SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs74728479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226165 | CAGCTGGCTGGCCAC[A/G]TAGACGATAATGCTG | 8853 |
rs74740619 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327224 | TCATCTTCTGACAGC[A/G]GAGGGGATGGGGACT | 8853 |
rs74801050 | in-del | -/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9375106 | GAGGCCCCATCTCTA[-/CA]AAAAAAAAAAAAAAA | 8853 |
rs74836872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373440 | TGCCCACTCAGTTCC[A/G]TCTGGGTGCTGTGGG | 8853 |
rs74849304 | snp | C/T | 0.030665 | 0.119967 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373108 | CAGTGCACGGGTTAG[C/T]GCTGTGTGGACGGGG | 8853 |
rs74862001 | in-del | -/CA | 0.386431 | 0.209491 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316969 | TCCCACACACCCCCC[-/CA]GTCACACCCTCTCAT | 8853 |
rs74867938 | snp | A/G/T | 0.0184529 | 0.0942665 | intron-variant | ASAP2 | GRCh38.p7 | 2:9403236 | TTAATAACAACCTAC[A/G/T]CTTTTCTCCATTTCA | 8853 |
rs74873794 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351113 | TGGCCCTGCTCCTTG[C/G]GGGCACTGTAGTCCT | 8853 |
rs74901074 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254034 | AATATAGTGAAACCC[C/T]GTCTCTACTAAAAAT | 8853 |
rs74918022 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9215271 | TCTGTGTGGTTCATT[A/G]TTGACTGAAATGTCA | 8853 |
rs74921310 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345251 | GCAGGACTCTGGGGA[C/T]CAGAAATCCATGAGA | 8853 |
rs74944996 | snp | A/C | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387213 | AGAGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAC | 8853 |
rs75042501 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351311 | AGGGTCTTCAACAGG[G/T]CCCTTGAAACTTCAG | 8853 |
rs75061115 | snp | A/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267926 | AAAAAAAAAAAAGAA[A/T]GATTATAAAGCCTGG | 8853 |
rs75073451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342500 | CACACCATAATCACA[A/G]TTAATTCAAAATGAG | 8853 |
rs75101012 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | ASAP2 | GRCh38.p7 | 2:9208731 | GGCAGATGGGGATGG[G/T]TGAATGAAATTTTTT | 8853 |
rs75114369 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351783 | AACTGCGGGTAATTA[C/T]CACTCCACCTCACCC | 8853 |
rs75121199 | snp | A/C | 0.0486741 | 0.148216 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378678 | TTGGCCCCACATGCT[A/C]AGCAACAACAGGGAT | 8853 |
rs75127033 | snp | G/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305501 | TTGGTGGAGAGGCTG[G/T]AGTAGTGGGGTATAG | 8853 |
rs75170319 | snp | C/T | 0.145978 | 0.227331 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375539 | CACAGGCTCATCCAT[C/T]TTTAATGGAGAGCAC | 8853 |
rs75171306 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330824 | AGCAACAGACCACTT[A/G]TGGAAAAGTGAAGTA | 8853 |
rs75189183 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9220849 | TGATGTGAGGTAGGG[A/G]TCCAACTTCATTCTT | 8853 |
rs75203841 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240925 | CTACTAGGTGACTCA[C/T]GGGCAGGTAGCATGG | 8853 |
rs75227558 | in-del | -/ATCA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317818 | ACACTCACACAATCA[-/ATCA]CACCCTTAGTCCCTT | 8853 |
rs75228444 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394838 | AGTGTCTGGAGCCTT[C/T]GCTGAAAGGACTCGA | 8853 |
rs75276642 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329774 | CCAGAGCAGGCTGTG[A/C]CACCAGCAGCCTACC | 8853 |
rs75296927 | snp | A/C | 0.0655868 | 0.168795 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337541 | AAAAATTCTAACCCT[A/C]CCTGTGTAATAACAG | 8853 |
rs75321072 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315150 | TTTGGAGAAATATGA[A/G]GATGAAACATGGAAA | 8853 |
rs75321088 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255694 | CAGAGCTGGTGCCAG[C/T]ACCATGTGGTGCTCC | 8853 |
rs75330699 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313887 | GTGTAAAATATGCTA[C/T]TATGTGGTATTCTTA | 8853 |
rs75336283 | snp | C/T | 0.000298919 | 0.0122217 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9401339 | CAACCCCGATGAGCT[C/T]ACCTTCTCCGAGGGG | 8853 |
rs75384948 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401468 | CTGGCTGGAGAGACG[A/G]GCTTGCAGGTGAGGT | 8853 |
rs75385207 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280124 | CAGGGGAGCTTGCCC[A/G]TGCTCAGGTGCAGAT | 8853 |
rs75387670 | snp | C/T | 0.0333238 | 0.124705 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230148 | GGATTTCTAGGCACT[C/T]ACAGTTTCAGAATAA | 8853 |
rs75388003 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320471 | CAGCCATGTTGCTGT[A/G]GTTCATTTTGATGAC | 8853 |
rs75460142 | in-del | -/TCAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317219 | CACTCACATCCACAC[-/TCAC]ACAATCACACAACCA | 8853 |
rs75463645 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337428 | AATAAGAATTGATCA[C/T]TTGGTCATTATTGTT | 8853 |
rs75477140 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229741 | CAAAGGGAGACTGGA[C/G]AGAGCATTCTGCAGG | 8853 |
rs75477606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9215254 | AATCTTATGAGAGGT[C/T]GTCTGTGTGGTTCAT | 8853 |
rs75486064 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268789 | GAGGGGAGAGGAGAT[A/G]GGACGGGAGAGCGGA | 8853 |
rs75488910 | snp | C/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302125 | ACCGCGCCCGGCCTT[C/T]TTTTTTTTTTTTTTC | 8853 |
rs75514341 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324600 | TTTTTAATAGCAGAC[A/G]CACTCTTCTCATAAT | 8853 |
rs75555464 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287602 | CAAGCCTTGACTCAG[A/T]TATGAGGGAGAGGAT | 8853 |
rs75555887 | in-del | -/ATCA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317039 | ATGCAATCATTCCCA[-/ATCA]CTCACATCCACACTC | 8853 |
rs75577775 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353414 | AATTTAAAAATAGTG[C/T]AGTATGGTGACATGT | 8853 |
rs75580202 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342721 | CTCAGAAATCCAAGA[A/G]GCTGCCTGTGCCTTG | 8853 |
rs75583680 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381202 | CCTCAGCCCCAGATC[A/T]TGTGGGTTGCTCAAT | 8853 |
rs75617317 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285044 | CACAGTGTGATGGTC[C/T]CTGGAGATGGGGCCT | 8853 |
rs75631220 | snp | G/T | 0.0766824 | 0.180169 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323522 | TCACGTACGTACTCT[G/T]GCTAAAATATTTATT | 8853 |
rs75698306 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332616 | CTCTCACTCTCGCTC[C/T]CTGTCTGACCGTAGG | 8853 |
rs75701656 | snp | C/G/T | 5.00332e-05 | 0.00500145 | missense | ASAP2 | GRCh38.p7 | 2:9388520 | CCACCAGCGCCCCCC[C/G/T]GCTTCCTCCACGGAA | 8853 |
rs75739053 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237414 | ACTGGGTCTTTTGGT[C/T]TTTTTTTTTTTTTTT | 8853 |
rs75747797 | snp | A/G | 0.000414319 | 0.0143871 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378913 | AGCCTGTGACACACT[A/G]TGCTCTCTCTCTGTT | 8853 |
rs75757576 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9273017 | CCCAGAGATAGTCAA[A/C]GCTCTTCTGAGCAAA | 8853 |
rs75823118 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373875 | ATGTACTCTGTGACC[A/G]GTGAGCTGCTGTTTC | 8853 |
rs75834907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214536 | TGAGCCGCTGCGCCC[A/G]GCTGCCTTTCCAGGT | 8853 |
rs75836447 | snp | A/G | 0.040671 | 0.13668 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323774 | GGTGGCCTGGGGAGC[A/G]CCTCTCTGCTCCACT | 8853 |
rs75870996 | in-del | -/CTC | 0.490287 | 0.0690083 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347072 | TCCACTTCCAGAGGT[-/CTC]CTCCTGCCTTTAGCA | 8853 |
rs75892964 | snp | A/C | 0.444444 | 0.157135 | intron-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212046 | CTTCCTCCCTGCCCC[A/C]TGGTGAATGCTGAAT | 8853 |
rs75909315 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221270 | ATCTTAACAATCTAT[C/T]ATAACCTCTTCTATC | 8853 |
rs75941749 | snp | A/C | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267900 | AAGACTCTATCTCAA[A/C]AAAAAAAAAAAAAAA | 8853 |
rs75987254 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9306526 | GAAGGGTTCCTAGGG[-/G]TGAGAGGGGCTTGAG | 8853 |
rs75997040 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254032 | CCAATATAGTGAAAC[C/G]CCGTCTCTACTAAAA | 8853 |
rs76008109 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371387 | TACTCATTTTGGTTT[C/T]TCCCACCGTAATATG | 8853 |
rs76025585 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277765 | CTCTTGTACATTCCA[C/T]GGGCTTGGACAAATG | 8853 |
rs76026369 | in-del | -/AC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318005 | CCCCAACACACACAC[-/AC]GTCTTTTCTCATTCG | 8853 |
rs76055763 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243511 | AGAAGTAACTGTTAA[A/T]ATACAACTTTGCTTA | 8853 |
rs76064913 | snp | C/T | 0.100231 | 0.200173 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323510 | TTCTTTCTGGCTTCA[C/T]GTACGTACTCTTGCT | 8853 |
rs76093336 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348345 | GGTCAGGCTGATCTG[A/G]AACTCCTGATCTCAG | 8853 |
rs76125556 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294828 | CGGCCCAGCTCCCCT[C/T]CTTTGTCATCTCTTG | 8853 |
rs76132998 | snp | G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265509 | GGATAGTACTTTTCA[G/T]TTTCTTTAATTCGAA | 8853 |
rs76133929 | snp | A/C | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354645 | AGTGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 8853 |
rs76137049 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282512 | TTTTTAGAACTAGAT[G/T]TCAGAAATAAGTCAG | 8853 |
rs76162549 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351374 | AATAGTCTTTCTGCT[G/T]CTCTGTGCTTTTCCT | 8853 |
rs76184126 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402597 | GCTTAGCCATGTGGA[A/G]AATACCTGCTCATTT | 8853 |
rs76209774 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212366 | GGCTGTGGTGAGGGA[A/G]GGCCTTATATGATGT | 8853 |
rs76236671 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244653 | TACTGGACTGAAGGA[C/T]AGAATCACTAACCTG | 8853 |
rs76238372 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366124 | TTGCTTTTGTCGATG[A/G]GTCTGGAGGGGTTCT | 8853 |
rs76255639 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386396 | TGCCTTAAAAAAAAA[A/G]AGCTGGAAGCAGTCT | 8853 |
rs76263433 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281768 | TTGTGAGTGGTTATC[A/G]TTCTTAACCCTTTCC | 8853 |
rs76282465 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355073 | TGTTAACATCTTAAT[A/G]CAGTTATCCAGTAGT | 8853 |
rs76342720 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251536 | AATAAGTAAAGATAA[C/T]GTGCATTTTACACTT | 8853 |
rs76359641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366656 | TCTAGGCTTTTGCCT[C/T]CTGACTGATGGCTTG | 8853 |
rs76370470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289289 | TTTGTTTCTTGCCTT[C/T]GTGTCGCTGCACTGA | 8853 |
rs76371508 | in-del | -/TTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240243 | ATGTCTTCCTCCCAT[-/TTT]AATTTTTTTTTTTTT | 8853 |
rs76403703 | snp | A/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271102 | CCGGCCCTGTTTTCA[A/T]TTTTTTTTATGGCTC | 8853 |
rs76419341 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302290 | CGATCCTTCTGCCTC[A/G]GCCTCCCGAGTAGCT | 8853 |
rs76425240 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334524 | AAATCTCAAATACTT[A/G]AGCTTATTGCATTTC | 8853 |
rs76439878 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372683 | AAAAACCAGTAAGAT[A/C]ATGATTCACCCACTT | 8853 |
rs76440887 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342746 | GCCTTGGGATGCAGT[C/T]GAAACTCTGACTCCA | 8853 |
rs76444524 | snp | A/T | 0.139564 | 0.224285 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383275 | AGTAAACAATTTTTT[A/T]AAAAAAAGACAGTGT | 8853 |
rs76455463 | snp | C/T | 0 | 0 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404744 | TGTGTAGAGTTTTTT[C/T]TTTTTTTGGCATTGT | 8853 |
rs76470744 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259657 | TCAGGCCCCCTGCCC[C/T]GAGGCTGGACCGCTG | 8853 |
rs76484209 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305529 | TAGATATTGGTGGAG[A/G]GGCTGTAATAGTGGG | 8853 |
rs76503717 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226379 | AGGGAGCGGGGTCAC[C/G]TCCCTGAGGCCATGC | 8853 |
rs76509009 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9216785 | TTTTTGTATTTTTTT[A/G]TAGAGAAGGTTTCAC | 8853 |
rs76541041 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350676 | AAGCCTTCCTCTGTC[A/T]AGTCTGAAGGCCACC | 8853 |
rs76600376 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328868 | AGACAAATTTCTAAT[G/T]AGATGTTTACAAAAT | 8853 |
rs76613341 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352224 | ACAAACACACACACA[A/C]ACACACACACACACA | 8853 |
rs76635501 | snp | C/G | 0.111576 | 0.20818 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294437 | GTGAGAAGGCCGGCT[C/G]CTCTCTCCTACCAAG | 8853 |
rs76650743 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9215611 | ATCCAAGTTTATGGA[A/C]CCCCTGGATTCAGAC | 8853 |
rs76662113 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355207 | CCCCAAATGTCCTTT[C/T]TTCTGTTCCAGAATT | 8853 |
rs76664994 | snp | A/C | 0.5 | 0 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213614 | TGGATGAGGAGGTAG[A/C]AGGGGGGGTGGTGGT | 8853 |
rs76669851 | snp | A/G | 0.0948562 | 0.196037 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377632 | TTTGACTCCCTGATC[A/G]TGGTTTGAGCCATGT | 8853 |
rs76670954 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275436 | GATCACTCTGTCATC[C/T]GTGGGAGTATCAGAG | 8853 |
rs76671984 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243587 | ACTTCCTAGGTCTAG[C/T]TTGGTGGAAACCAAA | 8853 |
rs76703680 | in-del | -/AA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311367 | TCTCTCAAAAAAAAA[-/AA]GAAAAAAAAAGTTTG | 8853 |
rs76774777 | snp | A/C | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375109 | GCCCCATCTCTACAA[A/C]AAAAAAAAAAAAAAA | 8853 |
rs76797410 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227492 | TTTAAAATAAGCTCT[C/T]ATTTGTATTTATACT | 8853 |
rs76823898 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299607 | CCAAGAGGATCATGG[C/G]GAAGGGAAGTCCCAG | 8853 |
rs76830222 | snp | C/T | 0.114036 | 0.209795 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323794 | TCTGCTCCACTCCAT[C/T]CCACCCGCAGCCTCA | 8853 |
rs76847510 | snp | A/C | 0.0766824 | 0.180169 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322864 | CCTCCAAGCCCTGTG[A/C]AGACTTCCTACCTCC | 8853 |
rs76903871 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316787 | CTTCCATTCCACCCA[A/G]TTTAATCCATGCGGA | 8853 |
rs76919748 | snp | G/T | 0.174932 | 0.238463 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397729 | AAAAAATCAAAAGGA[G/T]ATATATATATATATA | 8853 |
rs76954072 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318881 | AAAGTAAAGAGTTTC[C/G]GTCTCTCCAGGGAGC | 8853 |
rs76960479 | snp | A/C | 0.5 | 0 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9388500 | CCAGCCTGCAGCCCC[A/C]AGCACCACCAGCGCC | 8853 |
rs76991702 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368576 | TTGCCTTTGCCCGAG[C/T]CCCGGGAGGCAGGGG | 8853 |
rs76995309 | snp | A/C | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252917 | GAGACTCCGTCTCAA[A/C]AAAAAAAAAAAAAAG | 8853 |
rs77021823 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234640 | CCAGAAGCTGGGCTG[C/T]TTCTAATCAGTTAAA | 8853 |
rs77048896 | snp | C/T | 0.103082 | 0.202275 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363825 | GTGGTCTTCCAGCCT[C/T]GGCTTCCCAAAGTGC | 8853 |
rs77056688 | snp | A/C/G | 0.00716266 | 0.059414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363450 | CTGCCAACACTTGCT[A/C/G]TCTTTTGTCTTTTTG | 8853 |
rs77088468 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325283 | TGGCAGAGAAATCAG[C/T]GAGACAGCATGAGAC | 8853 |
rs77097987 | snp | A/G | 0.111928 | 0.208413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292636 | ATCTGCTCCTTCTCT[A/G]CTCGACAAGTCTTAC | 8853 |
rs77098033 | snp | A/G | 0.0341408 | 0.126114 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214205 | TCCAAGTGGATTGCT[A/G]GGGCCCTTCCAGGTA | 8853 |
rs77106027 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288227 | TCAGACCTTGAGCTT[A/C]AATCTTCTACCAAAT | 8853 |
rs77123349 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254033 | CAATATAGTGAAACC[C/T]CGTCTCTACTAAAAA | 8853 |
rs77152227 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310885 | TGGCCTATCTTTGTT[G/T]GCTCATCAGCTGTGA | 8853 |
rs77188829 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402600 | TAGCCATGTGGAAAA[G/T]ACCTGCTCATTTCCA | 8853 |
rs77214461 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254031 | GCCAATATAGTGAAA[C/G]CCCGTCTCTACTAAA | 8853 |
rs77298713 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245108 | TCACTTTGATACCCA[C/G]TTTGTAGGACTGCGG | 8853 |
rs77331530 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364109 | CATATGAAAAACAGT[A/G]TCACTGGTACTAGGG | 8853 |
rs77337435 | snp | C/T | 0.11228 | 0.208646 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290812 | CTGGGCTTGTTCACA[C/T]TCTGACAGTCTGTTT | 8853 |
rs77349882 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271363 | TAATATATGTTCTTG[C/T]ACCTGTCACCCTGTA | 8853 |
rs77350835 | snp | C/T | 0.133777 | 0.221342 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346104 | CTCCCCCTGCCCCCG[C/T]GACCCCAGGGCCATG | 8853 |
rs77474233 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338353 | TCTGTCTCTATCTCT[C/T]TCTCTCTCTCTTTCT | 8853 |
rs77488356 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341049 | CTTCGTCTCTCTTAG[A/G]AAAGTGGAGAGTACA | 8853 |
rs77491914 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381722 | AGCCTGGGCAACAGA[A/G]CAACACGCCATCTCC | 8853 |
rs77492666 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270482 | TTATGGGGTACATGG[A/G]ATATTTTGATACAGG | 8853 |
rs77493731 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222433 | TGTGTTCTCTGCAAC[C/T]GCAAACCCTTTCCAA | 8853 |
rs77521103 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305537 | GGTGGAGGGGCTGTA[A/G]TAGTGGGGTACAGAT | 8853 |
rs77526986 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276319 | CGGGCTGGGAAGACA[G/T]CAGGGGGAGGGGGAG | 8853 |
rs77577589 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280235 | GTGTCCCCTCACCCT[C/T]GTGGTGTCTTTCTTT | 8853 |
rs77711980 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324292 | AGCAGACTCTTAAGT[G/T]GTCAGCAGAGAGGAA | 8853 |
rs77712790 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383819 | ACATATACACCGTGC[A/G]ATACTGTGCAGCCAT | 8853 |
rs77739960 | snp | A/G | 0.127944 | 0.218179 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212363 | TGGGGCTGTGGTGAG[A/G]GAGGGCCTTATATGA | 8853 |
rs77740548 | snp | C/T | 0.0182019 | 0.0936463 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9405090 | AATAAAGTTGATTCA[C/T]ATCAACATTAGAACT | 8853 |
rs77819526 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9277172 | CTGAGGAGCACCGTG[A/T]ACTGGCACCTCTATG | 8853 |
rs77822720 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312479 | CTGCCCCCACCTCAC[A/G]ATGCCCCATCTTTTG | 8853 |
rs77869394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347983 | TAAAGCTGTTGCATC[C/T]TTTTTTTACCATTCC | 8853 |
rs77878163 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331224 | CCAGATTCCAGGGCT[C/T]AGGTTTGGCTGTTGA | 8853 |
rs77882822 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262528 | CCGTTTTTGAGGTCA[C/T]GCGGCTAGTAATTGG | 8853 |
rs77896350 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298834 | TTAGCTTCCTGGTGC[C/T]TCACACTTCAGTACA | 8853 |
rs77896360 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | ASAP2 | GRCh38.p7 | 2:9224969 | CAAAGGAGGGCATGG[G/T]AGGGCTAGCTTGAGT | 8853 |
rs77904775 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222853 | CACCTTTTCCTTGGG[A/G]ACTGGGATGCTTATG | 8853 |
rs77909952 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402598 | CTTAGCCATGTGGAA[A/G]ATACCTGCTCATTTC | 8853 |
rs77911357 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322107 | AGGGACCCTCCAGTC[A/G]CACTCCTTTCCGGAT | 8853 |
rs77984995 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343883 | ACTGTGGTAGATTCA[A/T]TCAGATTCTCAGCTG | 8853 |
rs77991637 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316696 | CCTGACTGAAGTTTC[A/G]CATCTTGAGTTGACT | 8853 |
rs78013848 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373225 | GTGTGATAAAAGTGC[C/T]AGAGCACAAGTTCAC | 8853 |
rs78014232 | snp | A/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272945 | ATGCAGTTTTGCTTA[A/T]TATAGCTCTATAGTA | 8853 |
rs78021400 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248537 | TTGACCCCAGTGAGA[A/G]TCAGCGTTTTGGGTC | 8853 |
rs78039204 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291583 | TCGTCATGTCATCCG[C/T]CTAGGGAGAGTCTCC | 8853 |
rs78046784 | snp | A/G | 0.040671 | 0.13668 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341453 | CAGGGTGATTTCATT[A/G]TCACCTTCTGGCATA | 8853 |
rs78066003 | snp | A/G | 0.111576 | 0.20818 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294433 | ATCAGTGAGAAGGCC[A/G]GCTCCTCTCTCCTAC | 8853 |
rs78078589 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320431 | GATTGTCCAAATAAA[A/C]CTTAATCCAGAAAAG | 8853 |
rs78078899 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310557 | TTCTAGATGGGATCC[C/T]TTTGGGCAAGATCAT | 8853 |
rs78095412 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230342 | GAGGGGCTGCGTGGG[C/T]CTGCTGCCACTGCGA | 8853 |
rs78100522 | in-del | -/TT | 0.132066 | 0.220435 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389316 | GGAGGCTGCTGAGAC[-/TT]TGATGCGGGGCGGGG | 8853 |
rs78108342 | snp | A/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281138 | AAGTATCTTGGAAGA[A/T]TTTTTTTTTTTTTAC | 8853 |
rs78108987 | snp | C/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385102 | GAAGTAGGCAGAGGG[C/G]CGGGGGCTTCACCTG | 8853 |
rs78110466 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242795 | GCCGTCTGGGGAAGC[A/G]TGATGCTGGGGAAGT | 8853 |
rs78131214 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351626 | GCAGAGGACCACGCC[A/G]GACTGTGTACTGTAG | 8853 |
rs78162467 | snp | C/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256162 | TTCTAGGGTCCCCTG[C/G]AAAAAAAAAAAAAAA | 8853 |
rs78175831 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392668 | TGATAAAAAGAAAGA[A/T]CATAAGCTGGATCCC | 8853 |
rs78182286 | snp | C/G | 0.0663309 | 0.169604 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267621 | GATTATGAAGGCCAC[C/G]TGCAGTTTCTCATGC | 8853 |
rs78213047 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267227 | ATGCTGAGTTTTGGG[A/G]CATGATTGATCCCAT | 8853 |
rs78245345 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338449 | CAGCCAAGGTCCACC[A/C]CAGCCATAATTTTCT | 8853 |
rs78272904 | snp | G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9391594 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTCACT | 8853 |
rs78278657 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373134 | CGGGGAGCATGTGCC[A/G]GGGGACGTTGAGGCA | 8853 |
rs78288734 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402859 | AATGGGGCCAACTTA[C/T]ACCTTTGCCACTTTA | 8853 |
rs78290084 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278512 | AGCGAGACCCCTTCT[A/C]AAAAAAAAAAAAAAA | 8853 |
rs78306708 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338446 | AGGCAGCCAAGGTCC[A/C]CCACAGCCATAATTT | 8853 |
rs78334531 | snp | C/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221811 | CTTTTTTTTGTTTTT[C/T]TGAGACGGAGTCTCG | 8853 |
rs78386604 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9283082 | AGATTCTTTTTTTTT[-/T]CCTCTCTTTTTTTGA | 8853 |
rs78409279 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303739 | TAAGGCTGGTGTCAG[A/T]TATCTACATTTTGGT | 8853 |
rs78423025 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352302 | CAAAAAAGGCTTGAA[C/T]TGAAGAGTTTCAGAA | 8853 |
rs78444842 | snp | C/G | 0.030665 | 0.119967 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371288 | CTCTGTGCTCCTATA[C/G]CATTTGGCTCTATTT | 8853 |
