGTGGCA[C/T]GTCCCGAGAGGGCAT | 50807 |
| rs367866080 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130129193 | CCTGAGGCCTCCCCA[A/G]CCATGTGGAACTGTG | 50807 |
| rs367866738 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130079276 | GAAGTTTGGGTCTGG[A/G]AGTGGCTCTCTGTCC | 50807 |
| rs367871006 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130091006 | GGCCAAGACCCTGTT[G/T]CGTGATGGGGTGACC | 50807 |
| rs367876241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422621 | CTCCCAAAACTCTCT[A/C]CCATGGATCAGCCTC | 50807 |
| rs367877901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096583 | CCTTCCAAAGCTTCT[A/G]TGAATAAATCTGAGG | 50807 |
| rs367879348 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130329072 | AGGCACTTCATTTTA[C/G]TCCTGACCAGATGGT | 50807 |
| rs367879701 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130073304 | CCGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG | 50807 |
| rs367886104 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130400396 | CAGACTCCTTAGACT[A/C]TTCATCATGTGTCCC | 50807 |
| rs367888152 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130414037 | AGAACAGAAGTTGCT[A/T]TAAAGTAGAGAAAAT | 50807 |
| rs367891174 | in-del | -/G | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229604 | ACTGAAAAGCACAAT[-/G]GACTCTACCTGGCAC | 50807 |
| rs367897590 | snp | C/T | 1.67075e-05 | 0.00289023 | missense | ASAP1 | GRCh38.p7 | 8:130179319 | GATCCACACCCTTTT[C/T]GGTCTTGATTTCATT | 50807 |
| rs367897760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150105 | ATGTTATCTCACTGA[A/C]TCCTCATATAATCTT | 50807 |
| rs367898966 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130432760 | TCTCTTTTTAAGATG[C/G]AGAAAAATCTTTCTT | 50807 |
| rs367910194 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130277220 | CAGCTGCCAAACAGC[A/G]TCAGCGAGAAAGGGG | 50807 |
| rs367911573 | in-del | -/T | 0.154993 | 0.231244 | intron-variant | ASAP1 | GRCh38.p7 | 8:130443215 | GGAGGCGAGGAGACC[-/T]CCCCCCCCCACCGGG | 50807 |
| rs367923041 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130057717 | CCTCCCAAAGTGCTG[C/G]GATTACAGGCGTGAG | 50807 |
| rs367941156 | in-del | -/ATT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130397146 | TATGAGAATTTTGTT[-/ATT]GTTGTTGTTGTTAAG | 50807 |
| rs367948174 | snp | C/T | 0.000552417 | 0.0166103 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214553 | ACATATGAAATGTCT[C/T]ACCAGATTTTTCAGC | 50807 |
| rs367957743 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130286963 | AGATGAAGAAGGCCC[A/G]TAGGGGGTCAAAAAG | 50807 |
| rs367970312 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319704 | GAACAGAGCAACGCA[C/T]GTATTAAAATAGCGG | 50807 |
| rs367975482 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130230099 | ACAAACAAACAAACA[A/C]ACAAACACCAACCCC | 50807 |
| rs367983503 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130369775 | CATTGCTGGTAGGAA[C/T]GTAAAATGGTGGAGT | 50807 |
| rs367984895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245372 | GTGCCTACAGCTTAA[G/T]GGCTGCATGGTTCTC | 50807 |
| rs367993156 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423152 | TCTGTCACCCAGGCT[G/T]GAGTGCAGTGGGTCA | 50807 |
| rs368004662 | snp | A/C | 0.000180038 | 0.00948612 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112365 | AATAATCAAGGACCA[A/C]CCTTCATGTGTACAG | 50807 |
| rs368006685 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325190 | AGATGAGTTCACATT[G/T]AACTCTTTCTTGGGG | 50807 |
| rs368012457 | snp | G/T | 1.78525e-05 | 0.00298763 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118286 | GTAAGTCAATAATAT[G/T]CTCTGCCAAGGGAGG | 50807 |
| rs368025819 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289592 | TTCATACTTTAAAAT[C/G]ATGGCCCTAAGTCAG | 50807 |
| rs368030677 | snp | A/T | | | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444516 | TTGTGCATATCTATG[A/T]CTACTTTCAAAGTCA | 50807 |
| rs368054173 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130109338 | GGGGCTTTGCTTGAC[A/G]GTAATTTAGGTCAAG | 50807 |
| rs368059983 | snp | A/G | 0.000136089 | 0.00824779 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118438 | AATAAGTCACCTTTT[A/G]AACTGATTTTCCACA | 50807 |
| rs368062057 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130155207 | TACACACACACGCGC[A/G]CACACACCCCTTCTC | 50807 |
| rs368062430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074421 | TGTATATGTTTATTA[C/T]GGAAAATTCCAAATA | 50807 |
| rs368069304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385450 | GCCCAAAGCCTCCTC[C/T]CCATGGGGAGATGCT | 50807 |
| rs368100010 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130232928 | TTTCTCTGGATGAGG[C/T]CAAAAGCCCTTGGAG | 50807 |
| rs368109805 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130426252 | TACCTGCTTCCCCTT[C/T]GCCTTCTACCATAAT | 50807 |
| rs368112734 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199708 | ACACTCTTACAGCTT[A/T]AAATGAGCTACTGAG | 50807 |
| rs368150938 | in-del | AA/C | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409270 | GTGTCTCAAAAAAAA[AA/C]ACAAAAAACCTCCTC | 50807 |
| rs368156010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353980 | CAAGCTCCGTCTCCC[A/G]GGTTCATGCCATTCT | 50807 |
| rs368157149 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130439117 | GTGGAAGAAGATGCC[A/G]GAAGGGAGAATCAGA | 50807 |
| rs368157988 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130333176 | TTATTTCCTAAGCAC[C/T]CCCAACCCTAGTCCA | 50807 |
| rs368179481 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130156156 | AATCCTTTAAGTAAT[A/G]AAGAGCATTCCAAAG | 50807 |
| rs368192921 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130314920 | ACTTTAAGAGAGAGA[C/G]AGAAAAAGTGGGTTC | 50807 |
| rs368208924 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130329449 | GGATCTTGGATTTAT[C/T]CATTCCATTTCCCAA | 50807 |
| rs368210998 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130312419 | AGCTAAATCTAACAC[A/C]CTTAAGCAAAATACA | 50807 |
| rs368218612 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130102482 | ATCTTTTGATGTGTT[C/G]TTGGATTCAGTTTGT | 50807 |
| rs368228049 | in-del | -/TC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130066597 | TTTCTTCTCTCTCTC[-/TC]CTTCCTTCCTTGTTT | 50807 |
| rs368230529 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130324751 | TCATCTGTTTTACCC[A/C]GACAGTTAAGGTTCT | 50807 |
| rs368235637 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130301606 | AAATATAAATCACAT[G/T]TTCACTACCCAAAAA | 50807 |
| rs368242256 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130233316 | TCCCAGGTAGTAACA[C/T]ATCCAGCCAACATGT | 50807 |
| rs368243254 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130254082 | GAATAATTCAACATG[G/T]ATTTACTGACTGCCA | 50807 |
| rs368250342 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130369192 | AGAAGTGTTTCAGAT[-/A]TTTTTTTTTATTTCT | 50807 |
| rs368250913 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130344355 | AGTGTTTTTTTCAGA[C/T]GAGAAAACATATTAT | 50807 |
| rs368259810 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130073038 | AAAACACAGTTAGAG[A/G]ATTATCCCCCACAGG | 50807 |
| rs368282751 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130215441 | CGTCTCTACAAAAAA[A/T]TAACAATTAGCTGGG | 50807 |
| rs368284183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084633 | ATACAGGCCTTGGAG[C/T]TGGAAATGGGTTCAA | 50807 |
| rs368285114 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130283587 | ACTCCATCACAGAAA[-/G]AAAAAAAAAAAAAAA | 50807 |
| rs368291744 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130142504 | AGTCTCTACCACATT[C/T]CAAGCACATCTGAGA | 50807 |
| rs368292312 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254881 | AGAACACAGGATGGC[A/G]TCAAATGATATTACC | 50807 |
| rs368293710 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130290960 | GACCTTCACAAGTAG[C/G]AGCTACTCCTCTTCT | 50807 |
| rs368315105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107673 | CTGCCTCAGAATCCT[A/G]AGTAGCTGGGATTAC | 50807 |
| rs368319615 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130400537 | GCTCACGCCTGTAAT[-/C]CCAGCACTTTGGGAG | 50807 |
| rs368334728 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130221378 | TGTTTCCCCTACCTC[C/T]TTTCTAGGAAGAGGA | 50807 |
| rs368345976 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406703 | GACCAGGATGATCTC[A/G]AACTCCTGACCTCAG | 50807 |
| rs368368780 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130151243 | AGGTGTGGTGGTGGG[C/T]GCCTGTAGTCCCAGC | 50807 |
| rs368385831 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130316237 | TGAGCTCCAGGACAC[C/T]AATACTTCAATAACT | 50807 |
| rs368394959 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130104787 | ATCCTTGTATATCTG[A/G]TTTTTAGTTACACAC | 50807 |
| rs368396574 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428705 | TACCACCATCATCAT[A/C]ACTACCACCATCATC | 50807 |
| rs368397441 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241141 | ATTTGAACTAGTTGA[C/T]TGCTCTGCCTAGAAC | 50807 |
| rs368424770 | in-del | -/AC | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215724 | ACTCCAGCCTGAGCA[-/AC]AGAGTGAGACTCTGT | 50807 |
| rs368438458 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122929 | TTAAAAAATGCTGGT[A/G]TGGACAAGAGTGCAC | 50807 |
| rs368450045 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130276732 | CACACACACACACTC[A/T]CTCTCTCTCTCTCTC | 50807 |
| rs368455671 | in-del | -/C | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347651 | CCACCCATCACATAA[-/C]CCCCTCATCCTGGCC | 50807 |
| rs368459423 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086385 | TGCTCAACACAATGC[A/C]CAGCACTCTGTGAGG | 50807 |
| rs368459708 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132905 | CTGATCCTTTATCAT[C/T]TCTCCTTTGAAATGG | 50807 |
| rs368462162 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130160709 | ATAAAATCAACAACG[C/T]TGAACTGCAGAACGA | 50807 |
| rs368465046 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130307590 | CAACAGGTAACCACC[C/T]TTCTATGAGAGAAAG | 50807 |
| rs368472545 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130433407 | GGAAGAGTAAAGCCC[A/G]GACACCTCTTTCACA | 50807 |
| rs368475118 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130285184 | TCCTACAGCAAGCAT[A/G]AAAAAAAAGTATTAG | 50807 |
| rs368475398 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130067294 | GTGGTCACATCTACA[A/T]GTAGTTTAGTGTGAG | 50807 |
| rs368480833 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130097642 | CACCCAGGCAGTGTA[C/T]TGCAGAAGTGACTAT | 50807 |
| rs368481922 | snp | A/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130429348 | CATTTCCTCTCCCCC[A/T]AGTTCCATGTGCCAG | 50807 |
| rs368485083 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130056888 | TCACTGTACCTTGGC[C/G]TGGCAGTTCCCATCG | 50807 |
| rs368503227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057727 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCC | 50807 |
| rs368505346 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130222288 | CTTACCAAACTGGGC[A/G]ATATTCACAAAACCT | 50807 |
| rs368514987 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130438565 | TCACACCCTGCCCAT[A/C]CCTTCCTGGGAGAGG | 50807 |
| rs368515998 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130437316 | ATGCCCCAGCTCACA[C/G]GTGAGGAACTATATG | 50807 |
| rs368522590 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130361937 | ATCATCTCTGTTGTC[A/G]CCATTATAATAAGAC | 50807 |
| rs368535457 | in-del | -/CG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130065868 | CCTGCCTTGGTCTAC[-/CG]CTATTGGACCTTAGG | 50807 |
| rs368540885 | snp | G/T | 3.35244e-05 | 0.00409403 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169088 | ATTAAAAAAATCAGA[G/T]ATTTACCACCAGTAT | 50807 |
| rs368547282 | in-del | -/ACACAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130284842 | TTCCTTTTACACTCT[-/ACACAC]ACACACACACACACA | 50807 |
| rs368551754 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130353657 | GGCAGATCACTTGAG[A/G]TCGGGAGTTTGAGAC | 50807 |
| rs368552608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281740 | GCATCTTATATTACA[C/T]TGGTGCAAAAGTAAT | 50807 |
| rs368557122 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130289283 | AATGAATAAGAAGGC[A/G]TCAGACTAACACTAT | 50807 |
| rs368557683 | in-del | -/CAGA | 0.0123036 | 0.0774623 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324750 | TTCATCTGTTTTACC[-/CAGA]CAGTTAAGGTTCTTG | 50807 |
| rs368562326 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130328133 | AGTGTCGTAAGTATT[C/G]TACATGCATTTCTCG | 50807 |
| rs368593713 | snp | C/T | 0.000108593 | 0.00736783 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091933 | GCCCCACACGCTGCC[C/T]GGCCCCAGCAGCTTT | 50807 |
| rs368600691 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130181983 | TGGAAAATCCACCGA[C/T]CAAGCCAATGAAAAA | 50807 |
| rs368606650 | in-del | -/AC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130267133 | ACAAACAAAAAAAAA[-/AC]AAAACAAAAAACAAA | 50807 |
| rs368608634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381509 | GTTCTTAGTAGCTAC[C/T]TGAAGTGGCTACTGT | 50807 |
| rs368615495 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130421517 | AATGAGATAGAAATG[C/T]TGCATGCCATTCTTC | 50807 |
| rs368630927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385044 | GATCTAACAGGATGA[A/G]CTTGAACAAGGAGCT | 50807 |
| rs368638780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344469 | GCTTCAAAAAATCAG[A/G]GGAAGGAGGCAGAAA | 50807 |
| rs368642584 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341657 | CAGAGCATCACCTGA[C/T]GAGGCTGGTGCAAAG | 50807 |
| rs368645063 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130380946 | CTGGAGTGCAGTGGC[A/G]TGATCCTGGCTCACT | 50807 |
| rs368649164 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130277887 | CAGACTGCCAGTGGA[A/G]TTCACAGAGATGTAG | 50807 |
| rs368661219 | snp | G/T | 0.0298908 | 0.118541 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339197 | TCAACACTTAACCAG[G/T]AGCCACCCACCCTCT | 50807 |
| rs368663777 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130226564 | TCAAGGTCATTTTGA[A/C]TTTGGAGTTGTTCTT | 50807 |
| rs368664809 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238253 | GGAAACAAGGACCAC[A/G]ATGCTCAGTCGCTTT | 50807 |
| rs368665180 | snp | C/T | 5.015e-05 | 0.00500724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112057 | GAGTCACAAGCCCTT[C/T]GAGGATGGAGTCACA | 50807 |
| rs368685632 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130307814 | GTAACCGGTGATGGC[A/G]GAGCTTGAAATCAGG | 50807 |
| rs368687270 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130337065 | AGGGACAATCACAAA[C/T]AGCTAACCCAGTCAG | 50807 |
| rs368691466 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130204898 | CCAGTGCCTGGCATA[C/T]AGTCACCACAGTATA | 50807 |
| rs368692750 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130126231 | AATGGACTCTTGAGG[-/T]TTAGCCTAGGGGCTA | 50807 |
| rs368704952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130193327 | TGAGCCAAGATTGTG[C/T]CACTGCACTCCAGCC | 50807 |
| rs368709007 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130142977 | CCTGAATTAGAGCTA[A/C]GTACGGTAGTGGTGC | 50807 |
| rs368709045 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130411908 | AGGAGCAGCACCCCA[C/G]TGTCCCAGCCTCCAC | 50807 |
| rs368715768 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123373 | TTGCCAGGCTAAAAG[C/G]AATCTCCCATTGTCT | 50807 |
| rs368721211 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130423142 | AGAGTCTCGCTCTGT[C/T]ACCCAGGCTGGAGTG | 50807 |
| rs368726713 | snp | C/T | 4.95987e-05 | 0.00497965 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130126088 | TGAAAGCCAGGTGGG[C/T]TCTGTGGAAAGAATG | 50807 |
| rs368737943 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130058483 | GTAAAGCAAAATCTG[C/T]AGCTTCTGCATAATG | 50807 |
| rs368739122 | in-del | -/ATT | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183642 | CCACCGTGCCTGAAA[-/ATT]ATTATAAAATCAGTA | 50807 |
| rs368757728 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428430 | CCATCACCATCATCA[C/T]CATCACCACCACCAC | 50807 |
| rs368762313 | in-del | -/CTGAAAGGCCTTTCAGCT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130282583 | TCCCCTTTTGGCAAA[-/CTGAAAGGCCTTTCAGCT]CTGGCATGTGTACAT | 50807 |
| rs368771502 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130400660 | GCTGGGCGTGATGGC[A/G]GGCGCCTGTAGTCCC | 50807 |
| rs368796486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258442 | TAATTCACTAAACTT[C/T]CTCCACCCTTAAGTC | 50807 |
| rs368803236 | snp | A/G | 4.94336e-05 | 0.00497135 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079986 | CCTACAAGGAAAACC[A/G]AAGGTGAAAAGGTAT | 50807 |
| rs368826336 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130150203 | ACAGATGCCACAGTC[C/T]ATTATCTTAGCCACT | 50807 |
| rs368832433 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130324731 | TTTCAGTGGTACTTA[A/C]AACTTCATCTGTTTT | 50807 |
| rs368839248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098501 | GGTGCCTGCCACCAC[A/G]CCCGGCTAATTTTTG | 50807 |
| rs368849348 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130285743 | TTCTATAGGCAATAG[C/T]CAGACTTTCTGTAAA | 50807 |
| rs368849907 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130357596 | GCCGCTGAGGGGTGC[A/G]TTCACTGCCCATCTC | 50807 |
| rs368855476 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130312412 | AGACGAGAGCTAAAT[C/G]TAACACACTTAAGCA | 50807 |
| rs368859919 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170640 | GAAAAATACTACCTT[C/T]AGAAAGTTTTTCAGC | 50807 |
| rs368860046 | snp | C/T | 9.92605e-05 | 0.00704418 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130188118 | ACTTACTCCTTTGAC[C/T]CCCTTTAGGTCTCCT | 50807 |
| rs368883994 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354816 | CCAAACCGTGAACCC[-/CT]GAGCCATGTGTGACC | 50807 |
| rs368893182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130351380 | ATAATAAGAATGCTA[C/T]TAGAATAAGCTTTTA | 50807 |
| rs368906113 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173148 | TTGGAGGCAAGCCCC[C/T]TGCAGAAAGTAATTT | 50807 |
| rs368913466 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130152945 | CAAAAAAATCCTGGT[G/T]GCCTTTTATTATCCC | 50807 |
| rs368915438 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130193663 | CATCAATGCCTCAAA[A/T]CCTTTGTGAAATGAA | 50807 |
| rs368922112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205487 | CAAGGTATACCTGTA[C/T]TGACAAACAGAAAAT | 50807 |
| rs368941641 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216963 | AATGCAACACTGTTA[C/T]ACTGTGCATCAGATC | 50807 |
| rs368955563 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130328352 | GTCTTAAAAGCAGTG[A/G]AAGTGCAGGTGACAA | 50807 |
| rs368956523 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130063732 | TAAGAAGAGATGGTC[A/G]ATTCCTAGCCCAAGG | 50807 |
| rs368963253 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130169862 | GGAATTCAGATCCAG[G/T]TCTGCCAGATTCTGA | 50807 |
| rs368966337 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130133798 | CCAGTGAAAGGCACA[C/T]GGCAGTTTCCTTCCT | 50807 |
| rs368977622 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130145066 | TGGCGCTGAGGTTAC[C/T]GCACCCAATGAATGT | 50807 |
| rs368989712 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130310138 | AATACAGTTTTTTTT[-/G]GGGGGGGGGAGGGGG | 50807 |
| rs368999901 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130101350 | GAAAGAGATTGCATC[G/T]AATCTGTAGATTGCT | 50807 |
| rs369005040 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130424336 | AGCCTATTGGTCTGA[C/T]GGCCTAGCCCCCACT | 50807 |
| rs369021071 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130213177 | AATCCAAAAGCACAG[A/G]AACATTAGAGCCAAA | 50807 |
| rs369028130 | in-del | -/AG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130353863 | GCGACAGAGTGAGAG[-/AG]CCTGTTTCACGGAGA | 50807 |
| rs369067119 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130130752 | GATGATCTGCCTAAG[G/T]TTAAAAAGCCACTAA | 50807 |
| rs369079591 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130366056 | TAGGTGACTTGCCCA[A/G]TGTTCCCTGACAGAT | 50807 |
| rs369098363 | in-del | -/ACAGTAGTGTAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130179837 | TTGAGGTAACTAAAC[-/ACAGTAGTGTAC]TTGTACTGTGCACTG | 50807 |
| rs369099478 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130260055 | AAAAGGACAATGTTG[G/T]TCATTTATACATTGT | 50807 |
| rs369101001 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130239546 | CGATAGGCTGAAACT[A/G]AAAACAGTCTCATCA | 50807 |
| rs369115421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208105 | TTTTGAAAAAATTAT[A/G]GACTCACCAAAAAAT | 50807 |
| rs369136268 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216013 | AGGAAAGGAAAGGAA[A/T]GGAAAAAGGAAAGGA | 50807 |
| rs369147878 | snp | A/C | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195519 | AGTGATAGAGTGTGA[A/C]CCTGTCTCTTAAAAA | 50807 |
| rs369148439 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130382310 | AAAAAAAAAAAAAAA[-/G]AAATTAAAGATATCA | 50807 |
| rs369154335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130433939 | AATTAAGGCGTGGAA[C/T]TAAAATTCAAGTCTG | 50807 |
| rs369158448 | snp | C/T | 4.23379e-05 | 0.00460078 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130358174 | AGACACAAGCGGGGG[C/T]GGGGGGTGAGTCACG | 50807 |
| rs369159843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341969 | GTGACAGGATCTCCA[C/T]GCCCAACACCTAAAA | 50807 |
| rs369180178 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | ASAP1 | GRCh38.p7 | 8:130116734 | CTAGGGCAGTTTCTC[C/T]AGCCTGGTTAACTGA | 50807 |
| rs369183344 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130248227 | GGCGGGTGCCGGGGG[A/G]GTTGGAGGGGGGAGT | 50807 |
| rs369184127 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130282208 | AAAGCAGAAGTGTCT[A/G]AAATCCTGCAAGTAT | 50807 |
| rs369194714 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130263597 | TTGCTCACTTAGGGA[A/G]CCTAACTGAAATGGT | 50807 |
| rs369198429 | in-del | -/CTT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130263954 | CTCACACACATTCTT[-/CTT]GCCACAGACCTCTGT | 50807 |
| rs369205202 | in-del | -/CA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130128138 | TTATAAGAGCATGGT[-/CA]TTTTTTTTTTTTTTT | 50807 |
| rs369209048 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130393028 | AATAAACCTTTTTTT[-/T]AACATGACAGTTATA | 50807 |
| rs369221686 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130246564 | CAGCGGCCTTGTGAA[A/G]AAGGTGCTTGCTTCG | 50807 |
| rs369228683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055133 | CCCAGAGAGGTGACA[C/T]GCTCTCCCACAGGCG | 50807 |
| rs369234601 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130168389 | GTGGCTCACGCTTGT[A/T]ATCCCAGCACTTTGG | 50807 |
| rs369235575 | in-del | -/CCAAGG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130178654 | AATAATAGGCCAAGG[-/CCAAGG]TGGATCGCGAGGTCA | 50807 |
| rs369241849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111190 | CCAGCCTGGGCAACA[C/T]AGCAAGACCTCATCT | 50807 |
| rs369241895 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130149190 | GCCAAAGATTTGTTG[G/T]AACTGGTATTTTGAA | 50807 |
| rs369244273 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130148486 | AATGAAGATAGTGAT[A/G]CCTATCCTGTAGGGC | 50807 |
| rs369250753 | snp | G/T | 1.64749e-05 | 0.00287005 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130112230 | CCTTGGAGTGCTGAA[G/T]CCTGGCAGTGCCAGC | 50807 |
| rs369259234 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130345343 | ACTGGCTGCCCCAGA[C/T]GCATGATGTAAATTA | 50807 |
| rs369270541 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130177497 | ATGAAAGATAAAAAA[C/T]TCCACCCAATACTAA | 50807 |
| rs369270890 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077509 | TTCTGTCCCCTGATG[G/T]CCTAAGAGTTGGTTG | 50807 |
| rs369301556 | snp | G/T | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296263 | CAGAGGTTTACCTGG[G/T]TGAACACCAGAAAAA | 50807 |
| rs369311823 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130090297 | AAGAGGATTAAAACT[A/T]AAGAGAAATTTGGAA | 50807 |
| rs369344384 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130121359 | TGTCCTATGTTTAGC[A/T]CCATCCCTGACCTCT | 50807 |
| rs369355364 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084560 | GAAAGAGAGGGGGCA[C/G/T]TGGCTCAGCAGCGAA | 50807 |
| rs369359437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066143 | TTAGTAAGAATGACA[C/G]AGGTATTTCCTTTGC | 50807 |
| rs369370292 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228309 | TCCACTTCAGAACTC[A/T]GGGAAAAAGCATCAC | 50807 |
| rs369391571 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130233522 | ATGAGAACAATGGTA[A/C]TTACCTTATTGGCTT | 50807 |
| rs369401009 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130274982 | TAATAAGCATAGACT[C/T]TTGAGACTGTAGCTC | 50807 |
| rs369424190 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130317197 | ATGTGCAAAAGCTGT[C/G]AGTTTCTTCTTACAT | 50807 |
| rs369426017 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130233821 | AGGAGAATATAATAG[A/G]TGCTCAATAAATATC | 50807 |
| rs369427305 | snp | A/T | | | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445391 | TGGTTGCTTATTTTT[A/T]ATCTGCCCCCCACTC | 50807 |
| rs369431376 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130107542 | TATGTATGTATGTAT[G/T]TATGTATGTATGTAT | 50807 |
| rs369455130 | snp | A/G | 1.80657e-05 | 0.00300542 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130061023 | AAAGATTTCGGGCGG[A/G]ATGGTGGCTTTGTCT | 50807 |
| rs369457830 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086299 | ACCTTTCTGCGCCCC[A/G]AAGTTGAGATAATAG | 50807 |
| rs369465825 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130303441 | CTTTGCCCTCTGTCA[A/C]CTAATTGCCAGTATC | 50807 |
| rs369467760 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130281542 | TACAACTAAGTACTG[C/G]TCCAGATTTTCAGGC | 50807 |
| rs369475818 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130139868 | AAATCTAGATTTCTC[C/T]GGTGTTTCTGAACAA | 50807 |
| rs369479713 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130431148 | CCCCCCTCCAAATGA[A/T]CCCCATGCCAGCCAA | 50807 |
| rs369485158 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130435463 | CAGGCACTGCAGCAG[A/G]TGAATGCACAGGACG | 50807 |
| rs369493501 | in-del | -/AAAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130306888 | ACCTCAGAGCCTAAC[-/AAAC]TAGAAACATGTTTCC | 50807 |
| rs369494090 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130153865 | CATAAGAATGTTCAA[C/T]TGATTACTTTTGTTA | 50807 |
| rs369496645 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205878 | CAAATCTAACCCCAA[A/G]GATTTTGGACCTGAA | 50807 |
| rs369509976 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130063984 | TGGGGAGGAGGAGAG[C/T]GACCACCAAGGAGGG | 50807 |
| rs369511687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355564 | CATTCTTAAAGTTTC[C/T]AAATATCTCAGTTGT | 50807 |
| rs369524160 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130264917 | GTAAATGACCCCCAA[A/G]AATCAAAGGAAAAGA | 50807 |
| rs369550751 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130212200 | ATAATGTTTTCTTAG[C/T]AACCAAACTACAGTA | 50807 |
| rs369563612 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130130624 | CGTCGCTTTGAGTTT[C/T]ATAAGATAAAAAATA | 50807 |
| rs369564023 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130140450 | AGGGGTTTGTTGTAC[A/G]TATTATTTTATCATC | 50807 |
| rs369571236 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130166910 | TGCCTGTTTTGGCTG[C/T]CCAGAAAGACAGAAG | 50807 |
| rs369578516 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130148175 | CACTGCAAAGAACTG[C/T]TATTCATGAAACTTT | 50807 |
| rs369595615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074674 | CTACCTTAGGACCAC[A/G]GCCACCATGCCAGGC | 50807 |
| rs369606217 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130292377 | AGAAGTATGAATAAA[A/G]TATGAATGAGGAACC | 50807 |
| rs369606621 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130256256 | TGCACACTAACACTT[A/C]AGAGATGTTTTCCTC | 50807 |
| rs369606885 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130363983 | GGCTCATGTTCCCAT[A/G]GTCTACATAAACTGC | 50807 |
| rs369615605 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130093087 | TGAACAACATTTATA[C/T]AGACACTGATTTTTA | 50807 |
| rs369620806 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130431418 | ACATCCTACCTCAAA[C/T]GTTAGGTTCCAACCA | 50807 |
| rs369622432 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130330725 | TGTGTAGGTATCTCT[A/G]TGGGGAAAGGGACAG | 50807 |
| rs369644334 | snp | A/G | | | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054532 | CCAGTAAGGCGCGCC[A/G]GGTCCGAGGCTACCC | 50807 |
| rs369650873 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130059275 | CTCAAGCAATCTTCC[C/T]GCCTTAGCCTCCCAA | 50807 |
| rs369657420 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130272557 | CTGCACCCCCATGTT[C/T]ACTGCAGCACTATTC | 50807 |
| rs369662578 | in-del | -/GT | 0.0448719 | 0.142907 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162646 | ACACGGTGAAACCCC[-/GT]CTCTACTAAAAATAC | 50807 |
| rs369669338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143700 | AGAAATGCATGCAGA[A/G]ACAGAATGAGTCAAT | 50807 |
| rs369672186 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130209550 | GTCTTGCTCTTACAG[A/T]AAAAAAAAAAAAAAG | 50807 |
| rs369672285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130125168 | CTGTCTGAGAAGTCA[C/T]ACTTTATTTTAAAAA | 50807 |
| rs369674965 | in-del | -/CTTT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130100338 | TTTCTTTCTTTCTTT[-/CTTT]TTTTTGAGACGGAGT | 50807 |
| rs369677211 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130389030 | ACTCACAGGATTGTT[G/T]TAAGGATTGAATGAG | 50807 |
| rs369685199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099304 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 50807 |
| rs369690604 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130162055 | TTCTCCTACTTTGGC[C/T]TTCCGAGGTGCTGGG | 50807 |
| rs369692977 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130060015 | CCTAGGAGACTGAGG[C/T]TGCAGTGAGCTGTGA | 50807 |
| rs369698061 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124766 | AAAGTCTTGGGTTTA[C/T]TGCATGGCAAACGTT | 50807 |
| rs369703991 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130088165 | GAAGGAGTTTCGCTC[C/T]TGTTGCACAGGCTGG | 50807 |
| rs369709406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283756 | GGAAGGGTCAGATAA[C/T]AGGATGCCTTAAAAC | 50807 |
| rs369718244 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428491 | CACCACCATCTTCAT[C/G]ACCATCACCATCACC | 50807 |
| rs369719252 | in-del | -/TTCT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130419953 | TGCACCACCTTCTTC[-/TTCT]TTTTTTTTTTTTTAA | 50807 |
| rs369720584 | in-del | -/AGAGAGAG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130300154 | CACACACACACACAC[-/AGAGAGAG]AGAGAGAGAGAGAGA | 50807 |
| rs369767530 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130245713 | AGTAGGGCTCAATAA[A/G]TATCTGTCAAATAAA | 50807 |
| rs369779679 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130375450 | CTGTAATCCCAGCAA[C/T]TGGAGAGGCTGAGGC | 50807 |
| rs369796423 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130391659 | GCACTATCACAGGGC[A/T]GACCAATGCATGCAT | 50807 |
| rs369797574 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130201674 | GGAGGGGGTGTGCTA[C/T]ATGGCTAGGCCTTGG | 50807 |
| rs369808528 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376817 | CTGAGGCAGGAGAAT[A/C/G]GTTTGAAGCCGGGAG | 50807 |
| rs369809376 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130167851 | TTAAATAACCTATCT[A/C]AGCTAGATAGTTAAC | 50807 |
| rs369811062 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130224231 | CCATGTGCCAGCCAT[A/G]TAAAATACAGTGAGC | 50807 |
| rs369813223 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130274228 | CTTGAAATTATTAGA[C/G]GATGACAAATGACTG | 50807 |
| rs369814507 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130309506 | AGATGAGGCACGGTA[C/T]GCAACTGCTGCTGCA | 50807 |
| rs369818706 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130355400 | AAAAAAGGTCATCAA[C/T]AGGAAGGTACTTACT | 50807 |
| rs369826274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419296 | TGGGCCTCACTGGCT[C/T]AAAACCATCCCCATC | 50807 |
| rs369830284 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076328 | TAATTACATGTAAAT[A/G]TAAAAATGATAGATC | 50807 |
| rs369851080 | in-del | -/ATTTTT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130190529 | TTTATTTTTATTTTT[-/ATTTTT]TGAGACAGAGTCTCA | 50807 |
| rs369858887 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130115682 | CTGTCGAAGATTCCA[C/T]TCATATTCTACGTGG | 50807 |
| rs369877347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168256 | ATGATTTTTGGGCAA[C/T]AACTTTACCATTTCT | 50807 |
| rs369877650 | in-del | -/CT | 0.0103295 | 0.0711199 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073218 | AACACGGAGAAACCC[-/CT]GTCTCTACTAAAAAT | 50807 |
| rs369889005 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130080868 | AAATTCCTGGCCTCC[C/G]GTGATCCACCTGCCT | 50807 |
| rs369903993 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130079237 | CTTTCAGAAACTCTG[A/G]ATAAGAGCTGACTCT | 50807 |
| rs369909770 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130263666 | AGTGAGTATTATTAA[C/T]CTCTGCAGGCCACAG | 50807 |
| rs369923310 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130230274 | CCAGCAAAACGGAGG[A/G]AGTGCATACACAGGC | 50807 |
| rs369925856 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359493 | GCCACAGGATTGGTA[C/T]CTGTAATTCAAGCCA | 50807 |
| rs369931326 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130206739 | CATTTTCTAAAACCA[C/T]TGCTGCCTTGGGACT | 50807 |
| rs369939872 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130115125 | AAATACTAGTCTAGA[C/T]GTTGCTGTAAAGGAA | 50807 |
| rs369952696 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130217082 | CCCATACTCTCAAAG[C/T]AAGGCAGGAAATATG | 50807 |
| rs369953908 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130162775 | GTGAACCGAGATTGC[A/G]CCACTGCACTCCAGC | 50807 |
| rs369959679 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130342073 | CTTCCAAGAGTTAGC[C/T]GAAAGCAGACTTTGG | 50807 |
| rs369965933 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130279064 | CGAAAGCCATGTCTA[C/T]CACGGGACAGAACAA | 50807 |
| rs369966700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144691 | AGCTCTCACATCCCC[C/T]GTGTGATCCTTCAGA | 50807 |
| rs369967250 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130346961 | CTCCCCATGTTTCAA[A/C]ACAATGAAGACAATT | 50807 |
| rs369972164 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130389011 | GGAAATAACAATACT[A/G]TCTACTCACAGGATT | 50807 |
| rs369973172 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130265489 | GAAGCAGGAGGTTTG[C/T]TTGAGTCTAGGAGTT | 50807 |
| rs370023155 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130259291 | TTAAACAATCTTCTA[C/T]TTTCTACTCCTTTTA | 50807 |
| rs370035434 | snp | C/T | 0.000153988 | 0.00877328 | missense | ASAP1 | GRCh38.p7 | 8:130127990 | CATCCTCAATAATGG[C/T]TTTTGTCAGGTCTTC | 50807 |
| rs370043472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090499 | CCTCAATTGTTCTTG[C/G]CTGGCTTGTGGGAAC | 50807 |
| rs370050750 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130113489 | TTATAATGATTATCA[C/T]ATTGTATTATAATTT | 50807 |
| rs370052553 | snp | A/G | 1.65384e-05 | 0.00287557 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130188181 | GTGGCTCAAACCCTG[A/G]AGCTGAAAAAGCAAA | 50807 |
| rs370064066 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130077573 | TTTTTTTGAGACACA[A/G]TCTTGCTCTGTCACC | 50807 |
| rs370075900 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130223299 | GACTTGGGTCTGAAT[C/T]CCCACTCTGGTTCTA | 50807 |
| rs370084562 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428683 | CCATCATCATCACCA[C/T]CAGAACTACCACCAT | 50807 |
| rs370090813 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130404724 | TCATGGGACTTTGTA[A/G]TACTTCCCACTAGAG | 50807 |
| rs370096905 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ASAP1 | GRCh38.p7 | 8:130051759 | AGGTCTGCTCCACTG[C/T]GTGGCAGCACTAGTT | 50807 |
| rs370137967 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130062321 | AGAAGAAACAGATAA[-/A]CCTCATGTTGTAAAT | 50807 |
| rs370139587 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128121 | TAAGAGGAAAAAAGT[A/C]TTTATAAGAGCATGG | 50807 |
| rs370147047 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130169592 | ACAAGAATTCAAAGC[A/T]ATAATACCAACGGGT | 50807 |
| rs370148642 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353758 | ACCTGTAGTCCCAGC[C/T]GCCCCAGGAGGCAGA | 50807 |
| rs370155967 | snp | A/G | 0.000115351 | 0.00759355 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079861 | TCTGTCCATTGCATC[A/G]ATGGATCCAACAGGG | 50807 |
| rs370157059 | snp | A/C/G | 0.000176966 | 0.00940488 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214748 | GAACTATTATTTGCC[A/C/G]CAATGAAAAGTTACT | 50807 |
| rs370157357 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130210290 | CTTCTAATGTTTTTT[-/T]GGTTTGAGAAAATAG | 50807 |
| rs370166518 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130401101 | TGGCCAGGCTGGTCT[C/T]GAACTCCTAACCTGA | 50807 |
| rs370183457 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130374057 | AAAAAAAAAAAAAAA[C/G]CAGCCATGTCCAAGC | 50807 |
| rs370200462 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130260623 | GATGTAACTGGAATT[C/T]CAGACTGTGGGGAGC | 50807 |
| rs370204449 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072442 | TTTTTCTCTTGCCTG[C/T]TGCCATGTAAGACGT | 50807 |
| rs370211953 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130198186 | TCATCCAGGCTGGAG[C/T]GCAGCCTTGCTCACT | 50807 |
| rs370233523 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397969 | TTACTGGCACATAAG[C/T]AATAAGCAGTTATCA | 50807 |
| rs370233968 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130287335 | GTAAGGTTACTTCAG[A/G]TTAGGAAGAGCTTGA | 50807 |
| rs370238400 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130411542 | TGTTTCCTTGGATCA[C/T]CTCCCAAAGAAACTA | 50807 |
| rs370239442 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130136691 | TACTCACAGTCAAGC[A/G]TTGGTTTAGTTCAAT | 50807 |
| rs370246015 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130373827 | ACTCCAGCCTGGGTG[A/G]CAGAGTGAGATGGAG | 50807 |
| rs370251675 | snp | A/C | 1.64754e-05 | 0.00287009 | missense | ASAP1 | GRCh38.p7 | 8:130116719 | GTCTCTTTGCTATGT[A/C]TAGGGCAGTTTCTCC | 50807 |
| rs370253429 | in-del | -/AGA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130125700 | ATGTAGTTTTGAAGA[-/AGA]CCATCCCAAAAGAAA | 50807 |
| rs370255698 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130203850 | GCAGACAGAAGGCTG[C/T]TAATTCTCTCCAATC | 50807 |
| rs370260713 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130258600 | CTCTGTGAGTTGGGT[-/T]ATGTCTCCTACTCCC | 50807 |
| rs370262385 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130269191 | CAACTGAAATTGGCC[-/T]TTTTGTCTAGGATGC | 50807 |
| rs370265735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347927 | CCAATGTATTTCATT[C/T]TGCTGGGGAAGGGGA | 50807 |
| rs370266431 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130118756 | CAAACATTTCTCTTT[G/T]AGAAGTTATTTTAAT | 50807 |
| rs370279171 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130300890 | CATCTGTCACAATGA[C/T]GATTAATCTCTAAGA | 50807 |
| rs370279563 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130244651 | GCGAGTGAAACATAG[C/T]CTGTCTGTATGGCAC | 50807 |
| rs370279699 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130395822 | CAGGCACCCGCCACT[A/G]CGCCCAGCTAATTTT | 50807 |
| rs370293242 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130091167 | ATTCCTGAATATTCA[-/A]CTGTATGCCAGGCGT | 50807 |
| rs370313904 | in-del | -/TATATATATATA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130256740 | GAATATACACATTCT[-/TATATATATATA]TATATATATATATAT | 50807 |
| rs370323900 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130095294 | CTTTTTAGGCCAGTG[-/A]TTTTTTTTTTTTTTT | 50807 |
| rs370330355 | in-del | -/AATTA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130200276 | GAAGTTGGGTAAATA[-/AATTA]TAGTGCAAATATAAG | 50807 |
| rs370360522 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130127310 | CAACCTCTGCCTCCT[A/G]GGTTCAAATGATTCT | 50807 |
| rs370363112 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130288190 | CATGCTGGAAGCTGC[C/T]TGAGGCTTTTCATCT | 50807 |
| rs370367108 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130145434 | GCGATTCTCCTGCCT[C/T]AGCCTCCCGAGTAGC | 50807 |
| rs370369085 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108728 | TCAAAGGTTAAAAAG[A/T]AACTAATCTTGGCAA | 50807 |
| rs370374288 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130402674 | CCAGGGCGAAAAACC[A/G]AGAGACATCTCAGTT | 50807 |
| rs370381133 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130175757 | GAATGAACATGACTT[G/T]GAGCAAAATACTGAT | 50807 |
| rs370385000 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130230100 | CAAACAAACAAACAA[A/C]CAAACACCAACCCCA | 50807 |
| rs370386563 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130056975 | GTCACTCACAGCCTG[A/G]GTACCTAGCAGGGCC | 50807 |
| rs370387896 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130054907 | TGCCCACAGACCTGG[C/T]GGTGGAATCCCAGGC | 50807 |
| rs370388781 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130104683 | ATTTATGTTCAAGTG[C/T]TATTTCTTTATGGCA | 50807 |
| rs370392750 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130078143 | TACAGGCGCACCCCA[C/T]TATGCCCGGCTAATT | 50807 |
| rs370395376 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130434737 | ACAAACGCAATGACA[C/T]GCAAAAATTCCATCC | 50807 |
| rs370406902 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130209256 | TAGTGAGGAAATTTA[C/T]GTCTGTAAGTTAGGC | 50807 |
| rs370409056 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130432724 | TCCCACAAAAGAAGA[A/G]GGGCTTTTTCTTCCT | 50807 |
| rs370427586 | snp | C/T | 3.41285e-05 | 0.00413075 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214512 | TATGACGTAATATTT[C/T]GGAAAGGCTGTAATT | 50807 |
| rs370432005 | snp | A/T | 1.64795e-05 | 0.00287045 | missense | ASAP1 | GRCh38.p7 | 8:130112273 | GAGATGCTGGAGGAG[A/T]GGCAGAAGCTCTGAG | 50807 |
| rs370437731 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130416862 | CCCATTCTGGTATCA[C/T]GGCAGCCTGAGCTGA | 50807 |
| rs370443525 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130209033 | AATTGCAATTCCCCT[C/G]TAGGCATGTGTTCTT | 50807 |
| rs370449722 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130181914 | AAGTTATGGTGGTGG[G/T]AGGGGAAACCAACTC | 50807 |
| rs370453917 | in-del | -/AAAGGGAAATGAG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130132064 | AGAAAGGGAAATGAG[-/AAAGGGAAATGAG]GAAGAGAGAATGAAA | 50807 |
| rs370462139 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130099361 | TTTTTTTGTATTTTT[-/T]AGTAGAGACGGGGTT | 50807 |
| rs370469053 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130242947 | TGGTATCTGTGGGGA[C/T]CCTGGAACCAATTTC | 50807 |
| rs370478322 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130103319 | TTGTCTAGCTAAAGG[C/G]TTGTCAATTTTTTTC | 50807 |
| rs370493253 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130279723 | TACAGATGAGAAAGA[A/G]TTAGCAATGTAGTAG | 50807 |
| rs370501641 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130056346 | CTGACAGAGGCTGGA[A/G]GTACCCCTGGGCCTC | 50807 |
| rs370505581 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086151 | CTGTGAGGAGAAATG[A/G]CCAGTGGGCCTGCAT | 50807 |
| rs370511153 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130199101 | TAAGTCCCTTCTCCC[C/T]AACCTCCTGTTACTC | 50807 |
| rs370511197 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130261019 | TGCAGTCCACATTTA[C/T]TCAATTATATATTCT | 50807 |
| rs370516214 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130245254 | TATCTGCAAATAAAG[A/G]TTTTAAGATGTTTAT | 50807 |
| rs370517090 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130159806 | TCCCTATATGAGAGA[C/T]TGGAAACATTTTCTA | 50807 |
| rs370527553 | in-del | -/TTCA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130397105 | TCATTCATTCATTCA[-/TTCA]CATATTTATGAGAAT | 50807 |
| rs370545773 | in-del | -/C | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218656 | CAGAACCTTCTGTGA[-/C]CCAAATCCTTATGCT | 50807 |
| rs370549584 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130061867 | GTTGACCCATTTCCA[C/T]AGCTCTTTGTACAGC | 50807 |
| rs370561613 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130219413 | CACACTGCAGAGTAC[A/C]GTAAGCCATCTGAGG | 50807 |
| rs370574684 | in-del | -/CAC | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428434 | CACCATCATCATCAT[-/CAC]CACCACCACCATCAT | 50807 |
| rs370580190 | in-del | -/AA/AAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130188723 | GTGAGAGACTCTCTC[-/AA/AAA]AAAAAAAAAAAAAAA | 50807 |
| rs370606297 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130277100 | TGCAGGCACCGAGGG[C/T]CCCCCATCCCAGACT | 50807 |
| rs370611434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324655 | TTAGGAAGCATAATT[C/T]GTAAAATCCATTAAA | 50807 |
| rs370614651 | snp | A/G/T | 0.000282666 | 0.0118856 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401846 | CGCTGTATCTCCCAC[A/G/T]CCGAGTTTTCTGGAC | 50807 |
| rs370620800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155562 | AGGGTTTTGCCATGT[C/T]GCCCAGGCTGGTGGG | 50807 |
| rs370621218 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130301310 | CTCCTTTATTCCACC[C/G]ACAAACAAAACAGTG | 50807 |
| rs370621318 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130352554 | AGGGAACACACACAG[A/G]AGTCTGACTGGCCTG | 50807 |
| rs370627115 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130155402 | GACAGGGTGTCACTT[G/T]GTAACCCAGGCTAGA | 50807 |
| rs370628399 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130135892 | TTCATACAGATGCTG[A/C]AGAATACAGTTTCGA | 50807 |
| rs370628646 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118267 | AAGGGAAAGAAAAGT[A/G]TAAGTAAGTCAATAA | 50807 |
| rs370632287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154248 | GATTCACAAAGGGAA[C/G]TAAATGGTGACCAAA | 50807 |
| rs370637428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109867 | TGTCTCACCAGCAGA[C/G]AGGCCAAATCTCTGA | 50807 |
| rs370645920 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130196959 | AAATAAAAATAAAAC[G/T]GATGCCTCGTCATTA | 50807 |
| rs370662930 | snp | C/T | 3.29468e-05 | 0.00405861 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167529 | TGTAAACATGTAAAC[C/T]ACTTACTTCTTTCTG | 50807 |
| rs370667603 | snp | C/T | 1.65154e-05 | 0.00287358 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152841 | AACTAGATATAGTAA[C/T]TGATTCACTCTGGGA | 50807 |
| rs370673744 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130213633 | GAACAGCTCCTCTTC[A/T]CCAGGGCAGGGCTAA | 50807 |
| rs370682878 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130231913 | GCCCCACTCCTACTG[A/T]ACTGACCCAGGGTCT | 50807 |
| rs370686530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234022 | CTGGAACAATTCGAG[A/G]GTAAGGGTCTGAGAG | 50807 |
| rs370694062 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437896 | ACCAGGATCCCGCCA[C/T]TGGAGGGACATACTT | 50807 |
| rs370701705 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130190556 | AGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG | 50807 |
| rs370701738 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130141706 | CGCACGCTACCACAC[A/G]AGGCTAATTTTAAAA | 50807 |
| rs370704369 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130390145 | AGCATGAGAACCAGG[A/T]AAGAATGCTCACTAT | 50807 |
| rs370706125 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130265791 | CTGAGGTGGGGATAT[A/C]ATCTGGGCCTGGGAG | 50807 |
| rs370707442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168727 | CACTCAAATGTGATG[C/T]TAACTGAATCGTAAA | 50807 |
| rs370726586 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086429 | TGGCCTTATAAAATA[-/T]TACGTACGTAGTTTT | 50807 |
| rs370735646 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130145770 | AGATGTGGAAAATAA[G/T]GCACCAAAAGGTTAA | 50807 |
| rs370736600 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082958 | TTATAACAATCAAAA[A/C]GTCAAGGAAAATTTT | 50807 |
| rs370740218 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130178821 | CTGAACCCAGGAGGC[A/G]GAGATTAGAGTGAGC | 50807 |
| rs370741726 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130344105 | AATGACAGTGCAGGG[C/T]TGCAGTCAACACTAT | 50807 |
| rs370744928 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380083 | AGCACCTACCTGTTG[C/G]GCACCCCAGGTCTCA | 50807 |
| rs370746147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130067082 | GAATTCTGCTGCTCA[C/T]TGAAAGCAAACTCAA | 50807 |
| rs370752677 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130099156 | GTAGCTGGGACTATA[C/T]GTGTACGCCACCAGG | 50807 |
| rs370759139 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130115860 | TGTAGGTGTACTATA[C/G]GCAACACTCTGCTTA | 50807 |
| rs370774397 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130105527 | TCAAGAATACAGTAC[A/G]TTATTAACTACAGGC | 50807 |
| rs370779716 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130076319 | GTGACACTTTAATTA[C/T]ATGTAAATGTAAAAA | 50807 |
| rs370787865 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130168878 | GTCCTAGGTTTGTAC[A/G]GACATATCATTTAAT | 50807 |
| rs370789875 | snp | A/G | 4.94238e-05 | 0.00497086 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130079967 | GGATGGACCCCCATC[A/G]TTACCTACAAGGAAA | 50807 |
| rs370789983 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130142508 | TCTACCACATTCCAA[A/G]CACATCTGAGAAACA | 50807 |
| rs370790135 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130319737 | GGATGGAAAAACCAA[C/T]ATCAGTAACAGGAAT | 50807 |
| rs370806786 | snp | A/T | 0.00167644 | 0.0289035 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066621 | CCTTGTTTCTTTTTC[A/T]TTCATTCATTCATTC | 50807 |
| rs370809770 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130275243 | GTCTTCAGATGAAGT[A/T]ATATTCCTGGCCCTA | 50807 |
| rs370811484 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130170014 | ATTTTCTCTGCCCTA[C/T]TGGAAGCTTCTCTAA | 50807 |
| rs370824294 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428604 | CATCATCACCACTAT[C/G]ACCATCATCATCACC | 50807 |
| rs370841685 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130248258 | GCGGAATGAACAGGC[A/G]GATACGGCTCCTACA | 50807 |
| rs370843045 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187993 | TCCAAGAGCATTTTT[-/A]ACGCTGAAAATGTTC | 50807 |
| rs370855529 | in-del | -/AAACGA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130163308 | AACTTATAAAAACGA[-/AAACGA]TTATATTCTGTAAAT | 50807 |
| rs370860564 | in-del | -/C | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409273 | TCTCAAAAAAAAAAA[-/C]AAAAAACCTCCTCTC | 50807 |
| rs370865931 | snp | G/T | | | utr-variant-5-prime, intron-variant | ASAP1 | GRCh38.p7 | 8:130361742 | GCACCTCTCATTTTC[G/T]CAAATACTCTGAAAA | 50807 |
| rs370867193 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130307466 | GTAGACTAGGGATGG[C/T]TGTTCCTCCTCCAGT | 50807 |
| rs370870868 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130337736 | CCATTTTTATAAGTC[C/T]TTTACTTTCCTCTCC | 50807 |
| rs370874044 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130069905 | GGCAGAAGACCCAAA[A/G]CTTTTTGCGCAAGAG | 50807 |
| rs370879143 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130266670 | CAGTTATAAAAAACA[C/G]AACTAATTTCCCCAA | 50807 |
| rs370883529 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130292923 | TATAAAAACATTTTA[A/C]AACTCGAATGTACTA | 50807 |
| rs370900149 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130393916 | CATAAATTGTGAAGA[C/T]TTCATGGACACTTAT | 50807 |
| rs370945499 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432911 | GGACATCTGAAGATC[A/T]ATGTCCTGCCAGCAA | 50807 |
| rs370961045 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130204782 | ATGTCACACGAGAAG[A/C]AAATAAACCATGTTA | 50807 |
| rs370961685 | in-del | -/ACT | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428599 | AACTCCATCATCACC[-/ACT]ATCACCATCATCATC | 50807 |
| rs370993932 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409254 | GTGACAGAGTGAGAC[A/G]GTGTCTCAAAAAAAA | 50807 |
| rs370994927 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130131573 | GTTTGAGGCCAGCCT[A/G]GGTAACAACAGCAAG | 50807 |
| rs370996302 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130090863 | AGCAACGGGACAATA[C/T]AACTTTCCCCCAAAA | 50807 |
| rs371002150 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130169427 | TTTGAATTTGAAGGA[C/G]AGAGAAGGACACATT | 50807 |
| rs371007379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395811 | GGCTGGGATTACAGG[C/T]ACCCGCCACTACGCC | 50807 |
| rs371018530 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | ASAP1 | GRCh38.p7 | 8:130116713 | CTTTTAGTCTCTTTG[C/T]TATGTCTAGGGCAGT | 50807 |
| rs371024958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395909 | GATCTTAGGTAATCC[A/G]CCCGCCTCCGTCTCC | 50807 |
| rs371034215 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096349 | AAAGCTGAAACAAAA[G/T]AAAATGGAACACAGC | 50807 |
| rs371048740 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130169288 | AATAAATTATGGCTG[G/T]CAGTTGACATTTGAT | 50807 |
| rs371079188 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130230096 | CAAACAAACAAACAA[A/C]CAAACAAACACCAAC | 50807 |
| rs371080637 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130367181 | AGGTGTGAGCCACCA[C/T]ACCCGGCCGCTAGAT | 50807 |
| rs371090872 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130420691 | CTGAGGTCAGGAGTT[C/G/T]GAGACTAGCCTGGCC | 50807 |
| rs371093778 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130328573 | TTTTAAGACAAAAAG[C/T]TGTAAAAACCCAATT | 50807 |
| rs371094237 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130374325 | TGAATCTTCATTGTT[C/T]TCCATGAAGCTAATA | 50807 |
| rs371099262 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130204564 | CTGCAGCTCCTGCTC[C/T]CTCCCATTTCCAGGT | 50807 |
| rs371104200 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130056673 | TGTGCCCATGCCTAT[A/G]TGTGTGTGCACACAT | 50807 |
| rs371108775 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130089464 | TCCTCATGGGCTGAG[A/G]AGAGATGAGAGGTTT | 50807 |
| rs371110040 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130071921 | TATGTATTAGTTTTC[A/G]TCCACAGTTGCTGGC | 50807 |
| rs371113320 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130271428 | AAGAAATTATATATA[A/C]CTTTTACATAGTTTT | 50807 |
| rs371116332 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391703 | AAGGCACTCAGAGTA[C/T]GTCAGTGGCAATAGA | 50807 |
| rs371119942 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130145079 | ACTGCACCCAATGAA[C/T]GTGCTAGATAGTCAT | 50807 |
| rs371127154 | snp | C/T | | | missense | ASAP1 | GRCh38.p7 | 8:130127975 | CTGGGAGCCGCTGGA[C/T]ATCCTCAATAATGGC | 50807 |
| rs371127788 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130143652 | TAACAGAAAGTGGCT[-/G]GTTTAGCTAGGAAAA | 50807 |
| rs371128901 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130399814 | AGAGAAAGTCAGTGT[-/C]TTTTTTTTTTTTTTT | 50807 |
| rs371129336 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130328148 | CTACATGCATTTCTC[A/G]CCTATCATCATAACA | 50807 |
| rs371132799 | snp | G/T | | | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052718 | ACATGCAGCTTTTGT[G/T]TTTTTTTTTTGTTTT | 50807 |
| rs371132952 | in-del | -/GGT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130200730 | TTTCAACAATGAAGT[-/GGT]ATTATTTTTGTACGT | 50807 |
| rs371153344 | snp | A/G | 4.95946e-05 | 0.00497944 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130118217 | ATCTGCAGTTCGGAC[A/G]GCAAGGTGAAGGGCT | 50807 |
| rs371154312 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178152 | GAAAGATCAAAGGAA[A/T]TTATGAATTTAACTT | 50807 |
| rs371160274 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131105 | TAGGTTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 50807 |
| rs371168308 | snp | C/T | 6.59402e-05 | 0.00574158 | missense | ASAP1 | GRCh38.p7 | 8:130112103 | CCATACCTTTCCCGG[C/T]GTTCCTAGGAGGCAG | 50807 |
| rs371189969 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130056790 | TCCCTCTTGGCAGGA[C/T]GGGGCTCAGGCTGCC | 50807 |
| rs371194105 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353008 | TCCCTGGGCCTAGCA[C/T]ACTGCTGGGCACATA | 50807 |
| rs371216224 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130328748 | ACCTCACAGCCTCCC[A/G]AGTAGCTAGGAGTAC | 50807 |
| rs371226890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236528 | TTTTCCACAACCATC[A/G]CCAATATTGATTTTC | 50807 |
| rs371227571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064018 | GGTCAGGGAAGGCCA[C/T]TCTGATATGGCAAGA | 50807 |
| rs371235388 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130196028 | TTTACTAACTGATCA[G/T]ATCCCAAAGAAGGAA | 50807 |
| rs371239040 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130367878 | TGTATTTGAACCCAC[A/G]TAACAATGAGCTGTA | 50807 |
| rs371240376 | snp | A/C | 1.64741e-05 | 0.00286998 | missense | ASAP1 | GRCh38.p7 | 8:130137030 | CAACTTGGCTGGTTG[A/C]CTGTTAGACTGGAAA | 50807 |
| rs371241715 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130241076 | ACAGCAGAGTGTAAG[A/G]GCAGATGTTCTCAGA | 50807 |
| rs371252479 | snp | C/T | | | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444356 | TGGATGTTAATTCCA[C/T]CCTCATAGGTTTGAT | 50807 |
| rs371265015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240751 | TCTCTTTAACATTAC[A/G]TAACTAAGGATCAGG | 50807 |
| rs371276368 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130246236 | GAGTGAAGGGAGATG[A/G]GTGAAGTATGGGCCT | 50807 |
| rs371277729 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130115518 | AATGGCCCTGATACA[C/T]TGGATCATAAAACCA | 50807 |
| rs371291960 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130117878 | AGCCTGTAGGCCATA[C/T]CTGGTTCACTGTCTG | 50807 |
| rs371305665 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353604 | GCCAGGCGTGGTGGC[C/T]CATGCCTGTAATCCC | 50807 |
| rs371311323 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278539 | GCCAATAAGAAAACA[A/T]TCTTTGCAAAAGTCT | 50807 |
| rs371311643 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130249144 | CAGCCAGGTACTTCC[A/C]CAGCCTCTAGCAGTT | 50807 |
| rs371314071 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130276746 | CTCTCTCTCTCTCTC[-/T]CTCTCTCTCTCTCTC | 50807 |
| rs371314814 | snp | A/G | | | intron-variant, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130357904 | GGCGGCTCCCTGAGG[A/G]GGTGTGGCGCCCCCG | 50807 |
| rs371317749 | in-del | -/CA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130373019 | AGACACACATACACA[-/CA]GACACACACACACAT | 50807 |
| rs371322604 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216029 | GGAAAAAGGAAAGGA[A/T]AGGAAAAAGGAAAGG | 50807 |
| rs371330312 | in-del | -/GAGGACATTATGTTAAGTAAGGCAGT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130391148 | ATAAGGATGAACCTT[-/GAGGACATTATGTTAAGTAAGGCAGT]AACAAAAAGACAAAT | 50807 |
| rs371349911 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084168 | AAGACAGGACTGACC[A/G]TGCTGGCTCATCAAC | 50807 |
| rs371350837 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130315623 | GCTGTGCTCCCATGA[A/G]GTGTCTGGAGTGCCT | 50807 |
| rs371367579 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428736 | ATCATCACTACCAAC[A/G]TCACCACCATCAGCA | 50807 |
| rs371369694 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244932 | TGAGGCAGAGAGAAG[A/C]AGAACAGAAATAGGA | 50807 |
| rs371375198 | in-del | -/GAGA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130284911 | AGAGAAAGAGAGAGA[-/GAGA]CAGAGAGACATACAC | 50807 |
| rs371380356 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130156722 | CATACTTACTGTCCG[C/T]ATGATCTTAGTCAAA | 50807 |
| rs371383742 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130191401 | GATTTTACTCACACA[C/T]AAGTGTATTCAACTG | 50807 |
| rs371385253 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130385971 | CTTGTCCAATCAGAA[C/T]AGTCCATGGCCTTGT | 50807 |
| rs371395794 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130150122 | CCTCATATAATCTTT[A/G]TGTGTTAAATACTTT | 50807 |
| rs371400355 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130238568 | TTACTGAGCACTTAC[C/T]AGACATCAGGTATAA | 50807 |
| rs371407271 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130302650 | CAGCCAAGCCCTGGA[G/T]AGACACCAGCTGAGG | 50807 |
| rs371415484 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130113296 | TTCCTCCGACATCCA[G/T]ACTCTACCATGACTC | 50807 |
| rs371436020 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130344887 | CTAATAATGCAAAGT[A/G]TCATGAAATTATCCA | 50807 |
| rs371446645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151991 | TGTTGGGAGGATTAA[C/T]TGAAATAAAGTTTAT | 50807 |
| rs371455028 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130077064 | AAGGAAATGGAAGGG[A/C]ATGGGGGTGTTGGCG | 50807 |
| rs371464294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107957 | AGGCAGCCATGGTCT[C/G]GCTTGACACAGACTG | 50807 |
| rs371466599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092453 | GTAACACAGCAAGAC[A/G]CCATCTCTATAAAAA | 50807 |
| rs371467413 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130301958 | AGACTGTAACCTCCA[C/T]GATGGCAGGGGTGTC | 50807 |
| rs371469024 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130242284 | AAAAAAAAAAAAAAA[-/C]AACTTTTTTTTTTTT | 50807 |
| rs371475210 | in-del | -/AC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130188692 | GAGCCGAGATCMMCA[-/AC]CTGCATTCCAGCCTG | 50807 |
| rs371476155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438514 | GCTGTGCTAGGAAAT[A/G]GACTGGGGGCAGACT | 50807 |
| rs371478154 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130260687 | CAGATACTTGGTGGA[C/T]GAGCCTCAAAAGCAT | 50807 |
| rs371482375 | in-del | -/AAAGAAAAAAAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130283584 | AAGACTCCATCACAG[-/AAAGAAAAAAAA]AAAAAAAAAAAAAAA | 50807 |
| rs371491649 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430493 | GCTGACCCTCGGTCT[G/T]AGCAGTTGAAACGTC | 50807 |
| rs371508029 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130135253 | CCTAACACTTTGGGA[C/G]GTTGAGGTAGGAGGA | 50807 |
| rs371510882 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241765 | TTCAAATAGTTATTC[C/T]GTGAACTTTCTTTAA | 50807 |
| rs371512220 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130174921 | ATATCTGGGTGTTTC[C/T]GTGTTTTGTTTATTG | 50807 |
| rs371512778 | in-del | -/AT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130425335 | AGACTCCATCTCAAA[-/AT]ATATATATATATGTA | 50807 |
| rs371518001 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082352 | CTTCAAGGTAGGGCA[-/T]TTATTTTTTTTCTTA | 50807 |
| rs371519072 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130108937 | GGCGCCACTACGCCC[A/G]GCTCATTTTGTATTT | 50807 |
| rs371522597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073322 | TTGAACCTGGGAGGC[A/G]GAGGTTGCGGGGAGC | 50807 |
| rs371543733 | snp | C/T | 0.000116158 | 0.00762009 | utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130401952 | ATCTCATGTCTCAGC[C/T]GTCACATCAGAAAAC | 50807 |
| rs371549973 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130174570 | CAGAACCAACCATGC[A/C]ACTAGGTTCAGAACT | 50807 |
| rs371553753 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130058011 | TCCCTCGATGAATGT[A/G]AGCTCGTCATCGTTG | 50807 |
| rs371562394 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130374450 | CAAGGCAGGAGGATT[C/G]CTTGAGCCCAAAAGT | 50807 |
| rs371565205 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130221773 | CTCCATATCCTAAAG[C/T]AGGACAGGCCTAGGT | 50807 |
| rs371567152 | in-del | -/ACA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130232456 | AAAACTTAGAGAACA[-/ACA]CAGGAAAACTGAATG | 50807 |
| rs371569866 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130211960 | AGCCCCAGGAGGGTG[C/T]TGAGTGCTGCTCAGC | 50807 |
| rs371574685 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130251797 | TTTCAATTGCACTGA[C/T]AAGTTTAAAATTCCA | 50807 |
| rs371592077 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264667 | TTCAATTCACTTCAC[A/T]ATGTGCTAATAAATA | 50807 |
| rs371593615 | snp | A/T | | | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052692 | TAGACACTAACTCCA[A/T]GTAATTTTAGACATG | 50807 |
| rs371599666 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130283323 | CAGTGGTTCACGCCT[A/G]TAATCCCAGCACTTT | 50807 |
| rs371605788 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130289176 | GGGCGACAGAGCAAG[A/T]CTCCATCTCAAAACA | 50807 |
| rs371608694 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130302993 | AAATTTAAGTCACCA[C/T]GGGAAAAAAAAGAGT | 50807 |
| rs371610566 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130354602 | CCGTTTAGGGAAAAC[A/G]CTTATGCTCTCCTAG | 50807 |
| rs371611897 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130418377 | ACATGGTGAAACCTC[A/G]TCTCTACTAAAAATA | 50807 |
| rs371617321 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130390368 | ACAAGTCCCTTCCAG[C/T]CTAAACAATCTAGGA | 50807 |
| rs371620831 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130354849 | TTCGCCCCAAAAGGT[A/G]AAGCCCAGAAGTAAA | 50807 |
| rs371625409 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130245232 | CCAAAATTGAAAGTT[A/G]GTATGTTATCTGCAA | 50807 |
| rs371629515 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130138627 | GGATCACCTGAGGTC[A/G]GGAGTTCCAGACCCG | 50807 |
| rs371655182 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130422878 | CTATTATTCTTAACA[C/T]GGAATGATAAAGATG | 50807 |
| rs371665980 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130381096 | TTGCCATGTCGTCCA[A/G]GCTGGTCTTGAACTC | 50807 |
| rs371669129 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130422867 | ACTGCTGCCTTCTAT[C/T]ATTCTTAACATGGAA | 50807 |
| rs371689737 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133699 | CAAACAAAAAAAAAA[A/C]CAAAAAACTCCAACC | 50807 |
| rs371694422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297934 | AATTGGCCAGAGAGG[A/C]CATTGTCTGGCCCAA | 50807 |
| rs371695424 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130171085 | TAAAACTTCTCAGTA[C/T]AGAATTTTAAAAGTT | 50807 |
| rs371730109 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130057638 | TATTTTTAGTAGACA[C/T]GGGGTTTCACCATGC | 50807 |
| rs371737012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247810 | CTTTCCACTTAGCTT[C/T]AGGCACACCCTGGGA | 50807 |
| rs371739209 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054363 | GAGAATACTGCATTG[C/T]TAGGAACAGAGTCAA | 50807 |
| rs371742001 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130165848 | GATTAGTGTCACTAG[C/T]GCAGGGCTTCCCATG | 50807 |
| rs371744480 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130137659 | ACAATGACAATTACT[-/A]CCTGTGAGGCAATGC | 50807 |
| rs371751832 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129233 | AACTTCTTTCCTTTA[A/C/T]AAATTACCCAGTCTA | 50807 |
| rs371761909 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130188062 | AAGAGGAAAAAAAAA[-/A]TTAATCCTTTCAAGT | 50807 |
| rs371778904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062347 | TAAATGTCACAGGCT[A/G]TACTAGGGCTGTTTC | 50807 |
| rs371782956 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130087354 | GTGAAACCCCGTCTC[C/T]ATTAAAAATACAAAA | 50807 |
| rs371788003 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119801 | TCGTCATGAGCTTCA[G/T]TTTTTTTTTTTTAAT | 50807 |
| rs371807923 | in-del | -/TCT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130284840 | TCATTCCTTTTACAC[-/TCT]ACACACACACACACA | 50807 |