rs78448775 | snp | A/T | 0.0667028 | 0.170006 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383276 | GTAAACAATTTTTTT[A/T]AAAAAAGACAGTGTC | 8853 |
rs78450765 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365310 | CACCCTTCGGGGATC[C/T]AAGGGGCCCAGTTAA | 8853 |
rs78474421 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323476 | AAAAGTAGAGAAAAA[C/T]CACTAAATGTCTAGA | 8853 |
rs78475568 | snp | A/C | 0.0722614 | 0.17581 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352248 | ACACACACACACACA[A/C]ACACACACACCACTG | 8853 |
rs78505509 | snp | A/G | 0.084364 | 0.187256 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317039 | ATGCAATCATTCCCA[A/G]TCACTCACATCCACA | 8853 |
rs78514957 | snp | A/T | 0.0777841 | 0.181223 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403502 | AGTAATTGTTTTTAT[A/T]ATTTGTGGTTTTCAT | 8853 |
rs78581833 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398865 | TATCTGCCTCTTTAA[A/G]GAAAAAGTCTGCTCA | 8853 |
rs78624469 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332689 | CTCCCTCTCCCTGGG[C/T]GGTTTTGCATTTATC | 8853 |
rs78633623 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341509 | TCCCTTATCCTGTTC[A/G]TGAGACCTGAAAATC | 8853 |
rs78647844 | in-del | -/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281136 | AAAGTATCTTGGAAG[-/TT]ATTTTTTTTTTTTTT | 8853 |
rs78680915 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365883 | TGAGGCCACAGGAAG[A/G]GCGACGGACTGGGCT | 8853 |
rs78681468 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326759 | ATTGGCTTAGTGGCC[A/G]CACAGTATTTTCTGT | 8853 |
rs78705158 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319125 | GCAGACGGGGCTGGA[A/G]GGGCGTTTGCTCATG | 8853 |
rs78705616 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337986 | TTTGGAGAAGATCCT[A/G]TTTACACAGTTAAAC | 8853 |
rs78718696 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298903 | AGAAAAATGAACGTA[A/C]GGGAAGACTGGGATG | 8853 |
rs78733073 | snp | G/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305491 | GGTATAGATATTGGT[G/T]GAGAGGCTGTAGTAG | 8853 |
rs78737303 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364356 | CTACAAAAAAAAAAA[A/G]GTTAGCTGAGTATGG | 8853 |
rs78741835 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399238 | TTGCCTTCCCCTTCC[C/T]TTCCTCCCTGGTCTT | 8853 |
rs78773801 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231868 | GAGAGCTGGGCTGTG[C/T]CCCTCCCACCCACTT | 8853 |
rs78792604 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331031 | GCAGAGTAAGAGCTC[A/G]CAGCCGTGCGTGTTT | 8853 |
rs78821377 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9280541 | ACAGAAGACGCACAG[A/G]AATCCTACATCAACA | 8853 |
rs78838506 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359652 | AATTTAAAAGTTTAC[A/G]TGTAGGGAATTTAAC | 8853 |
rs78846345 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327092 | CTCCTTGGGCTGCAG[A/G]GAGACCTCAGCCAGC | 8853 |
rs78897974 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337050 | GGTTATTTACAGCTT[C/T]GCAGGAAAGTAATAA | 8853 |
rs78960434 | snp | C/T | 0.030278 | 0.119257 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226201 | CAGAAATCAACATTA[C/T]AATAAAACTCTTAAA | 8853 |
rs78968854 | snp | C/T | 0.135143 | 0.222054 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355064 | TTTCCCTTCTGTTAA[C/T]ATCTTAATACAGTTA | 8853 |
rs78989801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234669 | AAATGAGTAGGTAGA[A/G]CCAAGGTGAAGGAAG | 8853 |
rs78990137 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326971 | AATTTGATACATTAC[C/T]AAATATTTAATATCA | 8853 |
rs79044067 | in-del | -/AAAA | 0.232651 | 0.249397 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344433 | ATTTTTGTTGTTGTT[-/AAAA]AAAAAACACATTAGG | 8853 |
rs79066860 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331766 | AGCGATTTTTTTTTT[-/T]TYAAAAAAAATACAA | 8853 |
rs79067858 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256819 | CCTCTGTGTGACAGA[A/G]GAGTTGGGTTTTAAA | 8853 |
rs79069313 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235444 | TGTTATTTCACTCGC[A/G]GAGTTCAGATGTTGT | 8853 |
rs79103917 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9334912 | TGTGTTTTCATGCCG[A/T]GCCGCCCACGTGGAG | 8853 |
rs79114090 | in-del | -/CT | 0.242201 | 0.249878 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343405 | ACTGGCACTGGTGGC[-/CT]CTCCTACTCTCAACT | 8853 |
rs79118327 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214184 | CCTTTTCTGTGTAAT[A/G]TGGCCTCCAAGTGGA | 8853 |
rs79125280 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368203 | CTCTATCCAGAGCGC[A/G]TTTTATGACAATGCG | 8853 |
rs79127269 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268207 | TAGCATTCTGTTGTA[C/T]GAATGTCCATCATCA | 8853 |
rs79136417 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278516 | AGACCCCTTCTCAAA[A/C]AAAAAAAAAAAAGAA | 8853 |
rs79157769 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318111 | TGGAGACTGGGGCCT[A/G]GGGCCCAGAGCACCA | 8853 |
rs79178116 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212945 | CTTGGGCGTTTGTGA[A/G]GCAGAGCTGCCTGGC | 8853 |
rs79194352 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357370 | TGTAGTCCCAGCTAC[A/G]TAGGAGGCTGAGGCA | 8853 |
rs79221312 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377946 | CGCAGCAGGGGTTTC[A/G]TAAACATTTGGTTGA | 8853 |
rs79250389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379727 | AATAATCAGACCTCA[C/T]TGACTGAGGCTTATT | 8853 |
rs79285835 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330315 | GTGAAACAAGCCAGC[C/T]GCAGAAAGACAAATA | 8853 |
rs79329830 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338319 | TCTCTGTCTGTCTGT[G/T]TCTGTCTATCTCTCT | 8853 |
rs79342201 | in-del | -/TA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9403128 | TTTACCTAAGTAATT[-/TA]CCTTGTCGGAAGAGT | 8853 |
rs79349755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344196 | ATCACCTCCCTCCTC[A/G]AGGGCTACTGTGGCC | 8853 |
rs79380613 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380605 | GCCTCGACTAGGTCA[A/G]ACTCACTGTGGATTT | 8853 |
rs79383218 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367926 | ATCCCATTTTACTGA[A/T]GAAAACTCTGCCGCT | 8853 |
rs79388546 | snp | C/T | 0.030278 | 0.119257 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373439 | CTGCCCACTCAGTTC[C/T]GTCTGGGTGCTGTGG | 8853 |
rs79396378 | snp | A/C | | | intron-variant, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9287096 | CAACAGTTGGAGGAG[A/C]TGAGATTCAAAACCA | 8853 |
rs79444693 | in-del | -/G/GTTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275088 | ATTTGTCTGTTTTTT[-/G/GTTT]TTTTTTTTTTAAGAG | 8853 |
rs79478027 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303429 | GCGAGCTGAAGAGCA[A/G]GGTGACTTGGCTTGT | 8853 |
rs79486305 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262976 | TCCTGGGGAAATCAG[A/C]CTGGCTTAGGATTCC | 8853 |
rs79511504 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359004 | GATATGTTGCCAGAT[G/T]GGTTTGGATAATTAG | 8853 |
rs79533074 | snp | A/G | 0.103438 | 0.202533 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288205 | CCAACCTACCAAGCA[A/G]AAAAGCTCAGACCTT | 8853 |
rs79540965 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382488 | CTGCACATGTAGAAC[A/G]GAACTAGCTATCTAC | 8853 |
rs79547913 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274824 | CAGATTGTAGAAAAG[C/G]AAGTTTATGCACTCA | 8853 |
rs79560769 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248555 | AGCGTTTTGGGTCTC[C/G]GTTTCTTCCTCTGTA | 8853 |
rs79579727 | snp | G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364357 | TACAAAAAAAAAAAA[G/T]TTAGCTGAGTATGGT | 8853 |
rs79588973 | snp | C/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305494 | ATAGATATTGGTGGA[C/G]AGGCTGTAGTAGTGG | 8853 |
rs79589871 | snp | C/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238681 | TTGTTTCCCTTTTTG[C/G]CCAGTTTTTTTTTGG | 8853 |
rs79594362 | snp | A/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264195 | GACCCTGTCTCAAAA[A/T]AATAATAATAATAAT | 8853 |
rs79600977 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252599 | CCGCCCCCCAAAAAA[A/G]GCCTTCGGAAGACAG | 8853 |
rs79601624 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222663 | CGGGCTGTCAGAACC[C/T]GTAGCTTTGGTTTGC | 8853 |
rs79615401 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212111 | TGATGCCACTCCTCA[C/T]GGGTTCCAGGTCCTG | 8853 |
rs79659186 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339883 | CACATTCACTCTAGG[A/G]GAGGAGGGACCTGTT | 8853 |
rs79665353 | in-del | -/TTGT | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406087 | GCCTTCAGTGTGTGT[-/TTGT]CACTGAGTGGACCTC | 8853 |
rs79719463 | snp | G/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305569 | TTGGTGGAGGGGCTG[G/T]AGTAGTGAGGTATAG | 8853 |
rs79726561 | in-del | -/GCCCAAAACCTTA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9259555 | AGGGCACAGTTTTCA[-/GCCCAAAACCTTA]AGGAACAAAAATGAA | 8853 |
rs79727792 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354473 | GTGCAGTTTTTACAC[A/G]TCAGAATGCAGAAAT | 8853 |
rs79730536 | snp | C/T | 0.140919 | 0.224948 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341232 | AGGCCTTCACCTGGT[C/T]AGGCGTTTTGTACAG | 8853 |
rs79748173 | snp | C/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334043 | CTGTCTTTCTCCTTT[C/T]TTTTTTTTTTTTTTT | 8853 |
rs79751932 | snp | G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238679 | GTTTGTTTCCCTTTT[G/T]GGCCAGTTTTTTTTT | 8853 |
rs79755039 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325835 | TCTGCAGAGCTGGCA[C/G]TTGGAGGGGTCAGGC | 8853 |
rs79769175 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318159 | CTTATGGGTGGAGCC[A/G]TGATTGAGAGTCAGA | 8853 |
rs79805479 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399962 | TCTCTGATAAAAGGG[G/T]ATGAGAAAGGGGCAG | 8853 |
rs79810957 | snp | C/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302121 | AGCCACCGCGCCCGG[C/T]CTTTTTTTTTTTTTT | 8853 |
rs79811466 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319379 | CCTCTACAGAGGCCT[C/T]TCAGGGTCTCCTTCA | 8853 |
rs79822951 | snp | C/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369029 | AAGCTTTTTTTTTTT[C/T]TTCTGGGAGACGGAG | 8853 |
rs79824969 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294315 | CTAATTTTTTTAAAA[A/G]GAAAAAAACTTAACC | 8853 |
rs79825515 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379144 | GCGCTGCTCTTGGAA[A/G]CAGGGCCAACCCTGT | 8853 |
rs79865770 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239647 | GCACCATTTATGTGC[C/T]GGCCATTTGGACCCA | 8853 |
rs79908288 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341746 | TTGTTCTCAGCAACG[C/T]TGAAAGCTGGATTTG | 8853 |
rs79922391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233813 | ATCATCCCCATGTTT[A/G]AAGAAGAGGGGAGTG | 8853 |
rs79960426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228912 | TGTCAAATTTCTGTG[A/G]CATTTCCAGCAGCTT | 8853 |
rs79997117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377046 | CCTTGGTATTTCTGG[A/G]GAAGGAATCGGACGC | 8853 |
rs80008657 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225578 | GGGCTGAGCATGTCA[A/G]TTGGAAATTGATTCA | 8853 |
rs80029340 | snp | A/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267925 | AAAAAAAAAAAAAGA[A/T]TGATTATAAAGCCTG | 8853 |
rs80048273 | snp | A/G | 0.0879971 | 0.190408 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382294 | TGACCTGTCTCATTT[A/G]ATCTTCATAGCTACC | 8853 |
rs80164902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342683 | AAATTAAAAAGTTTT[A/G]TGCTTCAGAATCTTT | 8853 |
rs80165485 | snp | A/G | 0.135825 | 0.222405 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382523 | CTTGAGAGAACTGAG[A/G]AAATAGCCACACAGA | 8853 |
rs80177391 | snp | A/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331767 | AGCGATTTTTTTTTT[A/T]CAAAAAAAATACAAC | 8853 |
rs80181094 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237170 | AGCTTTTTTAAAAAA[A/T]GAGAGTTAAAAAAAA | 8853 |
rs80224131 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315196 | GGAGAGTGTGAAATG[C/G]AGGAATAAGTAGTTT | 8853 |
rs80270860 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396021 | ATCCAGACACCGTCC[C/G]TTTTGCCCTCTCCAA | 8853 |
rs80285875 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336818 | CAGGAGCCAGAATGC[C/T]GTCCAAGGTGGCTGC | 8853 |
rs80287320 | snp | C/T | 0.108402 | 0.206034 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287128 | GTGAGCGTCCCGTCT[C/T]TGCTTCTGACTGCTG | 8853 |
rs80288965 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358014 | CTATCATCTGCTAAA[C/T]GTATGGTAGGTCATG | 8853 |
rs80295949 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315347 | AAGGAGCAGTGAGGC[A/G]CAGCCAAGGCAGTGG | 8853 |
rs80317053 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273561 | AATTTTATTATTATT[C/T]GAATCAGTCTCCTGG | 8853 |
rs80340978 | snp | C/T | 0.0619672 | 0.164753 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358734 | TACTGGAAGCTCAAA[C/T]CTGCCCTGTTCTCTT | 8853 |
rs80354795 | snp | C/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347982 | CTAAAGCTGTTGCAT[C/T]TTTTTTTTACCATTC | 8853 |
rs111070422 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406113 | TGGACCTCTGTGACA[C/T]CT | 8853 |
rs111206548 | snp | A/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317133 | TCACAACCACACAAC[A/T]CACATCCCAATCACA | 8853 |
rs111206549 | snp | A/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317444 | CACATACTCACATTC[A/T]CACACACACATGTGC | 8853 |
rs111229580 | in-del | -/CTTT | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352376 | CTCAGGGTTTTAGGC[-/CTTT]CTGTTTTCTGAACTA | 8853 |
rs111230434 | snp | A/C | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340678 | TCGACAAGCTTGTCA[A/C]TCACAGGAATTGTCT | 8853 |
rs111238496 | in-del | -/GGT | 0.394354 | 0.204112 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289989 | TGGCAGGAAGAAGCC[-/GGT]GGTGAGAGGCATCCT | 8853 |
rs111241007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370871 | GGTGAAGGAAACGTC[A/G]TGAATCCAGCATGGC | 8853 |
rs111254075 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350681 | TTCCTCTGTCAAGTC[G/T]GAAGGCCACCTTTGC | 8853 |
rs111266397 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292163 | AGTGAGTATAGCAGC[C/G]CTGAGGAGGTGGGGA | 8853 |
rs111281823 | snp | G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305291 | GTATAGATGTTGGTG[G/T]AGAGGCTGTAGTAGT | 8853 |
rs111286552 | snp | C/G/T | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241602 | TGGTGGCGCCGTGAT[C/G/T]GCACCACTGCACTCC | 8853 |
rs111300023 | snp | C/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393842 | TGTCTTACAAATGTA[C/T]ATTTTAAGTCCACAG | 8853 |
rs111318830 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323963 | AATGGCACATGGAAA[C/T]AGCTGCCACCTCTGC | 8853 |
rs111321038 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309238 | AAATGTCCATCAGCA[A/G]GTGTCTGGCTAGACG | 8853 |
rs111321820 | snp | A/G | 1.64751e-05 | 0.00287007 | missense | ASAP2 | GRCh38.p7 | 2:9358809 | TGCATCGAGTGTTCC[A/G]GAATCCACCGAGAGC | 8853 |
rs111387721 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363651 | TGCAGTGGTGCCATC[C/T]CGGTTCAGTGCAGCC | 8853 |
rs111393668 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347043 | TTGGAGGGGAAAACC[C/G]TCTCCAGGGAATCTC | 8853 |
rs111401686 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403360 | GCATTAACAGTTATG[C/T]TCCTGTTTCGTTATT | 8853 |
rs111424665 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386950 | GGGCTCACGCCTGTA[A/G]TCCCAGCACTTTGGG | 8853 |
rs111440832 | snp | C/T | 0.000100624 | 0.00709238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323293 | CAGCCCAGGCTGTGC[C/T]GGCTCTGCCCTCACC | 8853 |
rs111447041 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244188 | GTGGTCTGAGCTACT[A/G]GGGAGGCTGAGGTGA | 8853 |
rs111459392 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367263 | GTCTCGAACTCCTGA[A/G]CTCAGCCGATCCACC | 8853 |
rs111467356 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212654 | TCCTTTGTGGAGCAT[A/G]TACATGCATTCCAGG | 8853 |
rs111470184 | snp | G/T | 0 | 0 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405843 | TGGTTGGCCAGCATG[G/T]TATCTTGACCAGACA | 8853 |
rs111472084 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305877 | GAGGCTGTAGTAGTG[A/G]GGTATAGATATTGGT | 8853 |
rs111502596 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356520 | AGACCGCGGCAGGGG[A/G]GAGGGGCGGGAAGAT | 8853 |
rs111503103 | in-del | -/A | 0.306182 | 0.243605 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253424 | CCGCGTTGGCTTCCC[-/A]AAGTGCTAGGATTAC | 8853 |
rs111504121 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299827 | AGATTATAGCCAGCC[A/G]GTGACTCTTACACAG | 8853 |
rs111513876 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205203 | TCCCTCATAGCCTCA[C/T]AGAGACCAGCCCTCT | 8853 |
rs111533527 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395301 | AACATGGCAAAACCC[C/T]ACCTCTACTAAAAAT | 8853 |
rs111550032 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273898 | ATTTATTAGTCCTGC[A/C]AAGGCTGTCTAGTCC | 8853 |
rs111550779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352517 | CTAGGCCCCTCCAGC[A/T]TGCTCCACAGGGAGA | 8853 |
rs111579113 | in-del | -/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334202 | GTATTTTTGTATTTG[-/T]TTTTTTTTTTTTTGT | 8853 |
rs111585104 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324660 | GATTAATCCACTCAT[A/G]CAGTGACCTCCCAAA | 8853 |
rs111610870 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399424 | ACCCATTTATCCAGG[A/G]CTGCCAGGTGGCAGG | 8853 |
rs111622914 | snp | G/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323525 | CGTACGTACTCTTGC[G/T]AAAATATTTATTCCT | 8853 |
rs111645735 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345667 | AGGCCTAGTAGTGCA[C/T]GCAAGCCAGCAGCCT | 8853 |
rs111647876 | snp | C/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376610 | TTGCAGGCAGGGATC[C/T]GCCTTGTGGTGCTGA | 8853 |
rs111657541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384451 | TTGGAGGTAGTGTTA[A/G]ATCCCACAGGCTGGG | 8853 |
rs111722400 | snp | A/G | 0.040671 | 0.13668 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304952 | GGTATAGATATTGGC[A/G]GAGGGGGTTGTAATA | 8853 |
rs111757593 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348399 | CAAAGTGCTGGGATT[A/G]CAGGCGTGAGCTACT | 8853 |
rs111758381 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279759 | ATTGTGTCACAGTGC[C/T]CTTTCCGTTTCTCTT | 8853 |
rs111761084 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344893 | GCAGGAGTTGTTCTC[C/T]GTGTGTGATGGTATT | 8853 |
rs111766041 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304562 | TGCAGTTGTGGGGGT[A/G]TAGATACAGGGTGGA | 8853 |
rs111767974 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319417 | TGCCCGGAGAGAGCT[A/G]TTCAGACACATTCCC | 8853 |
rs111780748 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378764 | TTCTGCTAAGGCTTC[A/C]CCAGCCATGTAGGCA | 8853 |
rs111782004 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270185 | AGGCGGCAGCTGCAG[C/T]GCAGGCCCTGCTCCT | 8853 |
rs111811427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213237 | CCAGCCACAGAAGAT[A/G]TGGGAATAGAACAGC | 8853 |
rs111844553 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346654 | TGTTTGTTTGAACTC[C/T]GATTGACTGCCTCAG | 8853 |
rs111848425 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245070 | AACTTTTACCTCTTA[C/T]TGGTAGTGTGGCCTT | 8853 |
rs111849326 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340325 | CGCGCCCGGCCAGCC[A/T]TGTCTGCAACTTTAT | 8853 |
rs111849937 | snp | A/C | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241207 | ACATATTTATCTTTT[A/C]GGATACAATCTTTCT | 8853 |
rs111850407 | in-del | -/G | 0.21695 | 0.247806 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287781 | TCCAGCCTTCTCCCC[-/G]CTGCTGGCTAACAAC | 8853 |
rs111868166 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353901 | GATCACTTGAGTCCA[A/G]GAGTTTGAGGCTGCA | 8853 |
rs111870634 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366469 | TGCTTGGATTGTATG[A/C]TGCCTGGCTATAAAC | 8853 |
rs111871825 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213183 | GAAAAGCCTCTCTGC[A/G]GAGGTGACATTTGAG | 8853 |
rs111880801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391294 | TGCCAGCACAGACAC[A/G]TGCCAAGTGCCCCGT | 8853 |
rs111891888 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305284 | TAGTGGGGTATAGAT[A/G]TTGGTGTAGAGGCTG | 8853 |
rs111902053 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263679 | TCCTTAAACTGCAGG[A/C]GGCTGCAGCCTCTCG | 8853 |
rs111911978 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360888 | TTTAACAGTTGACTC[A/T]TATGAGCTGGTAGGA | 8853 |
rs111921070 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368694 | GGTGACCAAATAGAA[A/G]TTTTTTTAGGAAGAA | 8853 |
rs111927318 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257581 | TGGAGTGCAGTGGCA[C/T]GATCTCCATTCACGT | 8853 |
rs111949232 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313800 | AAGCCCAGGCCAGCT[G/T]GCCTGACCACCTAAA | 8853 |
rs111952838 | snp | C/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354382 | AAGCCGTCCGCTTAT[C/T]TGTAGCATCTTTAAA | 8853 |
rs111962980 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358060 | GCTGTGAGGGGAAAA[C/T]GTGGCTTTGAACTCA | 8853 |
rs111963005 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367754 | GCAACAGAGCAAGAC[A/G]CTGTCTCAAAAAAAA | 8853 |
rs111985865 | snp | G/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372019 | GTTAAACAGACCTGT[G/T]CCCATGTTTGTGTAG | 8853 |
rs112015215 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364233 | TCTTATGAGACCAGG[C/T]GCAGTGGTTCACACC | 8853 |
rs112016986 | in-del | -/A | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357106 | AAACACAACCAAAAT[-/A]AGAGTGGACAGTTGA | 8853 |
rs112027475 | in-del | -/A | 0.296873 | 0.245566 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375282 | GTGAGACCTTGTCTC[-/A]AAAAAAAAAGGAAAA | 8853 |
rs112061025 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230538 | GCTTTCCCTGGGCAG[A/G]CTCAGCCTCCTGCAG | 8853 |
rs112067433 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248087 | GCTAGGTGGAGAAGG[G/T]GTGGCTGATGGAAGG | 8853 |
rs112099715 | in-del | -/GT | 0.494896 | 0.0502606 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250592 | GGCAAATGCAGTGTG[-/GT]TGTGCTCTTTCATTT | 8853 |
rs112122995 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346193 | AGCGCTTAGGGAGGC[A/C]GAGGCGGGCAGATCA | 8853 |
rs112147503 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324515 | TTCTTGCTGGTGGGC[A/G]CTCTGCAGAGTCCTA | 8853 |
rs112210735 | in-del | -/TGTT | 0.5 | 0 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406084 | CAGGCCTTCAGTGTG[-/TGTT]TGTCACTGAGTGGAC | 8853 |
rs112224776 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380606 | CCTCGACTAGGTCAA[A/G]CTCACTGTGGATTTC | 8853 |
rs112235631 | snp | C/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305130 | TATTGGTGGAGGGGG[C/T]TGTAATAGTGGGGTA | 8853 |
rs112251882 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279619 | CCCCTGTCATCCTCC[A/G]TGCTGTCTGTCCCAC | 8853 |
rs112273103 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212448 | TAAGGCACTAAGCTG[A/G]TTCATTCTGGTCTTC | 8853 |
rs112284449 | snp | G/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348138 | TTTGTTTGTTTGTTT[G/T]TTTTTTTCTTTTTGA | 8853 |
rs112299514 | snp | G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387074 | AGCCGGGCTTGGTGG[G/T]GGGTGGGGGGGCGCC | 8853 |
rs112318965 | snp | G/T | 0.481165 | 0.0951993 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305458 | GTATAGATATTGGTG[G/T]AGAGGCTGTAGTAGT | 8853 |
rs112321735 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217261 | TTCTGGCAAATCCTT[C/G]TTGCTTCTCGTTTCC | 8853 |
rs112355974 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354353 | GCTCTTCTCCCTCAC[A/G]GCTGAAGCTCTGGAA | 8853 |