| rs371839198 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130418184 | GAGAATAGGAGCATA[A/G]GTCTTTCTTTAATGT | 50807 |
| rs371860558 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130211184 | ATTTTCTATAATGTG[C/G]AGGAGGGGGGAGTAA | 50807 |
| rs371863827 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130433992 | TCAAGAGTATGGGTA[C/T]TGAACACAGATCGCC | 50807 |
| rs371866696 | snp | C/T | 5.30227e-05 | 0.00514865 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060570 | GGGCCTGAACATTGT[C/T]CCACCCACCGTATTG | 50807 |
| rs371869785 | snp | A/G | 6.1393e-05 | 0.0055401 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130357983 | CGCGGCGGCAGCGGC[A/G]AGCGTGGACGGCGGG | 50807 |
| rs371885840 | in-del | -/AAAAAAAAAAG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130283605 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAG]AAGGCAGGATGCAGA | 50807 |
| rs371915173 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130313239 | AGATAATTTCTAAGC[A/C]ATTCTGGTGGGTCCC | 50807 |
| rs371931863 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130151492 | TAGACAGGATTTCTG[A/G]TATCAGATGGGTAGC | 50807 |
| rs371946602 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130350351 | CCCTGCATGGTTTCT[A/G]TCTCATCTTTGGGCC | 50807 |
| rs371950171 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092457 | CACAGCAAGACGCCA[A/T]CTCTATAAAAATTTA | 50807 |
| rs371950328 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130319232 | TTATGTTACTGTTGC[A/G]TTGGATCACATAGCC | 50807 |
| rs371953387 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353105 | ATGAATGTTCTATAC[-/T]ATTTCCCTCCCCTAT | 50807 |
| rs371958790 | in-del | -/AT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130261235 | GATGTATGTGTACAC[-/AT]GACATCATAGCCCCT | 50807 |
| rs371990350 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130381602 | GACGCCTGGCTTGGA[A/G]AATGCGTCCTCCAAG | 50807 |
| rs371996467 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130338998 | GCACTAATGAGCAGC[C/T]TATTCCCCACCTAAG | 50807 |
| rs371999286 | snp | A/C | | | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130053162 | AACGATGGAAGAGGG[A/C]TTTTCCTAAGGGTTG | 50807 |
| rs372013445 | snp | A/T | | | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082636 | AGCCTCCCAAGTAGC[A/T]AGGACTACATGCATG | 50807 |
| rs372013866 | in-del | -/AAATA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130362868 | AAATAAAATAAAATA[-/AAATA]GCCTATTTTCATGCA | 50807 |
| rs372023283 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130269178 | GGAGAATTAAGGCCA[A/G]CTGAAATTGGCCTTT | 50807 |
| rs372029119 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130195403 | AAAAAAAAAAAAAAA[-/G]ATGAGCTGGGCATGA | 50807 |
| rs372040689 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130183312 | ACAATGGAACAATGC[C/T]TTCAACATTTAGAGA | 50807 |
| rs372041832 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388866 | AATATAGTAGCACAC[A/G]GAGTAAAAGTGAAAA | 50807 |
| rs372043775 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130396538 | TTTTGAAAGGATTTT[C/T]GCAGCAGAACTTGAA | 50807 |
| rs372051048 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130228429 | CACAATGGGCCAGGA[A/G]CAGTGGCTTACGCTG | 50807 |
| rs372057464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368785 | AGATGCGGGAGAGTC[A/G]TGGTGACCTCATTTG | 50807 |
| rs372066319 | snp | A/G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070186 | GGACTACAGGCGCCC[A/G/T]TCACCATGCCCGGCT | 50807 |
| rs372067178 | snp | A/C | | | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445352 | TTCATAGCCCTTGTC[A/C]CTGTTTAATGTAGCC | 50807 |
| rs372070704 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078348 | CGCCCCGGATGGAGT[A/G/T]CAGAGGTGCGATCAT | 50807 |
| rs372081525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205890 | CAAGGATTTTGGACC[C/T]GAATGAGATATATAC | 50807 |
| rs372082746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226734 | AGTTCCACAGGGCTA[C/T]TACTCAGCATTTAAA | 50807 |
| rs372085992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228164 | AGAAACGAAGGACTT[G/T]TTAAGAAATACTCAG | 50807 |
| rs372090741 | snp | A/G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130188756 | AAAAAGAAAAGAAAA[A/G/T]AAAATTGAATTTAGG | 50807 |
| rs372093079 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130247432 | AGCCAGGATTCCAAA[G/T]CAGGTCTTCCTGATC | 50807 |
| rs372095195 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130161101 | AAAATGGTTGACAAA[C/T]CTCAAATGTGTATGT | 50807 |
| rs372096038 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272512 | GGGTATTTCTCCAAA[C/T]GAAAGGAAATCAGTA | 50807 |
| rs372111620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130216587 | TGCTGGTTCTTCATC[C/T]CTCTGACCTCATCAT | 50807 |
| rs372113887 | in-del | -/TG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130180413 | ATGGTTAAAAAAACA[-/TG]CTCTAAACATACACC | 50807 |
| rs372115031 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370690 | TAAACAAAATGTGGT[A/C]TATCCATACAATGGA | 50807 |
| rs372116992 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130363360 | GCGAGACTGCATCTC[A/T]TTTTTTTTAATAAAA | 50807 |
| rs372125458 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130058194 | CGCTGAGCCTTGATT[G/T]CCTCACCCTTGAAGG | 50807 |
| rs372141914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381099 | CCATGTCGTCCAGGC[C/T]GGTCTTGAACTCCGG | 50807 |
| rs372144596 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130396800 | ATGATAATGACAGGG[C/T]GTCTGCTTGACATTT | 50807 |
| rs372154207 | in-del | -/AAAGGGGGA | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432171 | GGAGGGGAGGAGGGG[-/AAAGGGGGA]GAAGGGAGAGAGGGA | 50807 |
| rs372164524 | in-del | -/TT | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090143 | CTGCTAGTCTTGCTC[-/TT]GAGTGATGTGAAAAT | 50807 |
| rs372166121 | snp | C/T | 1.65198e-05 | 0.00287395 | missense | ASAP1 | GRCh38.p7 | 8:130214650 | CGACTTAAAAAATTA[C/T]TCCCAAACTTATCAA | 50807 |
| rs372184982 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130133566 | GAGGCTGAGGCAGGA[A/G]AATGGCGTGAACCCG | 50807 |
| rs372191659 | in-del | -/G | | | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052735 | TTTTTTTTTGTTTTT[-/G]TTTTTTTTTTTTTTT | 50807 |
| rs372195634 | in-del | -/GGGGAGGGGGG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130071001 | AGAGAGAGAGAGAGA[-/GGGGAGGGGGG]GAGAGAGAGAGAGAG | 50807 |
| rs372200439 | snp | A/C | 0.00318978 | 0.0398085 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052687 | AAGAATAGACACTAA[A/C]TCCATGTAATTTTAG | 50807 |
| rs372205776 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359232 | TTTTTTAACTTGCAG[A/G/T]AAAGCCGAGGGTCAG | 50807 |
| rs372219824 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150914 | CATGGTAACTGACTA[A/G]AAACTCACCATCTAT | 50807 |
| rs372225223 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130228017 | GGAAATGCAGTATTG[C/T]TAGACACTATCAACT | 50807 |
| rs372244635 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130215165 | TCGGCCTCCAAAAGT[G/T]CTGGGATTACAGGTG | 50807 |
| rs372275969 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130268537 | CACACACACACACAA[A/C]TGTGTAACTATAGAG | 50807 |
| rs372282566 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130344364 | TTCAGACGAGAAAAC[A/G]TATTATGGTTCAGGT | 50807 |
| rs372283206 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216476 | TGCATAAACAATAAC[C/T]CCCACTGCCTTGAAA | 50807 |
| rs372288658 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180733 | TTCTAGGCAAATGGT[A/G]GAAAAGTCCATTCTT | 50807 |
| rs372313527 | in-del | -/AAAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130150028 | TTCAGTATTGTCAGC[-/AAAA]AACATCCAATAAACT | 50807 |
| rs372321835 | snp | C/T | 0.030278 | 0.119257 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334238 | ACACATATAAAGAGG[C/T]ACTCTTTGATTTTCA | 50807 |
| rs372325689 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130432993 | TCGCTCACTCGCCCC[C/T]GCAGTATGCTGCTCA | 50807 |
| rs372328287 | in-del | AA/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130144756 | AGTAATTCATTCTAG[AA/G]GTAGATGGCTGAATT | 50807 |
| rs372329179 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130329611 | CTGTGCAAATATGTT[A/C]CTGGCTCATAATAAA | 50807 |
| rs372329385 | in-del | -/TC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130097768 | TCTCCTGAGACTCTC[-/TC]CCAGGAACTGACATT | 50807 |
| rs372329680 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130412531 | TCCTGTACAGCCTGC[A/G]GAGCCATGAGCCAAT | 50807 |
| rs372340089 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130281792 | GTAATGGAGGCTGGG[C/G]GCGGTGGCTCACGCC | 50807 |
| rs372370074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406708 | GGATGATCTCGAACT[C/T]CTGACCTCAGGTGAT | 50807 |
| rs372372205 | in-del | -/TGTTTTTGTTTT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130340971 | TTTTGTTTTTGTTTT[-/TGTTTTTGTTTT]GTCGCTGGGGGGCAG | 50807 |
| rs372376137 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130138751 | TGAGGCAGGAGAATC[A/G]CTTGAACTTGGGAGG | 50807 |
| rs372376151 | in-del | -/T/TTT | 0.311859 | 0.242226 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143411 | TGTGTGAGATGTCTG[-/T/TTT]TTTTTTTTTTTTTTG | 50807 |
| rs372396833 | in-del | -/AAAGAAAAAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130283584 | AAGACTCCATCACAG[-/AAAGAAAAAA]AAAAAAAAAAAAAAA | 50807 |
| rs372405849 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130065098 | GTTACCCGGCTGGTC[C/T]CCACTCCTGGGCTCA | 50807 |
| rs372407691 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130097162 | AAAAAAAAAAAAAAA[A/G]TCCTTGAAAACTGTA | 50807 |
| rs372412532 | in-del | -/TGTATGTATGTATGTATGT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130107517 | TTTTTTTTTAAAAAA[-/TGTATGTATGTATGTATGT]ATGTATGTATGTATG | 50807 |
| rs372413914 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130063785 | GGGTTACCATTCCAC[C/T]CCTATTTGCTGGGCA | 50807 |
| rs372417489 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130130634 | AGTTTTATAAGATAA[A/C]AAATAACTTGGCACT | 50807 |
| rs372421444 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130156279 | GTATAAGCATTTCAA[C/T]TTTTTACTCTTCCAC | 50807 |
| rs372424201 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130392453 | GATAAATAACTAACA[A/G]TAACAATTAGTATTT | 50807 |
| rs372425500 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130199654 | CATCAATAAAGTGTG[A/T]GGTCTCTAAAAAGAC | 50807 |
| rs372432020 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130237280 | AAGACAGTACAAGAC[A/G]CTGAAGAAATCTTAA | 50807 |
| rs372438826 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130163011 | ACATTTGTTAAGTTT[C/T]CAAATGGGCCTAACA | 50807 |
| rs372442132 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130300147 | ACACACACACACACA[C/G]ACACACAGAGAGAGA | 50807 |
| rs372450484 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258905 | TGTTTCTTATGCCTT[C/T]CCTACTCCTCTCCTC | 50807 |
| rs372455375 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093616 | CGGTTGCAATGAGCT[A/G]AGATCATGCCACTGC | 50807 |
| rs372460445 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130437414 | GCTTTTCTTACATTA[C/T]CTCAGTTAAGTCAGT | 50807 |
| rs372471481 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130329541 | AGTGGCATGGGTGGG[C/T]GGCTATACAACTCGC | 50807 |
| rs372476705 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130215112 | TCACCAAGTTGGTGA[C/G]GCTGGTCTCAAACTC | 50807 |
| rs372478259 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130385399 | GAATTAAGAGCCAAC[C/G]GTGGGGCACCTTAGA | 50807 |
| rs372481405 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130251106 | ATGTTTTTTGGAACA[C/T]CAATATAGAACACTA | 50807 |
| rs372481861 | in-del | -/TT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130403571 | TTTTTTTTTTTTTTT[-/TT]GTGAGACAGTTTCAC | 50807 |
| rs372489595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206441 | TATTTGAGGGGAAAG[A/G]AAAGAAGAAAAATAA | 50807 |
| rs372508034 | snp | C/G | 7.4912e-05 | 0.00611967 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236916 | TCATTTTTAGTAAGT[C/G]CTTACCTTGACCAGA | 50807 |
| rs372526703 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130344643 | TTGGGAGGCTGAAGC[A/G]AGATCACTTGAGCCC | 50807 |
| rs372562245 | snp | A/C | 1.65195e-05 | 0.00287393 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152848 | TATAGTAACTGATTC[A/C]CTCTGGGACATGCGA | 50807 |
| rs372569409 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130317884 | GGACCCTATAATCCT[A/G]AGGAGGAGGGAGTGG | 50807 |
| rs372595665 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130419461 | ATGTTATAAGAAAGA[C/T]GTGAAGCTAAAAACG | 50807 |
| rs372607787 | in-del | -/AAAG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130180023 | GAGAGAGAGAGAAAG[-/AAAG]GAGAGGGAGGGAAGG | 50807 |
| rs372614462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227814 | TTTAAGTTCAGATAA[C/T]GTGTGTCGTCGTTCT | 50807 |
| rs372616096 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130372973 | ATACACACACAGACA[C/T]ACACACATACGCACA | 50807 |
| rs372633636 | snp | A/G | 1.648e-05 | 0.0028705 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130115709 | GTGGACGTGTGGATT[A/G]AACTTTCCAGATTTA | 50807 |
| rs372635460 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130233632 | CGCTACCTCAGATCC[C/T]TCTTCCTATTTCACC | 50807 |
| rs372640637 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130094655 | AGTCACAAGCCATGA[A/G]GGGCAGAGCTGGGAT | 50807 |
| rs372646764 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130126748 | CGTGTGTCACTATCA[C/T]ACATGTACACAATAA | 50807 |
| rs372653731 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130124737 | ACATACATGCAACCA[A/T]GTCTTTGAGGGAAAA | 50807 |
| rs372655178 | in-del | AA/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130267134 | CAAACAAAAAAAAAA[AA/C]AAAACAAAAAACAAA | 50807 |
| rs372655442 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130108379 | AACGCTTAAAAGGTT[A/C]GTTCTTTTAAGCATG | 50807 |
| rs372667545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339331 | CGCTGGAAACTTTCA[C/T]ACCTGTTTAAAGACC | 50807 |
| rs372670447 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130148778 | CAAACAATTCAAAAC[C/T]ATAGAAATGATAATA | 50807 |
| rs372681200 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130404252 | AGATGCCAACAGCAA[C/T]TGAATCTTCCTGAGC | 50807 |
| rs372690340 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130087093 | GGGGCTAATCATCAG[C/T]ATAGAAAGTGTGATC | 50807 |
| rs372696638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130346984 | AGACAATTTTATTTC[A/G]TATGTAACTGGGCAG | 50807 |
| rs372699093 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130870 | GCAACATAGATCTCA[A/T]TTTAAAAAAAAAAGC | 50807 |
| rs372699806 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130205518 | TCAAATAATCAGTTA[G/T]GGTACAGATATACAA | 50807 |
| rs372703291 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130305960 | TCACTTCTTCCCCCA[A/G]ACAATATTCACTCAA | 50807 |
| rs372703669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340903 | ATCATTGCGATGAAT[A/G]ACAAAATCTTTCCAA | 50807 |
| rs372707721 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150208 | TGCCACAGTCCATTA[C/T]CTTAGCCACTAAACA | 50807 |
| rs372721566 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130289754 | TAGCTGGGGCTGGCT[-/G]GTTTTAGAATTCATA | 50807 |
| rs372728574 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130194565 | ATTAGCAGTCCCCAA[A/C]CTTTCTGGCACCAGA | 50807 |
| rs372729816 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130320229 | AATATCAATGAGCAT[A/G]TATGTCATGTGCCTC | 50807 |
| rs372732881 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130177640 | AGGTGAAAACTTTCT[A/G]CTTCAATATATTATT | 50807 |
| rs372757390 | in-del | -/AGG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130351595 | GTGTTTAGTCATGGC[-/AGG]AGGAGAAGTGGGAGC | 50807 |
| rs372767377 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084137 | GCACAGAGCAGTCAA[C/T]AGTCCCTGCTAGCGA | 50807 |
| rs372781541 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130063333 | CAGGTATGTACCACC[A/G]CACTCAGCTAATTTT | 50807 |
| rs372798999 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130284191 | GGGGGCCCTAAAGAA[C/T]AAATCCCTTTTAAAA | 50807 |
| rs372800715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110901 | AACCTGTGGGAGCAC[A/G]AGCTGAGCACACAGG | 50807 |
| rs372806853 | in-del | -/TTTC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130403555 | TCTTTTTCTTTTTCT[-/TTTC]TTTTTTTTTTTTTTT | 50807 |
| rs372809847 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130223082 | TAAGAGGTAAAGGTG[C/T]CATAATTAATATAAA | 50807 |
| rs372810166 | in-del | -/TG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130175217 | GTTTTTCTGGCCATT[-/TG]TGTGTGTGTGTGTAC | 50807 |
| rs372813588 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130165870 | CTTCCCATGTTTTAT[A/G]GGAGTTGTTTTGTTT | 50807 |
| rs372828103 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130168455 | TTCAAGACTAGTCTG[G/T]GCAACACAGTGAAAC | 50807 |
| rs372847158 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130256976 | AGCTGGAGTGCTAAA[C/G]GTGGTAAAGAAGCAT | 50807 |
| rs372847595 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130254422 | GGTACTAATTCAAAG[C/T]AAGACTTGCATAAAT | 50807 |
| rs372851250 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059017 | GAAATGAAAATTTTG[-/C]ATCAGTGGTGCTTGG | 50807 |
| rs372868568 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189298 | TACCTAATAACCAAT[C/T]CCTCTTTATTCCCTC | 50807 |
| rs372880992 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130212254 | CCCTCACCAGGAATG[C/T]CACCACCACTTTCAA | 50807 |
| rs372889196 | snp | G/T | 1.65756e-05 | 0.00287881 | missense | ASAP1 | GRCh38.p7 | 8:130060616 | GGTACGGGCGTCTCT[G/T]GCAGAGTAGGCGTGA | 50807 |
| rs372905924 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130177038 | TCACTGTCCAGCCCC[A/G]TTATGATTAATAATG | 50807 |
| rs372915930 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130217432 | TCTACTGCAGTATTT[C/T]CTACCACATCCTATA | 50807 |
| rs372926643 | in-del | -/AAGAAAAGAAAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130197455 | TGTCTCAAAAGAAAA[-/AAGAAAAGAAAA]GAACTGACACCAATG | 50807 |
| rs372932730 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070197 | GCCCGTCACCATGCC[C/T]GGCTAATTTTTTCTA | 50807 |
| rs372935524 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366821 | CCTGGTATATAGTAA[A/G]TGATCAATAAACATT | 50807 |
| rs372945568 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130220491 | TTAGAATATGCCACC[C/T]CAAAACAAGCCACTT | 50807 |
| rs372954793 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130208134 | ATTGTAAAACTAGTA[A/G]AGAGGTCCCTTGTAC | 50807 |
| rs372961113 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130133787 | CTCTGTTCACCCCAG[G/T]GAAAGGCACATGGCA | 50807 |
| rs372967211 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216008 | AGGAAAGGAAAGGAA[A/T]GGAAAGGAAAAAGGA | 50807 |
| rs372969751 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130439995 | CCCACAACAACGCCA[C/G]CATACACCCAGCTGT | 50807 |
| rs372971749 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130441454 | AGATACAGCAGTGGT[-/T]GGGTGAAAAAACGGC | 50807 |
| rs372979570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060436 | CCACAGGCTCTAATC[C/T]ACCATCATGCTTGAA | 50807 |
| rs372993351 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130389637 | CTGGTACCAGCCAGA[A/C]CTACCTAAGCTGGAA | 50807 |
| rs373002422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419161 | CTTCAGTCAAACAGA[C/T]GGTCCAAGGACTCCC | 50807 |
| rs373002977 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130371370 | ACTCTCTGTACAAAT[G/T]GTACTCTGCTGATGT | 50807 |
| rs373008215 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130351806 | CCCCACCTCCGACAC[C/T]GGGGACTATGTTTCA | 50807 |
| rs373010313 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130403829 | AAAGTGCTGGGATTA[C/T]AGGTGTGAGCCTCTG | 50807 |
| rs373013450 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130434357 | AAAAAAAAAATCTTG[C/T]CACTTACTAACTATA | 50807 |
| rs373015939 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130260314 | CTACTAGACCATAAA[A/T]GAGCTCTGTGCCATT | 50807 |
| rs373025408 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130275401 | GGCAGCAGCACTTAC[A/G]TACTTTCAGATGGAT | 50807 |
| rs373027408 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130116702 | ACACTGGGTAGCTTT[C/T]AGTCTCTTTGCTATG | 50807 |
| rs373031430 | in-del | -/TT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130363636 | TCTGAATTCATTCAT[-/TT]ATAACAGTCCTGAGA | 50807 |
| rs373039821 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130346479 | GGATGAGTCTGAGTA[C/G]AAAGAGCATAAATTG | 50807 |
| rs373042938 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130294185 | AACCAAAATGAACTA[C/T]AGCCTTTCAACCACT | 50807 |
| rs373046859 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130213661 | TAACTTGGAAAAGCA[C/T]GATATAAATAGTTTT | 50807 |
| rs373047080 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130234683 | AGGGGGAACATTTGG[A/G]AAAGAGTCACATGGA | 50807 |
| rs373048576 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130326722 | TTAAGACAGCCAGAC[A/G]GCAAATGAGCAGAAA | 50807 |
| rs373059051 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130245570 | AAACACCACCAAGCT[A/G]TCAACTTCCCAAGCC | 50807 |
| rs373062629 | snp | A/G | 1.81355e-05 | 0.00301122 | missense | ASAP1 | GRCh38.p7 | 8:130061043 | TGGCTTTGTCTAGGG[A/G]GAGATGATCTGTTTT | 50807 |
| rs373065648 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130287982 | TCTAGTCACCTCCAC[A/G]CACAGTCAACCAAGC | 50807 |
| rs373067358 | snp | C/G | 3.29886e-05 | 0.00406118 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152831 | AGTCAAACACAACTA[C/G]ATATAGTAACTGATT | 50807 |
| rs373076566 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130130754 | GATCTGCCTAAGGTT[-/A]AAAAAGCCACTAACC | 50807 |
| rs373099060 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130312629 | AGGTGGGTACTATTA[A/T]AATTTCTATTTATAG | 50807 |
| rs373107534 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130408328 | AGTACCCTTCCCAAC[A/G]TGAGTGGGCATCATC | 50807 |
| rs373120415 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130212503 | CAACGGGTTCAGAGA[C/T]AGAATGTTTGGGTTC | 50807 |
| rs373135007 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130366280 | TAAAGTTTGGCACAC[C/T]ATCACTTAACTGACA | 50807 |
| rs373150711 | in-del | -/TCTC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130170749 | CTCTCTCTCTCTCTC[-/TCTC]GGCAGGGTCTCACTC | 50807 |
| rs373154278 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130299061 | CTAAGAGGACTGTGG[A/G]AAGTGGGTAAAGAAG | 50807 |
| rs373154942 | snp | C/G | 3.29995e-05 | 0.00406185 | missense | ASAP1 | GRCh38.p7 | 8:130116927 | AGCTTCAAACACTCA[C/G]GTTTACTGTACATAC | 50807 |
| rs373157209 | in-del | -/GAAAAATGAAGGGAGGGAGG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130396396 | ATGAAGGGAGGGAGG[-/GAAAAATGAAGGGAGGGAGG]AAGACAAGACCAGCA | 50807 |
| rs373163371 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130309551 | AGCAGTGAGGCAAGA[A/C]AGAGGCGTGACCAGG | 50807 |
| rs373163421 | in-del | -/GCCTGCACACAAAAGC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130275469 | CTGAGGCGTCCCAGC[-/GCCTGCACACAAAAGC]TCTCCTCCTGGCTAG | 50807 |
| rs373177921 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130283317 | GGGTACAGTGGTTCA[-/A]CGCCTGTAATCCCAG | 50807 |
| rs373179823 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130154190 | TTTAGGGGTCTTCCA[A/G]AGACAGAATGGTGCC | 50807 |
| rs373195103 | in-del | -/CAT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130267057 | AAAAAAAGTAGTCAT[-/CAT]TAAGAGGACAAAGAA | 50807 |
| rs373209987 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364635 | CTCATTACAAGCCCA[A/G]TTCAAATGCAAGCTT | 50807 |
| rs373211583 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130163347 | AAGACGTTCCTTATA[A/T]ATTTATTACTAGCTT | 50807 |
| rs373215394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434549 | ATAATAGCTATCACT[A/G]TTGATTCCAAGTCCA | 50807 |
| rs373219886 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130318973 | ATTAAAAGCTAGGAG[G/T]CTGCTTTATCTGAGT | 50807 |
| rs373234414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234812 | TCATCACATTACAGA[G/T]AACTGACCATTCTTC | 50807 |
| rs373235629 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130245768 | AGAATTAAAGCTGTA[C/G]AGAAGAAAACTGGAA | 50807 |
| rs373243909 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084759 | CCCACTTCCAATAAG[C/T]AGATATGTAATAAAA | 50807 |
| rs373245183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130265639 | CAGCACTTTGGAAGA[C/T]TGAGGTGGGCAGACT | 50807 |
| rs373270716 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216020 | GAAAGGAAAGGAAAA[A/T]GGAAAGGAAAGGAAA | 50807 |
| rs373274115 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130292237 | ATGAAGGACCAACAC[A/G]TGCCAGACAATGGGG | 50807 |
| rs373295136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059860 | AGATGGGAGGAGTGC[C/T]TGAGCCCATGAGTTC | 50807 |
| rs373295293 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130089495 | AGGGGAACATAAGAG[C/T]GTTGGAAAGGTGCGT | 50807 |
| rs373302489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275103 | ATGAATAATCCTAAC[C/T]ATCTCTAGATCTTAG | 50807 |
| rs373306138 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130355606 | CAACAAGATTTTGTG[C/G]TATGCCCCCAAATTT | 50807 |
| rs373324535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130172828 | GATAAAAATGAAAAT[C/T]CCTGCCAATTACAAG | 50807 |
| rs373331805 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130440513 | CTCTGTCAAAAAAAA[A/G]AAAAAAAGAGTCAAT | 50807 |
| rs373341512 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130201029 | GTGTCAATATCACCT[A/G]GAAACTTGTTGGTTA | 50807 |
| rs373344494 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130207255 | TGTTATGTCTGGAGT[C/T]GGCTTTGATTAGGAA | 50807 |
| rs373346393 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296776 | AAAGAAAAAAAAAAA[-/A]TTAAGCTACTTTCCA | 50807 |
| rs373350265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247961 | CAACCACAACACCAC[A/G]TGGAGATGCACAGGC | 50807 |
| rs373355613 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130300543 | AGTTTCTGATTTAAT[A/T]GTCTAGGATGTGGCC | 50807 |
| rs373384942 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130342434 | ACCCAGCACATTCTA[C/T]CAAGAGTGGACCTTG | 50807 |
| rs373391488 | in-del | AATTTTA/T | | | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082681 | GTTAATTTTAATTTT[AATTTTA/T]ATTTTTTTTGTAGAG | 50807 |
| rs373391941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055924 | CTTTGTGAATTTCAC[A/G]TCACAGTTAGCATGT | 50807 |
| rs373392364 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323043 | TGCAATGAAATTATC[A/G]TGCATCTGCTGGAGT | 50807 |
| rs373404280 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130218792 | AAGTATAGGCTAGGT[A/C]ATGGGTCCTGTATGT | 50807 |
| rs373406517 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130404830 | TAGAAGTGACAGTGT[A/G]CTGTTCCCAAGTCTA | 50807 |
| rs373418546 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130304515 | AAAGCCAACCTTCAC[A/G]CATCTGCACTCCCTG | 50807 |
| rs373427521 | in-del | -/TCT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130087888 | TGACAGCTCACATCT[-/TCT]CTGAAGACTAGAAAA | 50807 |
| rs373431556 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130055089 | TTATACAGTTTACAA[C/T]CTTCATTTTACAGAT | 50807 |
| rs373441482 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334409 | CTCCCAAAAGTTCTA[C/G/T]TTGTGTTTCACATAG | 50807 |
| rs373456352 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130167069 | AGAATTTTGGGAGGC[C/T]GAGGTGGGAGAATTG | 50807 |
| rs373512822 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400021 | GACAGAGTTTCTCCA[G/T]GTTGCTTAGGCTGGT | 50807 |
| rs373515324 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392910 | CATTTCCCATCAGGC[C/T]CCACCTTCAAAATTG | 50807 |
| rs373516805 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130415741 | TGCAGTGAGCCAAGA[A/T]CACACTCCAGCCTGG | 50807 |
| rs373529897 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130190564 | ACTCTGTCGCCCAGG[C/G]TGGAGTGCAGTGGCA | 50807 |
| rs373540496 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130128077 | CTTTGCTATTTGTCA[A/G]TACTGATATCCATCT | 50807 |
| rs373542586 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130408851 | AGAACTCAAACTTGA[A/C]AGAGCTCGATTTCAA | 50807 |
| rs373547373 | snp | A/T | 6.62306e-05 | 0.00575421 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130127931 | GGGACAAAAACCTGA[A/T]GAGCCACAATCGCAG | 50807 |
| rs373556518 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130324008 | TCAGTTATCACCCTA[C/T]TCCTCCAGGGGCTCA | 50807 |
| rs373566250 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130304793 | GCAGCCAGAGGGATC[C/T]GTTTTAAGTGTAAAT | 50807 |
| rs373571176 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130060269 | TCACTGTATTTAATC[A/G]TCTGTGAGCTCAAAT | 50807 |
| rs373579964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406543 | CTGGAGTGCAGTGGC[A/G]CGATCTCTGCTCACT | 50807 |
| rs373581350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292030 | CTAAAAGCTGCTGGA[C/G]AGGAGCTGAACTGAG | 50807 |
| rs373589102 | in-del | -/ACACAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130300114 | AAGTAAAAGAAAAAT[-/ACACAC]ACACACACACACACA | 50807 |
| rs373598811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411796 | AGCAAGGCCAGCACC[A/G]TAGGCATGTTTTATG | 50807 |
| rs373601626 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130279556 | AACAAGCGCAGGGTT[C/T]AAATTCCAGCTTGGG | 50807 |
| rs373604257 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130431641 | AGTCAGGCACCTCTT[A/C]CTAAGTGCCCATTAC | 50807 |
| rs373605337 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130219129 | TACCGCTATATATCC[A/G]TGACTACTTACAATA | 50807 |
| rs373606923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432831 | CCAGAGCTCTGTCAG[C/T]TGCCCACACCTAACC | 50807 |
| rs373611327 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130380886 | CTACACCTGGCTACT[A/T]TATTTATTTATTTAT | 50807 |
| rs373614267 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130129277 | TAGCAGTGTGAGAAC[A/G]GGCTAATAGAATGAT | 50807 |
| rs373614908 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130340394 | CACTTCAGAAATAAA[C/T]ACAAATTAACTCACC | 50807 |
| rs373622049 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314627 | GGCAGGCTTTCCAAA[C/T]CACAGCATGCTGCGC | 50807 |
| rs373622810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165874 | CCATGTTTTATGGGA[A/G]TTGTTTTGTTTTAGA | 50807 |
| rs373645293 | snp | C/T | 0.000116919 | 0.00764499 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401988 | GGATAGGGGGCAGGA[C/T]AAAAAGGGGACAAGA | 50807 |
| rs373647034 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130327777 | GGAGTGACTCTGACA[A/G]TTACAGGACTTCCTT | 50807 |
| rs373656601 | snp | A/G | 3.29957e-05 | 0.00406162 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057906 | GTGGTGCCTGCCCAG[A/G]CATGCTGTATGAATG | 50807 |
| rs373660266 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428502 | TCATCACCATCACCA[C/T]CACCACCATCAGCAG | 50807 |
| rs373660815 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347441 | CCTTATATTCCTACT[C/G]ATTCTCCCAACAGCT | 50807 |
| rs373665471 | in-del | -/CT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130399586 | CTCAGGTTGGCCTCT[-/CT]GCCTCCAGCCTCTCA | 50807 |
| rs373667541 | in-del | -/ACACAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130420236 | TGGCCATAATGAAAT[-/ACACAC]ACACACACACACACA | 50807 |
| rs373673680 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130134890 | TGTTCCCTATTTGTT[C/G]TGAGACTTAACCATG | 50807 |
| rs373683173 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130174430 | TAAATTACTGTAACA[C/T]AACAAGATCTTCAAA | 50807 |
| rs373686845 | snp | A/G | 0.00208218 | 0.0321987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169118 | TAAAAAAAAAAGAGT[A/G]TTTGTTTCCTTATGT | 50807 |
| rs373710288 | in-del | -/TAAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130090267 | TCAAACCTTAAGAAA[-/TAAA]GCCACTTAAACAAGA | 50807 |
| rs373711709 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130265860 | AGTCTCAAGCCTGGG[A/C]GAAAGTGAAACTGTC | 50807 |
| rs373727139 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130232166 | GCCTTGGAAATCACA[C/T]GGCATCACCTCTACT | 50807 |
| rs373736043 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130323596 | AAACCGTTTTGACTC[C/G]TCCTACCTCCCTCTA | 50807 |
| rs373739033 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130242079 | CCATCTAGGAGTGCT[A/C]TGAGCATTCAATACA | 50807 |
| rs373759936 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130288982 | ACGAGGTCGGGAGAC[C/T]GAGACCACCCTGGCT | 50807 |
| rs373762107 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130243742 | TACCTTCTCTCTTTT[G/T]TTCTGCCATTCAGGT | 50807 |
| rs373774615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126453 | TGGATTCTATAGCCA[C/T]CATTAACCTCCAAGT | 50807 |
| rs373781366 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130188532 | GGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 50807 |
| rs373781606 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393075 | AACTTATCTTCTTTT[C/T]AATGGCTGCATTATT | 50807 |
| rs373791824 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388371 | GGTGGCTGTAAGCAG[A/G]GGTGCAGCATGAGCT | 50807 |
| rs373805063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177132 | TGTCCCAGAACTGGG[C/T]ACAGTAGCTGATCTT | 50807 |
| rs373813056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342314 | CCCTCAGTTTTCTCA[C/T]CTGTAAAATGAAGTT | 50807 |
| rs373830152 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130179983 | AGAGAAAGAGAAAGA[G/T]AATGAGAGAGAGAGA | 50807 |
| rs373835779 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130366521 | TCTCTGACAACATTT[C/T]CCCCTGGGTACAGAG | 50807 |
| rs373841964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295081 | CCAGCCTGGGCAATA[C/T]AGCGCAACCCAGTCT | 50807 |
| rs373844121 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130268262 | AGACTGAGGCAGGTA[C/G]AGCACTTGAGCCCAG | 50807 |
| rs373848285 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130311654 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAAG | 50807 |
| rs373862065 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227187 | CCTCATTGGGTTCTT[G/T]TTCTGCTAATGAGGT | 50807 |
| rs373862474 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130115946 | AGAGCCTTCTTTATT[C/T]TGATGACTTGTCTCC | 50807 |
| rs373865575 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130337415 | CTTTTTGCTTTTTTA[G/T]AAGTCTCCAGTGTAA | 50807 |
| rs373869640 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130279262 | AAATTACTCTTTCCT[C/T]ATGTAAGGTCTGAAT | 50807 |
| rs373874069 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130247435 | CAGGATTCCAAAGCA[A/G]GTCTTCCTGATCTCA | 50807 |
| rs373882976 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130196240 | CCAGCTACTCAGGAG[A/G]CTGAAGCAGGAGAAT | 50807 |
| rs373890283 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130226256 | CCTGTCCTGTGACCC[A/G]GAAAATAATTTGTTT | 50807 |
| rs373906758 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130173921 | CTACTAAAAAAAAAA[A/G]AAAAAAAAAATTAGC | 50807 |
| rs373908570 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ASAP1 | GRCh38.p7 | 8:130051687 | AAGCTGAGGGGCTCA[C/T]GCTTCTCCTGGGCTT | 50807 |
| rs373912003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258536 | AGTGGAAACAACAGA[A/G]ACGAGAGCCCAGATA | 50807 |
| rs373918669 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261073 | TCAATTACTAGTCAC[A/T]GACCCCACTGTGAGG | 50807 |
| rs373921020 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428615 | CTATCACCATCATCA[C/T]CACCACCACCACCAC | 50807 |
| rs373922463 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130225077 | TTTTTGCATTTTATT[A/G]TCCATTAACATTTCC | 50807 |
| rs373940667 | in-del | -/TTTTTGTTTTTG | 0.0432578 | 0.140562 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340949 | AAAATACTAGGTTTT[-/TTTTTGTTTTTG]TTTTTGTTTTTGTTT | 50807 |
| rs373958338 | in-del | -/AAAAAT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130147073 | TCTACTAAAAATACT[-/AAAAAT]TAGCTGGCTGTGGTG | 50807 |
| rs373963043 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130416578 | ATCTTCTGGGGGCTG[C/G]TGTAAACTAGATTTC | 50807 |
| rs373969153 | in-del | -/AA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216016 | AAAGGAAAGGAAAGG[-/AA]AAAGGAAAGGAAAGG | 50807 |
| rs373978183 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078562 | AAGTGCTGGGATTAC[A/G]GGTGAGCCACTGTGT | 50807 |
| rs373981458 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130141558 | TCCTTCTCACTAAGG[A/T]CACACACATTTTTCT | 50807 |
| rs373984764 | snp | A/T | | | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082370 | ATTTTTTTTCTTATT[A/T]TTTATTTATTTATTT | 50807 |
| rs373988882 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112811 | ACACAATAATTACTT[A/T]CAGATCTGTAAATAC | 50807 |
| rs374029385 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130178040 | CTAATTTGTCTAACC[C/T]AAGCTTTGTGCTTTT | 50807 |
| rs374029593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337773 | CTTGAAATCTCACCC[A/G]TCCACCAAAACATTC | 50807 |
| rs374032882 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130105474 | TGCATCTTTTTCTTT[C/G]TAGCGAGAACATTTA | 50807 |
| rs374043724 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130257786 | TTTGGACTCAAGAGC[-/A]CCCCCCCCCCATTAT | 50807 |
| rs374081574 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130101343 | GTATTTTGAAAGAGA[C/T]TGCATCGAATCTGTA | 50807 |
| rs374086443 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130319837 | AGAGGGCAAAAGTTT[C/T]TAATGACATGACAAA | 50807 |
| rs374090167 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130088491 | AACACAGAGAGGCGG[C/T]GGCAGTGGGGAGATG | 50807 |
| rs374098608 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130424941 | GAGGTTGCAGTGAGC[C/T]GAGATCTCACCACTG | 50807 |
| rs374098865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130075389 | GTTACTTCACTGAAG[A/G]ACTCTAGAGAGTGGT | 50807 |
| rs374100833 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070328 | AGGCGTGAGCCACCG[C/T]GCCCGGCCGACTGCA | 50807 |
| rs374101908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062664 | CTTCAAAATACCCCA[C/T]CCTCTTCACCTGCAG | 50807 |
| rs374123247 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130230097 | AAACAAACAAACAAA[A/C]AAACAAACACCAACC | 50807 |
| rs374167908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395886 | AGCTAGGCTGATCTC[A/G]AACTCCTGATCTTAG | 50807 |
| rs374174596 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130355817 | TGCAAAAAGTAACCA[C/G]TCAAGAGAGTGCAAC | 50807 |
| rs374186855 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130400255 | CAGGTCAACCCTGTG[A/C]CAGTCAGTCTGCCAG | 50807 |
| rs374192264 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130432167 | AGGAGGAGGGGAGGA[C/G]GGGAAAGGGGGAGAA | 50807 |
| rs374198472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143725 | GTCAATCCCAATTAA[C/T]GTTTCTGTGTTTCCT | 50807 |
| rs374207325 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130124924 | AATCCTGAAGTGAAC[C/T]AGGGAGCCGAGTATC | 50807 |
| rs374207993 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130241499 | GCTTATGAAATGAAG[C/T]GACAAATGACTGAAT | 50807 |
| rs374218422 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130397620 | AAAAGCTGACCCCTT[C/T]TTAGTGCCAGTTAAG | 50807 |
| rs374226776 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130227413 | GCATGCCACCATGCC[C/T]AGCTAATTTTTTTTT | 50807 |
| rs374227698 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130390044 | GTTCCTTGACCCTAC[C/T]ACAACTTAAAGAATT | 50807 |
| rs374280290 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130222525 | CCAAATCCTATCCTT[C/T]TCCACTGACACACTC | 50807 |
| rs374282820 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130231382 | TAATAAAATTATATA[C/T]CACTGTCATTTTTTT | 50807 |
| rs374284949 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130338504 | AAAGAACATTATCCT[G/T]ACTACTCCCCAATAG | 50807 |
| rs374298604 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130120320 | GTGTTGATGGATGGA[A/G]CAGCAGACTTAAAAA | 50807 |
| rs374302118 | snp | A/G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130260703 | GAGCCTCAAAAGCAT[A/G/T]GATCAATTTGGCCTC | 50807 |
| rs374304784 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130164982 | TCTTCTAAACATATT[C/T]TGCAATGAGTGATGA | 50807 |
| rs374312924 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083051 | AAGTGATTATTAATG[C/T]AGGTTGCATGTGCTA | 50807 |
| rs374320003 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130262380 | AGCCTGGGCAACAGT[A/G]AGACTCCATCTCAAA | 50807 |
| rs374320835 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245075 | GCCAACAGAGGAAGA[C/G]GGACCTGGCAGCCGC | 50807 |
| rs374330233 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130062992 | AACCAACAAACAACA[A/C]TGATATGTAGCCAAT | 50807 |
| rs374331213 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130145462 | AGCTGGGATTACAGG[C/T]ACGCGCCACCACACC | 50807 |
| rs374332893 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108924 | GGGATTACAGGCAGG[C/T]GCCACTACGCCCGGC | 50807 |
| rs374335042 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216030 | GAAAAAGGAAAGGAA[A/T]GGAAAAAGGAAAGGA | 50807 |
| rs374346520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384215 | ACCTCAAGTTACCAG[C/T]AGGGAAGGGCCTCGC | 50807 |
| rs374350526 | snp | A/C | 1.70898e-05 | 0.00292311 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168948 | TTTACTGAAACTTAT[A/C]CATGAAAGCAAGTTA | 50807 |
| rs374356189 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130141858 | AAGTAGCTGGGACTA[C/T]AGGCATGCCTCACCA | 50807 |
| rs374360256 | in-del | -/AA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130165001 | ATGAGTGATGATAAA[-/AA]CAGCATGAGAAAGGA | 50807 |
| rs374373913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249353 | GTCACTGTGACTGTC[C/T]ACTTTATATTCCTGG | 50807 |
| rs374374441 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130390830 | ACTATTGGTGGGAAT[C/G]TAAACTGGTACAGAA | 50807 |
| rs374376108 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130169495 | AAAGAGAAATATGAT[A/G]GAACTACAGATAAAG | 50807 |
| rs374383935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130061227 | CCAGGCAGTTTTACA[A/G]AGACAAAGTTTGAAA | 50807 |
| rs374385121 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069368 | GGCCTCCTGAGTAGC[C/T]GGGACTACAGGCATG | 50807 |
| rs374386882 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130254841 | TTCTTAAGTAGCAAC[-/A]AACCAATCTAACAAC | 50807 |
| rs374427400 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107590 | TCTCATTCTGTCGCC[C/T]GGGCTGAAGTGCAGT | 50807 |
| rs374437530 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130184341 | CTAAAGCTAGAAAGA[A/G]CAAGAAAATACTGAG | 50807 |
| rs374447314 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130328696 | TGTGATCATAGCTCA[C/G]TGCAGCCTTGAACTC | 50807 |
| rs374459886 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130207250 | TCGTTTGTTATGTCT[A/G]GAGTTGGCTTTGATT | 50807 |
| rs374461722 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130104724 | AGCATTTCAAACAAC[A/G]ACTATAAAGATAATT | 50807 |
| rs374478872 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130071791 | TCCTCATCATCCTGG[A/G]AGACATTCATACACT | 50807 |
| rs374495059 | in-del | -/GCTGTGAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130147124 | CCAGCTACTCAGGAG[-/GCTGTGAC]GCTGTGACATGAGAA | 50807 |
| rs374496361 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130313761 | TGATCCACATTCTGC[A/T]TGAACTAAAAAACTC | 50807 |
| rs374501815 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130087050 | CACCTTCTACCTCCT[C/T]CTTAAAGGTCAGCAT | 50807 |
| rs374502981 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130232072 | TGAGTATCCTCAATA[C/T]GGTAGCTGGCTTCCT | 50807 |
| rs374503818 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130056791 | CCCTCTTGGCAGGAC[A/G]GGGCTCAGGCTGCCA | 50807 |
| rs374505834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072438 | CTCATTTTTCTCTTG[C/T]CTGCTGCCATGTAAG | 50807 |
| rs374506272 | in-del | -/ATTATAAAGTTAGTAAAGTCAATACTAGA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130219218 | TTTTTAACATACTGT[lengthTooLong]ATTATAAAGTTAGTA | 50807 |
| rs374516394 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130187815 | AGGAGCCCGAGGTTC[A/C]GAAGGGCTGGGTCCC | 50807 |
| rs374540690 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130235946 | GACCCTTTACAGATA[G/T]GAGATCATTAAATCC | 50807 |
| rs374540912 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130057649 | GACACGGGGTTTCAC[C/T]ATGCTGGCCAGGCTG | 50807 |
| rs374541758 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130090632 | CAACATGTCTATCCT[A/G]ATAGTAAAGAACATG | 50807 |
| rs374548959 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205039 | TATCAAAGAGATATT[C/G]ATTAGCAAAATGTTA | 50807 |
| rs374565262 | snp | A/G | 6.59087e-05 | 0.00574021 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130115700 | ATATTCTACGTGGAC[A/G]TGTGGATTGAACTTT | 50807 |
| rs374570433 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428460 | CCATCATTATCACCA[C/T]CATCATCACCACCAC | 50807 |
| rs374595355 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130142422 | ACTTACTTTCATAAT[C/T]GGGGAAAAGAGAAAT | 50807 |
| rs374613658 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130158722 | GTATTTTAAGCAGGC[A/G]AATGACATCATATGC | 50807 |
| rs374614135 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130331603 | CATTTGTAAAAAAAT[A/T]GGACGTCCACCCACA | 50807 |
| rs374620610 | snp | C/G | 3.31197e-05 | 0.00406925 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092184 | GGAAGATTAATCCCA[C/G]TCTCACAGATACAAA | 50807 |
| rs374623731 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130193284 | TGAGACAGGAGAATC[A/G]CCTGAACCTGGGAGG | 50807 |
| rs374628235 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130121681 | CCCAGCTATTCGGGA[A/G]GCTGCGACAGGAGAA | 50807 |
| rs374634457 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085619 | CGCACCCAGAGTCCC[A/C]AGTTACTTGGGAGGC | 50807 |
| rs374645581 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130283129 | TTGGCAAGTGGGCCA[C/T]TACGTTGTGAGCTCT | 50807 |
| rs374648752 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130277106 | CACCGAGGGCCCCCC[A/T]TCCCAGACTCTCCAG | 50807 |
| rs374650212 | snp | C/G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130064339 | CAGTATTTGTACAAG[C/G/T]ACAGGATGTGGTGTG | 50807 |
| rs374655037 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130187421 | ATGCACGTTACACCA[-/T]TTTTTTTTTTTTTTG | 50807 |
| rs374656924 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130200786 | GATGCAAAATCACAA[A/G]AGGGTGATATAATTA | 50807 |
| rs374657898 | snp | A/G | 0.000153988 | 0.00877328 | missense | ASAP1 | GRCh38.p7 | 8:130076386 | ACTCTTGGGCCAAGG[A/G]CAGTCTTTGCAGAAC | 50807 |
| rs374662461 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130072822 | GTGTGTGTGTGTGTG[C/T]GTGCGCGCGGGGGGG | 50807 |
| rs374685265 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130139718 | TGGGCAACAGGGTGA[A/C]AGAGCAAGACTCCAT | 50807 |
| rs374693184 | snp | A/C/G | 0.00431982 | 0.0462743 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169116 | TATAAAAAAAAAAGA[A/C/G]TATTTGTTTCCTTAT | 50807 |
| rs374698749 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216950 | CAACACAGCATCCAA[C/T]GCAACACTGTTATAC | 50807 |
| rs374706459 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130160426 | CCCCCAAATAAAAGG[A/G]GAACCTTCTAAGCAA | 50807 |
| rs374713415 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130284784 | TAATATTCCCTCCCC[C/G]CATAAGAATACTGGA | 50807 |
| rs374716830 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130261487 | GGTGGTGGGAGGCTC[A/G]GAAAATACGGGAATG | 50807 |
| rs374726067 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130056884 | TTATTCACTGTACCT[G/T]GGCCTGGCAGTTCCC | 50807 |
| rs374728801 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130238754 | AAGGCAAGGTGAGAA[A/C]GGTTAAGTAACTTTC | 50807 |
| rs374735552 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130198461 | ATTGCACCACATTCT[C/G]TCCATCTCACAGTTC | 50807 |
| rs374752620 | in-del | -/CT | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214933 | TGAGACAGAGTCTCA[-/CT]CTGTCTCCCAGGCTG | 50807 |
| rs374763178 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130109652 | AACAGAAGGAAATGA[A/C]AAAAAACATAGGGGC | 50807 |
| rs374763236 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130098595 | TCTCATGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 50807 |
| rs374777066 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130350478 | GAAGCCAATCACCTC[A/C]ATGAGGTAACACTTT | 50807 |
| rs374779393 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130057691 | CCGACCTCGAGATCC[A/G]TCCGCCTCAGCCTCC | 50807 |
| rs374784320 | in-del | -/TTTC | 0.0269764 | 0.112962 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100315 | ATTTATATGTCGTGT[-/TTTC]TTTCTTTCTTTCTTT | 50807 |
| rs374801167 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130145353 | GACGGAGTCTCGCTC[C/T]GTTGCCCAGACTGGA | 50807 |
| rs374802345 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130058017 | GATGAATGTGAGCTC[A/G]TCATCGTTGTCTGCC | 50807 |
| rs374808160 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130433486 | CAGCTATGACTGTTC[-/C]TTGGTAACTCTCCCA | 50807 |
| rs374812167 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130131281 | CTCAGTGAGAAGAAA[G/T]TTTTTCATTCAATTT | 50807 |
| rs374814896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150060 | ACGGTAATAGCAGCA[A/G]TAAGTATTAACAGAA | 50807 |
| rs374849615 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130392098 | TTGAGGGGAAAGACT[C/G]TAACTTATATATCAA | 50807 |
| rs374853248 | snp | A/G | 0.000100653 | 0.00709339 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127905 | ATGTTGTAAAAGCTC[A/G]TTCAAATATGGGGAC | 50807 |
| rs374858568 | snp | A/C/T | 4.06514e-05 | 0.00450826 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128126 | GGAAAAAAGTCTTTA[A/C/T]AAGAGCATGGTCATT | 50807 |
| rs374862783 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130357042 | GGGATGCTTTATGGC[A/G]CTTATTGATGATGCT | 50807 |
| rs374871503 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130350004 | CTCTCTGAGGCTCCC[C/T]GGACAAACAGACAAT | 50807 |
| rs374883028 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130363111 | CAACCCCTATCTCAG[C/T]GTTCTGAGAATTCAA | 50807 |
| rs374884985 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130101306 | GGATTGCTTTTTTCT[A/G]TTTCTATGAGGAATG | 50807 |
| rs374894635 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130077974 | CTAGTTCACAATCAG[A/C]TTGATTTTGTTTAAA | 50807 |
| rs374900830 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130362070 | AAAAAAAGGCAGCAG[C/G]AACAGTGGTGGCTTA | 50807 |
| rs374901878 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130153683 | GTGGCACTGCTTTGG[A/G]CAGTAAAAATGGGAA | 50807 |
| rs374908183 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130147736 | AGGATGTGGTCTGAC[C/T]CTCCCCCTGTTCAAA | 50807 |
| rs374910614 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130292279 | AAGAAGACTCTTTCT[A/G]GATCCTCAGGAATCT | 50807 |
| rs374912967 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130078161 | TGCCCGGCTAATTTT[C/T]GTATTTTTCGTACAG | 50807 |
| rs374918960 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130133839 | GCTCACCTGCTCCTC[C/T]TACAATAATGGTCAA | 50807 |
| rs374921983 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130082144 | ACCTCCTGGACAGAA[C/T]GTTCTGTAATTCTAT | 50807 |
| rs374923290 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130161966 | CTACCATGTCAGGCT[A/G]ATTTTTGCTTTTTTG | 50807 |
| rs374936074 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171503 | CCTTGAGACTCACTC[A/G]TTATCAAGAGAACAG | 50807 |
| rs374950116 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130424130 | ATAACAAAAGAAACT[A/G]TAAAAGGCCTTGAGG | 50807 |
| rs374980690 | in-del | -/GAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130236005 | CCTCACGTTACAGAA[-/GAA]AAATGGAGGCTCAAG | 50807 |
| rs374986766 | snp | G/T | | | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052735 | TTTTTTTTTGTTTTT[G/T]TTTTTTTTTTTTTTT | 50807 |
| rs374994149 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217672 | GCTGGACTTTCAAAG[C/T]TGCGGCTTGGTTAAT | 50807 |
| rs374996775 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ASAP1 | GRCh38.p7 | 8:130328845 | ATGTCGCTCAGGTTG[A/G]TCTCAAACTTCTGGC | 50807 |
| rs375001637 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130309033 | AAATGACTTACACGC[A/G]TAATAAAAGAGGTGA | 50807 |
| rs375012618 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079545 | GCAAAAGGAGTCAAG[A/T]GGAAAAGTAACAAAG | 50807 |
| rs375018436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233621 | CACCTTCCTCACGCT[A/G]CCTCAGATCCTTCTT | 50807 |
| rs375031418 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130347890 | CCATGAATCCTTCCA[A/G]TAAGTCCCCATTTTG | 50807 |
| rs375048587 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130278349 | TTAAAAGGGTGTGGC[A/C]GGTTAAGTCCACCAC | 50807 |
| rs375057120 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130156963 | TCATTGTGATTTCGG[A/G]AGAGTAGTGTTAAAA | 50807 |
| rs375063316 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130417867 | ATCCCTGCAGGAAAG[A/C]CTCGCTGTACTGGTG | 50807 |
| rs375085445 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130429892 | CTCAATTTGTTGTTC[A/T]CTATAATAGCTGCCT | 50807 |
| rs375093248 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130433601 | ACTTTGATTTTTCAT[C/T]TTCATATCCTAAGTG | 50807 |
| rs375105720 | in-del | -/TTTT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130107180 | GTCTCTCTCTTCTTC[-/TTTT]TTCTTTTTTTTTTTT | 50807 |
| rs375106063 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130193453 | AATAATACACAGAAA[C/T]CTGTTGATACCAATT | 50807 |
| rs375110067 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130113321 | TGACTCCTTCCCTTG[C/G]CACGTGGTGTTCTGG | 50807 |
| rs375125726 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216072 | AGGAAAAAGGAAAGG[A/G]AAGGGAAAAGGAAGA | 50807 |
| rs375126217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406227 | ACAAAAGAAAAGAAA[C/G]TTCATGATCTTAAAG | 50807 |
| rs375130287 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179375 | AAAACAGGGTTTTGC[A/G]TTGATTAATTCCAGA | 50807 |
| rs375136739 | snp | A/G | | | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445359 | CCCTTGTCACTGTTT[A/G]ATGTAGCCTACATGA | 50807 |
| rs375158404 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396801 | TGATAATGACAGGGC[A/G]TCTGCTTGACATTTG | 50807 |
| rs375162091 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130258538 | TGGAAACAACAGAGA[C/T]GAGAGCCCAGATAAC | 50807 |
| rs375164769 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130400655 | AATTAGCTGGGCGTG[A/G]TGGCAGGCGCCTGTA | 50807 |
| rs375178856 | snp | A/T | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083440 | CAGCTTCTTACCAGG[A/T]GTGGTTAATTAGGGG | 50807 |
| rs375181440 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130192079 | TTTCAAAGACAAAGG[G/T]ATTTCTACCAAGACA | 50807 |
| rs375188317 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130403755 | GACAGGGTTTCGCCA[C/T]GTCGAGCAGGCTGGT | 50807 |
| rs375195650 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130246007 | AGTCAGTCACATCAC[G/T]TATCAATAATGAAAT | 50807 |
| rs375196484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313788 | ACTCATGACTTTATA[C/T]TATCAGTTCTGATAT | 50807 |
| rs375201336 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228782 | TATATAAACAATGGG[-/A]AAAAAACCTTTAAAA | 50807 |
| rs375203590 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130099415 | TCGATCTCCTGACCT[C/T]GTGATCCGCCCATCG | 50807 |
| rs375213519 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130143585 | AAATGTTTCAATCAG[C/G]GAAGCTCTGGGTACA | 50807 |
| rs375215201 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130205591 | ATATAAAATACACGG[C/T]TTTTTTTTTTTTTTT | 50807 |
| rs375219422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130182605 | AGATCTCTAATGATG[C/T]ATATAAACTTTTAGT | 50807 |
| rs375221275 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130303335 | TATATTTAGACTAGG[A/G]CTTTCTCAACCTCAA | 50807 |
| rs375236473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102439 | TCCTTGCATCCCTGC[A/G]ATAAATCACACTTCA | 50807 |
| rs375237829 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130264669 | CAATTCACTTCACTA[C/T]GTGCTAATAAATAAT | 50807 |
| rs375242418 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130326625 | TTAACAGGGTGTCCA[C/T]CCGGAGGCCAACAAA | 50807 |
| rs375257287 | snp | A/G | 0.000798722 | 0.019968 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114114 | ATGATCTGAGATAAC[A/G]TAAGTGCTTAAATCT | 50807 |
| rs375273415 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130068340 | CAAAGGAGAAAATTA[C/T]GCAGGGACAACAGAA | 50807 |
| rs375296393 | snp | C/G | | | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444217 | AGGATAGTATAGGAA[C/G]AGTATGGAGAGTAAT | 50807 |
| rs375340242 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063814 | CATGTGCCGTGCCCA[G/T]CACCCTTTCAGGCAC | 50807 |
| rs375348270 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130119405 | ATGGATAACATGCCC[A/G]AAGTCTGAAAGGGTG | 50807 |
| rs375355497 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076491 | TAAATCAAATCAAAG[G/T]TATTTACATAATCAT | 50807 |
| rs375356661 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130413097 | GGAAACTGAGGCAAA[C/T]ACAGGATGAGTATCT | 50807 |
| rs375358944 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155194 | ATTATGGAAACAATA[A/C]ACACACACGCGCGCA | 50807 |
| rs375366798 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130255221 | TAGGACACCTGGTAC[C/T]GGCAAAAAGAAAAAC | 50807 |
| rs375376988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156677 | TACCCTGGCATTAAG[C/T]CAGAAGACCCAGGTT | 50807 |
| rs375381624 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130276726 | CACACACACACACAC[A/T]CACTCTCTCTCTCTC | 50807 |
| rs375384875 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130120558 | GCCAGAACTAGGCTT[A/C]AAGATGCAAAGTTGC | 50807 |
| rs375402140 | in-del | -/ATC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130346524 | TAAACCTAGTTCATC[-/ATC]TGTGAAATGAAGAAA | 50807 |
| rs375420447 | snp | C/T | 7.18881e-05 | 0.00599491 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060538 | CCAACTTGCAAAGTG[C/T]GGAATAGGGTTCCTA | 50807 |
| rs375428366 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130317915 | AGAGGAGAGCTGAGG[A/C]AGGGCTGGTGAAGAA | 50807 |
| rs375435793 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241130 | CTGCTCAGGACATTT[C/G]AACTAGTTGATTGCT | 50807 |
| rs375463150 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130136798 | TGGAAATTAAGAGAC[C/T]TGGGGCATCTTCCTA | 50807 |
| rs375472618 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070462 | AATATTAATTGGACA[G/T]GCCCAAGCCTGCAGA | 50807 |
| rs375476236 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130425945 | AGAGTTCAGCCGTCC[C/T]CACCACTGCCGCTGC | 50807 |
| rs375481713 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130392966 | AGAGGGGTCAAATAT[C/T]CAAACCATGGCACCG | 50807 |
| rs375495211 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130366865 | ACTATTTGCATTCTA[A/G]ACAGGTACTATGCTA | 50807 |
| rs375501142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296234 | CCACTCTGGGGATGA[C/T]GTTTCTTGCTAAACA | 50807 |
| rs375506486 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317715 | GCTCTGTTGCTACGC[A/C/G]TTTGTTTCACTAGTG | 50807 |
| rs375509677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415645 | ATACAAAAATTAGCC[A/G]GGCATGGTGGCAGGT | 50807 |
| rs375511368 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130057746 | AGCCACTGTGCCCGG[C/T]CAGCTCCACGGCTGT | 50807 |
| rs375520435 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130329620 | TATGTTACTGGCTCA[C/T]AATAAATGTCCAACT | 50807 |
| rs375541551 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130441487 | GGAAAAATGAGAACC[C/G]AGCAGCAGGATCCAA | 50807 |
| rs375543848 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130128168 | TTTTTTTTTTTTGCC[A/C]CTGCAAAAAAAAAAA | 50807 |
| rs375545649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130113519 | TATTTCCTCTTAAAG[C/T]TGTTAAGGCTTGAGG | 50807 |
| rs375557813 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121640 | ATACAAAAAACTAGT[C/T]GGGCATAGTGGCGCA | 50807 |
| rs375560122 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130376793 | TTGTAATCCCACATA[C/G]TTGGGAGGCTGAGGC | 50807 |
| rs375563715 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130324866 | GCATCCTCAGCTAGT[C/G]GCACAGTGCATGAGC | 50807 |
| rs375586966 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130281521 | CAAGTCTAGGTACTG[C/T]AAATCTACAACTAAG | 50807 |
| rs375587939 | snp | G/T | | | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130053774 | ATTCATAACACAATA[G/T]GTCAATCCATACTCT | 50807 |
| rs375589497 | snp | A/C | | | downstream-variant-500B | ASAP1 | GRCh38.p7 | 8:130051866 | GTTCACATCAACGGG[A/C]GCACAAGTGGACGTG | 50807 |
| rs375605178 | in-del | -/ATTCTCCCTAAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130161768 | GGATTTTCTTGCAAA[-/ATTCTCCCTAAA]TATTTCCTTTTAAAA | 50807 |
| rs375615314 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130239584 | GAGGTGACGACTATA[C/T]ACCAGTTTTGAGATA | 50807 |
| rs375621645 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130149067 | TGCCCAGGCTGGTCT[C/T]GAACTCCTGGGCTCA | 50807 |
| rs375624198 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130111694 | CAGAGAACTGAAACT[C/G]CACTCCACATTATAA | 50807 |
| rs375625978 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130130804 | GTCCCAGCTACTGGG[C/G]AGGCTGAAGCGGGAA | 50807 |
| rs375628504 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130077003 | TGTAGTGCACAGAAG[C/T]AACTCTTCCCACATG | 50807 |
| rs375630517 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130395824 | GGCACCCGCCACTAC[A/G]CCCAGCTAATTTTGT | 50807 |
| rs375632312 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130093749 | TAGATACCTAGTAAT[A/C]CAGAAGGGCTCCAAA | 50807 |
| rs375634619 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130316144 | CTGTTCCCATCCACA[A/T]GTTCACCTGTGACCA | 50807 |
| rs375635694 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130056261 | TGGGGGGGCTTCAGA[A/G]CCCACCTCCTCGTCA | 50807 |
| rs375667996 | snp | G/T | | | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052729 | TTGTGTTTTTTTTTT[G/T]TTTTTGTTTTTTTTT | 50807 |
| rs375676655 | in-del | -/GTGTGTGTGTGTGTGTGTGTGTGTGT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130064909 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGTGTGTGTGTGT]AAGAATCACAGCTCA | 50807 |
| rs375677758 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130272726 | AACTGGATGTCACTA[C/T]GTTAACTGAAATAAA | 50807 |
| rs375678001 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130271571 | AATTAGCTTCCAACA[C/T]CTACCAACCTGCATC | 50807 |
| rs375688132 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130126872 | CAGTGCTTAAGAATA[A/C]CAGGTTTGCATCCTT | 50807 |
| rs375692700 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130321579 | ATCCTAAAGCACTCA[-/T]CTACTCTAACTACAT | 50807 |
| rs375717700 | snp | C/T | 1.76176e-05 | 0.00296791 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214743 | AGTCTGAACTATTAT[C/T]TGCCACAATGAAAAG | 50807 |
| rs375733888 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130442069 | TCCAAATCCACTTAG[A/T]GGCGTTAGGTGATTT | 50807 |
| rs375734794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176982 | GGCGTGAGCCACCGC[A/G]CCCAGCCGTCTCTCT | 50807 |
| rs375738443 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130411327 | AGGCACAGGCTCGGA[C/G]TGCCAGGAAATGAAT | 50807 |
| rs375757814 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130416606 | TTCTCTTAGAAATCA[A/G]TCAAGGCTTCCCACC | 50807 |
| rs375758437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389325 | ACTACTCTGCAGTTC[C/T]GCCATGTGATGCCAA | 50807 |
| rs375769341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396461 | TTCCTTCCTTTATGT[A/G]TTTAACTGAAGTATA | 50807 |
| rs375769881 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130407047 | TACCTCATGCAGTCA[C/T]AGCAAGAATTAATAA | 50807 |
| rs375771361 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130361281 | CTCCTAGTAACTGAT[A/G]CTGTCATCTTGGGCC | 50807 |
| rs375778653 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130423103 | CAACTATTACAATCC[A/G]TATTTATACTTTTTT | 50807 |
| rs375784511 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428645 | CCACTGTCATCATCA[C/T]CACCATCATCACCAT | 50807 |
| rs375788296 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130221734 | ATGTCAGCCACTGAA[A/C]CTTACAGGGTACCCT | 50807 |
| rs375789864 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130189527 | TCCATTGTGTATATA[C/T]ACTGTATTTTCTTTA | 50807 |
| rs375813037 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130381366 | TAACCCAATATATTC[A/C]AAATACTATCATTTC | 50807 |
| rs375814798 | in-del | -/TCA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130252257 | TCATAATTTAGAACA[-/TCA]AGTTACATGTATTAT | 50807 |
| rs375816805 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148303 | TTACAAACTTCATGA[C/T]CCTGAGCATGGGATT | 50807 |
| rs375817086 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130279809 | GTTAAGCAGGAAACC[A/G]GTCCACTAAAATAGT | 50807 |
| rs375834793 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130075690 | ATCACTTGTGTTGTA[A/G]TAAGAAGACTGAAAT | 50807 |
| rs375841076 | in-del | -/T | 0.322007 | 0.239405 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052735 | TTTTTTTTGTTTTTG[-/T]TTTTTTTTTTTTTTT | 50807 |
| rs375858484 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324700 | AGTCTATGGATACAA[C/G]AATAGGGCTGGGAAA | 50807 |
| rs375870270 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130262333 | TCGGGGGATGGAGGT[C/T]GCAGTGAGCCGAGAT | 50807 |
| rs375891724 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399106 | AGGATGGGACGTGCC[C/T]TTCTCTGTCTCGTTC | 50807 |
| rs375896300 | snp | C/T | | | missense | ASAP1 | GRCh38.p7 | 8:130127935 | CAAAAACCTGATGAG[C/T]CACAATCGCAGCAAA | 50807 |
| rs375902782 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130286002 | TGATATATCTATTAT[G/T]TTTAGCCACTTACTG | 50807 |
| rs375905460 | snp | C/T | 0.000153988 | 0.00877328 | missense | ASAP1 | GRCh38.p7 | 8:130112211 | AGGAGAGCCGCTGTT[C/T]GTCCCTTGGAGTGCT | 50807 |
| rs375909106 | snp | A/G | 0.000463369 | 0.0152141 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118156 | AGAGAAAACAAAAAC[A/G]ATACCAGTTTTGTAC | 50807 |
| rs375912759 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130252006 | CCTTTCAAAACAACT[A/G]TTGCCATTTCCTCAA | 50807 |
| rs375913152 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130081802 | TCAATGTGCTCTTCA[C/T]TACCCATCAAGACGC | 50807 |
| rs375922826 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130088752 | AGCTATCCAGCAAAA[C/T]GCTAGGCTGAGAATA | 50807 |
| rs375923613 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297406 | ATCCACATATAAGTG[C/G]ACCAGCACAGTTCAC | 50807 |
| rs375932762 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130138979 | TCATCTTTTTGGATG[C/T]TGATAAAATTGCTGA | 50807 |
| rs375945770 | snp | A/C/G | 4.03871e-05 | 0.00449358 | missense, synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, intron-variant | ASAP1 | GRCh38.p7 | 8:130358050 | GGTGTTCCTGCAGTT[A/C/G]TGCAGCCGCGTGGTG | 50807 |
| rs375981753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093662 | TCACAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 50807 |
| rs376002736 | snp | C/T | 3.71768e-05 | 0.00431127 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112349 | AATAAGAAGGTGAGA[C/T]AATAATCAAGGACCA | 50807 |
| rs376023437 | in-del | -/A | 0.0718919 | 0.175435 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311895 | AAACAAAAACAACTC[-/A]AAAAAAAATAGTAAT | 50807 |
| rs376038180 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168353 | AAAACAAAACAAAAA[A/C]CCTTATAAATCAAAG | 50807 |
| rs376048218 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130205689 | ACTTGAGGTGGGGCA[A/C]CTAATAGTCTTTATA | 50807 |
| rs376050808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437551 | GGTCTCAGGAGAGAA[C/T]AACTATAATGGAATG | 50807 |
| rs376055653 | in-del | -/TT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130335349 | TTTATGACCCCTATT[-/TT]ACAGAGGAGAAACCA | 50807 |
| rs376058564 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216012 | AAGGAAAGGAAAGGA[A/T]AGGAAAAAGGAAAGG | 50807 |
| rs376073943 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130353586 | AAGATTTCTAAACTC[A/T]GGGCCAGGCGTGGTG | 50807 |
| rs376084805 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130323275 | ATTACGGACTGGACA[C/T]TCATTTAGGGATGTG | 50807 |
| rs376087798 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306630 | GGGCACAAGCGGAAC[A/G]AACTCAGCTCTCTGC | 50807 |
| rs376089112 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130284100 | GGCACGGAGGACAGA[C/G]GTTCTAATGGACAAA | 50807 |
| rs376115525 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130260894 | ATAAACTATATTGTG[A/G]TGCATAAAACCAAAT | 50807 |
| rs376119897 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130240637 | AAGTATGTATCCGCA[A/G]TTGGACAACTCAAAA | 50807 |
| rs376120963 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130286502 | GTAGTTACAGAGGGT[A/G]TCTGAAGGCCAGAAT | 50807 |
| rs376140494 | snp | A/G/T | 2.73385e-05 | 0.00369709 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130358000 | GCGTGGACGGCGGGG[A/G/T]TCCCGGCCCGACCTA | 50807 |
| rs376152004 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130071848 | ATTGTGTATATATAT[A/G]TTTTTTGATATAAAG | 50807 |
| rs376152116 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130366372 | AAGCCACCCACCCTT[C/T]ACCCAGAGAAGCTTC | 50807 |
| rs376159843 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130346565 | ACCCCACAGGGCTGT[A/T]GGGAGGATTATATGA | 50807 |
| rs376180853 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278645 | CTGGGACATACGATA[A/C/G]AACAGTCGAGAGACA | 50807 |
| rs376189522 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130220451 | TTACCCTTGATCATA[-/C]AACTCATAAATAAGG | 50807 |
| rs376198413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299473 | GTATGCCCAACACTA[C/T]ATGGCACAGTACCTT | 50807 |
| rs376202341 | snp | C/T | 3.30028e-05 | 0.00406205 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116841 | GTACCATGCAACACA[C/T]GCTTACTACAGTCAT | 50807 |
| rs376207443 | snp | C/T | 0.000182963 | 0.00956284 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401845 | CCGCTGTATCTCCCA[C/T]GCCGAGTTTTCTGGA | 50807 |
| rs376210075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130210206 | GAATACAGAAGTAGA[C/T]ATGAAAATATAGCTA | 50807 |
| rs376212749 | snp | C/T | 4.94222e-05 | 0.00497078 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054720 | GGACAATCTTAAGGT[C/T]CTGCGTTTTGCTAGT | 50807 |
| rs376213135 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130361909 | TGTGCACCTGGCTTT[A/G]TATAAAGCAAGCATC | 50807 |
| rs376215195 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130278789 | TCTGGGCCACCCAAC[A/T]TCTACTCACCGTACC | 50807 |
| rs376225205 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084462 | GAAAGTTGGAGATAC[C/G]TCCTGGGCAGGCAAT | 50807 |
| rs376250708 | in-del | -/CT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130079027 | GCTGAGGCCTTGTCT[-/CT]ACAAAAAAATAAAAA | 50807 |
| rs376258648 | in-del | -/GA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130299692 | TTAAAGAAACAGAGA[-/GA]TCAAGAAGACAAAAA | 50807 |
| rs376269560 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130279355 | CCAGATCCATGGCTG[C/T]CCCACATGGAGTCTT | 50807 |
| rs376283057 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428630 | TCACCACCACCACCA[C/T]CACTGTCATCATCAC | 50807 |
| rs376284626 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130364066 | GGTAATAATAATAAT[-/T]AAAAAAAGCCAATTC | 50807 |
| rs376287760 | snp | C/G/T | 0.0010673 | 0.0230765 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180924 | AAAAAAAAAAATACA[C/G/T]TCATGTACAATACCA | 50807 |
| rs376302759 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130257045 | ATGTACCTTCTTATA[A/G]CCCATAATTTTATAA | 50807 |
| rs376317332 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130146016 | TGGCTAAGTTTTGTG[-/T]TTTTTTTTTTTTTTT | 50807 |
| rs376330948 | in-del | -/CA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130366184 | AGAAACTCCCGTCTA[-/CA]ACAGATTATGTTGTC | 50807 |
| rs376333264 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130163431 | TACATCAAACTAATA[C/T]GCTTTTAAAGATGAA | 50807 |
| rs376335866 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402058 | CAAGATCGGATTTCA[A/T]ATGGAGGCTGCACCT | 50807 |
| rs376353418 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130167309 | TCAAAAAAGTAAAGA[A/C]AAAAGAAAAAAAAAA | 50807 |
| rs376357013 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086607 | TCAGGAGTTTGAGAC[C/G]AGCCTGGGCAATATG | 50807 |
| rs376357537 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130192483 | TCTATTCTACACAGA[C/T]AGCTGAAATAATTTG | 50807 |
| rs376369476 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130115062 | ACCATGCCTAGCTTC[A/G]TGGTTAATTTTATGT | 50807 |
| rs376378084 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130393077 | CTTATCTTCTTTTTA[A/T]TGGCTGCATTATTTT | 50807 |
| rs376380166 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130383232 | TCAGAATTCTCCCCC[A/G]AAGGATTCCCCAGGC | 50807 |
| rs376398321 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130287145 | TAATTGAACAAAGCT[-/G]ACTACATATCACCAA | 50807 |
| rs376407052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055945 | GTTAGCATGTGTGTG[C/T]GGCACCATCTTTACA | 50807 |
| rs376417360 | snp | A/G/T | 0.000313031 | 0.0125072 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079887 | CAGGGGAAATGAAGC[A/G/T]CTGAGATGGCTTACC | 50807 |
| rs376435121 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130350366 | GTCTCATCTTTGGGC[C/G]TCAGTCTCCACCTCT | 50807 |
| rs376437320 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259643 | AATGAACCATCATTA[C/T]CTTGTCATGCTAGCT | 50807 |
| rs376447407 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130356037 | ACACTTGCATTATAG[C/T]TAACTCTATTTTTCT | 50807 |
| rs376453356 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130310960 | GCCAGTATCTACTAA[A/G]GCGGCAGTGTTTCTC | 50807 |
| rs376467538 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234714 | GGGAGCCCTCAGCAC[A/G/T]GTAAATACAGCAGCA | 50807 |
| rs376501112 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130103596 | ACAACCTCTGCCTCC[C/T]GGGTTCAAGTGATTT | 50807 |
| rs376515748 | in-del | -/GAGAGAGAGAG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130262418 | AAAAAAAAAAAAAAA[-/GAGAGAGAGAG]AGAGAGAGAGAGAGA | 50807 |
| rs376524339 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359531 | CTTTGATAGCCTTAG[A/G]ATGGAAGGCTGAGCC | 50807 |
| rs376525515 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130124206 | GAATATGTATTTTCC[C/T]TCATTTGACTTAGAA | 50807 |
| rs376532965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316908 | GCAAATAACAAAATG[C/T]GGTGCAGGCTCTCCA | 50807 |
| rs376556009 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130375725 | CTTTGTTTTTTTAAA[C/T]CTCCTTTAATTCTTA | 50807 |
| rs376556200 | snp | A/G | 3.3264e-05 | 0.0040781 | missense | ASAP1 | GRCh38.p7 | 8:130060610 | GGCAGTGGTACGGGC[A/G]TCTCTGGCAGAGTAG | 50807 |
| rs376558131 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130077750 | TGAAAGGTGTGTGCT[C/G]CTTTCTGTCCTGGCT | 50807 |
| rs376561263 | in-del | -/AATTACCCAGTCT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130072589 | GAAAACGGACTAATA[-/AATTACCCAGTCT]CAGCACCCCTTCCCC | 50807 |
| rs376571389 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130334782 | TCTCTTTTCAGACTC[C/T]GGAAAAACTGGGCAT | 50807 |
| rs376587799 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130253914 | TAATCCCAGCTACTC[A/C]GGAGGCTGAGCCATG | 50807 |
| rs376592542 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130223319 | CTCTGGTTCTAACTG[G/T]GCATATATAACCTTG | 50807 |
| rs376612973 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130341019 | AGGGGTGGTTTTTTA[A/G]AGTGTTTTTTAACCG | 50807 |
| rs376613852 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130331809 | AAACACATACACACA[C/T]ACATGCAAACACACA | 50807 |
| rs376634452 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130279142 | AGCCCTTGATTCACA[A/G]TGAGACAGAGAGGGG | 50807 |
| rs376636861 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130218479 | CTTCCTTCCCTCCCT[A/G]GACACAGCCATTATC | 50807 |
| rs376640216 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428597 | TCAACTCCATCATCA[C/T]CACTATCACCATCAT | 50807 |
| rs376646208 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130287684 | CGTAAGCCCTATCTC[A/C]CAAGTTTGGGTGCAA | 50807 |
| rs376660286 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130424105 | ATTACAAAAATATAA[C/T]TTAAAATGGATAACA | 50807 |
| rs376665594 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130357473 | CACCAGAGACTAACA[C/G]GGAGGACTCCTGGAG | 50807 |
| rs376672210 | snp | G/T | | | missense | ASAP1 | GRCh38.p7 | 8:130167612 | TTTTCTTCATCCTGG[G/T]TCTGTTTTATCTATG | 50807 |
| rs376701821 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130332085 | GCACCTCTCTTGGAG[A/G]CCTGTTAACTTGGTT | 50807 |
| rs376715545 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130055571 | GCTATGTACTATCAC[C/T]TGTTTTCTGGTTACC | 50807 |
| rs376741802 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130355219 | TTCCAAGAGTGCTCA[G/T]CACAGAGATTTAACT | 50807 |
| rs376743913 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130055530 | TAAAGTGTTGTTCTA[G/T]CCAGTAAAAAAAAAA | 50807 |
| rs376751216 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128097 | GATATCCATCTGTTG[A/G]TAAAAACATAAGAGG | 50807 |
| rs376753964 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130056677 | CCCATGCCTATGTGT[A/G]TGTGCACACATGTAT | 50807 |
| rs376769113 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130096173 | AAATACTATATATAA[C/G]ACCCCAGAAATGCAG | 50807 |
| rs376781067 | in-del | -/GAGA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130284897 | ATACTGAGAGAGAGA[-/GAGA]AAGAGAGAGAGAGAC | 50807 |
| rs376786284 | in-del | -/AA/AAA | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085735 | CAAGACGTTGTCTTT[-/AA/AAA]AAGAAAAAAAAAAAA | 50807 |
| rs376787342 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130128580 | AACAGTGAAAATGAA[A/G]GGATATTTCATTAGC | 50807 |
| rs376792802 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130385753 | CTAAGGAAGCTGATT[C/T]GAACTTGAGCTACTA | 50807 |
| rs376798218 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130275123 | CTAGATCTTAGACAA[G/T]AATGAAATGAGAGCA | 50807 |
| rs376805040 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130079190 | ACAGAGAAAGGCCCT[A/G]TCTCAAAAAAAGAGA | 50807 |
| rs376825464 | snp | A/G | 0.000280512 | 0.0118396 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130127943 | TGATGAGCCACAATC[A/G]CAGCAAATGTCATTC | 50807 |
| rs376827163 | in-del | -/GTTT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130223858 | ACATGATAAACATTT[-/GTTT]ATCATCTTATCTTCA | 50807 |
| rs376831769 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070187 | GACTACAGGCGCCCG[C/T]CACCATGCCCGGCTA | 50807 |
| rs376837465 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130298105 | CATTCTGCTCTAACA[-/A]TTTTTGGCCTCTAGG | 50807 |
| rs376855708 | snp | C/G | | | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082552 | TCTGTCACCCAGGTG[C/G]GAGTGCAGTGGCATA | 50807 |
| rs376858344 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130112878 | GAGGTATCTCTGGTA[C/T]TTGCGCTTGTGGTGA | 50807 |
| rs376869205 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408435 | CATGCATCTTCTTTT[A/C/T]TGGACACTGGCGCTC | 50807 |
| rs376889213 | snp | C/G | 0.000282446 | 0.0118804 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401861 | GCCGAGTTTTCTGGA[C/G]AGGATGGGCTAGAGA | 50807 |
| rs376906435 | in-del | -/AC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130420236 | TGGCCATAATGAAAT[-/AC]ACACACACACACACA | 50807 |
| rs376920672 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130246485 | ATTCTGTTATCATAA[C/T]AGTGAGTGAGTTCTC | 50807 |
| rs376922207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074362 | GTATGTGGGTGTGGT[A/G]GAGGAGGCTGCAGGA | 50807 |
| rs376923239 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130078028 | ACGAAGTCTCGCTGT[C/T]ACCTAGGCTGGAGTG | 50807 |
| rs376930435 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130305761 | GTTACACTAGCCTTA[A/G]GTCAGAAATAGAAAG | 50807 |
| rs376932627 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130319109 | CTCTGTAGCAATTAC[C/T]GTGGTTATTTGGAGA | 50807 |
| rs376944212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425671 | ATGGCTCCAAATTCA[A/G]TCTTAGGGATCAGAG | 50807 |
| rs376952376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360481 | CCTCTATTGGCTGTA[C/T]TGAACCTGCACTGTG | 50807 |
| rs376970128 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236781 | CAGTCGAGATAAGAG[-/AA]AAAAAGAGAAATTTC | 50807 |
| rs376971513 | snp | C/G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130305415 | CCAGTGGTGCGATCT[C/G/T]GGCTCACCGCAAGCT | 50807 |
| rs376984388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130363615 | ATTGGTGGTTATATA[C/T]GTAATGTCTGAATTC | 50807 |
| rs376991828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072323 | TCTGATGGGAGATAA[C/T]TGAATCATGGGGGCA | 50807 |
| rs376992566 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130277601 | CAAAAAATAAGTGTC[A/C]TAATAGTCTAAATCT | 50807 |
| rs377002166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162457 | TTTAATCCAACAAAA[C/T]CACAGGAAAATTACT | 50807 |
| rs377006156 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130150002 | AGCAGGAGGGTTTGC[C/T]TGTCAACAGATTTCA | 50807 |
| rs377012735 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130107481 | TGAGCCACCATGCCC[A/G]GCCCATAGTCTCTCT | 50807 |
| rs377017556 | snp | A/C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130223881 | TCTTATCTTCATGAA[A/C/T]GAAGAAAAATCTTCC | 50807 |
| rs377023191 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130088497 | GAGAGGCGGCGGCAG[G/T]GGGGAGATGACCATG | 50807 |
| rs377026288 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158810 | GATCTCAGCTCACTG[C/T]AAGCTCTGCCTCCAG | 50807 |
| rs377029718 | snp | C/T | 1.692e-05 | 0.00290856 | missense | ASAP1 | GRCh38.p7 | 8:130214696 | TTTCTTCATTTTGTA[C/T]ATGATCTAAAAACAA | 50807 |
| rs377046652 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130260866 | GAGAAAGAAGTTTTA[C/T]ATTAAAACAGACATA | 50807 |
| rs377057500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285819 | GCCTCTGGTTTCTGA[C/T]GTAACTTTATCACGT | 50807 |
| rs377058881 | snp | C/G | 1.64749e-05 | 0.00287005 | missense | ASAP1 | GRCh38.p7 | 8:130112240 | CTGAATCCTGGCAGT[C/G]CCAGCTTGTCCTGGG | 50807 |
| rs377060284 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130424467 | AGCTCTCTGACTTTG[C/T]TCTTCCCTTCAAAAA | 50807 |
| rs377062859 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130377440 | CAGAAGGGGTGTTTT[A/G]TACTGAAGATCAGTC | 50807 |
| rs377065744 | snp | C/G/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432088 | AGGGGGAGGGGGAAG[C/G/T]GGGAGGAAAGGGAAG | 50807 |
| rs377071899 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130225319 | ACTTTTTTGGGTTTC[C/T]GGCCTTATGTTCCTA | 50807 |
| rs377082352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263118 | CTTGGCATATAGTGT[C/T]TGATTACGTGTGTTG | 50807 |
| rs377083458 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130065382 | GAAGCTCCTTGAACC[-/C]AGTCCTCTAGGGTTT | 50807 |
| rs377084245 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130130605 | TGTATTTTAATACTT[C/T]AAACGTCGCTTTGAG | 50807 |
| rs377098521 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116640 | CACTTTTAAGGCAGC[C/T]AATGTCTAATAAATC | 50807 |
| rs377099619 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130420461 | CATTCAAATAAATAC[C/T]TGTAAATGAATGTTC | 50807 |
| rs377101279 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162614 | ATGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 50807 |
| rs377103476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130071105 | TTCTCCCCTACCCGA[C/T]GCAGTGATCCTAGGA | 50807 |
| rs377110418 | snp | A/G | 3.31384e-05 | 0.00407039 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115607 | AGTTGTTGAGAATTC[A/G]AGGACATAATTTACA | 50807 |
| rs377111058 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130114987 | TTGCTCTCGAATTCC[C/T]GGTCTCAAGCGATAG | 50807 |
| rs377113599 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130227883 | AATTAGAAGAAATGT[G/T]AGCTGTATCTGAAGA | 50807 |
| rs377117935 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130376682 | AGTGAGCCAAGATTG[C/T]GCCACAGCACTCCAG | 50807 |
| rs377122000 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336235 | CTTAATAATCACAGT[C/G]GGGGAGAAGAAGGCA | 50807 |
| rs377139229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130125011 | ACACAAGACAGATCA[C/T]GATTGCTTAGTGAAC | 50807 |
| rs377152364 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130099259 | TCTCGGCTCACTGCA[A/G]GCTCCACCTCCCAGG | 50807 |
| rs377156987 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130212009 | CACGAAGATCCAGAA[C/T]CCTGACCCCCTCGGG | 50807 |
| rs377158161 | in-del | -/AC | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299291 | GGGAAACTGAAAAAA[-/AC]AGTTACTTATGTTTC | 50807 |
| rs377161273 | in-del | -/GTAAATACAGCAGCACCTCG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130234734 | TACAGCAGCACCTCG[-/GTAAATACAGCAGCACCTCG]TGGCTGTAAAGCAAG | 50807 |
| rs377164325 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130059999 | AAGAGGATCACCTGA[A/G]CCTAGGAGACTGAGG | 50807 |
| rs377184299 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130059239 | GCATGATTACGCTCA[C/T]TGCAGCCTCGATCTC | 50807 |
| rs377193540 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130074260 | AAATTGGCTGGGATT[C/T]GCTACAGAATTACTG | 50807 |
| rs377197989 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130434122 | GGAGTTCGAGACCAA[C/T]TTGGGCAACACAGCA | 50807 |
| rs377210674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434524 | AATGACACATATTAA[A/C]GAGCAATACATAATA | 50807 |
| rs377215465 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208833 | GACTTGACTCAACTT[G/T]GGAAAGTGTGTCTGC | 50807 |
| rs377243179 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130438516 | TGTGCTAGGAAATGG[A/G]CTGGGGGCAGACTCT | 50807 |
| rs377251281 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077420 | ACCAGGAGGCCTGCA[G/T]GCCTGAGAAGCAGCA | 50807 |
| rs377253873 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130393664 | GGGAGGCTGAGGCAT[A/G]AGAATCACTTGAACC | 50807 |
| rs377254112 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130208267 | TTTACTAGAATTCCC[C/T]CCATTTTTGCATGCA | 50807 |
| rs377255281 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108150 | ACAGCACGCTACTTT[C/T]GTGCAGGTTATCTGC | 50807 |
| rs377277087 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130273599 | AGGATCTTGGTATCT[A/G]CTTCTCTGGGTATCT | 50807 |
| rs377290860 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130338606 | TGTGGAATTTTTTCC[A/G]TTTCTTTTATTAACA | 50807 |
| rs377300005 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130352923 | AATGCCAGACCCAAA[C/T]TTGATTTCCAGTTTC | 50807 |
| rs377318588 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130270797 | TACAGATTTTAGTCC[A/G]CTGTTTCTCTCTACC | 50807 |
| rs377318972 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216025 | GAAAGGAAAAAGGAA[A/T]GGAAAGGAAAAAGGA | 50807 |
| rs377320798 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130091155 | TCATTCTCAAGTGAT[-/T]CCTGAATATTCACTG | 50807 |
| rs377322504 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130059302 | CCAAGTAGCTGGGAT[C/T]GCAGGCATGTACCAC | 50807 |
| rs377326199 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224559 | TACACACACATACAG[A/C]CACACAAATATAGGT | 50807 |
| rs377327163 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130202264 | ATTACATTTGTGATG[C/T]CAGCTGCTGCCAGGA | 50807 |
| rs377335721 | in-del | -/AAAC | 0.00319233 | 0.0398243 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199839 | TCAACAAAGTAACAA[-/AAAC]AAACAAACAAACAGT | 50807 |
| rs377341560 | snp | A/C/T | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130221704 | TAATTTGTCTTTTGT[A/C/T]CATATAATTTGCAGA | 50807 |
| rs377359300 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130135289 | TAAGCCTAGGAGTTC[A/G]AGACCAGCTTCAGCA | 50807 |
| rs377361416 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130078834 | TCGCTCTCCTCACCT[A/G]CAAAACTGAGGATAA | 50807 |
| rs377367871 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130173286 | CCATAAAAAGCAAAG[A/G]GTGACATGCTGTCAT | 50807 |
| rs377378639 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128119 | CATAAGAGGAAAAAA[C/G]TCTTTATAAGAGCAT | 50807 |
| rs377386876 | snp | A/C/G | 0.000230716 | 0.0107381 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079856 | AGAATTCTGTCCATT[A/C/G]CATCAATGGATCCAA | 50807 |
| rs377390432 | in-del | -/GT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130233013 | TGTTTTACTCATTTA[-/GT]CATTTTTAAAGAATT | 50807 |
| rs377390444 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400541 | CGCCTGTAATCCAGC[A/C]CTTTGGGAGGCCGAG | 50807 |
| rs377394844 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130306329 | ACTTCTATTTAGCAA[C/G]TCACTGTAAATGCAC | 50807 |
| rs377418394 | snp | A/T | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297127 | AATAATAATCTAATT[A/T]AAGCATAGTTACCAT | 50807 |
| rs377430668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244526 | AAACCTAACTAGTCT[A/G]AAAATATGTCTCATC | 50807 |
| rs377447337 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130300582 | TAAGAGTTTCTAGCA[C/T]GATTCTAACACACAG | 50807 |
| rs377448540 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229764 | CCCAAAATAGGCTGG[C/G]CGTGCTGGCTCACAC | 50807 |
| rs377458853 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130136518 | TCCCAAGTCTACATC[C/T]GTGCTTCTTAACCAC | 50807 |
| rs377463752 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130175156 | TTTCATTGAGGTTTT[C/G]ATTTGTACTTAACAC | 50807 |
| rs377466521 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130154890 | TACTTTCTTCTAGAA[A/G]TACTGGCCAGGGAAA | 50807 |
| rs377493886 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428490 | CCACCACCATCTTCA[C/T]CACCATCACCATCAC | 50807 |
| rs377495622 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130135778 | TAACTAGGGGTTTTT[A/G]GCTTTTTGAAGTCAT | 50807 |
| rs377496997 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130398667 | TATAGCACTTACCAT[-/G]TACCAGGCACTGTTC | 50807 |
| rs377507496 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387409 | AGCATGGTGGCGCTC[A/G]CCTGTAATCCCACTT | 50807 |
| rs377509961 | snp | A/G | 3.3145e-05 | 0.0040708 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134250 | TGTAAACAGAGAGGT[A/G]CTTTTTCAATCCAAG | 50807 |
| rs377520332 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130245582 | GCTATCAACTTCCCA[A/G]GCCAAAGAAAAGGTA | 50807 |
| rs377537247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169247 | TTATAAAACTAATTA[C/T]GGCATTTTATAAAGA | 50807 |
| rs377539037 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130244891 | AGGAAGGAATGGGAG[C/T]AAGGGTGCAGACAGG | 50807 |
| rs377554978 | in-del | -/ATG | 0.0130921 | 0.0798413 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098405 | CTGGAGTGCAGTGGC[-/ATG]ATCTTAGCTCACTGC | 50807 |
| rs377557464 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130330704 | TTTCCTTTCCCAGTT[G/T]AAATGTGTGTAGGTA | 50807 |
| rs377559678 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130312728 | TGAACTGATCTTTCT[A/G]ATTCTAAAGCCCATG | 50807 |
| rs377570614 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130371548 | GCCAGTGAGATGTAA[C/G]CAGAAATGCTATGTA | 50807 |
| rs377571025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278644 | ACTGGGACATACGAT[A/G]AAACAGTCGAGAGAC | 50807 |
| rs377572616 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130261928 | ATATCATATATATAT[A/C]ATAAACAGAATGAAC | 50807 |
| rs377575832 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130279618 | ACTAACCTCTTTCAG[C/G]TTTAGTTCCTTCATC | 50807 |
| rs377600620 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130196595 | TGGTACTTCCAGGAC[A/T]CCTACATGCACACAA | 50807 |
| rs377620406 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081623 | CTCACTACACTGCAC[A/G]TCTGCTCAATAGCAC | 50807 |
| rs377622334 | snp | C/G/T | 0.000216663 | 0.0104061 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130061020 | CTGAAAGATTTCGGG[C/G/T]GGGATGGTGGCTTTG | 50807 |
| rs377628880 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130113229 | CAAGGCAGCTGCCTG[C/T]CTCTCCCCACCCAGC | 50807 |
| rs377634508 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130407747 | TGCAGGAATCGGGGA[A/C]ATAAATCATTTGGTA | 50807 |
| rs377668252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055837 | ACAGAGTCAACCAGG[C/T]CTGCCCAGCTCTCCT | 50807 |
| rs377673761 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130230095 | ACAAACAAACAAACA[A/C]ACAAACAAACACCAA | 50807 |
| rs377708431 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130333198 | CCTAGTCCAAATCAG[C/T]TGGATTTAAAAGGCT | 50807 |
| rs377708571 | in-del | -/GATT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130113888 | TGGGCTCAGGTGATT[-/GATT]CTCCCACCTCTGCCT | 50807 |
| rs377709714 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130121739 | CAGTGAGCAAAGATC[A/G]CATCACTGCACTCCA | 50807 |
| rs377713045 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130104613 | CGTGGCAAAACTGCT[C/G]GCAAGTATACCCTTT | 50807 |
| rs377718141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409211 | AGGTTGTAGTGAGCC[A/G]AGATTGCGCCACTGC | 50807 |
| rs377719005 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130064435 | ACTGCCTTTAACAGA[C/T]GGGGACACTGAGGAA | 50807 |
| rs377722646 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130390029 | GTTGTTAAAATGCAG[A/G]TTCCTTGACCCTACT | 50807 |
| rs377724830 | in-del | -/CAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130132400 | CTATACCCATAACAA[-/CAA]GTCATCAATCACTTC | 50807 |
| rs377731752 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130431761 | TAGCAGAGTATGCAG[C/T]ACAACAGCTGGCAAA | 50807 |
| rs377751105 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130421088 | CCATCCCTTACTAGC[G/T]GTGTGACCTTGGGCA | 50807 |
| rs386360989 | in-del | -/A | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081597 | AGGGCTGAAAAAAAA[-/A]CTAACTGATCCTCAC | 50807 |
| rs386414003 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130081591 | GAGGGCAGGGCTGAA[-/A]AAAAAACTAACTGAT | 50807 |
| rs386414004 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130081596 | CAGGGCTGAAAAAAA[-/A]ACTAACTGATCCTCA | 50807 |
| rs386730004 | multinucleotide-polymorphism | CTT/TTC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130066614 | CTTCCTTCCTTGTTT[CTT/TTC]TTTCTTTCATTCATT | 50807 |
| rs386730005 | in-del | ATT/TCAGCCTCAGC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070141 | TCCCGGGTTCACGCC[ATT/TCAGCCTCAGC]CTCCTGCCTCAGCCT | 50807 |
| rs386730006 | multinucleotide-polymorphism | CAC/GAG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130074484 | ACACACACACACACA[CAC/GAG]AGAGAGAACGAGAGT | 50807 |
| rs386730007 | multinucleotide-polymorphism | GA/TG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130093288 | GTGCCAGGTATTCCA[GA/TG]CTGGGCACTTTCACT | 50807 |
| rs386730008 | multinucleotide-polymorphism | CA/TG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130133356 | ACCTGGTCAGGTGAG[CA/TG]CAAAACTCCAACCCA | 50807 |
| rs386730009 | in-del | GGGTG/TC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130143497 | CAATATACACAGATG[GGGTG/TC]TTCATTTTACACACC | 50807 |
| rs386730010 | multinucleotide-polymorphism | AT/GC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130158153 | ATGTACATGTCTCAG[AT/GC]TAAGCCAAGGAGTAC | 50807 |
| rs386730011 | in-del | A/TTAT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130163350 | ACGTTCCTTATATAT[A/TTAT]TACTAGCTTAAGTAA | 50807 |
| rs386730012 | multinucleotide-polymorphism | CA/TG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130244152 | CCCCAACAGGTAGCA[CA/TG]GTATCAGACCTATTA | 50807 |
| rs386730013 | multinucleotide-polymorphism | ATC/GTG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130245547 | CTAAGGATTTAGTCC[ATC/GTG]CAAGAAAACACCACC | 50807 |
| rs386730014 | in-del | A/CAAAAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130267102 | AGTGAGACTCTGTCT[A/CAAAAC]AAACAAACAAACAAA | 50807 |
| rs386730015 | in-del | CTGCTGAAATCTGCTTCTCTGCCAGATCCATGGCTGTCCCACA/GACTTG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130279319 | AGTCACCCACACCTT[lengthTooLong]TGGAGTCTTGAATAT | 50807 |
| rs386730016 | in-del | AC/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130312461 | AGGAGGGGAAAAAAA[AC/T]CCATTAGGAATTCTG | 50807 |
| rs386730017 | in-del | CA/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130320685 | ATGTAGCTTTCCACA[CA/T]ACCAGGAAGAAGTAT | 50807 |
| rs386730018 | in-del | AGGACA/CC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130389359 | GGCTGGTTAAAGTCC[AGGACA/CC]AGGGAAAAAATGGCT | 50807 |
| rs386730019 | multinucleotide-polymorphism | CGC/TGG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130392785 | TGTGCAGAGATCAGA[CGC/TGG]TGAGAGAAGGAGGTG | 50807 |
| rs386730020 | multinucleotide-polymorphism | CA/GT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130395452 | ATGACTGCTGTCCTT[CA/GT]AAGAGAGAAGAGAGG | 50807 |
| rs386730021 | multinucleotide-polymorphism | AC/TT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130396119 | CACAGACCCTGGCAC[AC/TT]AGTAGGTCGTCAGAA | 50807 |
| rs386730023 | multinucleotide-polymorphism | AC/GT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130408441 | TCTTCTTTTTTGGAC[AC/GT]TGGCGCTCCTGGTTC | 50807 |
| rs386730024 | multinucleotide-polymorphism | CG/TA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130423992 | TTCTAAAATTGACTG[CG/TA]GCGATGGCTGCACAA | 50807 |
| rs386730025 | multinucleotide-polymorphism | GC/TT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130426124 | GTTTCTAATGGTTTA[GC/TT]ACCATCCCCCTAGTG | 50807 |
| rs386730026 | in-del | A/CT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130437621 | ATTTAGATAGATAGA[A/CT]AACTACAATGAAATA | 50807 |
| rs386730028 | in-del | ATT/TTAAA | | | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444331 | TGAGCCTCAGTTTCC[ATT/TTAAA]TATGAAATGGATGTT | 50807 |
| rs397701086 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130115780 | AATTTAAATGCTGAA[-/A]ACATCCCAATATTAT | 50807 |
| rs397718112 | in-del | -/T | 0.0016 | 0.028239 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169103 | ATTTACCACCAGTAT[-/T]AAAAAAAAAAGAGTA | 50807 |
| rs397733859 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130113638 | GGTAGTTAACTGCTT[-/T]ATAAGGAAAACTCAG | 50807 |
| rs397748124 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130113637 | AGGTAGTTAACTGCT[-/T]TATAAGGAAAACTCA | 50807 |
| rs397751789 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130090299 | AGGATTAAAACTTAA[-/A]GAGAAATTTGGAAAG | 50807 |
| rs397778920 | in-del | -/AT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130218864 | TATATATATATATAT[-/AT]GCATATGTATGTATG | 50807 |
| rs397793523 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130055551 | AAAAAAAAAAAAAAA[-/A]GGCTGCTATGTACTA | 50807 |
| rs397834435 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130262414 | aaaaaaaaaaaaaaa[A/G]agagagagagagaga | 50807 |
| rs397892008 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130149028 | TTTTTTTTTTTTTTT[-/T]GTAGAGATAGGGTTT | 50807 |
| rs397892104 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130073405 | CAAAAAAAAAAAAAA[-/A]CAAATACAAATGTGG | 50807 |
| rs397892137 | in-del | -/T | | | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082519 | TTTTTTTTTTTTTTT[-/T]AAGAGACAAGTTCTT | 50807 |
| rs397892211 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130417076 | ATACACACATGCAAA[-/A]GTGCAACCCATGTAC | 50807 |
| rs397892398 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130350079 | TGGCTTCTAATGAAA[-/G]GCTGCTAGCCTAACA | 50807 |
| rs397892569 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130414788 | TTGAGACAGGGTCTT[-/T]CCTCTGTTGCCCAGA | 50807 |
| rs397892645 | in-del | -/A/G | 1.66535e-05 | 0.00288556 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115781 | ATTTAAATGCTGAAA[-/A/G]CATCCCAATATTATA | 50807 |
| rs397949496 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130196358 | AAAAAAAAAAAAAAA[-/A]GTTGTAGGTCACACT | 50807 |
| rs397950322 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130288325 | CACTCCTTAGGGTAA[-/A]TTCCATTCTTTTACA | 50807 |
| rs397963972 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130139935 | TTAAAAAAAAAAAAA[-/A]CAACAAAAAAACACC | 50807 |
| rs397967421 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130195402 | AAAAAAAAAAAAAAA[-/A]GATGAGCTGGGCATG | 50807 |
| rs397974926 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130182850 | AAAAAAAAAAAAAAA[-/A]CCCAACTGAGCAAAA | 50807 |
| rs398009908 | in-del | -/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170204 | TATCTTTTTTTTTTT[-/T]GAGATGGAGTCTCTC | 50807 |
| rs398009909 | in-del | -/AAT | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171443 | GGCAGGAGAGAGAAT[-/AAT]GCCAGCAGGAGAAAT | 50807 |
| rs398009910 | in-del | -/AAAGG | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130216072 | AGGAAAAAGGAAAGG[-/AAAGG]GAAAAGGAAGAAAGA | 50807 |
| rs398009912 | in-del | -/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332927 | GAAGTTTTTTTTTTT[-/T]AAAGGGAAAATAATA | 50807 |
| rs398009913 | in-del | -/T/TTA | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352230 | TTTTTTTTTTTTTTT[-/T/TTA]AAGACTACAATCTCC | 50807 |
| rs398009915 | in-del | -/A | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374056 | AAAAAAAAAAAAAAA[-/A]GCAGCCATGTCCAAG | 50807 |
| rs398009917 | in-del | -/A | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381552 | AGTTTGAGCACCAAA[-/A]GAGAATGGAGAATTG | 50807 |
| rs398047411 | in-del | -/T | 0.5 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080495 | TTTTTTTTTTTTTTT[-/T]GAGACAGTCTCACTC | 50807 |
| rs398068270 | in-del | -/AA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130074125 | GTTCTTAAAAAAAAA[-/AA]GGGGGCAATTGTGAG | 50807 |
| rs398068271 | in-del | -/AA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130135535 | AAACAAAACAAAAAA[-/AA]GAACATGCCATGGGT | 50807 |
| rs398068272 | in-del | -/CA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130286389 | TTCTACTTCCATTCA[-/CA]GTTTAAGTCCATCAC | 50807 |
| rs398073394 | in-del | -/AACA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130123612 | ACAAACAAACAAACA[-/AACA]CTGTAAAAAACTAAA | 50807 |
| rs398087011 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130219207 | ATGTCTTTTTTTTTT[-/T]TAACATACTGTATTA | 50807 |
| rs398096149 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130247233 | CAGAGTCTGATTTTG[-/G]TTCATTCTTGTCTCT | 50807 |
| rs398113025 | in-del | -/AC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130188693 | AGCCGAGATCACCAC[-/AC]TGCATTCCAGCCTGA | 50807 |
| rs398113026 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130209564 | TAAAAAAAAAAAAAA[-/A]GAAAGGCTATTTTCA | 50807 |
| rs398113027 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130405283 | TTATAGATGAAAAAA[-/A]TCATAACTCACAAGA | 50807 |
| rs527240114 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130330968 | AGATGATATGGTGTA[C/T]CAAAAATGGGCTTTG | 50807 |
| rs527244536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136494 | ACAGATATAGTGGCA[C/T]ATCTGCATTCCCAAG | 50807 |
| rs527244643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129583 | TCAACAGACAATACA[A/G]AGGTTCAGAACTGAG | 50807 |
| rs527248224 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130353450 | GGAACTTAGGCACCT[G/T]TTTTAATCAGACCAA | 50807 |
| rs527253719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227588 | TTTAATCATCAATCC[A/G]TGTCAGTAAAACATT | 50807 |
| rs527254461 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130420699 | AGGAGTTCGAGACTA[C/G]CCTGGCCAACATGGA | 50807 |
| rs527254711 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130254925 | AAAATAATACCTTAT[A/G]TCTTGCCATTTTTAC | 50807 |
| rs527269789 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321229 | ACAGAGACAGGTGAC[A/T]GCAAAGAAGCAGGCC | 50807 |
| rs527271264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178048 | TCTAACCCAAGCTTT[A/G]TGCTTTTGACATAAT | 50807 |
| rs527272446 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130168721 | AAGGAACACTCAAAT[G/T]TGATGCTAACTGAAT | 50807 |
| rs527272520 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ASAP1 | GRCh38.p7 | 8:130052022 | TGTCATCTATATACC[C/T]GAAAGCACAGCCAGA | 50807 |
| rs527273948 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130268002 | TTCCCTCTGTCCAAG[A/C]ATCTCACTTCCATAC | 50807 |
| rs527301239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226851 | AAATACACAATACAC[C/T]TTGGTTTACTGATGG | 50807 |
| rs527303083 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082922 | TAGATATCAAATCTT[A/G]TACTTTCCCACTTAA | 50807 |
| rs527304461 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407108 | TGGTTGGCTCCCCGT[A/G]ACTGATGAATGCATG | 50807 |
| rs527304595 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130351484 | TGTTGTTATAAAGGA[A/G]TATCTGAGACTGGGT | 50807 |
| rs527328676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130185030 | ACCACAGAAAATGTC[C/T]AGCCTTCTCCATTAT | 50807 |
| rs527330456 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090095 | ATAAAAAATGCTCCC[A/T]GACCCATCAACAATG | 50807 |
| rs527332241 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130401793 | TTCCAGTGCTTGTGT[C/T]TGATAAAATTTTGCA | 50807 |
| rs527337187 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401117 | GAACTCCTAACCTGA[A/G]GTGATTCTCCCGCCT | 50807 |
| rs527363293 | in-del | -/AAAC | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084772 | AGTAGATATGTAATA[-/AAAC]AAACAAACAACAAGA | 50807 |
| rs527369344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130894 | AAAAAGCCACGCTCA[C/T]GCCTGTAAGCCCAGC | 50807 |
| rs527378660 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130057216 | CTGATTCCCAGCCTG[A/G]GGACAGTGTGGAATG | 50807 |
| rs527380701 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130099430 | CGTGATCCGCCCATC[A/G]TGGCCTCCAAAAGTG | 50807 |
| rs527382428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364096 | CTAGTCCCAAATGTA[C/T]TTAATTCAATTTAAA | 50807 |
| rs527382618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130410 | TAAATAAAGAAGTTT[C/G]TCATGATAATCAGAA | 50807 |
| rs527396267 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130389030 | CTCACAGGATTGTTG[-/T]TAAGGATTGAATGAG | 50807 |
| rs527401147 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058885 | GGCCGTGCGGGTGGG[A/T]TGGAGAAGCCTGGCA | 50807 |
| rs527407702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084719 | TGTGCCTAATTTCCT[C/T]ATCAGTAACTGGGAC | 50807 |
| rs527416749 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130233075 | TATACTATACTTGTT[C/T]GTGACTGCAGAAACC | 50807 |
| rs527430691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349084 | TGGCCTGGGTCAAAG[C/T]GGGCAGCACTGGTCA | 50807 |
| rs527441533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301780 | ACGACTGTCTTTCCA[C/T]GTCAACAGATATGCA | 50807 |
| rs527482651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164034 | TCTACTACAGAAGCC[C/T]AAAATTTCTAATGCA | 50807 |
| rs527483789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164528 | CCTGGGAGGCAGAGG[C/T]TGCAGTGAGCGAGAT | 50807 |
| rs527484666 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342746 | TAAAAAAGATGCCAA[C/G]TCTCAGAAACAAGTT | 50807 |
| rs527496226 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171370 | ACTCACAGTTCCACA[C/T]GGCTAGGGAGACCTC | 50807 |
| rs527504242 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130209977 | GAAAACTTGAATTTG[C/T]CACGAGCTGACAGTT | 50807 |
| rs527511330 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118074 | GAAAAAGCTTGCCAA[A/T]TCCCGATCTAGGCCA | 50807 |
| rs527519056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085359 | CACCTTACTTTGCTA[A/C]CTTTATTCTCCCTTT | 50807 |
| rs527534703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111561 | TTTGAGATGATTACA[A/G]AAGAAGTACTAGGCG | 50807 |
| rs527555638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391603 | GCACCTAGGCAGGTA[C/T]TAGGGGACAGGAGAG | 50807 |
| rs527556545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180949 | ATACCAACAGCAGAT[C/T]CTAATACAAACTATG | 50807 |
| rs527566781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130433533 | TGGTGCCAAATTATT[A/G]ACAGTTACATATCTT | 50807 |
| rs527568390 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130426072 | TTCCCAGTGTCGGAG[A/G]AGGGGCCTTGTGGGA | 50807 |
| rs527572413 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130306532 | CACATGATCAATTGG[A/T]CAAAGGTCTAAGTAG | 50807 |
| rs527574819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130200703 | GTCTTTTTCTCCCTA[C/T]ATTTTCTGAGTTTTC | 50807 |
| rs527584295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130207560 | AAATGAACACAAGGA[A/G]GGATTACTAAACCCT | 50807 |
| rs527585451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385578 | GTTTTCTCAGTTACC[A/G]GGTGGGTAGGAATCT | 50807 |
| rs527586527 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341761 | TCACCAATGGTTCAC[A/C/G]AACAGGCTTTAGGGA | 50807 |
| rs527607438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130294956 | GTTGTTGGATTAACA[A/G]CGAGAGGAATAATAA | 50807 |
| rs527627505 | in-del | -/AAAAC | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415480 | ACCCTGTCTCTTAAA[-/AAAAC]AAAACAAAACAAAAC | 50807 |
| rs527629386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343485 | CTTTTGGAGAAACTT[A/G]AATCGAGACCTCAAA | 50807 |
| rs527643439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130212428 | CAGTACTTCTGCTGA[A/G]GGAAACAGCACAACC | 50807 |
| rs527647091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307837 | AAATCAGGAATTTCT[A/G]GCTCCAAATTTCTTA | 50807 |
| rs527648043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299449 | ATTGTGTCTACTGCC[A/G]TCTTGGTTGTATGCC | 50807 |
| rs527648648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354824 | TGAACCCCTGAGCCA[C/T]GTGTGACCCTTCGCC | 50807 |
| rs527659847 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431145 | CATCCCCCCTCCAAA[G/T]GATCCCCATGCCAGC | 50807 |
| rs527674735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259682 | AGCTATGCCCCACTG[C/T]CTCACATGACTTCCA | 50807 |
| rs527677691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394191 | CCGGTGAGCTGGGCG[G/T]AACAGAGCCATATTT | 50807 |
| rs527678127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399910 | CCAAAACCTCTGCCT[C/T]GCGGGTTCAAGAGAT | 50807 |
| rs527683887 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130225935 | CCAGGCTGTAATGCC[A/G]CGGCATGGTCATAGC | 50807 |
| rs527688139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348108 | CTTACAGCCCACTGC[A/G]TGCTGGGTGCTATAC | 50807 |
| rs527709679 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428850 | TTTTCTAGGGCTGTC[-/A]TTAAAAAGTACCAAA | 50807 |
| rs527710599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122854 | ACAGGACATAAAAAC[A/C]CATGTTGTTATGACA | 50807 |
| rs527712158 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259010 | AGCATGTGTCCATTT[C/G]CTTATGGTATTTTAA | 50807 |
| rs527714866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394504 | ATTTTAATGTCGTCC[C/T]GGTCCTGTGGTCCTG | 50807 |
| rs527725603 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083107 | GGGCTGCAAAGGCCC[G/T]CTGGCTCTGCTGTGG | 50807 |
| rs527725819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130075886 | TCCTTTGCCACCCAC[C/T]TGCTGGGGACTTTCT | 50807 |
| rs527739228 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109636 | ATGGTTCTATCAGCT[A/C]AACAGAAGGAAATGA | 50807 |
| rs527741943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253437 | TTTTTCCCCAAAGTT[C/T]CCAACAGATACATAG | 50807 |
| rs527742040 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130276648 | TGGATTTGTGATTGG[G/T]ATTTGCAGGCCAAAC | 50807 |
| rs527742589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246258 | TATGGGCCTCCTATC[A/G]TATCAACAACCTTTT | 50807 |
| rs527743077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389818 | CAATCCTTCCACCTC[A/G]GCCTCCCAACTACCT | 50807 |
| rs527771734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293344 | AATAAGTGGTTGCCC[C/T]ACCAGGTAAGACTGG | 50807 |
| rs527771838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431529 | ATTTCCTTCCCTTCC[C/T]TCCATTCTTTACTGG | 50807 |
| rs527774663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197955 | TTCTTGTTCAGCCTG[C/T]TGCCACTGGACTCTC | 50807 |
| rs527778196 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205497 | CTGTATTGACAAACA[C/G]AAAATTCAAATAATC | 50807 |
| rs527783181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383738 | AACAGAAGACAGAGG[C/T]CTGACCACACCAGTG | 50807 |
| rs527787037 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130360327 | CTATGGCATCTTGGG[C/G]CCTCAGCTGCCTCAC | 50807 |
| rs527802676 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070143 | CCGGGTTCACGCCAT[C/T]CTCCTGCCTCAGCCT | 50807 |
| rs527806202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292863 | CTGTAAAGCAGAGAT[A/G]AGATGATCTCACAAG | 50807 |
| rs527807489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213007 | AAAGTGAACTGTCAG[C/T]CTTGTTTTGCTTCCT | 50807 |
| rs527808535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299960 | TAAGGGATGGAGGGA[C/T]TGTGAAATGAGCCAC | 50807 |
| rs527816190 | in-del | -/CAG | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130298228 | ATGAGAAACCTGTAA[-/CAG]TGGTGTCCATATCCA | 50807 |
| rs527825780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341344 | GTCTAAGCGCTTGAG[C/T]TGACTTAACCAAGCA | 50807 |
| rs527828897 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424995 | GAGATTCCGTCTCAA[G/T]AAAAATAAATAAATA | 50807 |
| rs527834813 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130242236 | CACCTCTGAAACAAA[C/T]ACTCCTATACCAAAG | 50807 |
| rs527837500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149584 | CTGAATCACTTTGAT[A/G]AGAACAATTTGCAAA | 50807 |
| rs527837884 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130439050 | TTAAAATAGGGAGAG[A/T]AGCCTAGATTATACA | 50807 |
| rs527846845 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425439 | TGAGAATCCTTTGAA[C/G]CCGTGAGGCAGAGGT | 50807 |
| rs527867700 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334652 | GAAAAAAACACAAGA[G/T]GAATGAAAAGGTCTA | 50807 |
| rs527868295 | in-del | -/CAT | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428669 | TCACCATCCCCCCAC[-/CAT]CATCATCACCATCAG | 50807 |
| rs527869705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239988 | TCTGCTTCTGGAGGA[C/G]AATAACCTATCGGTT | 50807 |
| rs527872366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058212 | TCACCCTTGAAGGGC[A/G]GGAAGAAGAGTGTCT | 50807 |
| rs527882219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411774 | GGGCCTGACTCAGCG[G/T]CTTCCCAGCAAGGCC | 50807 |
| rs527893313 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148896 | CTGGAGTGCAGTGGC[A/G]CAATCTTGGCTCACT | 50807 |
| rs527902342 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130265421 | ACTAAAATTTTTAAA[A/C]AAGTAACAGGGTGTG | 50807 |
| rs527904632 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155635 | TACAGGCATGAGCCA[A/C]TGCGCCCAGCCAGCA | 50807 |
| rs527906217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335416 | AAACTGACAAATAGT[G/T]AGCAACATAGCCAGG | 50807 |
| rs527909002 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063890 | GCTCACATTCCACGA[C/G]AGGGTGACAAGTAAA | 50807 |
| rs527914250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130198761 | ATTAAGGTTTTTACT[A/G]ACTCCAAAGGCCACT | 50807 |
| rs527917687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377633 | CCTCCTTCTCCTGCT[A/G]ACCTGCTCCAGACAC | 50807 |
| rs527919635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130103227 | AATAGTCTCCTACAA[C/T]GACCTTTGTATTTTT | 50807 |
| rs527934280 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130184210 | AAAATGTAAACACTG[A/T]AACTAGTTTAATAAA | 50807 |
| rs527944854 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059377 | CTGTATGTTGCCCAG[C/G]CTGGTCATGAATCCT | 50807 |
| rs527953397 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ASAP1 | GRCh38.p7 | 8:130051658 | GCCTCTGAGCCTCAT[C/T]TGTCAGCTCTGTAAA | 50807 |
| rs527956137 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143415 | GTGAGATGTCTGTTT[G/T]TTTTTTTTTTGACAT | 50807 |
| rs527963601 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130311924 | ATTTGAATACGATCC[A/C]TAATGATTTATTAAT | 50807 |
| rs527972471 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097077 | GTTGCAGTGAGCCGA[A/G]ATCATGCCACTGCAC | 50807 |
| rs527988266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287077 | GAGCATTTTTAGTAA[C/T]GGGGCCAGAAGGAAC | 50807 |
| rs528002329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370863 | TATAGAGACAGAAAG[C/G]AGATTAGTGGTTATC | 50807 |
| rs528028864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130142832 | ACTCTGGCAATCTAC[C/T]GGAGAAAGCAGAGTG | 50807 |
| rs528041080 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130327024 | GATGAATGCCCCCAG[A/G]AGGCAGCATCTGAGT | 50807 |
| rs528058220 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339971 | CACAGAGCCAGGCTC[A/T]CCTTGCCTAAATTCT | 50807 |
| rs528058327 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237809 | CAAGTTTAAAATGGG[G/T]CATAGTCAATATACT | 50807 |
| rs528084627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062662 | ACCTTCAAAATACCC[C/G]ACCCTCTTCACCTGC | 50807 |
| rs528096886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417218 | CAGAAAACAACCCAC[A/G]TACAACTGCACACAT | 50807 |
| rs528105135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130196483 | CCCAACAAGCCACCC[C/T]GTCCTGCTGGAGCAG | 50807 |
| rs528109475 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251900 | TGGAGAGGCTTTGGA[C/G]AAATGGCCACAAACC | 50807 |
| rs528129202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325638 | GTTTAGTGAGACACT[A/G]ATACGTAAACAACTA | 50807 |
| rs528139732 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284452 | GTAACTCAACTTTTC[A/T]CTAAAGGTGAGGGAA | 50807 |
| rs528142847 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130145880 | GGGGTCTCACTCTGT[C/T]GCCCAGGGTGGGGTA | 50807 |
| rs528146299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189939 | TAAACCTGTGGGCCA[C/T]TTGTAGGTCTTCTTT | 50807 |
| rs528151075 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376187 | GGAAGCACAGATAGG[A/G]CCTCCTAACCACAAG | 50807 |
| rs528155642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057310 | TGGCTGAGGGACCAC[A/G]GGCAACATGCTCAAC | 50807 |
| rs528162676 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094706 | GCGAGGCACTCACCC[A/C]ATCAAATGATGCTGC | 50807 |
| rs528166880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141168 | CAGGAGAGAAAAAAG[A/G]AAACAAAACAGGAGA | 50807 |
| rs528176430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056635 | CTGTCTAGGCCTGAA[A/G]GAAGAAAAGTCAAAG | 50807 |
| rs528179259 | in-del | -/GACA | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127710 | TAGTATTTTGGCAGT[-/GACA]GACACCTAGGAGAGC | 50807 |
| rs528203915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285185 | CCTACAGCAAGCATG[A/G]AAAAAAAGTATTAGT | 50807 |
| rs528207026 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197128 | AGTGTCAGTGGATCG[A/C]GACAGAACTGACACC | 50807 |
| rs528212027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189434 | TATCTTTCTGTACTT[A/G]GCTTATTTCACCTAA | 50807 |
| rs528223617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417597 | CATGAGACAGAAAAC[A/C]CCACAAGTCCTGGCT | 50807 |
| rs528227831 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130304551 | CGCTGTCCAATTTAC[A/G]TTTACACAACCAATA | 50807 |
| rs528229847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148035 | AAATTCTTAGAACAC[C/T]TGCATTATCTTCATG | 50807 |
| rs528239466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133971 | TTGCCCTCGAAAAGC[C/T]CTTGGTCTCTAAAGG | 50807 |
| rs528241409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130232494 | GAGAATTTTCCATTG[A/G]TCTAAGTAGTTCACA | 50807 |
| rs528249269 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409662 | TGACAATGCCGAGGC[A/T]GCTGGACCTTAGCTT | 50807 |
| rs528249590 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130439665 | AGTTAAAAGCATCTT[C/T]GAGGAGATAAAGACA | 50807 |
| rs528253275 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130133370 | GTGCAAAACTCCAAC[C/G]CAGGGGCCGGGCGCG | 50807 |
| rs528258510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175880 | AGAAAATAAGCTCTC[C/G]GTAAATGTTAGCTAT | 50807 |
| rs528277875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130326483 | GGTTTCAATACACAC[A/C]ACGAACAGACTGGAT | 50807 |
| rs528280261 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183161 | ACTCTTCGTAAAACC[C/T]TTTACAGAGACAAGA | 50807 |
| rs528286679 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130181327 | AGATTCATATACATT[C/G]TCTTAAATTTTGGTA | 50807 |
| rs528299368 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130250659 | ATAAGGAGAGAAAGA[C/T]CTAATTTGGCAGAGG | 50807 |
| rs528313419 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130415725 | CCCAGGAGGCGGAGG[C/T]TGCAGTGAGCCAAGA | 50807 |
| rs528314891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319981 | TATATAATGCATAGA[A/G]AAGTACATTTTAACA | 50807 |
| rs528315327 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130151992 | GTTGGGAGGATTAAC[C/T]GAAATAAAGTTTATG | 50807 |
| rs528317699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272885 | AGAATGGCTGGTTAA[C/T]GAGTACAAACATACA | 50807 |
| rs528329965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399501 | CCTATAATAGAAAAA[C/T]TTTGAAAATAAAAGT | 50807 |
| rs528338653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130265965 | TAACATCCATAGTGA[A/G]TAAGCAGTAAGCATG | 50807 |
| rs528341643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130182396 | CCTCAAACTATAGGG[C/T]TCTCTGTCTCCCTCA | 50807 |
| rs528370625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130089053 | ATGCCCTCAGAAGGA[A/G]TTCATGTACTAGGAA | 50807 |
| rs528372444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082416 | TAAGTTGCCCAGGCT[A/G]GTCTTGGACTCCTGA | 50807 |
| rs528381267 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128395 | TACAAGGAGACTGCA[A/T]TTCCGTGTGGGCATA | 50807 |
| rs528382330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219199 | GGTCTCACATGTCTT[C/T]TTTTTTTTTAACATA | 50807 |
| rs528392326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273412 | AGAAGGGGAAAGTAA[A/G]GAAGCAAAGTAGCAG | 50807 |
| rs528403898 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130399955 | CTCCCAAGTAGCTGG[A/G]ATTACAGGCATGTGC | 50807 |
| rs528413581 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130381404 | ATTGAAAGAAAAATT[A/T]TTAATGAGACAGAGT | 50807 |
| rs528431961 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130268319 | AGCAAGACTTTGCCT[C/G]TACAAAAATATTAAA | 50807 |
| rs528432552 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130252531 | AACAAGGCAGAAATG[A/G]TACATACTCTCAGTA | 50807 |
| rs528434175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086709 | CTCAGGAGACTGAGG[C/T]GGGAAGATAGCTTGA | 50807 |
| rs528445582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130230036 | GTTACTGCTCTCCAG[C/T]CTGGGCAACACAGTG | 50807 |
| rs528464280 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130432478 | TGTAGTGAACCCAGA[A/G]TCTTCTAGATGCCAT | 50807 |
| rs528465669 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324155 | AGTTTCTAATCAGGA[A/T]GATCTGGACGGTTCT | 50807 |
| rs528487083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100577 | CAGGCAATCTACCCA[C/T]CTCGGCCTCCCAACG | 50807 |
| rs528494401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318107 | TTTTTTATTTTTATT[A/C]TTTCCTGAGAGAGGG | 50807 |
| rs528494831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229467 | GAGGCAGCAAGATAT[A/C]GGTAAAGCCATAGAA | 50807 |
| rs528506295 | snp | G/T | 6.02367e-05 | 0.00548769 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237019 | AAAAAAGGGGGAAAA[G/T]ATATTAGAAGATTTG | 50807 |
| rs528510068 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130243460 | CTCTCTCTCTCTTTG[A/G]AGGAAGAAAGGAAAG | 50807 |
| rs528512377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188350 | GTAGGTTAGGCGACA[C/T]AATTATCACTACTTT | 50807 |
| rs528517619 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277422 | GAAGTTGAGAGGAAA[G/T]AACCAGAAAGTTCAG | 50807 |
| rs528524878 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409125 | AAATTAGCCAGGCAT[A/G]GTGGCAGGCGCCTGT | 50807 |
| rs528530070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318688 | CTCCTTTTACAGTTA[A/G]GTCCCTTTCCCAAGG | 50807 |
| rs528531923 | snp | A/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410076 | TGCATGCTATTTTCC[A/T]TTGGCTACAGCTTCC | 50807 |
| rs528533678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403681 | CCTCAGCCTCCCAAG[C/T]AGCTGGGATTACAGG | 50807 |
| rs528542798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087203 | ACAAATGTCGGGGAA[A/C]CAAAGAGGGGTATAG | 50807 |
| rs528551503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272133 | CACACCACTGCACTA[C/T]AGCCTAGGGGACAGA | 50807 |
| rs528558311 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384682 | AGATGGGGTTTCACC[-/A]TGTTGCCCAGGCTGA | 50807 |
| rs528562711 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130312625 | TTACAGGTGGGTACT[A/T]TTATAATTTCTATTT | 50807 |
| rs528566853 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139894 | AACAATCTTACCAAC[A/C]GATACAACCAAGAGT | 50807 |
| rs528581514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130441507 | GCAGGATCCAAATAC[C/G]GCTGAGACCTAGGTG | 50807 |
| rs528583008 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130271378 | CTGCACTGCTTGTAG[G/T]CCACACAGTTCCAAG | 50807 |
| rs528584168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130358244 | GAACCCCGGCGCGCA[A/G]CCCGCCACCCGCCGC | 50807 |
| rs528585608 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130304751 | CACCCTCTTTCCACC[G/T]CATACTCTCACAATC | 50807 |
| rs528586223 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130095821 | ATGGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTC | 50807 |
| rs528588267 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130383995 | TACGGTTCATGGTGA[A/G]GACTGCCCTTTGTAA | 50807 |
| rs528598433 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311880 | AATCTACTTTTAAGT[A/G]AACAAAAACAACTCA | 50807 |
| rs528609546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223739 | TACCATCCCACACTC[C/T]AGAGTCTCACTTCCT | 50807 |
| rs528612360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352112 | AGGTTTGTTTGCCTT[C/T]TGTTGTATTATCTTC | 50807 |
| rs528618417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217503 | TATATGTATATTATA[C/T]GTGTATATATGTGTA | 50807 |
| rs528620232 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130210178 | CAACTAAAACAATAA[A/C]TTGCAACAAAATGAA | 50807 |
| rs528632856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074374 | GGTGGAGGAGGCTGC[A/T]GGATACTATTCTGTG | 50807 |
| rs528635759 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081041 | GCTTATGCTCTGGCC[C/T]GTGAGACTTAAGACA | 50807 |
| rs528636409 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435335 | TTCTTCAAGCACATG[C/G]ATTTTCTTTCTTTCT | 50807 |
| rs528641135 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352621 | CTGATACTGGTTGTA[G/T]GACCTGGGCAGAATA | 50807 |
| rs528667834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217204 | CCTCCTCTGTTGTGG[C/T]GCACAGAGAAGCATG | 50807 |
| rs528679961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130346038 | GAGAGGTAGACTTAA[A/C]CGTATTTGGAAAACT | 50807 |
| rs528687193 | in-del | -/AAG | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130219714 | TGTGATCCATCCGTT[-/AAG]AAGACACATTCTTTC | 50807 |
| rs528692029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258050 | AAAAGATCAGCTTTT[C/T]CTATAGAAGGCCCTG | 50807 |
| rs528699860 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130191979 | TGAACAACAACTAAT[A/T]TTACACACCGGAAGG | 50807 |
| rs528713156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114221 | CTTGTGCGAACATCA[C/T]AGAGTATACTTACAC | 50807 |
| rs528713682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127606 | GTCCAGGCTGGGAGT[A/G]GTGGACAGTGATACA | 50807 |
| rs528717723 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257708 | AAAGCATTAATATAC[C/T]AAAATTCATTACATT | 50807 |
| rs528718999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080311 | TAAATTTCAAGTTCA[C/T]CAAGAGGCCTCATGC | 50807 |
| rs528724713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393115 | TTTGTTTTTCATCCT[C/T]CTGCCCCTAATTTGT | 50807 |
| rs528726361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264405 | TCTCAGTCAGCAAAG[A/G]CAGTCGTGCGTGCCA | 50807 |
| rs528747833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130429756 | CAGAAGGAGAACACC[C/T]CCACTCCCCCGCAAC | 50807 |
| rs528761345 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130167140 | CAAACTCCATCTCTA[C/T]AAAAAATACAAAAAT | 50807 |
| rs528770946 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350034 | TGAAGGCAAAGGTCT[C/G]GGTAGTGTTTGAACA | 50807 |
| rs528773918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204000 | TGTCCATATCTTTTG[C/T]GAGGAGGTACAGCAT | 50807 |
| rs528776376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130113509 | TATTATAATTTATTT[C/T]CTCTTAAAGTTGTTA | 50807 |
| rs528780463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130210944 | GCTTCTCTGACCTCA[A/G]TGAAACCCTGCCACT | 50807 |
| rs528795652 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121391 | CCCACTGGGTGACAG[C/T]AGCACCTGTCCAAGT | 50807 |
| rs528803032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339442 | TGAGTACATCGATGC[A/G]GTCAGGGAGGGGAAT | 50807 |
| rs528807417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430265 | TTTGCTAAGTGGATA[C/T]GAAGGACTCACCAAG | 50807 |
| rs528812543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068432 | GTAACTATGGAAACT[A/G]GAGGGTATAGTGCGA | 50807 |
| rs528819891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347009 | GGGCAGTGAAGAAGC[C/T]GTTCAATGGAAGTAA | 50807 |
| rs528842474 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130302280 | TGGAAACCAGCCAGG[A/G]CTGCTAAAAGAATAA | 50807 |
| rs528843619 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130063985 | GGGGAGGAGGAGAGT[A/G]ACCACCAAGGAGGGT | 50807 |
| rs528856401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165414 | CCCGTACTCCCTTCT[A/G]CCTGGGTCTTTTTAA | 50807 |
| rs528870907 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238233 | TTCCTCGGATTTCTG[A/G]GCTTGGAAACAAGGA | 50807 |
| rs528883770 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130156612 | TTATGCCTTGCATAT[C/T]CTTAGAGTGATAACA | 50807 |
| rs528885776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391715 | GTATGTCAGTGGCAA[C/T]AGATATCTAACAGGT | 50807 |
| rs528885903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262296 | GCTACTTGGGAGGCT[A/G]AGGCAGGACAATAGC | 50807 |
| rs528887132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130351162 | GAGGTAAAAAGATAA[C/T]TAATAGATGCCTTTC | 50807 |
| rs528892723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130172358 | TGACAGGTACACCAA[G/T]ATCCCAGAAATCACC | 50807 |
| rs528915263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396692 | ACACGTTTCCCGTCC[A/G]TGTGCAGCATGCATT | 50807 |
| rs528919742 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130186105 | CAAGTTCATGCACTG[C/T]TGTCTCTGGGCAGCG | 50807 |
| rs528920414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078605 | AACCTTTTATGAGTG[C/T]TTTTGGAGTGTCAGA | 50807 |
| rs528927969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392289 | GACTATCAGAGTGCT[C/T]GATACAGAGAAGCTG | 50807 |
| rs528935221 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086074 | TGTGCTGCTTGCCAG[A/C/G]AGAACCATGCTAAGT | 50807 |
| rs528941643 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130256392 | CGGGGAATACATCTG[C/G]AGAGGATCTGGGGGG | 50807 |
| rs528942901 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248932 | GCATTTCTTTTTTGT[G/T]GCTTTCTATTTTTTA | 50807 |
| rs528955361 | in-del | -/A | 0.42666 | 0.176893 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437105 | GCAAGATTTCATCTC[-/A]AAAAAAAAAAAAAAA | 50807 |
| rs528961203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208931 | TGCCATCCCCCTAAA[A/T]AAAAAGAGGTACAGA | 50807 |
| rs528969510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296438 | ATGCTTACTCCAGGG[A/C]AAAACTCTGTGGAGG | 50807 |
| rs528979102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269492 | CAGGAAAGAAACAAG[A/G]ATGTTAAACTTATGT | 50807 |
| rs528987604 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130369774 | ACATTGCTGGTAGGA[A/C]TGTAAAATGGTGGAG | 50807 |
| rs528990145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158513 | AGAGCAAGGTCCTGT[C/T]CCCTCCCTCCAAAAA | 50807 |
| rs528993872 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130405433 | CCCATGAGTCTGTGA[C/T]GTACCAACCTACCTC | 50807 |
| rs528995941 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119851 | ATTGGTATATTTTGA[A/G]TTAAAGGATGTACAG | 50807 |
| rs529003381 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208426 | ACTGCTGCTCCCTTT[A/C]CTAACCGCTGGTAAC | 50807 |
| rs529005241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130303174 | CAGGAAGCATGCTAA[C/T]ATCTTAGACTGTTTC | 50807 |
| rs529016085 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215699 | CAGTGAGCCGAGACC[A/G]CGTCACTGCACTCCA | 50807 |
| rs529030124 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130427786 | CCCTTCAGTTTGAAT[A/G]TCCTCTCAATGCAAT | 50807 |
| rs529035825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428385 | CCACCTTCTGGGTGA[C/G]TCTTTAGGCCAAATG | 50807 |
| rs529043331 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292906 | ACAGAGAAAAGGATC[C/T]ATATAAAAACATTTT | 50807 |
| rs529064841 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130314169 | AAAGGTAAGCTTCCT[A/C]CCCCCACTTACACCC | 50807 |
| rs529065791 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130161205 | GGACTTTTTTTTTTT[-/A]ATTTTTCCCCAAGGG | 50807 |