rs112379758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366049 | GACAGCCACCTTCCT[A/G]CCCCCTTGGTTTCTG | 8853 |
rs112395514 | snp | A/C | 0.211212 | 0.246973 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387195 | TTCCAGCCTGGGCAA[A/C]AGAGAGAGACTCTGT | 8853 |
rs112410870 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297126 | TGGGATCTGTTGCCG[A/G]CACCACGGGTTGTTG | 8853 |
rs112420874 | snp | C/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234909 | CTAGAAATACCCTAT[C/T]TTTCATGACTCACCA | 8853 |
rs112450819 | snp | C/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305368 | TTGGAGGGGCTGGAG[C/T]AGTGAGGTATAGATA | 8853 |
rs112483192 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356152 | TTGTTTGTGGAATTT[A/G]ACACAGCGTTGCTCT | 8853 |
rs112496540 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293700 | TGTCGTGGTGGGCAC[C/T]GTGCTAGGTGTTAGA | 8853 |
rs112497197 | snp | G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225044 | CAGGGTTGTCCCTGT[G/T]TGGTCAGGGCAGGGT | 8853 |
rs112564101 | snp | C/T | 0.0150105 | 0.0853224 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374987 | AAAAAAAAAAAAAGG[C/T]CGGCCACGGTGGCTC | 8853 |
rs112575096 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330732 | CGCTTCCTTGCTGAT[A/G]TTTTATTTTTAAGAA | 8853 |
rs112601720 | snp | C/G | 0.181659 | 0.240478 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395811 | ATGGGGTTTCACCGG[C/G]TTAGCCAGGATGGTC | 8853 |
rs112625474 | in-del | -/T | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341459 | GATTTCATTGTCACC[-/T]TCTGGCATAGGGTCT | 8853 |
rs112635628 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355859 | GCAGGTTTATTTTGC[A/G]TTAGAATGCCACCGT | 8853 |
rs112654989 | snp | G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332563 | CTGACGAGAAGTCTC[G/T]GAGCACTTGATTCCA | 8853 |
rs112662087 | snp | C/G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276896 | TGCTGGCCCATGGAA[C/G/T]GTGCTTAGTAAGAAT | 8853 |
rs112671741 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303019 | ATTAGTAAGGCTTGT[C/G]TCGTCACTCAATATA | 8853 |
rs112686778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274048 | TGGAGGTTAGAAACA[A/G]GATGGAGTCAGTTAT | 8853 |
rs112689564 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358264 | CTGTTATTGCTACTA[C/T]CAGCATGCTGAACAC | 8853 |
rs112694656 | snp | G/T | 0.00318978 | 0.0398085 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406010 | AGCCCATGTCCTCAG[G/T]CTTCCTCAGGCCTTC | 8853 |
rs112697510 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346989 | GCTGAGAACTCAGCT[G/T]GTCACACAGCGTGTG | 8853 |
rs112701611 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397689 | GAACTAAGAATGGCT[C/T]TTATATTTGTAATTG | 8853 |
rs112710270 | snp | A/C | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394646 | ACATACACCACTTAT[A/C]TCTCTATTCCGTATA | 8853 |
rs112712547 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360417 | TTTAATCTGATACCA[A/G]ACCTCACACTTAAAC | 8853 |
rs112721165 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320875 | ACTACGGTTTCTACA[A/G]GAAGTAGAATTGGTT | 8853 |
rs112727793 | in-del | -/TT | 0.23031 | 0.249223 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281137 | AAGTATCTTGGAAGA[-/TT]TTTTTTTTTTTTTTA | 8853 |
rs112733076 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345022 | TTTAATTTTAATTTT[A/T]ATTTTTTATTTTAGC | 8853 |
rs112736867 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214399 | TGACTGCCACCATGC[C/G]CGGCTGATTTTTGTA | 8853 |
rs112737265 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329962 | CTGCTTGTCTCCATG[A/G]TGACATCTTCCTTGT | 8853 |
rs112741445 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314454 | TCACATATTCGATGC[C/T]CAAAAAAATATTTCA | 8853 |
rs112747713 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9375107 | AGGCCCCATCTCTAC[-/A]AAAAAAAAAAAAAAA | 8853 |
rs112756582 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362551 | CACTTAAAATCTACT[C/G]TCTTGAGCCTGGTGT | 8853 |
rs112795100 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363608 | CTCTTTTTTTTGACA[A/G]GTTCTTGCTCTGTCG | 8853 |
rs112814147 | snp | G/T | 0.0984431 | 0.198823 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210812 | GTGATCCGCCCGCCT[G/T]GGCCTCCCAAAGTGC | 8853 |
rs112814594 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214951 | AAATGTTTTAATGCA[A/G]AGAACAAAATAAGAT | 8853 |
rs112819187 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249734 | GCTGCAGGCAGGCAT[C/G]CCCGGGCTGGCGGGG | 8853 |
rs112829430 | in-del | -/TT/TTAAG | 0.00199481 | 0.0315187 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405883 | TCTGCTTTGTGTGTC[-/TT/TTAAG]TTAAGTTGGCAATGT | 8853 |
rs112871597 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305417 | TAGTGGGGTATAGAT[A/G]TTGGTGGAGAGGCTG | 8853 |
rs112871861 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369750 | GTAGAATTAATGACA[C/T]GAGTCTTCCCAAAGG | 8853 |
rs112880564 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305505 | TGGAGAGGCTGTAGT[A/G]GTGGGGTATAGATAT | 8853 |
rs112888538 | snp | A/G | 0.5 | 0 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406079 | TTCCTCAGGCCTTCA[A/G]TGTGTGTTTGTCACT | 8853 |
rs112910928 | snp | A/G | 0.263535 | 0.249633 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210931 | GAGGCCAAGGCGGGC[A/G]GATCACTTGGGGTCA | 8853 |
rs112939434 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345534 | CCTGGCATGACTAGA[A/G]CTGGTGATAACCACA | 8853 |
rs112949838 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9396584 | GCCTCACCTCTTTTA[C/G]GTTTAATTTTTAAAA | 8853 |
rs112969783 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350196 | GTGATCGCTTGGTGT[C/T]GTGTGTGGGGGAGAG | 8853 |
rs112970379 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351535 | TGTGTGGCAGGGTTA[C/G]AGTCTAGGGGAAGAA | 8853 |
rs112995317 | snp | C/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271112 | TTTCATTTTTTTTTA[C/T]GGCTCTTTTCAGTTT | 8853 |
rs112998657 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363890 | ATTACTTCTTTTCCA[A/G]TGGAATGGAAGTTGC | 8853 |
rs113001067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355742 | TTGGGGGCCAACTCT[A/G]TAGTGAGTTAAAATG | 8853 |
rs113004487 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354375 | GCTCTGGAAGCCGTC[C/T]GCTTATTTGTAGCAT | 8853 |
rs113013803 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347738 | AATAACTCTAATTAG[A/G]TATCCTCTTTGCCAG | 8853 |
rs113018258 | in-del | -/A | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258664 | GTGGCTTGAGCAGGC[-/A]GAAACCCCCGGAAGC | 8853 |
rs113037728 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | ASAP2 | GRCh38.p7 | 2:9403110 | ACAAAAATCATTTGG[A/T]TGTTTTACCTAAGTA | 8853 |
rs113056348 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317948 | TTACACACCCACAAC[A/C]CCCTCACTCAGTCGT | 8853 |
rs113073326 | in-del | -/AACTTA | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365920 | CCCTGGGTGATACAG[-/AACTTA]AACACTCCCTCCTCT | 8853 |
rs113077304 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302187 | TTTTTTTTTTTTTTT[C/T]TTTGAGACGGAGTCT | 8853 |
rs113082089 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290451 | CTGACCTCAAGAGAT[C/G]TGCCCATCTCGGCCT | 8853 |
rs113085589 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332897 | AATACAGGAACAAGA[A/G]TATAAAATAAAGAAT | 8853 |
rs113108833 | snp | C/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338805 | GGAAGCAGTGTCTGC[C/G]CAGTGCGGGCTGGGC | 8853 |
rs113133857 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354237 | ACCTTCCAGGTCCAC[A/C]TGGCAGGTTAGCGGC | 8853 |
rs113149790 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348863 | TAAGTTGTGGTTCTT[C/T]GCTGCTCTTAAAGAT | 8853 |
rs113153550 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262777 | CAGAGCCTGGCATGC[C/T]GACTGGGACAGAAGC | 8853 |
rs113163671 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365684 | CAAGAAAAGGGGCCT[C/T]CTGGCCAAGGGACTG | 8853 |
rs113167452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397022 | AATAAAAATAAAATA[C/T]GCATATCTGTGCCCT | 8853 |
rs113171957 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373964 | TGCAGGTGTGTTGAC[A/G]CACATACGTCTCATG | 8853 |
rs113195045 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334898 | CTTCTGTGTAATCCT[A/G]TGTTTTCATGCCGTG | 8853 |
rs113196129 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400197 | ATTCCACAGCCCTCC[G/T]GCCCCCTCCCCTCCT | 8853 |
rs113202473 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307810 | AGTTTGTGTTAAACA[C/G]TTAGGATCAGCATGG | 8853 |
rs113205990 | snp | A/G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392909 | CCAGCTCTGCCACCC[A/G/T]TGACGAGAGCTCTTC | 8853 |
rs113228510 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249763 | GGGAGCTGCATGCAC[C/T]GCCACCCCCAGAGGA | 8853 |
rs113238701 | in-del | -/GT/TG | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335072 | CTGATTGGTTCTGTT[-/GT/TG]GTGTGTGTGTGTTTT | 8853 |
rs113268385 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316943 | CACAATCACACCCTC[A/C]CTCTCACACCCTCCC | 8853 |
rs113273568 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382027 | CTTACTCTGTCACCC[A/G]GGCTGGAGTGCAGTG | 8853 |
rs113299696 | in-del | -/C | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370167 | CATTTTGTGTGGCAT[-/C]GTCTTTGAGAAACGG | 8853 |
rs113302093 | snp | C/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392669 | GATAAAAAGAAAGAT[C/G]ATAAGCTGGATCCCT | 8853 |
rs113307685 | snp | C/G/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271437 | ATTGCAGGCAAACTT[C/G/T]TTAAACGCCTTCACT | 8853 |
rs113315551 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281877 | GCACCAGATGAGTTC[C/T]GAGCTCTTGTGCATT | 8853 |
rs113317859 | snp | A/G | 0.117886 | 0.21224 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334067 | TTTTTTTTTTTTTTG[A/G]GAGACAGTCTCACTC | 8853 |
rs113334439 | snp | A/G | 0 | 0 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403460 | CACTGCTCTGTTTTA[A/G]AAACTCAGAGGCAAT | 8853 |
rs113336456 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318337 | AGACTTTTCATTAGC[C/T]CTCTATTCATTTGTA | 8853 |
rs113346114 | snp | C/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305548 | TGTAATAGTGGGGTA[C/T]AGATATTGGTGGAGG | 8853 |
rs113376723 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323821 | CTCAGCCCTTCCCTT[A/G]GTGAGGCGGAGACAG | 8853 |
rs113383374 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399608 | AGAGGCATGGACAGC[A/G]CTGACCCAGAGTGCT | 8853 |
rs113395008 | snp | A/C/G/T | 0.0190172 | 0.0958846 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361862 | GAGCCACTGCGCTTG[A/C/G/T]CCTCAAGCCTTTTAA | 8853 |
rs113412498 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355282 | TCTCTTGCAGTCTGT[A/G]TCGGTTCTGTAGTCT | 8853 |
rs113413334 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253370 | AGATTCACCATGTTG[C/G]CCAGGCTGGTCTCCA | 8853 |
rs113414289 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354260 | TTAGCGGCCAGTAGA[A/G]CCAGAGCCCTGGCCA | 8853 |
rs113446247 | snp | A/C | 0.5 | 0 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406005 | CACTGAGCCCATGTC[A/C]TCAGTCTTCCTCAGG | 8853 |
rs113489643 | snp | A/G | 0.0001146 | 0.00756881 | missense | ASAP2 | GRCh38.p7 | 2:9393511 | ACGCCGCCCCCACCC[A/G]TTGCCAAGACGCCCA | 8853 |
rs113502884 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380983 | GCTAGGGAGTCTACA[A/G]GGAAACCTAGGGGGA | 8853 |
rs113509261 | in-del | -/AG | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369210 | TTTTAGTAGAGACAG[-/AG]TTTCACCATGTTGGC | 8853 |
rs113512311 | snp | G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305596 | ATAGATATTGGAGGG[G/T]CTGGAGTAGTGAGGT | 8853 |
rs113520099 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395707 | CCGCTTCCCAGGTTC[A/G]CACCATTCTCCTGCC | 8853 |
rs113543532 | in-del | -/AAAAAA | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264190 | GTGAGACCCTGTCTC[-/AAAAAA]AAAAAAATAATAATA | 8853 |
rs113557667 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384990 | GACTGTAACAAGGGA[G/T]TTGAGAGTTACGAGC | 8853 |
rs113588477 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372685 | AAACCAGTAAGATAA[C/T]GATTCACCCACTTAT | 8853 |
rs113600135 | snp | A/C | 0.0150606 | 0.0854603 | upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9204862 | GGCTTATGCAGTAGG[A/C]AAGTTAGATTTCTAA | 8853 |
rs113658783 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9347077 | TTCCAGAGGTCTCCT[C/G]CTGCCTTTAGCAGCC | 8853 |
rs113676450 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279453 | TTGAAGTCCTGGTAC[C/T]GTAATATTGATGACC | 8853 |
rs113681351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369468 | AGTGGGTGTCCGGCT[C/T]GCCTTAGACTTCAGC | 8853 |
rs113717598 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362850 | CTGTCTCAAAACAAA[A/G]TTTTTAAGTATACAG | 8853 |
rs113719312 | in-del | -/TCTCTG | 0.0767118 | 0.180198 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334018 | CATTATTTCTCTCTC[-/TCTCTG]TCTCTGTCTCTGTCT | 8853 |
rs113720607 | in-del | -/T | 0.278664 | 0.248351 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369018 | ACTTGACGGAGAAGC[-/T]TTTTTTTTTTTTTCT | 8853 |
rs113740402 | snp | G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305424 | GTATAGATATTGGTG[G/T]AGAGGCTGTAGTAGT | 8853 |
rs113751391 | in-del | -/TTTTTTT | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216283 | CAATGTCAGTTCATA[-/TTTTTTT]TTTTTTTTTTTTTCT | 8853 |
rs113764906 | snp | C/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241303 | ACTGTTGTGCATGTA[C/G]AACATTAATTCTTTG | 8853 |
rs113771291 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361440 | AACCTTATTCCTTAG[C/T]CCTTCAGTTAAGCAG | 8853 |
rs113808818 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364324 | ACCAACCTGGGCCAC[A/G]TGGCAAAACCCCATC | 8853 |
rs113819312 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319468 | GGAGAACAGGTCAGC[A/G]GAGTTAGCCCAACTC | 8853 |
rs113831650 | snp | C/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396894 | GTAATCCCAGCTACT[C/T]GGGAGGCAGAGGCAG | 8853 |
rs113833731 | snp | C/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317871 | CACGATCACTCATAC[C/T]CACATTCACTCACAT | 8853 |
rs113838749 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344312 | CAGTTTGGGAATATT[C/G]GTTTCCTGACATTTC | 8853 |
rs113843535 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210953 | TTGGGGTCAGGAGTT[C/T]GAAACCAGCCTGACC | 8853 |
rs113862530 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372851 | TTGAGACACAGCAGT[A/T]AGCCGAACGTGCACA | 8853 |
rs113885167 | snp | A/T | 0.227369 | 0.248974 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345016 | TTTAATTTTAATTTT[A/T]ATTTTTATTTTTTAT | 8853 |
rs113896055 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356122 | GGTGGTGGGACTTTG[A/G]GCTGGACTCAGCCGT | 8853 |
rs113903318 | snp | C/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305334 | TTGGTGGAGGGGCTG[C/T]AGTAGTGGGGTATAG | 8853 |
rs113905796 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236308 | TAAAGATCATTTCGG[A/G]CCACTTGAATATATT | 8853 |
rs113912695 | snp | G/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399435 | CAGGGCTGCCAGGTG[G/T]CAGGTTCGAGATGAG | 8853 |
rs113932877 | snp | G/T | 0.030278 | 0.119257 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374083 | CAGTGTGTGGTGGGA[G/T]TGGGATTTGAACTCA | 8853 |
rs113952023 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305471 | TGTAGAGGCTGTAGT[A/G]GTGGGGTATAGATAT | 8853 |
rs113955333 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298904 | GAAAAATGAACGTAC[A/G]GGAAGACTGGGATGC | 8853 |
rs113978482 | snp | A/G | 0.00430699 | 0.0462055 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356158 | GTGGAATTTAACACA[A/G]CGTTGCTCTTGTTTT | 8853 |
rs113979812 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305304 | TGTAGAGGCTGTAGT[A/G]GTGGGGTATAGATGT | 8853 |
rs114000195 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293840 | CCTCAACTGGTACAG[G/T]GTGAGCATCAGAAGA | 8853 |
rs114001078 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272421 | TTAGATTTTTTCCTA[G/T]AGAGTTGTTTGAGCT | 8853 |
rs114012647 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310052 | CAGCCTCTGCTAAGA[A/G]TGCTCTTAATTGATA | 8853 |
rs114013651 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342519 | ATTCAAAATGAGTCA[A/G]AGAGCTAAATGAGAG | 8853 |
rs114026753 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391328 | GTATGGCTCCCTGTG[A/G]CTCTTGTGCAGGGCT | 8853 |
rs114043305 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339401 | ATGTCATGGTCTCCC[C/T]GTCTGTCAAATAGGA | 8853 |
rs114055122 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221142 | TGGCTATTGAGGCTC[C/T]CTTGCATTTCCATAT | 8853 |
rs114056859 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287718 | GAGGGAGGTGAGGAC[A/G]TGGGCTCGAAGGCCC | 8853 |
rs114066379 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331050 | CCGTGCGTGTTTCCA[C/T]GTGTGGGAGCGCCTC | 8853 |
rs114129192 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349865 | CATATGTGTATGTAT[C/G]TGGATTAATCCCAAA | 8853 |
rs114137583 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226966 | GCTGTTGTCAGTGGA[A/G]CAGAGGTGTCGCCCA | 8853 |
rs114142070 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342681 | TAAAATTAAAAAGTT[C/T]TGTGCTTCAGAATCT | 8853 |
rs114164991 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307165 | ATCAGCATCGCCTGC[A/G]TGGCTTGTTAGACCA | 8853 |
rs114173607 | snp | C/T | 0.13446 | 0.221699 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404745 | GTGTAGAGTTTTTTT[C/T]TTTTTTGGCATTGTA | 8853 |
rs114206547 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311921 | GCATGGAAAGGCAGA[A/G]GCAAGCAGGCTGATG | 8853 |
rs114207906 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261528 | GGAGTTGGGCCCTAG[A/G]TGTGATTTTAGAGTA | 8853 |
rs114211223 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239648 | CACCATTTATGTGCC[A/G]GCCATTTGGACCCAT | 8853 |
rs114216629 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319753 | GAATTTCCAGTGGCT[C/G]AGTAGTTTTTGAGGC | 8853 |
rs114219704 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347758 | CTCTTTGCCAGATTC[A/G]CAGGATTGCCACACC | 8853 |
rs114284749 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374400 | GGCCTTCCTGGGGGA[A/G]GAGGCGCAGGGCATG | 8853 |
rs114297959 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ASAP2 | GRCh38.p7 | 2:9208589 | TATAACTTGGGTAGC[C/T]TTCCTTCTCTCCATT | 8853 |
rs114302698 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373843 | CCTCAACCTTCAGAA[C/T]TGGGATTGTAAAATG | 8853 |
rs114304607 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245299 | CCAGTGTGTTGCTGC[C/T]GTGGCTGTTGCATTT | 8853 |
rs114305567 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322363 | ATGCTACTTGGGTCT[G/T]CTGGTGTCTACTTCA | 8853 |
rs114306743 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282636 | GGAGAAGTCCCCATA[C/G]TGTTTTGATCACGAG | 8853 |
rs114313423 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | ASAP2 | GRCh38.p7 | 2:9223006 | TCTTTAAAAGATCCT[C/G]TTCCATCCAGAGGAG | 8853 |
rs114327972 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212328 | TGTGGATGTGCAAGG[C/G]TGCAGGTGGTCCCAG | 8853 |
rs114333844 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240198 | TATTGAACTAGTTTG[C/T]CTTCAATCACGACAT | 8853 |
rs114342339 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324838 | ACTTATAGATAATAT[A/G]TATAGCTGGATCATG | 8853 |
rs114388223 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289300 | CCTTTGTGTCGCTGC[A/C]CTGAACTGATGGGCT | 8853 |
rs114404021 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226673 | ATGTCACTTCTTCTT[C/T]CCTCTTAAGCCCTGG | 8853 |
rs114407907 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227844 | GGATTTCAAGGTTCA[C/T]ATATGCATTGTTTGT | 8853 |
rs114410789 | snp | C/T | 0.133777 | 0.221342 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346223 | AGCTGAGGTCAGGTT[C/T]GAGGCCAGCCTGGCC | 8853 |
rs114423764 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366802 | ATCATCCAGCTATTA[A/G]GCTACCCCACATAAT | 8853 |
rs114424818 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269447 | ATAGTGGGCTTGGCC[C/T]GCACCATTCAGCCTG | 8853 |
rs114427019 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309354 | GTCATGCGCAGTCCC[A/G]AAATCATGATGCAAG | 8853 |
rs114488702 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252234 | AGGTCAAAGAGCAGA[A/T]GACAACTGAGAGTAA | 8853 |
rs114493018 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328072 | TAAACATTGAGAACA[C/T]GTTCAATGAAGGAAG | 8853 |
rs114493019 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365368 | TCCTGAGCTCAGCGG[C/T]CAGGGAAGTCTGGTT | 8853 |
rs114495069 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342231 | AAAAAGAAGAACAAA[A/G]TTGGAGGATTCACAT | 8853 |
rs114520054 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329610 | AGGACAAGGGTGGAT[A/G]TGGGCAATTGCTTGT | 8853 |
rs114560213 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317935 | CACAGTCACACCTTT[A/T]CACACCCACAACACC | 8853 |
rs114562118 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305025 | AAGATATTGGTGGAG[A/G]GGCTAGTGTAGTGAG | 8853 |
rs114580436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288330 | ACGTATGTCATCTCC[A/G]CAGTGTTCATGGTAG | 8853 |
rs114590162 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228442 | ATTCCCTGTTTTTTC[G/T]CATTCCTTTTGGTTG | 8853 |
rs114613331 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267969 | CTCCAAGCGCGCCCC[A/G]CAGGCCTGTCCCATC | 8853 |
rs114618992 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308315 | GCAAGAATGAGGCGG[A/G]AGGTGCCACACACTT | 8853 |
rs114620477 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217576 | TCTTTCCCCAGCTTC[G/T]CAGAAGAAATCATGT | 8853 |
rs114625827 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324514 | CTTCTTGCTGGTGGG[C/T]GCTCTGCAGAGTCCT | 8853 |
rs114633245 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379130 | TGTCTGCCATCCAAG[C/T]GCTGCTCTTGGAAAC | 8853 |
rs114654115 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296410 | AAAATCCATGCATGC[A/T]TTTGGCGTCCAGCAG | 8853 |
rs114656346 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367798 | TAATGTTTAACATGT[C/G]AGAAGATTGATTGGC | 8853 |
rs114735502 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317166 | CACTCACATCCACAC[A/T]CTCACCACACTCAAC | 8853 |
rs114739386 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219302 | TTTGCCCTGTGATTC[A/G]GTTGTGTTTATGTTG | 8853 |
rs114756843 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341837 | TCATCCCATGAATGC[A/G]TGTGTGCCCTAGTTT | 8853 |
rs114762012 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369717 | CAGAAACAGCATTTT[C/T]TGTGGAATAAGCCTG | 8853 |
rs114772672 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312125 | CCATCACCTCAAATC[C/T]GTTTTAGGACATTTT | 8853 |
rs114777850 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320579 | TAGGATGTTATTTTC[A/G]GGAAAGTTCATTGAG | 8853 |
rs114803399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363106 | CCTTCAGGTTCATCC[A/C]TGTTGTCACAAATGA | 8853 |
rs114805600 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321433 | CAGGTCCATTCAGCC[C/T]AGGGAGGCCCCCACC | 8853 |
rs114810299 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212188 | TGAGGTGGCAGGAAT[A/G]GAACACCAAGAAGAA | 8853 |
rs114823318 | snp | A/G | 0.140242 | 0.224618 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304732 | GGCTGGACTAGTGGG[A/G]TATAGGTATTGGTGG | 8853 |
rs114855313 | snp | C/T | 0.077417 | 0.180873 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216888 | ATAGGCGTGAACCAC[C/T]GTGCCCAGCCTCCCC | 8853 |
rs114859857 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321306 | ATACTCCTTCTATCC[A/T]TGGGAATCTTACATT | 8853 |
rs114862022 | snp | A/G | 0.000477598 | 0.0154457 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356114 | AGTTACATGGTGGTG[A/G]GACTTTGGGCTGGAC | 8853 |
rs114863471 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341693 | TCACAGAGACGCTGT[A/G]CAGGTGAGCAGTATT | 8853 |
rs114871982 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316087 | ACTTTGAGAGGCCGA[G/T]GAGGGCAGATTGCTT | 8853 |
rs114875337 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327139 | CCCTACCCCACCCCC[C/G]CCCATCCTTTACAGC | 8853 |
rs114916377 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319502 | GGCGGGAAGGCATCC[C/T]AGGCAGAGGAAAGGC | 8853 |
rs114922994 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230625 | CTGAGATGCTGGATG[A/T]GGTGCCTGCATCCCC | 8853 |
rs114982502 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335941 | ATAAAGTTCCCTGTT[C/G]GCAGTTTGGTGAGCT | 8853 |
rs115040713 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252254 | ACTGAGAGTAATTGA[A/T]GAACCAGGGACTGTA | 8853 |
rs115054112 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221386 | GAGTGCAATGGTGCA[A/G]TCTTGGCTCACTGCA | 8853 |
rs115055226 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254990 | TGTGTGTTTAACTTT[A/C]TCAAATGCTGCCATC | 8853 |
rs115060291 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374683 | AACCGTTAACATGGC[C/T]TTAGACAAAGGGAGG | 8853 |
rs115063906 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342977 | TCTTCAGTTCCTGAG[G/T]GCTCTTGTTCTCAGC | 8853 |
rs115070971 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357015 | CATTTATAAAATGAA[A/G]AAGATGGAGGCTTGG | 8853 |
rs115076442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260363 | ATCCCTGTGCACCTT[C/T]GGGCCCTCCCTCAGC | 8853 |
rs115089830 | snp | A/G | 0.140581 | 0.224783 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306670 | CCAGCCAGGAGTCAA[A/G]CCTCTGCTCCTGGCT | 8853 |
rs115115036 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242967 | ATAAGCAGCGTTGTG[C/T]GCTTTCTTTATTTTG | 8853 |
rs115127742 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399273 | TTCTGCTTCTCCAGC[C/T]CCCGTCCTGTGCCTG | 8853 |
rs115145782 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347148 | CTTGATTCACTTCCT[C/T]GCTGCCATGCAGAAA | 8853 |
rs115158394 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331755 | CCTGGGCGACAGAGC[A/G]ATTTTTTTTTTTCAA | 8853 |
rs115182589 | snp | A/G | 0.0333238 | 0.124705 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226811 | CCTAACATCATCGGT[A/G]TGTGATCTCTCTCCC | 8853 |
rs115194279 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326921 | ATAAATTCCTGGGAG[G/T]AGAATTTCTAGGTCA | 8853 |
rs115209871 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306960 | TCGGAGGCCTGCAAA[A/G]CCAGAATCTTAGTGT | 8853 |
rs115213507 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332388 | ACCTCAAGGAGGGTA[C/T]GGGAAGGTCAGCACT | 8853 |
rs115247947 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338471 | TAATTTTCTTCTGCC[C/T]CTGGGTTCGCGTATC | 8853 |
rs115255475 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273568 | TTATTATTCGAATCA[C/G]TCTCCTGGAGCATTC | 8853 |
rs115255537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232407 | TGGCTTTGTGCCCCC[A/G]TACCCCTTTCGCAGC | 8853 |
rs115291098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248513 | TTTATTCTGCCACCT[C/T]CTTGCTAGTTGACCC | 8853 |
rs115304718 | snp | A/C | 0.108402 | 0.206034 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286319 | AGGAAGATTACATGA[A/C]CCTGGGAGGTTGAGG | 8853 |
rs115310356 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313166 | ACTGCTGAAATGAAC[A/G]AAGAACGAAAGCAAG | 8853 |
rs115311832 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269621 | CAGAGGTGGTGGCAC[C/T]GCCCTCAGGCGGTAC | 8853 |
rs115320308 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219721 | TACCATAGAATTCAC[A/T]TACCATAAAATTCAC | 8853 |
rs115328114 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341525 | TGAGACCTGAAAATC[A/G]CTCTGATTAATATGC | 8853 |
rs115344518 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337221 | TCAAGACCTAACTCA[A/G]CAGTCTCCTAGTTGT | 8853 |
rs115345393 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375086 | ATCAGCCTGGGCACC[A/G]TAGGGAGGCCCCATC | 8853 |
rs115368949 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292290 | TTTGGGAGGCTGAGG[A/T]GGGTGGATCATGAGA | 8853 |
rs115376568 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256590 | TTTAAAAAAGAATGT[G/T]GCCATCTGTTTCTAT | 8853 |
rs115390045 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278976 | GGTAACCAAGGAGAA[C/T]GGAGGGTTCGGCTGG | 8853 |
rs115393275 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233192 | TTGCTTTGGTGATAG[C/T]GATCGATGTCTGTGT | 8853 |
rs115407458 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289643 | TTCACAGGGAGGTCA[C/T]TGGGGTGACGTTTAG | 8853 |
rs115408416 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240509 | CCTTGGCCTCCCAGA[G/T]TGCTGAGGTTTCAGG | 8853 |
rs115408747 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317789 | CCTCACACACCCATA[C/T]ACAATCGCATTCACA | 8853 |
rs115440420 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303800 | GGACTTGGATACTGT[A/T]TCTTTTTGGGGTTGG | 8853 |
rs115471437 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334086 | ACAGTCTCACTCTGT[C/T]GCCAGGCCAGAATGC | 8853 |
rs115471563 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249124 | TGTGGCTGAGGCCAC[A/C]CAGCCAGTCTGTGGT | 8853 |
rs115475730 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257484 | ACCAGTACATGATGT[C/T]GGAAAGAACAGGCTA | 8853 |
rs115499783 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361896 | TATCCAGATTGTTTT[A/G]TTTTGCTTAGACAAT | 8853 |
rs115504666 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293124 | ATCCAGTAAACTAAA[A/T]AGCACACAACAAAAC | 8853 |
rs115534094 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252165 | GCCAGGGAGGGCAGG[A/C]GTGCCTGACACCAGC | 8853 |
rs115536382 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260939 | GGAATTGGTTACCCA[A/G]GGTGGTTAGGGGGGT | 8853 |
rs115563616 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222619 | GTTTTTTGGCAAATA[A/G]GAATGAGGTGTGTTT | 8853 |
rs115593224 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366189 | ACTGCAAGGTAGCAC[A/G]TTTCTCTAGCATTGG | 8853 |
rs115600785 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388990 | TACCCATGATCCCCA[C/T]AAAAGATATTGGGGA | 8853 |
rs115606610 | snp | C/G | 0.0168055 | 0.0901129 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362630 | GATTGTTTGAGTCTG[C/G]GAGTTCAAGACCAGC | 8853 |
rs115623695 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212603 | GGTGATCCTCAATTC[C/T]TCCCATGCACCCCAC | 8853 |
rs115638247 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218822 | CTCTGTTTTTTTCTT[C/T]ATCTTGACTATTTAT | 8853 |
rs115648823 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296979 | GAGTCTGGTGAGTTG[A/T]GCCATCATTTGGTGA | 8853 |
rs115649771 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323518 | GGCTTCACGTACGTA[C/T]TCTTGCTAAAATATT | 8853 |
rs115705572 | snp | A/G | 0.0244538 | 0.107838 | intron-variant, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9287015 | ACAGCCTTGTGAGTT[A/G]GGTCCTGTCCATTGA | 8853 |
rs115708867 | snp | A/C | 0.0221141 | 0.102801 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212955 | TGTGAAGCAGAGCTG[A/C]CTGGCTCCACTCCCT | 8853 |
rs115709662 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339701 | CCTCCTTGTTGGTCC[A/G]TCCTCTGGCCCTATG | 8853 |
rs115722653 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314460 | ATTCGATGCCCAAAA[A/C]AATATTTCAGTATAC | 8853 |
rs115746996 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358352 | TGTTTTAAGCCTATT[C/T]CCCTTTTACAAGTAG | 8853 |
rs115756803 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219353 | AGGGAGTTAGGAGAG[C/T]GGGATTGGAGTTGTA | 8853 |
rs115760216 | snp | C/T | 0.031825 | 0.122064 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352533 | TGCTCCACAGGGAGA[C/T]CCTGCTAGATGCCAT | 8853 |
rs115769960 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313325 | TTGGAATTAAATAAC[A/G]AATAATCTCAAAATA | 8853 |
rs115777100 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9333001 | GAGTTCATGCCCCAC[A/G]GCCTGTGTGTCCCTC | 8853 |
rs115781433 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307870 | CGACTGTGCTGCCAG[A/G]GACGGGCTGGGCGCA | 8853 |
rs115797457 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291311 | AAATATGTTTTCAGC[C/T]GTTTAGTTGGGATGA | 8853 |
rs115834840 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306881 | ATTGGTGCCCCAGGG[A/G]CCCTGGCCGGACATC | 8853 |
rs115849799 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381751 | CCACAAAAACGTTTC[A/G]AATTAGCTGGGTGTG | 8853 |
rs115873622 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251172 | AAGGAGATTTTGAAA[A/G]GAGGAACGTGGCCAG | 8853 |
rs115881863 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286308 | GAGGGTGAGGCAGGA[A/C]GATTACATGAACCTG | 8853 |
rs115886239 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319128 | GACGGGGCTGGAGGG[A/G]CGTTTGCTCATGAGC | 8853 |
rs115901755 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346198 | TTAGGGAGGCCGAGG[C/T]GGGCAGATCAGCTGA | 8853 |
rs115956330 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317093 | CATCCACACACACAC[C/T]CAACCACACTCATAC | 8853 |
rs115967869 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361459 | TCAGTTAAGCAGTAC[A/G]TAGGGTGTCAGGTGT | 8853 |
rs115974268 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341548 | TAATATGCGCGGCAC[A/G]AACAGTGTTAGCGGT | 8853 |
rs115997527 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228781 | CTAATATATGTAAAT[A/G]TATGCTGCTCAGTTG | 8853 |
rs116022440 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383549 | CAGGTGTGAGCCACT[C/G]CACTGGATGGTAAAC | 8853 |
rs116045222 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370382 | AGTGTTTGTGGTGTC[A/G]CATTTCCTTGAGAAT | 8853 |
rs116061603 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289460 | AAATATTCTTGACCC[A/G]TAATGGAAGCACACA | 8853 |
rs116065247 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332669 | TTCTTGGAGCTGTAC[A/G]CCTGCTCCCTCTCCC | 8853 |
rs116073581 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246981 | ATGTAGCTGGGGCCA[C/T]GGTATATACTACCAC | 8853 |
rs116096562 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370628 | CCCCTCACAGAGGCA[C/T]TGGGGGCATGAGCGG | 8853 |
rs116096796 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378822 | GCGATGATTTACAGA[A/G]ACCGTTCACTCGGGG | 8853 |
rs116106999 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301414 | CTCCAGAAATGTGAC[A/G]TGTGTGAAATTAAAG | 8853 |
rs116139429 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302266 | CAGCCTCTGCCTCTC[A/G]CGTTCAAGCGATCCT | 8853 |
rs116169004 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375331 | TCTGTGGAATCAGCA[A/G]TACTGACCAAAGCTG | 8853 |
rs116184640 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241483 | GTGGCTCATGCCTAT[A/T]ATCCCAGCACACTGG | 8853 |
rs116189886 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279902 | CATATATATTTTTTA[A/C]ACCCATGCAACTTTT | 8853 |
rs116193316 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239015 | AGTGGCCTCCTGCCC[A/G]TCCCTCCCAGCCCCT | 8853 |
rs116196812 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372675 | AAGATCATAAAAACC[A/G]GTAAGATAATGATTC | 8853 |
rs116225086 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299866 | ACTTAATTCTTATGA[C/G]AATCCCATAAGGTCA | 8853 |
rs116225519 | snp | C/G | 0.0637235 | 0.166737 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275528 | AACGGCTACTGCCCA[C/G]CTTTAGCCCTGAATG | 8853 |
rs116229781 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381967 | GCACTGTACATCCAC[A/G]AGCTCATTTAATCTT | 8853 |
rs116242135 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313688 | CAAATTGACCTGCGC[C/T]GGTGACTCTGATTGT | 8853 |
rs116252778 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256387 | CAGTGTCAACTGTAC[A/T]TAAAGAAATTAGCGT | 8853 |
rs116252892 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349659 | AGCCACGAACCAGGA[A/G]AGTCTAGTACAACCC | 8853 |
rs116261539 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319239 | GCCAGCCCTGACAGA[C/T]GTGCACCACGGAAGG | 8853 |
rs116266099 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322219 | TTGAGAACCTACACA[A/G]TGCAGGACACACAGA | 8853 |
rs116281144 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243862 | AGTAATTAGGAAATA[G/T]TGTAGTAAAAATAGC | 8853 |
rs116285991 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312678 | CAGAGTTTCCACTTG[A/G]TAGTTTACTTACCTA | 8853 |
rs116295232 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364413 | CAGGGAGGCTGAGGT[A/G]GGAGAATCACCTGAG | 8853 |
rs116317068 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287677 | CCTGCAGCGGGTGGA[C/T]GGCCTCTGTCTCTGA | 8853 |
rs116335641 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316908 | TTTGCCTAGCAACAC[A/C]CCCCCAACACACACC | 8853 |
rs116348020 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265391 | TTTTGAGTATTTTTG[C/T]TTTATTGTTTAATCT | 8853 |
rs116348394 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293830 | TTCCCACTGACCTCA[A/G]CTGGTACAGTGTGAG | 8853 |
rs116348797 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218593 | AGGGAGAATGTTGAG[A/G]CCTTGTACTGTATTC | 8853 |
rs116354966 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320196 | ATTGCAGAAATTAAT[A/G]CTCCTTTCAGGGCTA | 8853 |
rs116388136 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365893 | GGAAGGGCGACGGAC[G/T]GGGCTGAGCTACCCT | 8853 |
rs116389360 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399199 | GTCGACAGACGGGAG[C/T]GTACAGTGGAAAGAA | 8853 |
rs116390180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276682 | AGCTGGGATTACAGG[C/T]ACACCCACCAACACG | 8853 |
rs116410812 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238489 | ACTTTCATCCACCTT[C/T]CCATGGGGGCTGCTC | 8853 |
rs116412225 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231476 | CCTGCTACCCGTTCG[A/C]TGAGATGCCAGTGAG | 8853 |
rs116482008 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401174 | TTCTCAGGCCTAGGT[A/G]CGGGACTCCTGAGAC | 8853 |
rs116502976 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281530 | TATTTCTAACCACCC[C/T]CAAGCGTCGTTTGCT | 8853 |
rs116504383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278948 | GCAGGCAGGGGCATC[C/T]TGGAGCCTTGCTGGT | 8853 |
rs116504716 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248208 | ATCCCACGCTAACCA[C/T]GGAGGCCACGCAGGC | 8853 |
rs116515525 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389603 | CTGGGTGTCTCACAG[A/C]CCCTCACACGGCTCT | 8853 |
rs116534449 | snp | A/G/T | 0.00179503 | 0.0299047 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323272 | CGGTGGTGAAGGCAG[A/G/T]TCCTACAGCCCAGGC | 8853 |
rs116546057 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313441 | CATGTGTGTACTCCC[C/G]CTTCATGAAAAACCT | 8853 |
rs116557420 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212409 | TCTTGAAGTCCAGGC[A/G]GTTACCTGTGGGTTA | 8853 |
rs116567340 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345496 | GTTCTTTCCATGGCA[A/G]CGTTATACATACTAT | 8853 |
rs116584568 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296589 | TCAGGCACACGACTT[C/T]GTCGAAGATGAATAC | 8853 |
rs116602404 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363268 | ACAAGATGGTGAAGA[C/T]GTGTCTTCAACAAAC | 8853 |
rs116636618 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238079 | GAGCCATGGCTCTGG[C/G]CTCCGACTGCTGGGG | 8853 |
rs116652548 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254676 | ACCGTCCCCGGCCTA[C/T]AAACTAAACTTTATC | 8853 |
rs116667354 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343047 | TTTGGGGATGTGCTT[C/T]GTTCTCCAAGGATGG | 8853 |
rs116718707 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328795 | CGAGAGACACAGTGA[G/T]GTACAGTGCTGGCAT | 8853 |
rs116728748 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325619 | ACTTGAGGAGTAATT[C/G]GTTCCCCACTTGGCT | 8853 |
rs116732931 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310828 | AGGACATTGTGAAGA[C/G]ATGGCTGTTTGGCTG | 8853 |
rs116758074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376834 | TGGAAGAGTTGTACA[C/T]GATTTCACCGGTGTT | 8853 |
rs116760385 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321302 | TTTGATACTCCTTCT[A/C]TCCATGGGAATCTTA | 8853 |
rs116788871 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313082 | AAAAAAAAAGCTGCA[A/C]TTGGTTGTTGAGTGT | 8853 |
rs116814211 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360616 | TAAATACTCCCACAA[C/T]GGCCAATTTCAAGCT | 8853 |
rs116835949 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262899 | AGAAAACTCGGCTAT[C/G]TTACATCTCCTCTCC | 8853 |
rs116836658 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216756 | GTGAGCCACCATGCC[C/T]GGTCCCTGATTAATT | 8853 |
rs116888231 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298161 | TCCTGTTTTTCTTCT[C/T]CAGTTTCTCCTAAAG | 8853 |
rs116950540 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230314 | GACCCAGAGGACCAG[C/T]GTTGGGGACCCAGAG | 8853 |
rs116955299 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217271 | TCCTTGTTGCTTCTC[A/G]TTTCCTGTTTGCCTC | 8853 |
rs116965888 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378834 | AGAAACCGTTCACTC[A/G]GGGACTGTCTGCCTT | 8853 |
rs117018353 | snp | C/T | 0.0256364 | 0.110376 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300331 | ACCATGGAATCCGGA[C/T]GAAACTAACTTGTCT | 8853 |
rs117047834 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392722 | CCTCTCTGTGTAGCT[A/G]AAGGCCTCATTCTTC | 8853 |
rs117123457 | snp | A/C/T | 0.0165278 | 0.0893908 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227350 | ACCCTCCCTCAGTGT[A/C/T]GTTCAGCAGTGAGCC | 8853 |
rs117168599 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354413 | GAGAGTGTAGTGGAG[A/G]GGATTCTTGCTTGAA | 8853 |
rs117169111 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217331 | TTCTTTCCTCTCCTC[A/G]CTGCTCTGCTGACAT | 8853 |
rs117172598 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402014 | GGGCGGTGGATGAAC[C/T]GGCTTGAATGGGGCG | 8853 |
rs117199651 | snp | C/G | 0.0599851 | 0.162463 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231602 | AGCCTGCGCCTGCCT[C/G]TTCTTCCTCCTGTCA | 8853 |
rs117220472 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377535 | AGATCTGGGAGTCCC[C/T]GTGGTTTGGGGCATA | 8853 |
rs117309678 | snp | C/G | 0.0596104 | 0.162024 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253118 | AAGTTTTTAAAGTCA[C/G]CTGAATTGAGGTCTA | 8853 |
rs117336786 | snp | A/G | 8.31359e-05 | 0.00644678 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380831 | TCCCACCACAAGGAC[A/G]GGGTGGGGCACCTGT | 8853 |
rs117347802 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317719 | ACACACACCCATACA[C/T]AATCACATTCACACT | 8853 |
rs117389657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320232 | GGGATAAGTAAGTTT[A/G]TCTTGCACAGAAGTG | 8853 |
rs117423990 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283791 | CAGCTGCCTTCTCCC[C/T]GTACCCTCACATGGC | 8853 |
rs117453994 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383711 | GTTTTCACATGCACA[C/T]GTATGTTTATTGCGG | 8853 |
rs117523410 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251155 | CTGGTAAACAGATCG[C/T]GAAGGAGATTTTGAA | 8853 |
rs117640178 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239152 | ATCAGATGCTTTTTC[C/T]GCACTGACTGAGATG | 8853 |
rs117714731 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382683 | ATCCTTTAGATCTCA[A/G]ATATCCTTTGCCTGT | 8853 |
rs117739749 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | ASAP2 | GRCh38.p7 | 2:9220015 | TTTTTAAGATTCATC[C/T]AAATCATAACATGGA | 8853 |
rs117781451 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300485 | ACCCTGTGGCTTTGC[C/T]AGTTTTTAATACTTC | 8853 |
rs117781511 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235809 | CCTGAGGGTAGAACT[C/T]GGAGAACTTGGTTGG | 8853 |
rs117811912 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269964 | GAGATTGGAAGAGGC[C/T]CCTCGGTAACTTGAG | 8853 |
rs117839702 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300315 | ACTTGGAGCACTCCA[C/T]ACCATGGAATCCGGA | 8853 |
rs117840958 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278790 | TGGAGAAGAAATCTG[A/G]GGCTCGGGAAGCAAT | 8853 |
rs117891152 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259268 | ACATTCATCCCTCAA[C/T]GCTGAGAATAAATGG | 8853 |
rs117935201 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335703 | CTCTTTCTGTAATGA[C/T]GTCTCTGTGTGCTAA | 8853 |
rs117954442 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238800 | GACCTAAAACACCCC[A/G]AAAGCTTCCCTCTTG | 8853 |
rs117982037 | snp | C/T | 0.0142736 | 0.0832652 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404171 | AGTAGAATTCTGTGG[C/T]GCAGACCATGCTGTA | 8853 |
rs118062344 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268861 | CCAGGGCAGCATCTT[C/T]GGGTTCTAAGAAGGA | 8853 |
rs118077348 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216043 | GGTAGGTCCTACAAC[C/T]CAGCTCTCCTATTTG | 8853 |
rs118090627 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355844 | TGAATGAGGGAAAGG[G/T]CAGGTTTATTTTGCA | 8853 |
rs118130511 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292640 | GCTCCTTCTCTACTC[A/G]ACAAGTCTTACCTGT | 8853 |
rs118172004 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239282 | CAGATTTGGTGTCAT[C/G]ATGTTGGGATTTGAG | 8853 |
rs118200130 | snp | A/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317446 | CATACTCACATTCTC[A/T]CACACACATGTGCAT | 8853 |
rs118200636 | snp | C/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317445 | ACATACTCACATTCT[C/G]ACACACACATGTGCA | 8853 |
rs118202180 | snp | C/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317441 | CTACACATACTCACA[C/T]TCTCACACACACATG | 8853 |
rs118202859 | snp | A/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317452 | CACATTCTCACACAC[A/T]CATGTGCATTCACCT | 8853 |
rs118203078 | snp | A/C | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317336 | ACAATCATATCTTCA[A/C]TCACACACACCCTCA | 8853 |
rs137855711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219303 | TTGCCCTGTGATTCG[A/G]TTGTGTTTATGTTGT | 8853 |
rs137868681 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289242 | CCCCATGCTCTGGAC[A/C]CACCAAGCGCCTTGA | 8853 |
rs137884443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327403 | CCTTGTAAGGGAAAT[A/G]TCTCAGGACGAGAGA | 8853 |
rs137905963 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257326 | GTCTCAAACAGTGGT[A/G]GGAAGGATATACCTA | 8853 |
rs137926225 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253895 | TGAGAAAGAGACCAC[A/G]TTCACATAACTTTTA | 8853 |
rs137930394 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371933 | CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTG | 8853 |
rs137935465 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323023 | AAACGTGTGGTGAGC[A/G]TTGGTCTCGCCAGGC | 8853 |
rs137957835 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368173 | AGTTACTGGTTCTCC[C/T]TGTCTCTGTCTGTAC | 8853 |
rs137999103 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228169 | TGTATGGTTGATAGG[A/G]ACATACTCTTTGGCC | 8853 |
rs138037452 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334923 | GCCGTGCCGCCCACG[G/T]GGAGTGTGGCGTTCC | 8853 |
rs138052116 | in-del | -/GTGG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305472 | GTAGAGGCTGTAGTA[-/GTGG]GGTATAGATATTGGT | 8853 |
rs138080408 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338782 | AGCACTCGTGGACAT[C/T]AGCTCCAGGAAGCAG | 8853 |
rs138084537 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266801 | AAGATTGCCCAAAAC[C/T]ACCTCCCAGAGTTAG | 8853 |
rs138114893 | snp | C/G/T | 0.00438571 | 0.0466605 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273913 | AAAGGCTGTCTAGTC[C/G/T]CCAGGCAGGAAGAGG | 8853 |
rs138123121 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262193 | GAAAAAAAAATGTAT[C/T]AGTGGAAATGAAAGG | 8853 |
rs138154882 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267987 | GGCCTGTCCCATCGT[A/G]ACGCCCTCAGAAGCT | 8853 |
rs138160232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339991 | CTTACAAGCCACTTT[A/G]CAGGGTAGGCAATGT | 8853 |