| rs529084081 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066666 | TGGGTGTTTAGAATA[A/G]TTCCTATACCTACCA | 50807 |
| rs529099630 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130331215 | TTTCGAGTGGAAAGA[A/G]CGAGTAGGGCCCTAT | 50807 |
| rs529110400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187798 | GGTCATGCTGATGAA[A/G]CAGGAGCCCGAGGTT | 50807 |
| rs529111707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073562 | GAAAGCAGTTAAGGG[A/G]GTCGGGAAGGAACTG | 50807 |
| rs529114775 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130090401 | CCTTTTTGATGAAAT[C/G]TGGGGATCCCGAAGG | 50807 |
| rs529122742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106670 | TGTTTATGCATCTGA[C/T]GAGTACTGACGAGCA | 50807 |
| rs529123470 | in-del | -/TGACTA | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130303695 | TTTACTTTATGACTC[-/TGACTA]TATGACATTCTGAAA | 50807 |
| rs529131621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283926 | ACTCATCAGATGTAG[A/G]AAATCCCCAGAATCT | 50807 |
| rs529135419 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380260 | CTGAAGGTGACCTTC[A/C/G]GGAGATGCTAGAGAA | 50807 |
| rs529138370 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112625 | ATAAGCAAACACCTT[C/T]AGAATGCAGGACTTT | 50807 |
| rs529141063 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130054914 | AGACCTGGCGGTGGA[A/C]TCCCAGGCTTACCCT | 50807 |
| rs529143859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195476 | AGGACTGCAAGATTA[C/T]AGTGAGCTATGATCC | 50807 |
| rs529151369 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130322169 | AAGCAAAATTTAAAA[A/G]TCAATAAAACAACTT | 50807 |
| rs529153542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130061353 | GATTGCAGAGAATCG[A/G]AAAGTACAGAGTTCT | 50807 |
| rs529165990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289817 | ACTTATTGTTTATTA[C/T]ACAACATACCCCACA | 50807 |
| rs529166413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146237 | GGTTCCTTGGTTTTA[C/T]ACCTTCAAATTTGTA | 50807 |
| rs529173786 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373767 | CAGGAGAATTGCTTG[A/T]ACCCAGGAGGCAGAG | 50807 |
| rs529183404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415624 | GAAACCCCATTTCTA[C/T]GAAAAATACAAAAAT | 50807 |
| rs529189297 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295264 | CTCCAGCCTAGGCAA[C/G]AGAGCAAGACTGTCT | 50807 |
| rs529199124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107181 | GTCTCTCTCTTCTTC[C/T]TCTTTTTTTTTTTTT | 50807 |
| rs529200358 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130057052 | TTTAATGTAAAAGGA[G/T]TTTTCATAGATATTT | 50807 |
| rs529204237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283345 | CAGCACTTTGGGAGG[C/T]TGAGGCGGGTGGATC | 50807 |
| rs529206016 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216879 | GCAATGGCAAATACA[C/T]TCTGCTTCTGAAATG | 50807 |
| rs529229669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342647 | GTTACAAACACAAAA[C/T]GTAACAAACTCACAT | 50807 |
| rs529236266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240716 | AGAATGTAAAGTTGT[A/G]CCATACGGCATTATT | 50807 |
| rs529237882 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248053 | GTGACTGATTGGTAG[A/G]AAAATCCTTGAAAAG | 50807 |
| rs529240374 | in-del | -/GAGAAAAC | 0.000265287 | 0.011514 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118142 | TCAGGTAATTCAACA[-/GAGAAAAC]AAAAACGATACCAGT | 50807 |
| rs529248677 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335587 | AACAGTGCCTAAAGA[A/G/T]CATACAACCACCCTA | 50807 |
| rs529254071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130294868 | AAAAGATAGTAAGAT[A/G]CCTTCTTTTTAAAAT | 50807 |
| rs529256507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287289 | CTTGATGGATGGATG[C/T]TGGGGGATAATAAAA | 50807 |
| rs529261821 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339643 | ATCAATTACTTAAAA[C/T]ATAAAACACAATGCT | 50807 |
| rs529267593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236105 | ATCTGTCCAACTTCA[C/T]GGCCTGCGCTCTTTC | 50807 |
| rs529271678 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247775 | CAGCATAGTGAGTGT[A/C]AGTTAAAACCACAGA | 50807 |
| rs529285173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111043 | GCCAGCCCTGTGAGA[C/T]ATTTGACAACTCACA | 50807 |
| rs529292450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130065373 | AGCTTTCTAGAAGCT[C/T]CTTGAACCCAGTCCT | 50807 |
| rs529303197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130207452 | GCAACTCCAAGAGGA[C/T]ACGGCCCTTGTCTGT | 50807 |
| rs529308180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130420508 | CGATGGCCAGGAGGT[A/G]GAAACAACCCAAAAC | 50807 |
| rs529308293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156581 | GAAGAAGTCAAGGGG[A/G]TGAATTTGTGCCAGT | 50807 |
| rs529326909 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130155907 | ATGGTCTCGTATAAA[C/T]AGATAATTCCAACTT | 50807 |
| rs529328135 | in-del | -/GT | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076037 | TAAGTGGTAGAGCTG[-/GT]GTGTTGGTTCCCAAG | 50807 |
| rs529331537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130071504 | TACTTGCTAGACTTG[C/T]ATTGCTGCTTGTAAT | 50807 |
| rs529339926 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130129028 | TGGATCAAGGTGGCG[A/G]TTTCCCCCATGCTGT | 50807 |
| rs529341699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130329176 | ACCCTCAACCACTGC[C/T]GCTGCCTCATCTCTG | 50807 |
| rs529352237 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052575 | CAGTAAGCTGGGTTA[C/G]AGAGAACTCAAATTC | 50807 |
| rs529354886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341486 | AGTAAAACCTGGGAC[A/G]GAAAACTGCTGACTG | 50807 |
| rs529361772 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130107840 | AGGCATGAGACACCA[C/T]GCCCGACCACCATAG | 50807 |
| rs529362919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130193136 | CATTTTGGGAGGCCG[A/C]GGCGGGCGAATCACT | 50807 |
| rs529368401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281499 | TAAGAACAGGGGTTT[A/G]TATCTCCAAGTCTAG | 50807 |
| rs529369748 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111445 | ACACAGAACCTGGGT[G/T]AGAATCCCAGGCTGA | 50807 |
| rs529374333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378811 | AGACAGCAAGATCTG[C/T]CACCTCCCTACTTCC | 50807 |
| rs529376774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098078 | CTAAAACACAGTATT[C/T]AAAATTTATCTTGTA | 50807 |
| rs529388278 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143664 | GGCTGTTTAGCTAGG[A/C/G]AAATCATCAAATAAG | 50807 |
| rs529389885 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130200665 | CTCCATAACAGATAA[A/G]ATTACTGTTGATTTT | 50807 |
| rs529391858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379486 | ACACGCAGCCTCTGG[A/G]AATTGTGACTGGCAT | 50807 |
| rs529394366 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241321 | CCAGTTTTTCCATAG[C/T]GTTACCACATCCTGA | 50807 |
| rs529398648 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364410 | CAATATAAAGCAGGT[A/T]CTGTATTATTCCCCA | 50807 |
| rs529406759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372700 | ATTTTGTATGCACTA[G/T]GGATGGCTAGAGCTG | 50807 |
| rs529410204 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066016 | CCAATACATCTGATC[A/G]TATCAGTATTATCAT | 50807 |
| rs529412980 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137235 | ATCTGTAGGTTTCTG[A/C]CCTCAAATATAAGCT | 50807 |
| rs529420400 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287936 | CTGTTAGGTCCCTAC[C/G]CCAGCCTATCTCTTC | 50807 |
| rs529437596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130235167 | AGACTACTTGAGTTT[C/T]TCTCTTTTTCAAAGG | 50807 |
| rs529441570 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130053217 | ATTAACATCTCTCAC[C/T]CATTGCCAAGATTCT | 50807 |
| rs529454553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130330095 | GGAAATGAATCACTC[C/G]CACACACGTCCCCAA | 50807 |
| rs529457293 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130317372 | TAGGGGAAAAGAAAC[C/T]TCTACGATAAACTGA | 50807 |
| rs529459153 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130286364 | TGTTTATCTCACTGC[A/G]TATATGACATTCTAC | 50807 |
| rs529460281 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228493 | ATAGCTTGAGCCCAG[C/G]CGGTCAAGACCAGCC | 50807 |
| rs529488690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322681 | TATTCATTTAGTGCT[C/T]ATTATGGCAAATCCT | 50807 |
| rs529495653 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130264969 | AGGAACACAGGCAAA[A/G]TATGGGAGGAGAAGC | 50807 |
| rs529504282 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130261323 | AGCACCCAGATATGT[A/T]AGCCTCCATCATGGA | 50807 |
| rs529506661 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130282098 | AAGGAATGGCATGGC[A/C]AAAATCGCAATTACT | 50807 |
| rs529515875 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428210 | CTCACTCTCTAGACT[A/G]GGAATATTTACTTTG | 50807 |
| rs529529886 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179041 | GTAAGTATTTGTCTT[C/T]TTGTAAGGAAGACAA | 50807 |
| rs529534751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364930 | ACAACAGAGCAATCC[A/G]GTCTCAAAAAATAAA | 50807 |
| rs529537505 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316259 | TCAATAACTTTTCCA[A/C/T]CTAATCACAATTCTT | 50807 |
| rs529546570 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269307 | ACACCCAGAGAGAGA[A/C]GGCCAATGCAGATTT | 50807 |
| rs529546869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137836 | ACTGGTCAAAACACT[C/T]TCCTGCCTGCCCATG | 50807 |
| rs529557735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130186389 | ATCCTGCTGCTATTG[C/T]TGCCTACAGAAATGT | 50807 |
| rs529565699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171532 | AGCATGGGGGAAACT[G/T]CCCCCATGACTCAAT | 50807 |
| rs529582265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124468 | GCAGGCTCCATATGT[A/G]AGTCTAGGTTAAACT | 50807 |
| rs529594956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131027 | CCAGGCGTGGTGGCA[C/T]GCGCCTGTAGTTCCA | 50807 |
| rs529603996 | snp | A/C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130311761 | AGCGAAACTCCGTCT[A/C/T]AAAAAAAAAAAAAAG | 50807 |
| rs529610692 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130279680 | CTAGATCTTTCTCTA[C/T]TGTAAAAATATTGTA | 50807 |
| rs529617570 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130235574 | GAGTTATAAATTAGG[C/T]ATATAACTTAGGCCA | 50807 |
| rs529617918 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356985 | CTTTCCACCCAATGG[A/T]GCCATTTTCAGTTGA | 50807 |
| rs529631519 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130390803 | GATATGGAGACATGG[C/G]AACTCTTGTGCACTA | 50807 |
| rs529644280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058765 | ATTTTAAAAAAAGCA[A/G]GCTGTCTCTTTAAAT | 50807 |
| rs529646634 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130124684 | TTCTGAAGGGCCTCT[A/G]ATCATTTTATGTAAT | 50807 |
| rs529655240 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130283803 | GATTTGGTTGATGGG[A/C]AAAGTAGAATCACTG | 50807 |
| rs529657578 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130360105 | TATGTGCCCTGGAGA[C/T]TGAGTAATGCCAAGG | 50807 |
| rs529657809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233448 | TCCATTATTTGCTAG[G/T]TATGGTACCCTGAAC | 50807 |
| rs529689895 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191440 | TCCATCCATCCATCA[C/T]TAATAAGATATCTAC | 50807 |
| rs529699719 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183325 | GCCTTCAACATTTAG[A/T]GATAAAATTATTATT | 50807 |
| rs529703939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321206 | ATAGTGAATAAGCCC[C/T]AGTGGCTACAGAGAC | 50807 |
| rs529717161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239924 | GAAGGCAAGTCCAAG[C/T]TTCCCCTGAATCAAC | 50807 |
| rs529720459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130089890 | GATTTCAACAATCAA[A/T]AGTCCATGCCATGTG | 50807 |
| rs529731624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280089 | GTAGTGTTCTTGACT[A/G]TTTTGCTGACAAGGA | 50807 |
| rs529733579 | snp | C/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219841 | GTAGACCTGCGTGGA[C/G]TGCAGTGGCATGAAC | 50807 |
| rs529739872 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444980 | GAGCGAAAACAGAAG[A/C]CTGAAATGAACCTGC | 50807 |
| rs529740646 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130125462 | CTCACAATTTCTTCC[C/T]TTACTACCTAAAGAA | 50807 |
| rs529740780 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130103573 | CAGTGACGCGATCTC[A/G]GCTCACTACAACCTC | 50807 |
| rs529780293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129576 | TTTATTCTCAACAGA[C/G]AATACAGAGGTTCAG | 50807 |
| rs529794244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220470 | TCATAAATAAGGAAA[C/T]TTAAATTAGAATATG | 50807 |
| rs529795845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213246 | AATAATTCTATGTTC[G/T]ATATTTATTTTCTTT | 50807 |
| rs529810268 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438265 | GCTACACAGCACATC[A/G]TGGTGTGTTTCCTTT | 50807 |
| rs529821957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130240 | CTAAGTTAGGGTTTA[C/T]AATACTTTATAGATG | 50807 |
| rs529825411 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226774 | AACATCACTCTCCTA[A/T]AGCAGAAGCAGAAAT | 50807 |
| rs529829232 | in-del | -/TG | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169186 | GAAAATACACTTATC[-/TG]TGTATATATATACTC | 50807 |
| rs529838767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130315467 | ACTATCCACTAATAA[C/T]GTTCAGAATTGCAAC | 50807 |
| rs529844612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348981 | TGGAGAGGACTCGAC[A/G]AGTGGGGTGTAGAAG | 50807 |
| rs529848426 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130308055 | AATTTGCTTCTAGCA[A/T]AACATTCTTGAATTT | 50807 |
| rs529850338 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130232673 | ATGTTTACTAGTACT[C/G]ATAAAAGTTTATGTG | 50807 |
| rs529853675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077124 | GTAGAAGTGGAAATT[C/T]GGCCCTAGCTCCCCT | 50807 |
| rs529859915 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130056721 | TCTGGGTATTCTTAG[A/G]TACTGCTGGCTCAAC | 50807 |
| rs529887432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130230186 | CATGATGTACATTCC[C/T]CAAAGATAGAAGAAG | 50807 |
| rs529895744 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400531 | CGGTGGCTCACGCCT[A/G]TAATCCAGCACTTTG | 50807 |
| rs529908720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170407 | TGATCTGCCCACCTC[A/G]GCCTCCCAAAATGCT | 50807 |
| rs529910635 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163183 | TACTAGGCACTCAAT[A/C]AAAAACAAGCAACTG | 50807 |
| rs529914745 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130204791 | GAGAAGAAAATAAAC[C/T]ATGTTAAGCCATGGA | 50807 |
| rs529915109 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130177379 | AAAGTCAGGTGAAAT[A/C]AGTTTTGCTGCCAAA | 50807 |
| rs529919804 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432170 | AGGAGGGGAGGAGGG[A/G]AAAGGGGGAGAAGGG | 50807 |
| rs529922065 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333279 | TTGATGGGATTACTT[A/G]AGATTTTTCATCTTT | 50807 |
| rs529929631 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130354328 | AGAGAGCTCATATGA[C/G]AGGTAAATGTAAGCA | 50807 |
| rs529936041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117770 | TCTCTTTTAACCTCT[C/T]CTAACGGTTAGCAAA | 50807 |
| rs529937409 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130360819 | GCTCATGTGCCATAG[C/T]TGACAGAACATGGTC | 50807 |
| rs529943504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130267861 | AGAAACTCAGGAAGT[A/G]TCCAGCCCAGAACTG | 50807 |
| rs529945213 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130058800 | TGGGTGGAGTGCCTC[C/T]TCCTCTCTGTCCCCT | 50807 |
| rs529948007 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395154 | ATCTGGAAGCACTCA[C/T]TCAGAGTAACACAGA | 50807 |
| rs529953103 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118366 | CACTCTCATATTCTC[-/TT]GATTTAGACATGGCC | 50807 |
| rs529955442 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384430 | ACCCCACTGCTGGGC[A/G]GGGGGCAGAAAGTGG | 50807 |
| rs529955891 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213895 | GGGATGCCCACACAC[A/G]ACTGCCTGGCAAACA | 50807 |
| rs529963274 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130228702 | TGAGACCCTGTCTTA[-/A]AAAAAAAAAAAAAGA | 50807 |
| rs529979304 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130102563 | GGTAGTTTTCTTTTT[C/T]TGTTGTGTCCTTGTC | 50807 |
| rs529980049 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130206900 | AACTTCTTTGCTAGG[A/C]TCACAGGAATGATGC | 50807 |
| rs529996882 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206471 | AAAAAAAAAACAACT[G/T]TAACACAAACCACAA | 50807 |
| rs530004876 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130363665 | GATGCAAGTATTACA[A/G]TAATGGAAACTGAGA | 50807 |
| rs530006518 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130294306 | AGTTCTGAATGAGGG[G/T]AATGCCACGGAGCGT | 50807 |
| rs530007833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306371 | CTTTCCAGTCACTTG[G/T]ATTAATAGCTCCTTT | 50807 |
| rs530027278 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391085 | TATGTACATACAATG[C/G]AATGTTATTTAGCCT | 50807 |
| rs530029083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070468 | AATTGGACATGCCCA[A/G]GCCTGCAGAGTGCAG | 50807 |
| rs530030371 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220628 | GATGGCTTGAGCCTA[C/G]GAGTTTGAGACCAGC | 50807 |
| rs530030757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130398705 | TTTAGCTTAACTCAA[C/T]TAGTGCTCAAAACAA | 50807 |
| rs530041063 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130223163 | CTACTTAATGGGTAT[A/C]ATAAGGCCTTGAGAA | 50807 |
| rs530056791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130082123 | GGAGAGGCTGGCAGG[C/G]TGCTCACCTCCTGGA | 50807 |
| rs530063249 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130265095 | TCTCATGGCAACAAA[A/G]GGCTGCTGGCAGCTT | 50807 |
| rs530086809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436409 | CAAACAATCCTCCCA[C/T]GTCAGCCTCCCGAGT | 50807 |
| rs530088892 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130443892 | AGGGGCCCCAGACCT[C/T]GGCCGGGGTCGGGCG | 50807 |
| rs530101921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252042 | AAGGATGTGTATTAT[C/T]AAATGTTCTAAATCA | 50807 |
| rs530102891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394178 | TAAACTTTGACCACC[A/G]GTGAGCTGGGCGGAA | 50807 |
| rs530123066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299284 | GAGCCCAGGGAAACT[C/G]AAAAAAACAGTTACT | 50807 |
| rs530129009 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280028 | CTCAAACTGGCACTT[-/A]ACATGTTCCTTATTT | 50807 |
| rs530133621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204653 | CTAGGAAAGCTGTGA[A/G]AAGTATGCATACGCT | 50807 |
| rs530148251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389242 | ATAAGGAAACTTGCC[C/T]AGCACCACCCAGTAA | 50807 |
| rs530151960 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409417 | CTCCCTACCAACCCT[C/G]ATCAGCCCTGATTTA | 50807 |
| rs530164971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130161527 | TGGCTTTGACATGGA[C/T]GCTCACACTCTCACC | 50807 |
| rs530166828 | in-del | -/A | 0.0248432 | 0.108648 | intron-variant | ASAP1 | GRCh38.p7 | 8:130267041 | GCCACCCACCCCCTC[-/A]AAAAAAAAGTAGTCA | 50807 |
| rs530180320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430965 | GAGGACATAGACTTG[C/T]GCCTCCCTCAGATAG | 50807 |
| rs530183480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292813 | GTGTGACTCTAGGCA[C/T]GTCACATAACCTCTC | 50807 |
| rs530188077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130212377 | GGTGTGGAAAAAGGG[C/T]TGTAGCTTGAGGTAT | 50807 |
| rs530201751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437030 | GAATCACTTGAACCC[A/G]GGAGGGAGCAGTTGC | 50807 |
| rs530212813 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130200687 | GTTGATTTTTATTTT[A/T]GTCTTTTTCTCCCTA | 50807 |
| rs530221406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070105 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAAGCT | 50807 |
| rs530221724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063524 | CTCAGGGTACACTGG[C/T]CCAGGTGACTCAACT | 50807 |
| rs530228824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382768 | GAGAATTGCTTGAAC[A/G]TGGGAGGTGGAGGTT | 50807 |
| rs530228902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122046 | GGCACCCATATGACC[C/T]GTTCCAGCTGCCTGG | 50807 |
| rs530234833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219127 | GTTACCGCTATATAT[A/C]CATGACTACTTACAA | 50807 |
| rs530238805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307103 | CACCCTATTTGTGTT[C/T]TCCATAAAAGTTATC | 50807 |
| rs530246348 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334105 | AGGAGACGTGAAAAT[A/G]CAAGAGGCTTCCAGT | 50807 |
| rs530259901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347652 | CACCCATCACATAAC[C/T]CCCTCATCCTGGCCA | 50807 |
| rs530267817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431478 | ACTGTGCTATTGGTA[C/G]CATTCACATCCTTGC | 50807 |
| rs530268707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146877 | CTATGAAAGAAGAGG[C/T]ACCCCAAATGGGCTC | 50807 |
| rs530275239 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389736 | GACAGGGTCTCCTTC[C/G]GTTGCCTAGGCTGGA | 50807 |
| rs530287937 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130356516 | CAGACGAGTATAACA[C/G]ACTGGCAGTTCACAA | 50807 |
| rs530305056 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130208032 | GTATACTAAACACTT[G/T]CCCCTACTTTTCTCT | 50807 |
| rs530305436 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166102 | ATACAGCTTACTACA[C/G]CCTCCACTTCCTGGG | 50807 |
| rs530324728 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130057263 | GGCTCTGGGGTCAGG[A/G]CCGATCTGGAATCTT | 50807 |
| rs530327495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341218 | ATGGGTGCAGGGCGC[C/T]AGGAAGGCCACCCTG | 50807 |
| rs530329170 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063838 | CAGGCACTTGGGACA[C/G]AGCTGATGGAAAGAA | 50807 |
| rs530340449 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252807 | TAAAGACCAAAAAAA[G/T]ACTCATGAAAACACC | 50807 |
| rs530345095 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130169391 | TCTATACATAGAACA[G/T]TTCTTCCCAGTTAAA | 50807 |
| rs530345272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293210 | ATTCTGATTCAGCAG[G/T]TCTGACGAGGAGGCT | 50807 |
| rs530347105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197892 | TTAAGGGGAGTGTTA[A/C]GTGAAAATCCTATAT | 50807 |
| rs530400658 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286371 | CTCACTGCGTATATG[A/T]CATTCTACTTCCATT | 50807 |
| rs530400949 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130349860 | TTATTTATCAAATGG[A/G]GAAACAGAGGCTTAG | 50807 |
| rs530401710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244319 | AATATGAACTCCTTG[C/T]TGCCTTGCCCTCTCC | 50807 |
| rs530418929 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130097924 | CTGGAAATTCATTCA[C/T]TTATACCTAAATAGA | 50807 |
| rs530437441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377572 | GCTCTCAAGGAGCCT[A/G]TGGTCAATCAGAGTA | 50807 |
| rs530446909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109506 | TAGGGGTCCTTCAGA[A/C]CCCTAAATTCAGTTG | 50807 |
| rs530447641 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130225822 | ATACACAGAAACTAA[C/T]ATGGAGCCTTTGGTT | 50807 |
| rs530456475 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246632 | TTCCCCAGCCACGCG[C/G]AACTGTGAGTCAATT | 50807 |
| rs530462905 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130166888 | TATTTCCCTGGCAAA[G/T]GAGACATGCCTGTTT | 50807 |
| rs530472771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297904 | AACTGGCAAAGTGAC[A/G]TGCTCTTGTAGCTAA | 50807 |
| rs530475766 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130141296 | TCGCAGGCCCCTTCT[C/T]GCACTCAGCTCCTGT | 50807 |
| rs530497822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130338605 | GTGTGGAATTTTTTC[C/T]ATTTCTTTTATTAAC | 50807 |
| rs530521069 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160717 | AACAACGTTGAACTG[A/C]AGAACGAGAACATGG | 50807 |
| rs530531561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062085 | GGCAGGCTGTAAGCA[C/T]TATGCAGTAGTACTA | 50807 |
| rs530533145 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130429827 | AGTTTTGAAGAATAA[C/T]GCATGTATACTTCGC | 50807 |
| rs530534161 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130143888 | ATTAGTACCCAGAAA[C/T]GAAATTATTTCCTCC | 50807 |
| rs530540291 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375284 | TTAATATTCTATTGG[A/C]CACTGCAGGAATGGG | 50807 |
| rs530550036 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146451 | ACTGGCTCCAAAGTT[C/T]GCCCTCTTACAACTG | 50807 |
| rs530556245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203337 | TGCAGGGTGTACATG[A/G]CTCAAAGCACCCACC | 50807 |
| rs530567627 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333016 | ACATTCACAGTGATT[A/C]AAGCACAAAGCGGTT | 50807 |
| rs530574095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130367991 | GTTTTCTTCTTAACA[C/T]ATGCTATTTAGTTAA | 50807 |
| rs530586267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130231112 | TTTCCTTGTGCACTA[C/T]GAGCTTTTTCTTAAA | 50807 |
| rs530587393 | snp | C/T | 0.000798881 | 0.01997 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108141 | GTATGCCACACAGCA[C/T]GCTACTTTCGTGCAG | 50807 |
| rs530589805 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130184851 | ACACTACCTTATCTC[A/G]TCCTCACAAAAACCC | 50807 |
| rs530602564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062604 | CCTTGGCTGTGAGTC[A/G]CACTGATGGGGCAAG | 50807 |
| rs530603639 | in-del | -/TAA | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106270 | AATATCAAGCTACTC[-/TAA]TGACTGTCTTCCCAT | 50807 |
| rs530604355 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130424856 | AAATTAGCCGGGCAT[A/G]GTGGCAGGTGCCTGT | 50807 |
| rs530613971 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100751 | TACAAGTCCCTTGTA[A/T]GATGAATAGTTTGCA | 50807 |
| rs530620047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237698 | TGATTCTTAATCCAG[A/G]TACAGGATATACCAT | 50807 |
| rs530632862 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068648 | TCCAGACACACAGGA[A/G]GCTATTCCTGCGGTA | 50807 |
| rs530645365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195768 | TGGACAAAAATAGCC[A/G]TTTATTCCTTACAAT | 50807 |
| rs530651490 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423790 | TTATTTGCTTCTTTA[C/T]CTTTTCTTGTTCTTT | 50807 |
| rs530653142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203836 | GGGACAAAGATCATG[C/T]AGACAGAAGGCTGTT | 50807 |
| rs530656154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278307 | AAGCTGTAGTCACAT[C/T]CCATAATCTAGACAT | 50807 |
| rs530661496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153766 | ACTACAATGATATAA[C/T]AATAACTCCTCTCTA | 50807 |
| rs530672701 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130298300 | CAACATGATGTACAA[C/T]ATAGATGAAGACTCC | 50807 |
| rs530673940 | in-del | -/ACTA | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334867 | AAAAATCATCATCCC[-/ACTA]ACAAAGTACCTTTGT | 50807 |
| rs530675106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404357 | CAGGATAGCCAAAAC[A/G]ATCTTGAAAATGAAG | 50807 |
| rs530686202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175143 | GTGTGAAGTGCTATT[C/T]CATTGAGGTTTTGAT | 50807 |
| rs530694768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087762 | AGGCAAGCGATCAGC[A/G]TGAACCCATTGATCT | 50807 |
| rs530709317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189849 | TAAAAGCCATTTTAG[C/G]TGGCTTGAGATGATA | 50807 |
| rs530711394 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324990 | CCCCAAAACCCAGAA[C/T]ACTGGCTGCTCACCG | 50807 |
| rs530717698 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417079 | ACACACATGCAAAGT[A/G]CAACCCATGTACAAC | 50807 |
| rs530718481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333400 | TGAGGTCAGGAGTTC[A/G]GGACCAGCCTGACCA | 50807 |
| rs530738915 | in-del | -/TCT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130072980 | CGTTTGTCACAGAAA[-/TCT]TCTTCTGTGTTGATG | 50807 |
| rs530748855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325525 | ATGTGATCTAAAAGT[C/T]CAAACACACCTGTCT | 50807 |
| rs530749285 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318768 | ACTTCAAATATAGAC[G/T]AGACACTTAAAAAAG | 50807 |
| rs530771528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101560 | CTATCGTAAAAGGGA[C/T]TGCTTTCTCAATTTT | 50807 |
| rs530779906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413613 | TAGAAGACTGTAAGT[C/T]TGAAAAATGAGGAGC | 50807 |
| rs530782701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099975 | CACTGCAGTAAACAT[A/G]GGGTGCAGGTATCCC | 50807 |
| rs530785983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319373 | TCCCTGACAGACTGT[C/T]GTATTAGTGAATGAA | 50807 |
| rs530791346 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130439176 | CAACACTGCCGGCTT[C/T]GGAGGTGGAAGAAGG | 50807 |
| rs530806688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095526 | GGCAGGTCTTGAACT[A/C]CCAACCTCAAGTGAT | 50807 |
| rs530816380 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133951 | AGATGCATAAGGCAC[G/T]GTCCTTGCCCTCGAA | 50807 |
| rs530817507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415605 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCATTT | 50807 |
| rs530819227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130225194 | GAAACTTTTATAATA[C/T]GTGTTGCAAATATTT | 50807 |
| rs530823505 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081248 | CAGAGGCACACAGGT[-/G]GAGGTAAGTGTGCTA | 50807 |
| rs530823521 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137667 | AATTACTACCTGTGA[-/G]GCAATGCTTAATGAA | 50807 |
| rs530830513 | snp | A/G | | | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130294900 | AACATGTCTGGAAGT[A/G]AAAAAGATGAACAAA | 50807 |
| rs530832573 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413596 | AAGCCCAGATCAGGC[C/T]TTAGAAGACTGTAAG | 50807 |
| rs530836041 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130443336 | GCTGCGAGAGGAGCC[C/G]GGAGCCCGCCCCGCG | 50807 |
| rs530837304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278682 | GAAAAAAACTCTAAT[C/T]AATTCCTGGGATATT | 50807 |
| rs530850369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283170 | CTGTTGGAGAGAGGA[A/G]AAATATATCCACACC | 50807 |
| rs530855017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224625 | TGGGATATTACATAC[A/G]ACCACCATGGCTTGC | 50807 |
| rs530858137 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130100224 | ACTGGAAATAGATAA[-/T]TATCTCATTGTGGTT | 50807 |
| rs530859186 | in-del | -/AAG | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123939 | AGCCAAAAAAAAAAA[-/AAG]AAGTTTTTTGGAAGG | 50807 |
| rs530861724 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130194840 | CTATGCAGCAAGGTT[C/G]CTAACAAAGACAATG | 50807 |
| rs530864588 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130341705 | CTTCAACTTGACTGC[C/T]CAGCCCAGTGAAGGA | 50807 |
| rs530873824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317494 | TTCAAAGTAAGAAGT[A/G]AAGGGGCTGGACCTG | 50807 |
| rs530883874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373655 | GGAGTTTGAGACCAG[C/T]CTGGCCAACATGGTG | 50807 |
| rs530886082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145444 | TGCCTCAGCCTCCCG[A/G]GTAGCTGGGATTACA | 50807 |
| rs530890727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132502 | TTCCCCTACGTTCCT[A/G]AGCCAGCTCAGCCTT | 50807 |
| rs530913219 | snp | A/C | 0 | 0 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054330 | CTTTGCTAATGTTGC[A/C]TTTTCAGTAACACAA | 50807 |
| rs530922529 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130177837 | ACAGCTGTCAACACA[C/T]ACAAGGTCGCAGGCA | 50807 |
| rs530928715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366661 | GGTTCAATCTCAGTG[C/T]TGCCATTTAACAGGA | 50807 |
| rs530929884 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130243188 | AAGCCTGGTAAGGCT[G/T]CTGATAAGATTGATA | 50807 |
| rs530932967 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130093223 | GTTAAGGGAGTAGTG[C/T]ATTTGATCTTAGTTT | 50807 |
| rs530934716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130235466 | TGTGGCATCTCCTAG[C/T]TATTTATTTCACTCA | 50807 |
| rs530937265 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130268014 | AAGCATCTCACTTCC[A/C]TACACCCCAAGGAAA | 50807 |
| rs530950268 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145049 | GGGCTCCTGCTAAGA[C/T]GTGGCGCTGAGGTTA | 50807 |
| rs530956012 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408614 | TTATTATAAGGGTGA[C/G]CCAATTCCCTATAAT | 50807 |
| rs530961250 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079817 | CTTTGAGCAGCGCTG[C/G]GAAATTCATGAAAAC | 50807 |
| rs530963455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223652 | TGGGGTTATTAAAGG[A/C]AATAGATGAGAAAGA | 50807 |
| rs530965226 | snp | C/T | 1.9985e-05 | 0.00316103 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, intron-variant | ASAP1 | GRCh38.p7 | 8:130358056 | CCTGCAGTTGTGCAG[C/T]CGCGTGGTGAAGCTG | 50807 |
| rs530974503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130441245 | AAGAAAAACTCGATT[A/C]CAGATAAATCTGAGA | 50807 |
| rs530974955 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130111732 | AGGTTCTGGAGCCAC[A/G]TGGACCTCAGATTGA | 50807 |
| rs530977639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107057 | TCTAAGCAAGGTAGA[C/T]ACCTAATCCTTATTT | 50807 |
| rs530978093 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311816 | TATAATTATAGAAAG[A/C]AAAGATTTTAGGCTA | 50807 |
| rs530999424 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277355 | CAATAACTATAAGCC[A/T]TACTAGTTCTTCATA | 50807 |
| rs531003776 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130157134 | ACAAGGAGCTGAGCC[C/T]GAGGCTTTTCAGCAA | 50807 |
| rs531010315 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402783 | CTCTCCCCACCTCCA[C/G]TGGTCCAGCTCTGGA | 50807 |
| rs531019171 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437703 | TTGACCAAAAATTCA[C/T]GATTGGTTTTGAAAG | 50807 |
| rs531023245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229796 | TGTAAATCCCAACGC[G/T]TTAGTAGGCAGAGGT | 50807 |
| rs531027660 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366019 | TTCATTTTTTGGATA[A/T]GGAAACTGATTCCCA | 50807 |
| rs531029885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276807 | GAGACCCTAAACTAT[A/G]AGAAGGTGGAAAGTG | 50807 |
| rs531041468 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409936 | CATTGCCCATAGAGA[A/G]CTCACAGTCTGGTGG | 50807 |
| rs531056458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239164 | TCACATACCTGTCAT[A/G]CTGCATGTCATGCTT | 50807 |
| rs531064442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130357615 | ACTGCCCATCTCCTA[C/G]TCCCTTGCTGGTGAC | 50807 |
| rs531067162 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130183123 | AGATTGCAAACAGAA[C/T]GCACATACCGTGGCA | 50807 |
| rs531073311 | snp | C/G | 1.64735e-05 | 0.00286993 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130054740 | GTTTTGCTAGTCAGA[C/G]AGGATATGAACAAAG | 50807 |
| rs531087071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215769 | CAACAACAACAACAA[A/C]AAACAATTAGCTGGG | 50807 |
| rs531089697 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130210007 | TTCCAAATAATGTTC[A/T]TTTGCATGGTTTCAG | 50807 |
| rs531092738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087136 | AAGACCTGTCAGCCA[C/T]GGCTACTCTGCAAAG | 50807 |
| rs531105667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130174075 | CCTGGGTGACAGAGT[A/G]GCAAGACTCCGTCTC | 50807 |
| rs531106597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352079 | TTGACTTGTGTGTGG[C/G]AGAGAAACATTATGG | 50807 |
| rs531120803 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120253 | CGGCCCAAGCCTGGC[G/T]TCTGAGGCCTCTGCT | 50807 |
| rs531122500 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126720 | ACTACCTGCTTGCCA[A/T]TTCCTGACACTACGT | 50807 |
| rs531124667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130216778 | TACCTATTCAGTATC[C/T]CCACTAACTATGTTG | 50807 |
| rs531137062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311342 | AAGTAGAGAAATTTA[C/T]GTCTAAAATAACAAT | 50807 |
| rs531143925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130345249 | ATTCACTACTTACCA[C/T]CCATAAAGAAAAATC | 50807 |
| rs531151183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435274 | TGAGTCTCAATTCAG[C/T]GATATTCTTCAGCAT | 50807 |
| rs531165465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130271202 | TAAAACTGAACTCGA[C/G]CAGAAGAGCTATACT | 50807 |
| rs531175371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180399 | TTCAAACTGGACATA[C/T]GGTTAAAAAAACATG | 50807 |
| rs531197737 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166601 | GTATCTCTAATAGTA[A/T]CCATACCACTTTAGG | 50807 |
| rs531202601 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130260596 | CACTCCTGTGGCTTC[G/T]CCCTCTATTGAGATG | 50807 |
| rs531205838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397707 | TACCCACTGATGTGG[A/G]AACTTTTCCCCCATC | 50807 |
| rs531207198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401162 | GCCAGGATTACAGGC[A/G]TGAGCCACTGCACCC | 50807 |
| rs531240655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316820 | GCATTTAAGCTTCTG[C/T]TTATTTGGGATTTTC | 50807 |
| rs531244088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387204 | CTCTGGATGACCCAG[A/G]AAGAAGAAATGTGAA | 50807 |
| rs531252748 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091411 | CAGGGAGTGGGAGGG[C/T]CCTCAGGAGGCAGAG | 50807 |
| rs531256713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080209 | TGAGCAGCTGCTCTG[G/T]GGCAAGGCCTCAAAG | 50807 |
| rs531283807 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130385899 | CACATCCTTTGGTTC[C/T]TGTGGGTCTCACTTT | 50807 |
| rs531285116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432979 | TCTGCTACACCTGGT[C/T]GCTCACTCGCCCCCG | 50807 |
| rs531293156 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130326588 | AAGCTTAAACAGCTC[A/G]CTCCACGCTAGTCAA | 50807 |
| rs531299872 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438810 | ACACAGTGGAGGCTG[A/T]CTCCCACAAGTGCAT | 50807 |
| rs531300231 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130302212 | AATCAGTAAAAAGGC[A/C]TTGATTGTCCAGTCT | 50807 |
| rs531303248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309754 | AAACAGAGATTGGCT[C/T]TAAAGGAAGAACAGA | 50807 |
| rs531303457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356880 | GAGGTCCGTCCTTGG[A/G]GTGGGGGGCTTACAT | 50807 |
| rs531326406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078540 | ATCCTCACACCTTGG[C/T]CTCCCAAAGTGCTGG | 50807 |
| rs531327565 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130395673 | GAGACAATACATTTC[-/T]TTTTTTTTTTTGAGA | 50807 |
| rs531332776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316199 | CTCCTCTTCTGAGGG[C/T]TATGCCAACCATCTT | 50807 |
| rs531345251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078598 | CTTTAAAAACCTTTT[A/C]TGAGTGCTTTTGGAG | 50807 |
| rs531358130 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295682 | ATAAGCTGCAACTGT[A/G]TGATGTGCATGAGGT | 50807 |
| rs531361686 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130299352 | CTGTTTTAATGCTAC[A/G]CGTATGCACAGGGAA | 50807 |
| rs531374474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269084 | AATACATTTCTGTTT[C/T]AGACTTTTAAAGAAG | 50807 |
| rs531374479 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130165049 | GATCAATGTATTACT[C/T]GTAAAACTCTGTGAT | 50807 |
| rs531375868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059567 | CTCAAGCGATCCACT[C/T]GCCTCTTCCCAAAGT | 50807 |
| rs531401987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072958 | TGTGTGGGGAAAAAT[C/T]CCCACACGTTTGTCA | 50807 |
| rs531409701 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165353 | ACAATAAACAAAAAA[A/C]CCCCAAAAAACCTCA | 50807 |
| rs531411057 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130062041 | GATTACATGGGTTAA[C/T]ATATGCAAAGAATTT | 50807 |
| rs531411552 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130060259 | TGCTCATTTGTCACT[A/G]TATTTAATCATCTGT | 50807 |
| rs531414831 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439262 | CAAATTCTTCCCAGC[A/G]CTGCCAGGAGTAACA | 50807 |
| rs531426927 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130348503 | GACCACAAACAGCAC[C/T]ATGACAGAGGGCTGT | 50807 |
| rs531434916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079108 | GCTGAGGCAGGACCA[C/T]CTCTTGAGCCCAGGA | 50807 |
| rs531443208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391681 | TGCATGCATGGTTCC[C/T]GCCTTCAAGGCACTC | 50807 |
| rs531444232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208346 | CATGTATAGATAACT[A/G]CAACAATCACCACCA | 50807 |
| rs531449739 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222259 | GTTTATCTAACTGAC[A/T]CTATGTGTTATACCT | 50807 |
| rs531464911 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130194218 | GTCTTTCCAACTAAC[C/T]TCCCAGGAAAACGTA | 50807 |
| rs531477242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130433732 | AGAATTCTTATCTCA[C/T]TTTGAAACCCACTAA | 50807 |
| rs531478810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160961 | CCTCTAGATTCAGGA[A/T]AAACTTTGGGTGACA | 50807 |
| rs531478907 | snp | C/T | 0.000595208 | 0.0172409 | missense | ASAP1 | GRCh38.p7 | 8:130060623 | GCGTCTCTGGCAGAG[C/T]AGGCGTGAGGTCGTT | 50807 |
| rs531487419 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130427076 | AGTCATTACTGGGCA[G/T]AGACGGCAGAGCAGG | 50807 |
| rs531490835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130386263 | CAGTCATTTCTGGGG[C/T]CAGGTTTTACCCCTG | 50807 |
| rs531512375 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130181901 | TCAAGTCTTCTTTAA[C/G]TTATGGTGGTGGTAG | 50807 |
| rs531520045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066606 | TCTCTCTCCTTCCTT[C/T]CTTGTTTCTTTTTCT | 50807 |
| rs531539352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157516 | TGCTTTCACCCTCCA[C/T]GACTCTGCTTTGCTT | 50807 |
| rs531539364 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130320723 | TCTCTAGTATCACAT[C/T]AAAAAAAAATGGAGA | 50807 |
| rs531540852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344346 | CACCGAGGAAGTGTT[A/T]TTTTCAGACGAGAAA | 50807 |
| rs531541287 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130244882 | GAACAAGCCAGGAAG[G/T]AATGGGAGTAAGGGT | 50807 |
| rs531544793 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130319946 | TATTTACATGTTCTA[C/T]ATAAAGTCTTCACTA | 50807 |
| rs531557252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337639 | TCCTTCCCATGAAAA[C/T]TGAAGTACTAAAGGC | 50807 |
| rs531561577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293424 | CTTCCAACATCCATC[A/G]CTCATGCCCCAGCAA | 50807 |
| rs531570708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119322 | CCCCCAGGCCAGGCA[C/T]TGAGCTCCAAAGGGG | 50807 |
| rs531573895 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246972 | AGGTCCAACCTTTGC[C/G]TCTTGGAAGAAACAT | 50807 |
| rs531576070 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254003 | TCCAGTTTGGGCAAC[A/T]AGAGTGAAACTTCAT | 50807 |
| rs531577235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341415 | TTAATGGCAGAGACT[C/T]GGAGACTTGAGGGTC | 50807 |
| rs531580655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385598 | GGTAGGAATCTCAAC[C/T]GGTCTCTGACTCTCT | 50807 |
| rs531598198 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163878 | TATAGACAAATCACT[G/T]TCTTATTTGAAAATC | 50807 |
| rs531630092 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130260320 | GACCATAAATGAGCT[A/C]TGTGCCATTCTCTTC | 50807 |
| rs531660726 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384363 | CTGGTCTGCATACAA[A/G]CATCCATTCTGTGTT | 50807 |
| rs531666718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058877 | CCCTTCTGGGCCGTG[C/T]GGGTGGGTTGGAGAA | 50807 |
| rs531667707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110990 | ACCTCTCAATTATCC[C/T]TACTGGCTGAGGCAA | 50807 |
| rs531670245 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130242277 | AAAAAAAAAAAAAAA[A/C]AAAAAACAACTTTTT | 50807 |
| rs531675734 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249433 | ATGACTCTGGAGATG[C/T]TAATTCTAGTAGCTA | 50807 |
| rs531681763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130065309 | GTGTGTCGCCCTCCC[A/G]GCACGTGAGCGAGTT | 50807 |
| rs531683131 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432112 | AGGGAAGAGGGGGAG[A/G]GGGAAGAGGAGGAAA | 50807 |
| rs531692859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425037 | AAAAGAGTGGACAAA[C/T]AGTGTGGGTCAGGCC | 50807 |
| rs531696686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378302 | TGACTGATGAATGAT[A/G]GAAGCACTAAAAGAA | 50807 |
| rs531715828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384991 | ACACACACCATGGCT[C/T]TATGGAGGCCGGGGC | 50807 |
| rs531722855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155652 | GCGCCCAGCCAGCAC[C/T]TGATCTTTGTGAACA | 50807 |
| rs531727202 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130204222 | GATCTAGGTTGCACG[C/T]TACTTATGAGAATCT | 50807 |
| rs531727725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395097 | CAAGAATGTCCCTGC[C/T]GCAGCACAAGAAAAA | 50807 |
| rs531728382 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117635 | ACTCTTATACTTCCA[C/T]CAGTATATCCCAAAC | 50807 |
| rs531732882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247543 | AAAAAAAACAACAAC[A/G]AGGATTCAGTCATCA | 50807 |
| rs531740532 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130193688 | ATGAAGCAGCAAATT[-/A]AAAAAAAATACATTA | 50807 |
| rs531752118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425465 | GAGGTTGCAGTGAGC[C/T]GAGATCTCACCACTG | 50807 |
| rs531764989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117108 | TGAGACCTAATTATT[A/G]TAATAGAGAAAATTA | 50807 |
| rs531776208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126530 | GAGCACTTCTTAGTA[A/G]TAAGACAGCTGTAAA | 50807 |
| rs531809842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150205 | AGATGCCACAGTCCA[C/T]TATCTTAGCCACTAA | 50807 |
| rs531816089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287196 | ACACATTTTTGTATA[C/T]TGCCTGTCCAAAGCA | 50807 |
| rs531820873 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130335994 | TGAAATTTCCAAGTG[A/C]GACAGGAAAAGAGAG | 50807 |
| rs531832481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128886 | ATAGTGTTTTGTGAA[A/G]TCAACAACAAAAAAA | 50807 |
| rs531834075 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218367 | ATATAATTAGTTAAT[C/T]GAATATACATGTATG | 50807 |
| rs531852958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110301 | TAGAGGCTCTCTGAA[C/G]AGGCATAGGCTGTGC | 50807 |
| rs531853078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130294098 | AAGCAACGTTCCATA[C/T]GAAGAAACAATGGCT | 50807 |
| rs531856561 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275469 | CTGAGGCGTCCCAGC[A/G]CCTGCACACAAAAGC | 50807 |
| rs531857291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287811 | GAGGGCTGTGTTTGG[G/T]TTTTGTCACCTCTAT | 50807 |
| rs531866228 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130198887 | TGAACTACACTCATA[A/T]CCAAGCTCCCAATTT | 50807 |
| rs531888068 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130339317 | GAACAAATTTAAGAC[A/G]CTGGAAACTTTCACA | 50807 |
| rs531892905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274850 | TTGGCTCTTAGCTAC[A/G]CCTACTGTAGTTCTT | 50807 |
| rs531898218 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130314044 | TGAATATAGAAGTAC[C/T]GCATGTAAATGGACA | 50807 |
| rs531899223 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137175 | TCAGCAAAGAAGAAA[C/G]AGACATCTGAGCATT | 50807 |
| rs531923567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130328177 | CAATTCTGTGAAACT[C/G]GTACTAAATGAGGAA | 50807 |
| rs531928466 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052433 | TTTTTTCATAAGGTT[C/T]CATATCTTCAAAATA | 50807 |
| rs531928537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144148 | CTACAGGGACATATA[C/T]TTTTGGCATACAATC | 50807 |
| rs531931352 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130420284 | CACACACACACAATA[C/G]CAATAACAAGTCTTG | 50807 |
| rs531941445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234622 | AGCCTTTGTATGAGC[C/T]GCTGAGTGATGTGGT | 50807 |
| rs531962726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321365 | GAGGGTCTGGTTCAG[C/T]ACCAAAGATTCCAAA | 50807 |
| rs531964885 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130238605 | TTATATTTATAAAAC[A/C]TATCAATTATATAAG | 50807 |
| rs531972053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141196 | AGAAACTCTGGAAAC[A/G]TCTATGTATCTATTG | 50807 |
| rs531985231 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104991 | AAAAGTTATATCTAT[A/C]CAACTTGGGACAATA | 50807 |
| rs531990961 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407190 | TATCCTAGAAGAAGC[A/T]GAAACTCAGACATTG | 50807 |
| rs531993319 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130107586 | AGAGTCTCATTCTGT[C/T]GCCCGGGCTGAAGTG | 50807 |
| rs531996519 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063810 | TGGGCATGTGCCGTG[A/C]CCAGCACCCTTTCAG | 50807 |
| rs532000165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417607 | AAAACCCCACAAGTC[A/C]TGGCTTCAGGGGAAA | 50807 |
| rs532001217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130326587 | AAAGCTTAAACAGCT[C/T]GCTCCACGCTAGTCA | 50807 |
| rs532002380 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130422997 | GAGGTCACAGTTGAC[A/G]GCAAAGTCAGGTCTA | 50807 |
| rs532002488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322073 | GCTACTGTGCTGCCA[C/G]GGTTCTTCATCTCTA | 50807 |
| rs532016434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238570 | ACTGAGCACTTACTA[A/G]ACATCAGGTATAAAA | 50807 |
| rs532018189 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238194 | GGCCAGGTGAGCACC[A/G]GACTCATACTGGACT | 50807 |
| rs532020225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130477 | ATTCAAATTTGGTGG[A/C]ATGAAATGGCTAAAT | 50807 |
| rs532025116 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130440005 | CGCCACCATACACCC[A/T]GCTGTTCAAGCCAGA | 50807 |
| rs532025538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098505 | CCTGCCACCACGCCC[A/G]GCTAATTTTTGTATT | 50807 |
| rs532036052 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410862 | GGAACCTGTGTCATC[A/T]TCTTTTTCTGTTTTT | 50807 |
| rs532036739 | snp | A/G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130416393 | AATGAATTAATTAAT[A/G/T]AATGCCTAAACAAAC | 50807 |
| rs532047342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130185107 | CTAACTTATAACAGC[A/C]TAAGTCCCAGTACAT | 50807 |
| rs532052101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109354 | GTAATTTAGGTCAAG[C/T]TTCCTTGAATTTCGA | 50807 |
| rs532058432 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130121178 | CAGTTTACCTTCAGC[A/G]CTCAGTGGATCTATT | 50807 |
| rs532061002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096253 | TAGTAACCAGTCCCA[C/T]AGCATTAAAAGGGAT | 50807 |
| rs532063228 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130401882 | GGGCTAGAGATCACT[C/T]ACCGATTCCATAGTG | 50807 |
| rs532065267 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130425419 | CTGTTTGGGAGGCTG[A/C]GGTATGAGAATCCTT | 50807 |
| rs532067748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320070 | ACTTTTCTGTATTTT[C/T]CACATTTTTATAATG | 50807 |
| rs532069583 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227817 | AAGTTCAGATAACGT[C/G]TGTCGTCGTTCTGAG | 50807 |
| rs532070062 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130101700 | CTCCCTACTAGCTGG[A/G]GACTACAGGCATGTG | 50807 |
| rs532077085 | in-del | -/TAGT | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154275 | CAAATCATTCACAAA[-/TAGT]TAGTAACAAGTGATA | 50807 |
| rs532081241 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130076027 | CACACAGCTACTAAG[C/T]GGTAGAGCTGGTGTT | 50807 |
| rs532088133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130369454 | ACATTTGGGATTTTC[A/G]GATTGGGAATGCTCA | 50807 |
| rs532100280 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130417835 | CTTTCAGGCTTACAT[-/C]CAGACACAATTCAGC | 50807 |
| rs532106464 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148692 | AATATGTCAACTATA[A/T]TTCTTATACTTTCTG | 50807 |
| rs532127593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226715 | CAAGAAAAGATACTC[A/G]AAGAGTTCCACAGGG | 50807 |
| rs532128886 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057453 | AAAGCCCCATGGCTG[G/T]TTTTCTTTTTTTTCA | 50807 |
| rs532129172 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130361030 | TTCACTCCAAGAAGG[A/C]CTTCCTTCCTCTAGG | 50807 |
| rs532133070 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130237501 | ATTTCTTTTAGTGTT[-/A]AAAAAAAAAATTAGT | 50807 |
| rs532136546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246100 | CTGCGAGTTGTAAAG[C/G]AAGTCTTACAAAGTC | 50807 |
| rs532146618 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380911 | TTTATTGAGACAGGG[-/TC]TCTCTCTCTCTTGTC | 50807 |
| rs532148428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129042 | GGTTTCCCCCATGCT[A/G]TTCTCATGATAGTGA | 50807 |
| rs532158028 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219298 | TGTGTACAAAATTAA[C/G]GGTTTACCCAGCAGA | 50807 |
| rs532159296 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154960 | ACATTTGGTTAACGT[C/G]ACTAACTCTCTGCAA | 50807 |
| rs532166202 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130089802 | TCTCACATACATGCA[C/G/T]GTACACCAACATATG | 50807 |
| rs532167780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148092 | CCCGGAATCCCTTAC[A/C]GCCCTCTCTACCCTA | 50807 |
| rs532180589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130135255 | TAACACTTTGGGAGG[C/T]TGAGGTAGGAGGACT | 50807 |
| rs532185993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376966 | ATCCAAGTTGAAATG[C/G]GGCAAGAGATGTGAA | 50807 |
| rs532186664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257683 | GCTGTATCTCCTTTC[A/G]AAAATTCAAAAAGCA | 50807 |
| rs532192158 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278762 | AAACAGAAGAGAGGG[C/G]GAGCTGTTGTTTCTG | 50807 |
| rs532202399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314144 | ATGCAAGGCTCTCAC[C/T]TGGGGTCAAAAAGGT | 50807 |
| rs532207615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405310 | AAGATATGAAATAAC[A/G]TGTCCAAGACAGTGT | 50807 |
| rs532217773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273497 | CATCCAATACACTGG[C/T]TGTGCATCAGAATTA | 50807 |
| rs532219236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134504 | CCTTGTGTATATTAT[C/T]GCTAATCTTCACAAA | 50807 |
| rs532219607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130279867 | TGAGCTATTTACAAC[C/T]TTTTGCCTCTCTTGA | 50807 |
| rs532220281 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130382547 | TTGTATCCCCAGCAC[A/G]CAGTGCTACCACCCA | 50807 |
| rs532225665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377415 | ATGTGTGATCGACAA[A/G]CAGACATTGCAGAAG | 50807 |
| rs532242610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130266150 | CTCAATGAAAGGTGA[A/G]CTAGGGAAGAGAAAA | 50807 |
| rs532247598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130190793 | AGTGCTGGGATTACA[A/G]ACGTGAGCCACCGCA | 50807 |
| rs532249960 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370162 | AAAAAATTACCCAAG[C/G]ATGGTGGCGCACACA | 50807 |
| rs532254230 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130103419 | CTGCTCTGATCTTTT[G/T]TCTTTCCTTTTACTA | 50807 |
| rs532256641 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130279382 | TCTTGAATATGGCAA[C/T]GAGGGAATGTGAGGA | 50807 |
| rs532270036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123523 | AGAATCTGTGCATCC[C/T]GGAAATACATTTCTA | 50807 |
| rs532273833 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130400127 | GCCTGGCCGAAAGCC[A/G]GTGTCTTGTGTGAGA | 50807 |
| rs532275486 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130250885 | CCATTTGTAAAATGG[C/T]AAATTTGGAAAATAC | 50807 |
| rs532276366 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130253859 | AACCCCGTCTCTACT[A/G]AAAATATAAAAATTA | 50807 |
| rs532278426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394576 | CCTTGTAAAGTATGC[A/G]ATCTCTGTGACCCAC | 50807 |
| rs532283340 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141652 | TCCCAGGCGAAGTGA[C/T]TGTCCTACCTTAGCC | 50807 |
| rs532284976 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130360154 | TTACCTTCTAGGACA[C/G]AACTAGACAACTCAC | 50807 |
| rs532290213 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056170 | GATTAATCATGTCCT[A/G]TTTTTCAGAGGAAAG | 50807 |
| rs532292841 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130129401 | AAAACAACTGATAGA[A/G]GAATTGCCCGACTTT | 50807 |
| rs532305554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348217 | TAATAATAGAGCTAA[C/G]AAGAGCTTACATTTT | 50807 |
| rs532307869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355351 | CAGTTTTTCAGTTGC[A/G]CTCTATGTATGTGCA | 50807 |
| rs532324918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083865 | ACGGCATCATCTCAG[C/T]TCACTGCAACCTCTG | 50807 |
| rs532329359 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130218430 | AATGATTCCCTATTC[A/C]CCTACTCCTGTCCCT | 50807 |
| rs532330312 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130273955 | AGGATGAAGGGGGGC[A/G]GAGGAGCTGGGGTCC | 50807 |
| rs532331031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320620 | ACACTGAGAAGTCTA[A/G]GGCTGTATGAAGGAG | 50807 |
| rs532332976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130266799 | AGACACTATGAACGA[C/T]AGACAGATATAAATA | 50807 |
| rs532346299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431563 | GTTCCTATTCGTTAT[C/T]TAAGATTCGGCTCAA | 50807 |
| rs532347745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403707 | ACAGGTGTCCGCCAC[C/G]ACGCCCAGCTACTTT | 50807 |
| rs532360783 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130105602 | ATCTAATGGTTTTCA[C/T]AGTATAAAGCTTAAA | 50807 |
| rs532383469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399963 | TAGCTGGGATTACAG[A/G]CATGTGCCACCATGC | 50807 |
| rs532383606 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130089206 | GAAAGATGACTAAAC[A/T]TTAACATAAAGAAGT | 50807 |
| rs532384971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397852 | GGTGGCTGGTAATCT[A/G]AATGGTATTTACCTC | 50807 |
| rs532389627 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176760 | CAATGGCGTGATCTC[A/G]GCTCACTGCAACCTC | 50807 |
| rs532392796 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130208804 | GTCATATTCTTTTGA[A/G]CTTCTGAATCTATGA | 50807 |
| rs532399535 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359212 | ATCTTTCATTTGCAC[-/T]TTTTTTTTTTAACTT | 50807 |
| rs532399686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400504 | AGGAAAAAAAAAAAG[A/G]CCAGGTGGGCACGGT | 50807 |
| rs532423119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130398591 | GTGGCAGTAGCAGTA[A/G]TAGTAGAAGTACTAG | 50807 |
| rs532434015 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130421926 | TGAGAAATCCTGTGA[A/G]TTCCAAATAAACATA | 50807 |
| rs532442479 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130308781 | GCATGGTGGCTTACA[C/G]CTGTAATCCCACCAC | 50807 |
| rs532448136 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130386547 | ACCCTGTAGATACAC[A/G]ATCGCCACGCGTCGC | 50807 |
| rs532450277 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219829 | GGTCTTGCTATTGTA[A/G]ACCTGCGTGGAGTGC | 50807 |
| rs532455535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130357739 | ACAGTGCATGCCAGG[A/G]ACAGGACTTCCATCT | 50807 |
| rs532465983 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130298014 | CTGTGGGAGTCCAGG[A/C]AAATCACTTCCCTTC | 50807 |
| rs532467663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076584 | TGGAGTGTAGTGGCG[C/T]GATCTCTGCTCACTG | 50807 |
| rs532475220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438161 | GAAACCGTCTGTTTC[C/T]GGGGAGGATCTGGGA | 50807 |
| rs532480740 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | ASAP1 | GRCh38.p7 | 8:130443222 | AGGAGACCTCCCCCC[A/C]CCACCGGGCGGCCTC | 50807 |
| rs532482523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229399 | GGAAAATACAATCCT[A/G]CTTTGATGAGACATA | 50807 |
| rs532493641 | snp | G/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081114 | GCTGTCAATTGAGGA[G/T]AATAGTTTCTAAACT | 50807 |
| rs532501855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130305467 | CTCCCGGGTTCAAGC[A/G]ATTCTCTTGCCTCAG | 50807 |
| rs532502287 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133649 | GCCTGGGCGACAGAG[C/T]GAGACTCCGTCTCAA | 50807 |
| rs532506253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130442468 | CAAAACAGAAAGGCT[C/T]TGGGATGAAGGTTGC | 50807 |
| rs532509522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359453 | GAAGAAGAAGAAGAA[A/G]AAAAAAGCTAGGCCT | 50807 |
| rs532521987 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224524 | TGTATCTCAGTGAAA[A/C]CTTAGGATTAAAAAA | 50807 |
| rs532527369 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130298337 | CAGACAGGCAGGACA[A/G]GCCCTCATTTTCAAG | 50807 |
| rs532534566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217611 | ATTACCTATGGTTCA[C/G]TTCTGCATCCCTACC | 50807 |
| rs532539326 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130353131 | CCTATGAACTGCCCC[C/T]TTCTACCCTGTTAAA | 50807 |
| rs532560144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130230936 | ACCATGGTAAGACAC[C/T]GAACCTAATTACCAA | 50807 |
| rs532567010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130075467 | CTAGGCAACGGAGCA[C/T]TAGACTGGGGTCACA | 50807 |
| rs532583420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430784 | TTGGAAGAAGAGCAA[C/G]AAAGAAAGACAATGA | 50807 |
| rs532583473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423963 | GTTTTTTTTGAAGGG[C/T]GGTGATGAAAATGTT | 50807 |
| rs532584808 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130412542 | CTGCAGAGCCATGAG[C/T]CAATTAAACCTCTTT | 50807 |
| rs532586122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094499 | AGGCGTGAGTCACCA[C/T]GCCTAGTCTAAATTT | 50807 |
| rs532591472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068738 | GGACTGTCCAACTCT[A/G]CCTACAAATGTCAAG | 50807 |
| rs532592012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393183 | TTTGTAGCGGTTTAC[C/T]ATTTTAAATGATGCT | 50807 |
| rs532593091 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130194457 | TTTTAGGTGATTATT[C/G]TGCCACGAAGATGGA | 50807 |
| rs532599441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160916 | ACACAGAAAATATCA[C/T]TGTAAAGATAATACC | 50807 |
| rs532605336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340044 | TCATTCTACTGGGTC[A/G]CAGGCTTTGGAGATA | 50807 |
| rs532605924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081929 | ATAAATAGTATAATC[A/G]CCCCTCATTTTATAT | 50807 |
| rs532614525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435465 | GGCACTGCAGCAGGT[A/G]AATGCACAGGACGCA | 50807 |
| rs532625145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114355 | ACAACTGTAACACAA[C/T]GGTAATTACTTGTGT | 50807 |
| rs532641007 | snp | A/G | 1.74078e-05 | 0.00295019 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128112 | GTAAAAACATAAGAG[A/G]AAAAAAGTCTTTATA | 50807 |
| rs532650889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360112 | CCTGGAGATTGAGTA[A/G]TGCCAAGGCCCCTGC | 50807 |
| rs532650939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352677 | ACAAAATACTTAACT[A/G]CTGTAATCCTGAATT | 50807 |
| rs532655599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127684 | TTATATACCTGGACC[G/T]TATAGGAAAGGTAGT | 50807 |
| rs532656224 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205006 | GCCTTAAGGCTGTGA[A/G]GGTGAGACCAGCTCT | 50807 |
| rs532671375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313379 | CTCTCAATGAGATCA[C/T]GTATAAATTGAGTCC | 50807 |
| rs532680942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285313 | GAGTTGTAAACCACC[A/G]AGTTGGAAAGAAAAA | 50807 |
| rs532685611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299126 | ATAAGCTGGATGCCC[A/G]TGTGTCCGTGCCTCT | 50807 |
| rs532688912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224983 | CTAATTCTCTTCAAC[C/T]ATATCAGCACATAGA | 50807 |
| rs532692006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424411 | TCGGAGAGCACTCCA[C/T]TTCCCAAGAGCCCTT | 50807 |
| rs532701169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211736 | ATGACATTTTTTAGT[A/G]TTTAGCATAGACCTT | 50807 |
| rs532710523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333622 | AAACAAAACAAAACA[A/G]AACAAAAAACAAACG | 50807 |
| rs532715704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292073 | AACTGAAGAATTTGA[A/G]TTTTATTTCCTACCC | 50807 |
| rs532729802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130161439 | GAAAATCATAGATTC[C/T]GTGTTCAAAAGCATG | 50807 |
| rs532736556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245574 | ACCACCAAGCTATCA[A/G]CTTCCCAAGCCAAAG | 50807 |
| rs532740495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168229 | AATATATACGCTTTT[A/C]TTTACCCCCAAATGA | 50807 |
| rs532745623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434771 | AACGGCTCTCTGTGA[C/T]GGCTCGGCCCATATT | 50807 |
| rs532746541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197369 | AGGAGGTTGAGGCTG[C/T]AGTGAGCTGAGATCA | 50807 |
| rs532769290 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251343 | GAAGTGCTTGAACCT[C/G]GGGGGAGGAGGCTGA | 50807 |
| rs532770894 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258535 | TAGTGGAAACAACAG[A/G]GACGAGAGCCCAGAT | 50807 |
| rs532779834 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397192 | GTTGCCCAGACTGGA[C/G]TGCAATGGCACGATC | 50807 |
| rs532782458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130256481 | TCAAGAGTTGAGAAA[C/T]ACAGAGATAATCTTG | 50807 |
| rs532783263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121990 | TCTCCCGCCACATCT[G/T]CCTTCATGACATAGC | 50807 |
| rs532799616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130345173 | ATGAGAATATATTAT[A/G]ACAGAGCGCAGAAAT | 50807 |
| rs532809437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063447 | CCTGGCTTTGGTGTG[A/C]CAATGTGACTGTTGG | 50807 |
| rs532819739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120187 | AGGTCAAAGTCCTTT[C/T]TAGGATGGCTAGAGC | 50807 |
| rs532829297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130172155 | CAGCAAAGTGTGGGG[C/T]AGTTAGCATGTGCTC | 50807 |
| rs532830616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387056 | TAAAAACAGAGAAAA[C/T]TGTTCTCTCCTCAAA | 50807 |
| rs532832485 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130061400 | ATGTAGCCATTTAAA[A/T]TTCTTTTATATAGTT | 50807 |
| rs532857296 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114997 | ATTCCTGGTCTCAAG[C/T]GATAGTTCTGCCTTG | 50807 |
| rs532861905 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376245 | CTGGGTGCTCCACCC[C/T]GAATGCCAGAGCATC | 50807 |
| rs532861967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382825 | GCACTTCAACCTGGG[C/T]GACAGAGCAAGACTG | 50807 |
| rs532866919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104961 | TCTAAGCTGCCACAT[A/C]GGAAGGGTAATGACA | 50807 |
| rs532867312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381051 | ACCACACCTGGCTAA[A/T]TTTTGTATTTTTTTG | 50807 |
| rs532867627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417325 | CCGCAGCAGCAGGGC[C/T]GTTCCCTGTGGGCCC | 50807 |
| rs532868268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289900 | TCCAGTACGTTTCTA[C/G]TTTAGCTTCTAAAAG | 50807 |
| rs532894391 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130067589 | TCTGTAGAGACAAGG[A/T]CTCATCTCATCATGT | 50807 |
| rs532900771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130216707 | GCTGATAACTCCTAA[A/G]TTGATATCCCCAGCC | 50807 |
| rs532902202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112716 | CCTGCTCAACCCTTT[A/C]ACGTTGAAGTTCTTT | 50807 |
| rs532904689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297244 | GTGGGAGATTAGTTC[A/G]TCTCCCCCCATGCAT | 50807 |
| rs532936107 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130186276 | TATATTCCTAAGACA[C/G]CAAGTCCCTAACAAT | 50807 |
| rs532943355 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130061929 | CCAATTTTAGCTCCA[C/T]CACTTACTAGCTGTG | 50807 |
| rs532951192 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130324692 | GGCCTCCAAGTCTAT[A/G]GATACAAGAATAGGG | 50807 |
| rs532972441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428757 | ACCATCAGCAGCACC[A/G]TTATCATCCCCATTA | 50807 |
| rs532992804 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079768 | GTGAACGTCTGGTTT[C/G]TTGTTGTGGCCTGCC | 50807 |
| rs532995436 | in-del | -/T | 0.413914 | 0.188765 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332916 | CAGCTAAAAAAGAAG[-/T]TTTTTTTTTTTAAAG | 50807 |
| rs533001628 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381607 | CTGGCTTGGAGAATG[A/C]GTCCTCCAAGCTAGA | 50807 |
| rs533004879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130416395 | TGAATTAATTAATGA[A/G]TGCCTAAACAAACAC | 50807 |
| rs533009318 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180596 | TGGCAGGTTCCCAAA[A/C]GGCTTGGAGAAAAAT | 50807 |
| rs533012807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107242 | GGTTGGAGAGAAGTG[C/G]CACAATCTCGGCTCA | 50807 |
| rs533016339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068228 | TTGTTGTCTATAATG[C/G]CTAAAATAAAAGAGG | 50807 |
| rs533026443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056308 | CTCTGACAGGCTTCA[C/T]GCCAGGGGCTGGCCC | 50807 |
| rs533038209 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130116824 | AATAATCAAATTACA[A/G]TGTACCATGCAACAC | 50807 |
| rs533052091 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130346818 | CCAGCAGTGAGTGCT[C/T]ATTTTGATTTGTACT | 50807 |
| rs533054395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375211 | GTCTTGTGCTTAGTC[A/G]CAGGGCTCTAAACCC | 50807 |
| rs533060381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093971 | TGCTTTAGGTTTAAA[C/T]TGCCAGGCTATATAA | 50807 |
| rs533064157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120420 | GAATCTCAGTTTCTT[G/T]ACCTGTAAAATATTA | 50807 |
| rs533069338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277462 | TACAAATTCAAAATA[C/T]GAATTCCATTTTTAC | 50807 |
| rs533090244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130243406 | AAGATGCTTTGTAAG[A/G]ATTCACTGACATGAA | 50807 |
| rs533098965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130367855 | CAAAAATATGATTTC[A/G]CCTGCAATGTATTTG | 50807 |
| rs533107376 | snp | C/T | | | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444152 | CACTTCCTCTCTGCT[C/T]TTATAATTTTATTTT | 50807 |
| rs533116195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244885 | CAAGCCAGGAAGGAA[C/T]GGGAGTAAGGGTGCA | 50807 |
| rs533118029 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295383 | ATTGATTAGCCAGGA[A/G]CCACCAATGGAAAGA | 50807 |
| rs533131055 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100677 | TCCTTTGCCCATTTT[A/G]AAATCACATTATCAT | 50807 |
| rs533136038 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130329303 | GTTGTGGAACAGACA[C/T]TGGGTGGGAACCTCC | 50807 |
| rs533138460 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415681 | TAATCCCACCTACTC[A/G]GGAGGCTTAGGCAGG | 50807 |
| rs533140233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234763 | AGGGTCTCCCTTTTG[C/T]AGCTCACAAGCATAG | 50807 |
| rs533150120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423135 | TTGAGACAGAGTCTC[A/G]CTCTGTCACCCAGGC | 50807 |
| rs533158728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130242090 | TGCTCTGAGCATTCA[A/G]TACATTAATGTGCCT | 50807 |
| rs533176526 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409360 | TGTACTAATCGCTAG[C/G]TCTTTCAGTTTCCAT | 50807 |
| rs533181480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324392 | AGGGATGAAAAGGTT[C/G]AATATCATTAACCAA | 50807 |
| rs533192434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248684 | GGGAGGAGACAAGCT[A/G]GGTATTACATCACAA | 50807 |
| rs533193345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111998 | CTCAAATGTACCTTG[C/T]AATTCTTACCTCAAA | 50807 |
| rs533193428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105836 | TGTGCCACATTGCTC[C/T]GTCAACTGACTTCCA | 50807 |
| rs533193911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374594 | TGCTTTTTAACAAGC[C/T]TACATACTTGTCGAC | 50807 |
| rs533194931 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130188341 | GACACCTCTGTAGGT[G/T]AGGCGACACAATTAT | 50807 |
| rs533200609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130201219 | AGAAGGAAAGACTTA[C/G]AGCCAGAGAGCAGAA | 50807 |
| rs533204757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130147436 | AAAATCCTCACTAGA[A/G]ATTCAGTGTCAGGGT | 50807 |
| rs533210131 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318169 | TCATTGTAGCCTTGA[C/T]CGCCCAGGCTCAAGT | 50807 |
| rs533231626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140548 | TCTCATTTCTAAGCA[C/T]GGACTATTTCAAAGT | 50807 |
| rs533239682 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366885 | GTACTATGCTAGATT[A/C]CTTTTTTTTTTTTTT | 50807 |
| rs533249591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133116 | ACAGTTTATAAAACT[C/T]GGTCCAAATTACCCC | 50807 |
| rs533291104 | in-del | -/A | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214231 | CTAAAGGTTATCTTT[-/A]AAAAAAAAATCAATG | 50807 |
| rs533304078 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414773 | TCTTTTTTTTTTTTT[C/T]TTGAGACAGGGTCTT | 50807 |
| rs533309382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130357080 | TGGGCAAATATCCTA[C/T]TTTTATCGTGGCCCC | 50807 |
| rs533315904 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151151 | GCCGAAGCGGGCAGA[C/T]CACAAGGTCAGGAGT | 50807 |
| rs533325458 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130317500 | GTAAGAAGTGAAGGG[A/G]CTGGACCTGTCTGTG | 50807 |
| rs533326377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130365890 | TGGAGAGATCCAGAA[A/G]AGAGTAAGATCCACA | 50807 |
| rs533353534 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066563 | TTTTCTTTCTCATTC[A/T]TTCTTTCTTTTTTCT | 50807 |
| rs533356344 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270473 | AATAACTTCCCTCAT[G/T]TAAAAGGTTAATTGG | 50807 |
| rs533356860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060146 | ACCCCGAGAGGGAAA[C/T]TGGTTTCTCGTGACC | 50807 |
| rs533362487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414151 | ACAGAAAGGTAGGAA[A/G]AGGGAATTCTGAATG | 50807 |
| rs533365021 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122704 | TCTGGCTTCAAAATC[-/A]TATGACCCTAACCAC | 50807 |
| rs533367709 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130303678 | CTGAAAAGGCTACAT[A/G]CTTTACTTTATGACT | 50807 |
| rs533377234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150744 | AATTAGCTGGGCGTG[A/G]TGAAGTGTGCCTGCA | 50807 |
| rs533379936 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130089432 | AGTCCTGATCTCTCA[C/T]AGTTCAAAGGCCCTG | 50807 |
| rs533384588 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241402 | AGAAGAATGGAAGTT[C/G]TATGAAAGCAGGGGC | 50807 |
| rs533390477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317417 | GGTTTGTTGAAACTG[C/T]AGGAACAGGGTCTAC | 50807 |
| rs533392069 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083080 | TATACATGAGTAAAT[C/T]TGAGACCAACAGGGC | 50807 |
| rs533405425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379609 | TTGAACATGTAGTTC[A/G]GGTAGGAAAATTGGA | 50807 |
| rs533409593 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281572 | CTAAAAAACTTATCC[A/G]AAGTGTAAAAAATAG | 50807 |
| rs533411976 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130371615 | AGCTGGAAGAGGACT[-/C]CTGTTATCCTTCCCT | 50807 |
| rs533421111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322794 | ATACGTATAACTAAC[A/G]AAGGGCAGAATGTGG | 50807 |
| rs533421274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109337 | GGGGGCTTTGCTTGA[C/T]GGTAATTTAGGTCAA | 50807 |
| rs533421602 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187081 | ACCTCTTAGCCCTAA[C/T]AAGGATATGCTAGAG | 50807 |
| rs533424095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173431 | GCTTCTCTGTTCCTC[C/T]TTTCTCTCTTCTCTC | 50807 |
| rs533435044 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415732 | GGCGGAGGTTGCAGT[C/G]AGCCAAGATCACACT | 50807 |
| rs533435253 | snp | A/T | 0.000803213 | 0.020024 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275927 | GATAATACCAGTCAC[A/T]TTTTTTTGCAGAAGT | 50807 |
| rs533438828 | snp | A/G | 1.64841e-05 | 0.00287085 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130126001 | TTCCAAAGACTGAAT[A/G]CGAGAAATATGAACC | 50807 |
| rs533441560 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130212925 | AAAGCAAGACATCAA[C/T]GCGAAAACACCCATC | 50807 |
| rs533445500 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288851 | TGGTTAAGCAAATTA[C/T]GATAAATTCACAGAA | 50807 |
| rs533448958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132435 | TCCTATTCCATCCTC[C/G]TGTTTCTGTGCCATC | 50807 |
| rs533451712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091539 | GCCTTGATATAGGGA[A/G]CTTGCATTTATCTGA | 50807 |
| rs533454982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215731 | CCTGAGCAACAGAGT[A/G]AGACTCTGTCTCAAA | 50807 |
| rs533483076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130186469 | AAAATACATATCTCC[C/T]CCCACCCCACCCTAC | 50807 |
| rs533490499 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130365048 | ACTATCAATCCCTGA[C/T]AGCATTCAGGGACTA | 50807 |
| rs533493091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223007 | ACTGAAGCTCCTAGG[G/T]GCCTTAATTTCTTCA | 50807 |
| rs533503646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407813 | TGTTTTTTATTCAAC[A/G]GAAGTGACTCCACGA | 50807 |
| rs533512931 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130064144 | TGACATGATTGAATG[C/T]GGAAGGCTCCAGTGT | 50807 |
| rs533517027 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347897 | TCCTTCCAATAAGTC[C/G]CCATTTTGCTTTAAC | 50807 |
| rs533527279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220035 | CTCATGTGTTCCTCC[C/T]ACATTGGCCACCCAA | 50807 |
| rs533528175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086105 | TGATCGCCTTCTCCA[C/T]ACTTCAGCTTCATGG | 50807 |
| rs533529760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130092963 | AAAAAAAAAATTAAG[C/G]CTTTTCTAAATAATG | 50807 |
| rs533534216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130138641 | CGGGAGTTCCAGACC[C/T]GCCTGATCAACATGG | 50807 |
| rs533534743 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130310508 | TTAAACCACAAAGGC[A/C]ATTAAGTCATAAAAG | 50807 |
| rs533536496 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314758 | AAGGGAGCTAAGCCA[A/C]AGATACTAAACATTA | 50807 |
| rs533545336 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179665 | TGTGGTCAAAAACTG[G/T]AAAGATTGATTGTTT | 50807 |
| rs533546725 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ASAP1 | GRCh38.p7 | 8:130172436 | CTACTGAAATAAACA[C/T]TTTTTAAAAATAAGA | 50807 |
| rs533552941 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130300781 | ATTCTTGAAAGCCCA[C/G]CACTGGGCTGGCTTC | 50807 |
| rs533576174 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384539 | GCTGGAGTGCAATGG[C/T]GCTATCTTGGCTCAC | 50807 |
| rs533593231 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130260996 | CCTCAATCAACTTTA[C/T]GCAGAGATGCAGTCC | 50807 |
| rs533598008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276599 | CACAGCTGAGACAAT[C/T]TGGAGTAAATACTTA | 50807 |
| rs533609869 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130406465 | TTATTTATCCTTTCA[C/T]ACTTTAGTTCTTTTT | 50807 |
| rs533610028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179111 | ACACTGAAGATGGAA[A/G]ACACTATTTCTTATC | 50807 |
| rs533615147 | in-del | -/TT | 0.0126979 | 0.078662 | intron-variant | ASAP1 | GRCh38.p7 | 8:130391565 | TAGCTTTGGAAAAAC[-/TT]TGGTTCTCAATCTAT | 50807 |
| rs533615165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163293 | GGATTCAGACACTAA[C/T]AACTTATAAAAACGA | 50807 |
| rs533617859 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187599 | TCTTGTACTTCTTCT[G/T]TAGACATGGGGGTCT | 50807 |
| rs533619077 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206040 | TTTCCATATATCTCA[A/C]ATTTTTATAATAAAT | 50807 |
| rs533634381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109919 | AGCCATGAAGAACAC[C/T]CTTGGTTTTTGTAGG | 50807 |
| rs533638136 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359450 | AAAGAAGAAGAAGAA[A/G]AAAAAAAAAGCTAGG | 50807 |
| rs533644668 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117237 | TACATGTATTAGTTC[A/C]TTGAATCTTTACAAC | 50807 |
| rs533678213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425111 | CGAAGTGGGCGAAAT[C/T]ACTTGAAATCAGGAG | 50807 |
| rs533678349 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205396 | AGAAAAAAAAAAAAA[A/C]AAAACAAAAACCATA | 50807 |
| rs533687808 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130205165 | TCTCCCTTCTCCACT[C/T]TCCCTTTTCCTTCTT | 50807 |
| rs533701014 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419097 | GCCAGGGTCCCGCAC[C/G]CATTGTCTCACCCCA | 50807 |
| rs533707088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130294353 | ATTTCCCCTGGTGTA[C/T]AGTCACCTCCTCTGT | 50807 |
| rs533707714 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249456 | AGTAGCTAAAATTTT[A/C]TCTTTTCTGAACAAT | 50807 |
| rs533709847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335057 | ATGAGACGGATTAAC[A/G]ATCACTGATTTATTC | 50807 |
| rs533712417 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130213180 | CCAAAAGCACAGAAA[C/T]ATTAGAGCCAAAGTT | 50807 |
| rs533718349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215196 | TGAGCCACCGCACCT[C/T]GCCTTTCCCTTTTTC | 50807 |
| rs533720616 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434284 | AGGATGCAGTGAGCT[C/G]CCATAGCGCCACTGC | 50807 |
| rs533732235 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355081 | ATGGGGTTTCCCTAT[C/T]TTGGCCAGGCTGGTC | 50807 |
| rs533758262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400111 | AGGCGTGAGCCATCG[C/T]GCCTGGCCGAAAGCC | 50807 |
| rs533763743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259900 | TAAGGCTTTCAAATT[A/G]AGTGCATTTATCTAT | 50807 |
| rs533767631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278711 | TTTTATCCATATGCA[C/T]TAAATATCCTTTCTA | 50807 |
| rs533789727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105206 | ACTCACAATAAAAAA[C/T]AACAATCCAACAACA | 50807 |
| rs533796015 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219401 | AGAAGGGAGGAACAC[A/C]CTGCAGAGTACAGTA | 50807 |
| rs533796414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394734 | CTCTCTTTTGTACTC[C/T]GTCTCTTTATTTCTC | 50807 |
| rs533799058 | in-del | -/CTAATC | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175491 | CGGCCTCCTAAAGTG[-/CTAATC]CTAGGATTATAGGTG | 50807 |
| rs533821965 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169533 | AAAAGTCAAAATTCA[C/T]TCAGTTCCTCAAAGA | 50807 |
| rs533827234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390079 | ACACTAAAGGGAGGG[C/G]CTGAGAATCTGATTT | 50807 |
| rs533834392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130192413 | AGGAAAAAAAAGGTT[A/G]AGCAACACTAACTGG | 50807 |
| rs533850424 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130315183 | AGTTCACAAGGAAAA[C/T]AGTAGGCAGTCCCAA | 50807 |
| rs533878661 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130328305 | AAAGACTATGCTCTT[A/T]ACCACTGTGACAAAT | 50807 |
| rs533884845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240802 | CTTCCAACCTTGATA[C/T]GAAGACTTTTTACTT | 50807 |
| rs533894472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069633 | TCCAATTTTAGCATA[C/T]GTGCTGCCGAAGTGA | 50807 |
| rs533906331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130196799 | AAAATAATGAGCCAG[C/T]TCCCAGTAGTTAAGT | 50807 |
| rs533907116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070208 | TGCCCGGCTAATTTT[C/T]TCTATTTTTTAGTAG | 50807 |
| rs533911723 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130176208 | AAATTCACTGTTGAA[A/T]ACCAGCTGACTTTGT | 50807 |
| rs533914849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424167 | AAAAATCAATAAATG[C/T]GAGCTGAGCTTGAAA | 50807 |
| rs533920550 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388740 | GGTCAGATGATTCGC[A/T]GAAGCTGAGTTGACT | 50807 |
| rs533923321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341677 | CTGGTGCAAAGATTA[A/G]ATAATTCCGTGTCTT | 50807 |
| rs533927940 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130170888 | CATGCCTGGCTCATT[C/T]TTATTTTTGTAAAGA | 50807 |
| rs533932186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154710 | TGTGCATTTAACTAC[C/T]AGAAGCACAGTTTGT | 50807 |
| rs533932505 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286794 | AACGAATGCACAAAT[C/G]AGCAAACAACTTTAA | 50807 |
| rs533939955 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130173076 | TTCTTAAGGATATCA[A/C]GTATTAATCAGTTAA | 50807 |
| rs533954339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199044 | CTTCCTCTGTCTCCA[C/T]GTCACTTTCTCAGTG | 50807 |
| rs533956633 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245087 | AGAGGGACCTGGCAG[C/G]CGCAGCTTATATGAA | 50807 |
| rs533957760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382405 | CTAGACCAATGCTCA[A/G]AAAAATACAAGGTGC | 50807 |
| rs533968961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390739 | CAAGCATTCATACCT[A/G]CTAGGATGGCTACTA | 50807 |
| rs533973897 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130244965 | TCCAATTACAGCAGT[C/T]TGAGGAGTTGAGGTG | 50807 |
| rs533990463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149869 | AAAAAGGTCTGGGCC[A/C]AAGCCAGTGAAAAGT | 50807 |
| rs534001604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376470 | CGGTGGCTCACGCCT[A/G]TAATCCCAACACTTT | 50807 |
| rs534007434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384554 | CGCTATCTTGGCTCA[C/T]TGCAACCTCCCCCTC | 50807 |
| rs534009205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064094 | ATCTGGTGGGGGTTG[C/T]GAGAAGAACCACCAG | 50807 |
| rs534012210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286135 | ATGAAGAAAAGAAGG[C/T]TCAGGGCACAGTAAT | 50807 |
| rs534025420 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130440922 | AAGGAATCACTCATC[A/T]GTTAGAGGTTGTTTC | 50807 |
| rs534034830 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056936 | CAACGTGAAAACCAA[C/T]AGATGTGTGGACTGC | 50807 |
| rs534046640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285803 | CCGTGGAAAGTTTTC[C/T]GCCTCTGGTTTCTGA | 50807 |
| rs534050058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101999 | TGTGTTTTTTGGTGA[C/T]GTCTTTAGGTTTTTC | 50807 |
| rs534065056 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130127366 | GGATTACAGGTGCCC[A/G]CCACCTCGCCCAGCT | 50807 |
| rs534067441 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280968 | TATGTTTACAGATTC[A/T]CTTTTTCCAAATAAC | 50807 |
| rs534069477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130184708 | AACTAGTAAAAGCAC[C/T]ATCTGATGTTTTAGT | 50807 |
| rs534076087 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130326108 | ATAGTTCTAAGTAGT[A/T]GAGGGTTGCTGGAAA | 50807 |
| rs534084222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141784 | ATGCAGTGGCACAAT[C/G]ATGGCTCACTGCAGC | 50807 |
| rs534089514 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097617 | GCATACAGCCAGGGC[C/T]CAGGAAGTGCACCCA | 50807 |
| rs534091006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130411050 | ATTTTGAGTAGAGAC[A/G]GGGTTTTGCCATGTT | 50807 |
| rs534093773 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191837 | ATATGGATAAGATAA[C/T]GAGGGAGCAGAGAGG | 50807 |
| rs534097369 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130278010 | AGTATGGTTCTCAGC[A/G]AGGCTGAAGATTTAT | 50807 |
| rs534097527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130371310 | GTTAAGATTCAAACA[A/G]AAGTCTATCTAATTT | 50807 |
| rs534104199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280475 | CATCCTTGACACACA[A/G]TCTGCCACAGTAGAG | 50807 |
| rs534111687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319637 | TGTTCAAAAGCCCTA[C/G]ACCCAGCAACTCTAC | 50807 |
| rs534117498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130225455 | TTTTTAAAGTTTTAT[C/T]CACTTCAATATTTAA | 50807 |
| rs534118243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150304 | CCACAACAATGTGTT[C/T]TGGCAGGAATAAAAT | 50807 |
| rs534127140 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405440 | GTCTGTGATGTACCA[A/C]CCTACCTCCACTCTT | 50807 |
| rs534132634 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130142987 | AGCTACGTACGGTAG[C/T]GGTGCTGGTGGCCAG | 50807 |
| rs534147552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130412558 | CAATTAAACCTCTTT[C/T]CTTTATAAATTACCC | 50807 |
| rs534155258 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130182842 | AAGGCAAAAAAAAAA[A/C]AAAAAAAACCCAACT | 50807 |
| rs534162169 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204699 | TTCCCCTGTAGAGAA[G/T]GGGGAGCTTCCATGC | 50807 |
| rs534167136 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130279512 | ATCATAAAAGCAGCA[C/T]AGTGCAGTGAAAATA | 50807 |
| rs534173752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273137 | TAAATACAGTGTATC[A/G]ATAAGAACAGAGGGG | 50807 |
| rs534175735 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130416873 | ATCACGGCAGCCTGA[A/G]CTGATGGGGCAACCT | 50807 |
| rs534177077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314267 | CTTCATACCACTTTT[C/T]ATGATGCTCTCAAAA | 50807 |
| rs534191602 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130088034 | CTGAATAATGGCCAC[A/C]CAAAGTTATCGAGTC | 50807 |
| rs534201172 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130192479 | ACCCTCTATTCTACA[A/C]AGATAGCTGAAATAA | 50807 |
| rs534208329 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082818 | CTGTCTTGGCCTCCC[A/G]AAGTGCTGGGATTAC | 50807 |
| rs534230196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252089 | ATAGAAAGTTAGAAG[C/T]AACCTAAATCCAACA | 50807 |
| rs534239193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183389 | TTTCTTGCCCAGGCT[A/G]GAGTGCAGTGGTCCG | 50807 |
| rs534240902 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153774 | GATATAATAATAACT[C/T]CTCTCTAGGAAGGGG | 50807 |
| rs534245306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238714 | GATAAGGAAATGTAG[C/T]AGACCTTCAATAAAT | 50807 |
| rs534248730 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296190 | GAGTCTTGCTTAGGG[-/T]ACTAGCTTCTGAAAG | 50807 |
| rs534252756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102635 | TAGGAAAAATTCCTT[C/T]GTCTTCAATTTTTTT | 50807 |
| rs534260847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405878 | TCTAGGTTCATCAGA[A/G]AAAATATTAAGGCAT | 50807 |
| rs534264372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399678 | ACCTAAAAATTGAAG[G/T]AATTACAATGCCCTA | 50807 |
| rs534274268 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139933 | ATCTTAAAAAAAAAA[A/C]AACAACAAAAAAACA | 50807 |
| rs534287292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424518 | GCTCAGCGTTTGTTT[C/T]TGTTTTTTTTAAACA | 50807 |
| rs534302720 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109055 | GTTGGGATTATAGGC[A/G]TAAGCCACCGCACCC | 50807 |
| rs534303923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377109 | ACATCACTTAGAATT[C/T]CTGAGCCCAGGAATG | 50807 |
| rs534304311 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130306710 | TCATTCATATATTTA[A/G]GGTAAACTTTAAGTA | 50807 |
| rs534305588 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130433727 | AAATGAGAATTCTTA[C/T]CTCATTTTGAAACCC | 50807 |
| rs534309424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130230433 | TTAAACAGCATTCTT[C/T]TGAATCCCTCTAGTT | 50807 |
| rs534319941 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130435248 | CATTCCAAACTAGAA[C/T]TCAGGACTTCTGAGT | 50807 |
| rs534329373 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139435 | GAAAAATTTAATAAT[G/T]TTTAAGCTGACCAGG | 50807 |
| rs534336892 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237262 | GCTAAGCTATGCACA[A/C]GAAAGACAGTACAAG | 50807 |
| rs534341495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134171 | TGATGGCCCACAGGC[A/G]GGAAAGAAGCATGGA | 50807 |
| rs534352180 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055418 | CCAGGTAGGATGCAT[A/T]CAGACCATTAAGCTG | 50807 |
| rs534360700 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130094527 | TTTAAAAAAAAAAAA[C/T]GTTTATGGATACGAA | 50807 |
| rs534365007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130367359 | GACCAATGAATGTAA[A/T]GTCCAAGTAAAAGTA | 50807 |
| rs534367420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277723 | CAGCCATTAGCTCCA[A/G]TTGGGAAATGATTTC | 50807 |
| rs534370790 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130097382 | GTCCTCCCTTGTTAA[C/T]GGCCCTCCCTGCACA | 50807 |
| rs534378062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233074 | CTATACTATACTTGT[C/T]CGTGACTGCAGAAAC | 50807 |
| rs534397005 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127167 | AAGGTGTGGCTGAGT[A/G]GGAAGGAAGGAAAAT | 50807 |
| rs534401487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368114 | GACAGCATCCAGCTT[C/T]TGTTCCCTAATATTT | 50807 |
| rs534401539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359004 | ACTGCGAGGGCCGCC[C/G]ACCCCGCGAAGGAAG | 50807 |
| rs534406946 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130395919 | AATCCGCCCGCCTCC[A/G]TCTCCCAAAGTGCTG | 50807 |
| rs534416065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130232233 | TGTACATTCAAGGGG[A/G]AAGGGGATTAGGCTC | 50807 |
| rs534417691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141385 | CTCCTGCAGGCCCTC[A/G]GAGAGCTCCCTGCTC | 50807 |
| rs534418518 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130071060 | AGAAAGCAGAGTTTC[C/T]CCAAATCATCTAAGA | 50807 |
| rs534423281 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130162165 | GGTTCACTAAGTCCT[A/C]CCTAATAGATATTTT | 50807 |
| rs534423568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320216 | ACTGCCAAAATGGAA[C/T]ATCAATGAGCATATA | 50807 |
| rs534423986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130442681 | AAGTTAACGATGATG[G/T]TCTGCAGTTGACCAT | 50807 |
| rs534426292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130271853 | ATGAAGATTGTGTGC[C/G]ACTCTGAGCTTTCCT | 50807 |
| rs534443749 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130443712 | CGACGCGAGCGGCTC[C/G]CACGATCCCGCTCGG | 50807 |
| rs534451661 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130103643 | GAGTAGCTGGGATTA[C/T]AGGCGTGTGCCACCA | 50807 |
| rs534456363 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176898 | TTTTGCCATGTTGGT[C/G]AGGCTGGTGTTGAAC | 50807 |
| rs534462049 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130076930 | AATGATAAAGCCCAA[A/C]TCCTCCACTTCAAAG | 50807 |
| rs534468247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224011 | GACTCTTTCAATGTA[A/G]GTGTAACCTACCAAG | 50807 |
| rs534476921 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130266411 | TAGGGGGGAGGGTTC[C/T]GTGTACTGTACTTGC | 50807 |
| rs534477693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074640 | AGTCTGTCCCCGAGG[A/G]GGTGGGAGGGTACAA | 50807 |
| rs534479503 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130218478 | CCTTCCTTCCCTCCC[C/T]AGACACAGCCATTAT | 50807 |
| rs534485598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121064 | CTGAGTCTTAAACAT[C/G]TCATATTAAAACTGA | 50807 |
| rs534502493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258327 | GTCCCTGTTTACACC[C/T]ATTGCCCTGGCATAT | 50807 |
| rs534532395 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130312598 | ACAGGCATTATCTCA[A/C]TGAACCAACCATTAC | 50807 |
| rs534534533 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130348798 | TAACCTAGCTGCCAT[G/T]CTCTGTACCAGTCAG | 50807 |
| rs534551016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073288 | CCAGCTACTTGGGAG[A/G]CCGAGGCAGGAGAAT | 50807 |
| rs534561942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388004 | GAAGAAAACATACGG[C/G]GAGCAACCAAAGAGA | 50807 |
| rs534566078 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130299438 | ATCACTAACAAATTG[C/T]GTCTACTGCCGTCTT | 50807 |
| rs534568033 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130161022 | TTATTTCAGGTCATA[C/T]GGCGTGAGAACAGAA | 50807 |
| rs534582284 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130109041 | CGGTCTCCCAAAGTG[C/T]TGGGATTATAGGCGT | 50807 |
| rs534586509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094176 | CAAAATGTGTTTATA[C/T]ATGCTATTCCTCAGC | 50807 |
| rs534588547 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130215316 | TAAGAAACTATGATT[G/T]ACTGGGTATGGTGGC | 50807 |
| rs534590851 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141479 | CTCCCCATGATGTTC[C/T]ATTTTTGTACACCCT | 50807 |
| rs534592112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204182 | CATAGGAGACGGAAC[C/T]CTACTGTGAACTGCA | 50807 |
| rs534599266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130291498 | ACAGAAGGTGTGTGA[C/T]GGAGACACTGACAAA | 50807 |
| rs534609795 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130370487 | ATACATTTGTTGTTT[G/T]TAAGCCATCCAGTCT | 50807 |
| rs534609852 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130346406 | TCTCAGCAGAAGCCT[A/C]TTTCCTGTTTGTTCT | 50807 |
| rs534616826 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130176772 | CTCGGCTCACTGCAA[A/C]CTCTGCCTCCTGGAT | 50807 |
| rs534618865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318348 | TGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCAT | 50807 |
| rs534626467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146494 | TCTAATCTGTTGGAG[C/T]GAAGAAAAATATTCT | 50807 |
| rs534626492 | in-del | -/T | 0.415235 | 0.18761 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114770 | TGTTTTGAAGGTTAA[-/T]TTTTTTTTTTTTTTT | 50807 |
| rs534629508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325062 | TACCCTAACCCAAAC[A/G]TGCCTATACATTTAG | 50807 |
| rs534630869 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062190 | TCCTGGCACAAGGGC[C/G]AAGGACATAGCCTGC | 50807 |
| rs534632533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188709 | TGCATTCCAGCCTGA[A/G]TGAGAGACTCTCTCA | 50807 |
| rs534637304 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130195688 | CAAACAGAGGGAGGC[C/T]GAGGTCTATCTTTCA | 50807 |
| rs534644310 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130298115 | CTAACATTTTTGGCC[A/T]CTAGGGTGCAAAATA | 50807 |
| rs534671963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311407 | GCATTGTATTCTATC[C/T]TTTCCTAGTCTTTTT | 50807 |
| rs534675031 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079539 | AAATCTGCAAAAGGA[G/T]TCAAGTGGAAAAGTA | 50807 |
| rs534690772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402515 | CAGAGCACAGGAAGT[A/C]TGGGATAAAAGATGT | 50807 |
| rs534707298 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130310732 | GCAAGCATGTTAAAC[A/C]GTACTACTTCATGCC | 50807 |
| rs534724509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278346 | AAATTAAAAGGGTGT[A/G]GCAGGTTAAGTCCAC | 50807 |
| rs534725153 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130180874 | TTTCTCTTTCTCAAT[C/T]TTTGTACTGTAATTA | 50807 |
| rs534726169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396878 | TGGTTGAGGAGGGTC[C/T]AAAGTTTAGGTCACT | 50807 |
| rs534748754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403802 | CAGGTGATCTGCCCA[C/T]CTTGGCCTCCCAAAG | 50807 |
| rs534749406 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130370987 | GGTGATAGTTCTATC[A/C]TTTTGTGAATACACT | 50807 |
| rs534755513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130312041 | TGAACACCAACCACT[A/G]TAAATATGTGGATCA | 50807 |
| rs534764261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130231262 | GACAAAAATGTAAGG[A/G]AATGAGAAAATCAAT | 50807 |
| rs534769856 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081351 | GGCAGTTGTGGAGCC[C/T]CAAGCTGCAGGCACC | 50807 |
| rs534779342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127832 | TATGTGAGTGTGTCC[A/G]TAGGGGTTAAGGTTT | 50807 |
| rs534782598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112389 | TGTACAGAGGGCCTC[C/T]GCAGGGCGGGCTCAG | 50807 |
| rs534812923 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130102176 | TCCTTGTCTTCTTCC[A/C]GTTCTTAGAGAAAAA | 50807 |
| rs534820816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217142 | AAGTGATGCATACCA[C/T]GTTCTCTTGGAAGCA | 50807 |
| rs534825255 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208617 | TGTAAAAGACAAAAG[A/T]TCTTGCACGTACTTG | 50807 |
| rs534842824 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130221707 | TTTGTCTTTTGTCCA[C/T]ATAATTTGCAGATGT | 50807 |
| rs534853216 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130443509 | GCGGGTTCGGCCGGG[C/T]GCTCGCGGCTCTCGG | 50807 |
| rs534855895 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130375441 | GGCTCATGCCTGTAA[C/T]CCCAGCAATTGGAGA | 50807 |
| rs534857629 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130396681 | CAGCTCCAGGGACAC[A/G]TTTCCCGTCCATGTG | 50807 |
| rs534859404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175173 | TTTGTACTTAACACC[A/G]ACTAATGATGTTGAG | 50807 |
| rs534874379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393887 | TTACATCTGTCTTTA[C/T]TGTAATCTCTGAACA | 50807 |
| rs534891960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430102 | CTGAGCACCAGGGCC[C/T]CGATCCTTCTGGACC | 50807 |
| rs534907462 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353596 | AACTCTGGGCCAGGC[C/G]TGGTGGCTCATGCCT | 50807 |
| rs534915913 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130298567 | CTTCTAAAAAGCAAA[A/T]CAGAGCATGCCAATC | 50807 |
| rs534932246 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130353825 | GCAGTGAGCTGAGAT[C/T]GCACCACTGCACTGC | 50807 |
| rs534937173 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130348247 | TCCTCCACCCAAAAC[A/G]CATCTGGCAGGGAAA | 50807 |
| rs534938604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249864 | GCCCCTCAGATGTCT[C/T]TGGTTCTCAGCTTCC | 50807 |
| rs534943310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244409 | CCCATTCCTGGAGAC[C/T]GTGCAAGAATCCAAA | 50807 |
| rs534943609 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236770 | GTTTGGGCTGACAGT[A/C]GAGATAAGAGAAAAA | 50807 |
| rs534950596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339656 | AACATAAAACACAAT[A/G]CTATAATCAGGAAGT | 50807 |
| rs534950654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211366 | TTTGTAGGTAGCCCT[G/T]GGGAGTTTTCACATA | 50807 |
| rs534969494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381216 | ATATCTTTTGTAGAG[A/G]GGAGGTCTCACTGTG | 50807 |
| rs534970302 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350832 | GGAAGCTGGAAGCAG[A/C]CAGCCAGACAGCCCT | 50807 |
| rs534973048 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130339277 | TATCTCAAGGTAAAA[A/T]AACGTAAAGAAAAAT | 50807 |
| rs534986699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223239 | GCACAACCTAGACAA[C/T]ATTTGGTGAAAGATC | 50807 |
| rs534990653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130302717 | CTTCATTAAACAAAC[A/G]GTTCTCTGGAGAAAA | 50807 |
| rs534991641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422788 | GGTTCAAATCTCCAC[C/T]GTCATTTGTGAATTC | 50807 |
| rs534998919 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130323240 | AATGGACTGCTATGC[C/T]GTTCTATTCAAGCCT | 50807 |
| rs534999397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396396 | AATGAAGGGAGGGAG[A/G]AAGACAAGACCAGCA | 50807 |
| rs535000556 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107343 | GTCCTCCACCACACC[C/T]GGCTAATTTTTGTTT | 50807 |
| rs535002111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165735 | TATAGACTTCTCTCA[C/T]TTGACCAATCCCCAG | 50807 |
| rs535007483 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374696 | AGCACAGATGTTAAA[C/G]TTGCGCTGAGCAAGT | 50807 |
| rs535011112 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195294 | TAATCCAAGCAATTG[C/G]CGGGGGCCAAGGTGT | 50807 |
| rs535033745 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098252 | CAGCCTTGACAACAG[-/C]TTGCTTCCCTTCCTC | 50807 |
| rs535035070 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130089925 | ACTGTCACTGTGGCC[A/G]AGGACAGATGATGAT | 50807 |
| rs535049228 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130364910 | ACCTCAGCACTCCAG[C/T]CTGGACAACAGAGCA | 50807 |
| rs535050629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332289 | CACCAATGGCAGGGA[A/G]TATAATGAAAACTCT | 50807 |
| rs535054937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415818 | GGAAAATATTCATGA[A/G]ACCTAACACTGGCCC | 50807 |
| rs535062013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270812 | ACTGTTTCTCTCTAC[C/G]TTTAAAAGCCATTTC | 50807 |
| rs535062052 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262729 | CCAAAAGCTCTAAGA[A/G]AGCAGACCTCAAATA | 50807 |
| rs535071864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130113426 | GAGAAGGCAGACTGA[A/G]GCAGCTGCTTGGTCC | 50807 |
| rs535083086 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130182504 | CCTCAGACACTGACA[A/T]TTGGAAAACCCCTAA | 50807 |
| rs535090773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157004 | ATACTTTTGCTTCAA[C/T]AGATATGTAATAGTA | 50807 |
| rs535101149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248264 | TGAACAGGCAGATAC[A/G]GCTCCTACATCTACA | 50807 |
| rs535106170 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120282 | CTGCATGTGTCTTAT[A/G]TAAAGTGTGAAAGGC | 50807 |
| rs535116588 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115472 | CTTAATATAGCTGTT[A/G]AATGGTGCCCAATAA | 50807 |
| rs535119079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126286 | GAACTGAAAACAAAA[G/T]TAAGCACTTTATCCT | 50807 |
| rs535122975 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130064215 | AGGCAGACAGGGTAG[G/T]AGGCTCCAACTGTCC | 50807 |
| rs535127580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263147 | TGATCACAAAACTTA[A/C]CTTCAAAATGCCCAA | 50807 |
| rs535137133 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130345784 | GAAGACTAGCCTGGG[A/C]AACATCACAAAAAAG | 50807 |
| rs535139413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254995 | CCCATCTTCCCTTTC[C/T]GGGAAAATTAAGGCT | 50807 |
| rs535154572 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106123 | GCACTAGGTGATTCA[A/C/T]GTGCAATGCCTTACA | 50807 |
| rs535168824 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130193527 | GAGATTTTTGCATTT[A/T]AAAAAAATTGTAATA | 50807 |
| rs535179480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297380 | TTTCAATCCACGTTT[A/G]GCTGAAGAAAATCCA | 50807 |
| rs535184358 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130427148 | AAACAGCTTGGCCAC[G/T]CTGTTCAGTGGCTAT | 50807 |
| rs535190474 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289562 | AAAAGACTGGGGAGG[A/C]GAAGACTGGAAGGCT | 50807 |
| rs535192542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066231 | TTACAATGGCCATGA[C/T]TCAGTCATTTCTGGA | 50807 |
| rs535194107 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422274 | GGCGTGGAGATGAAG[C/G]CGATGAGGACTCTGG | 50807 |
| rs535201406 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318157 | TGCAGTCACAGCTCA[C/T]TGTAGCCTTGACCGC | 50807 |
| rs535201727 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413625 | AGTTTGAAAAATGAG[G/T]AGCCTGAATCATCTC | 50807 |
| rs535204814 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130200982 | GACAATCCTTCCTAG[A/T]GGTTCTCAAAAGTGT | 50807 |
| rs535244650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159482 | AAAAAATTAGCCAGG[C/T]GTGGTGGCAGGCGCC | 50807 |
| rs535245522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091761 | TTTAGGAAGTGCTCA[A/G]CACCTTTTAGTTTTT | 50807 |
| rs535249922 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130282454 | TATTTTTGAAATTTC[A/C]TCTGAAACTGCTTAA | 50807 |
| rs535260634 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387258 | AAACCCAGGTCCGGC[A/G]AAAGTGGTGGCTCAC | 50807 |
| rs535273523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408233 | TGCCCAGATAGCTGG[G/T]AAAACAGCATTTCTG | 50807 |
| rs535301700 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098863 | GTCACTCTACAGTGT[A/T]ACAGAACACAGGAAC | 50807 |
| rs535305461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144513 | CTTATCACACTGTTT[C/T]CCTGTCAAGCCAAGC | 50807 |
| rs535319350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284022 | GGAGGACTGGGTATG[C/T]GATGAGGACAGCTTT | 50807 |
| rs535328955 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130325412 | GTGTGAATTTGGTAA[-/C]CACACCACAAGTATC | 50807 |
| rs535331345 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203362 | CCCACCTGGCTTGTA[A/C]AAGGGAAGCCTGAAG | 50807 |
| rs535340656 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130293293 | CATTCCCCAGTGTGA[A/G]TAGCAAAAAATGGAT | 50807 |
| rs535353999 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130429802 | CCATTAAGATTCTTT[G/T]GGAAAAATGAGTTTT | 50807 |
| rs535357312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130061662 | TTTGTGCCCCTGTCT[C/T]GGGTTAACCTCTGTT | 50807 |
| rs535364764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153112 | GCAACCTCCATCTCC[C/T]GGGTTGAAGCGATTC | 50807 |
| rs535381767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187228 | ACTCTAAACAAAAAA[A/C]CACTTACAACTTTGT | 50807 |
| rs535383610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439751 | CCGCAGGGGGAAGAA[C/T]GTAAGCAGACACTCA | 50807 |
| rs535384939 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072658 | GCAGTATCCTTTATG[A/G]TAAACTGGTAAATGT | 50807 |
| rs535386655 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130435390 | GTGCTAGACTTGGTG[A/C]TAGGCACTAGGGATT | 50807 |
| rs535398380 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130227668 | TTATTATATATATTA[C/T]ACTATATATAACACA | 50807 |
| rs535401021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408830 | CTGGTTAGTGGTGGC[A/G]GACTCAGAACTCAAA | 50807 |
| rs535403621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130426497 | TCATTCAGAGCAAAA[A/G]CTAAAGTCCACAAAA | 50807 |
| rs535404581 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343019 | AAAGGTTTTCAGCTG[C/G]AGAAATGTCCTGTGA | 50807 |
| rs535412207 | in-del | -/A | 0.0254951 | 0.109989 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180908 | CCAATGTCATTATTT[-/A]AAAAAAAAAAATACA | 50807 |
| rs535420985 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150559 | GGGAGAGCTCTGCAG[C/T]AGAAGGCAAAGAGAG | 50807 |
| rs535426720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229053 | GCAACAGACAAACTA[A/G]CCGAGCAAAGTCATC | 50807 |
| rs535429082 | in-del | -/AAATAAATAAAT | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418540 | GTGACCTCTGTCTCA[-/AAATAAATAAAT]AAATAAATAAATAAA | 50807 |
| rs535436282 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130157056 | ACAATATTAACTTTT[C/T]GTTTGATGACAGAAC | 50807 |
| rs535460040 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385265 | GAGGTCAGGAGTTCC[A/T]GACCAGCCTGGCCAA | 50807 |
| rs535462766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245767 | AAGAATTAAAGCTGT[A/T]CAGAAGAAAACTGGA | 50807 |
| rs535468584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111269 | ACACCTGTGGTTCCA[A/G]CTACTTGGAAGGCTG | 50807 |
| rs535471339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058924 | GCAGTGACTGCGTGA[A/G]CAACTGAGAGGCCTG | 50807 |
| rs535473665 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130142100 | CTACCTGTGAGGGAA[A/G/T]TCTTCAGTTTCTTTT | 50807 |
| rs535493850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130328250 | CACATAATTAGTATG[C/T]AGTGCCACAACAGAG | 50807 |
| rs535496851 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379035 | TGTACGCTAATGAGA[C/T]GGCCAAAAAGATGTC | 50807 |
| rs535497954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149710 | AAAGAAGCCCTTTAT[A/G]TTTTTCTCAGAAAAC | 50807 |
| rs535498357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105026 | TGAAGATTTTATCAC[C/T]TTCTAATAGTTTTCT | 50807 |
| rs535506363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370365 | TATTTTTCAGCCATA[G/T]AAGGACACAATGAGA | 50807 |
| rs535517893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281793 | TAATGGAGGCTGGGC[A/G]CGGTGGCTCACGCCT | 50807 |
| rs535532076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362339 | TTCATCACAGGCTCC[C/T]GATGCCCTCATGGAA | 50807 |
| rs535543973 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372318 | AAGGAAGATGATAAA[G/T]CTCAAAGACTTCTTT | 50807 |
| rs535558716 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274977 | AGACATAATAAGCAT[A/C]GACTCTTGAGACTGT | 50807 |
| rs535579269 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ASAP1 | GRCh38.p7 | 8:130051781 | GCACTAGTTGTGACA[C/G]CTACGTGACAGAAGT | 50807 |
| rs535580029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130329742 | CACACAGATGCATTA[C/T]TTCCAATAAAAATGT | 50807 |
| rs535591852 | in-del | -/AGCGCCTGCACACAAA | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275466 | CCCCTGAGGCGTCCC[-/AGCGCCTGCACACAAA]AGCTCTCCTCCTGGC | 50807 |
| rs535593913 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280895 | TTAACCATAACCAAG[A/C]ATCCATGTCAGTGAT | 50807 |
| rs535595599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130135848 | ACTCAATAAATCTCT[C/T]GGTCATGAAAATCAC | 50807 |
| rs535607736 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130141846 | CCTCAGCCTCCCAAG[C/T]AGCTGGGACTACAGG | 50807 |
| rs535611529 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130419704 | AGCCCCAGCAGAAGA[A/C]AGGAGGGAGGGAGAG | 50807 |
| rs535620774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234159 | ACATGTTCTCCTACA[A/G]TATCAGTCTAACAGG | 50807 |
| rs535624733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228685 | CAGCCTGGGCAACAG[A/G]GTGAGACCCTGTCTT | 50807 |
| rs535625183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258715 | TGCTCAACAAATAGT[A/G]CTTATCAGTTCTGAG | 50807 |
| rs535633542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130235529 | CCTACCACAGTGTGG[A/G]AGTTCATTGAAATAA | 50807 |
| rs535649979 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130227160 | ATTATATGTAAAATC[A/G]AGATAATAAAACCTC | 50807 |
| rs535651720 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130423642 | AGGAGAGTCCCTATA[C/T]ATTATATGAAGGAAT | 50807 |
| rs535666040 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234925 | AGAGAAGGCACTCAA[G/T]AATTCATCTAGCTGT | 50807 |
| rs535668669 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395330 | AGATCTTAGCCACCC[C/G]CTCATCCATGAATGT | 50807 |
| rs535670512 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130167009 | AACTAGGATTGAAAA[C/T]CTATAGTCATGGGGC | 50807 |
| rs535685801 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275663 | ATATAAAGATTCTTG[A/C]ACAATTAGAGAAACG | 50807 |
| rs535687563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401335 | ACTGCAACCTTTGCC[C/T]CCTGGGTTCAAGCAA | 50807 |
| rs535697602 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373206 | AAAAACCATGTAAAT[A/C]TCTAGACAGACACAT | 50807 |
| rs535698216 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170187 | CAAGACATTTTAAGG[A/T]ATATCTTTTTTTTTT | 50807 |
| rs535701693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111976 | CCTGACAACACGATC[C/T]GCGCCACTCAAATGT | 50807 |
| rs535703538 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130087767 | AGCGATCAGCGTGAA[A/C]CCATTGATCTAAAAA | 50807 |
| rs535704302 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130148990 | TACAGGTGTGCACCA[C/T]CATGCCCAGCTAATT | 50807 |
| rs535704374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395816 | GGATTACAGGCACCC[A/G]CCACTACGCCCAGCT | 50807 |
| rs535710498 | in-del | -/AATA | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336172 | GATAAATGTTTGCTG[-/AATA]AATTCAGTGATCAAT | 50807 |
| rs535722142 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085604 | CTGGGTGTGGTGTGA[C/T]GCACCCAGAGTCCCA | 50807 |
| rs535722912 | in-del | -/AAAAAAAAAAAAAA | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130060092 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAA]TAGAGAGAGAGAGAA | 50807 |
| rs535727312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269946 | AGGCGAAGGCAGTTA[A/G]ATCACCTGAGGTCAG | 50807 |
| rs535729564 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130190717 | GAGATGGGGTTTCAC[C/T]ATATTAGTCATGCTG | 50807 |
| rs535744421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130294546 | GGGACAGCAATAGCA[C/T]CTTCATGCAGTCAGA | 50807 |
| rs535748144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063239 | TGGAGTGCAGTGGTG[C/T]AATCAGGGCTCACTG | 50807 |
| rs535749911 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078070 | TCTCGGTTCACTGCA[A/C]CCTCCACTTCCCAGG | 50807 |
| rs535754873 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130357151 | CCCATACCACTCTCT[C/G]ATTAACTCACTGAAA | 50807 |
| rs535756841 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178725 | CCAGTCTCTACTAAC[A/T]ATACAAAAAAAAAAT | 50807 |
| rs535766923 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099490 | CGGCCAGGCCCAGCT[A/G]ATTTTTTAAGAAAAA | 50807 |
| rs535772329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301802 | AGATATGCATATGCA[C/T]TGTTGTTGAGAGTAT | 50807 |
| rs535772748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208310 | GTATGTCTTTGTGTA[C/T]AGTTCTATGGCATTC | 50807 |
| rs535776183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124176 | AGTCTCCTATTATTT[A/G]TTTTTGAGATTTATG | 50807 |
| rs535787776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236511 | CCCCCTCCTCTCTAA[C/T]TTTTTCCACAACCAT | 50807 |
| rs535790203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130138251 | CTCTCTGGACCATTT[C/T]TCAAGATCTTTCTCC | 50807 |
| rs535799554 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349838 | AATACTCAAAAAGCA[A/T]TGTCATTTATTTATC | 50807 |
| rs535809978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309838 | CTCCCAACCATGTCC[A/G]CAAAAATCAAAGACT | 50807 |
| rs535815231 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411932 | CCTCCACCCTGTCCA[A/G/T]AGAAAAGGGAACCAG | 50807 |
| rs535815596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218850 | TGTAGTCTCTTTCCA[C/T]ATATATATATATATG | 50807 |
| rs535823769 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130281306 | CCTATCACTTATAGC[C/T]TTCTCCATTGCTTTT | 50807 |
| rs535824494 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353789 | GGTGAGAGAATTGCT[C/T]GAACCTGGGAGGCAG | 50807 |
| rs535842929 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226125 | TCAGGCAATTCTCTC[A/G]CCTCAGCCTCCCAAA | 50807 |
| rs535846147 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306767 | CAGCTATACTCACAA[G/T]GCTCGGACCATGTAA | 50807 |
| rs535849538 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097597 | TATGTCAGAAGTGTG[-/C]CCCGGCATACAGCCA | 50807 |
| rs535855077 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130412432 | GCTTGGGCCATGTGA[C/T]GTGCCTGTTCCCCCT | 50807 |
| rs535858145 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176822 | CAGCCTCCCAAGTAG[C/G]TGGGATTACAGGTAT | 50807 |
| rs535862169 | in-del | -/ATA | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056102 | GATCACTGCTTGATT[-/ATA]ATAATATTAACAGAT | 50807 |
| rs535868928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058521 | AGCATAAACAAATTT[G/T]TCAGTCCCCTCATGC | 50807 |
| rs535876586 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130064543 | CTTGCTCCTCTAACC[A/G/T]TGCTTTTCCCTCTAC | 50807 |
| rs535881091 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130444225 | ATAGGAACAGTATGG[A/G]GAGTAATTGTGTGGG | 50807 |
| rs535895383 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130382063 | AGGCCGAGGCGGGCA[C/G]ATCACGAGGTCAGGA | 50807 |
| rs535901217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321445 | AAATCCCTCCTCAGT[C/G]AATAGGAATGTGAAC | 50807 |
| rs535903111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314990 | TGAATTTCGGTTACC[A/G]ATTTGTAAATAAGTA | 50807 |
| rs535904355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177670 | TTTTATTTTTGAAAG[A/G]CACTTATATAAGGTA | 50807 |
| rs535923554 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129935 | TGAAGTTAGAAACTA[C/G]AAATTGTTTTGTTAA | 50807 |
| rs535936564 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130212525 | TTTGGGTTCAAGTCT[A/G]TAACACATACTAATA | 50807 |
| rs535949093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437852 | GGAAGTACTGACAGG[C/T]ACTCTTCTTTATCCC | 50807 |
| rs535953329 | snp | C/G | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083470 | GTGCAGATTTTGGAC[C/G]TAGACAAGTGTGGCT | 50807 |
| rs535961217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274528 | CCTAAATGGAAAACA[C/G]GTAAGGGGATACTTA | 50807 |
| rs535968126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129085 | CTGATGGTTTTATAA[A/G]GGGCTCTTCCCTCTT | 50807 |
| rs535971245 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219318 | TACCCAGCAGACTTT[C/T]AACAGGCACAGAGAG | 50807 |
| rs535972910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347869 | TCATGTTCCATAAAA[C/T]ATCTCCCATGAATCC | 50807 |
| rs535978121 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130355979 | TCAATGTACTCTAAC[-/A]TGACACTGAACTTCT | 50807 |
| rs535988021 | snp | C/T | | | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130053211 | TGTGAAATTAACATC[C/T]CTCACTCATTGCCAA | 50807 |
| rs535994346 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130256248 | CTTGAAGATGCACAC[G/T]AACACTTCAGAGATG | 50807 |
| rs535995791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211988 | AGCTGGGGGCTGCAG[A/G]TGCTGCACGAAGATC | 50807 |
| rs536001552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309800 | AACTGGACTTTTAAT[C/G]ACAAGCTGTACTGCC | 50807 |
| rs536008012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341014 | GGTGGAGGGGTGGTT[G/T]TTTAGAGTGTTTTTT | 50807 |
| rs536012062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077419 | CACCAGGAGGCCTGC[A/G]TGCCTGAGAAGCAGC | 50807 |
| rs536024032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130300486 | AGCACACTGGAATCA[C/T]CTGGCAGCTTTAAAA | 50807 |
| rs536027611 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220763 | TCAGTTCAGCCATGG[C/T]TGAGGAGGGCCTCAG | 50807 |
| rs536030506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424769 | TAGGTCAAGGTGGGC[A/G]GATCACGAGGTCAGG | 50807 |
| rs536033457 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130400770 | CGCTCCAGCCTGGGC[A/G]ACAGAGCCAGACTCC | 50807 |
| rs536037078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246456 | GTGACTGGATCATGG[A/G]GGTGGTTTCCCCCAT | 50807 |
| rs536046371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130315678 | CAAGTTCAATGACAG[A/C]TATGCCCCCTAGCAA | 50807 |
| rs536050085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084164 | GCGAAAGACAGGACT[C/G]ACCGTGCTGGCTCAT | 50807 |
| rs536057128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253555 | AAGCTCTTTAGATTA[A/G]TGATCTCCTAGAAGA | 50807 |
| rs536058029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090820 | ATAACCCGGGGTGTC[C/T]GGGCCAGATGGTGAA | 50807 |
| rs536058739 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130066477 | CAGCCTCCCAAAGTG[C/T]TAGGATTAAAGGCTT | 50807 |
| rs536059180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334289 | TATCAAGCACATCAA[A/G]TATGTTCCTTGGGTA | 50807 |
| rs536064204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220146 | AACAAGAATGAAATA[A/G]TATGAGAATGAAATC | 50807 |
| rs536092471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438465 | TTTGGAACAAGGTTT[C/T]AGCCATACAAAAGGA | 50807 |
| rs536103889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239462 | GAGCTGGAATTTGAA[C/T]CCAGGTCTTTGACAA | 50807 |
| rs536118004 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254431 | TCAAAGTAAGACTTG[A/C]ATAAATGATAGCTGC | 50807 |
| rs536119751 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085764 | AAAAAAAGGAAAGAG[G/T]TTCAATGAAATGCAA | 50807 |
| rs536134606 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349157 | GATTATACAGTTACA[A/C]TGAGTTGACAGTCTG | 50807 |
| rs536140339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110406 | ATTATTGTATTCAGT[C/G]TGGAGGCTTCTCACA | 50807 |
| rs536149522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199019 | CGTGCTTTACTCTGT[C/G]TGGAACACTCTTCCT | 50807 |
| rs536155795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432618 | CATTTTTCTGCTCTG[A/G]CACCCTCAACACATC | 50807 |
| rs536155796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438930 | AGGCTGCAAAGATAT[C/T]CTCATCCTAATCCCC | 50807 |
| rs536160955 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376808 | CTTGGGAGGCTGAGG[C/T]AGGAGAATCGTTTGA | 50807 |
| rs536183096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301414 | GCATTTTAATGTAAA[C/T]TGTGTTCTAGAATGC | 50807 |
| rs536186650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155772 | TTCCAGTCTGCATAG[C/T]TCCTGAATGGACATA | 50807 |
| rs536196583 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130361118 | GGTAGTCGTCTAGCA[C/T]CTGTCACCTCCACTG | 50807 |
| rs536208681 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082651 | TAGGACTACATGCAT[C/G]ACCCACCATGCCTGG | 50807 |
| rs536219720 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130279658 | AATAGACTTGACTAG[A/G]TAATTTCTAGATCTT | 50807 |
| rs536223263 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203458 | CACCAGGCTGGGCTG[A/T]AGGACCTCCCAACAG | 50807 |
| rs536224591 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130416719 | CAGGAGATTTGGCTC[A/G]GCTACCTGCTTAGGC | 50807 |
| rs536237880 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197775 | TTAGTTCCTTGTCTA[A/T]GAGAAACGTCCAAGT | 50807 |
| rs536241290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393267 | TTAGGAAAATCATGA[A/G]GAAATGTTCTGATGG | 50807 |
| rs536247286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153539 | CATGCCTGGCTAATT[C/T]TTACATTTTTTGTAG | 50807 |
| rs536252766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167393 | AAGGAACTAAAATAC[A/G]GTTTCTACATGGGGC | 50807 |
| rs536255978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245226 | ACAGCCCCAAAATTG[A/G]AAGTTGGTATGTTAT | 50807 |
| rs536268460 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130224597 | CCCTTTCTCCCTTTT[-/A]AAAAAAAATAAATGG | 50807 |
| rs536285263 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074572 | GCCTGCCCTGATAGG[G/T]CAAGTCAGATGGAAG | 50807 |
| rs536293695 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076607 | GCTCACTGCAACCTC[A/G]GCCTCCTGGGTTCAA | 50807 |
| rs536294192 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176052 | CCGACAATGTTCATG[A/T]CTGAAATTGAGCAGT | 50807 |
| rs536295045 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273529 | TTGGGAAACTTGCTA[C/T]AAACACAGCAGCCAG | 50807 |
| rs536318243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259198 | CTGAATTTTCTTCCT[C/T]TGTGCTTTGGGATTT | 50807 |
| rs536320597 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076062 | CCCAAGTCTCTCTGA[G/T]TATGTTTATAAGGGG | 50807 |
| rs536323288 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381852 | CCCTGCACGCAGGCC[A/T]CTGCATGCTTGTTCC | 50807 |
| rs536323431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169432 | ATTTGAAGGAGAGAG[A/G]AGGACACATTAACCA | 50807 |
| rs536336241 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130326037 | CTGCCATGGCGGAGC[G/T]GGCTTAGGAACCTAG | 50807 |
| rs536338693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354466 | TAACCAAGTAGACTT[C/T]CATTTATCATGTTGG | 50807 |
| rs536344562 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130279950 | TTTATAAACATCAAC[C/T]ATGTGCCAGGTTAGA | 50807 |
| rs536373098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130291331 | ATTCCAGGAAAAATA[A/C]TTCTGTAAGACCTAG | 50807 |
| rs536384538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307403 | TTAATCTATAATATG[C/T]ACAACCTATGGCAAG | 50807 |
| rs536390633 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130247559 | AGGATTCAGTCATCA[G/T]GCCACTAGACAATCA | 50807 |
| rs536402379 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070193 | AGGCGCCCGTCACCA[C/T]GCCCGGCTAATTTTT | 50807 |
| rs536405315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417380 | CAGATGCCCTTCCAG[G/T]GGCCCTTCCAAAGGA | 50807 |
| rs536415296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431603 | CTTGTAACAAGTCTT[C/T]TCTGACCCTCCCTGC | 50807 |
| rs536415299 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205393 | ATAAGAAAAAAAAAA[A/C]AAAAAAACAAAAACC | 50807 |
| rs536416660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293047 | GAAAATCAGCCCTAA[C/T]TGGCAGCCCTGCTTA | 50807 |
| rs536421911 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130302449 | AAGAGGCAAAACTCC[A/C]AACAAATAAAAATTC | 50807 |
| rs536433440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211400 | TCTCACTTGATCGTA[C/T]TTTCTATAATCACAG | 50807 |
| rs536439449 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130202295 | AACCCCACTTGTGGG[A/G]AACCAAAAGCACAAT | 50807 |
| rs536450862 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130438043 | GGAGCTGAAGGGGCT[C/G]GCAGGGTGACCCCAG | 50807 |
| rs536454298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410497 | TCCTCATGCCAGCAG[A/G]AGCAGGCTCAACCCA | 50807 |
| rs536458153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162645 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 50807 |
| rs536480036 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189566 | ACTGTTGATGGACAC[G/T]TAGGTTGATTCCGTA | 50807 |
| rs536481560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253167 | AAATAACATGGTTTG[A/G]AACACAAAATCTAGA | 50807 |
| rs536482163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197246 | CCGCCTAGGCGACAT[A/G]GTGAAACCCTCATCT | 50807 |
| rs536486587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390072 | ATTAGAAACACTAAA[A/G]GGAGGGCCTGAGAAT | 50807 |
| rs536494712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069780 | TTTTAAAAGTTGCAA[C/G]GTAGAGATTACAATG | 50807 |
| rs536533791 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130306234 | GCAGGCAATCTAGCA[A/G]AGTAGGCACTTAGAA | 50807 |
| rs536534810 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130333932 | TGTTGGGCCACAGTG[A/T]GCACAGAGCAGCTGG | 50807 |
| rs536545585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191113 | GATTTTAAGATGGCA[C/T]AAAGAGGAATCTACA | 50807 |
| rs536557632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130198116 | TTAATCAAATTTAAC[G/T]AGGTTTATTTTCATA | 50807 |
| rs536559169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109825 | TTCAAATCCCTTATA[A/G]AAGTCATGAGAAGGC | 50807 |
| rs536560056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360496 | CTGAACCTGCACTGT[A/G]CCTCCAGCGAGATGC | 50807 |
| rs536564255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130182072 | AACTCTTTAATCATG[C/T]CACCTTGGCAGTCGA | 50807 |
| rs536566426 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102568 | TTTTCTTTTTTTGTT[C/G]TGTCCTTGTCTGGTT | 50807 |
| rs536567074 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130443643 | GAGGCGCGGGAGCCG[A/G]GCGCGGCGCAGGAAG | 50807 |
| rs536568740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130190155 | TTTAACTTCATATGA[C/T]CCCACTTGCGTTTGC | 50807 |
| rs536575100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095066 | ACCTCCTGAATCATT[C/T]CAAAAATTAAGTAAT | 50807 |
| rs536586600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404879 | GATGCACCACAAAAG[A/G]AATATGTCTCCATAG | 50807 |
| rs536594670 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283542 | AGGAGATCACGTCAC[C/T]GCACCACTCCAGCCT | 50807 |
| rs536603995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211190 | TATAATGTGGAGGAG[G/T]GGGGAGTAAGAAAAG | 50807 |
| rs536620488 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236607 | ACTGAAGCCACTGAG[A/T]TACAGGTTGACCAAA | 50807 |
| rs536621372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130113877 | GCCTTGAGTTCCTGG[A/G]CTCAGGTGATTCTCC | 50807 |
| rs536625938 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130134872 | CAGAAATGATTCATT[C/T]ACTGTTCCCTATTTG | 50807 |
| rs536636157 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130223058 | ACATCTGCCCTGCTG[A/T]TTGGCCACTAAGAGG | 50807 |
| rs536638143 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054531 | ACCAGTAAGGCGCGC[C/T]GGGTCCGAGGCTACC | 50807 |
| rs536646152 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160978 | AACTTTGGGTGACAG[A/G]ACAATCAAATGTCTG | 50807 |
| rs536650817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130305653 | TGCTGAGATTACAGG[A/C]ATGAGCTACCACTCC | 50807 |
| rs536670458 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130182103 | AGAGGCATAACAGGG[A/C]TTTTAACAGAAAGAA | 50807 |
| rs536671421 | in-del | -/TGCTTCG | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246573 | TGTGAAGAAGGTGCT[-/TGCTTCG]TCTTTGCCTTCTGCC | 50807 |
| rs536680075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130250564 | TGAGTTTAGACCCAA[C/T]TGTTTATTCATCAAA | 50807 |
| rs536684865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422500 | CACAGTGTACTTTCC[C/T]GCCTTCTCCCTTGCC | 50807 |
| rs536685491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258293 | TCTGCACGTGACCCA[C/G]GATGGTTTGTCAAGG | 50807 |
| rs536691645 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130437525 | CCACTGAGCCATCCT[G/T]CATCCCCCAAGGTCT | 50807 |
| rs536698294 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130114885 | GCTCAAGCAATCCTC[C/T]TGCCTCAGCTTGTCA | 50807 |
| rs536709591 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180060 | GAAGGGAGGGAGGGA[A/G]GAGAAGGGGAAGGGG | 50807 |
| rs536713910 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130170235 | TTCGTTGCCCAGGCT[A/G]GAGTGCAGCGGCGTG | 50807 |
| rs536724337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388694 | AAGCCAAAAGAAAAC[C/T]GTGTTTTTAGAGGAA | 50807 |
| rs536725618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277614 | TCATAATAGTCTAAA[C/T]CTAACAGGGCACCAA | 50807 |
| rs536725833 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270998 | GCCAAACAAATCACA[A/C]TGGGGGCAATCTGAG | 50807 |
| rs536736267 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130170244 | CAGGCTGGAGTGCAG[C/T]GGCGTGATCTCAGCT | 50807 |
| rs536747945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353293 | AACAAATGCTGTTCA[C/T]GGATTATACTCAAAT | 50807 |
| rs536762243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382282 | CAGAGCGAGATTCTG[C/T]CTCAAAAAAAAAAAA | 50807 |
| rs536763551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277056 | ACCCTCACCCGTCCA[C/T]ATCAGAATCACATGT | 50807 |
| rs536765717 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130367112 | GGCCAGGATGGTCTC[A/G]ATCTCTTGACCTCAT | 50807 |
| rs536781634 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173780 | TCAAAAAGAAAAAAA[-/T]AAAATAAAAAGGCCG | 50807 |
| rs536784935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340124 | TAAAACCAACATTTC[A/G]GCACAGTGGGTTCTA | 50807 |
| rs536787878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229720 | TTTAACAGAGCAAAT[C/T]TGTTGTTCATCCTAA | 50807 |
| rs536797679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424018 | GCACAACTCTGAATA[C/T]ATTAAAAACCACTGA | 50807 |