rs138160336 | in-del | -/CATATTTTTTACACATA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279874 | CATATTTTTTACACA[-/CATATTTTTTACACATA]TATATATTTACACAT | 8853 |
rs138176579 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240782 | AGTGCTGTATGATTT[C/T]TCCTTGGCATATCTG | 8853 |
rs138185439 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384685 | AGGTGCGTAGGGCAA[C/G]GTGTGGGGGAGGGGA | 8853 |
rs138197009 | in-del | -/T | 0.040671 | 0.13668 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337547 | CTAACCCTCCCTGTG[-/T]TAATAACAGTTGATA | 8853 |
rs138198279 | snp | A/G | 0.000759414 | 0.0194713 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279434 | TGTGTGGAAAATGTC[A/G]CATTTGAAGTCCTGG | 8853 |
rs138201520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301619 | AGTGTTAGAGGATTG[C/T]TAGTGAAAGATGTCC | 8853 |
rs138226715 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308886 | TCTGGTGGTTTATTC[A/C]GGCCATTTTAGTCAG | 8853 |
rs138235416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390606 | TAGTGTCTGATTTGC[A/G]CTCTGCCCCCAACCT | 8853 |
rs138272038 | snp | C/T | 0.000204922 | 0.0101202 | missense | ASAP2 | GRCh38.p7 | 2:9356310 | AAGTGCAGAGGATGA[C/T]GGGCAATGACGTCTG | 8853 |
rs138305232 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9392043 | AAGCGTATTTTTTGT[A/G]GAGACAGGGTTTTGC | 8853 |
rs138309057 | snp | C/T | 1.73105e-05 | 0.00294193 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9379004 | CTACTGCTGCCTGAC[C/T]GACAATGCCGAGTGC | 8853 |
rs138316502 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284837 | TTAGATGTAAGTGGT[A/G]TGTGTTACGACAGGC | 8853 |
rs138320476 | snp | A/C | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213828 | TGTTGCTGTCTAGAG[A/C]TACTTAGTGTCAGAA | 8853 |
rs138342574 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404240 | TGCCTTCCCTTCTAG[C/G]CCAGGAGAATGTTTA | 8853 |
rs138362812 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322034 | GACCAGTGTCTGGAC[A/G]GTCTCTTGCCTGTGA | 8853 |
rs138393410 | snp | C/T | 0.000117205 | 0.00765432 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9401372 | TGTGATCATCGTGGA[C/T]GGGGAGGAGGACCAG | 8853 |
rs138405112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9208689 | CTACTTTTAGCAGCA[A/G]GGCTTACAGATGATG | 8853 |
rs138435141 | snp | A/C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219781 | TAGTGTACTCACAAA[A/C/G]TTGTGTAGCCATCAC | 8853 |
rs138441156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248110 | ATGGAAGGGGGGCGG[C/T]TGACAGCAGCAAGAG | 8853 |
rs138442474 | in-del | -/CCCCCCCCCC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338449 | AGCCAAGGTCCACCA[-/CCCCCCCCCC]CAGCCATAATTTTCT | 8853 |
rs138447760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318020 | CGTCTTTTCTCATTC[A/G]CACCCAGCATTCGCT | 8853 |
rs138468316 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256627 | GTGCAAATCAGAATT[C/G]TCTCTGTCTTGTGTA | 8853 |
rs138478307 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315729 | GCACGGCCTTCTGTT[A/T]GTCCTTGTTCCTTCC | 8853 |
rs138504180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245411 | GCTTACTTGGGGGCA[C/T]TCACTGTGCTAGGTG | 8853 |
rs138509979 | in-del | -/GTGT | 0.0770498 | 0.180522 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318973 | AGGATCCTAGCAAGG[-/GTGT]GTGTATTTTCCTGCT | 8853 |
rs138530455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367400 | AGCAGAACATGGAAA[C/T]GAAAATATGTTTTCT | 8853 |
rs138531553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291944 | AAGAGCTGAAGATAG[C/T]GACAATGTCATTAGC | 8853 |
rs138533081 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355552 | GTAGGATTTTATATT[C/T]GACCATTATTTAACA | 8853 |
rs138544235 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328500 | AAAGAGAAATGATAC[A/G]ATGTTAATGCAGTGT | 8853 |
rs138569542 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352717 | TGAATCTGGCCACAC[A/C]CAAGCTCTGTGGCCA | 8853 |
rs138583018 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362223 | TCGGCTGACTTGCTT[A/T]TTGAAGTATGTTTTA | 8853 |
rs138586564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289573 | GCAGTAGCCCAGTCT[C/T]CACTCTTCACCCTCT | 8853 |
rs138601518 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372054 | TGCCTTCGGGGCCTC[C/G]AAGCCCTGGGCAGAT | 8853 |
rs138614019 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270663 | TCAAATACTAGATCT[C/T]ATTCATTCTGTCCAC | 8853 |
rs138666336 | in-del | -/ACACACACACACAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352213 | TTAAAACACACACAA[-/ACACACACACACAC]ACACACACACACACA | 8853 |
rs138722190 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302037 | ACCACGTTAGCCAGG[A/C]TGGTCTCGATCTCCT | 8853 |
rs138775716 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232634 | CTCTTACTTAGTGAT[A/G]CATCCTCAGCACCCA | 8853 |
rs138797986 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238228 | CCTTGTATTTGTTCT[C/G]TTTTTAAAACCTCAG | 8853 |
rs138799468 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301150 | GCTTTTGCTTTCCCT[C/T]GGGCATTTAAAACAT | 8853 |
rs138800658 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315244 | CAACCCCAGACAAGC[C/T]TGCCATAGCCCTGAA | 8853 |
rs138814217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347952 | CACTGATAATCTCTG[C/T]CTGCATGGCAAACTC | 8853 |
rs138817502 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274202 | CAAACAAGGCTAATT[C/G]AACTTCATCCTTCCA | 8853 |
rs138837877 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297701 | ATGGGTAAATGCATT[C/T]GTCTTCTTAAGGGCC | 8853 |
rs138838825 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355323 | TCATGATGCCTTCTT[A/G]AAGAGTATTGACCTG | 8853 |
rs138855584 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270983 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 8853 |
rs138861043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343725 | ATGTTGGGATTACAG[A/G]CATAAGCCACTGCGC | 8853 |
rs138871231 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228969 | CAGAGGTGGAAGATC[C/T]GGTATCTCAGGAGGG | 8853 |
rs138890246 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9391655 | TCTTGGCTTGCTGCA[A/G]CCTCTGCCTCCCGGG | 8853 |
rs138929075 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339621 | CTTCCCTCATGGTGT[C/T]GCGCTCTTAGAGGTT | 8853 |
rs138932956 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248566 | TCTCGGTTTCTTCCT[C/G]TGTAAAACCTCAGAG | 8853 |
rs138967260 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336707 | GAATGTAGGCCCTGA[C/T]GCTTTGATATTCCCA | 8853 |
rs139005993 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238873 | TTGCCTGGCATTTCT[A/G]CATAGATGATTTTGT | 8853 |
rs139023855 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | ASAP2 | GRCh38.p7 | 2:9223391 | CTTGGATCCTTCAAG[C/G]ATCTGTATACTAAGC | 8853 |
rs139044586 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243132 | TTGTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 8853 |
rs139071135 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353428 | GCAGTATGGTGACAT[A/G]TGCCTTTGGTCCCAG | 8853 |
rs139091519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281619 | ACCCTCTTTGAAGTT[C/T]GTGGAAGTCAGTTCC | 8853 |
rs139118931 | snp | C/T | 8.24763e-05 | 0.00642116 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9385286 | TAATTCTCACGTTCA[C/T]GTTGAATATGAATGG | 8853 |
rs139188126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218059 | AGTCCTATAGTGACA[C/T]GCCTCCAGGTTCCAC | 8853 |
rs139193419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286630 | ATCAAGAAAAATAAC[A/C]ATCTTTTTGTGGAAG | 8853 |
rs139197875 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212918 | CGGAACCCCGGCTGC[A/G]CACTGGAGTTGCTTG | 8853 |
rs139214182 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325640 | CCACTTGGCTCTGTC[A/G]TTGCTTCCTGTGGTA | 8853 |
rs139218899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284258 | CTTAGGATTTGGAGG[C/T]TGAATCAGTTTCCAC | 8853 |
rs139235213 | in-del | -/C | 0.349452 | 0.229367 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327129 | ACTTGGGTACCCCTA[-/C]CCCACCCCCGCCCAT | 8853 |
rs139237158 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318870 | CTATTTTGGAAAAAG[A/T]AAAGAGTTTCGGTCT | 8853 |
rs139255739 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321732 | AGAGAGTCATCTGGT[C/T]CTGAAAAGAAAAGGT | 8853 |
rs139273043 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249189 | TCCAGTTTCTTTCCT[C/G]TGTCAGACAGCAATG | 8853 |
rs139294738 | in-del | -/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317442 | ACACATACTCACATT[-/CA]CTCACACACACATGT | 8853 |
rs139311300 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247030 | TGTTTTTGTAGAGAT[G/T]GGGTCTGTGTTGTCC | 8853 |
rs139321453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331155 | CCCTGCTGGGTACAC[A/G]CGGGCCTCTGCACAC | 8853 |
rs139323215 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259795 | CGACAGGCAAAGTAG[C/T]CCTGCACATCTGGGG | 8853 |
rs139329859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363344 | TGGTTCTAGTTTTTC[A/G]AGGAACCTCCATAAC | 8853 |
rs139342967 | snp | C/T | 0.17332 | 0.23795 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398025 | GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCGTG | 8853 |
rs139347518 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318243 | TTTGAAATATTTTTT[C/G]TTCACTGCAATGATT | 8853 |
rs139367850 | snp | A/G | 8.27068e-05 | 0.00643013 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374917 | TGGTGTGGATCTTAC[A/G]GAAAAAATCCCACTG | 8853 |
rs139371661 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356915 | GGGCTTTATAGTAGG[A/G/T]TGTGATTTAAGGAAT | 8853 |
rs139383113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316193 | CAAGCATGTTGGCCC[A/G]TGCCTATAGTCCCAG | 8853 |
rs139435328 | in-del | -/CA | 0.0115144 | 0.0749975 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373060 | TGAGACCACGTATCT[-/CA]CACACACAAGTCAGC | 8853 |
rs139453791 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382736 | CTGTTTTTTCTGTAC[G/T]GTTACACTGTTGTCA | 8853 |
rs139473354 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392529 | CAGAGGTTTCCAAGG[C/T]GAACACACCAAAGGC | 8853 |
rs139475533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309867 | AATGTGAAGAGGGGC[A/G]TGTAGCTATTATCTG | 8853 |
rs139485860 | in-del | -/TCAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317121 | TCATACCCCACGCAA[-/TCAC]TCACAACCACACAAC | 8853 |
rs139511854 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316615 | AGTGGGTTTCGAGCT[C/T]GTTTTCCACTTGAGG | 8853 |
rs139517275 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306844 | GTTCCAGCTTAGAAG[A/G]CATGTGGGCAGGGTT | 8853 |
rs139573064 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211269 | TTTTGTACAATTTTA[G/T]CAAACTTAGCAAAGT | 8853 |
rs139600571 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318983 | GCAAGGGTGTATTTT[A/C]CTGCTGGGAAGGTCG | 8853 |
rs139618845 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249365 | GACAGCAATGCCTTC[C/T]CCATATATGTTCATT | 8853 |
rs139661093 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9235986 | TGCTGGTGGCATCTG[A/G]TGGGTGGAGGCCAGG | 8853 |
rs139673224 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262906 | TCGGCTATCTTACAT[A/C]TCCTCTCCCCTGTTT | 8853 |
rs139699055 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230697 | AGCTGGGAGTAAGAG[C/T]AGATATGTGCAAGGC | 8853 |
rs139716137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299907 | TCCCCACTTTACAGA[C/T]TAGATAACTGAGGCC | 8853 |
rs139736627 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340286 | TCCGCCTCCCAAAGT[G/T]CTGGGATTACAGGCA | 8853 |
rs139764290 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257910 | TGGAAAAATACCTTT[A/G]TGAGTGTTACTTTCT | 8853 |
rs139798798 | in-del | -/C | 0.164873 | 0.23506 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291229 | TCACCTTGATTATTT[-/C]CTTAGGATAGATTTC | 8853 |
rs139801652 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298544 | CTCATCCCCCTTCAT[A/C]CTTATCCTAGAGTGG | 8853 |
rs139804849 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294897 | AGCAGGACCATGGAG[G/T]TTGCGTTCCTGTTTC | 8853 |
rs139818574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248684 | CACTGCTTCTACTGT[G/T]TACTCTGCTTGTAAC | 8853 |
rs139828035 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370016 | GCTAATTTTTTGTAT[C/G]TTTAGTAGAGATGGG | 8853 |
rs139864581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246990 | GGGCCACGGTATATA[C/T]TACCACACCCAGCTG | 8853 |
rs139865509 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338323 | TGTCTGTCTGTGTCT[A/C/G]TCTATCTCTCTCTGT | 8853 |
rs139881591 | snp | C/G | 0.000313084 | 0.0125078 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356175 | GTTGCTCTTGTTTTT[C/G]TAGATGGATGTCTGT | 8853 |
rs139883054 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286315 | AGGCAGGAAGATTAC[A/T]TGAACCTGGGAGGTT | 8853 |
rs139894145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238799 | TGACCTAAAACACCC[C/T]GAAAGCTTCCCTCTT | 8853 |
rs139908630 | snp | C/G/T | 0.0001155 | 0.00759854 | missense, synonymous-codon | ASAP2 | GRCh38.p7 | 2:9380790 | CAAGCGCCTCAAGCA[C/G/T]GAGCACTGTGAGGAG | 8853 |
rs139927188 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365106 | TAAGAAATACATACT[A/T]TGTAAACTACATCAA | 8853 |
rs139930676 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282170 | TTTGAGGCCCCGCAC[A/G]TAACAGCCTGGCATG | 8853 |
rs139947151 | snp | C/G | 0.00261376 | 0.0360562 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400858 | CCCCCTTTCCTGCCT[C/G]TCTGCTCTAGCCAGG | 8853 |
rs139980237 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349266 | ATAGGAGTTATTCCT[A/G]TATCTAAGACCCCAC | 8853 |
rs139989241 | in-del | -/AA | 0.16618 | 0.23553 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261380 | TTGGACAAGTCACTT[-/AA]ACTCTTTGAGTCAGT | 8853 |
rs139999557 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301731 | GTTGCAGCATGAGAT[C/T]TGAGGTGACCCTGGG | 8853 |
rs140018946 | snp | A/G | 6.59065e-05 | 0.00574012 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9358844 | GGTTCATTATTCCAG[A/G]ATGCAGTCCCTGACC | 8853 |
rs140044415 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235109 | GTCCCCGCCCGACAT[A/G]TGCCAACTGGAGCTT | 8853 |
rs140064358 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229590 | GCTGGCTGCTTTTCT[A/G]TAGGAGCCTGAATCT | 8853 |
rs140091080 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340179 | AGGTACGCGCCACCA[C/T]GCCTGGCTAATTTTT | 8853 |
rs140100102 | snp | C/G/T | 0.000131755 | 0.00811543 | missense, utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207196 | TCACCACCCGCACGG[C/G/T]GCAGTGCCGGAACAC | 8853 |
rs140109222 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341407 | TCAGATTTGCCTGCA[C/T]GCTTCAATTGGCCTA | 8853 |
rs140112567 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268825 | CTAGGGCTGCCTGAG[G/T]GCTGCAGGCCTCTGC | 8853 |
rs140132196 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264835 | TAAAAACTAATACAG[A/C]AATTTAAAAAATACA | 8853 |
rs140136435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337810 | TGTTTTGTTCTTGAT[A/G]TTTTCTGCTCTCTGT | 8853 |
rs140136482 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385762 | CTGAAATCATCAGAC[A/G]ACCTTTAGAGCTCAC | 8853 |
rs140156598 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381008 | GGGGGACCCACCCCT[C/T]GCAGTGAGACTTGGG | 8853 |
rs140165937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242558 | CATCTTGTATTGGGC[A/G]GTGTGTGGGCTCTGT | 8853 |
rs140179635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309345 | AATCGCACAGTCATG[C/T]GCAGTCCCAAAATCA | 8853 |
rs140189620 | in-del | -/TG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265712 | TTTGCTTTTACAATT[-/TG]TGTGTGTGTGTGTGT | 8853 |
rs140227385 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371359 | ACATATATTTTTCTG[A/T]TGAATTACTTCTTAC | 8853 |
rs140228177 | snp | A/T | 4.94344e-05 | 0.00497139 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9376973 | CTCTCTTCACATTGT[A/T]GACTTTTTAGTTCAG | 8853 |
rs140228765 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237355 | TGATACCTTTGAAAA[C/G]ATTAAGATGGTTCTG | 8853 |
rs140236738 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334278 | GGTCTGGAACTCCTG[C/G]TCTCTAGTGATCCTC | 8853 |
rs140237073 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346435 | AGCAAGACTCCATCT[-/C]AAAAAAAAAAAAAAA | 8853 |
rs140252961 | in-del | -/T | 0.0138799 | 0.0821421 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245097 | CCTTGGGCAAGTCAC[-/T]TTGATACCCACTTTG | 8853 |
rs140258989 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239219 | TGAATTACATTTTTA[A/G]CACTGCAACTACTCT | 8853 |
rs140273873 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378005 | ACATTTTCAGGGGGC[A/G]GGAGAGGGAAGGTCC | 8853 |
rs140279663 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347364 | TTTGGTTTGGTTTGG[A/T]TTTGACTTGATTTCT | 8853 |
rs140302523 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275912 | CAATATTGTTTTAAC[A/G]TGGCACTTAGCCACA | 8853 |
rs140305748 | in-del | -/CT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338291 | TCTCAAGTATGGTTG[-/CT]CTCTCTCTCTCTCTC | 8853 |
rs140310742 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349726 | ACTTACATTTATTAA[C/T]CCAAATCCTTCACGC | 8853 |
rs140314593 | snp | C/T | 0.000494576 | 0.0157176 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374827 | GAAGCACGCGGATAA[C/T]GCGGCGAAGCTTCAC | 8853 |
rs140323308 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273228 | TCAATTTCTTACATC[A/G]TCGTTTTATAGTTTT | 8853 |
rs140323900 | snp | C/G | 0.00755907 | 0.0610114 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205145 | ATTAGTCTGGTTAAT[C/G]CTGTACTAGACATCA | 8853 |
rs140361147 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396538 | CACCTTGGCCTTTCA[C/G]AGTACTGGGATTACA | 8853 |
rs140369800 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394300 | CTCCCGAGTAGCTGG[A/G]ACTACAGGTGCCTCC | 8853 |
rs140374555 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313172 | GAAATGAACGAAGAA[C/T]GAAAGCAAGCCGACC | 8853 |
rs140396824 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244546 | GTGCGACACAGTTAA[C/T]GTCCACGGGAAGAGC | 8853 |
rs140407404 | in-del | -/TGA | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212590 | ACCAAGAATTTGGGG[-/TGA]TCCTCAATTCTTCCC | 8853 |
rs140436271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240707 | TTCCCTTAGATCTTA[A/G]CAACCTCAGCATAGG | 8853 |
rs140447747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207977 | CTGCTAAGCAGTACG[C/T]TCTCCAGGTCCTGGG | 8853 |
rs140451791 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393900 | ACACAAGGCTTCTGG[G/T]TTCTATTTGCTGCTC | 8853 |
rs140454191 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354029 | CTAGGAGGATGGTTC[G/T]GTGGCAAGGCCGGCC | 8853 |
rs140456165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308506 | AGTGATTTTCCTGTT[G/T]AGAGTTTCCTTGTAT | 8853 |
rs140473585 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317859 | CTCACACACCTACAC[A/G]ATCACTCATACCCAC | 8853 |
rs140498084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222164 | TGCACAGAATAGGTG[C/T]TCAGTAACTTTATTG | 8853 |
rs140507748 | snp | A/G | 4.94474e-05 | 0.00497205 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9335122 | GGATGAAGAAAGAAG[A/G]CAGTTGATACAGCTT | 8853 |
rs140583550 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253357 | TTAGTAGAGACAGAG[A/G]TTCACCATGTTGGCC | 8853 |
rs140589866 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225768 | CCGTGGGAAGTGGTT[A/G]TAGGGGTCTGGATTA | 8853 |
rs140608826 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292878 | AGATGAAAAAGGAGG[C/T]GATTGAAGGTGAGTT | 8853 |
rs140643421 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367183 | CTACAGGTGCACGCC[A/G]CCATGCCTGGCTAAT | 8853 |
rs140669638 | snp | C/T | 1.65132e-05 | 0.00287339 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9350846 | CAACCTGCTAACCTG[C/T]CAGGTGAAGACCAAC | 8853 |
rs140680943 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221283 | ATCATAACCTCTTCT[A/G]TCTATGAACTTGGAA | 8853 |
rs140693928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295644 | CTCCTGAGGAGCTGC[A/G]TTTGCGGGTGTGTGT | 8853 |
rs140714839 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227532 | TCAAACGCTATTCGG[A/G]TGGGACAGGGCTCAT | 8853 |
rs140732073 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304194 | CATCTGCACACAAGC[C/G]TGCTTGCAAGGTTTA | 8853 |
rs140734906 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9223424 | GTAAGGCCTTATCTG[A/G]AACATGCAGGCTTCA | 8853 |
rs140738565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329930 | CTTTTCTTCCTCCTG[C/T]GTTGCCACCACACCG | 8853 |
rs140742552 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291490 | TGTACAGCCGACAGC[C/T]GGAGGAAATGGTCTC | 8853 |
rs140744556 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338075 | TCCCCATCCCACGTC[A/G]TCCATCCGATGGTGT | 8853 |
rs140776835 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326095 | CATTAAAATCATGTT[A/G]AAAGGCCGGGCAGGG | 8853 |
rs140780364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332582 | CACTTGATTCCACTA[C/T]GGGGCTCATGCTCAC | 8853 |
rs140837371 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307873 | CTGTGCTGCCAGGGA[C/T]GGGCTGGGCGCATCT | 8853 |
rs140864383 | in-del | -/C | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362766 | AGGATCACCTGAGCA[-/C]CCAGGAAGTTGAGGC | 8853 |
rs140949927 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244766 | TGTAGGAAGAACAGG[A/G]GATGGATTTAATGTG | 8853 |
rs140966207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354500 | AAATTGGCCAGGTGC[A/G]GTGGCCCACGCCTGT | 8853 |
rs140967236 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283972 | TAATATATGAATCTG[A/G]GGGAAGGGACGCAAT | 8853 |
rs140984635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255586 | TCCTTGCCGTGGATT[C/T]GGCAGATGGTGTCGT | 8853 |
rs141013484 | snp | A/G | 0.00132998 | 0.0257531 | intron-variant | ASAP2 | GRCh38.p7 | 2:9403224 | ACATTTGGAATTTTA[A/G]TAACAACCTACACTT | 8853 |
rs141016017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275408 | CGGTTGACCCAAACT[C/T]CTGTAGACACAAGAT | 8853 |
rs141054152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271704 | GGAAAGTAGGGAAGC[A/G]ACGGGGCCCAAGGGG | 8853 |
rs141076503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288616 | TCAGATTGCTTTGCC[A/G]ACATGAACTCTTCCT | 8853 |
rs141091679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219252 | TTCTCATCATTGGAA[G/T]ATGTGCTCTCTAGTG | 8853 |
rs141105677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277598 | AAAATTGAATGGAAA[A/G]TACAGAAACTTTCCA | 8853 |
rs141117730 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291973 | CAAATGAAGAAACGG[-/T]TTTTTGCTGTGGGAG | 8853 |
rs141123604 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327315 | TCGTGGTCACTAATG[A/C]ATTCTCCAAGTTAAA | 8853 |
rs141123652 | snp | A/G/T | 0.000152013 | 0.0087171 | synonymous-codon, missense | ASAP2 | GRCh38.p7 | 2:9393582 | GCCTGGGATCTCACA[A/G/T]ATCAGGCCCCCACCT | 8853 |
rs141142654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281156 | TTTTTTTTTTTACTG[C/T]GTTCACTTGGACTTT | 8853 |
rs141143089 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274026 | CCAGGAATGAACAAG[G/T]ACAGCTTGGAGGTTA | 8853 |
rs141144910 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317715 | GCCCACACACACCCA[C/T]ACACAATCACATTCA | 8853 |
rs141148036 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9269946 | CAGCTCAGCTGAGCA[A/G]CAGAGATTGGAAGAG | 8853 |
rs141155415 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397210 | ATGCTGCTGTTTTTC[A/G]AGAGAAACAAATCAC | 8853 |
rs141167822 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398939 | GTTAGGGATGACTGC[C/T]GGCCAGGGGGTCAGC | 8853 |
rs141182305 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9224249 | TCTGAATACTCTGGC[A/G]CTTCCTTTTTGGGGT | 8853 |
rs141183525 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9375836 | CTCTCTGAGAGGGGC[-/G]GGTTCCCTGGAACCC | 8853 |
rs141186048 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266222 | CACAGTCATAGCCCA[C/T]TGCAGCCTCGACTTC | 8853 |
rs141188584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318704 | CGTTCTCATTGGGAC[G/T]ATAGGATGGCTCTTT | 8853 |
rs141195207 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395200 | ATTTGGGGCCAGGCG[C/T]CATGGCTCACGCCTG | 8853 |
rs141229599 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261940 | CCAGTTGGACCAGAG[C/T]GCCTCACCCCACCAT | 8853 |
rs141234593 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314522 | TATTCTAGGCCAAGC[A/C]CCATGCTAAGAGCTC | 8853 |
rs141271431 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383543 | GGATTACAGGTGTGA[A/G]CCACTCCACTGGATG | 8853 |
rs141292097 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9401276 | TCTCCTGACCCAGAC[C/T]AAGTTGAAGCCTAAG | 8853 |
rs141300447 | in-del | -/GTGG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305707 | GGAGAGGCTGTAGTA[-/GTGG]GGTATAGATATTGGT | 8853 |
rs141315866 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301366 | TGTGAATTTTCTCTG[C/T]GGTGATGCAGGATGA | 8853 |
rs141350576 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9223195 | CTATATTTTAAAATT[A/G]ATTTATTATCTTCTA | 8853 |
rs141376199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331909 | GATAAGGCTCAGCCC[C/T]GGATGCTGCAGAAGC | 8853 |
rs141387850 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267171 | TTTATTTTAGATCGG[A/G]GGGTACATGTGTAGG | 8853 |
rs141404910 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384208 | CAGAGTCAGTTTTAG[A/G]GAGGGACTATTACCA | 8853 |
rs141420711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260263 | TGGTCTTCATCTGTA[A/G]CAGTGACTCCCGCAG | 8853 |
rs141459252 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256862 | GAGAGTCAGTATGAC[C/T]GTCTCTTAGCCGCTT | 8853 |
rs141467215 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375376 | GGAAGACGGCACGGA[G/T]AGGGGTACTGGGGTA | 8853 |
rs141487278 | in-del | -/CA | 0.332568 | 0.235971 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317385 | CCCCCAACTCACATC[-/CA]CACACACACCCTCAA | 8853 |
rs141513917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309273 | TGTAGCCATATGATG[A/G]AACAGTGCTGGCCAA | 8853 |
rs141544600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253459 | ATGAACCACTGTGCC[C/T]GGCCAAAATTCACGT | 8853 |
rs141547459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250393 | TCCTGGAGTTCTCGC[A/G]GTGCCCCAGGTGCCA | 8853 |
rs141588173 | in-del | -/TGGCTC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9238070 | GTGTGGGAGGAGCCA[-/TGGCTC]TGGCCTCCGACTGCT | 8853 |
rs141589412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248880 | AGTGTTAGGTGGCAA[C/T]GAGGCTGGCTCTGTG | 8853 |
rs141609809 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368033 | CTCAGTGCCGCTTCA[C/G]TCTACCAGAACTACC | 8853 |
rs141616685 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316230 | AGGAGGCTAAGGTGG[A/G]AGGATCGCCTGAGCT | 8853 |
rs141617855 | in-del | -/C | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296094 | GCTGCAGCACTAAGG[-/C]TGTCTCTGGTGGAGT | 8853 |
rs141621527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246041 | AGGGTGGTGTGACCC[C/T]GTTGGGGGAAGGAGC | 8853 |
rs141636809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248025 | CAGGAACTGGAAGTC[A/G]ACAGAAAAGGCCTTG | 8853 |
rs141649221 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362821 | TGCACTCCAGCCTGG[C/G]CAACAGAGTGAGACT | 8853 |
rs141664050 | snp | C/T | 0.000955157 | 0.0218327 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356159 | TGGAATTTAACACAG[C/T]GTTGCTCTTGTTTTT | 8853 |
rs141676079 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288543 | GGTATGACGTGGCAA[A/C]AATGAAGGGCTGAAA | 8853 |
rs141680861 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289578 | AGCCCAGTCTCCACT[C/T]TTCACCCTCTCACCT | 8853 |
rs141686039 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359439 | GGAGGAGACAGAAGC[A/T]TTTTCTGTGAAGTGG | 8853 |
rs141692216 | in-del | -/TTAT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9290194 | AGACATATTCTAATG[-/TTAT]TTATTTATTTATTTA | 8853 |
rs141708233 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296877 | TTAAAAGGAGAAGGA[A/G]CTGCTGTGTGGGGCT | 8853 |
rs141714475 | snp | C/G | 1.64874e-05 | 0.00287113 | missense | ASAP2 | GRCh38.p7 | 2:9388328 | AAGACCGGCCCATCA[C/G]CTTCTACCAGCTGGG | 8853 |
rs141726512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355385 | TCTCTAGTGTTTTCT[C/T]ATGAGTGGATTGAGG | 8853 |
rs141770269 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284278 | TCAGTTTCCACTGTT[C/T]TGTTCAGCTACAAAT | 8853 |
rs141801887 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234498 | AGGAGGAGCTCAGAA[A/G]CAGGGAGAGATCACT | 8853 |
rs141818006 | snp | A/G | 0.0103295 | 0.0711199 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403649 | AAAATGTTTGCATTA[A/G]TGAATAAATTCTTCC | 8853 |
rs141827510 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343353 | CATCTTGCTCCCCTC[A/T]CGTTTCCTTTAAGTC | 8853 |
rs141891003 | snp | C/T | 0.000313928 | 0.0125246 | missense | ASAP2 | GRCh38.p7 | 2:9385269 | GCCTTATCTGGAAGA[C/T]TTAATTCTCACGTTC | 8853 |
rs141894530 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352236 | ACACACACACACACA[A/C]ACACACACACAAACA | 8853 |
rs141917478 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238523 | CCCTTGTCTTACTGG[A/G]AATGTCTTTCTCAAG | 8853 |
rs141934520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348552 | TATTTAACCTGAATA[A/G]CAAACAGTTATTAAT | 8853 |
rs141936395 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275223 | TACAGGTGCATGTTC[C/G]CATGCCCGGCTAACT | 8853 |
rs141948077 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9344434 | TTTTTGTTGTTGTTA[A/G]AAAAAAAACACATTA | 8853 |
rs141959626 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236580 | TAAACATTCTTAATG[G/T]CTAAAGAGGATTTTT | 8853 |
rs141972913 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238229 | CTTGTATTTGTTCTG[C/T]TTTTAAAACCTCAGC | 8853 |
rs142010601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348114 | TGATGACACTTTTTT[A/G]TCTGTTTGTTTGTTT | 8853 |
rs142012658 | in-del | -/G | 0.0119091 | 0.0762411 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251651 | GGGAAGGGAGCAGCT[-/G]GGGGGCGCACCTTGT | 8853 |
rs142049447 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343831 | TTCATTGCTAGTCCT[C/T]GCTTACCCTAAGAAG | 8853 |
rs142051646 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9241414 | TGAGTTCCTTATCCA[-/T]TATCAGGGTTGGGGA | 8853 |
rs142055964 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386846 | TAGTTTAATGAAGCT[A/G]GCATTTGAAATAGAA | 8853 |
rs142056712 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271992 | GTTTCCAAATCTTGG[A/C]CATTGTGAACAGTGC | 8853 |
rs142056804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232507 | GTGCAGAGAACTTGT[C/T]TGATTTGTTTAACCA | 8853 |
rs142092290 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270324 | AGCATGGTAGTTGAG[A/T]GCCTGGGTCTGGTTA | 8853 |
rs142115918 | snp | C/T | 0.000412014 | 0.014347 | synonymous-codon, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9297443 | GCACTTTTCAAAAAC[C/T]TGGTAAGCAGCTCTG | 8853 |
rs142116939 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341986 | TTACTGATTGCTCAC[A/G]TGGAGTTTTTTGGTT | 8853 |
rs142120526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272216 | CCACATCCCCACAAG[C/T]ATTTGTTATTGCCTG | 8853 |
rs142131432 | snp | C/T | 0.00498264 | 0.0496638 | synonymous-codon, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207113 | CGAGGCGATGCCGGA[C/T]CAGATCTCCGTGTCG | 8853 |
rs142153749 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339134 | CAGTGAGCCAAAATC[A/G/T]CACTGCTGCACTCCA | 8853 |
rs142162544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394253 | CACTGCAAGCTCTGC[C/G]TCCAGGGTTCTTGCC | 8853 |
rs142173764 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217604 | TGTTCTTCTTAGAGG[C/T]ATGTTTTTGTTTTTT | 8853 |
rs142179326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386212 | ATTAGATGGATGGAT[A/G]GGTCAGTAGGTAACC | 8853 |
rs142195073 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254832 | TTCACCAAGTGATGG[A/G]CATTTGGGTTCTTTC | 8853 |
rs142269601 | in-del | -/T | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301257 | AGGCGTGAAAGAATG[-/T]TTATAAAGCAGTTGG | 8853 |
rs142286914 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358330 | TATCAGCATCTGTAG[A/T]TGCATATGTTTTAAG | 8853 |
rs142312863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259336 | TCCCTGCCTGTTGCT[A/G]CACTTCCCCTCCCTT | 8853 |
rs142333654 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289444 | ATTCTTTAGTAACCA[G/T]AAATATTCTTGACCC | 8853 |
rs142344442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218806 | TTTTTTTGGCTGTCG[C/T]CTCTGTTTTTTTCTT | 8853 |
rs142347590 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | ASAP2 | GRCh38.p7 | 2:9388399 | GATGCTGCAAACCTT[A/G]CCAAGGAGAAGCAGA | 8853 |
rs142349008 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374166 | GGAGTCTGAGCATGT[C/T]GCCACATAAAGGCCA | 8853 |
rs142352838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299475 | GCTCCCATGTGTCAT[C/T]TCTCTGAAACTCCTA | 8853 |
rs142364139 | in-del | -/TCAA | 0.4021 | 0.198407 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317336 | CAATCATATCTTCAC[-/TCAA]CTCACACACACCCTC | 8853 |
rs142414110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9215448 | GAATATAAACAATAC[A/G]AGATATTTCTAATAA | 8853 |
rs142424565 | snp | A/G | 0.030278 | 0.119257 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212526 | GGTGGCCAGCTCGGC[A/G]TCTGCGGTAGGATTT | 8853 |
rs142427441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327626 | ACTTCAATATTTAAT[C/T]ATCTGACTGTCAGAT | 8853 |
rs142427466 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285701 | TGACATATCAGTGGG[G/T]GGAAAAATTCATCTC | 8853 |
rs142462823 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9303833 | GGGAATGCTGTGATA[C/T]GGTAACCCCCATACA | 8853 |
rs142464364 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252041 | CCAGTAGGTGTTAGA[A/G]TGTTAGCCTGTACAA | 8853 |
rs142480376 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236288 | GGTAATCAAGTGCCA[C/T]GAAGTAAAGATCATT | 8853 |
rs142480883 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320989 | CCTAGAGTAGAGAGA[A/G]TCGAGCTACAGGGAA | 8853 |
rs142510578 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346712 | TAGTTCATGCTTTTA[C/T]AGCTCTGAAGTCAAG | 8853 |
rs142519115 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318062 | GCAGCAGACAGAAGA[C/G]TCTGCCTTTGTTTCC | 8853 |
rs142584693 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239682 | AGGGGCACAAAACCA[C/T]TGTTTTTTGTTGTTG | 8853 |
rs142591836 | snp | C/T | 3.32165e-05 | 0.00407519 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374938 | AATCCCACTGGCCAA[C/T]GGACATGTAAGAGTG | 8853 |
rs142596288 | in-del | -/AGG | 0.195214 | 0.243923 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279062 | CAGCTTGCATGCTGC[-/AGG]AGGAGGAGTTGGTTT | 8853 |
rs142606196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276972 | GGGTGTCTTCCACTG[C/T]CTGTGGGGAGGCTTA | 8853 |
rs142607335 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249202 | CTCTGTCAGACAGCA[A/G]TGGCCTCATGTCTTG | 8853 |
rs142609985 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360833 | GCATAATTTTTAATA[A/G]TAGCAGTGCTTAACA | 8853 |
rs142630928 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397108 | ATTATTTCTGCCTCT[A/G]TACCAAAGTGGCCAC | 8853 |
rs142664793 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289967 | GGTGTTGGAGAAGGC[A/G/T]GAGGAAGTGGCAGGA | 8853 |
rs142694391 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352879 | TGCTAGAGTCCATTG[C/T]CATCTTTGAAAAGAG | 8853 |
rs142754327 | in-del | -/TCAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317337 | AATCATATCTTCACT[-/TCAA]CACACACACCCTCAC | 8853 |
rs142778233 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271054 | TGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 8853 |
rs142791085 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283810 | CCCTCACATGGCAGC[A/G]AGAGAAAGCAAGATG | 8853 |
rs142821052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308942 | TCTGCCTGGATACCC[A/G]TTCTTTCAGATAAGC | 8853 |
rs142821299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268389 | CATCTGTCCTTAGGC[A/G]CACACTTTCCTCAGC | 8853 |
rs142824026 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402933 | TTCATTCATTCATTG[A/G]AAAATGGCAAGTGGG | 8853 |
rs142826187 | snp | A/G | 0.000697084 | 0.0186563 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320350 | AATGTGAGTGTTCTC[A/G]TTTTTAAATTTACGT | 8853 |
rs142841882 | in-del | -/TTTTCT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9235320 | CCCCGGGCAGAGTTG[-/TTTTCT]TTTTAAGAGGTAGCC | 8853 |
rs142847031 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229236 | CTGCAGGGCTGGTGG[C/T]GGGGCAGGTGGCCGG | 8853 |
rs142852307 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385029 | GTGGATGAAAACTAA[C/T]ACAGTTTACAAAGCC | 8853 |
rs142852762 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294737 | TTTGAGGGACACCAC[A/G]AGGCTGCATAGAGTC | 8853 |
rs142872024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337149 | CTGATTGCACAGAGG[A/G]ATCAAATGAACCTCC | 8853 |
rs142937603 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339744 | TTGCCCCTCTTCCTT[C/T]TTCACTATCTGACTC | 8853 |
rs142943813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380560 | CTTCTGTATTTAGCT[A/G]TAGTTCTATACAATT | 8853 |
rs142948637 | snp | C/T | 0.000115318 | 0.00759249 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9358808 | CTGCATCGAGTGTTC[C/T]GGAATCCACCGAGAG | 8853 |
rs142960664 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231014 | CCTGCCTGTTTCTGG[C/T]GGGGAGATGCTGCCC | 8853 |
rs142975974 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340537 | TGCTTGGCTCAGCAA[G/T]GCTTCCAGCTCCCAG | 8853 |
rs142979861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269652 | AGTGGGGCCCATGAA[C/T]GGAGGAAGAGAAGCA | 8853 |
rs142980329 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336781 | GTGGGCTAGCGGTAA[C/T]GAGGAGGAGGTAGTG | 8853 |
rs142988043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370168 | CATTTTGTGTGGCAT[A/G]TCTTTGAGAAACGGA | 8853 |
rs143005706 | in-del | -/TG | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309618 | AAGTCATACTTTAAA[-/TG]TGTGTGGTTTATTGT | 8853 |
rs143052280 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362042 | CTGACACACCGTTAA[C/G]AACCATAAAGTATTA | 8853 |
rs143138736 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245076 | TACCTCTTACTGGTA[C/G]TGTGGCCTTGGGCAA | 8853 |
rs143148546 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267046 | CAACTCTAATTTCTT[G/T]TCTTTAAAAGATGCT | 8853 |
rs143162624 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216693 | CTCGAACTCCTGACC[G/T]CAAGTGATCCACCCA | 8853 |
rs143188135 | in-del | -/CT | 0.423881 | 0.179625 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317563 | ACATCCACAATCACA[-/CT]CTCACACACCCACAC | 8853 |
rs143191815 | in-del | -/G | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278970 | CTTGCTGGTAACCAA[-/G]GAGAACGGAGGGTTC | 8853 |
rs143205613 | snp | C/T | 0.0162398 | 0.0886349 | upstream-variant-2KB, intron-variant, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9206191 | CGTTTATCTTGTGCT[C/T]TTGGGCACACTGTGT | 8853 |
rs143225194 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247278 | AGGATGAACTCTTCG[C/T]TCCTCAATTAAGGAG | 8853 |
rs143226789 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9242106 | GTTCGTTGTGTTTGC[C/T]ATCTTGGAAGAGAGG | 8853 |
rs143271616 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280441 | GAGCTGTGCAAGCCA[A/C]AATCGGGAAGAATCT | 8853 |
rs143290006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352284 | ATACCTGTGTCTAGC[C/T]AGCAAAAAAGGCTTG | 8853 |
rs143300065 | in-del | -/GTTCCC | 0.0142736 | 0.0832652 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270250 | GTTTTTTACACATAA[-/GTTCCC]GTTCCCGTGAAAGTT | 8853 |
rs143301124 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309037 | TTGTGTTAGAGTCCC[A/G]TTGGCCCAGAGCGCA | 8853 |
rs143304380 | snp | C/T | 0.00016497 | 0.00908063 | missense | ASAP2 | GRCh38.p7 | 2:9374892 | TTGGATTGCTCCAAG[C/T]TTATGCTGATGGTGT | 8853 |
rs143313845 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9246996 | CGGTATATACTACCA[C/T]ACCCAGCTGATTTTT | 8853 |
rs143322114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351834 | TCCCTGTTCCCCTTC[C/T]CATACCCTCTGTGTG | 8853 |
rs143328114 | snp | C/T | 0.093777 | 0.195178 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398044 | ATTACAGGCGTGAGC[C/T]ACTGCGCCCGGCCTC | 8853 |
rs143340599 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252592 | AACACCCCCGCCCCC[A/C]AAAAAAAGCCTTCGG | 8853 |
rs143350818 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286364 | AACTGCACCACTGCA[C/T]TTCATCCTGGGTGAC | 8853 |
rs143353188 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243563 | CAGGCAGATGAATTG[C/T]ATTAAAATACTTCCT | 8853 |
rs143354243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275590 | TCTTCTTTGCGTAGC[C/T]TCTCCCTGAATGCAC | 8853 |
rs143357417 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366445 | TGTGCTCACCTGGGG[A/C]CAGTGTCCTGCTTGG | 8853 |
rs143359879 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291059 | TTTTTAAACTTGGCT[A/T]TCTGCTCCTACCATA | 8853 |
rs143361746 | snp | A/T | 9.01283e-05 | 0.00671238 | missense | ASAP2 | GRCh38.p7 | 2:9378961 | GGAACCTGGATAAAC[A/T]GACAGGGAAAGGCAG | 8853 |
rs143373289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356754 | GAAGTAGCTTTAAGC[C/T]GCTGTCTGGCTCTGT | 8853 |
rs143417697 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396020 | CATCCAGACACCGTC[C/T]GTTTTGCCCTCTCCA | 8853 |
rs143429874 | in-del | -/TTTTTAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9344999 | GTTTATGTTTTTTTT[-/TTTTTAA]TTTTAATTTTAATTT | 8853 |
rs143445554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283012 | TCCCCACCCATTTTC[A/C]TCAAGCCTTAGCTCT | 8853 |
rs143466595 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405240 | ATATTAACGACCCTG[C/G]TAATATCCTTTCTTA | 8853 |
rs143510008 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338591 | CTGGCCTCCATGTCA[A/C]CCTCAGTGGAGGACT | 8853 |
rs143555851 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228808 | GTTGGCCAAGAAATT[A/G]TGAACGGCACTCTTC | 8853 |
rs143584385 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234370 | GGGGAGAACATTTAG[C/T]CAGAGCCTGTCGCAT | 8853 |
rs143591778 | snp | C/T | 1.6546e-05 | 0.00287624 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9344800 | CATATCCCATGGTAC[C/T]GTAAGTATTCTCTTT | 8853 |
rs143610339 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342963 | TTTCTCCCTTTGACT[C/G]TTCAGTTCCTGAGTG | 8853 |
rs143629144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390544 | ATCTGTGTCTGCTTC[C/T]AGCCAGAAATATGTT | 8853 |
rs143642854 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266991 | ATAAATTACTCCTGA[A/T]GTTCACTTTCATTTT | 8853 |
rs143646720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225571 | TTATGGAGGGCTGAG[C/T]ATGTCAGTTGGAAAT | 8853 |
rs143647167 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212493 | TGCCTTAGGTAAATA[C/T]TGATCTACTCCTGAG | 8853 |
rs143682059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262307 | AATGACTGAGACGGT[C/T]CTGGGGTAACAGCGT | 8853 |
rs143703956 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334934 | CACGTGGAGTGTGGC[A/G]TTCCCACGCCTGTCC | 8853 |
rs143720635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274709 | TGCACCATAATGAAG[A/G]GTGTGTTTCTGAATA | 8853 |
rs143739158 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395440 | AGATCACGTCATTGT[A/C]CTCCAGCCTGGGCAA | 8853 |
rs143739667 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379795 | GTCAAGAGATCGAGA[C/T]CATCTGGCCAACATG | 8853 |
rs143741595 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315646 | ATTCCTCACTCACCT[C/G]TCTGGCTGCCAGGAC | 8853 |
rs143741693 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329512 | TGATGGGGAGAGAGA[C/G]AGTGGTGTTGGTTAG | 8853 |
rs143741858 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383121 | GGCCACGGGACTGTT[-/T]GAGTCATGAGTCAGG | 8853 |
rs143746814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230520 | ACAGCTGGACTGCAA[A/G]CTGCTTTCCCTGGGC | 8853 |
rs143753578 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219131 | GGTTGTGTTAGTGAT[A/G]ATCATGGGGTTTTGT | 8853 |
rs143771190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257924 | TGTGAGTGTTACTTT[C/T]TATGTTGTTGCAATA | 8853 |
rs143782203 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227267 | AAGGGCATGTGCTCT[C/G]TGAAGTGGGGGACTT | 8853 |
rs143783270 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327171 | GAGAGCCAGGGCATG[A/T]ATCAGCAGCTTTTCC | 8853 |
rs143783702 | snp | A/C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269101 | ATATTTTAGGTTTGG[A/C/T]GGGCCTCAAGGCGGT | 8853 |
rs143802721 | in-del | -/CACACT/CACT/CT | 0.0252325 | 0.109451 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317452 | ACATTCTCACACACA[-/CACACT/CACT/CT]CATGTGCATTCACCT | 8853 |
rs143833181 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337824 | TATTTTCTGCTCTCT[A/G]TAAGGAGAATACTAC | 8853 |
rs143852559 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318399 | AATAAGGCACAGTAC[A/G]TGCACCGGCCAGGTT | 8853 |
rs143868663 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248652 | AGATACCCAGGCCCT[A/G]GCTGGGCATGGGAAT | 8853 |
rs143875080 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264851 | AATTTAAAAAATACA[A/C]ATTTTGGCCAGACAC | 8853 |
rs143886220 | snp | C/T | 0.00188259 | 0.0306227 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9393504 | GACCCCCACGCCGCC[C/T]CCACCCGTTGCCAAG | 8853 |
rs143920944 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381303 | TGGCCTTGCCGGGGG[C/T]TCCCCAGCTTGGCTT | 8853 |
rs143931072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209315 | TTCTGAGGTAAATCA[A/G]TGTGGATTTCTTTAA | 8853 |
rs143959533 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376295 | GCCCTCACCTCCTGT[C/T]TTCTGTATCTGTCCT | 8853 |
rs143993133 | in-del | -/G | 0.0433465 | 0.140692 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323696 | GAAGTCCAGTCACCT[-/G]TTTTGACTTCCTGCT | 8853 |
rs144014982 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248511 | TGTTTATTCTGCCAC[C/G]TCCTTGCTAGTTGAC | 8853 |
rs144061845 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315784 | AACTGCGCTTTTCAG[C/T]ATTTAAAAATTTAAT | 8853 |
rs144070875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292571 | TTAACAGTGGGAACA[C/T]ATAGGACTCCCTGGT | 8853 |
rs144079124 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368734 | AGGCAGGTTTCGCAG[A/G]TGCTGTGCGTGTGTG | 8853 |
rs144086633 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318918 | ACCTGTGGGAGGAGT[C/T]GGGCTTTCTAGCTGG | 8853 |
rs144090082 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205146 | TTAGTCTGGTTAATG[C/T]TGTACTAGACATCAA | 8853 |
rs144104687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309426 | CCGTATATAAAATTC[C/T]GGAAAGTGCAGTGTT | 8853 |
rs144104764 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355622 | TCAAAGCATATTATT[A/C]TTAGAATTTCTCATA | 8853 |
rs144182619 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239420 | CCTTTTTACTCTTTC[A/G]TTATATTTTGGGTAG | 8853 |
rs144198040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354131 | TATCCGCGAACCCCA[C/T]AGGCACCCTGGGAGG | 8853 |
rs144234685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349909 | CATCTTGAAGTGACC[A/G]GTGGCCAAGGGAAGT | 8853 |
rs144251472 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229569 | AGCGGTTGTGGCCAG[C/T]ATTGAGCTGGCTGCT | 8853 |
rs144258461 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9298798 | GTGGATAAGCCCTTT[C/T]CATGCACACAGAGCT | 8853 |