| rs536798850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141004 | AGCACTTTCTTGACA[C/T]TTAGTACTAATTTAT | 50807 |
| rs536800100 | snp | C/T | 0.0425829 | 0.139564 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130358727 | CTCCCCGCCCGCGCC[C/T]CGCCCCCGGCCCGGC | 50807 |
| rs536814056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080055 | TGGCCTGTAGACAGG[C/T]ATTGCTCAGGTTCCA | 50807 |
| rs536830972 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130145025 | CAAATAGAAAAAAAG[A/G]GCTTACTGGGGCTCC | 50807 |
| rs536832561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333678 | GTATGGCAGGGCATA[C/T]TGCCATCATGAAACA | 50807 |
| rs536841298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056800 | CAGGACGGGGCTCAG[A/G]CTGCCAAGGAAGGGG | 50807 |
| rs536858943 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130086786 | TCCAGCCTGGGTGAC[A/T]GAATAAGACCCTGCC | 50807 |
| rs536860094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245625 | AGCTCGCAAAAGTCT[A/G]CTCTCCTACGTAGGC | 50807 |
| rs536860674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215520 | AGGCCAAGGCGGGCC[A/G]ATCACGAGGTCAGGA | 50807 |
| rs536867063 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325890 | CACAAGCTTTAGGGA[G/T]TACTAAATATGCCAG | 50807 |
| rs536868025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397440 | GCCACCATGCCCAGC[C/T]CGTATATTTATTTTA | 50807 |
| rs536871058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132725 | TTCTCAAGGCTTTGC[A/G]TAGCCTTGGCATACA | 50807 |
| rs536885232 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130271716 | ACTAAACTTGCTTTC[A/T]TTACCAGGATTTCGT | 50807 |
| rs536886237 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130119941 | TTGCTCAAAAATATG[C/T]ATTCCACCTGTGGAA | 50807 |
| rs536886665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101858 | GATTACAGGCATGAA[A/G]CATCACACCCGGCTT | 50807 |
| rs536897469 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130068364 | AACAGAAAGTACCTC[C/T]GAGACTTGTGGTTAC | 50807 |
| rs536899831 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130121580 | TGAGGTCGGGAGTTT[A/G]AGACCAGCCTGATCA | 50807 |
| rs536906827 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130182618 | TGCATATAAACTTTT[A/C]GTCTTTGGGTACCTT | 50807 |
| rs536907255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392959 | GAGGTTTAGAGGGGT[A/C]AAATATCCAAACCAT | 50807 |
| rs536916847 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130440160 | GCTGTCCAGTTCTAA[A/G]CCACCATCCTCTTTC | 50807 |
| rs536925798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273086 | TACACATCCTATGCA[C/T]GTAAGAAAATTTCAC | 50807 |
| rs536931553 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134057 | AGTAGTGAGCTATAA[A/C]CCCAGAGAGGGTGAG | 50807 |
| rs536949314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263998 | TGACAACTTAGGTTC[C/T]AGCCCCTGTTAAAAC | 50807 |
| rs536961223 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130375224 | TCGCAGGGCTCTAAA[C/T]CCTTGGATCCCCCAG | 50807 |
| rs536970357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278868 | CCTCTTACTTTTAAG[C/T]CTTTTCATAAAGGCC | 50807 |
| rs536974234 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130217996 | CCTGCAGTGGTTGTC[A/G]GCATCTCAGGCTGAG | 50807 |
| rs536983834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130304986 | TCCAACCTCTTCTTC[C/T]TCACACGCTCTACAC | 50807 |
| rs536999988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262133 | TGGGCGCGGTGGCTC[A/G]CACCTGTAATCCCAG | 50807 |
| rs537000318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130365225 | GAACTCAGAGATAAG[C/T]ACAATTTGCTCAAGG | 50807 |
| rs537002414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131158 | CAAGACTCTGAAAAC[A/G]AACAAACAAACAAAC | 50807 |
| rs537012504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415351 | TATACACCTATAGTC[C/T]CAGCTACTCTGGAGG | 50807 |
| rs537039463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130061449 | TATTTTCTATAGATA[C/T]AACTTTTACTTGCTT | 50807 |
| rs537044844 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130136816 | GGGCATCTTCCTAGA[C/G]CAGCACATGCAGGAA | 50807 |
| rs537050907 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091641 | AACCATTCTGGCTGT[A/T]GTGAGGAAAATGGAT | 50807 |
| rs537050982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228656 | AAGTGAGCCAAGATC[A/G]TGCCATCGCACTCCA | 50807 |
| rs537055343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323675 | TCCTCTATGGTCCCA[C/T]AGTCCTTTGCAGACA | 50807 |
| rs537057798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130409016 | CTTGTAATCCCAGCA[A/C]TTTGGGAGGCCAAGG | 50807 |
| rs537059347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099773 | CTGCAACCTGACCTC[A/G]GGTGATCCACCCGCC | 50807 |
| rs537061772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332238 | TTTTCAATGAAGATG[C/T]TGAGTGCTTGTTATC | 50807 |
| rs537068294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152334 | CTGTTGGTTTAAAAA[C/G]GGCAAAACTTACTGT | 50807 |
| rs537072690 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130137479 | AGCACCAACAGTTGG[C/T]ACTTTTAATGCTGTA | 50807 |
| rs537076009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195256 | AAAATCATTTCAGGA[C/T]GAGGAATGGTGGCTC | 50807 |
| rs537079555 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439092 | GGAATCACTTTAAGG[G/T]TCCTTCAAGGTGGAA | 50807 |
| rs537081530 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130102829 | TAGTTAGCACCACAG[A/G]TAGGTACCACCGTGC | 50807 |
| rs537084584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107290 | CGGGTTCACGCCATT[C/T]TCCTGCCTCAGCCTC | 50807 |
| rs537111019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188665 | TTTAAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 50807 |
| rs537125841 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130266402 | AAGTGGTTGTAGGGG[A/G]GAGGGTTCTGTGTAC | 50807 |
| rs537127933 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366317 | ATTTGGGGCAAGAGG[A/G]CTGTGCCCCACAGTA | 50807 |
| rs537128566 | snp | A/C | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295944 | CCATCATCTTTGCCT[A/C]TCAAAGCCCCTTCCT | 50807 |
| rs537135030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130125170 | GTCTGAGAAGTCATA[C/T]TTTATTTTAAAAATT | 50807 |
| rs537139093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350109 | ATCAGGGAAAGCTAC[C/T]GCGGCCTCGCACAGT | 50807 |
| rs537139817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215377 | CTAACGTAGGCAGGT[C/T]GCTTGAGCCCAGGAG | 50807 |
| rs537143446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439729 | TGGGAGAGAGGAAGA[C/G]CATCCCCCGCAGGGG | 50807 |
| rs537143528 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130357115 | GCTTCTGCTGCTCCT[G/T]GGCTTTCAGGTTCCT | 50807 |
| rs537162770 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284001 | CTGTATCCACAAAAA[A/C]CTTGTGGAGGACTGG | 50807 |
| rs537177805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350710 | GATCAGGCTTTCAGG[C/T]TGGCAAACGCCAGAG | 50807 |
| rs537196519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124622 | AGGCAGCAGAGGACC[C/G]AGGAACCATTTTGCT | 50807 |
| rs537202896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208593 | TTACAGGGGTATAAA[A/G]AACGTGGATGTAAAA | 50807 |
| rs537218259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087326 | GGAGTTTGAGACCAG[C/T]CTGGCCAACATGGTG | 50807 |
| rs537219393 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434377 | TACTAACTATATGAC[C/T]TCAGGGAAGTTAGCT | 50807 |
| rs537241889 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158795 | GGAGTGCAGTGGTGC[C/G]ATCTCAGCTCACTGC | 50807 |
| rs537246864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249060 | TGTGCCTCTATGTCA[A/G]GTTATTCTGCAGCAT | 50807 |
| rs537248325 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094034 | ACACAATGGAAGCCT[G/T]ATGCTTACCCCAAAT | 50807 |
| rs537251121 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344569 | GCATGTGCAAAAATT[C/T]AAGTTAACAGCAAGC | 50807 |
| rs537253784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130230287 | GGAAGTGCATACACA[A/G]GCTCATACACACAGT | 50807 |
| rs537267729 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130231424 | ATATTAAAGGATTTA[-/C]AAGCCTCAACTTTCA | 50807 |
| rs537284601 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130394284 | CCTGAGAAAGAGAAT[A/G]CGCCCCTGAGGGTAG | 50807 |
| rs537284679 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410405 | CAAGAAGAGAACAAC[A/G]AAATAAACTTGAGAG | 50807 |
| rs537303749 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130374010 | TTTGGTGCTCAAAGG[A/C]CTTGGAGAAAGTGTA | 50807 |
| rs537308679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130242614 | GGATGAAAAAGTGAC[A/G]TAAGTTCTCATGCAG | 50807 |
| rs537318932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130386610 | CTTACCAAACTCACA[C/T]TGTTTGGGAACTTCT | 50807 |
| rs537327237 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428069 | GCACCCGCCCCACCA[C/T]TGTCTACATGGTGAC | 50807 |
| rs537328341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121009 | TTTGTTAATGCTACT[A/G]TCTATTTACCTAGAT | 50807 |
| rs537332569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080706 | GGTGCAATCTCAGCT[C/T]ACTGCAGCATCGGCC | 50807 |
| rs537338374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435038 | GCTGGAAGGCACGCT[A/G]TCCCATCGGCCTTGA | 50807 |
| rs537339064 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070774 | GGTTTATAGAGGATC[A/G]TGCTACCTGAGGAAC | 50807 |
| rs537341645 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130345439 | TTCCACTGGCAGATG[C/T]ATGTCTTGTTTGTGT | 50807 |
| rs537341750 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130369506 | AGTATTCAAAATATA[C/T]AAACTTTTGCAACCC | 50807 |
| rs537341854 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087902 | TTCTCTGAAGACTAG[-/A]AAAAACAATGGCCAA | 50807 |
| rs537342304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130442591 | TCACGCCAAGATAAC[C/T]TAACAGAGTAGACAG | 50807 |
| rs537343027 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296941 | TAACTGTCTTTTTTG[C/G]GGGGCTAAGTGGATG | 50807 |
| rs537343131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359557 | GAGCCTGTCCTCTGC[A/G]ACACACACCCACCGC | 50807 |
| rs537350603 | snp | C/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435532 | CATTACTAATGTTCT[C/G]TTACAGATTTCAGTT | 50807 |
| rs537356345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380482 | AGGGAACCAGGGTGC[A/G]CCAAGGGGACCCAGG | 50807 |
| rs537375148 | in-del | -/T | 0.499984 | 0.00279548 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077537 | TGCTGCTGCTGCTGC[-/T]TTTTTTTTTTTTTTT | 50807 |
| rs537383658 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352718 | TAAAATGGAGCCATT[C/G]ATGATAGTAGGGTGA | 50807 |
| rs537395475 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130118895 | TAGATATAGTTACAA[A/T]GTAAACGGGCACATA | 50807 |
| rs537396717 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213991 | GTTAGGGATTCTTCC[G/T]GTCATTTACTTTGGA | 50807 |
| rs537398011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127072 | TCAGTGTTAGCTGTT[A/G]CCAATACACTGGTAA | 50807 |
| rs537399030 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130361201 | AAATATGAGCTGTTA[C/T]TAAAAGCCAAAAGTC | 50807 |
| rs537406189 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130275191 | ATGGTAGCTCCTTTT[C/T]TTCTTCCAAATGCTT | 50807 |
| rs537408131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070962 | GAGGGGTAGAGAGAG[A/G]GGGAGAGAGAGGGGG | 50807 |
| rs537413518 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130391298 | GAAGAGAAGGAGTTG[C/T]CATTTGATGGGTACA | 50807 |
| rs537415894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301369 | GTGACTCTAATCCAC[A/G]TACACTGCTGCTCCT | 50807 |
| rs537423425 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401597 | CTATAGCACCTTATA[G/T]TGTTGCTGGTGTCAC | 50807 |
| rs537425486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171729 | GATAGTCAAAGCAGC[A/G]GCTTCATTGAGCATG | 50807 |
| rs537430893 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309999 | GCTCTTTTCTAAATC[A/G]TAATATCCCAATCGT | 50807 |
| rs537436719 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390096 | TGAGAATCTGATTTT[C/T]AACAGCTCCCCAGGT | 50807 |
| rs537448212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395291 | ATATTACATACGTTT[A/G]ACACGTCCTCTTGCA | 50807 |
| rs537457896 | snp | A/C | 0.000991399 | 0.0222422 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134357 | TATCTAAAATAAAAA[A/C]AAAGAAAAATAAGTG | 50807 |
| rs537459948 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130236095 | GAAAGCCCACATCTG[C/T]CCAACTTCACGGCCT | 50807 |
| rs537462035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402060 | AGATCGGATTTCATA[C/T]GGAGGCTGCACCTTT | 50807 |
| rs537480472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269444 | ATAGTGACAGTTCAA[C/G]TGGCTGTCTACACAT | 50807 |
| rs537481285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130260928 | CTTTTCCCCCCCTCA[A/G]GATAAAACACTGTAT | 50807 |
| rs537482479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275975 | CCGGACTTCATCAGC[A/G]GCTCCAAGAACAGAT | 50807 |
| rs537488751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077390 | AACAAGAGGTTTTGG[C/T]GATTCTCAGAGGACA | 50807 |
| rs537490501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130170870 | ACTACAGAGGCACCC[C/T]ACCATGCCTGGCTCA | 50807 |
| rs537499649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396338 | GAGTGTAGGACCTGG[C/T]ACACAGTCGCTGCTT | 50807 |
| rs537510187 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179662 | TTATGTGGTCAAAAA[A/C/T]TGGAAAGATTGATTG | 50807 |
| rs537512314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130156910 | ATACAGATTTTAACC[A/G]TTTCACTTAGAATTA | 50807 |
| rs537513589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130172502 | TAAAGGTGAGTTTCA[A/G]TGAGAATGCTCTACA | 50807 |
| rs537521946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078951 | GTAATCCTAGCACTT[C/T]GGGAGGCTGAAGCAG | 50807 |
| rs537527585 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425684 | CAATCTTAGGGATCA[C/G]AGAATGACAGGCTAA | 50807 |
| rs537531145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086182 | TTTGCGAGCACAGAG[C/T]GGTGCGTGGAGAGGG | 50807 |
| rs537541995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269917 | GCTCACACCTATTAT[C/T]CCCGCACTTTGGGAG | 50807 |
| rs537544707 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130364440 | ATGTTATATGCATGG[C/G]AAACCTGAAGCTTAG | 50807 |
| rs537551031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385217 | ACGCCTGTAATCCCA[A/G]CAGTTTGGGAGGCTG | 50807 |
| rs537558577 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130313119 | ATAACCAAGTGCTTA[C/T]GTTCTCCTAGTTTAG | 50807 |
| rs537571927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130071818 | CACTATGATGGACTG[A/G]ACTAATTATTAATGA | 50807 |
| rs537576894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342899 | ATACTTCCCACCCTA[C/T]TTCTCTGCCAAGTGT | 50807 |
| rs537579854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214766 | ATGAAAAGTTACTTT[A/G]AACACCGATCACTAC | 50807 |
| rs537579959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130294449 | GAAATAACATGAGCT[A/G]GACAGACCTGGGTTT | 50807 |
| rs537596220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131958 | AAATAAAATATTGAA[A/G]ATCTGAGTTTGAGTC | 50807 |
| rs537613883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130412691 | GAGTCTTGCTTTGTC[A/G]CCCAGACTAGAGTGC | 50807 |
| rs537621903 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241489 | GCTCAAAAATGCTTA[C/T]GAAATGAAGCGACAA | 50807 |
| rs537635520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396840 | AAAGAGGGAGGAGGA[A/G]TCACAGAGGTTTCTC | 50807 |
| rs537642696 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059666 | TCTGGATATAGAGTA[G/T]GAAACATTTCATGAA | 50807 |
| rs537645354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130302425 | GATGAGAGAGAAATG[C/T]TAAAAATGAAGAGGC | 50807 |
| rs537653452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337359 | TGATTTCCTGTACCA[A/C]CAACCACCTGCATTT | 50807 |
| rs537683062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105382 | GCACTTGAGCATTCC[C/T]GGAGTTTTGGCATGG | 50807 |
| rs537692889 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079435 | GCCTAAAAAAAAAAA[A/T]ATTAGAAACAGAACT | 50807 |
| rs537721723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421615 | GACAGCAACAAAGCT[C/G]CAGGGGGCAGCAGGG | 50807 |
| rs537740964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098695 | TTTATAGGATACATA[G/T]TGATATTTCAATACA | 50807 |
| rs537741840 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144636 | CCCTCCAGATGCACG[-/T]TTCCAAATTCCAAAC | 50807 |
| rs537764216 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130209194 | GGTATGATTTGATCC[C/G]TACACAACCAATAAA | 50807 |
| rs537764890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281717 | CTCATTTTCCTCTAA[A/G]AAACTCTGCATCTTA | 50807 |
| rs537766878 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296745 | AGAGCACAAGGCCGA[A/C]TACAGAATTAGTTTA | 50807 |
| rs537774354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288933 | GGCTCATGCTTGTAA[C/T]CCCAGCACTTTGGGA | 50807 |
| rs537785242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422243 | GGTGGAGGAAGGGGA[A/G]GAAAGGGAAGAAGGG | 50807 |
| rs537789736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234804 | ACAAACCATCATCAC[A/G]TTACAGAGAACTGAC | 50807 |
| rs537793477 | in-del | -/AAAGA | 0.173643 | 0.238054 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283584 | AAGACTCCATCACAG[-/AAAGA]AAAAAAAAAAAAAAA | 50807 |
| rs537794273 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130202305 | GTGGGAAACCAAAAG[C/G]ACAATGTTTTAAAAG | 50807 |
| rs537795463 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130345955 | TGCAGCACAACCTTC[A/C]AGAAATTTAGTAACT | 50807 |
| rs537799416 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349138 | ACAGAGCCCACTAAG[G/T]GCTGATTATACAGTT | 50807 |
| rs537811423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124163 | GCTACTAGTTAAAAG[C/T]CTCCTATTATTTGTT | 50807 |
| rs537821089 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206207 | AAATAAGGGGATACC[A/T]GGTAGATCAAACGCT | 50807 |
| rs537822420 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130307019 | AGGATGCAGCTCAAA[C/T]ATAATTTCCTTAAAG | 50807 |
| rs537846457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057714 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 50807 |
| rs537851024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063957 | GGAAGGGAGAAAAGA[A/G]TGCTGGCTGGGTGGG | 50807 |
| rs537856910 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155204 | CAATACACACACACG[C/G/T]GCGCACACACCCCTT | 50807 |
| rs537859168 | snp | A/C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130441056 | AGGGCTTAGCATGGC[A/C/G]CAGGTGCTCAATGCA | 50807 |
| rs537865356 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238874 | TGAGACAAAAAACAG[C/G]GTTTCCAGACTGCAA | 50807 |
| rs537878636 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390867 | ATGGAAAACAGCCTG[A/G]CTGTTCCTCAAAAAA | 50807 |
| rs537889586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070175 | CTGAGTAGCTGGGAC[C/T]ACAGGCGCCCGTCAC | 50807 |
| rs537893293 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377196 | ACAGGCATAGGAAGG[A/T]TACAGTGAACTTTGG | 50807 |
| rs537903244 | in-del | -/CAGGC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130264373 | GATGGACACGACTCT[-/CAGGC]CAGGCCAGCCAAGTC | 50807 |
| rs537914184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191565 | TCACTACACAGCCAA[A/C]TCTACTACATTATGC | 50807 |
| rs537924166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273589 | AGGAGCTCACAGGAT[C/G]TTGGTATCTGCTTCT | 50807 |
| rs537926162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280196 | AAGATGATTTTACCA[A/G]ACCAGTGCTTGCTCA | 50807 |
| rs537930359 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377699 | GATTCAGGCAAAGGC[A/T]TGTGGTAAAATGCAG | 50807 |
| rs537934912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370023 | AAGAGACCCCAGGCC[A/G]GGCACAGTGGCTCAC | 50807 |
| rs537939732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287422 | CCTCCTTTATGAATA[C/T]TGTCTTTGTTCTACC | 50807 |
| rs537942116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342196 | GGTGAGGAGGATGAA[A/G]AAGGCAAATTGGCAA | 50807 |
| rs537949382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378563 | TGCAGGGAGGGATTG[A/G]AGCTGAGGTCAGACG | 50807 |
| rs537954205 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130110568 | TGATTTAAAAACATA[C/T]ATTTTAGTACAATGT | 50807 |
| rs537959175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058436 | CTTGCAGAATGACAG[A/C]AGAGTCTAAAAATGT | 50807 |
| rs537969186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286595 | CTATACAGTGAGCTT[G/T]GCGGTGAGGGTTTAA | 50807 |
| rs537980608 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335758 | GTCAGGGAGAGATAG[C/T]CTGAGGTTAAGAAAA | 50807 |
| rs537997020 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281116 | TTTGGGGGCAGATAA[A/C]CTGGGGCTGTATGAC | 50807 |
| rs538014396 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130127747 | GGGCTTTCCAGGTAG[A/C]GAAAACAGCATAGGT | 50807 |
| rs538021780 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234424 | CAATAAGCTGTACCA[C/T]CCCCATCCACAAAGA | 50807 |
| rs538022198 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090307 | AAACTTAAGAGAAAT[C/T]TGGAAAGGAGGTTAA | 50807 |
| rs538038587 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130191705 | ATATTATAACCTACT[A/G]CAAGCAGCTGTTGTG | 50807 |
| rs538040535 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314354 | CTGTATTGCTAGGCA[A/T]GGCACTGAGCTCCTT | 50807 |
| rs538045170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150463 | GATTCCTAAGAAAAG[C/T]AAATAGATACAACAT | 50807 |
| rs538050213 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130182833 | ACTATAAAAAGGCAA[-/A]AAAAAAAAAAAAAAA | 50807 |
| rs538051293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248158 | TGGTATTTCTAATCC[C/T]AACTCTGGCCCATTG | 50807 |
| rs538060803 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240935 | ACAGAGGCACTACAT[A/G]AGAGCTGACAGCCAA | 50807 |
| rs538068015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227933 | TGGGTGCACAGTTGG[C/T]GAGTCTGAGGGAAGG | 50807 |
| rs538076021 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130130522 | GACTCACAGTGATCA[C/T]TTGTGACATTAACTT | 50807 |
| rs538084221 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130378971 | TGGTCTTTGTCCTTG[A/T]CTTCTGGCACAGAAC | 50807 |
| rs538093811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108337 | GGGAATGAACTGTAA[C/T]TAGCATATCAGGTGT | 50807 |
| rs538095444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176956 | CAGCCTCCCAAAGTG[C/T]GGGGATTACAGGCGT | 50807 |
| rs538111448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400686 | GTCCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG | 50807 |
| rs538111564 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130117114 | CTAATTATTATAATA[A/G]AGAAAATTATGATGT | 50807 |
| rs538112457 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130053525 | TGACTTGAAGGTGGA[C/T]AGAGCTTAAGACTGG | 50807 |
| rs538112772 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275623 | ACTGGCAGGATGCAA[A/C]TTCAGTTAAAAAAAA | 50807 |
| rs538115123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130315598 | GAAATAGACCACTTG[C/T]TGCTTCCCAGCTGTG | 50807 |
| rs538120896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372168 | TTAAATTTCATCTCA[A/G]AAATTGTTTCAGAGA | 50807 |
| rs538130717 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246322 | GAATTCAGCAATGTG[C/T]ACAGAGAAAGGAAAA | 50807 |
| rs538134527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091088 | ATGGGAATTTGTCAT[A/G]TGCAGTCAATGTCAC | 50807 |
| rs538149371 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052848 | TGTAAATGAATGACC[A/G]GGACACTGAGCAACC | 50807 |
| rs538154997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060258 | CTGCTCATTTGTCAC[G/T]GTATTTAATCATCTG | 50807 |
| rs538160887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364532 | AGCCACCATGCTCTG[C/T]TGGCTTATCAAAGAC | 50807 |
| rs538164332 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130185667 | CCAGGAGGCAGAGGC[C/T]GCAGTGAGACGAGAT | 50807 |
| rs538175474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130230894 | TCCCCACTGAAAACC[A/G]CAGGATTAAAATAAG | 50807 |
| rs538213766 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130333759 | TCATACAGATAAAAT[G/T]ATCAGACTATTAGAT | 50807 |
| rs538214913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130239367 | CAAAAGTCCTGTGAA[A/G]TAAATATTCTTATTA | 50807 |
| rs538241144 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319045 | AGCAGTCACTCCTAT[A/G]ATCAGCACCACTGTC | 50807 |
| rs538271264 | in-del | -/CATGC | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131240 | GCCAAATGAGTCTAA[-/CATGC]ATCTGCTCTTTGTGA | 50807 |
| rs538275124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102665 | TGGAACAGTTTAAGA[A/G]TTGGTGCTAGTTTTT | 50807 |
| rs538279338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130198016 | ATGTCTCATTTGCTG[A/G]CTCTGGGTCTTTTCT | 50807 |
| rs538280116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133396 | GCGCGGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 50807 |
| rs538298865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183632 | CAGGCATGAGCCACC[A/G]TGCCTGAAAATTATT | 50807 |
| rs538300756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359665 | TCTGTCGCCCAGGCC[A/G]GACTGCGGACTGCAG | 50807 |
| rs538307360 | snp | C/G | 0.00795532 | 0.062565 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130443867 | CCGGCAGCCACGAGG[C/G]GGGCGTGGGAGGGGC | 50807 |
| rs538310389 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258423 | CTGTCACAGACCACC[C/G]TGATAATTCACTAAA | 50807 |
| rs538310642 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167702 | CCAAAAATACCACTC[A/C]TCAAAATTCTATTAT | 50807 |
| rs538312704 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130396788 | ACAGCCTGTGGCATG[A/G]TAATGACAGGGCGTC | 50807 |
| rs538319697 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130310184 | GAGATAAAGATAGAG[A/G]GATTAAATGGTAGAA | 50807 |
| rs538332775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128456 | ACTCAATGAGGGACC[C/T]ATCCAATGCAAGGAT | 50807 |
| rs538345423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211444 | AGGAAAAAAACCCGA[A/G]GCATCTCAATGATGG | 50807 |
| rs538356224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370325 | CAAACAAACAAACAA[A/C]AAAAACAGAGAGCAG | 50807 |
| rs538358514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191040 | AGTGCAATCTATAAC[C/T]GGGAAATAGTTTTTT | 50807 |
| rs538362778 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130103336 | TGTCAATTTTTTTCA[C/T]CTTTTCAAAAAAACA | 50807 |
| rs538365504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353699 | ACATGATGAAACTGC[A/G]TCTCTATTAGAAATA | 50807 |
| rs538370556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130142007 | ATAGCCATGTACCAC[C/T]GTGCCCAGCCCTCAA | 50807 |
| rs538378816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233164 | TCTGAGACATGACCA[C/T]GGAAACTACTATTGG | 50807 |
| rs538382358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217932 | CCAATGAAACGAAAT[A/G]AGGCCCTAGCCAGCC | 50807 |
| rs538386993 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130195405 | AAAAAAAAAAAAAGA[A/T]GAGCTGGGCATGATG | 50807 |
| rs538389789 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320300 | GTGGCTGTCGCCTGT[A/C]ATCCCAGCACTTTGG | 50807 |
| rs538391410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327468 | CTCACAGCACAGGCA[C/T]GTAAGACCACAGGTG | 50807 |
| rs538396138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127862 | TTTCAATAACTAGAT[C/T]GTTTTATATTCTACA | 50807 |
| rs538401127 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130171768 | GGCCTAAGTGCCAGA[C/T]CTGGAGAGGTTGGCA | 50807 |
| rs538404617 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347364 | GGGAGGTGACACTTG[C/G]AGAGGGAAGGGCAGA | 50807 |
| rs538409918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226886 | GTAGGTAATTGCAAT[G/T]CTTTGAGATGTGGTC | 50807 |
| rs538415871 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130087857 | AAATCCTAGGCACAG[C/T]GGGGAGAGGAGTACA | 50807 |
| rs538417259 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405979 | CTAGGTTCATCAGAA[A/C]AAATATTAAGGCATA | 50807 |
| rs538426421 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320804 | TACCAATGGAAAAGA[C/G]TAAAATTATCTATCC | 50807 |
| rs538434926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252286 | TTATAATAATGTAAA[C/T]TATCTAGAACTGTAA | 50807 |
| rs538446041 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259110 | CACAAAATTCATGAC[A/C]TGAGCTGATTTGAGA | 50807 |
| rs538446355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195818 | GTATACAAATAGCCC[A/G]TTATCCTAGTCACTG | 50807 |
| rs538446622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226404 | CACTTCCCTGAGCCT[C/T]AGTTTCCTTACATTT | 50807 |
| rs538446836 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097383 | TCCTCCCTTGTTAAC[A/G]GCCCTCCCTGCACAG | 50807 |
| rs538452003 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134920 | GGGGTAGCCCCAACA[A/C]CCCCAACACTAGACA | 50807 |
| rs538454295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393976 | CCTATGCCTGTCTTT[A/G]CTTTAATCTCTTAAT | 50807 |
| rs538455765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314936 | AGAAAAAGTGGGTTC[C/G]AACCCCAGGTCTTCC | 50807 |
| rs538458421 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171006 | AAGGTGTGAGCCACC[A/G]TGCCTGGCCTAAACC | 50807 |
| rs538487246 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130399689 | GAAGTAATTACAATG[C/T]CCTATGTGCCTACTT | 50807 |
| rs538488201 | in-del | -/CAAG | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311542 | AAGGCGGGAGGATCA[-/CAAG]CCTGAGGTTGGAAGT | 50807 |
| rs538497406 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130400727 | AGCCGGGAGGCGGAG[C/T]TTGCAGTGAGCCGAG | 50807 |
| rs538498079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252993 | TTTAGCTTCCCACCA[A/G]TTCTAAGATCCTATA | 50807 |
| rs538500833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130161131 | TATAGGGAATCAATA[C/T]CTCAGTGAAACCCAA | 50807 |
| rs538523811 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162597 | GCTGAGGCGGGTGGA[A/T]CATGAGGTCAGGAGA | 50807 |
| rs538531692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130267325 | CAAGCAATTCATGGA[C/T]CTTGAAGAATAGGGG | 50807 |
| rs538533876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438384 | CACACTCCCTCCTGA[C/T]CTCTCCTGGGGCCAA | 50807 |
| rs538540849 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130057347 | CCGCTTTAGTATTTA[C/T]ATGAAAAATCAGAAA | 50807 |
| rs538546397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130285833 | ATGTAACTTTATCAC[A/G]TTCTGTTCCTGCTGA | 50807 |
| rs538552529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340376 | TCAGGAAGCAACCAC[C/T]GCCACTTCAGAAATA | 50807 |
| rs538555082 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130382826 | CACTTCAACCTGGGC[A/G]ACAGAGCAAGACTGT | 50807 |
| rs538555534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383376 | CTACAAGCCAGGAGT[C/T]TGTAAGCACAGAACC | 50807 |
| rs538558993 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355712 | TAATAATGCACTACT[A/T]CCACATATGTAAGCA | 50807 |
| rs538559317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348574 | CCTGGATTCTGTTAA[A/G]ACCAAGTAGAGTCAA | 50807 |
| rs538570354 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130308179 | CAAAAGTCTACTCCA[A/T]ACTTAGATTCTATAA | 50807 |
| rs538590198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133776 | CCTTTTATTGACTCT[A/G]TTCACCCCAGTGAAA | 50807 |
| rs538592914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333777 | CAGACTATTAGATGC[A/G]TTTATTCATTCAGTA | 50807 |
| rs538613039 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130119660 | AGCCTGGATCCAGCT[A/G]TACCTGAATCCACCC | 50807 |
| rs538613599 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130215109 | GTTTCACCAAGTTGG[C/T]GAGGCTGGTCTCAAA | 50807 |
| rs538634404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159596 | GGTGAGTATGAGGTC[A/C]GCACTTGCCTGCTGC | 50807 |
| rs538635274 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094896 | TCTAGGGACTTTCTG[A/C]TGCAGATGCAGTTCC | 50807 |
| rs538651519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140879 | CCCACGAATACCAGA[A/G]GGGAGTGGTATGTTC | 50807 |
| rs538661200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404803 | GACTTGCTGTAGCCA[A/G]TGGAATGTGGCTAGA | 50807 |
| rs538670228 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130369066 | GATAATGATATTTAC[A/G]TCAAAGGATTGTTAT | 50807 |
| rs538675698 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130098693 | TATTTATAGGATACA[C/T]AGTGATATTTCAATA | 50807 |
| rs538690603 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130174337 | ACTACCTATCACTAC[A/G]CTTAACACATAAATC | 50807 |
| rs538692514 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130079910 | GGCTTACCTCGACTG[C/T]TGGGATAGTCCCTCA | 50807 |
| rs538699724 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063380 | ACGTGCAGGGCCATG[-/C]TGTCCCCAGCTTCAG | 50807 |
| rs538700444 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130265378 | GAGCTTGAGACCAGT[A/C]TGGGTAACATAGCAA | 50807 |
| rs538710217 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360479 | TCCCTCTATTGGCTG[G/T]ACTGAACCTGCACTG | 50807 |
| rs538718387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218756 | CATGAAATGTGACGT[A/G]AGTGAGGCAGAAGAC | 50807 |
| rs538727238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130429107 | GTCTTCCCTCTGTGC[A/G]TATCTGCCTCTAGGT | 50807 |
| rs538741480 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107420 | TCGATCTCCTGACCT[A/C]GTGATCCGCCCGCCT | 50807 |
| rs538746132 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130334297 | ACATCAAATATGTTC[A/C]TTGGGTAACGGAAAA | 50807 |
| rs538748325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130290478 | TCTTTTCTAACTGTA[C/G]GATCCAAACCTTCCT | 50807 |
| rs538751662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130345430 | GCTTTCCTTTTCCAC[C/T]GGCAGATGCATGTCT | 50807 |
| rs538753626 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175381 | GTGTGCCACCACACC[A/T]GGGTAATTTTTTATT | 50807 |
| rs538758584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203036 | CAATGAGAAATTACA[C/T]ACTGAAATATAAATT | 50807 |
| rs538763365 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130145844 | AGGTCAAAGTAAAAC[-/T]TTTTTTTTTTTTTTT | 50807 |
| rs538764024 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112887 | CTGGTATTTGCGCTT[C/G]TGGTGATGGCATTAG | 50807 |
| rs538767408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313661 | TTCAGCTACAGAAAA[C/T]AAAAAATAAAATTAA | 50807 |
| rs538772703 | snp | C/G | 0.133435 | 0.221162 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074488 | ACACACACACACACA[C/G]AGAGAACGAGAGTAG | 50807 |
| rs538779819 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130305827 | CTCAAATGGACTTTA[C/G]TACCAGCTGTTTCAC | 50807 |
| rs538782337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130067943 | ACATTTGGTATCAGC[A/G]AAGCAGGATTTGTTG | 50807 |
| rs538786920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130429819 | GAAAAATGAGTTTTG[A/G]AGAATAACGCATGTA | 50807 |
| rs538795822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130075996 | TAGTGAAGCTACTAC[A/G]TCACCTGCCCAAGGC | 50807 |
| rs538799382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423369 | TGTATACTTGCAAAA[C/T]TGCTCATAGAAATAC | 50807 |
| rs538805158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130298806 | ACAAGGCTGGGTGCC[C/T]TGCCATGGTCTCCCA | 50807 |
| rs538810256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204036 | AGAGCACGGGTCCCC[A/G]GTCCCCAGGCCACGA | 50807 |
| rs538820226 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325836 | ACAAAACCAAGGCTC[C/T]GAGAAGAGACCACAA | 50807 |
| rs538822367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332441 | GATTATGTCATTGTA[C/T]TTTAGTTTACAGTTT | 50807 |
| rs538854690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333113 | TCTCAAAACTCAAGG[A/G]GGAATTACAATTATA | 50807 |
| rs538858517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324714 | AGAATAGGGCTGGGA[A/G]ATTTCAGTGGTACTT | 50807 |
| rs538866897 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130168702 | CTTTCTGCAACTGCT[C/G]ACCAAGGAACACTCA | 50807 |
| rs538867270 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130280032 | AAACTGGCACTTACA[C/T]GTTCCTTATTTTATT | 50807 |
| rs538875304 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130416793 | GCCACAGTGGTAAAA[A/C]AGAAATCATAATGAC | 50807 |
| rs538881804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130075044 | TTGCGGTAAAGCCCC[A/G]TGGGCACTGGGAAGT | 50807 |
| rs538902473 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101817 | AGCTCAAGCAATGCA[C/G]CCACCTCATCCTCCT | 50807 |
| rs538913416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424218 | CCTCACATGAGACTG[C/T]GGCTGCCCATTCTCT | 50807 |
| rs538917116 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130436145 | AACAGAAACCCTAAG[A/G]AAAGAAAAGGACCCA | 50807 |
| rs538920152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109092 | AGAACCAGTGTTAAT[A/G]AACGTACAGTAGAAG | 50807 |
| rs538933414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205316 | GCCACAAGCTGAAAA[C/T]GCAATCCTATTTAAA | 50807 |
| rs538936621 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130118052 | TTTTTATATCTAGCA[C/T]GACACAGAAAAAGCT | 50807 |
| rs538946570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130069679 | TAATACAACATTATC[A/G]AAGCTTGGGTGGACC | 50807 |
| rs538946876 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130299570 | TACATGTTTAGTTGC[A/T]ATACTATTGAGATGG | 50807 |
| rs538956674 | snp | C/T | 0.00020286 | 0.0100692 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340985 | TTGTTTTTGTTTTGT[C/T]GCTGGGGGGCAGTGG | 50807 |
| rs538957183 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094228 | AAAAAAAATTTTTTT[G/T]GAGACAAGGTCTTGC | 50807 |
| rs538966275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100964 | GTAGTTTTATAGTTT[C/T]GGGTATTATGTTTAA | 50807 |
| rs538969501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368253 | AACTTATTTTCAATA[C/T]CATATTATTTTCATG | 50807 |
| rs539003695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166784 | TCCAGCCTCTACCAT[A/G]CATTCTATGCTCTTT | 50807 |
| rs539010450 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410074 | ACTGCATGCTATTTT[C/G]CATTGGCTACAGCTT | 50807 |
| rs539022492 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288843 | ATGGGAGATGGTTAA[C/G]CAAATTATGATAAAT | 50807 |
| rs539025217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249955 | AATCACGTATTTTCA[A/G]ATCCTAGGAACATTA | 50807 |
| rs539038053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385853 | ACTCCTGCCGGTGAA[C/T]GCATTTCAAATTCCC | 50807 |
| rs539042229 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060474 | ACATAAGGGTCAGGT[A/G]AGCAAGCTCTCACTT | 50807 |
| rs539043320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130242479 | TACTTTGGCCTAATT[C/T]TGGTTTAGACTCTGA | 50807 |
| rs539044348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151585 | TCTGAGGAATTCCTC[C/T]GAAGAATCACTGAAA | 50807 |
| rs539048330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158615 | AACAGAAAAGAAGCC[C/T]CATGTGGCAGGATCA | 50807 |
| rs539050630 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314162 | GGGTCAAAAAGGTAA[A/G]CTTCCTCCCCCCACT | 50807 |
| rs539056478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151013 | AAATAAAAATTATCT[A/G]ATTTTTCATTCATGC | 50807 |
| rs539078189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379893 | ACCAGCCAGACACCA[C/T]GCCCTGAGCCTGGCA | 50807 |
| rs539094290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066429 | TTGCCCAGGCTGGTC[C/T]TGAACTCCTGGGCTC | 50807 |
| rs539096036 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130197717 | AGATGCACCTGAATG[C/T]GTGTTCTGAGTTAGG | 50807 |
| rs539101475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130152500 | GATAATATTATGAAA[G/T]CAAAATACCGTATTC | 50807 |
| rs539118164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375083 | TTCCTAACTGCTCCA[C/T]ATTGCCACTCTCAGC | 50807 |
| rs539119938 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130133998 | AAGGGCTGCAGACAT[A/G]CACCACAGGATCACA | 50807 |
| rs539120428 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070122 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 50807 |
| rs539120707 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130113106 | AGAGCTGGTGGGAAA[C/T]CTTGCTCTTTAGACA | 50807 |
| rs539131911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276248 | GGGGGCACTGGGCCG[C/T]TCCAGCTGTAACAAT | 50807 |
| rs539133993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283436 | TACAAAAAGTAGCTG[C/G]GCATGGTGGCATGCG | 50807 |
| rs539143621 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381244 | GTGTTGCGCAGGTTG[G/T]TCTTAAACTCCTGGT | 50807 |
| rs539149147 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187339 | TTTGCTGAAAATTAA[G/T]AAATAGTTTTGAAAT | 50807 |
| rs539154825 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376018 | AATACACATTGGCAC[A/G]CCATACACAAATTAA | 50807 |
| rs539156406 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130053936 | GCTTCTAAATGCATG[C/T]GTAATGTAGAGGCTA | 50807 |
| rs539156458 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130060732 | TGTGACCTCAGAGGG[C/T]TGCTGAGCCTTGGGT | 50807 |
| rs539163411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374014 | GTGCTCAAAGGCCTT[A/G]GAGAAAGTGTAACTC | 50807 |
| rs539169008 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130282591 | TGGCAAACTGAAAGG[A/C/T]CTTTCAGCTCTGGCA | 50807 |
| rs539170566 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130165398 | GACTGAAATCTACCA[C/T]CCCGTACTCCCTTCT | 50807 |
| rs539176097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415980 | CCTGTAAACTTAGAA[A/G]GATCAACCAATTTCC | 50807 |
| rs539188736 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284072 | CACATCCGCCTTAAA[G/T]TTCCAGTTCACTGGC | 50807 |
| rs539192367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339537 | GGTAAGTCTCCTCCA[C/T]TTGAAGGCAGTGCTC | 50807 |
| rs539193382 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145100 | AGATAGTCATCCACG[C/G]AGGCATTTCTGCAAA | 50807 |
| rs539214612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387803 | ACTTAGCAGCAGCCA[C/T]TGATTTTATTTCAAC | 50807 |
| rs539221030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062277 | ATCCTAAAAATATAA[C/T]GTATTCAGAAAGACA | 50807 |
| rs539225547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153939 | TGGCTCATGCCCGTA[A/G]TCCCAGCACTCTGGG | 50807 |
| rs539233534 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130139875 | GATTTCTCCGGTGTT[C/T]CTGAACAATCTTACC | 50807 |
| rs539233679 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130167278 | TCTAGCCTGGGTGAC[A/G]GAGTGAGACCCTGTC | 50807 |
| rs539238031 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153289 | TCCCAAAGTGCTGAG[A/T]TTACAGGTGTGAGCC | 50807 |
| rs539243630 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130408952 | CATTTCCTGATTGTT[C/G]ATAGAGGTAAGTCAA | 50807 |
| rs539247916 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130141696 | GCACTATATGCGCAC[A/G]CTACCACACGAGGCT | 50807 |
| rs539258038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068493 | ATCAGCTTCCTGAGG[A/T]ACCTTTACTAAAACG | 50807 |
| rs539258624 | in-del | -/GCACACATG | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173489 | CATGCAAGGGCTACT[-/GCACACATG]GCTCATGCCTGTAAT | 50807 |
| rs539265005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381818 | GCCTTTGCACGTGCT[A/G]TTCCCCTCAGCTGGA | 50807 |
| rs539276304 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317688 | CCTCCATTGTGAGCT[G/T]TGAGGCCTGGGGCTC | 50807 |
| rs539279443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130138342 | TTCCAAAGCGAACTG[C/T]TTTAGGGGAGGAAGT | 50807 |
| rs539297205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276937 | CTCAATGGCAGACGA[C/T]GGAAGGACTCTGCCT | 50807 |
| rs539301454 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366269 | TTGTAACAGTATAAA[G/T]TTTGGCACACCATCA | 50807 |
| rs539301683 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130092196 | CCAGTCTCACAGATA[C/T]AAAACAGCCAGTATG | 50807 |
| rs539303253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173682 | CTGAGGTGGGTGGAT[C/T]GCTTGAACCCAGGAG | 50807 |
| rs539306747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130375651 | CCTACCAGCAAGAAA[C/T]GGAGGGCAAAGAAGG | 50807 |
| rs539308384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189515 | GCTGAATAATATTCC[A/G]TTGTGTATATATACT | 50807 |
| rs539309446 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402980 | ATAAAAACAGAGAAG[G/T]GTATCATATACCCCC | 50807 |
| rs539310850 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056688 | GTGTGTGTGCACACA[A/T]GTATATACATATGTA | 50807 |
| rs539320417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130196565 | TGACAGAAGAGCAGA[A/G]CACAGCTCTACAAAT | 50807 |
| rs539326423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263242 | CTGAACCAGGGAAGG[C/T]AGCATGACCCAAAGG | 50807 |
| rs539331299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079590 | TATCAAAAATAAAAA[C/G]TCATTCTGACAGGAA | 50807 |
| rs539362342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179978 | AAAAGAGAGAAAGAG[A/G]AAGAGAATGAGAGAG | 50807 |
| rs539413176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413432 | ATTTCTGAAACAGGA[C/T]GTGTCTCCTATCAAT | 50807 |
| rs539413365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228104 | TCATAAACAGACAAG[A/G]AAAAAAATCATCTCT | 50807 |
| rs539416408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144635 | TTCCCTCCAGATGCA[C/T]GTTCCAAATTCCAAA | 50807 |
| rs539421431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091017 | TGTTTCGTGATGGGG[C/T]GACCCCTAAGTCGCT | 50807 |
| rs539433799 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130421815 | TATTACTAACTAATA[C/T]ACCATCCCAGTCTCC | 50807 |
| rs539446297 | in-del | -/AA | 0.0325976 | 0.123435 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320723 | CTCTAGTATCACATT[-/AA]AAAAAAAAATGGAGA | 50807 |
| rs539450703 | snp | A/C/G | 0.000131798 | 0.00811675 | missense | ASAP1 | GRCh38.p7 | 8:130112258 | AGCTTGTCCTGGGGG[A/C/G]AGATGCTGGAGGAGT | 50807 |
| rs539453125 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422173 | CTTCAGAGACCAACC[C/T]GAGCCACAGTGTGGA | 50807 |
| rs539468080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322226 | GTGAAAAATTGCATA[A/C]GAAACTGAGAGATAA | 50807 |
| rs539476984 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083699 | TTATTCACAGCTCTT[C/T]AATGGCATGAAACAG | 50807 |
| rs539488041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373367 | TTAGACCTTCAACAA[A/G]CTGAACACAGCAGTT | 50807 |
| rs539488780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372034 | TGTATATTTAAGAGG[C/T]TTAGGGATCCTACTG | 50807 |
| rs539494915 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130107972 | GGCTTGACACAGACT[A/G]ATCTGCCTTAGTTTG | 50807 |
| rs539495620 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130363731 | GCCTGGCAGACTCTA[A/T]ATCCAATGCTTTTTC | 50807 |
| rs539501875 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130289771 | TTTTAGAATTCATAC[-/T]TTTGTAGATTTCAGA | 50807 |
| rs539502282 | in-del | -/TAAT | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130181473 | TTCAATTATTTCAAA[-/TAAT]TAAAGTATATAATGG | 50807 |
| rs539510314 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130219158 | TACAGAGCGATGTCT[C/G]TAATATCAAACAGAA | 50807 |
| rs539513995 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085961 | TGTGGTTCTGGCAGG[C/G]AAAAAGCCTGGGGTG | 50807 |
| rs539519768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261088 | AGACCCCACTGTGAG[A/G]AAGCCATGCCAGTGA | 50807 |
| rs539529681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355811 | CATCTATGCAAAAAG[C/T]AACCACTCAAGAGAG | 50807 |
| rs539531012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364473 | GTTACCTGTCAAGTA[A/G]TGGAGCAGGACTCAA | 50807 |
| rs539566542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323028 | GATCAGAATAGGCAA[C/T]GCAATGAAATTATCG | 50807 |
| rs539571114 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404419 | AAAGAAATCAGGACA[A/C/G]TGTGGTACTGGCATA | 50807 |
| rs539582256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222881 | TGCTCCTAACTAGTG[G/T]ACTTGGTAAAGTGCA | 50807 |
| rs539583972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130235688 | GGAGCAAAATGAAGG[C/T]ACCAGGGTGCAAAAT | 50807 |
| rs539587947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130331252 | TTAGACCATTCTCTG[A/G]AAGGTTAGTTGACAT | 50807 |
| rs539602865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317333 | CCTTCTCAGCCAAAA[C/T]TGGGCAAGAGAGAAT | 50807 |
| rs539606044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132100 | GAAGGAGAAACAATA[C/T]TCCAAGGTGACTGTG | 50807 |
| rs539608216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229643 | TATTCAACAAATGGC[A/C]GCTATATTTATTTTT | 50807 |
| rs539611201 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124560 | TACTCCCAGGACAGA[A/C]AAGGACACAGGATTA | 50807 |
| rs539622272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164783 | ACTAAAATTCTTGGA[A/G]CTTCCTTTAATGGAG | 50807 |
| rs539626753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430063 | TAAGTCTTAGCTTCC[A/G]TTTCCTCCTCCAAAT | 50807 |
| rs539644671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187925 | AAGTGCCTAATCTCA[C/T]TCCTCTGTCAATACC | 50807 |
| rs539645510 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229103 | TTCTGTCTTATGGCA[C/G]TGATTATCAATGAAA | 50807 |
| rs539647859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236505 | ACTTTGCCCCCTCCT[C/T]TCTAACTTTTTCCAC | 50807 |
| rs539659528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130396209 | TACTAAGAGACTTGA[A/G]CAAATTAGATGCTCA | 50807 |
| rs539665044 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130180174 | GGAAAAAAATTTGAC[A/C]AAGTTCTCCACTTTA | 50807 |
| rs539673129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392513 | TTCATGTGTTTTAGA[A/G]GTACTATCCCATTTA | 50807 |
| rs539678382 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130093601 | GAACCCAGGAAGTGG[C/T]GGTTGCAATGAGCTG | 50807 |
| rs539679157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261626 | CACTCTGGCCCATCT[A/G]AATTAGAGGCTGATA | 50807 |
| rs539681765 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130392891 | TCCGCCTCCATGACC[C/G]AAACATTTCCCATCA | 50807 |
| rs539687427 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130062659 | AAAACCTTCAAAATA[A/C]CCCACCCTCTTCACC | 50807 |
| rs539693049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432677 | CAAGATGGCTGCCAC[A/G]GTTCCAGGTATCACA | 50807 |
| rs539693210 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407261 | AATCCCACTAAGGGA[A/C]CTTCTGAGAGACTGT | 50807 |
| rs539699549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385338 | AATAGAGCCAAAGCA[A/G]AACAGAGACTTGAGT | 50807 |
| rs539699591 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130255961 | CCTCCCACACACACA[C/G]AACAGCTGGTTCTTA | 50807 |
| rs539709976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157838 | AGAACCACTCCCATC[C/T]CCCACACCACCTGCA | 50807 |
| rs539711345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130065531 | AGATTCTGTTTCCTG[A/C]GGCCTAACACATCCA | 50807 |
| rs539719425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130433881 | AAAGCTTAGGCAGGC[C/T]AAGAGAAAGGCTAAA | 50807 |
| rs539724812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434502 | GAGGAAAACTGCTTA[C/T]AACAGTAATGACACA | 50807 |
| rs539729668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130357759 | GACTTCCATCTTCTG[C/T]CCTCCCTGGAGTGTC | 50807 |
| rs539741720 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130137439 | GTCCATGGAAATGCA[C/T]CTTTCTGGAACCTAC | 50807 |
| rs539743678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350634 | AGTTACTAGCAGTGT[C/G]CACTAATTTTTCCAC | 50807 |
| rs539748275 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130068217 | ATCCCTGGTTATTGT[G/T]GTCTATAATGGCTAA | 50807 |
| rs539764370 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130358284 | CGCGCGGCTCCCGTC[C/G]CCGGCAGCGGCGAGA | 50807 |
| rs539764406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072743 | GTTGTAGGAGCCCCA[C/T]CTTGTAGCCAGTCAG | 50807 |
| rs539767502 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130214177 | TGTATGTTCGACACA[A/G]AAATCATCATTCTTT | 50807 |
| rs539777746 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130183145 | ACCGTGGCACTTGAA[C/G]ACTCTTCGTAAAACC | 50807 |
| rs539781372 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165140 | TGCATTTCATCATGT[A/T]CACATTCCTTTGGCT | 50807 |
| rs539800608 | snp | A/C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130200257 | ATAGAAATATTCAAA[A/C/T]CAGGAAGTTGGGTAA | 50807 |
| rs539810500 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108979 | GGGGTTTCTCCATGT[C/T]GGTCAGGGTGGTCTC | 50807 |
| rs539813844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130115552 | TCAATCAATCTCACC[A/G]AAAATGGATCTTGTC | 50807 |
| rs539813996 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130256884 | TTTATTTAATATACC[A/G]CTGGGAGTAAAATTA | 50807 |
| rs539828759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406786 | CTGTGCCTGCCCTAG[G/T]TCTCTCATCTTTAAA | 50807 |
| rs539829158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090412 | AAATCTGGGGATCCC[A/G]AAGGCCTTACACAGC | 50807 |
| rs539854234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130212163 | TGTGTAAACTCCTGG[A/G]ACTGCCTTTTATTCA | 50807 |
| rs539864816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400879 | CCCGTAAAATGAATG[C/T]AGAAATTCTTTTTTT | 50807 |
| rs539866947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130185430 | GATTGTAGAGGACAA[C/T]ACAGAAAAATGAACA | 50807 |
| rs539874713 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130356239 | CTTATCACACCCTTC[A/C]CAAACAGAATACAGC | 50807 |
| rs539879461 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130329774 | TTGACCACTTATGAC[A/G]TGTTGCACTTCTCTA | 50807 |
| rs539887968 | in-del | -/A | 0.0670745 | 0.170406 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323870 | AGATTACCAGGCATT[-/A]AAAAAAAACCACTTA | 50807 |
| rs539891588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178617 | GAAGACTCCAGGTGG[A/G]AATACATGGTGCAAA | 50807 |
| rs539905099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246568 | GGCCTTGTGAAGAAG[A/G]TGCTTGCTTCGTCTT | 50807 |
| rs539906204 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124237 | TACAAACCACCGTCC[A/C]TCTGGTCTACAAATA | 50807 |
| rs539910351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214262 | GTAGAGATGTGGAAG[A/G]GAATTCAGGTTAAGC | 50807 |
| rs539918351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424903 | GAGGCTGAGGCAGGA[A/G]AATCGCTTGAACCCG | 50807 |
| rs539922244 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439025 | AATCAAGGTTGCTAA[C/G]CTGTTGACCTTAAAA | 50807 |
| rs539922971 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130258908 | TTCTTATGCCTTCCC[C/T]ACTCCTCTCCTCCCC | 50807 |
| rs539923104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084961 | ATTAAATAAAAGTAC[A/C]ATTCTAACTCCCAGT | 50807 |
| rs539925714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130198503 | CCTCGTCTGCAAGGC[A/G]GTCTCCATAAACTGT | 50807 |
| rs539927630 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417600 | GAGACAGAAAACCCC[A/G]CAAGTCCTGGCTTCA | 50807 |
| rs539934540 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334009 | GGGAAAAGCAGTAGT[C/T]AGGAAGGGTCTCTTC | 50807 |
| rs539946435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109330 | AGCACAAGGGGGCTT[C/T]GCTTGACGGTAATTT | 50807 |
| rs539948273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220987 | GAGGTCCCTCCCCCA[A/T]CATGTGGGGATTACA | 50807 |
| rs539951440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341107 | AAGTCACTAAGTCTA[C/G]TGACAAGATGCATTA | 50807 |
| rs539968361 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130255641 | TCAAATAACAAAAAG[A/T]TGCTTTTATGAAAAA | 50807 |
| rs539979100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401366 | TTCCACTGCCTCAAC[C/T]TCCCGAGTAGCTGAG | 50807 |
| rs539980613 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208597 | AGGGGTATAAAGAAC[A/G]TGGATGTAAAAGACA | 50807 |
| rs539985003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130072190 | CTGACCATGTGGAGG[C/T]TCCTGGAGTTTCCAG | 50807 |
| rs539985838 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130326529 | TTGGTGCAACACTGC[C/T]GAACTCCTGTTGCAA | 50807 |
| rs539987846 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130293130 | GTCTACAGAATTGCC[C/G]TTTCTTTTCCAAAGC | 50807 |
| rs539989099 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130374088 | TAAGCACAGAACTTA[A/G]AAGTCAAAAGACCTG | 50807 |
| rs540008037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301949 | GTAATGAGAAGACTG[C/T]AACCTCCACGATGGC | 50807 |
| rs540018713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191342 | GAGACCTGCAGGAGC[A/C]GATTATAGATGGAAA | 50807 |
| rs540038857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134402 | AGGGTACTTTCAGGT[A/G]CAACACAGATTTAAG | 50807 |
| rs540044722 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309911 | TCCAGAACTCAGCAT[C/G]AGTCTTTAGACATAT | 50807 |
| rs540047457 | snp | C/T | | | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445214 | TGGCTGTTCTTGGCA[C/T]GCAGCTCACAGCCCA | 50807 |
| rs540051371 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130232546 | TTTAAAATGTCCTCA[A/T]ACACAACAAGGAAAA | 50807 |
| rs540052148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130142269 | ATCTGATATAGCTCG[A/G]AGAATAACAGCTGGA | 50807 |
| rs540066386 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164193 | CCTGCAAACGATAAT[G/T]TGATGGGGTTTTAAA | 50807 |
| rs540067235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130103648 | GCTGGGATTATAGGC[A/G]TGTGCCACCACGCCC | 50807 |
| rs540071888 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130365465 | ATGGGAGTCCTAAAA[A/C]CTTGCGATCTATAGG | 50807 |
| rs540083789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078195 | GGGTTTCACCATGTT[A/G]GCCAGGCTGGTCCTG | 50807 |
| rs540085326 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130310962 | CAGTATCTACTAAGG[C/T]GGCAGTGTTTCTCTG | 50807 |
| rs540087879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085521 | AGGAGGATCACCTGA[A/G]CCCAGGAGTTCGAGA | 50807 |
| rs540095759 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130384973 | ACAGTGTCCCACGTA[A/C]ATACACACACCATGG | 50807 |
| rs540107519 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130361609 | TATTGTGCTTTGGTA[A/T]GTATATACCTCCTCA | 50807 |
| rs540115972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130426603 | TCCAGCCACACTGGC[C/T]TCCTTGAGGTACCTT | 50807 |
| rs540119722 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130423162 | AGGCTGGAGTGCAGT[A/G]GGTCAATCTCGGCTC | 50807 |
| rs540122324 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288372 | AAAAAAAAAATTCCT[C/T]GTTGAAACAACTGTT | 50807 |
| rs540122955 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370576 | AGAAATGAAAACATA[G/T]GTGCACATAAAACCT | 50807 |
| rs540127122 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130105291 | TAGTAGGTATAACAA[A/G]TAATCTAGAGGTGAT | 50807 |
| rs540132275 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130368498 | TTCTAGACTGTCAGT[C/T]ATGTCTCTACTTTCC | 50807 |
| rs540134993 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130347664 | AACCCCCTCATCCTG[A/G]CCAAAGCTGACTGGA | 50807 |
| rs540136176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208486 | TGGATGACTTTGACT[G/T]TAGTCATAAAAATAC | 50807 |
| rs540143253 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274555 | CTTAACCCCGCCACA[A/C]AATATCAACTTGACA | 50807 |
| rs540145857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354920 | AGACGTAGCCTCACT[C/T]TGTCGCCTAACCTGG | 50807 |
| rs540146262 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130342831 | CCAAGAACCTGGTTG[C/T]CCCCCACCCTACACC | 50807 |
| rs540176411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130427278 | AGTTATCATGGCCTC[C/T]CAGGAGCCACCATGT | 50807 |
| rs540184399 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165357 | AAACAAAAAAACCCC[-/A]AAAAAACCTCACAAT | 50807 |
| rs540192983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063420 | CCCTGTTCCACATCC[C/T]CTCTCCGCACTCCTG | 50807 |
| rs540196913 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130171959 | GAAAAGTTTTGAAGG[C/T]AGAGCATTTAAATTT | 50807 |
| rs540197841 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284841 | CATTCCTTTTACACT[C/G]TACACACACACACAC | 50807 |
| rs540199508 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130272097 | TTGAGCTTGGGAGAT[C/G]AGGCTGCAGTGAGGT | 50807 |
| rs540209078 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409775 | AAGAGGTCACTGTGA[A/T]GGACCCACAACCCAA | 50807 |
| rs540209513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399911 | CAAAACCTCTGCCTC[A/G]CGGGTTCAAGAGATT | 50807 |
| rs540211548 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154897 | TTCTAGAAGTACTGG[C/G]CAGGGAAATGTCTGA | 50807 |
| rs540213705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389114 | GTGAGCATTAGCTAT[C/T]AGTATTGTTGTTGCT | 50807 |
| rs540223616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278173 | TGATGTTAGACAGCA[C/T]AAAGGGAATGAGCAA | 50807 |
| rs540226424 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130236746 | TTTCTGTTTTGGAAA[C/T]ACTAATAGGTTTGGG | 50807 |
| rs540233443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324874 | AGCTAGTGGCACAGT[A/G]CATGAGCATCTGGTG | 50807 |
| rs540244810 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410198 | GTTAGCAAAATAGAC[A/G]TGGTCTCTGCTTAAG | 50807 |
| rs540250120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389533 | GTGATGTGGTTGTGC[C/T]AGGTTAGAGTTGTAC | 50807 |
| rs540267683 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130094213 | CCTAGGTTTATCGTT[-/A]AAAAAAATTTTTTTT | 50807 |
| rs540270555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162090 | CAGGTGTGAGCACCA[C/T]GCTCGACCTAAATGT | 50807 |
| rs540284704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130383566 | TTTAATCTTCACTGC[A/G]GTGGCGTGTGGGATC | 50807 |
| rs540297396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148543 | ATTCTAAGTGCTGCA[C/T]AAATGGCAGTTCTCT | 50807 |
| rs540300591 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213925 | AGTTTCCTCCACCAC[C/G/T]CCCATCCCTGGGTCT | 50807 |
| rs540324620 | in-del | -/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130273947 | CCTCCATAGGATGAA[-/G]GGGGGGCGGAGGAGC | 50807 |
| rs540325090 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130114293 | GTATAGCCTATTGCT[C/T]CCAGGCTACAAACCT | 50807 |
| rs540327775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130279301 | CAGCACTAGGGGTTC[C/T]GAAGTCACCCACACC | 50807 |
| rs540330178 | in-del | -/A | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130307903 | ATAAAATGGATTTTT[-/A]AACTTTAGTGTTAAA | 50807 |
| rs540335093 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130234221 | CTGCACTATCCAATA[A/T]GGCACCCACTAGTCA | 50807 |
| rs540349143 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063801 | CCTATTTGCTGGGCA[G/T]GTGCCGTGCCCAGCA | 50807 |
| rs540356369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377871 | GAGGATCTGGGTGCC[C/T]GACTAATCTCTATGG | 50807 |
| rs540360992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197652 | CACTACTGTAGGGCA[A/G]GTGCCCTGATAGCAG | 50807 |
| rs540376314 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130404144 | TTGGATTTGTTTATT[G/T]GTGTATGTTGCAGCA | 50807 |
| rs540389221 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | ASAP1 | GRCh38.p7 | 8:130443215 | GGAGGCGAGGAGACC[C/T]CCCCCCCCCACCGGG | 50807 |
| rs540401078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081845 | ATTATTAACAGCAAC[C/G]ACCGTTTACTGAGCA | 50807 |
| rs540420329 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130123157 | ACTTGTTTTGTTCCT[A/C]ATCTTTTTGCATTAC | 50807 |
| rs540424397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058590 | GATCGGCCTGGGGCT[C/T]GGAGAAGTCTATGCA | 50807 |
| rs540429810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320565 | AAAAAGAAAAAGAAT[A/G]CATACATACATATGA | 50807 |
| rs540431994 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130103296 | TTTGGGTCTTCTCCC[C/T]TCTTTTCTTGTCTAG | 50807 |
| rs540435377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081071 | ATAGGAAATACACTA[A/C]TAATGTGTAATGAGA | 50807 |
| rs540440601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405647 | ACGTCACTAGACCAT[C/T]GTGAACCTTCAGAGA | 50807 |
| rs540442320 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096231 | GAGCTCAGAAGACTT[A/C]CAAAATTAGTAACCA | 50807 |
| rs540443331 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130219763 | ACTTCTGGCATCCAC[A/G]ACATTGTTGCAGAAG | 50807 |
| rs540473844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393729 | CCACTGCACTCCAGA[C/T]TGGGTGACAGAGCGA | 50807 |
| rs540506157 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130266751 | AAGACCTAAATAGTA[A/C]AATAAAATGAGAATA | 50807 |
| rs540525901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430749 | AGACACTGGGAAGGT[A/G]TATTCAGAATTGGTT | 50807 |
| rs540533923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183808 | GGAGGTAATGGGCCA[C/T]CAAAATATGGAACTA | 50807 |
| rs540542868 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130274110 | AAAGTCTATGACTCA[A/C]AATACCTTATATAAT | 50807 |
| rs540546307 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382155 | GCTGGGCGTGGTGGC[A/C]GGCGCCTGTAGTCCC | 50807 |
| rs540557716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347029 | AATGGAAGTAAAGCC[A/G]TTAGTCCTCACTGGA | 50807 |
| rs540561140 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226541 | GGATGATTCATTTCT[A/C/G]TAATTTCTCAAGGTC | 50807 |
| rs540569191 | snp | C/T | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306802 | ACATGTATTTGTATT[C/T]CCCATCTCTCTGTCT | 50807 |
| rs540569724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417012 | GTGTACATTTGCATA[C/T]ACGCATATGGACACA | 50807 |
| rs540571718 | in-del | -/GCCAGGGCAGGGACCCTTCCTGGAG | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419057 | ACATCAGGCCCTGCA[-/GCCAGGGCAGGGACCCTTCCTGGAG]GCCAGGGTCCCGCAC | 50807 |
| rs540582770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406371 | CCAGATCCTGTACTC[C/T]AACAGTATGACTTAT | 50807 |
| rs540595717 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353119 | CTATTTCCCTCCCCT[A/G]TGAACTGCCCCTTTC | 50807 |
| rs540602775 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333316 | ATAGTAAAAAGGCAT[G/T]GCTGGCTGGGCGCGG | 50807 |
| rs540606370 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130269239 | AAAGGCAGAGTCTGG[G/T]TTAGCTGTGGATAAA | 50807 |
| rs540610781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238136 | GGAAAATGGTCTTTC[C/G]TACCACCTTCCTTCA | 50807 |
| rs540613624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381931 | TCTCCTCCCACCCTA[A/T]TCCCCATCTCTTGTT | 50807 |
| rs540618664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218902 | GTATATACTGGCATA[C/T]ATGTCTCACATATAT | 50807 |
| rs540621412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140384 | TTAAAAAAAAACTTT[C/T]AGGTTTGGGGGTACA | 50807 |