rs144260355 | in-del | -/CACT | 0.33303 | 0.235809 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317216 | ACCCACTCACATCCA[-/CACT]CACACAATCACACAA | 8853 |
rs144275179 | snp | C/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237144 | ACTGGTTTCTGGCTT[C/G]AGTGAGTGGAAGCTT | 8853 |
rs144311595 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347253 | GCTCTGGAAGTCAGA[A/G]TCCAGAGGACCCCTC | 8853 |
rs144341226 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263769 | TCACTTATCTGTTCA[C/T]ACCGCATGACACCGT | 8853 |
rs144381151 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302824 | GCCTGGTCAGAAGAC[A/G]TTATAGCTAACCTTA | 8853 |
rs144381833 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345478 | AGCCCTGCACACCAC[A/G]CTGTTCTTTCCATGG | 8853 |
rs144383007 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259883 | TGATGAGCCCCTGCA[A/G]TGTCCTGCATAGTCC | 8853 |
rs144392623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245564 | TTGCTCGAATATCAC[C/T]ATACATCTTCCTGAC | 8853 |
rs144398518 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271650 | CAATTTCTTTTTCTC[A/G]GTGGAAATGGTCTGC | 8853 |
rs144428200 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392394 | GAATTCTAGAGCCGA[A/G]GTGCTCGTGACTTCC | 8853 |
rs144437063 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285179 | TTGAATCCCTGCATT[A/G]GAGCAGTGGTTATAA | 8853 |
rs144473121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300006 | GAGGCCAAGGTGGGC[A/G]GGTTGCTTTGAACCC | 8853 |
rs144524521 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317002 | CCACTCTCATACACT[C/T]TCACAACCACACTCA | 8853 |
rs144524705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289724 | CATTAATATAAGGCA[A/G]GATCAAAGAGGATGG | 8853 |
rs144543558 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9220104 | TTTGTTTATTCATTC[A/G]TCAGTTGATGGACAT | 8853 |
rs144568704 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225998 | CGCCCATGAGCTGGA[A/G]GAAAGGAGAAACAAT | 8853 |
rs144572148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329169 | AGGTCTTAAGGCAGG[A/G]AAAAGGCCAAGGTGA | 8853 |
rs144591310 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ASAP2 | GRCh38.p7 | 2:9223931 | ATAGTCAAAATCAGC[A/G]TCCTCTGATTTGGTG | 8853 |
rs144598595 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291602 | GGGAGAGTCTCCACC[A/G]GGCTGCTGCCATAGA | 8853 |
rs144599168 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290290 | TCTCGGCTCACTGCA[A/G]CCTCTGCCTCCTGGG | 8853 |
rs144605342 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222068 | GCTGGGATTAGAGGC[A/C/G]TGAGCCACCGCGCTG | 8853 |
rs144657542 | snp | C/T | 3.29489e-05 | 0.00405874 | synonymous-codon, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9297358 | GTTTGGCGGCAACTG[C/T]GTATGCAGAGATGAC | 8853 |
rs144677577 | in-del | -/ACAC | 0.0573587 | 0.15934 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317586 | CACCCACACACCCGT[-/ACAC]AATCACATTCACGCA | 8853 |
rs144687776 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287564 | TAGTATTTGTTCCTC[C/T]CTAGAGGAGGCTTTC | 8853 |
rs144688997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328073 | AAACATTGAGAACAC[A/G]TTCAATGAAGGAAGC | 8853 |
rs144689623 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9329931 | TTTTCTTCCTCCTGT[A/G]TTGCCACCACACCGT | 8853 |
rs144692276 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263476 | AGAGCTCCCAGAAAA[A/G]TCTCTAGGACTTTTC | 8853 |
rs144705289 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336791 | GGTAACGAGGAGGAG[A/G]TAGTGCGAGGGCAGG | 8853 |
rs144725775 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326444 | TATGTCAAATAGGTA[A/G]TACAGACCTTCTGTG | 8853 |
rs144781867 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9375291 | TGTCTCAAAAAAAAA[-/A]GGAAAACTGGGGCAC | 8853 |
rs144801520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269354 | AAATGTTCGTCTGGA[A/G]ACACCCTTAGCTCAC | 8853 |
rs144820582 | in-del | -/GGG | 0.382473 | 0.212016 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257293 | TGAAGTCTGAAAGCA[-/GGG]GGGACTGTTTTATAG | 8853 |
rs144827364 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386550 | TCATCCACGCTGCTC[A/G]CCTGATTCTCAGCAG | 8853 |
rs144841699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210029 | CCCTTATCCTGTACT[A/G]TGAAACTCACAGGTA | 8853 |
rs144849035 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240472 | GCTGGTCTCAAACTC[C/G]TGGACTGGAGCGATT | 8853 |
rs144869192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260469 | TTGGGGTAGGAGCTG[C/T]GGGTGGAGCGGGGCC | 8853 |
rs144885111 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277912 | TCCAATAAAATTATC[A/G]TTGTGGCATTAGAAC | 8853 |
rs144892988 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238208 | GTTTAGATTGTATGC[C/T]GGTTCCTTGTATTTG | 8853 |
rs144893725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376320 | TGTCCTTCTCCTCTG[C/G]TTCTCTCACCCACCC | 8853 |
rs144914923 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300302 | CCTAGGCAGGCCCAC[C/T]TGGAGCACTCCACAC | 8853 |
rs144922072 | snp | C/T | 3.65243e-05 | 0.00427327 | missense | ASAP2 | GRCh38.p7 | 2:9378952 | CGGGCAGTGGGAACC[C/T]GGATAAACAGACAGG | 8853 |
rs144938149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311199 | AAGTTTGAGACCAGC[A/G]TTGGCAACATGGGGA | 8853 |
rs144955499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243424 | AAAGATTTTTTTTAT[A/G]ATGTGCATTTTTGTC | 8853 |
rs144971908 | in-del | -/GTGTGTGTGTGT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361975 | TATCTCTTTCTCTGC[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTG | 8853 |
rs144985426 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274057 | GAAACAGGATGGAGT[C/T]AGTTATGTCAGATCT | 8853 |
rs145002903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271974 | TTAGTGGACACTTAG[A/G]TTGTTTCCAAATCTT | 8853 |
rs145025837 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395304 | ATGGCAAAACCCCAC[C/T]TCTACTAAAAATACA | 8853 |
rs145040266 | in-del | -/GGGGGG/GGGGGGGG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258698 | GACTCTCTTGTGGCT[-/GGGGGG/GGGGGGGG]GTTGCAACTTCTTTA | 8853 |
rs145045636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9391005 | GTTTCTGTTTTTGTT[C/T]GTGTGTGCACGTGTA | 8853 |
rs145065476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392572 | CTTTCCTGCCTCTCC[A/G]TCTGGTGGTCCAGGG | 8853 |
rs145074565 | in-del | -/CTT | 0.103438 | 0.202533 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300393 | TAAAAGGAATCCCTC[-/CTT]CTCCTTTATAAAATT | 8853 |
rs145085728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347646 | AACATCCGGGAGATT[C/T]GTTCAAAGCCCGAGT | 8853 |
rs145092926 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310064 | AGAATGCTCTTAATT[G/T]ATACAATGAGGTGTG | 8853 |
rs145093182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269968 | TTGGAAGAGGCCCCT[C/T]GGTAACTTGAGAGGA | 8853 |
rs145104334 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247164 | TTTTAATTGAGGAGA[A/G]AGGTCTTCTTCCTGA | 8853 |
rs145131887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307094 | GAATTGTTAGAAATG[C/T]GCAGCCCCAGCCTCC | 8853 |
rs145132337 | in-del | -/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260043 | AGGCTGGCCTCTCCC[-/CA]CGAGTCAGGCACCAG | 8853 |
rs145146471 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9223358 | CTGTTTTATTTGCTC[A/T]TTTAATTTATGAACC | 8853 |
rs145151047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287297 | TGATTACAGGGTCAG[G/T]GTGAGCCAGTACGTG | 8853 |
rs145166855 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219286 | AGCAGTGATTTTCAC[A/G]TTTGCCCTGTGATTC | 8853 |
rs145168343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260330 | TCTGCTGCTGGGGGC[A/G]GGAAGGATGCCTGGC | 8853 |
rs145169553 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358061 | CTGTGAGGGGAAAAC[A/G]TGGCTTTGAACTCAG | 8853 |
rs145173097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332201 | GGTAAAAGTTCTGTG[A/G]AGCTTGGAAAAGTGT | 8853 |
rs145197255 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327390 | ATCACATTATTTTCC[C/T]TGTAAGGGAAATGTC | 8853 |
rs145241401 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256925 | TTCCTGATCCTCCTG[C/T]TGCAGCCAAGGGCTG | 8853 |
rs145272524 | in-del | -/ACCC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322521 | TTAGCAGCCACGATT[-/ACCC]TGGTGGCTCTTCTTT | 8853 |
rs145276372 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323012 | TGCCTGTGCTGAAAC[A/G]TGTGGTGAGCGTTGG | 8853 |
rs145318451 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218653 | TTGGACCTTGGAGCA[A/G]GTGACTTCACTGGTC | 8853 |
rs145338512 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255310 | TACCTGAAGGGCTGT[G/T]CAGGAGAAATGGACT | 8853 |
rs145365491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368118 | TTGAGGCACAGGTCA[C/T]TGGGAGGAGTGGGTA | 8853 |
rs145368880 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236171 | GTCCTTGGCACCTGG[A/T]CTGCTTTGGGGCCCC | 8853 |
rs145382582 | in-del | -/TG | 0.0480414 | 0.147352 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335071 | TCTGATTGGTTCTGT[-/TG]TGTGTGTGTGTGTTT | 8853 |
rs145420401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251047 | GTCTGTAGAGTTTGA[A/G]TTGGAGACAGATTAG | 8853 |
rs145436685 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227630 | AGTAGTAGCCCTGAG[A/T]CTTTAACCAGGATCT | 8853 |
rs145471103 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365494 | GTTTCCCTGCCCCAC[C/G]CCAAACTCTCAAAAC | 8853 |
rs145510574 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382929 | GGCAAGCTGGCTGAG[C/T]GGTGGGAGGACAGGA | 8853 |
rs145511943 | snp | C/T | 0.014798 | 0.0847349 | missense | ASAP2 | GRCh38.p7 | 2:9393566 | CGAGCAAGCCTGCCC[C/T]GCCTGGGATCTCACA | 8853 |
rs145521866 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276673 | CTCCTGAGTAGCTGG[A/G]ATTACAGGCACACCC | 8853 |
rs145564656 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313618 | GCCTTCTTTCTTGCA[C/T]GTGCCTTGTTCTAGA | 8853 |
rs145607628 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308502 | CATCAGTGATTTTCC[C/T]GTTTAGAGTTTCCTT | 8853 |
rs145624005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389592 | TCCCTGCCGTCCTGG[A/G]TGTCTCACAGACCCT | 8853 |
rs145634845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308734 | TGTTCTAGCCAACTC[C/T]GCTGCTAATAGTTGT | 8853 |
rs145637776 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240717 | TCTTAGCAACCTCAG[C/T]ATAGGAATTTTTCCT | 8853 |
rs145646637 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212383 | GCCTTATATGATGTC[A/G]TACCGTTGAGTCTTG | 8853 |
rs145694494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319467 | TGGAGAACAGGTCAG[C/T]GGAGTTAGCCCAACT | 8853 |
rs145709413 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348142 | TTTGTTTGTTTGTTT[G/T]TTTCTTTTTGAGACG | 8853 |
rs145710262 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242846 | TTGTCAGGTGAGACT[A/G]TTACACGTGTTCAGA | 8853 |
rs145734851 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398637 | ACATGGTGAAACCCC[A/G]TCTCTACTGAAAATA | 8853 |
rs145770828 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219069 | TGCTGCTTTCGTTGG[A/T]CTCTTAATTAAAACT | 8853 |
rs145788296 | snp | C/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 2:9256039 | GTTTTGATGAAGGAA[C/T]CTGTGTAGACTTAAA | 8853 |
rs145842071 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219476 | TGACCTAAAAATTCC[A/G]TAGTTCTTTGTATTC | 8853 |
rs145861142 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256199 | AAGCAAGTAATTCTG[A/G]CAGCCCAATTAATTC | 8853 |
rs145875416 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300649 | TGTTTCATTTATTCC[C/T]CTTGGCAGCTGTGCA | 8853 |
rs145884515 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232603 | TCATAAGCTTCCTGG[G/T]GGCAGGGATTTTTGA | 8853 |
rs145896690 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295718 | GGTCTCAGAAATTCA[C/T]TTAATTTATCTAGAA | 8853 |
rs145938139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342088 | AGATAACAGTACTCC[C/T]CTAATTGATCTACAC | 8853 |
rs145947560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289497 | GAATAAAAGTAAATG[C/T]GGATACATTCTGTAC | 8853 |
rs145958844 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219434 | AACATGAGAGATTTG[G/T]ACTAGATGTTCTCTG | 8853 |
rs145970075 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216847 | CAAGTGATCCTCCTG[C/T]CTTGCCCTCCCAAAG | 8853 |
rs145974356 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286302 | GTTTGGGAGGGTGAG[G/T]CAGGAAGATTACATG | 8853 |
rs145985104 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323069 | CTTCAAGGCTGTCCC[A/G]TTGAGTTCTGTGCCA | 8853 |
rs146002507 | snp | C/T | 0.000928952 | 0.0215317 | missense | ASAP2 | GRCh38.p7 | 2:9400798 | GCTATGGTCCTGCAG[C/T]CCCCTGCACCCATGC | 8853 |
rs146011570 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318982 | AGCAAGGGTGTATTT[A/T]CCTGCTGGGAAGGTC | 8853 |
rs146018188 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9339199 | CAAAAACAAAAAACT[A/G]GGGACGGGGCAGGAG | 8853 |
rs146088081 | in-del | -/A | 0.0475351 | 0.146656 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383834 | ATACTGTGCAGCCAT[-/A]AAAAAAGGATGAGTT | 8853 |
rs146098573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268497 | CAAGGGGGGAGGTTC[A/G]TTATTGCTCTGGCTT | 8853 |
rs146124852 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380997 | AGGGAAACCTAGGGG[A/G]ACCCACCCCTCGCAG | 8853 |
rs146193634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253545 | AACGTAGCAGAGTGC[C/T]GTCACGCAGAACTCC | 8853 |
rs146221000 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249066 | CTGGACAAATTGCAT[C/G]TTTTGTGGCTGGGCT | 8853 |
rs146230275 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363191 | TTTTTAAAATCCATT[C/T]GTCCATTGGTGGCAT | 8853 |
rs146255280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356883 | TTTTATTTTTACATT[C/T]TGATAAAGCATATTA | 8853 |
rs146275239 | snp | A/G | 8.24165e-05 | 0.00641883 | intron-variant, synonymous-codon, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391141 | CCGGCAGCGATCTTC[A/G]TCAGATCCGCCAGCT | 8853 |
rs146277749 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379890 | CCAGCTACTTGGGAG[C/G]CTGAGGCAGGAGAAT | 8853 |
rs146312868 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238357 | GGACTTAGGGGAACC[A/G]CTTGATATTTGACAA | 8853 |
rs146339417 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235261 | ACACAGATGGCTGGT[C/T]GTCCTGTGCACCAGT | 8853 |
rs146347553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299743 | TTTACCTTTATTCAG[C/G]TGATATCTAGACCTG | 8853 |
rs146411567 | snp | A/G | 0.029116 | 0.117091 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332528 | AGTACACCATTCATC[A/G]TCATGCTGGAAACAG | 8853 |
rs146493726 | snp | C/T | 0.00914312 | 0.0669923 | upstream-variant-2KB, intron-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205924 | GAGGTTGGCTGGCTG[C/T]TGTAGCACGTTCTCC | 8853 |
rs146496900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218919 | TTCCCTCCTTGGAGA[C/T]ATCACTGGAGTTGAT | 8853 |
rs146500277 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277377 | AATTTAATTATGATT[G/T]TCCTGAGTTATTTAC | 8853 |
rs146515642 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397188 | CTCCCTGGGATTTAC[A/G]CTTTCCATGCTGCTG | 8853 |
rs146527447 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394415 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 8853 |
rs146562961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284130 | GTATTTCATCCACAA[C/T]TTCAATTCCTCTTTG | 8853 |
rs146595384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264610 | ACGTGAATATATCCT[C/T]GTGGTAAAGTTTTCA | 8853 |
rs146621018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260209 | TGAGGCCCAGGTGAT[C/T]AAGTAATTTGTGTGT | 8853 |
rs146629001 | in-del | -/C | 0.0763149 | 0.179815 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334375 | CATTCCTTTTCTTTT[-/C]CATGTCGCGGTCGCC | 8853 |
rs146630056 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375373 | AGAGGAAGACGGCAC[A/G]GAGAGGGGTACTGGG | 8853 |
rs146632022 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300008 | GGCCAAGGTGGGCGG[G/T]TTGCTTTGAACCCAG | 8853 |
rs146655894 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371167 | TGTTGAAAAAGAAAT[C/T]TACATCCCCCAACCC | 8853 |
rs146656171 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295959 | AACAAATGTTCCCTC[A/G]TTTTCCCACATTGTC | 8853 |
rs146689258 | snp | A/G | 0.00363864 | 0.042498 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9403297 | CAAAGGCGCATTCCC[A/G]GTGTCATTTGTGCAC | 8853 |
rs146714619 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247016 | AGCTGATTTTTTAAT[A/G]TTTTTGTAGAGATGG | 8853 |
rs146743270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279565 | ATGTTTTGTTTTGCC[A/G]GTCGTCTGATTCAGG | 8853 |
rs146750323 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354013 | ATGAGCATGGGCTTT[C/T]CTAGGAGGATGGTTC | 8853 |
rs146751355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283032 | GCCTTAGCTCTCTTT[A/G]ACTTCAGCGTAGCCC | 8853 |
rs146762742 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209399 | TATGTATGGTTTAAT[A/C]ACAATTGATGTGTAC | 8853 |
rs146776570 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350930 | GCCGCGCCATAGAGA[C/T]GTTGTCTTATGCTCT | 8853 |
rs146778579 | snp | G/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278016 | TGCTCTGAGGAGCTG[G/T]GCTGTGTTTCTGATG | 8853 |
rs146788349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397469 | GGACGGAGCCATGTC[A/G]TCAGCGCCCAGTGGA | 8853 |
rs146822411 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318221 | ACGTAATTCTGTCAT[G/T]GAATGTTTTGAAATA | 8853 |
rs146844203 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230662 | GCTTGGCGAGGAGGA[C/T]GGTCCATGTTTTCCA | 8853 |
rs146848319 | in-del | -/C | 0.207253 | 0.246318 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266018 | ACCTCAAGTGATCCA[-/C]CCCCCCACCCCCTGC | 8853 |
rs146854710 | in-del | -/ACACACACACAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352213 | TTAAAACACACACAA[-/ACACACACACAC]ACACACACACACACA | 8853 |
rs146855812 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227293 | GACTTGGGGTTGTGC[A/G]CCCCTGTGCCCTGCA | 8853 |
rs146859037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295311 | TTGATCTCTTTGAGC[C/T]CTAATTGCCTAATAG | 8853 |
rs146871842 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337854 | CTCTTTGGTATTTCC[A/G]TTATTTTTCTTTGTG | 8853 |
rs146957746 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266224 | CAGTCATAGCCCACT[G/T]CAGCCTCGACTTCCC | 8853 |
rs146962967 | in-del | -/T | 0.0777841 | 0.181223 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373251 | TTCACCAGGTGCCCC[-/T]GGAAGTCCTTCCTGG | 8853 |
rs146973120 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383724 | CACGTATGTTTATTG[C/T]GGCACTATTCACAAT | 8853 |
rs146980988 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262086 | ACTCCTGGGCTCAAG[C/T]GATCCTCCTGCCTCA | 8853 |
rs146990789 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301367 | GTGAATTTTCTCTGC[A/G]GTGATGCAGGATGAA | 8853 |
rs146995921 | snp | C/G | 0.000421481 | 0.0145108 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9378983 | GAAAGGCAGCACAGC[C/G]CTGCACTACTGCTGC | 8853 |
rs147021501 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228610 | CCTGAGCAGAGTTCA[C/T]GTGTGATATACAAAT | 8853 |
rs147077103 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359669 | GTAGGGAATTTAACG[A/T]CAAGAGCAATAGTCT | 8853 |
rs147082511 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253424 | CCGCGTTGGCTTCCC[A/C]AAGTGCTAGGATTAC | 8853 |
rs147087780 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288570 | GAAAGCTGCTTACCC[C/T]GGCAAAATGCACATT | 8853 |
rs147097723 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284438 | GAGATGGTGTCATTT[A/G]GGATAAAGAAGACGT | 8853 |
rs147099687 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355530 | CTGACACCAGCAGTA[C/T]GTAAGTGTAGGATTT | 8853 |
rs147109524 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404155 | GAAAGCAACTGTACA[C/G]AGTAGAATTCTGTGG | 8853 |
rs147128347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349569 | AATACTGATTTCTGA[C/T]GATCCAGGAATTCTC | 8853 |
rs147130151 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275797 | ACTGGGGATACAATG[A/C]ACAAATATCAGTGAC | 8853 |
rs147151630 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396398 | TCCCACCTCAGCCTC[C/T]GCATAGCTGGGACCA | 8853 |
rs147161168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393275 | ATCCTAACTTTAGGC[C/T]CCCAGCTTCCTTATT | 8853 |
rs147205169 | in-del | -/CTGG | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208408 | CGTTATTTTTTTTTT[-/CTGG]TTTTTTTTTTTTTTT | 8853 |
rs147223098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334981 | GGAAGGTTTGACCAG[C/T]GAGGGAGGCAGTTGT | 8853 |
rs147224150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262858 | AGGAATCAAAGTCCT[C/T]AGTCTCTTTCACGCG | 8853 |
rs147224955 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9220326 | CAAAGAGGCTGCACC[A/T]CTTGACATTCTTACC | 8853 |
rs147232807 | in-del | -/C | 0.0248432 | 0.108648 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338357 | TCTCTATCTCTCTCT[-/C]TCTCTCTTTCTCTTG | 8853 |
rs147233509 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329891 | ATCATTCCTGCTTTG[C/T]GATGCTTCTTCCTTT | 8853 |
rs147234236 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258462 | AAATGCAAGCTGTTT[C/T]AAAGGTGGTACTTTC | 8853 |
rs147256662 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372860 | AGCAGTTAGCCGAAC[A/G]TGCACAGCTTTGGGA | 8853 |
rs147306151 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275271 | GAGACAGGGTGTCAC[C/T]GTTGGCCAGGCTGGT | 8853 |
rs147329413 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316068 | TCATGCCTGTAATCC[C/T]AGCACTTTGAGAGGC | 8853 |
rs147340030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309501 | AAGGAGCTGGGGTTG[C/T]AAAAGGGGCACAAGA | 8853 |
rs147362303 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352904 | AAAGAGCTCTCATCC[C/G]TCCTCCTTCCCTGCT | 8853 |
rs147371192 | snp | A/C/G/T | 7.2871e-05 | 0.00603583 | missense | ASAP2 | GRCh38.p7 | 2:9393551 | AAGCCTTGAGCCAGC[A/C/G/T]GAGCAAGCCTGCCCC | 8853 |
rs147412286 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257854 | AGCAAAAAAAGAGAA[G/T]ACAAAGGTGGCATTT | 8853 |
rs147426668 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372614 | CATTGAAATATGAGC[A/G]ATGCATACATTTAAG | 8853 |
rs147437107 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254994 | TGTTTAACTTTATCA[A/C]ATGCTGCCATCCCAT | 8853 |
rs147437216 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298246 | AACAGCATCTTTTTC[A/G]TGTCCTCTGTTAGGA | 8853 |
rs147447022 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293949 | AATTGATCACCTTGG[C/G]GTTGCTGGGGATCAA | 8853 |
rs147449860 | snp | C/T | 0.130351 | 0.219509 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369165 | CTGGGATTATAGGCA[C/T]ATGCCACCACGCCTG | 8853 |
rs147541120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239171 | CTGACTGAGATGACC[A/G]TATGGTTTCCCTTTT | 8853 |
rs147542408 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281089 | CACTAAGAAATGGTA[C/T]GCCCAGTTTCATTGA | 8853 |
rs147573807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346872 | TCACTTCCATAGCTT[A/G]AGCTTCCTCTCAAAA | 8853 |
rs147574074 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9344435 | TTTTGTTGTTGTTAA[A/T]AAAAAAACACATTAG | 8853 |
rs147574097 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271984 | CTTAGATTGTTTCCA[A/G]ATCTTGGCCATTGTG | 8853 |
rs147575214 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231896 | CTTGACCCAGCGGAC[A/T]CTTTGGGAAGTGGCA | 8853 |
rs147582792 | in-del | -/ATC | 0.00993419 | 0.0697739 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405749 | TAAAAAAAGTACACT[-/ATC]ATCATACTGTACATG | 8853 |
rs147583746 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341659 | AGTTGAGTCTCCTGA[C/T]AGGTTTATTTTTAGT | 8853 |
rs147606089 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387589 | GGCCACCCTGTGGGG[C/T]AGCATAAGAAGGCAT | 8853 |