| rs540631603 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130118780 | TTTTAATTAAGATAC[A/G]CTTCTTTTCACCATT | 50807 |
| rs540640943 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130436994 | CCTGTAATCCCAGCT[A/C]CTCAGGAGGCTAAGG | 50807 |
| rs540641480 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132358 | TTCCTCCTCATTGAC[A/T]TCTAGTCACCTTTCA | 50807 |
| rs540652287 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130301240 | GACATGTTGTACCAA[C/T]GCCTGCTCTTTGAGA | 50807 |
| rs540653924 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101624 | CACCCAGGCTGGAGT[A/G]CAGTAGCGTAATCAC | 50807 |
| rs540658003 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377566 | GCCCCAGCTCTCAAG[C/G]AGCCTATGGTCAATC | 50807 |
| rs540665298 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130367813 | CTATATTACATGAAT[C/G]TGTCACAGTATTCTC | 50807 |
| rs540671969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263017 | TGCTTTTGTACAACA[C/T]GGAAACAGAAAAAGA | 50807 |
| rs540672431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130357880 | CCGTCCGAAGTCCCT[C/T]ATTCACCCGGCGGCT | 50807 |
| rs540702272 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130097785 | CCAGGAACTGACATT[C/T]TCTTCTCACTGAAGC | 50807 |
| rs540719633 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123197 | ATAAATTCCCAGGAG[C/T]GGGACTGCTGAGTCA | 50807 |
| rs540745234 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278613 | CAAGTTTTGCAGCTA[A/T]GAGTGCAAATATTGG | 50807 |
| rs540753134 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130341119 | CTAGTGACAAGATGC[A/T]TTACAGCAGAAGGTA | 50807 |
| rs540755461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094388 | GCTAATTTTTAAAAA[A/T]TTTTAAATTTTTAGT | 50807 |
| rs540771188 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130231797 | TGCAGTATGTCTCAC[C/T]GTGTTTTTTAAACAA | 50807 |
| rs540785370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068146 | ATCCAACTCCCCAGG[A/G]GTTGGGGCACTGGAT | 50807 |
| rs540789375 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130190393 | AATTTTCCCAGCACC[A/T]TTTATTGAAGAGGAT | 50807 |
| rs540789616 | snp | C/T | 0.000115394 | 0.00759499 | missense | ASAP1 | GRCh38.p7 | 8:130128023 | GGCTGTTCTCTCCCG[C/T]ACTCTGCTCTCCACG | 50807 |
| rs540789757 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130344116 | AGGGTTGCAGTCAAC[A/G]CTATCCATACTATGG | 50807 |
| rs540803338 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160551 | GTGAAAAGTGTTATG[A/G]TGTCGTGGAGGGTGA | 50807 |
| rs540807759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130386900 | TGACGTCCTTGTTGC[C/T]GTGGTTACCAACGCT | 50807 |
| rs540808471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218095 | GAAAGGCCACACGAG[C/T]TCAACCGAGAAGACA | 50807 |
| rs540809190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119974 | TGCTACTGTTTCCAA[C/T]AGCCCACAGTCAGGC | 50807 |
| rs540813130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130304269 | TTTTTTTATACTGCC[C/T]GGAAAAGAACGCCTT | 50807 |
| rs540821227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203195 | AGTCAATGTTTCTTA[C/T]ACAACAACAAAGTCC | 50807 |
| rs540823012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399189 | CTGTGAGGTGACCTT[A/G]GGAATAGAGGTTCAC | 50807 |
| rs540823068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224889 | ACATTTCAAGTTTTA[A/G]TTAATATTGCCACAT | 50807 |
| rs540846280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387487 | GTTGCAATGAGCCAA[A/G]ATTACACCACTGCAC | 50807 |
| rs540851257 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127612 | GCTGGGAGTGGTGGA[A/C]AGTGATACAAAATGT | 50807 |
| rs540852862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133884 | TGGCTGATATGTTTG[A/G]CCACCAAAAACTGAG | 50807 |
| rs540853347 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130443728 | CACGATCCCGCTCGG[C/T]GGCGGAGGGCGCGGG | 50807 |
| rs540853376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175563 | ATTCTGGATATCAGA[C/G]TCTTATCAGAAAAAT | 50807 |
| rs540856915 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257846 | TAGTTCTCCATGTAA[C/T]ATGTTAGTTATATGC | 50807 |
| rs540860121 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244218 | AAACAAATGGAAGGT[C/G]AAAGAATGAATATCT | 50807 |
| rs540866994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159701 | ATTACTGTTTCTTCT[A/G]AAGAGAGCTGGTCAA | 50807 |
| rs540894073 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277541 | ACAAACATTGAAAAC[-/T]CCTAAAGACAAGCAC | 50807 |
| rs540899142 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130250163 | TTCGGTGTCCCTATT[C/T]TGCATCCTCTGACCT | 50807 |
| rs540900735 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114914 | CAAATAGCACCACCA[C/G/T]GTTTTATTGATTGAT | 50807 |
| rs540906763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130353909 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 50807 |
| rs540908820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130075384 | AGTGTGTTACTTCAC[C/T]GAAGAACTCTAGAGA | 50807 |
| rs540923505 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130324483 | GTCTGACCCCTTTGC[C/T]CTACAGAAAAGGAAA | 50807 |
| rs540944761 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297726 | AAGAAAACAAAGCGG[C/G]GGGGCGGGGAGCAGA | 50807 |
| rs540945489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347562 | TGATCTGGGTATAAA[C/T]GGTGTGCTTCCCTAT | 50807 |
| rs540962158 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121964 | CCCTGCATCTCCCTC[C/T]TGCTCAGTTCTCTCC | 50807 |
| rs540987365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343386 | ACTCACTCCTTTTTC[C/T]CTTCACTACTCCTAC | 50807 |
| rs540993696 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111452 | ACCTGGGTTAGAATC[A/C]CAGGCTGAGAACTAC | 50807 |
| rs540995483 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119182 | CTCCTGAGCTCAAGC[A/T]ATTCTCCTGCCTTGG | 50807 |
| rs541003938 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130391583 | GGTTCTCAATCTATC[A/C]TGCTGCACCTAGGCA | 50807 |
| rs541005408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130416295 | GCAACCCCACACTCC[A/G]TCTCTTCCTCCTCTC | 50807 |
| rs541006721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130223564 | CAGGTTTTCTGTTTA[C/T]AAACTGTGATCTAGG | 50807 |
| rs541007678 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130366712 | ATTTAATTTAAATTA[-/C]TTTATTGTTAAAAGG | 50807 |
| rs541010350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311686 | GAATCGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 50807 |
| rs541014656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215712 | CCGCGTCACTGCACT[A/C]CAGCCTGAGCAACAG | 50807 |
| rs541023549 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130073094 | TGTTGTTGGTGAATT[C/T]GGATTATGGACGAAT | 50807 |
| rs541038335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130214808 | ATGGAAGCATAAACT[A/G]TATCAATTATTTATT | 50807 |
| rs541039128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086390 | AACACAATGCCCAGC[A/C]CTCTGTGAGGCACTT | 50807 |
| rs541074876 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130302143 | GCATGCAAAGACTCA[C/T]ACATTCTCTCATTTG | 50807 |
| rs541081374 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241968 | ACTCTTTGGAGCTAA[A/G]TTTTATGTTTACAGA | 50807 |
| rs541086336 | snp | A/C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130372007 | TCCCAACTAGTCCTC[A/C/T]GTGTTTGGGATTGTA | 50807 |
| rs541097383 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130096758 | GCCCTTAAACAGAGA[C/T]GGATGACAGGACTAG | 50807 |
| rs541104808 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130244661 | CATAGCCTGTCTGTA[C/T]GGCACACCTTTGGAA | 50807 |
| rs541113034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130441805 | TCTCCAACATTATCA[C/T]ATACTAAAAATGAAA | 50807 |
| rs541114620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080075 | CTCAGGTTCCAGAAC[A/G]GCATTTAAAAGACCC | 50807 |
| rs541126462 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130276778 | TCTAACAAAAAAGCT[C/G]CATGGCAGCATGAGA | 50807 |
| rs541131016 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428555 | ACCATCATATAACTA[A/C]CACCATCATCACCAC | 50807 |
| rs541143648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352362 | GCATTCTTGAGCAAG[A/G]GGAGCTGACGAACAA | 50807 |
| rs541156874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106351 | ACCACTGATAGGAAA[A/G]TATTTCCCATGCGAG | 50807 |
| rs541156898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337519 | CTCTCCAAATAATCA[A/C]ATCCTAACATGTCCA | 50807 |
| rs541160117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126546 | TAAGACAGCTGTAAA[C/T]ATTGAACACCAAATG | 50807 |
| rs541165037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130427430 | AAGCACCAATAAGCC[C/T]TTGCCGAGAATCCCA | 50807 |
| rs541176240 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130216627 | CCTCAGTCTTGGACC[C/T]TTCTTCTCTATTTTT | 50807 |
| rs541179094 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421692 | GAGAGACTCCCACCG[A/T]ACTAGAAATACACAT | 50807 |
| rs541180823 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130345721 | AATCCCACCACTTTT[A/G]AGAGGCCAAGAAAGC | 50807 |
| rs541189021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297729 | AAAACAAAGCGGGGG[C/G]GCGGGGAGCAGAGGT | 50807 |
| rs541192540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130113275 | CACACACAGTGCTTC[C/T]CTCCATTCCTCCGAC | 50807 |
| rs541200151 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130160820 | AAGGGCAAAAGAAAC[A/G]GAGAAAAAAGGCAGA | 50807 |
| rs541204185 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130244082 | ATCTGGCTGGAGGGC[C/T]GAATCAAGGGTGTAT | 50807 |
| rs541206321 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130201143 | ATGCAAGATCAAGTG[A/T]GAGAACCACTGCCTT | 50807 |
| rs541213354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130250754 | CATAAAAAAAACTGA[C/T]GGAGTTAAAAAAAAA | 50807 |
| rs541230643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130305032 | TCCTTTTGTTGTTTC[A/G]TGAATGTGTCAGGCA | 50807 |
| rs541233527 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130111571 | TTACAAAAGAAGTAC[C/T]AGGCGTAGAGCCTCT | 50807 |
| rs541254460 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379994 | TGCGACCTCACCCTA[A/C]TCCCCACCCCTGACA | 50807 |
| rs541261426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130235178 | GTTTCTCTCTTTTTC[A/G]AAGGGGTGTGTAGTA | 50807 |
| rs541262341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133447 | GGATCATGAGGTCAG[A/G]AGATCGAGACCATCC | 50807 |
| rs541270566 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323189 | CTGGATCATCACCAT[A/G]TTCCTGGGGAGGACA | 50807 |
| rs541282262 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130351526 | AAAGGAAATTCTGCA[G/T]GCTGTACAAGCATGG | 50807 |
| rs541287045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099286 | CAGGTTCACGCCATT[C/T]TCCTGCCTCAGCCTC | 50807 |
| rs541292022 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373525 | AACACTCTACTCAAC[C/T]GATCCCAACCTCAAA | 50807 |
| rs541295750 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130212956 | TCAGAGAAAACAGAT[-/C]TTCCTGCCCAAGCAA | 50807 |
| rs541295764 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130345383 | AAATGCCTCCCCGTC[-/A]ACTCGAAAGAAACAA | 50807 |
| rs541296112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130196107 | AGCACGCTGGAAGGC[C/T]GAGGCAGGCGGATCA | 50807 |
| rs541298575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130365710 | ATTTATATTTATCCA[A/G]CTAGACTGTGACCTA | 50807 |
| rs541321889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229289 | AGAAATAAAACTAAA[C/T]ACACACATATGACTG | 50807 |
| rs541322091 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130287285 | ACAGCTTGATGGATG[C/G]ATGTTGGGGGATAAT | 50807 |
| rs541324115 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107968 | GTCTGGCTTGACACA[C/G]ACTGATCTGCCTTAG | 50807 |
| rs541335481 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130357396 | GCCCTACCAAACCCT[C/T]CGGGTTAGGGAAGCC | 50807 |
| rs541335715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366455 | CTATTGTGATTGACA[C/T]AGTTCCTCCTCCCTT | 50807 |
| rs541336639 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107509 | TCTTTTTTTTTTTTT[A/T]TAAAAAATGTATGTA | 50807 |
| rs541336852 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130326130 | TGCTGGAAATCAGAG[A/G]AGGCTTTAAGGAGGA | 50807 |
| rs541338626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130113979 | TAGAGAGAGGGTTTC[A/G]CCATGTTGCCCAGGC | 50807 |
| rs541353175 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130138456 | CCAAAGAGGAAACAG[C/T]GCTTGGGAAGATTCC | 50807 |
| rs541355800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203542 | AGAGACTCAGGCAAC[A/G]TTGTGCAGAGGAATC | 50807 |
| rs541376021 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130412140 | ACTTTACAGAGGAAA[A/C]AACAGCCCTTACAGG | 50807 |
| rs541385870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287594 | CTAACCCACAAAGCC[C/T]AACAGCCAAGGAAGG | 50807 |
| rs541394106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191989 | CTAATTTTACACACC[A/G]GAAGGTTTCCCAATG | 50807 |
| rs541412168 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224378 | TTATAAAATATTTAA[-/G]TTCTATTTGTTTTTA | 50807 |
| rs541417505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059354 | TATTTTTTATAGAGA[C/T]GGTTTCTCTGTATGT | 50807 |
| rs541429740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130207495 | GCTGCATCCCTACAG[C/T]CTACCCACAGTGCTT | 50807 |
| rs541430893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321209 | GTGAATAAGCCCCAG[G/T]GGCTACAGAGACAGG | 50807 |
| rs541434268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130419810 | CCAAGTTTCAGCTCT[C/G]GCCAGGGCTCCTTCG | 50807 |
| rs541453550 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130313389 | GATCACGTATAAATT[A/G]AGTCCTCCTTCCAAA | 50807 |
| rs541462415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078996 | CCCAGAAGTTCAAGA[A/C]CAGCTTGGGCAACAT | 50807 |
| rs541462605 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150107 | GTTATCTCACTGAAT[A/C]CTCATATAATCTTTA | 50807 |
| rs541465644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130065007 | AGCTTCCCAAGCAGC[C/T]AGGACTACAGGCCTG | 50807 |
| rs541466232 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134548 | CTCATATTTTTACAG[-/A]AAAAAAAAACTGAGG | 50807 |
| rs541466520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130379569 | CCTAATTCCAGACAG[C/T]TAGGGTCAGAATTAA | 50807 |
| rs541475362 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157377 | GCAAGTCCTGCTGCC[A/C]CTGCCTCCATTATCC | 50807 |
| rs541475687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165189 | TTAGCTAGCATGAGC[A/G]GAACACTTAAGTCTC | 50807 |
| rs541489565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130386105 | GTGGGGTCTTTAAAC[C/T]GGTGGCTTTAGGACC | 50807 |
| rs541512947 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130259902 | AGGCTTTCAAATTAA[A/G]TGCATTTATCTATCA | 50807 |
| rs541514369 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130193952 | GCCTCTGCCTCCCAA[A/T]GTGCTGGGATTACAG | 50807 |
| rs541514647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130412884 | CCTGACCTTAGGTGA[A/T]CCACCCACCTCGGCC | 50807 |
| rs541515103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421062 | CAGCTTGTTGGACCC[A/G]AATCTCAGCTCCATC | 50807 |
| rs541527009 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130287273 | AAGGATGACAGGACA[A/G]CTTGATGGATGGATG | 50807 |
| rs541544441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275366 | TCAAAGATTCCTGGA[A/G]GGCAGTAATAATGGC | 50807 |
| rs541552276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407098 | AAGCAAAAAATGGTT[A/G]GCTCCCCGTAACTGA | 50807 |
| rs541559176 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066532 | TTTCTTTTCTTTCTT[C/G]CTTTCCTTCCCTTTC | 50807 |
| rs541577316 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | ASAP1 | GRCh38.p7 | 8:130051922 | GGACAGAAAGGGGCC[A/G]AAGGCCCACAGTTTG | 50807 |
| rs541580646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130194608 | GGAAGACAGTTTTTC[C/T]ACAGATGGCAGGGGT | 50807 |
| rs541581183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281195 | AAACTGGAAATGATA[C/T]GTACCCCCTCACAAA | 50807 |
| rs541589778 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414768 | ATAACTCTTTTTTTT[C/T]TTTTTTTGAGACAGG | 50807 |
| rs541595655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097724 | CATTCCTGGGCCCAA[A/C]AATTTAGTCTCTCAA | 50807 |
| rs541601545 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321781 | ACGTTTGTCTTTTAA[A/C]ATCAGTTATCTCATC | 50807 |
| rs541606338 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187063 | TTTAGGTCAGTGTAC[C/T]CAACCTCTTAGCCCT | 50807 |
| rs541606982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309532 | CTGCAGATGAGGCAA[A/G]ATAAGCAGTGAGGCA | 50807 |
| rs541610991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130221274 | AAGAAAGAAAGAGAA[A/G]GAAGGAAGAAGGGAG | 50807 |
| rs541611796 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130874 | CATAGATCTCATTTT[A/T]AAAAAAAAAGCCACG | 50807 |
| rs541631436 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130259864 | CCTTTGTGGATAATG[C/T]TCATGAGGATAAATA | 50807 |
| rs541639849 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130320839 | CCACTGATCAGATCA[A/G]TAGACATCAACACCA | 50807 |
| rs541647336 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130424829 | AAACCCTGTCTCTAC[A/T]AAAAATACAAAAAAT | 50807 |
| rs541649769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438686 | CCTGGGTTGAAAGTG[A/G]ACAATCGGGCCGACA | 50807 |
| rs541661404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401702 | ATGTGACAGAAAACA[C/T]AGTAGGCAGTCTACA | 50807 |
| rs541671118 | snp | A/C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130188820 | TATACTACAGTACAC[A/C/G]TATATGTGTACAAAT | 50807 |
| rs541678363 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130290766 | AATCCTTAACAGGAT[A/C]ATGATGATACTCCTC | 50807 |
| rs541693941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277199 | TGAGTGAGACTGGAG[A/G]GAAAGCAGCTGCCAA | 50807 |
| rs541704259 | snp | C/G | | | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052912 | GCTTCAGTACCGAGG[C/G]TGCTAAAGCTGCCAG | 50807 |
| rs541727791 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130061755 | CTGAAACTTTGCTTT[C/T]CTCCCACTTACTATG | 50807 |
| rs541735409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415427 | GACCTATGACTGTGC[C/T]ACTGCACTCCAGTCT | 50807 |
| rs541737503 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130294409 | TGGCCATTCAACATA[C/T]ACAGGTGAGAAGTGT | 50807 |
| rs541739561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179640 | CAGTGGATCTCAAAC[A/G]TATAGTTTATGTGGT | 50807 |
| rs541739859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318723 | AAAACTACTACGTGA[C/T]AGAGTTGGGGTTCAG | 50807 |
| rs541741849 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130264222 | TGCTAGCTAAACAAC[A/G]GAGGCTCCTAAATAG | 50807 |
| rs541744094 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130234664 | AGGGATGAAATGCAT[C/T]TTGAGGGGGAACATT | 50807 |
| rs541744213 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078423 | CCTCAGCCTCCCGTA[C/T]AGCCAGGTATGTACC | 50807 |
| rs541744473 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356545 | AAAGACAAAAAAAAA[C/G]AAAAAAGAAAAGAAA | 50807 |
| rs541745221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099791 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 50807 |
| rs541751766 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187522 | CCAGGCTCAATTGAT[C/G]TTCCCACCTCAGCTT | 50807 |
| rs541775691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130135017 | CTGCTATCCATGTAA[G/T]GGAAGGAGTGGGAAG | 50807 |
| rs541777327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273801 | CCCCAGGTGATTCCA[A/G]TGGGCAGCCAGGGTT | 50807 |
| rs541781215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350118 | AGCTACTGCGGCCTC[A/G]CACAGTGTGTCTTCT | 50807 |
| rs541801434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124323 | ATGGGTAAACTATGT[C/T]CCCTTTCCATAGATG | 50807 |
| rs541808419 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233928 | ACTCATAGGCCAGTG[A/C]AACAGTTCTTAATTT | 50807 |
| rs541813397 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335992 | AATGAAATTTCCAAG[A/T]GAGACAGGAAAAGAG | 50807 |
| rs541821760 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130256612 | GAGATAAAATTTCCA[A/G]GGCAAAAATGTATTC | 50807 |
| rs541833870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143181 | TTCTCTAAATATAGT[C/T]ATGACACTTTTCAAA | 50807 |
| rs541834792 | snp | A/G | 0.000198426 | 0.00995859 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130134328 | ATCTTCTGCCTGAAA[A/G]TGATATGTTCTATTA | 50807 |
| rs541840005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241052 | CAGGCCGAGTGGTAT[C/T]CCTCAGTCACAGCAG | 50807 |
| rs541840481 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226466 | AGATTAAAGACAAAA[A/T]CCTTGGAGGCAGAAA | 50807 |
| rs541852669 | snp | C/G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130075045 | TGCGGTAAAGCCCCA[C/G/T]GGGCACTGGGAAGTG | 50807 |
| rs541853534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130058810 | GCCTCTTCCTCTCTG[C/T]CCCCTGGTTTCTCCT | 50807 |
| rs541858671 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130221765 | CCTCTATACTCCATA[A/T]CCTAAAGTAGGACAG | 50807 |
| rs541874400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370806 | TCAGATACAAAAGAC[A/C]ACATACTGTATGATA | 50807 |
| rs541877196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130233312 | AGCTTCCCAGGTAGT[A/G]ACACATCCAGCCAAC | 50807 |
| rs541893231 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130183679 | ATACTGATTTACCAC[A/T]TTTATAAAAATGATT | 50807 |
| rs541908667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098351 | ATTCTCATCTTTAAA[C/T]ACTTTTTTGAGATGA | 50807 |
| rs541911119 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130371544 | TCTAGCCAGTGAGAT[G/T]TAAGCAGAAATGCTA | 50807 |
| rs541916104 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445407 | ATCTGCCCCCCACTC[C/T]CCCCACTGCATGGGT | 50807 |
| rs541930947 | in-del | -/CAT | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428649 | TGTCATCATCACCAC[-/CAT]CATCACCATCCCCCC | 50807 |
| rs541934856 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169187 | GAAAATACACTTATC[C/T]GTATATATATACTCA | 50807 |
| rs541935324 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130422518 | CTTCTCCCTTGCCTC[A/G]GGCTTCTCTGCAGTT | 50807 |
| rs541946781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083684 | GACACAAGGGTATTA[C/T]TATTCACAGCTCTTC | 50807 |
| rs541963394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394499 | TAGCAATTTTAATGT[C/T]GTCCCGGTCCTGTGG | 50807 |
| rs541967118 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130055262 | GGGCTAAAGAAAATC[C/T]CTTCTCTCCAGGCTT | 50807 |
| rs541967526 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130200871 | ATCAGATGTCATGTA[A/T]AAAAGTAAAAACAAT | 50807 |
| rs541974582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136440 | TTTTCCTTTAAGAGC[C/T]AGATTTTGCAGGGAT | 50807 |
| rs541974606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143941 | GCTTTACAAACAAGA[A/G]GTGAACATTAATTAC | 50807 |
| rs541979982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203239 | TTAGAAAGCACTGCA[C/T]TGGACAAGTTTCTTT | 50807 |
| rs541981322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176990 | CCACCGCGCCCAGCC[A/G]TCTCTCTTCCTCTTG | 50807 |
| rs541985855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070316 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCC | 50807 |
| rs541996041 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130183302 | AAAGTAGAAAACAAT[A/G]GAACAATGCCTTCAA | 50807 |
| rs541998431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394911 | CCAGGCTCACATGAC[C/T]AGCAAACAGCAGAAC | 50807 |
| rs542001644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129276 | ATAGCAGTGTGAGAA[C/T]GGGCTAATAGAATGA | 50807 |
| rs542004588 | in-del | -/AA | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314091 | GAATGCGTCACCTTC[-/AA]AATTTGGTCAGAAAA | 50807 |
| rs542009020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395704 | CAGAGTCTCACTCTG[C/T]CACACAGGCTGGAGT | 50807 |
| rs542010076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348660 | TGACACTGAAAACAA[A/G]CTATGAAGCACACAG | 50807 |
| rs542017742 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436674 | AGGCAAGGTGGCTCA[C/T]GCTGGTAATCCCAGC | 50807 |
| rs542021259 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130277 | CTGAAGTTATATGAC[C/T]TGCCTAAGGTTCTAG | 50807 |
| rs542037386 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130052923 | GAGGCTGCTAAAGCT[A/G]CCAGTCACAACCCAG | 50807 |
| rs542039749 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130058879 | CTTCTGGGCCGTGCG[A/G]GTGGGTTGGAGAAGC | 50807 |
| rs542058736 | snp | C/T | 3.29549e-05 | 0.00405911 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136948 | GAGAGAAAAAGGACT[C/T]ACGTGATATCAGGTC | 50807 |
| rs542060001 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171879 | GGAGTTAAAAGTATG[C/G]GTACAAAGTTAATCA | 50807 |
| rs542061457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130260098 | AAAAACCCATTAAGA[A/G]TCTATGTTTTTCTTT | 50807 |
| rs542067595 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162812 | GACAGAGGGAGACTC[C/T]GTCTCAAAAAAAAAA | 50807 |
| rs542073054 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180183 | TTTGACAAAGTTCTC[C/T]ACTTTAATATTTTCT | 50807 |
| rs542088631 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124666 | GCATTCTAAGAAAAT[G/T]TGTTCTGAAGGGCCT | 50807 |
| rs542089227 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130268839 | TATACTACTGTTTGT[G/T]AAACGAAATTCTTTC | 50807 |
| rs542137269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130199173 | ACTTTACAATTATCC[A/G]TGTGTTCCTTTACTG | 50807 |
| rs542142211 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130206608 | GACTCAAGCTCTTAT[A/G]CAAGCTATAGAATTG | 50807 |
| rs542152567 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269542 | TCCCAGTAATACATG[C/T]CACCTACCAAAGTCC | 50807 |
| rs542152579 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261361 | TAAGCAACTTTCAAG[A/G]GCATTTCTGCCTATA | 50807 |
| rs542165848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253886 | ATTAGCCAGCCGTGG[C/T]GGTGGGAGCCTGTAA | 50807 |
| rs542169745 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425861 | CTCCCTACAATGGCC[A/C]AGGTAGAACTGACCC | 50807 |
| rs542174333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130405505 | GCTGGGGTCGGGGGG[A/G]AGGCCACTGGGCCTA | 50807 |
| rs542178875 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130252072 | ATCATTAGCAGTGTT[C/T]TATAGAAAGTTAGAA | 50807 |
| rs542180474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082964 | CAATCAAAACGTCAA[A/G]GAAAATTTTATGTTT | 50807 |
| rs542181459 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121850 | ATAACTCAGATCACG[A/C]CACTCCTGTTTAAAA | 50807 |
| rs542182472 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130217169 | AGCATTTCAGATGCC[C/T]GTACTCAACTCTCCA | 50807 |
| rs542197863 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130376711 | AGCCTGGCAACAGAG[A/C]AAGACTCTGTCTCAA | 50807 |
| rs542221526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320390 | ACAAAACCCCATCTC[G/T]ATAAAAAATACAAAA | 50807 |
| rs542222183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130218044 | TCTGGTTACTATCCA[A/C]GTTCACTCAGAGGAG | 50807 |
| rs542222937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130075122 | TGTGAGCGATCTAGG[A/G]CGGAATCTGGGCACA | 50807 |
| rs542231351 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130199927 | CTCAATTTTTTAGTA[C/T]AGTCCATCCACAATG | 50807 |
| rs542236742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176483 | TACTACTTGATGTCT[C/T]AGAACATCTCTCTCC | 50807 |
| rs542245886 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130398761 | AGAACAGGAAGAAGC[C/T]GAGGCACAGAGAAGT | 50807 |
| rs542252699 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436743 | GGATTAGAGGCTGCA[A/G]TGTGCTATATTTGTG | 50807 |
| rs542265979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130210832 | ATAGCTGTCTTTACA[C/T]TGAGTTACCTTAAAA | 50807 |
| rs542272238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388201 | TGTGAGGAACAGAAC[A/G]GAGGCCAATGTGCTG | 50807 |
| rs542274149 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130169841 | CTAGTAAGCAGCAGA[A/G]CTGGTGGAATTCAGA | 50807 |
| rs542285824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354762 | AACACCAGCTCATCC[A/G]TTCCTGCCTCCCCAA | 50807 |
| rs542289265 | in-del | -/AC | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366183 | CAGAAACTCCCGTCT[-/AC]AACAGATTATGTTGT | 50807 |
| rs542291842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259649 | CCATCATTATCTTGT[C/T]ATGCTAGCTGACTAA | 50807 |
| rs542294040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130076226 | TAGGCATCCACTACA[C/T]GCCAGGTGCTGCTCT | 50807 |
| rs542294678 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430236 | AAGCATCTGGTCTAC[G/T]ACAGGATGGGCAGTT | 50807 |
| rs542303322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437661 | GTGTTGTTACACACA[C/G]GACAAGTTTTTACAG | 50807 |
| rs542303735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347433 | TCTGCCTCCCTTATA[G/T]TCCTACTGATTCTCC | 50807 |
| rs542307826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339916 | TCAGTCCTACAGACA[A/G]TACTTCTTCTGGACT | 50807 |
| rs542310931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382082 | ACGAGGTCAGGAGAT[C/G]AAGACCATCCTGGCT | 50807 |
| rs542311345 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASAP1 | GRCh38.p7 | 8:130420668 | GGAGGCCGAGGCAGA[C/T]GGATCACCTGAGGTC | 50807 |
| rs542317877 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114796 | TTTTTTTTTAAGATA[C/T]AGGGTCTTGCTCTGT | 50807 |
| rs542338733 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340592 | TTTGAATTTAAAAAT[A/G]TTCATTCCACATCTC | 50807 |
| rs542353205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122814 | AGCTGACCAGGTGGC[A/G]CTGATGCTGCTTCCC | 50807 |
| rs542354283 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130412433 | CTTGGGCCATGTGAC[A/G]TGCCTGTTCCCCCTT | 50807 |
| rs542355774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423869 | AAAGTAATTGTGCAG[A/G]AAGTACTTTAAAGGT | 50807 |
| rs542357223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307805 | CACAAAGGAGTAACC[A/G]GTGATGGCGGAGCTT | 50807 |
| rs542358249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348017 | CATCCATAAAAAGAG[A/G]AGTTGGACTAGATGG | 50807 |
| rs542363504 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130205485 | GACAAGGTATACCTG[A/T]ATTGACAAACAGAAA | 50807 |
| rs542366527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431481 | GTGCTATTGGTACCA[C/T]TCACATCCTTGCTGA | 50807 |
| rs542368727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130089635 | ATGTCAGCAGGAGGC[A/G]GGGAAGGGATAAAAC | 50807 |
| rs542386689 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130144014 | GGAAAGAGGTAAAAA[C/T]AAAATGACAAAGCTC | 50807 |
| rs542388745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333404 | GTCAGGAGTTCGGGA[C/G]CAGCCTGACCAACAT | 50807 |
| rs542388926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219607 | ATCTTTACTACATGC[A/G]AGTGCTAGAAGACTT | 50807 |
| rs542395169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341250 | TCTCAAAAATGGATG[C/T]ATGGCTCAAGTGTTA | 50807 |
| rs542417787 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130385583 | CTCAGTTACCAGGTG[A/G]GTAGGAATCTCAACT | 50807 |
| rs542419000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299948 | CTGGAAAACCACTAA[C/G]GGATGGAGGGACTGT | 50807 |
| rs542436571 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130129271 | TCCTTATAGCAGTGT[C/G]AGAACGGGCTAATAG | 50807 |
| rs542446706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238260 | AGGACCACAATGCTC[A/G]GTCGCTTTCTGGTCA | 50807 |
| rs542447841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130148419 | GGTACTGAAAATTCA[A/G]AGATGAGTAAGATGC | 50807 |
| rs542452290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130212822 | GAAAGGAACCTGCAG[C/T]GTAGCAAACCGTAGA | 50807 |
| rs542453445 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130360068 | ACAGCACCTCATTAA[-/CT]CTCAAATATTTACTA | 50807 |
| rs542459658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384288 | AGAGACCTGCTAGAA[A/G]GGGTTATTACACCTT | 50807 |
| rs542470260 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130439335 | TAGACTTCTGACCTC[C/T]AGAACTGTAAGATAG | 50807 |
| rs542477060 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431989 | GGGGAAGGGGAGGAA[A/C]GAAGGAGAGGGAGGA | 50807 |
| rs542481762 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130122733 | ACTACATTAGAGATA[C/T]TGGAGAATCACAGAC | 50807 |
| rs542484747 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130332222 | TGCATCTTTCTGGTG[C/T]TTTTCAATGAAGATG | 50807 |
| rs542513596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247356 | AGGTTTCTATTACCT[A/G]TGTTTGACAGATAAG | 50807 |
| rs542540650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117325 | GCAGAGAGGCTGAAG[C/T]GCTTGCTTTCAAGAT | 50807 |
| rs542540672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141490 | GTTCCATTTTTGTAC[A/G]CCCTGCTGTATTTTC | 50807 |
| rs542548171 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246651 | TGTGAGTCAATTAAA[C/T]GTCTTTTCTTTATAA | 50807 |
| rs542567077 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130250462 | ATGCTAAGCTTACTA[C/T]AGTTGCTTCATGTTC | 50807 |
| rs542568721 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335323 | TCCTCACTGTCATTC[A/T]ATAAGGTCACTTTAT | 50807 |
| rs542569122 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130360842 | ACATGGTCTTTTGAA[C/G]TATGAGCTACCCAGG | 50807 |
| rs542570860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102805 | ATCATCTTGCTTCAG[C/T]CTTCTACATAGTTAG | 50807 |
| rs542574955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130057789 | TAATAGTGTGTGACA[C/T]AGAAAAGACACCAAA | 50807 |
| rs542577642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130290760 | ATGACAAATCCTTAA[C/T]AGGATAATGATGATA | 50807 |
| rs542586213 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130236445 | GGCACACCTTCCAAC[A/C]AAAGAAAAGATGATA | 50807 |
| rs542597952 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130222014 | GACAACCATACCAAC[C/T]ATCCATCCTTGGCCA | 50807 |
| rs542598056 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130194171 | CTAGTCAATGAAAAG[G/T]CTACAGGAAAAATAA | 50807 |
| rs542610255 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130242991 | CTGATGATCATCAAA[C/T]TTGGGTTTTTACATC | 50807 |
| rs542610624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068650 | CAGACACACAGGAGG[A/C]TATTCCTGCGGTAAC | 50807 |
| rs542616675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130298225 | AAGCATGAGAAACCT[A/G]TAATGGTGTCCATAT | 50807 |
| rs542619749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130306046 | AACTAGGATTCTGGG[A/G]TCATAAAGTCCTCAG | 50807 |
| rs542620106 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332030 | CTTACACAGAGAAGA[G/T]AAGTTATCACTATGG | 50807 |
| rs542624616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393632 | ATGGTGGCACACACC[G/T]GTAATCCCAGCTGCT | 50807 |
| rs542629009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130161268 | ACACCTGAAATGTGA[C/T]AGTGTCGAGGTAAGC | 50807 |
| rs542633804 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130438496 | ACAACTGTAGGGATG[A/C]GTGCTGTGCTAGGAA | 50807 |
| rs542637617 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130324089 | ACTAACCCAAACCCT[C/T]TGAGTCAATCATCAA | 50807 |
| rs542639310 | snp | C/G | | | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295026 | CCCAGTGCTTTGGGA[C/G]GCTGAGGTGGGAGGA | 50807 |
| rs542647714 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254138 | AGGTGGAGTAAAATG[A/T]GACAAAAATGCAGCG | 50807 |
| rs542649262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074713 | GTAGGGGTGGACTCC[C/T]GTGCTGACTCAATGA | 50807 |
| rs542651589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130068049 | ATTCCTATGTGGCCA[C/T]GTGGTCACCCAGGGT | 50807 |
| rs542654158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258466 | TTAAGTCCCACGGAT[A/G]TTTTAAAACACTGAG | 50807 |
| rs542654851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380831 | TCAAGTGATCTTTCG[C/T]CTCAGATTCCTGAGT | 50807 |
| rs542658587 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130354190 | CCACCGCGCCCAGCC[A/G]GGAGGGAGATTTTTA | 50807 |
| rs542659612 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130196621 | CACAAGACTGTATTA[A/G]TTAATGAGGACATAA | 50807 |
| rs542661347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393996 | AATCTCTTAATCTCA[C/T]CATTTTCATAAGCTG | 50807 |
| rs542686797 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130383763 | CCAGTGGCATCCCTG[A/G]ATCCAGGAGAGCCCT | 50807 |
| rs542694192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167756 | TCCTTTATACTGTCT[A/C]ATTTTTGATATGATA | 50807 |
| rs542696371 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130326858 | ATATATTCAGAGACA[A/G]TCAGTGGCCTATTTC | 50807 |
| rs542698156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389054 | GAATGAGTTAATAAA[C/T]AGCAAGTGCTTAGAA | 50807 |
| rs542700914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297463 | AGTATGACTGCTCCT[A/G]TTTCACTGATGAGAA | 50807 |
| rs542705690 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430694 | CCAGAACACTGACCC[C/G]AGGCAGGAACTGTGG | 50807 |
| rs542709094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188920 | CTTCAACTGCTTCTG[C/T]CAGAGTAAGGAGGGC | 50807 |
| rs542712070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229824 | GGTGGGTGGATGGCT[C/T]GGGCCCAGGAGTTCA | 50807 |
| rs542714144 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086436 | ATAAAATATTACGTA[A/C/T]GTAGTTTTTTATCCG | 50807 |
| rs542717664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424327 | CCCACCCCCAGCCTA[C/T]TGGTCTGACGGCCTA | 50807 |
| rs542719320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195994 | TTGCTTCTTAAGGGG[A/G]GGCCCTGTATCTATT | 50807 |
| rs542724997 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197045 | ACTCATCACTCCCGG[C/T]CTGCGTGAACTGGGA | 50807 |
| rs542736121 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130171125 | ACCCTTGAATACTTC[C/T]GTTTTATCTCTTACC | 50807 |
| rs542745161 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410401 | CCCCCAAGAAGAGAA[A/C]AACGAAATAAACTTG | 50807 |
| rs542750169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100519 | TTTTTAGTAGAGATG[A/G]GGTTTCACCATGTTG | 50807 |
| rs542751013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180424 | AACATGCTCTAAACA[C/T]ACACCAATAAAACTT | 50807 |
| rs542753240 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130101007 | TCTTGAGTTGAGAGA[G/T]ACCCAGCTTTCTCAG | 50807 |
| rs542753749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417128 | AGTGAAACCCATGTA[C/T]AACTGCACACAGAAA | 50807 |
| rs542775140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333856 | ACCATGCCTATCCCC[C/T]AGAAGCTGAGATTAC | 50807 |
| rs542779965 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130298909 | CCGACCAGATTACAG[G/T]TATTAGGGCGGCAGA | 50807 |
| rs542780046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130291934 | AAAAACTGCAGCTGC[A/G]CCTGATGCTTGTCTA | 50807 |
| rs542783739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277384 | TATCCAGTGAATTTA[A/G]GACAACAAAAGATGA | 50807 |
| rs542790568 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318672 | GAAGTGGTATTATCA[A/C]CTCCTTTTACAGTTA | 50807 |
| rs542794754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224333 | ATTCTTTTTATATTA[C/T]CCTATGCATACTTTG | 50807 |
| rs542798600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063656 | GATGTGGATATCACC[A/G]TCATCCCCATCTTCC | 50807 |
| rs542799383 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130145621 | GGGCAGTCTTTAAAG[C/T]GAGGGCATCATTATG | 50807 |
| rs542801148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410009 | GTGATATCATCTGGG[C/T]GTGAACACAATGTCA | 50807 |
| rs542809596 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130147946 | TAATAATCGTTGTAA[G/T]TGTTAATCATAAGGG | 50807 |
| rs542812548 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197511 | TCCAGGCCACAGAGG[C/T]GGCTCGTTTTACACA | 50807 |
| rs542816619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130417587 | AGACATGCTTCATGA[A/G]ACAGAAAACCCCACA | 50807 |
| rs542832626 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130095687 | GCAGTGGTGTAATCT[C/T]GGCTCACTGCAACTT | 50807 |
| rs542834007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130102270 | TTTTGAGATATGTTC[C/T]TTCTATACCTAATTT | 50807 |
| rs542838801 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130312483 | AGGAATTCTGGTTTT[A/T]AAAAAAATACTGCAA | 50807 |
| rs542858395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130442192 | CTAAAGTGGTGAAGG[C/T]TGTGACGCAAAGAAG | 50807 |
| rs542867348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087168 | AGCTGAATGTCAGAG[C/G]TGCCCCTGAGACCAG | 50807 |
| rs542869216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130232429 | TTCACAGATTAATAA[C/T]GTTAAAACTTCAAAA | 50807 |
| rs542870039 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130304068 | AAATGAGACGGTACA[G/T]AAGAACTCTGGACTT | 50807 |
| rs542870558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130443034 | GGGCCGGGGGCCGCG[A/G]GGAACTTTCCTCGGC | 50807 |
| rs542886055 | in-del | -/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130069032 | GAGAACAGGGAAAGG[-/C]AAAAGTGAGAGCCAA | 50807 |
| rs542889053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121319 | CTGACATTTGGGGCT[A/G]GGTACATTCTTTTCT | 50807 |
| rs542890039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359415 | ATTTCTCACCATTCG[C/T]TGAGTATGAATTTGG | 50807 |
| rs542914298 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175496 | CTCCTAAAGTGCTAG[C/G]ATTATAGGTGTGAGC | 50807 |
| rs542927385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418059 | AGGGGAGGAGAACTT[C/G]CCCCAAGGCCACAAG | 50807 |
| rs542928409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130279113 | GGCAGGTAAAAGCAA[A/G]ATCTCCAAAATCAAG | 50807 |
| rs542930563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352458 | ACCTAACAGTATTTA[C/T]CAAAGACTGATGAGC | 50807 |
| rs542930926 | snp | A/G | 6.60873e-05 | 0.00574798 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130127937 | AAAACCTGATGAGCC[A/G]CAATCGCAGCAAATG | 50807 |
| rs542934263 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130442120 | TCTCAAAATATGCAG[C/T]TTGAAATAAGTGCAT | 50807 |
| rs542939857 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087563 | AAACCTCCACCTGGC[C/T]GAGGAAAGAGGCTAA | 50807 |
| rs542947678 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130190469 | TTGACTGTGAGCATG[G/T]GAATTTATCTCTGGG | 50807 |
| rs542960438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217379 | AAAGTCTTCCTTTAG[C/T]TGGAAACAATCCTTC | 50807 |
| rs542966790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130269755 | AGGCCTCTGGATTCA[C/T]GCAAGGGTAGAATTA | 50807 |
| rs542980255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095556 | TTCACCTGCTTCAGT[A/C]TTTCAAAGTGCTTGG | 50807 |
| rs542983232 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107476 | AGGTGTGAGCCACCA[C/T]GCCCGGCCCATAGTC | 50807 |
| rs542984659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319971 | TCACTATTACTATAT[A/G]ATGCATAGAAAAGTA | 50807 |
| rs542988925 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130127341 | TCTGCCTTATCCTCC[A/C]AAGTAGCTGGGATTA | 50807 |
| rs542991190 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130111402 | AAAATGTTCCTTATT[A/G]GAGAGTACAAGAGAA | 50807 |
| rs542998304 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130305387 | ACTCTTGCTCTGTTG[A/C]CCAGGCTGGAGTCCA | 50807 |
| rs543006205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131558 | GGCTTGAGCTCAGGA[C/G]TTTGAGGCCAGCCTG | 50807 |
| rs543008063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130332586 | ATGCTTTTGGAAATA[C/T]TCCAGAATGCAAAAC | 50807 |
| rs543044864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381460 | TATATTTTAGACTTA[C/T]AGGACATCTCCATTC | 50807 |
| rs543050621 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146605 | GAAACAAGGTTACTG[A/G]ATACATTAATAGCAA | 50807 |
| rs543054716 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130363823 | TATTTTTCCCAGCCC[A/G]GGCAACCAAAGGAAG | 50807 |
| rs543055422 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402288 | TCCTAAACATAAAAT[A/T]AAAGTGTGCTGATGG | 50807 |
| rs543060340 | in-del | -/TTTC | 0.123883 | 0.215858 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100318 | ATATGTCGTGTTTTC[-/TTTC]TTTCTTTCTTTCTTT | 50807 |
| rs543071772 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228813 | AGACCAGTGGCTATT[A/T]TTTTTTTTTCTTTTA | 50807 |
| rs543076752 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130172888 | TTCTGCTTCAATTAT[A/T]CAGACTGTTACATAC | 50807 |
| rs543086410 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179004 | GAGCTCCACAGGCGA[C/T]CAAATTTAGGAAGAA | 50807 |
| rs543098165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130277999 | AAATCCAAAGTAGTA[C/T]GGTTCTCAGCGAGGC | 50807 |
| rs543107202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130366667 | ATCTCAGTGCTGCCA[C/T]TTAACAGGATTTGTT | 50807 |
| rs543109396 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130116100 | ATTTTCTCATTCATA[A/T]AATGGGAGCAGGGAT | 50807 |
| rs543122525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055649 | CAATTTTATTGTCTG[C/T]TGCATTGGCCTGTAA | 50807 |
| rs543129654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262855 | ATTTCCTTGAATGAC[A/G]CGCTAATGAAAAATG | 50807 |
| rs543145347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130367757 | CGCTAAGAACTGTCT[A/G]GAGGTCTTCCGTCTG | 50807 |
| rs543173466 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146647 | ATCCATTTTGCAGGT[C/G]TCTTCCTGTTTCCTG | 50807 |
| rs543178339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085962 | GTGGTTCTGGCAGGG[A/G]AAAAGCCTGGGGTGG | 50807 |
| rs543185485 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296310 | GGGTGCTTCTCTGTA[C/T]GAAGGACAGGTATTC | 50807 |
| rs543191301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392244 | AGGGACTCTCATACA[C/G]ACTCCTAAAGGGAGA | 50807 |
| rs543196818 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130436734 | TTGAGCCCTGGATTA[A/G]AGGCTGCAGTGTGCT | 50807 |
| rs543197488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397050 | CTTGTTCTTTATTCC[C/G]TTGGACTTGAGTTTT | 50807 |
| rs543237576 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159081 | TGTGTGAAGGTGAAC[A/T]GCAGAAAAAGAAGAA | 50807 |
| rs543259484 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130140370 | TCTTTCTTTTTTTTT[A/T]AAAAAAAAACTTTTA | 50807 |
| rs543262752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165972 | TTTAAAAACTGACTA[C/T]AAAAATGCTGTATTT | 50807 |
| rs543277310 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130072023 | CTCTTGCCCTCTTAT[G/T]ACCTATCCCAAGGCA | 50807 |
| rs543283301 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359875 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 50807 |
| rs543288846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074052 | CCTAAGACACTTAGA[A/G]ACAAATCAATCAACT | 50807 |
| rs543290642 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130371629 | TCCTGTTATCCTTCC[C/T]TTCTTATTGCATCTT | 50807 |
| rs543291813 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130246269 | TATCATATCAACAAC[C/G]TTTTCATTAAACCAC | 50807 |
| rs543302768 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130346436 | TTTTTCATTAGCATT[A/G]CATGCATATCTGCAT | 50807 |
| rs543318408 | in-del | -/A | 0.0573587 | 0.15934 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237500 | ATTTCTTTTAGTGTT[-/A]AAAAAAAAAAATTAG | 50807 |
| rs543321509 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422496 | CTTACACAGTGTACT[C/T]TCCCGCCTTCTCCCT | 50807 |
| rs543323496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151943 | GCTTCAGTTTCTTCA[C/T]CTGTAAAATGAAGGT | 50807 |
| rs543328971 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216972 | CTGTTATACTGTGCA[A/T]CAGATCTTGTGACTC | 50807 |
| rs543353796 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382217 | TGTGAACCCAGGAGG[C/G]GGAGCTTGCAGTGAG | 50807 |
| rs543353824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112532 | TCACCACTATGAATA[A/T]TCACACTAGTGAAAC | 50807 |
| rs543366554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281804 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 50807 |
| rs543368682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130349507 | ACTCACTGAGAGGTA[A/G]GTACTTATCCCCATG | 50807 |
| rs543369612 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397314 | CCTGGCTAATTTTTG[C/T]ATTTTTAGTAGAGAC | 50807 |
| rs543378273 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130338459 | GAAGATACGTGTCAG[C/G/T]TAAATAAAGACAGGA | 50807 |
| rs543380714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130163341 | ATCATTAAGACGTTC[C/T]TTATATATTTATTAC | 50807 |
| rs543383542 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130398287 | GTCGCTATCCCCTAC[C/T]CACCCAAGGGTAGAC | 50807 |
| rs543385443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393066 | TGTTCTCATAACTTA[C/T]CTTCTTTTTAATGGC | 50807 |
| rs543391487 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130219520 | GTTTCTGAAGGAGAC[A/G]GACTGATAAGGCAGA | 50807 |
| rs543417774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130221146 | GGCTGAGGCAGGAGG[C/T]TTGCTGGAGCCTGGG | 50807 |
| rs543418354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316842 | GGGATTTTCCCCCTG[G/T]AATATGCAGCTCAAT | 50807 |
| rs543426449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222294 | AAACTGGGCAATATT[C/G]ACAAAACCTCTGGAC | 50807 |
| rs543428800 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130235769 | AAACAAGAGAATATT[A/C]GGTTTCCAGTTTCAT | 50807 |
| rs543434229 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123863 | TTGATCTCCTGACCT[C/T]GTGATCCGTTTGCCT | 50807 |
| rs543435847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130164257 | TAATTTTTGGAATAA[C/T]TCTGTATATCCTAAA | 50807 |
| rs543437501 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325913 | TATGCCAGAAACGGT[-/G]GTAAGTTATGCACCT | 50807 |
| rs543447000 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130405782 | TCCGTACCTCACCCA[C/T]GGCACTTGGAGACCC | 50807 |
| rs543454994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317371 | GTAGGGGAAAAGAAA[C/G]CTCTACGATAAACTG | 50807 |
| rs543466644 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117405 | TCTCTGGAGCCAATG[-/T]TTTGAGCCACTATGC | 50807 |
| rs543483715 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130329014 | CTAATGGTCAGAATA[C/T]GATATCTGCTGGAAT | 50807 |
| rs543503479 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130284413 | ATGAACCCCCATAAA[A/G]GCAAAAACGGGAGTC | 50807 |
| rs543514541 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130065901 | TAAACTTGTGCAGAG[C/G]TGTTTCGCACAGAGA | 50807 |
| rs543523023 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157243 | CCAGTTTAAATCTGT[G/T]AATTGTTAGTTGGGA | 50807 |
| rs543528566 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130434175 | ACAAAAATTAACTGT[A/G]CCTGGTGGCGCACAC | 50807 |
| rs543540219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343280 | CTACTAAGGCGGATA[C/T]GGGCTGATAAGGCAG | 50807 |
| rs543544977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132171 | TACCATGGGCACATT[A/G]TGCCTCTGTTTCCTC | 50807 |
| rs543549406 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130433381 | TCACTTAGGGAAATC[C/G]TGCCTATCTTGGAAG | 50807 |
| rs543563785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130254679 | CCTTATGTAAACAGT[A/G]CTAAATCAAGGACTT | 50807 |
| rs543579604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130303943 | ACCCTTGTCATGGTT[A/G]ATGAATCAGTATCAA | 50807 |
| rs543588861 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222937 | TAGCCAGATGCCAAG[G/T]GATTGAGAAACCTGA | 50807 |
| rs543593131 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130344410 | CCTTATCTTTTAGAA[G/T]TACATACTGAAGTAT | 50807 |
| rs543604203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079683 | GAACTGGGTAGACAG[A/C]GTTGCTGCTCAGAGA | 50807 |
| rs543607267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119790 | AAACTGCTTAATCGT[C/T]ATGAGCTTCAGTTTT | 50807 |
| rs543607673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241819 | ATGCTAACTGAGCAA[C/T]GGCAATACTGTTGCC | 50807 |
| rs543611210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130216317 | ATGAATTAGGTGCAC[A/G]TGAGAAACATTAATT | 50807 |
| rs543614100 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130131423 | TGTGGACTGCCATTA[C/T]CTCCTACAGCACTCA | 50807 |
| rs543617875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288555 | GAAGTCTGGACTGCA[C/T]ATCCATTAAACAAAT | 50807 |
| rs543618522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130386384 | CCACGGAGGTAACAC[C/G]TTCCATTGCCGAGTC | 50807 |
| rs543628772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321918 | GTGTGCAAGTGTCCA[A/G]CATTATACCTGGCAT | 50807 |
| rs543646244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248488 | GAAGAGATACACTGG[G/T]ACCCATCACACAGGG | 50807 |
| rs543649753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215631 | TGCCTGTAATCCCAG[C/G]TACTCGGGAGGCGGA | 50807 |
| rs543674861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109050 | AAAGTGTTGGGATTA[C/T]AGGCGTAAGCCACCG | 50807 |
| rs543683506 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203093 | TGAATTTGAATTAAA[A/T]AAAAAACACACACAA | 50807 |
| rs543695649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337697 | AAGACCTTCTGTAAT[A/G]CATCTGTTTTCATGC | 50807 |
| rs543700306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275780 | CAAATAAGGAGGCCA[C/T]ATCAGAGAAAAGATA | 50807 |
| rs543711498 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257405 | TATTTACATAGTTTG[C/G]CTAATGTTTCACAAA | 50807 |
| rs543714034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130250066 | CATGGAAATATATTT[A/G]GGAAAGTATCTGATA | 50807 |
| rs543715801 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130349158 | ATTATACAGTTACAC[C/T]GAGTTGACAGTCTGC | 50807 |
| rs543753531 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130186987 | GCAGCCATAAATGCG[A/T]GAACAACTGATAGTA | 50807 |
| rs543768888 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130259336 | TATTTTAGCTAATAA[C/T]AAGTTATTTCTCACG | 50807 |
| rs543773331 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425328 | CAGAGTGAGACTCCA[A/T]CTCAAAATATATATA | 50807 |
| rs543775672 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130198649 | ACCTCTGTAAGATGG[G/T]TCTTAGTCTCACTAG | 50807 |
| rs543791290 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130206685 | GCTGACCTAGAATAC[C/T]TCCGGGTGACTCCCA | 50807 |
| rs543806445 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213801 | AAAATCCAAATGATC[C/T]GTCCAGGTGGTGTTA | 50807 |
| rs543807003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078334 | CAGGGTCTTGCTGTC[A/G]CCCCGGATGGAGTGC | 50807 |
| rs543810066 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130177021 | ATGCTCCATGGTACC[C/T]GTCACTGTCCAGCCC | 50807 |
| rs543811666 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130229372 | ACAGTTTAAGTGCAA[C/T]AGCTTTATACAGGAA | 50807 |
| rs543815212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301644 | TTGTCCTTAAACTCT[A/G]GCAACCAGAAATAAC | 50807 |
| rs543820796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130814 | CTGGGGAGGCTGAAG[C/T]GGGAAGATCGCTCTA | 50807 |
| rs543830758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432744 | TTTTTCTTCCTACAT[G/T]TCTCTTTTTAAGATG | 50807 |
| rs543835777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130109996 | AAAGTACTGTATCCT[C/T]AGATGACCACGGTTG | 50807 |
| rs543843554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077661 | AGCGATTCTTGTGCC[C/T]CAGCTAACTGCATTT | 50807 |
| rs543856376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130097005 | GTGGCATGCACCTGT[A/G]ATCCCAGCTACTTGG | 50807 |
| rs543870688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130155546 | TAATTTTTGTAGAGA[C/T]AGGGTTTTGCCATGT | 50807 |
| rs543873022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130255390 | TCTCTATGTACCTAA[A/T]AAATGTTTTATGTGC | 50807 |
| rs543889991 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130339478 | AATAGCAAGTAGAGT[C/T]GGAAGTCAGCAAAAA | 50807 |
| rs543894614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130425994 | TAAGCATTTGCAGAC[A/G]GCAAATACTGCTTGA | 50807 |
| rs543899179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130384230 | CAGGGAAGGGCCTCG[C/T]TGATTAAAATAAAGC | 50807 |
| rs543900249 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104555 | CAATAGGATGGACAC[A/G]TCAGGTTATAAATGA | 50807 |
| rs543901867 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311552 | GGATCACCTGAGGTT[C/G]GAAGTTCGAGACAAG | 50807 |
| rs543912879 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130103693 | TTTTTAGTAGAGATG[A/G]GGTTTCACCATGTTG | 50807 |
| rs543922463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336146 | CCTGTGAAAACAATC[A/C]TATCACCCAAGATAA | 50807 |
| rs543925172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240396 | TAGAGAGACAGGGGA[C/T]ACTGTCCTTCAATCA | 50807 |
| rs543926835 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130155633 | ATTACAGGCATGAGC[C/T]ACTGCGCCCAGCCAG | 50807 |
| rs543938095 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130327852 | ATAGTTAAAAAACAC[G/T]GCATTGTATACTTCA | 50807 |
| rs543941322 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130252800 | AGGTATTTAAAGACC[-/A]AAAAAATACTCATGA | 50807 |
| rs543943771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370164 | AAAATTACCCAAGCA[C/T]GGTGGCGCACACATA | 50807 |
| rs543949039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130066457 | CTCAAGTGATCCTCC[C/T]GCTTCAGCCTCCCAA | 50807 |
| rs543959244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130329070 | AGAGGCACTTCATTT[C/T]ACTCCTGACCAGATG | 50807 |
| rs543965933 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130411716 | AATGAACAACTGCCA[C/G]TATTATGACAGCCCA | 50807 |
| rs543967749 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111961 | CTATTTCAAGCTGCT[A/C]CTGACAACACGATCC | 50807 |
| rs543968964 | snp | A/C | | | missense | ASAP1 | GRCh38.p7 | 8:130112142 | CCTCCGTGGTTGGTG[A/C]TGTGGGCGAGTCTGT | 50807 |
| rs543970379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130191899 | TAACTTCTTCCTAAC[C/G]CTTTCCTGTTGTTTT | 50807 |
| rs543973502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130302108 | CAGCTATAGTCTAAC[A/T]TTAGGTATAATATCT | 50807 |
| rs543976906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130321192 | AAAAAACATGGATTA[C/T]AGTGAATAAGCCCCA | 50807 |
| rs543982851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130227293 | GATCTCACTCTGTTG[C/T]GCAGGTTGGAGCACA | 50807 |
| rs543984991 | in-del | -/CTT | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130175789 | CTTTCTGAGCTACAA[-/CTT]CTTGAGTGTTGGGAA | 50807 |
| rs543994257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234624 | CCTTTGTATGAGCTG[C/T]TGAGTGATGTGGTCA | 50807 |
| rs543997633 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287839 | TATACCCCTAGCCCT[A/T]CCCACTCAGTCTAGC | 50807 |
| rs544001573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158036 | CAGGACTCAAAATAT[A/C]TTTGTTGAATGCATG | 50807 |
| rs544003360 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130174036 | GAGGGTGCAGTGAGC[A/T]GAAATCACGCCACTG | 50807 |
| rs544004690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130193032 | TAAATATTTATGTGA[C/T]AAAAGCAAGGTATAA | 50807 |
| rs544007789 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130400135 | GAAAGCCGGTGTCTT[A/G]TGTGAGATCACACAG | 50807 |
| rs544013411 | in-del | -/AA | 0.386884 | 0.209196 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121784 | GTGAAATTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 50807 |
| rs544029697 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347387 | AGGGCAGAGAAACTA[A/C]CATCTTCCAAGCGTC | 50807 |
| rs544031448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130241236 | TTTCCCCACAAAAGC[C/G]TTCTAAGGATACCCT | 50807 |
| rs544031811 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295369 | TCAAAGACTATCACA[G/T]TGATTAGCCAGGAGC | 50807 |
| rs544054689 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074657 | GTGGGAGGGTACAAG[A/G]TCTACCTTAGGACCA | 50807 |
| rs544059417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438247 | ACCCCTCGCAGCAAC[A/G]TGGCTACACAGCACA | 50807 |
| rs544073989 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130056464 | TTAGTGGCATCCCTG[C/G]CCACTAAACTTCCAT | 50807 |
| rs544079756 | in-del | -/AT | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130218850 | GTAGTCTCTTTCCAT[-/AT]ATATATATATATATG | 50807 |
| rs544081190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099162 | GGGACTATACGTGTA[C/T]GCCACCAGGCCTAGC | 50807 |
| rs544082425 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130287997 | GCACAGTCAACCAAG[A/C]ACCCATGCAGGGTGA | 50807 |
| rs544083519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130406971 | CTCCAATTTTCCCAG[C/T]GCAACAATCTGTCCA | 50807 |
| rs544098353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364861 | CTTGGGCTCAGGAGT[C/T]TGAGGCTGCCGTGAG | 50807 |
| rs544108120 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060484 | CAGGTGAGCAAGCTC[G/T]CACTTTTTCTTGTGT | 50807 |
| rs544111466 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130058447 | ACAGCAGAGTCTAAA[A/C]ATGTTTTTAGGAAAC | 50807 |
| rs544115677 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130184868 | CCTCACAAAAACCCT[A/G]AGAAGTAGGTAATTT | 50807 |
| rs544116918 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091468 | GGCCAGCCCTGAAGA[C/T]AGAGTGGCAGGAGAG | 50807 |
| rs544117306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348925 | AGCTCATTACCCCAA[A/G]GCCCCAGCAAGAATC | 50807 |
| rs544120918 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413988 | TCCTCTGCTGTAAGG[C/T]AGACAGGTGAATCGA | 50807 |
| rs544126457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407720 | CAGTCAGGACAGGAA[C/T]TCCTGATGCCATGCA | 50807 |
| rs544137259 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130193865 | GTAAATCCTTTTTTT[A/T]AAAAAGCAGATATGG | 50807 |
| rs544141986 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228183 | AGAAATACTCAGTTA[C/T]TTCCTGTCAGAGTAG | 50807 |
| rs544143682 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220420 | ATTACCATCCTCACT[A/G]TGTAGATATAAACAC | 50807 |
| rs544152270 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278921 | CATGTTTACAAAGCC[C/T]TTCCTCATCCATTAG | 50807 |
| rs544152311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272779 | CTTATGTTCTCACTC[A/G]TATGTGGGAGCTAAA | 50807 |
| rs544153011 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084084 | AGGCGTGAGCCACTG[C/T]GCCAGGCCGATAACA | 50807 |
| rs544157911 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414708 | TCTTTTTTCTTGATA[A/C/T]ACGTGTCTTATTTAT | 50807 |
| rs544158548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130286326 | CAATTAACTAAAAAC[A/G]AAGCTAGCATTTATT | 50807 |
| rs544160693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130334585 | GATAGCTTAAAGCTT[A/G]CTTCTAGCTGTAGCA | 50807 |
| rs544165767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322640 | GTTCAATATAATGCT[A/G]TCTGGATTCAGTTCG | 50807 |
| rs544195911 | snp | A/C | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130355878 | AATGTTTTCCTGGCC[A/C]ATACCTTCCTCAAGT | 50807 |
| rs544220442 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149346 | CATTACTTTGAATAG[C/T]TGGTAAAAGAATTTT | 50807 |
| rs544258224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176221 | AATACCAGCTGACTT[C/T]GTACTGAAAATCACT | 50807 |
| rs544260041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130377565 | GGCCCCAGCTCTCAA[A/G]GAGCCTATGGTCAAT | 50807 |
| rs544269152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313380 | TCTCAATGAGATCAC[A/G]TATAAATTGAGTCCT | 50807 |
| rs544276875 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130250271 | ATGCCTTTTTGGAGA[C/T]GAAGAAATTAAGTCA | 50807 |
| rs544277227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141446 | CTCCTCAGAGGAGGC[A/G]GTACCTGGCCTGACC | 50807 |
| rs544289459 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130183513 | GCCCAGCTAATTTTT[C/G]TATTTTTTAGTAGAG | 50807 |
| rs544292870 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130149964 | CCAGGCTGCTCTGGG[G/T]GCAGGAGAGTGCTGA | 50807 |
| rs544300482 | in-del | -/ATGA | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130235368 | TAAGTTCAGCATCTG[-/ATGA]ATTATCAAAAAGTGA | 50807 |
| rs544318902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130440256 | GTCAAAGCAATCTCA[A/G]AAATGTCCATCAGGC | 50807 |
| rs544326955 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130424246 | TCTGGTCTATACAGG[A/C]AAACTCAGTCAACCA | 50807 |
| rs544333561 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130370754 | GGCACATGCTACAAC[A/T]TGGATGAAACTTGGA | 50807 |
| rs544358117 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130254379 | GGAAACTCAAATGGT[A/G]AGAAGTAATCATACA | 50807 |
| rs544359896 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208753 | AAGGCTGATCTGCCA[A/G]TGATGAGGAATTCAT | 50807 |
| rs544373867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088800 | CATTTATTGGGTGCT[A/G]CCTATGGTTTTGGTT | 50807 |
| rs544374991 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299134 | GATGCCCGTGTGTCC[A/G]TGCCTCTGCAGGTCT | 50807 |
| rs544383380 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130399823 | CAGTGTCTTTTTTTT[A/T]TTTTTTTTTTGAGAC | 50807 |
| rs544393905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130265060 | GAATATTGTGAACTG[A/G]GCCAAGGATGTGGCC | 50807 |
| rs544400072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130436901 | TACCTAAGGTCAGGA[A/G]TTCAAGACTAGCCTG | 50807 |
| rs544407622 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130315189 | CAAGGAAAATAGTAG[A/G]CAGTCCCAAATCATG | 50807 |
| rs544409701 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130089846 | AAATTTAAAAAAAAA[A/T]TTAAATTGTTTTTTA | 50807 |
| rs544413510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130135275 | GTAGGAGGACTGCTT[A/C]AGCCTAGGAGTTCGA | 50807 |
| rs544420709 | snp | G/T | 0.000798403 | 0.0199641 | downstream-variant-500B | ASAP1 | GRCh38.p7 | 8:130051902 | GGTGGAATGCGGAAG[G/T]TGGAGGACAGAAAGG | 50807 |
| rs544421433 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394439 | TTTGGTCAGACCGGT[A/T]GCTCTCAAACATGTT | 50807 |
| rs544426109 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130143131 | TGTTCCTGAAGGCTG[C/T]CTTGAGCAGCATCTC | 50807 |
| rs544427973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130400515 | AAAGGCCAGGTGGGC[A/G]CGGTGGCTCACGCCT | 50807 |
| rs544429313 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130197832 | CCATACAGAAGATTG[A/T]GGCCCTGAGTTTTGG | 50807 |
| rs544431606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059211 | ACTCTGTTGCCCAGG[C/G]TAGAGTGCAGTGGCA | 50807 |
| rs544435887 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130362496 | ATGAGAAAATATGGA[A/T]AAGTAGGCTGATGCA | 50807 |
| rs544445790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130308789 | GCTTACACCTGTAAT[C/T]CCACCACTTTGGGAG | 50807 |
| rs544456573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130177087 | TACCTGGACAATTAA[C/T]TCCTGAGCGGAAAAG | 50807 |
| rs544465314 | snp | C/T | | | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082615 | CTCAAATGATCCTCC[C/T]GCCTCAGCCTCCCAA | 50807 |
| rs544472651 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130260432 | TTACTGACTAACAGA[C/G]CTGGTAAGACCTTAG | 50807 |
| rs544479858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070059 | TTTTTGTTTTTGAGA[C/T]GGAGTCTCACTCTGT | 50807 |
| rs544487824 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197794 | AAACGTCCAAGTCCC[C/T]GGCCCGAACTGTGGA | 50807 |
| rs544495664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130268614 | CATGTATTTGAAGAT[A/G]GTAACGGTTAAAACA | 50807 |
| rs544509344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130267771 | TTAGTTGTGACTGAT[A/G]TATTTTCTCCTTGAG | 50807 |
| rs544543248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130299895 | ATAGTATAAATAGAT[A/G]AGGTGGCTATTTTCT | 50807 |
| rs544547866 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162766 | GGGCTTGCAGTGAAC[A/C]GAGATTGCGCCACTG | 50807 |
| rs544564723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410672 | GAATTCACTCTCAGC[A/G]AGTATGCTGAGCGCA | 50807 |
| rs544564897 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130119246 | GGCCTGTACCCGGCC[A/G]TAACTCTCTATTTTA | 50807 |
| rs544565814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130116582 | AGTGTTAAAAAAAAA[C/T]GAATCTGCATTTTTA | 50807 |
| rs544567475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130127374 | GGTGCCCGCCACCTC[A/G]CCCAGCTAGTTTTTG | 50807 |
| rs544568707 | snp | A/G | | | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130236980 | CTGAAGGGCTGTTCT[A/G]TCTTGGTCTAGAGCC | 50807 |
| rs544570141 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130340863 | ACTCTTATGATGGCT[C/G]CTGCATGCTTCTTGA | 50807 |
| rs544587574 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130224570 | ACAGACACACAAATA[C/T]AGGTGTTTTCACCCC | 50807 |
| rs544591016 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133912 | GAGCAAAGGCCCCTC[A/C]TGAGGGCAAGGGATG | 50807 |
| rs544595810 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130225035 | CTGGCCACATGTGTA[A/T]AAAAAACTGCCTATA | 50807 |
| rs544597638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130232368 | GAGGGAGAAAATGGG[A/G]AAGGGAGAGGGACCA | 50807 |
| rs544600801 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359663 | GCTCTGTCGCCCAGG[C/T]CGGACTGCGGACTGC | 50807 |
| rs544601287 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141034 | TAGGTATATTGATTG[A/C/G]AGACTGTATAATCTT | 50807 |
| rs544606292 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130224135 | TGGCACATAGTGAAT[G/T]CTCAGTAAAATGCTC | 50807 |
| rs544606974 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130212793 | CTGTGTGTATGGCAC[A/T]TATACACACAGTTGA | 50807 |
| rs544611064 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130303383 | AACTGGATGACTCTT[C/T]GTTGCGGGGGTCTCC | 50807 |
| rs544623040 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292171 | AAAGAAAAGAAAGGC[-/A]AAAAAACAAAGTCTG | 50807 |
| rs544624541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126640 | ATTACTTCCATGTTA[A/G]CCAAATCTTCAGGTT | 50807 |
| rs544630107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130182208 | AAGCCTTTCAATTTA[C/T]CATGGTGACTTAAAC | 50807 |
| rs544631999 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130100147 | CATTATATAAGAGTT[C/T]CCCTTTCTCTGCATC | 50807 |
| rs544633666 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130216501 | TTGAAACATGTTCTT[C/T]GTCTGGCTTCCAGGA | 50807 |
| rs544634395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130231847 | AGCTCTTTTCTCAAG[C/T]CACACCTGACTTACG | 50807 |
| rs544634468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095389 | CACCGTGACCTCCCC[C/T]TCCTGGGTTCAAGTG | 50807 |
| rs544639924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130369266 | CCAAGACTAAACACA[A/G]AATTCACTTATGTTA | 50807 |
| rs544641464 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120435 | TACCTGTAAAATATT[A/G]GTAATCATAGCTGCC | 50807 |
| rs544646177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313824 | CAGTCTTTACTGGGG[A/G]AAAGGGAATGAATCC | 50807 |
| rs544649482 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352386 | CGAACAAGATCAGAC[A/G]TCAAACCCTGACCAC | 50807 |
| rs544653535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257626 | TTAATGCTGTTGCGA[A/G]AAAAAGGGATCTACA | 50807 |
| rs544662081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394505 | TTTTAATGTCGTCCC[A/G]GTCCTGTGGTCCTGT | 50807 |
| rs544667721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130250911 | AATACTACATTCTAA[C/T]GATATCTTTTTCCTG | 50807 |
| rs544682680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130216720 | AAATTGATATCCCCA[A/G]CCCAGAAAAACCCAC | 50807 |
| rs544683680 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397285 | AGCTGGGACTACAGG[A/C/T]GCCCACCACCATACC | 50807 |
| rs544686542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130087413 | CAATCCCAGCTATTC[A/G]GGAGACTGAGGCAGG | 50807 |
| rs544686942 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130081994 | CCAAGGTCAGGTCAC[A/T]GGTAAGGGTCAAAGC | 50807 |
| rs544703046 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393006 | GAAATTAAGTCACTT[A/C]CTCAAAAATAAACCT | 50807 |
| rs544703851 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130397644 | AGTTAAGCAAAGGAT[A/G]GGGGGAACTGCTTTA | 50807 |
| rs544704392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257929 | GGGCCCCAAATCCAA[A/G]TTCAACCTGCCATGG | 50807 |
| rs544721682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130088474 | GCAAAGGCAGTTCTG[A/G]GAACACAGAGAGGCG | 50807 |
| rs544723625 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166595 | TCCAATGTATCTCTA[A/T]TAGTATCCATACCAC | 50807 |
| rs544729235 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130166546 | AGTTTTCCATCTCTG[C/G]GTCTTGTAGGTTTCT | 50807 |
| rs544735501 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130387569 | AGCACAGGTCCCAAC[A/C]AATTTTTTAACTACT | 50807 |
| rs544738800 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130373604 | CTGTTATCCCAGCAC[C/T]TTGGGAGGCCAAGGA | 50807 |
| rs544748183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121115 | TCCCTTCAAAATACA[C/T]TGGGAAGTCAACCAC | 50807 |
| rs544748747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130096067 | AAACAAACACACAGA[C/G]AGACCTATCTATTGT | 50807 |
| rs544750948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128237 | TTCCAAAATAGCAAT[A/T]AAGTGAGGAAAAACA | 50807 |
| rs544760085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130225710 | TAACAAGTAGACTTG[A/G]GGTGTGGACATTCAA | 50807 |
| rs544772377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354655 | TTGTCAAGAGTAAAA[C/T]GGCACACATCAGTGT | 50807 |
| rs544773610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162282 | AGCAACAGTCCCTAG[C/T]AACAACAGTAGTAAC | 50807 |
| rs544773704 | in-del | -/A | 0.00164338 | 0.028618 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278667 | GAGAGACATTGGACG[-/A]AAAAAAACTCTAATT | 50807 |
| rs544782052 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130349791 | GACACATAAAGTCAT[C/T]TGATGAGTGCCTCCC | 50807 |
| rs544785216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154259 | GGAAGTAAATGGTGA[A/C]CAAATCATTCACAAA | 50807 |
| rs544787166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130146939 | CAATACAAAAGAATT[A/C]CAACGGCCAGGTGTG | 50807 |
| rs544797684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339310 | TCGGTAAGAACAAAT[C/T]TAAGACGCTGGAAAC | 50807 |
| rs544798744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381626 | CTCCAAGCTAGAAAA[A/G]AATCACTACGGTGGC | 50807 |
| rs544804088 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130398477 | CAGCAGAAGTGACAG[A/T]AGAAGCAGTAGTGGT | 50807 |
| rs544809183 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130200392 | GAGGATCCTTTCTCC[A/T]AACCCTGCACAAACA | 50807 |
| rs544823736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437619 | TTATTTAGATAGATA[A/G]ACTAACTACAATGAA | 50807 |
| rs544835344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130382043 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCG | 50807 |
| rs544839027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284381 | AGTGTAATTTAGCCA[A/C]AAAGTATGAGGTTCA | 50807 |
| rs544840250 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128779 | AGTTGATTAACTAGG[C/T]CTGAAATAACCACAA | 50807 |
| rs544847455 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153748 | AATAAATGAATGACA[A/G]GTACTACAATGATAT | 50807 |
| rs544852273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130389653 | CTACCTAAGCTGGAA[A/C]AACTCTACTCTCTGT | 50807 |
| rs544860178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130154988 | CAAGTAGTTTTGCAT[C/T]CATCTTACTCTCACA | 50807 |
| rs544863811 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130065137 | ACCCACCTTAGCCTC[A/C]CTAAGCGCTGGGATT | 50807 |
| rs544869633 | in-del | -/TCACT | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347185 | AGGAGCACCATGCCA[-/TCACT]TTGGATTTAGTGGCA | 50807 |
| rs544875936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376040 | ACAAATTAACAACAA[C/T]AACAAAAAGACATAA | 50807 |
| rs544881832 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130290897 | GGCTTGGGTTAAAGG[C/G]AGTAAGGATTTTAAG | 50807 |
| rs544884963 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431444 | AACCATAACGAACCA[A/C]TTGTAATTTCCAGCA | 50807 |
| rs544890147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278661 | AACAGTCGAGAGACA[C/T]TGGACGAAAAAAACT | 50807 |
| rs544892700 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130246121 | TTACAAAGTCCTACA[C/T]GTAACACGGGCAAAA | 50807 |
| rs544901383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244924 | AGACAAGTTGAGGCA[A/G]AGAGAAGCAGAACAG | 50807 |
| rs544910220 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376596 | CTGGCCATGATGGCG[C/T]GTGCCTGTAGTCCCA | 50807 |
| rs544916963 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130340639 | TAACGTCTAAGAAAG[A/C]AGTGTGACATGGAAC | 50807 |
| rs544918088 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341152 | GTCGACACAAAACTT[A/C]CAACTGACTGCTCCA | 50807 |
| rs544926837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056317 | GCTTCATGCCAGGGG[C/T]TGGCCCCACTCTGCT | 50807 |
| rs544927978 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094500 | GGCGTGAGTCACCAC[A/G]CCTAGTCTAAATTTA | 50807 |
| rs544954688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217278 | TGAATAAATGAATAA[A/G]TAGATATTTATCAAA | 50807 |
| rs544969467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130421898 | AAAAGGCTTCACCTG[A/C]ATACCTACTATGTGA | 50807 |
| rs544970395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123322 | ATGTCAGTTTCCCCA[C/G]AGTCTTGCTGAGTGG | 50807 |
| rs544973537 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130106442 | TTCACCCTTTCTACT[C/G]TTCTTCCTATCTACT | 50807 |
| rs544976939 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130274133 | TATATAATCATTTTT[C/T]ATTCTTCTCATACTA | 50807 |
| rs544983087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130368640 | TTCATGGAGGACTGA[C/T]ATAGATGCTAGGATA | 50807 |
| rs544984923 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108754 | GGCAAGCCTCAAAAA[C/T]CAGTTTTTTTTTTTT | 50807 |
| rs544997345 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130063203 | TTCTATTGAGACAGG[G/T]TCTCCCTCTGTTACT | 50807 |
| rs544999070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130305239 | TCTTGACTGCCTGTC[C/T]CCACTAAAAAACAAA | 50807 |
| rs545001066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206976 | GATTTTATTGGTTTC[C/T]TTTTCATGGTTAAAA | 50807 |
| rs545005690 | in-del | -/TGCTGGGCACTG | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437229 | TCAGTGCCTGTCATT[-/TGCTGGGCACTG]TGCTGGGCACAAAGG | 50807 |
| rs545005782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130312314 | CATGCCTAAAAGAGC[C/T]GGCTACCATCCACCA | 50807 |
| rs545006177 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130168642 | AAAAAACTCTATAAA[C/T]CTGCCTATTCAGAGT | 50807 |
| rs545007144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397568 | CCCCATGGAACATCA[A/G]GTAGGTTCACAACTA | 50807 |
| rs545024575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080178 | TTATTTCTGGTAAAG[A/G]AGTGTATCAAAGAGG | 50807 |
| rs545030088 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130326943 | ACACCAGACCCACTG[G/T]GGTTATTCCTTCCCC | 50807 |
| rs545035656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337627 | AAGAGGTTTCTCTCC[C/T]TCCCATGAAAATTGA | 50807 |
| rs545037319 | in-del | -/AAC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130219006 | TCTTGGGGTAATAAT[-/AAC]AATAATAATCATAAT | 50807 |
| rs545038110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130264279 | TGATGTTTCATTTCA[C/T]CTGGTCCTTCCATGG | 50807 |
| rs545039250 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130284434 | AACGGGAGTCAAATT[A/G]TAGTAACTCAACTTT | 50807 |
| rs545041229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289119 | TGAACCCGGGAGGCA[C/T]AGGTTGCAGTGAGCC | 50807 |
| rs545050367 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393527 | TTGGGAGGCCAAGGC[A/G]GGCAGATCACTTGAG | 50807 |
| rs545063478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130243038 | ATCCACTCAGTGTGC[C/T]AGACGCTTCAACAGG | 50807 |
| rs545070414 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130114028 | CTCAAGGCATCCACC[A/C]GTCTCACCCTCCCAA | 50807 |
| rs545076964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130296253 | TCTTGCTAAACAGAG[A/G]TTTACCTGGTTGAAC | 50807 |
| rs545078520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422434 | TAAATTCCCAGGCTC[A/G]GATCACCCACGCTTC | 50807 |
| rs545079918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435864 | ATCCACCATACACCA[C/T]TGGTCTGGGGTCAAA | 50807 |
| rs545090544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430165 | AGCAAAAGAGAGATT[C/G]TCAAACTCTCAGCTA | 50807 |
| rs545099244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130331005 | GAAAGACCTTAGCTG[G/T]CCATTGGCCAGACCA | 50807 |
| rs545110023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130074673 | TCTACCTTAGGACCA[C/T]GGCCACCATGCCAGG | 50807 |
| rs545117186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130210748 | GAGCTCAATCCCTAA[C/T]TGCACCATTTTGCAG | 50807 |
| rs545117429 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130193901 | TCCCTTGTTGGTCAG[G/T]CTGGTTTCCAACTCC | 50807 |
| rs545132274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323265 | AAGCCTGAACATTAC[A/G]GACTGGACACTCATT | 50807 |
| rs545134233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130331909 | CCAGAGAACCATAGA[A/G]CAGATCCCCAAATAT | 50807 |
| rs545150083 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130062500 | CGTTCCTCTCTTGGA[A/C]GTCTGAAATTGGCTA | 50807 |
| rs545158465 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108103 | ACCAACCCTTCAACA[A/T]CAAGCATCTATTGAC | 50807 |
| rs545167229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297874 | ACTGCTGCTGAAAAG[G/T]AGTGGGAAAAGTAAA | 50807 |
| rs545167939 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130321438 | GGAGTTAAAATCCCT[C/T]CTCAGTCAATAGGAA | 50807 |
| rs545168086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313530 | GTAACAGACTACCCT[C/T]GTGGGATTCTCAAAT | 50807 |
| rs545170862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130323831 | GAGACATCCTTGAGG[G/T]CATCTTTTTATCCTA | 50807 |
| rs545177374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130229767 | AAAATAGGCTGGGCG[C/T]GCTGGCTCACACCTG | 50807 |
| rs545178168 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130374415 | TGGCTCACACCTGTA[A/T]TTCCAGCACCTTGGG | 50807 |
| rs545180265 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130294725 | GCTAATGAAAACAGA[A/G]AATTATTTTAACTCC | 50807 |
| rs545182957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388128 | GTACAGGGACAAGGC[A/C]CTGGAGGCAGAAGAA | 50807 |
| rs545191592 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132482 | AGTATAGAGTATTTA[C/T]AACCTTCCCCTACGT | 50807 |
| rs545197875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204266 | ATGTGCTCAAATCAT[C/T]CCGAAACCATCCTCC | 50807 |
| rs545203656 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130433910 | AAAGCAGACTCTTCC[A/G]AGGCCACATGAAGAA | 50807 |
| rs545204923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130415530 | TGGTGGCTCAAGCCT[A/G]TAATCCCAGCACTTT | 50807 |
| rs545228998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130298150 | ACAAATAGCTAGTTG[A/G]CAAGTATGGATACTG | 50807 |
| rs545241769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409175 | GCTGGGGCAGGAAAA[C/T]AGCTTGAACCCAGTA | 50807 |
| rs545246732 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130066417 | GGTCTCACTTCATTG[C/T]CCAGGCTGGTCTTGA | 50807 |
| rs545259254 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130326668 | CACCAGCAACAACAA[A/G]TAAATGTAAATGTTC | 50807 |
| rs545267272 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409703 | CCCAACCGCCCGCCT[C/T]ATTTGTTGATTCAAA | 50807 |
| rs545277140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130357955 | CCAGCTCGGAGAGGA[A/G]ATCCTCCAGCTGCGC | 50807 |
| rs545282299 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130317955 | GCACCATTAGTCACT[G/T]TTACCAAAATAGCTA | 50807 |
| rs545294180 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123552 | TAAATACTTTTCTTT[-/G]TTCTGCTTTCCCCTG | 50807 |
| rs545307198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130061741 | AAGGGATACATAGTC[C/T]GAAACTTTGCTTTTC | 50807 |
| rs545312745 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130284922 | GAGAGAGACAGAGAG[A/T]CATACACTCATGAGT | 50807 |
| rs545319228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333344 | CGGTGGCTCACGCCT[A/G]TCATCCCAGCACTTT | 50807 |
| rs545319372 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130328124 | CTGGTGGCCAGTGTC[A/G]TAAGTATTCTACATG | 50807 |
| rs545329958 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130311803 | GATATAGGTTACTTA[A/T]AATTATAGAAAGCAA | 50807 |
| rs545348111 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381407 | GAAAGAAAAATTATT[-/A]ATGAGACAGAGTTTT | 50807 |
| rs545352552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130263529 | AGACACCAGGAGGTG[A/G]CTGGAATTAATCCCC | 50807 |
| rs545353418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130281905 | CCCCATCTCTACTAA[A/G]AATACAAAAAGTTAG | 50807 |
| rs545355048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112496 | CAAGGGAAGGATCTA[A/G]ATACCACACTTTCAT | 50807 |
| rs545358272 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325505 | GAGACATCTGTTCTT[A/C]AACTATGTGATCTAA | 50807 |
| rs545391371 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130053068 | GGTTTGTCATGCAAG[A/G]TTTATTTATTAGGTG | 50807 |
| rs545391650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130271175 | CCAATCAGCAGAGGG[G/T]CTGCTCGCTCCTAAA | 50807 |
| rs545400439 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151919 | AGCCAAGTTACAGCT[C/G]TTCTTTGTGCTTCAG | 50807 |
| rs545404418 | in-del | -/TT | 0.390464 | 0.206809 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136561 | CAATCACCTAGTGGC[-/TT]TTTTTTTTTTTTTAA | 50807 |
| rs545405443 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130407607 | AAAGCACCTGCCTGC[G/T]AAAGTGAACCAGAAT | 50807 |
| rs545406126 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086513 | ATAAACCTGTATTAA[G/T]AATTTATGGGCTGGG | 50807 |
| rs545422750 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133612 | AGTGAGCCGAGATTG[C/T]GCCACTGCAGTCCGC | 50807 |
| rs545425734 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159011 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 50807 |
| rs545429576 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ASAP1 | GRCh38.p7 | 8:130052030 | ATATACCCGAAAGCA[C/T]AGCCAGAGGAAGCCT | 50807 |
| rs545433205 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073374 | CAGCCTGGGCAACAA[A/G]AGTGAAACTCCGTCT | 50807 |
| rs545434874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244097 | CGAATCAAGGGTGTA[C/T]AGATCACCCTGTTGT | 50807 |
| rs545451988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130386747 | CAGGAGCGATGAAGA[C/T]TTAGGGAGCTCACTG | 50807 |
| rs545453358 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373624 | GAGGCCAAGGAGGGT[A/G]GATCACCTGAGTTTG | 50807 |
| rs545455458 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413894 | TTGCCAGATTCATTC[A/G]TTCATTCATTCATTC | 50807 |
| rs545464156 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130151246 | TGTGGTGGTGGGCGC[A/C]TGTAGTCCCAGCTAC | 50807 |
| rs545476832 | in-del | -/TTTT | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099181 | ACCAGGCCTAGCTAA[-/TTTT]TTTTTTTTTTGGTGG | 50807 |
| rs545479773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130414811 | TGCCCAGATAGGAGT[A/G]CAGTGGCAAGATCTT | 50807 |
| rs545480507 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130092544 | AGGTAGGAGGATCAC[C/T]TGAAGTCAGGAGTTC | 50807 |
| rs545481642 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130131314 | TCGAACACTTTCATA[C/T]GAAAAATAAACTCAA | 50807 |
| rs545483201 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195301 | AGCAATTGGCGGGGG[C/G]CAAGGTGTGGGAACT | 50807 |
| rs545484515 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178883 | ACAGAGTGAGACTCC[A/G]TCTCAAAGGAAAAAA | 50807 |
| rs545488732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380698 | ATTGTCAGCAGCCAC[A/G]GGAAAAAAGTTAAAA | 50807 |
| rs545490121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130322548 | TTAAATACAGAACTG[C/G]GGACTAGGAATCAGA | 50807 |
| rs545490162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085426 | TGTGTTAGTCTGTTA[C/T]AAAGTAGGTTATTAA | 50807 |
| rs545491968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130144089 | CATTATGGTCATTTC[A/G]AAGTTTTCATTCAAT | 50807 |
| rs545500258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098447 | CTCCCGGGTTCAAGC[A/G]ATTCTCCTGTCTCAG | 50807 |
| rs545509281 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130276758 | CTCTCTCTCTCTCTC[C/T]CTCCTCTAACAAAAA | 50807 |
| rs545512117 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130289674 | TGGTTATATTCCCAG[G/T]GTAGCCCATACAGCC | 50807 |
| rs545516820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275718 | TATGTTTAAATCTAT[C/T]ATATTTTCTAAATAT | 50807 |
| rs545537362 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130234797 | CTCAGGTACAAACCA[C/T]CATCACATTACAGAG | 50807 |
| rs545546023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130283031 | CAAGCCAGAAATCCA[A/G]TATTTATGTGAAATT | 50807 |
| rs545554323 | snp | A/C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130136352 | CTGAACCATGAAGTA[A/C/G]AAGAGTGACAGGGTG | 50807 |
| rs545554774 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130297158 | CAACTATGGGCCAGG[A/C/T]GCTGCACTGGTTTTT | 50807 |
| rs545564092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079057 | AAAATCAGCTGAGTA[C/G]AGTGATGCATGCCTC | 50807 |
| rs545572418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130310787 | TCTGCCCAAACTTGA[C/T]AGAAAATTTTCTGAA | 50807 |
| rs545579400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139501 | GAGGCTGAGGCAGGC[A/G]GATCACCTGAGGCCT | 50807 |
| rs545580540 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130402216 | CCTTCTGGCATTCTA[C/T]TTCTAGCTCTACGTT | 50807 |
| rs545584801 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130267429 | TAAGCTCTTTAGATG[A/T]AGAATCACATTAGAT | 50807 |
| rs545593676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130409649 | GAGGTATTCTCCCTG[A/G]CAATGCCGAGGCTGC | 50807 |
| rs545602664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130078487 | AGCAAGGTCTTGCTA[C/T]GTTGCCCAGGCTGGC | 50807 |
| rs545612517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091311 | GTAGGGAGGAAGCTG[C/T]GTTGGAGGGCGGGGG | 50807 |
| rs545615416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130055554 | AAAAAAAAAAAAAGG[C/T]TGCTATGTACTATCA | 50807 |
| rs545619971 | snp | A/G | 1.65247e-05 | 0.00287438 | synonymous-codon | ASAP1 | GRCh38.p7 | 8:130188151 | TAACAAAGAATCCAA[A/G]GTGAAGATCACATTG | 50807 |
| rs545627718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145890 | TCTGTCGCCCAGGGT[C/G]GGGTACGGTGGTGTG | 50807 |
| rs545652776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130367515 | ATTTGTGACTTTTGC[A/T]CCAAGATGTTTGTGA | 50807 |
| rs545654172 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130369297 | CATATAAACCTTATA[C/T]ACATAGCCTGAAGGT | 50807 |
| rs545669462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130271914 | TCTTTATGGAAATAA[A/G]AAAAGTCATGTTTTA | 50807 |
| rs545676718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130174044 | AGTGAGCAGAAATCA[C/T]GCCACTGTACTCCCA | 50807 |
| rs545678440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130201248 | AAATCACTTGCCTAT[A/G]GTCTAAGGCATAATT | 50807 |
| rs545682303 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130208670 | GCCCCAGTAGTTGGA[A/C/T]TGCCATTCCGCAGAT | 50807 |
| rs545687428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130256170 | ACTAGGTATTGTTTC[C/T]GTAAACATAAATCTT | 50807 |
| rs545694991 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130427448 | GCCGAGAATCCCACA[A/T]GTGGACAGGGTTCAG | 50807 |
| rs545696426 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130212030 | CCCCCTCGGGGTGAG[C/T]TGGCTTTCTGGGAGC | 50807 |
| rs545700889 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130428019 | CATCAACCTCTTCTC[C/T]AATCCTTCTCCAAGT | 50807 |
| rs545708764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439946 | ACAGAACTTGATTTT[C/T]TCCATGAGCATAATC | 50807 |
| rs545714133 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093664 | ACAGCGAGACTCCGT[C/T]TCAAAAAAAAAAAAA | 50807 |
| rs545724723 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130391744 | GTCATTTCAGTCCAA[C/T]ACAGTAAATGTAATA | 50807 |
| rs545730492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130318498 | TACCAGACATTTTCA[C/G]GAACATCTCCTTTCA | 50807 |
| rs545737315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392140 | AAAATCATTTGTGGA[A/G]TAGTTTTTAAGACTG | 50807 |
| rs545754934 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130178071 | GACATAATATTAATG[C/T]TGACCTCCTTAAATG | 50807 |
| rs545756671 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244863 | CTATCTGACACTCCT[C/T]TTGGAACAAGCCAGG | 50807 |
| rs545758624 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130204203 | GTGAACTGCATATGC[A/C]AGGGATCTAGGTTGC | 50807 |
| rs545763668 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130112021 | ACCTCAAAGCTGGCT[A/G]GACTATCAGCTCTGA | 50807 |
| rs545784511 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130080265 | ACTGGCTCAGGATCT[G/T]GTCCTTAGTTTGAGG | 50807 |
| rs545785415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130329918 | ATAATTTTCTAGTCA[A/G]CACATCCAGCAGCCC | 50807 |
| rs545786346 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130149787 | AGTCAGGAAAAGCCC[A/G]CTAAAACTGGCTAGA | 50807 |
| rs545796870 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130213462 | ATCTGTAAACTAACC[C/T]TTTGTATCTAATGGA | 50807 |
| rs545806870 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130184727 | TGATGTTTTAGTTTA[C/T]GTACATTTATCACTT | 50807 |
| rs545816278 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364174 | GGTTTGTTTGGAGAC[A/T]AAAAACTACTCTGGT | 50807 |
| rs545821308 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130367996 | CTTCTTAACATATGC[-/T]ATTTAGTTAACGTCC | 50807 |
| rs545823094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119275 | TATAGGTGAGGAAAC[C/T]AAGGCTCAGAAAGGC | 50807 |
| rs545823566 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130425056 | GTGGGTCAGGCCGGG[A/C]GCAATGGCTTATCCC | 50807 |
| rs545832347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259724 | TGCTTATAATGGACA[G/T]GAAGGGGCGACAGTG | 50807 |
| rs545841556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220291 | TTACTATTCCAGTAA[C/T]AATCGTTACAATAGC | 50807 |
| rs545858761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130253942 | ATGAGAATCGCTTGA[A/G]CCCAGGAGGTGGAGC | 50807 |
| rs545866525 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130086561 | GTAGTCTCCAGCACT[C/T]TGGGAGGCCAAGGCA | 50807 |
| rs545877663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130091823 | TCCCTTAAGAGACAG[A/G]TAGAATCATGTCATA | 50807 |
| rs545886089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130186723 | AGCCTTTCATGAGCC[C/T]CTTAGCCTCTCCAGG | 50807 |
| rs545886246 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130253128 | ATGGAGAATCACATA[A/G]CTACCAACTAGATGC | 50807 |
| rs545903638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130260310 | TGGGCTACTAGACCA[C/T]AAATGAGCTCTGTGC | 50807 |
| rs545908250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130268997 | CAAAGGCACTTAAAC[C/T]ACTAACAAAAAAAGT | 50807 |
| rs545922685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130221432 | GAAATGTCAGTACCA[A/G]GATGAGTCTGCATAA | 50807 |
| rs545925053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130267485 | AATAAGAATATGATG[A/G]TGATTTTACAGATAA | 50807 |
| rs545934506 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130216747 | CCACCCTCTGTAATA[C/T]AGACATATATTCAAC | 50807 |
| rs545936977 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130210128 | TTCTCTTTTCCCAAT[A/G]CAGATCTGTATGAGG | 50807 |
| rs545937475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395486 | CACAGGCAGAATGCC[G/T]CAGGACAACACAGGC | 50807 |
| rs545950012 | snp | A/C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130178330 | CTGGTAGAGTCTCCA[A/C/T]GTGTAGCTGGCACAT | 50807 |
| rs545960296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228768 | CTTTAACTTGAAAAA[C/T]ATATAAACAATGGGA | 50807 |
| rs545964172 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ASAP1 | GRCh38.p7 | 8:130117573 | CTGTTGCTTACAGAA[A/C]AGATAAAGAGAATAA | 50807 |
| rs545965833 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130157057 | CAATATTAACTTTTC[A/G]TTTGATGACAGAACA | 50807 |
| rs545971703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150159 | GGTCACAAAGTAAAT[A/G]GCAAAGTTGGCATTC | 50807 |
| rs546005527 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130088373 | GACCTCAAGTGATCC[G/T]CCCGCCTTGGCCTCC | 50807 |
| rs546007929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130433542 | ATTATTAACAGTTAC[A/G]TATCTTTCTCTTCTA | 50807 |
| rs546011504 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130061967 | GGGCAAATTACACAA[C/T]CTCTCTATGCTGCAA | 50807 |
| rs546034716 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130165905 | CTCATAAACCCCTTT[A/C]AGAAATTTTAGAAAT | 50807 |
| rs546037653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342515 | GATAGCTGCTATTTG[A/G]CCCCCTAGGGAAGCA | 50807 |
| rs546040089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130124399 | CAAATATGTGATAAA[C/T]GCTAGAACAGAATCT | 50807 |
| rs546042561 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248692 | ACAAGCTGGGTATTA[C/T]ATCACAACACTTATC | 50807 |
| rs546044302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130131469 | CTCACCACCAGCACC[C/T]AGAGAGAATGCAGGC | 50807 |
| rs546048388 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130063427 | CCACATCCTCTCTCC[A/G]CACTCCTGGCTTTGG | 50807 |
| rs546052009 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130095683 | GAGTGCAGTGGTGTA[A/G]TCTCGGCTCACTGCA | 50807 |
| rs546061288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130343487 | TTTGGAGAAACTTAA[A/G]TCGAGACCTCAAAGC | 50807 |
| rs546062740 | snp | A/C/G | 0.0115144 | 0.0749975 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401042 | CCTGCCACCACACCC[A/C/G]GCTAATTTTTTGTAT | 50807 |
| rs546064789 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP1 | GRCh38.p7 | 8:130357208 | GGCCCTGCCCCCCAC[C/T]CCCCACCAGCAACGC | 50807 |
| rs546074574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130158187 | ATCCACAAGTAATCA[A/G]AAAACAAGGAGCTTT | 50807 |
| rs546077171 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130390944 | TATATCCCCCGCCCC[A/C]CCAAAATTGAAAGCA | 50807 |
| rs546084667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130256193 | TAAATCTTCCTGTTC[A/G]CAAGAGTTGATGAAG | 50807 |
| rs546097999 | snp | A/C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130371238 | TAATAGATAGGAAAT[A/C/T]GAGACTCAGAGAGGT | 50807 |
| rs546101100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350870 | CTGCAACTGAGAGTA[A/G]TGGTTCTTTAGCCAG | 50807 |
| rs546104163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130215528 | GCGGGCCGATCACGA[A/G]GTCAGGAGATCGAGA | 50807 |
| rs546112603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059487 | AATTTTTTTGAGACA[A/G]GGTCTTGCTCTGTTA | 50807 |
| rs546122532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295555 | TTATATGAGATAATG[C/T]TTATGAAACATCTAG | 50807 |
| rs546124990 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130157617 | CCCCACCTCACGGAG[G/T]GGTTCCCTGTCCCTC | 50807 |
| rs546125460 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130430144 | TCAAAAAAGCTTCTC[C/G]AATTTAGCAAAAGAG | 50807 |
| rs546146012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130333516 | GGCTGAGGCTGGAGA[A/G]TAGCTTGAACCTAGG | 50807 |
| rs546149239 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130229113 | TGGCACTGATTATCA[A/G]TGAAAACCAGTTCAG | 50807 |
| rs546156787 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130192927 | GTGCCTATCAATAGG[A/G/T]CACTGGCTAAATAAA | 50807 |
| rs546178732 | in-del | -/AAACAAACAAACAAAC | 0.00795532 | 0.062565 | intron-variant | ASAP1 | GRCh38.p7 | 8:130230066 | GAGATCCTGTCTCCA[-/AAACAAACAAACAAAC]AAACAAACAAACAAA | 50807 |
| rs546179554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219710 | GAAATGTGATCCATC[C/T]GTTAAGAAGACACAT | 50807 |
| rs546180951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130238425 | CAGCTGTTCCCAAGG[C/T]ATATGTCACTGTTAA | 50807 |
| rs546182500 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213049 | ACACCACACTTTGAG[A/C]AAGGCCTCCAGTGAA | 50807 |
| rs546182602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130231291 | ATGGCTGTCTTCCTT[A/G]TAATGAAAAAGCTGC | 50807 |
| rs546188446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130084406 | CTCTCTCTGTGCAAT[C/T]TGGAAAAAGGTCTTA | 50807 |
| rs546201983 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130395082 | CAACCAGGGACCACA[A/C]AAGAATGTCCCTGCC | 50807 |
| rs546206541 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130429804 | TTAAGATTCTTTGGG[-/A]AAAAATGAGTTTTGA | 50807 |
| rs546210247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130169920 | TTTCTTGTCTCAGGT[A/G]GCACACTTCCACTCA | 50807 |
| rs546213502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287796 | CATAGGGAACGCTCA[A/G]AGGGCTGTGTTTGGG | 50807 |
| rs546214153 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130237813 | TTTAAAATGGGGCAT[A/G]GTCAATATACTTGGC | 50807 |
| rs546217574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130200390 | GAGAGGATCCTTTCT[C/G]CAAACCCTGCACAAA | 50807 |
| rs546219597 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | ASAP1 | GRCh38.p7 | 8:130420848 | CAGTGAGCCAAGATC[A/C]CGCCACTGCACTCCA | 50807 |
| rs546225446 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083851 | CAGGCTGGAGTACAA[C/T]GGCATCATCTCAGCT | 50807 |
| rs546228361 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130386287 | ACCCCTGGACTCCTC[A/T]CTTACCTAAGCCAGT | 50807 |
| rs546229777 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130197147 | AGAACTGACACCAAC[A/G]GGCCAGGTGCAGTGG | 50807 |
| rs546237490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307886 | AGTTGCCTTTCCTAA[C/T]ATATAAAATGGATTT | 50807 |
| rs546239853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130325098 | AAAATTCCACTGACA[A/G]ATTCTGGGGGGCGGA | 50807 |
| rs546261060 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130348822 | CAGTCAGGGCCAAGG[A/C/T]ATAAATGTTTCACCT | 50807 |
| rs546262943 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130204027 | GCATACTCTAGAGCA[C/T]GGGTCCCCAGTCCCC | 50807 |
| rs546265146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130070332 | GTGAGCCACCGTGCC[C/T]GGCCGACTGCATCTC | 50807 |
| rs546287219 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130292035 | AGCTGCTGGAGAGGA[C/G]CTGAACTGAGAACTG | 50807 |
| rs546297796 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130341864 | AAGAGCAGCAAGAAA[A/C/T]GAGAGTCAAACTAGG | 50807 |
| rs546306856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130206413 | ATCCAACCTGTACAT[C/T]ATCAGATATTCTTAT | 50807 |
| rs546312871 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432097 | GGGAAGGGGGAGGAA[A/T]GGGAAGAGGGGGAGA | 50807 |
| rs546322094 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301056 | TCATTCCCTATGATG[A/C]ATTTAAGGAGATGAT | 50807 |
| rs546325036 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130098419 | CATGATCTTAGCTCA[C/T]TGCAATGTCCACCTC | 50807 |
| rs546325307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130432707 | ATGCTAACCCCAGTA[A/C]GTCCCACAAAAGAAG | 50807 |
| rs546345578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213681 | TAAATAGTTTTCCTT[C/T]GGCACCTTTCAACCT | 50807 |
| rs546352364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130141176 | AAAAAAGAAAACAAA[A/G]CAGGAGAAACTCTGG | 50807 |
| rs546387403 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130130883 | ATTTTAAAAAAAAAA[-/T]GCCACGCTCACGCCT | 50807 |
| rs546388394 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130128400 | GGAGACTGCATTTCC[A/G]TGTGGGCATACTGAA | 50807 |
| rs546400499 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130134012 | TGCACCACAGGATCA[A/C]AGAAGGTTATGAAGA | 50807 |
| rs546403953 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247447 | GCAGGTCTTCCTGAT[A/C]TCAAGGTCTATATTC | 50807 |
| rs546404406 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130075634 | TTGCAGCTTTAAAGG[C/T]AAGGTATGGTAACAA | 50807 |
| rs546412090 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120051 | TGGCAGTAAAAACAG[C/T]TGAGCTGGTTGATGA | 50807 |
| rs546417865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130189975 | AATATATATTCAGAT[A/C]TTTTGCCCAGTTTAA | 50807 |
| rs546440274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130273438 | AGCAGGAGGCATCAG[C/G]AAGGAACTGCGGGGG | 50807 |
| rs546452449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130398947 | TCTATAACAATAACT[C/T]TCAATTTGGTAAGCA | 50807 |
| rs546452755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130225947 | GCCGCGGCATGGTCA[C/T]AGCTTGCTGTAGCCT | 50807 |
| rs546454873 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | ASAP1 | GRCh38.p7 | 8:130443516 | CGGCCGGGCGCTCGC[A/G]GCTCTCGGGTGGGAA | 50807 |
| rs546458503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130085289 | TGGCCCACTTCCAGA[C/T]ACTGTATGTGACTTT | 50807 |
| rs546459545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130354157 | GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCCTG | 50807 |
| rs546465933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130259019 | CCATTTGCTTATGGT[A/G]TTTTAATTTTTTGAT | 50807 |
| rs546486061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130192164 | AGAGAGCTATAGTCT[A/G]AGAGTCTACATTCTG | 50807 |
| rs546502702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130258806 | GTTTTGGGTTCTTAC[A/G]GTAAATAGATAACAT | 50807 |
| rs546510515 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130413113 | ACAGGATGAGTATCT[C/T]GCCAGAGTTTTTACA | 50807 |
| rs546513295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130105655 | TACTTTAAAAAGTAA[C/T]TAACCGTATAATTAT | 50807 |
| rs546513499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130336106 | CTGGGATTAAGATAA[C/T]GCAAAACAAAGTTTC | 50807 |
| rs546525768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130104963 | TAAGCTGCCACATAG[A/G]AAGGGTAATGACAAA | 50807 |
| rs546527593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130111324 | AGCCCCGGAGATGGA[A/G]GCGACTGAGAAAGGC | 50807 |
| rs546535137 | in-del | -/TAAAAGGCAAAGC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130144460 | ATGTTTTACAAAAAA[-/TAAAAGGCAAAGC]TGAATTCTGAACAAA | 50807 |
| rs546584882 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130278404 | GAAAAAGAAAATATG[A/T]CCCTACCTAAAAATG | 50807 |
| rs546592271 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130376224 | AGATGTGGTCACAAG[C/G]CTGGGCTGGGTGCTC | 50807 |
| rs546600849 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130403699 | CTGGGATTACAGGTG[G/T]CCGCCACCACGCCCA | 50807 |
| rs546601816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130266139 | GGGACTACAATCTCA[A/G]TGAAAGGTGAACTAG | 50807 |
| rs546608433 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130301807 | TGCATATGCATTGTT[A/G]TTGAGAGTATCTATT | 50807 |
| rs546611677 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130430622 | CCCTGAGGCAGCTCA[A/G]AGGATGGGCTGAGGG | 50807 |
| rs546618169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130219232 | GTATTATAAAGTTAG[C/T]AAAGTCAATACTAGA | 50807 |
| rs546621279 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130271484 | AAGGAAAAGGAGAGT[A/G]GGAAGTCAAAATCAT | 50807 |
| rs546630189 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130133270 | GCTACAGGAAAGAAG[-/A]GGGAATAAAGACAGC | 50807 |
| rs546644690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130173645 | TGGTGGTACATGCCT[A/G]TAGTCCCTGCTACTT | 50807 |
| rs546645679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130312627 | ACAGGTGGGTACTAT[C/T]ATAATTTCTATTTAT | 50807 |
| rs546645733 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130304814 | AAGTGTAAATATGGT[A/G]ATTCAGTGCTGCTTG | 50807 |
| rs546673261 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126298 | AAATTAAGCACTTTA[G/T]CCTTGTGAAAAAGTG | 50807 |
| rs546673876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130272897 | TAACGAGTACAAACA[C/T]ACAATTAGAGGGAAT | 50807 |
| rs546683827 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130394160 | GAACAAGAGAGATAA[C/T]CTTAAACTTTGACCA | 50807 |
| rs546684488 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130080379 | CACACAACTCACAAG[A/T]GGAATGTGCATGTGA | 50807 |
| rs546687795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397337 | GTAGAGACAGGGTTT[C/T]GCCATGTTGGCCAGG | 50807 |
| rs546695462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130182516 | ACATTTGGAAAACCC[C/T]TAATAAAAGAGCTGC | 50807 |
| rs546699751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093854 | CTTTCCTATTTCCCA[C/T]TGTCAATTACTAGTC | 50807 |
| rs546707292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130435375 | TTTATTGTCTTCCCT[A/G]TGCTAGACTTGGTGC | 50807 |
| rs546715671 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410456 | TCGGAGGGAGGCTAG[G/T]CTCACTAACTAGCCA | 50807 |
| rs546716338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130441511 | GATCCAAATACGGCT[A/G]AGACCTAGGTGGGGA | 50807 |
| rs546723873 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130277103 | AGGCACCGAGGGCCC[A/C]CCATCCCAGACTCTC | 50807 |
| rs546726167 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130243586 | CCACACCCTCCACTA[C/G]TCATTATGTTCCAGC | 50807 |
| rs546727966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130181670 | TCTTCTGTGTGTGGG[G/T]AGGGGGCCAGGGGAA | 50807 |
| rs546736650 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130265257 | GGTGTCCCATCATAC[G/T]TTCCCCAAAACAAGA | 50807 |
| rs546747013 | snp | C/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130352143 | AAGAGGTCAGAGACA[C/G]ACCCAAACATACTTT | 50807 |
| rs546754013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130410818 | CACCTAATTTCTGGC[C/T]GATCTTGAGTGATGA | 50807 |
| rs546757265 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130215086 | TTTGTATTTTTAGTA[A/G]AGACAGGGTTTCACC | 50807 |
| rs546758734 | in-del | -/TA | 0.00438332 | 0.0466095 | intron-variant | ASAP1 | GRCh38.p7 | 8:130094978 | TGAGCAACGCTGCAT[-/TA]TATATATGTATGAGA | 50807 |
| rs546785006 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130250688 | GGAGACCAAGAAGCC[C/T]GGGCTATACATTTGC | 50807 |
| rs546825581 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130314127 | TTTTTAAGAAAACAA[A/T]CATGCAAGGCTCTCA | 50807 |
| rs546828029 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130437231 | AGTGCCTGTCATTTG[C/G]TGGGCACTGTGCTGG | 50807 |
| rs546835368 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130350043 | AGGTCTGGGTAGTGT[C/T]TGAACATCCAACACC | 50807 |
| rs546835596 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130418427 | GTGGCATGAGCCTGT[A/G]ATCCCAGCTACTCAG | 50807 |
| rs546837146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130121434 | GTATCTCCAGACATT[G/T]CCAAGTATCCTCTGG | 50807 |
| rs546840766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130203368 | TGGCTTGTACAAGGG[A/T]AGCCTGAAGTCCAGC | 50807 |
| rs546845919 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130313630 | ATAATCAACGTCCTC[A/G]CAGAAAAGCAGACGT | 50807 |
| rs546869218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130075955 | AGTATTATTTTCCCC[A/G]TTTTACAGATGAGGA | 50807 |
| rs546870464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130307243 | AACACCCAGAACAAT[C/T]ACTATAAAACAGTAA | 50807 |
| rs546876351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130339510 | AAGGAGCTATCACAA[A/G]ATTCAACATGGGGTA | 50807 |
| rs546879878 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130217583 | TCCTACCACCAGACC[G/T]CAAGAGGCAGGGATT | 50807 |
| rs546881450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130347739 | TTCCCAGATATCCTC[A/G]CCTCAGAATCAGGCA | 50807 |
| rs546890955 | in-del | -/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130231412 | TCCTGCCCAGAAATA[-/T]TAAAGGATTTACAAG | 50807 |
| rs546896758 | snp | G/T | | | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445553 | ATGGGACCTCTGCCT[G/T]AGGTAGGGTGGTTCA | 50807 |
| rs546908519 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130167292 | CAGAGTGAGACCCTG[A/T]CTCAAAAAAGTAAAG | 50807 |
| rs546915201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130186440 | GTTGTCCAAGACTTT[C/T]ATTAAAAGCTTTAAA | 50807 |
| rs546918514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130250469 | GCTTACTATAGTTGC[C/T]TCATGTTCCTAGTTT | 50807 |
| rs546919822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130176561 | GACCTAGGGGACATT[C/T]GTCTACCAGATTGCA | 50807 |
| rs546922171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130394229 | TTCAAAAGCAAATGG[A/G]AGAAATATCGCTGAA | 50807 |
| rs546932007 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130431165 | CCCATGCCAGCCAAT[A/C]CTACTGCCTCCCCAT | 50807 |
| rs546933432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130107695 | TGGGATTACAGGCAC[A/G]GGCCACCAAGCCTGG | 50807 |
| rs546936846 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130325468 | CACTTATCATATTTT[A/G]TTCACTCTATAAGCA | 50807 |
| rs546939461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130204004 | CATATCTTTTGCGAG[A/G]AGGTACAGCATACTC | 50807 |
| rs546940673 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130188749 | AAAAAAAAAAAAGAA[A/G]AGAAAAGAAAATTGA | 50807 |
| rs546948533 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130082493 | AGGTGTGAGCCACCA[C/T]ACGTGGCCTTTTTTT | 50807 |
| rs546953968 | snp | C/G | | | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT2 | GRCh38.p7 | 8:130083106 | AGGGCTGCAAAGGCC[C/G]TCTGGCTCTGCTGTG | 50807 |
| rs546956425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130211879 | GTTTCTGGCCTTCAC[C/T]AGCCTAAGAGAACAG | 50807 |
| rs546965798 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130226425 | CCTTACATTTTCCCA[C/G]CACTAACTGTATTAG | 50807 |
| rs546969753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423344 | GATAATGCCTGGGGC[A/G]GGCAAGAAATGTATA | 50807 |
| rs546981919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130416738 | ACCTGCTTAGGCTGC[A/C]ACCTAATGGAAAGTC | 50807 |
| rs546982154 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130165188 | TTTAGCTAGCATGAG[C/T]GGAACACTTAAGTCT | 50807 |
| rs546992937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130392330 | GCTGACAGACAAAAG[A/G]AAGTCCCTTTGAATA | 50807 |
| rs546994616 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130385790 | CCTACATCCAGTTAC[C/T]TGGTTAGAGGGGTGG | 50807 |
| rs547014186 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093533 | TTAGCCAGGTGTGGC[A/G]GTGCACGCCTGTAGT | 50807 |
| rs547026850 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130141491 | TTCCATTTTTGTACA[A/C]CCTGCTGTATTTTCT | 50807 |
| rs547028409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130132622 | CTCTGTCCTTACACT[G/T]AGCACCTGCACCATG | 50807 |
| rs547030730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130230114 | AACAAACACCAACCC[C/T]AAACTAGCGGTCGTG | 50807 |
| rs547042453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130159101 | AAAAAGAAGAATGAG[C/T]GATACAAAGAGACCA | 50807 |
| rs547046018 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130395085 | CCAGGGACCACACAA[A/G]AATGTCCCTGCCGCA | 50807 |
| rs547050885 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130358255 | CGCAGCCCGCCACCC[C/G]CCGCCCGGCCTGGCG | 50807 |
| rs547066218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130245347 | TCAGAAACATTTAAC[A/G]TCTTCTACGGTGCCT | 50807 |
| rs547068986 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130070007 | TGAAAGTTGGTATAT[C/T]TGAACACACTTCATG | 50807 |
| rs547078730 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130217234 | GAATTTGTAGGGAGG[C/T]CCACAGTAGATGCAT | 50807 |
| rs547087033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130359430 | CTGAGTATGAATTTG[C/G]TTTAAAAGAAGAAGA | 50807 |
| rs547091587 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | ASAP1, ASAP1-IT1 | GRCh38.p7 | 8:130295822 | GGATTCATGGAGATA[C/T]CAGAAATCTTTTTGG | 50807 |
| rs547093347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130257718 | TATACTAAAATTCAT[C/T]ACATTTCTGTTTTTT | 50807 |
| rs547094076 | snp | A/G/T | 0.00398691 | 0.0444912 | intron-variant | ASAP1 | GRCh38.p7 | 8:130256437 | GGAACTTCCATCACC[A/G/T]CTCTGAATTCATTCA | 50807 |
| rs547098418 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130302351 | GAGGTTAAGGGGCTC[A/G]TTTTTTCACAGACAC | 50807 |
| rs547098565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130118873 | GTTTACTAATATATA[C/T]AAGTAATAGATATAG | 50807 |
| rs547107226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130126849 | AAAACCGCAAAAAAG[G/T]TATATCACAGTGCTT | 50807 |
| rs547116819 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130355634 | TTTTTTCTTATATTG[A/C]GTGTGGTAATGTTAA | 50807 |
| rs547119579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130397770 | TTTCAGCAGATGAGC[C/T]TGTGGGGCTGGGTTA | 50807 |
| rs547136721 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130288788 | AGCATTACTTATAGA[A/C]GGAAAGAAGGGAGGG | 50807 |
| rs547148982 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130061360 | GAGAATCGGAAAGTA[C/G]AGAGTTCTTAAGCCT | 50807 |
| rs547178133 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130422076 | TCTACCCAGAATCAG[G/T]CTGGTCAGGAACGGC | 50807 |
| rs547180212 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130248956 | TTTTTTAGAAACAGG[G/T]GTCTCACTATGTTAA | 50807 |
| rs547192923 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130120779 | GGCCATAGGAAGTAT[C/G]TGGCCTCTTACTAGG | 50807 |
| rs547201215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130201444 | GAGTACCAGGGAATA[C/T]GAGAATTCCTTAACT | 50807 |
| rs547206046 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130240151 | CCTACTTCCTTTTGT[-/G]GGGGGGGAGCGGGTA | 50807 |
| rs547211742 | in-del | -/TTGAG | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130161633 | AAAGAGGTTACAAAC[-/TTGAG]TTATTTTCTATTTGA | 50807 |
| rs547233001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130067542 | CTGGGACCACAGGTG[C/T]GGACCACCACACTCT | 50807 |
| rs547234128 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130054425 | CTTCTATTTGCAAAG[C/T]CAGCAGTTCCTATAC | 50807 |
| rs547235716 | snp | A/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130244970 | TTACAGCAGTTTGAG[A/G]AGTTGAGGTGTGGAG | 50807 |
| rs547236921 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130306987 | ACTCTTCTCATTCTG[A/G]CTCCTTCTGACATCT | 50807 |
| rs547244515 | snp | C/G | 0 | 0 | intron-variant | ASAP1 | GRCh38.p7 | 8:130160170 | AAGTCCGAGGCAGAG[C/G]TGGGGTCTGGGTCTC | 50807 |
| rs547256612 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130099649 | TGTCCTTCAGGGTCA[C/T]ACATGTTGTAGCACA | 50807 |
| rs547265440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130188481 | GCTTACGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 50807 |
| rs547265702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130179875 | ACTGGTCAAGATTTT[A/C]TATTGACACTGTTTG | 50807 |
| rs547269129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130153923 | AAGTGGTTGGGCATG[A/G]TGGCTCATGCCCGTA | 50807 |
| rs547273275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130381792 | CATTTCTGGAACACA[A/C]CCCCCTGAGGGCCTT | 50807 |
| rs547273685 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130251229 | TCAAGACCAGCCTGG[C/G]CAACATAGCGAAACC | 50807 |
| rs547273839 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130423935 | GGGGTGACTGCTAAT[A/G]AGTATGGATGGAGTT | 50807 |
| rs547288419 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130194401 | AAAAAAAAATCCTTT[C/T]TTGGAGATCTCAAAG | 50807 |
| rs547292545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130373796 | AGGTTGCAGTGAGCC[C/G]AGATCGTGCCACTGC | 50807 |
| rs547296674 | in-del | -/GAGGATGGAGTCACAAGCCCTTC | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130112035 | TAGACTATCAGCTCT[-/GAGGATGGAGTCACAAGCCCTTC]GAGGATGGAGTCACA | 50807 |
| rs547297900 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130194349 | ACCAATCTCAAGAGG[A/T]GGAAATTTTAGGAAA | 50807 |
| rs547299212 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130167234 | GAGGTCAAGGCTGCG[A/G]TGAGCCATAAGTGTG | 50807 |
| rs547321970 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130170373 | TTGATCAGGCTCGTC[C/T]TGAACTCCTGACCTC | 50807 |
| rs547323079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130119431 | GGGTGTAGTACTTTT[C/T]CCTTTTCTTGAGGAA | 50807 |
| rs547324168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145080 | CTGCACCCAATGAAT[C/G]TGCTAGATAGTCATC | 50807 |
| rs547327983 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130187826 | GTTCAGAAGGGCTGG[G/T]TCCCCAGTGGTCACA | 50807 |
| rs547339080 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130073126 | CTTTGGTAGGAGATA[C/G]AAATGTGGAGCTTTC | 50807 |
| rs547350985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130303184 | GCTAACATCTTAGAC[C/T]GTTTCTTCAGCTACA | 50807 |
| rs547374139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130270834 | AGCCATTTCCCTCAT[C/T]TGCTCAAATTAATTT | 50807 |
| rs547376914 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130234196 | TGTGATGATGGAGAA[G/T]TTTCTATTTCTGCAC | 50807 |
| rs547381567 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130079283 | GGGTCTGGAAGTGGC[G/T]CTCTGTCCTTTCCTT | 50807 |
| rs547411329 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130213894 | GGGGATGCCCACACA[C/T]GACTGCCTGGCAAAC | 50807 |
| rs547418604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130351181 | TAGATGCCTTTCTCA[C/T]GGGTCCTGCAAGACA | 50807 |
| rs547436593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130249540 | TTGTTCAACCTTTCA[C/G]ATTGGGTTTTATCAC | 50807 |
| rs547437711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130420523 | GGAAACAACCCAAAA[C/T]CTATCAGCCAAGGAA | 50807 |
| rs547440285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372026 | TTTGGGATTGTATAT[C/T]TAAGAGGCTTAGGGA | 50807 |
| rs547443406 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130427149 | AACAGCTTGGCCACT[C/G]TGTTCAGTGGCTATT | 50807 |
| rs547454966 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130339822 | ATTTCTAAGGCTCCT[C/T]CTGGCTCTAAAACTC | 50807 |
| rs547455495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130319442 | GGGTGGTGGGGATTG[C/T]TCCAGGCCCTGAATG | 50807 |
| rs547458365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130136710 | GTTTAGTTCAATGTA[C/T]AAATCCTAGATTCTA | 50807 |
| rs547461805 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130369939 | GTGATGGTATTACAA[C/T]GTGACACTTTTGAGA | 50807 |
| rs547483590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130242425 | AAGGCAAATGTTCTT[A/G]TATGTGTTATTCCTT | 50807 |
| rs547490207 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130322195 | AACTTCCAAAAGAAG[A/G]CTATGTAGGTATGCA | 50807 |
| rs547491276 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130346595 | AGACGATATGGGTAG[A/G]GCAATCAGCACAGTT | 50807 |
| rs547506129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130427828 | CCAACACAACCTGGA[A/G]GTGAAGGAGGTACAG | 50807 |
| rs547517386 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130314955 | CCCAGGTCTTCCACA[A/G]GTTAGCTGGGTGACC | 50807 |
| rs547519124 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130107845 | TGAGACACCACGCCC[A/G]ACCACCATAGTCTCT | 50807 |
| rs547520072 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130195038 | AAGCTTTTCAAATCC[A/C]TTATATAATTATTTC | 50807 |
| rs547523448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150258 | ACTTGTTAATTCAAG[C/T]CTTAAGAATGCATAT | 50807 |
| rs547534958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130337906 | TGGGGATGGCAATTA[C/T]AGCAACTATTTCTAT | 50807 |
| rs547556662 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130145482 | GCCACCACACCCGGC[C/T]ACTTTTCTGTATTTT | 50807 |
| rs547557471 | snp | A/G | 0.000148247 | 0.00860822 | missense | ASAP1 | GRCh38.p7 | 8:130112165 | GAGTCTGTGCTTGTG[A/G]AAACGAAGATCTGGT | 50807 |
| rs547574627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130275526 | GAAAACACCTTCTAA[A/G]CAGAGGTACACACAG | 50807 |
| rs547581722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364431 | TTATTCCCCATGTTA[C/T]ATGCATGGGAAACCT | 50807 |
| rs547582341 | snp | A/G | | | upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130445578 | GGTTCACTCGGTCCC[A/G]CAGCTCCCTGTGGCT | 50807 |
| rs547584654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130380954 | CAGTGGCGTGATCCT[A/G]GCTCACTGAAACCTC | 50807 |
| rs547592767 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130137839 | GGTCAAAACACTCTC[C/T]TGCCTGCCCATGTTC | 50807 |
| rs547606877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130236380 | ATACTTTTGCCTCCA[A/C]GGTGACAAAGTCACT | 50807 |
| rs547611218 | in-del | -/A/AA | 0.497981 | 0.041865 | intron-variant | ASAP1 | GRCh38.p7 | 8:130180908 | CAATGTCATTATTTA[-/A/AA]AAAAAAAAAAATACA | 50807 |
| rs547618463 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364955 | AATAAATAAATAAAA[A/T]AAAACACAAAAAACA | 50807 |
| rs547620744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098181 | TGGCAAGTCACAGCA[A/G]ATGAGCAGCTACGTC | 50807 |
| rs547626129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130093289 | TGCCAGGTATTCCAT[A/G]CTGGGCACTTTCACT | 50807 |
| rs547638864 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | ASAP1 | GRCh38.p7 | 8:130304374 | TGACACATTCACCCT[-/A]AAAAAAGGAACATCA | 50807 |
| rs547642481 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP1 | GRCh38.p7 | 8:130243293 | CTCTACCTTATTTTT[C/T]AGATGTTTAAGTACC | 50807 |
| rs547669267 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130262319 | ACAATAGCTTGAACT[C/T]GGGGGATGGAGGTTG | 50807 |
| rs547670562 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130425795 | TTCCTGTTCTAAAGC[A/G]GCTGACAGACTAACA | 50807 |
| rs547672005 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130064859 | TTCACAGAACTCAAA[C/G]AAACACTTACCTAAG | 50807 |
| rs547684448 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130124190 | TGTTTTTGAGATTTA[C/T]GAATATGTATTTTCC | 50807 |
| rs547687135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130139027 | CAATGGCATATGACC[A/G]CCTGAAAAGGCAGTG | 50807 |
| rs547700671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130324279 | TTAGGCTCACTTCTC[C/T]TTTAACAAAATGAAA | 50807 |
| rs547705772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130261558 | AACCCAGGGCATCTT[A/T]GATTGTGAGTAAAGA | 50807 |
| rs547720282 | snp | C/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130272764 | TAGAAAGAACAATAT[C/G]TTATGTTCTCACTCA | 50807 |
| rs547730621 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130127098 | GGTAATATAGTGCTA[C/T]TTGAAAATAAAAGTT | 50807 |
| rs547732041 | in-del | -/GAA | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130439243 | ACTGGAAAAGACAAG[-/GAA]ACAAATTCTTCCCAG | 50807 |
| rs547743094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130280908 | AGAATCCATGTCAGT[A/G]ATTTGTCTAACAGTC | 50807 |
| rs547752535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130320693 | TTCCACACAACCAGG[A/G]AGAAGTATCATTCCT | 50807 |
| rs547757127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130150698 | AGCTGGGCAACACAG[C/T]GAAACCCCTACCTCT | 50807 |
| rs547758838 | in-del | -/G | 0.00119784 | 0.0244435 | intron-variant | ASAP1 | GRCh38.p7 | 8:130108141 | TATGCCACACAGCAC[-/G]GCTACTTTCGTGCAG | 50807 |
| rs547764343 | snp | A/C/G | 0.00398691 | 0.0444912 | intron-variant | ASAP1 | GRCh38.p7 | 8:130192329 | ATTAAAATTTCACGG[A/C/G]GGGGAGCGATGGGGG | 50807 |
| rs547770063 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130059566 | CCTCAAGCGATCCAC[A/T]CGCCTCTTCCCAAAG | 50807 |
| rs547780636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130171569 | CACCTGGTCCTGCCC[C/T]TGACATGTGGGGATT | 50807 |
| rs547784568 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130210649 | GTGTCAGGTGGGCCT[C/T]TACCATCCACATAAT | 50807 |
| rs547786687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130350492 | CAATGAGGTAACACT[C/T]TGCTTTCCCACTTTA | 50807 |
| rs547820066 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130287300 | GATGTTGGGGGATAA[A/T]AAAAGATAAGATAGG | 50807 |
| rs547825765 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130317432 | TAGGAACAGGGTCTA[C/T]GACTCACTTAGCTGC | 50807 |
| rs547827959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130098590 | CCTGATCTCATGATC[C/T]GCCCGCCTCGGCCTC | 50807 |
| rs547858383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130065467 | CTCAAACCCACAAGA[C/T]GGGAAAAGATTAGAG | 50807 |
| rs547870740 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130090944 | AAGAGGTGAGACACA[A/C]AAACTAACAAATTTA | 50807 |
| rs547873759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130226789 | TAGCAGAAGCAGAAA[C/T]GTTCTCTCTTCTGGC | 50807 |
| rs547895672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130438280 | ATGGTGTGTTTCCTT[C/T]ACTCTCAGAAGATGG | 50807 |
| rs547902608 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130131830 | GCAAAGTGCAAAATG[C/T]GCAACTTCAGGGTGG | 50807 |
| rs547924193 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130315473 | CACTAATAATGTTCA[A/G/T]AATTGCAACAAATAG | 50807 |
| rs547931905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130060120 | ATAGAGAGAGAGAGA[A/G]AATACCCAGAACCCC | 50807 |
| rs547943399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130401353 | TGGGTTCAAGCAATT[C/T]CACTGCCTCAACCTC | 50807 |
| rs547960993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130372796 | GAGAGAGAATTCAGA[C/T]TGAAATGTATTACAG | 50807 |
| rs547968536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130228911 | GAAAACACCAGTGAG[A/T]AAAATCAGCACGGGG | 50807 |
| rs547975884 | snp | G/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130254859 | CCAATCTAACAACTT[G/T]AAACTTAGAACACAG | 50807 |
| rs547979551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130316314 | GTTTTGGTATCCATA[C/T]TGGTAAACATCAACT | 50807 |
| rs547981351 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130267914 | TCTTTCCTAAAACCA[C/T]GAACCTTCTTTGTGG | 50807 |
| rs547983591 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP1 | GRCh38.p7 | 8:130162930 | CTCTTCATCTGCCCA[C/T]ATAATTCCTAGGTCT | 50807 |
| rs548001091 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP1 | GRCh38.p7 | 8:130053246 | CTCTGCTTAAAAATA[C/T]TAGTTTTCTGTGCTG | 50807 |
| rs548003030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130356335 | AAAACTTATCTAGAA[A/G]GAAAATAACCACTCA | 50807 |
| rs548003621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130220479 | AGGAAATTTAAATTA[C/G]AATATGCCACCCCAA | 50807 |
| rs548003916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130309865 | GACTGACCAAGCAAA[C/T]TTCCTAGGTTTAGTT | 50807 |
| rs548005568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130213280 | ATTTGCTTATTCGCT[A/G]TGTAAGATTAATTCA | 50807 |
| rs548029803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130222344 | ACCTTTGATTCTCAG[C/T]GACTCTAATTATGGC | 50807 |
| rs548047777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130364026 | CTTTGTATGAGTGCT[C/T]CCCAATTGCACTCGT | 50807 |
| rs548065775 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP1 | GRCh38.p7 | 8:130301232 | TATTAAATGACATGT[C/T]GTACCAATGCCTGCT | 50807 |
| rs548066956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130310423 | GACCCCAGGAGTCAT[C/T]AAGCAAATACTCGGA | 50807 |
| rs548076041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130056894 | TACCTTGGCCTGGCA[A/G]TTCCCATCGGGAGAC | 50807 |
| rs548082881 | snp | A/C | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130391005 | ATAGCAGCATAATTC[A/C]TAACAACCAAAAGGT | 50807 |
| rs548083574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130440219 | TTTGCCCCCTATGAT[C/G]CATCCACTTTTCATA | 50807 |
| rs548094577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130077170 | TCACTTCCTCCACTA[C/T]AGCAAAGAGCTTGGT | 50807 |
| rs548099680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130335605 | TACAACCACCCTAGT[A/G]GAAAAAGAGATGGAA | 50807 |
| rs548100407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130123674 | CACTGTTGCCCAGGC[C/T]GGAGTGCAGGGGTGC | 50807 |
| rs548101567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130342665 | AACAAACTCACATGA[A/C]AAAGTGATGGGGTTC | 50807 |
| rs548106200 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP1 | GRCh38.p7 | 8:130308915 | GGCACGGTGGTGTGC[A/G]CCTCAAAAAAAAGAA | 50807 |
| rs548109032 | snp | C/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130127815 | TACGTGTTTTGTGTG[C/T]GTATGTGAGTGTGTC | 50807 |
| rs548123749 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ASAP1 | GRCh38.p7 | 8:130051631 | CCACATGTCTCCTGT[G/T]TGTGAATGAATGCCT | 50807 |
| rs548140712 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP1 | GRCh38.p7 | 8:130393863 | CCAAATTAATACTTT[C/T]ATAATTTCTTACATC | 50807 |
| rs548153797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130247794 | TAAAACCACAGAGGG[C/G]CTTTCCACTTAGCTT | 50807 |
| rs548159738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130129147 | GTGAAGAAAGACATG[G/T]TTGCTGCCCTTCCAC | 50807 |
| rs548165795 | in-del | -/TCA | 0.00636936 | 0.0560724 | intron-variant | ASAP1 | GRCh38.p7 | 8:130267053 | TCAAAAAAAAAGTAG[-/TCA]TCATTAAGAGGACAA | 50807 |
| rs548184218 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASAP1 | GRCh38.p7 | 8:130388715 | TTTAGAGGAAGGGAG[A/T]GATCAACTGGGTCAG | 50807 |
| rs548186607 | snp | A/T | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130136358 | CATGAAGTAGAAGAG[A/T]GACAGGGTGCAGTGC | 50807 |
| rs548189454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP1 | GRCh38.p7 | 8:130426061 | TAGAACTGTAATTCC[C/T]AGTGTCGGAGGAGGG | 50807 |
| rs548191563 | snp | A/G | | | intron-variant | ASAP1 | GRCh38.p7 | 8:130337892 | CAGCCAGTTCCCCAT[A/G]GGGATGGCAATTATA | 50807 |