rs147656958 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218668 | GGTGACTTCACTGGT[C/T]CTGCCTCAGTTGCGT | 8853 |
rs147677605 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325913 | AAGCAGAGGTGGGCT[C/T]ATCTAACAGTAAACT | 8853 |
rs147687213 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320586 | TTATTTTCAGGAAAG[A/T]TCATTGAGGGAAGTT | 8853 |
rs147689470 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251501 | ATCCCTGATGTCCGT[C/T]GGGTGGGTTTTGTAT | 8853 |
rs147710225 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365804 | GTTGAAGTGAGCTGC[C/T]ATAGAGCAGGAGGGT | 8853 |
rs147720071 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9360525 | GTCCTTCCCTATCAC[C/T]GTCCCCAACAAATGT | 8853 |
rs147778598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239464 | GTGTGGTGATGGAGG[A/G]GTGGTGGTGGGGGGA | 8853 |
rs147782103 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306765 | TTGGGAACTTTCAGC[C/T]GTTTGGTAATCATTG | 8853 |
rs147791391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349957 | GAAGTTTAAGACATT[C/T]TTATTTGATCTTTCC | 8853 |
rs147801449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237296 | CCTGAGGCTGGATTA[A/G]GACATTTCTCATTTA | 8853 |
rs147814676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347280 | CCTCTGTATGACTGC[A/G]TCTACAGAGAGGTTG | 8853 |
rs147816119 | in-del | -/T | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245536 | CTTAGTTTCTGAGTC[-/T]TTTTGGTGTGTGTTG | 8853 |
rs147827063 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342183 | AAGTTCATGTGGAAA[C/T]GCAAAGGACCCAGAA | 8853 |
rs147850846 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9344436 | TTTGTTGTTGTTAAA[A/T]AAAAAACACATTAGG | 8853 |
rs147865638 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249941 | CCACCGTCTCCTGCC[C/T]ATCAAAAGGCTACAT | 8853 |
rs147878438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364629 | GTTAATAAGCTGTCA[A/G]ATGTTAAAGCGGGTC | 8853 |
rs147939174 | snp | C/T | 6.59761e-05 | 0.00574314 | missense | ASAP2 | GRCh38.p7 | 2:9388318 | AACCGGCGGGAAGAC[C/T]GGCCCATCAGCTTCT | 8853 |
rs147984057 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9285398 | AAGGGTATCTGCATG[C/T]CCCACGTGTATACAA | 8853 |
rs147986820 | snp | A/G | 0.000790423 | 0.0198642 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356136 | GGGCTGGACTCAGCC[A/G]TTGTTTGTGGAATTT | 8853 |
rs147996716 | snp | G/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406031 | TCAGGCCTTCAGTGT[G/T]TGTCACTGAGTGGAC | 8853 |
rs148002526 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296851 | CTGCAAAGACCACTG[C/T]TGTTGCTGTATTAAA | 8853 |
rs148056019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234453 | GAACAAGGTAATGGC[A/G]GCGCGTGGCCTTGCA | 8853 |
rs148068757 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343031 | GTTAGTTCTTTCATC[A/G]TTTGGGGATGTGCTT | 8853 |
rs148108109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238430 | GCTACAGCCACATCC[A/G]CTTGAAAAAGCATTG | 8853 |
rs148122999 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348265 | GGGACTGCAGGTGCA[C/T]GCCACCATGCCCAGC | 8853 |
rs148130799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275141 | GCTATAGGGCAGTGG[C/T]GCAATCATGGTTCGC | 8853 |
rs148146124 | snp | C/T | 0.132751 | 0.2208 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395662 | GCCCAGGCTGGAGTG[C/T]GGTGGCGCGATCTTG | 8853 |
rs148149902 | snp | A/G | 0.000197844 | 0.00994397 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374830 | GCACGCGGATAACGC[A/G]GCGAAGCTTCACAGT | 8853 |
rs148151069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288584 | CTGGCAAAATGCACA[C/T]TCTGTAATGTAGCGA | 8853 |
rs148153343 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219164 | TCATTGAGTAATGTG[A/G]ACTGTTGAACTTCAA | 8853 |
rs148195271 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318703 | ACGTTCTCATTGGGA[C/T]GATAGGATGGCTCTT | 8853 |
rs148197138 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9398853 | TAAAAAGTTTACTAT[C/G]TGCCTCTTTAAAGAA | 8853 |
rs148206004 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | ASAP2 | GRCh38.p7 | 2:9224178 | TGAGCAGTGCGAGGG[A/T]AGGGAGGATTGCCTA | 8853 |
rs148216100 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261194 | GAAAGCAGGGGTAAT[G/T]CCGGGTGGTTATTTT | 8853 |
rs148228861 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377337 | CAGGTCATCGTACTG[C/T]GCAAGCAGTGTCCTG | 8853 |
rs148266417 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267142 | TCAATGAGATTTTTT[A/T]AAAAAATTCAACTTT | 8853 |
rs148287848 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207866 | CGGTTACCTGGGTCT[C/T]ACCTGCTTGAACCCG | 8853 |
rs148342436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309050 | CCGTTGGCCCAGAGC[A/G]CACTTCCCCCAGGTC | 8853 |
rs148342922 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241853 | ATCTAATAAGTGAGA[A/C]GAGAACTCAGGACCT | 8853 |
rs148352148 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352162 | AAGCTCAGGAGTAGA[C/T]GTCCAGCCTTGGTAA | 8853 |
rs148393859 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245727 | GCTTTCCTTCCTCCC[A/G]TCTCTGCAGTCTGAC | 8853 |
rs148394867 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338334 | GTCTGTCTATCTCTC[G/T]CTGTCTGTCTCTATC | 8853 |
rs148419154 | in-del | -/AG | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263294 | AGTAATGTGGGTGTC[-/AG]GGAACCCCAGGCCAG | 8853 |
rs148438487 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276926 | TGGTGGCTGACTTCT[A/G]ATGCTTCCAGAGAGC | 8853 |
rs148458025 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9220202 | AGACATATGTTTTCA[C/T]TTCTCTTGGGTATAT | 8853 |
rs148460945 | snp | A/G | 1.65789e-05 | 0.0028791 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374929 | TACGGAAAAAATCCC[A/G]CTGGCCAACGGACAT | 8853 |
rs148478884 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329457 | GGCAAGTAGGAAACA[C/T]GAGCCAATATTTAAC | 8853 |
rs148509844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226170 | GGCTGGCCACGTAGA[C/T]GATAATGCTGTACAC | 8853 |
rs148520974 | in-del | -/AAT | 0.438806 | 0.163867 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264196 | ACCCTGTCTCAAAAA[-/AAT]AATAATAATAATAAT | 8853 |
rs148532235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337015 | GGAGGTTTGGGAAAA[C/T]GGGCTGTTGTGAGAG | 8853 |
rs148534151 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263705 | TCTCGTTGTTCATGC[A/G]TCGTTTTTTCATAGT | 8853 |
rs148575549 | snp | A/G | 0.000451267 | 0.0150143 | synonymous-codon, intron-variant | ASAP2 | GRCh38.p7 | 2:9318574 | GGACAGTTTGCTGAA[A/G]GGGGACCTGAAAGGA | 8853 |
rs148583365 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269622 | AGAGGTGGTGGCACC[G/T]CCCTCAGGCGGTACA | 8853 |
rs148592829 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9306542 | GGTGAGAGGGGCTTG[A/G]GCCTGTTTCTGGGCC | 8853 |
rs148597801 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386677 | CCAGAACCTAGAAAG[C/G]GTTGGTGGTCCTGTG | 8853 |
rs148603412 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281090 | ACTAAGAAATGGTAC[A/G]CCCAGTTTCATTGAC | 8853 |
rs148605108 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210441 | TTAGTGAGTCCACAG[A/G]CCCCAGTGAGGGCTT | 8853 |
rs148645957 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311792 | ACCTGCCGAGAAGCG[C/T]GTCTGGCCCCCACGC | 8853 |
rs148647234 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243475 | GTTTAGGAACTCAGA[C/T]GGAAAATGTGACTGA | 8853 |
rs148656730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217004 | AGTTATTATCAAAAT[A/G]CTATAGGGGCCAGCA | 8853 |
rs148667240 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254800 | CCCTGAAGATAAGCG[A/G]TACTACTTGTTATCA | 8853 |
rs148668216 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353788 | TTTACCATCCTTGCT[C/T]CTAAACAGGGGCTTC | 8853 |
rs148670017 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9323786 | AGCGCCTCTCTGCTC[C/T]ACTCCATTCCACCCG | 8853 |
rs148715499 | in-del | -/AT/ATCA | 0.113334 | 0.209338 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317339 | TCATATCTTCACTCA[-/AT/ATCA]CACACACCCTCACAC | 8853 |
rs148721906 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358303 | TTATGTACATAGTAC[A/G]TTCTCTGTTATTATC | 8853 |
rs148732973 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373151 | GGGACGTTGAGGCAC[C/T]CGCCTTAACCTAGGC | 8853 |
rs148795500 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303386 | TGTCAGTGCTTGGGT[G/T]CCTCTAAGGTCTCTG | 8853 |
rs148796879 | snp | A/G | 0.031825 | 0.122064 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236231 | CTCTGTAAGTTTTGC[A/G]GTATGAAGTTGACCT | 8853 |
rs148804844 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346383 | AGAGTTTGTGGTGAG[C/T]CGATATCACGCCACT | 8853 |
rs148828641 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296214 | GAAATTAGGTAGCCA[C/T]GCAGATAGAAGTTGT | 8853 |
rs148830059 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228002 | AGGTACTGCTTATTT[A/G]TAATAACCAGATAAT | 8853 |
rs148838550 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338309 | TCTCTCTCTCTCTCT[C/G]TCTGTCTGTGTCTGT | 8853 |
rs148849496 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239642 | ACCGAGCACCATTTA[C/T]GTGCCGGCCATTTGG | 8853 |
rs148895137 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9342747 | CCTTGGGATGCAGTC[A/G]AAACTCTGACTCCAG | 8853 |
rs148909820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283809 | ACCCTCACATGGCAG[C/T]GAGAGAAAGCAAGAT | 8853 |
rs148914226 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant, missense | ASAP2 | GRCh38.p7 | 2:9389953 | GGCATCAATTTTCTA[C/T]GGCCCACAATCAAGA | 8853 |
rs148914998 | snp | C/T | 4.94597e-05 | 0.00497266 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9335147 | CAGCTTCGAGATATT[C/T]TGAAATCCGCATTGC | 8853 |
rs148919703 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212387 | TATATGATGTCGTAC[A/C/T]GTTGAGTCTTGAAGT | 8853 |
rs148932255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319634 | TGGGCCTTACCTGAG[A/G]CCATTGAAAAGCCAA | 8853 |
rs148964508 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219088 | TTAATTAAAACTTTG[C/T]TGTGCTTTGCTTCTC | 8853 |
rs148964512 | in-del | -/A | 0.108402 | 0.206034 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299836 | CAGCCGGTGACTCTT[-/A]ACACAGGATAGCTTA | 8853 |
rs148995137 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370164 | TAACCATTTTGTGTG[A/G]CATGTCTTTGAGAAA | 8853 |
rs149039180 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260470 | TGGGGTAGGAGCTGC[A/G]GGTGGAGCGGGGCCC | 8853 |
rs149039710 | in-del | -/T | 0.281313 | 0.248031 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271101 | CCGGCCCTGTTTTCA[-/T]TTTTTTTTTATGGCT | 8853 |
rs149048577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300503 | TTTTTAATACTTCAC[A/G]TATCACTGCAGGTCC | 8853 |
rs149051225 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376716 | TCAGGAGAAACAGGA[C/T]GAATCTCCAAATTGC | 8853 |
rs149095487 | in-del | -/GT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295652 | GAGCTGCGTTTGCGG[-/GT]GTGTGTGTGTGCACA | 8853 |
rs149109242 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238203 | GACAGGTTTAGATTG[C/T]ATGCTGGTTCCTTGT | 8853 |
rs149120238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247208 | GCTCGTGAGTTTTGA[C/T]GGCACAAGCTGCATG | 8853 |
rs149122636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347915 | CGGGAAAAAATAGAA[C/T]GGCACGATTAGAATG | 8853 |
rs149144970 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287459 | AACCTCCTTGTAGGA[C/T]GGATATCTGAAGGAC | 8853 |
rs149176537 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351773 | GCTCCCAGCAAACTG[C/T]GGGTAATTATCACTC | 8853 |
rs149195653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291013 | ACTTTTTGCAAAATT[A/G]AGACTAAATATCTAA | 8853 |
rs149241111 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322092 | TATAATTCTAGTCCC[A/G]GGGACCCTCCAGTCA | 8853 |
rs149243909 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404528 | CTCTATTTAGTAATT[A/G]CGAGGGTAAGATTCA | 8853 |
rs149245223 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279877 | TATTTTTTACACATA[C/T]ATATTTACACATATA | 8853 |
rs149278672 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219880 | GTCACCTGTACCCGA[A/G]TCCTTGGCAGTCACT | 8853 |
rs149291290 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328613 | AGGAGAGGATTCCAC[A/G]TGCAGGGGCTGCTCA | 8853 |
rs149301893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257766 | TGACCTCAAGTGATC[C/T]GCCCGCCTCGGCCTC | 8853 |
rs149302738 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233028 | TGCTGCCTCTTAGGA[A/G]TGGAGAATGCTGCCA | 8853 |
rs149312154 | in-del | -/CAAT | 0.326035 | 0.238157 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317037 | ACATGCAATCATTCC[-/CAAT]CACTCACATCCACAC | 8853 |
rs149314871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372590 | GCCCAGAACACTTCT[A/G]ATATTAAACATTGAA | 8853 |
rs149319662 | in-del | -/GTTTGG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343446 | GCTACTGTTTGTTTT[-/GTTTGG]TTTTTGTTTTTTTGA | 8853 |
rs149345731 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263395 | CTGCCCCACGCTGCC[A/G]TGTTTGTGCTGCTGC | 8853 |
rs149364578 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274392 | CAGTGGTGTGATCTC[C/T]GCTCACTGCAACCTT | 8853 |
rs149368554 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380065 | GTTTAAAAGTTTGTT[A/G]TATTGCAGTGCATGG | 8853 |
rs149433986 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349439 | AGAAATAGATCATTT[G/T]CTGTATTGGTTCCTG | 8853 |
rs149442402 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318325 | ATATACAGACCTAGA[C/T]TTTTCATTAGCCCTC | 8853 |
rs149443820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248620 | AGAACTAGGCAAGAC[A/G]CTGACGGTGAGGTCT | 8853 |
rs149506867 | snp | A/G | 0.103438 | 0.202533 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292445 | ATCACTTGAACCCAG[A/G]AGTTGGAGGTTGCAG | 8853 |
rs149535322 | snp | A/C | 0.000153988 | 0.00877327 | missense | ASAP2 | GRCh38.p7 | 2:9393493 | GCAGATCCCCTGACC[A/C]CCACGCCGCCCCCAC | 8853 |
rs149542865 | in-del | -/CAAT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317812 | ATTCACACACTCACA[-/CAAT]CAATCACACCCTTAG | 8853 |
rs149556484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298714 | CCAGGGTAAAGATCC[A/G]TAGATGCTGCCATGG | 8853 |
rs149566165 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229460 | CTGAGCTGGGAACCA[G/T]GGGCAGCTACAAAGG | 8853 |
rs149579002 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340111 | CACTGTAACCTCTGC[C/T]TCCTGGGTTCAAGTG | 8853 |
rs149631780 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345402 | GCTTATGAAAAGCCG[A/G]TCAGGATAAAGTTCC | 8853 |
rs149641248 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9392252 | AAGTTTTTCTCCAGT[G/T]TACAGAACTAAAGTC | 8853 |
rs149648361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214192 | GTGTAATGTGGCCTC[C/T]AAGTGGATTGCTAGG | 8853 |
rs149653067 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284991 | TGGTTTCTTACCATC[A/G]TTACCTGCACAATAA | 8853 |
rs149663920 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338123 | TGTTGGGGTGCTGGC[A/G]GAGTCCCAAAGCCTC | 8853 |
rs149673908 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382902 | ATTGCAGCAGAGAAA[A/G]AGTTTAATTATGGCA | 8853 |
rs149685664 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275927 | GTGGCACTTAGCCAC[A/G]TTTCAGGTGCTCCGT | 8853 |
rs149695867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316661 | GGCTCAGGGCTCTGA[A/G]TCCGTACTTGAAGGC | 8853 |
rs149697914 | snp | A/G | 0.029116 | 0.117091 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396747 | TGGCTCACACCTACA[A/G]TCCCAGCACTTTGGG | 8853 |
rs149732886 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211901 | ACCTTCTTGCCCAGA[A/G]CATTCATGTTTTTGG | 8853 |
rs149746025 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319311 | GGATCTGCGCACGAT[A/T]CCTGGGTCCCATCGG | 8853 |
rs149746982 | in-del | -/AGG | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315527 | GAGAGAGGGCTTTGT[-/AGG]AAGGAAGAGCATTGG | 8853 |
rs149755759 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249788 | AGAGGAGGGCAGGGC[C/T]GTGTGGGGATACTGC | 8853 |
rs149808153 | snp | A/G | 4.94246e-05 | 0.0049709 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9334765 | TGGACTCAAAGCCGT[A/G]GAAAGCCTCAAACCT | 8853 |
rs149822943 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370077 | ACTCCTGACCTCGTG[A/G]TCTGCCCACCTTGGC | 8853 |
rs149824074 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295037 | TAGTTTAAAAATAGT[A/G]TGTGGTTTGAAAGGA | 8853 |
rs149839966 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238956 | GCTTTCTCTTGCTGT[A/G]CTGTGTTCCCTGGGC | 8853 |
rs149905588 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353532 | ATTGCACTCCAGCTT[C/G]GACAACACAGCAAGA | 8853 |
rs149929172 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259154 | TCCCCTCGCTTCCTC[-/T]CTTGTTCTGTTAGCT | 8853 |
rs149950856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247080 | GGGCTCATGCAGTCT[A/G]CCTGCCTTAGCCTCT | 8853 |
rs149959205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287145 | GCTTCTGACTGCTGC[A/G]GCATGCTGCCTGGTG | 8853 |
rs149961030 | snp | C/G | 0.021333 | 0.101051 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394399 | TCGATCTCCTGACCT[C/G]GTGATCCACCTGCCT | 8853 |
rs149961218 | snp | A/G | 5.19116e-05 | 0.00509442 | missense | ASAP2 | GRCh38.p7 | 2:9374757 | CGTTTGGTTTCAGGA[A/G]TGCAAGAAAGGACTA | 8853 |
rs150035291 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331640 | GGATGCGGTAGTGCA[C/T]ACCTGTAGTCCCGGC | 8853 |
rs150054011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271591 | TTACTTGCATCAGCA[A/G]AGGAGTTTAAATAGT | 8853 |
rs150067192 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9218612 | TGTACTGTATTCCCC[-/T]GATAGCCTGAATCTG | 8853 |
rs150077291 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367363 | TAGAGAGCAGAAATA[G/T]CACAAGCGTCACTGA | 8853 |
rs150086919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265846 | GGCACGATCTTGACT[C/T]ACTGCAACCTCCACC | 8853 |
rs150118816 | in-del | -/GG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9335405 | CATGGCCTTAATGGC[-/GG]GGTGTATAAACCCTG | 8853 |
rs150127434 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372025 | CAGACCTGTGCCCAT[A/G]TTTGTGTAGGAGCTG | 8853 |
rs150138147 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297099 | CCCCTCTTGCATACC[A/T]CACTTGTTCTTTGGG | 8853 |
rs150138902 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270581 | TTGTGTTACATCTCA[A/G]TTATACTCTCTTAGT | 8853 |
rs150148434 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389588 | ATCTTCCCTGCCGTC[C/G]TGGGTGTCTCACAGA | 8853 |
rs150149053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307982 | TACGTGTGCATGCAT[A/G]TGTGTATGATAGACC | 8853 |
rs150202462 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314762 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 8853 |
rs150205249 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343531 | GACTCACTGCAACCT[C/T]GATCTCCCAGGCTCA | 8853 |
rs150209470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244848 | TTAGATCCTTTCTGA[A/G]GCATCATAAAAATCA | 8853 |
rs150254193 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248543 | CCAGTGAGAGTCAGC[A/G]TTTTGGGTCTCGGTT | 8853 |
rs150271421 | snp | C/G | 1.64863e-05 | 0.00287104 | missense | ASAP2 | GRCh38.p7 | 2:9374870 | GCCGTCAAAACGAGA[C/G]ATATTTTTGGATTGC | 8853 |
rs150274818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360865 | TTGGCTTGCAAAATT[A/C]CTGAAATTTTAACAG | 8853 |
rs150276629 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288830 | TTCTCCTTCCCTGAT[G/T]TGGTCTCAGAGCACC | 8853 |
rs150329957 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292295 | GAGGCTGAGGAGGGT[A/G]GATCATGAGATCAGG | 8853 |
rs150338897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334896 | CACTTCTGTGTAATC[C/T]TGTGTTTTCATGCCG | 8853 |
rs150343883 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237453 | TTCTTGCTTTGTTGC[C/T]CAGGCTGGGATGCAG | 8853 |
rs150356712 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9347435 | TCGTTTACAGTCAGG[A/G]AAAAAGGGCACATTT | 8853 |
rs150411312 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278813 | GAAGCAATAGGACCC[A/G]TCTTCTAACACAGCT | 8853 |
rs150415798 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384444 | TATCTACTTGGAGGT[A/G]GTGTTAGATCCCACA | 8853 |
rs150421722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9208663 | TCGGTGATTCCCCAG[A/G]TCACTTAATTCTACT | 8853 |
rs150433744 | snp | C/T | 0.328616 | 0.237317 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397844 | GCTCATTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 8853 |
rs150435010 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318008 | CCAACACACACACGT[C/G]TTTTCTCATTCGCAC | 8853 |
rs150467315 | in-del | -/CACT/CT | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317133 | CACAACCACACAACA[-/CACT/CT]CACATCCCAATCACA | 8853 |
rs150474489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213417 | TTGGGGAAGGAATTT[A/G]GATTTTGTTCTAGTG | 8853 |
rs150484340 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253413 | AGGTGATCCGCCCGC[A/G]TTGGCTTCCCAAAGT | 8853 |
rs150485587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227588 | ATCACAGAGGTTTAA[C/T]GGCTCTGTAAAATAA | 8853 |
rs150489633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322033 | TGACCAGTGTCTGGA[C/T]GGTCTCTTGCCTGTG | 8853 |
rs150517325 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246192 | TTCTCCAAACCCGTA[C/T]TCCTTAGACATTTAA | 8853 |
rs150522598 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316327 | GAAAAAAAAATTAGT[A/G]CACTGAATGGTGTAT | 8853 |
rs150532321 | snp | A/G | 0.00867759 | 0.0652954 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356160 | GGAATTTAACACAGC[A/G]TTGCTCTTGTTTTTC | 8853 |
rs150537290 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257623 | TCCCAGGTTCAAGCT[A/C]TTCTCCTGCCTCAGC | 8853 |
rs150569257 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249310 | CAGCCTGCCCGTGGC[A/C]TGTCTGTCTGCCCCA | 8853 |
rs150570523 | in-del | -/CT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317176 | CACACTCTCACCACA[-/CT]CAACACACACCCCAC | 8853 |
rs150574217 | in-del | -/TTCATG | 0.0263992 | 0.111815 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313418 | ACTCACTCGTGTACA[-/TTCATG]TTCATGTGTGTACTC | 8853 |
rs150593856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290164 | ACCTTGTCCAGGGAA[A/G]GCTTTGGGAGAGAAA | 8853 |
rs150603755 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302003 | TAGTTTTTGGTATTT[G/T]TAGTAGAGATGGGGT | 8853 |
rs150628027 | snp | C/T | 0.000791283 | 0.019875 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9323202 | CGGAGCGGAAATTGC[C/T]GAAGAGATGGAAAAG | 8853 |
rs150659342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337615 | GGTTGGTAGAAGCCA[C/G]TGCTCCTCATTCTCT | 8853 |
rs150665092 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238547 | TCTCAAGGGTCTTTT[C/G]TGGTGTACAGGTCTC | 8853 |
rs150679889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349169 | ATAAAAATAGCTGAG[G/T]AAATGTAGCTATTGT | 8853 |
rs150711314 | in-del | -/TG | 0.0023933 | 0.0345097 | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405435 | CAGACTAAGAGTAAC[-/TG]TGTGATCTGTTAAGG | 8853 |
rs150716152 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243054 | AAAGATGTGTACTTC[A/G]CTTTCCAAGAACAGG | 8853 |
rs150726596 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281419 | AGGCGCTAGTGCTTC[G/T]GTGTCAGGAAGCTGG | 8853 |
rs150738837 | snp | C/T | 0.000894765 | 0.0211325 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400009 | GTAAATCTACTTTTT[C/T]CCTGTCTTTGTAGGG | 8853 |
rs150746027 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9224589 | ATCTTCTAAGGATGA[A/T]CGAAATCTCCACTCT | 8853 |
rs150771036 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254119 | GCTGAGGCAGGAGAA[C/T]TGCTTGAAGCCAGGA | 8853 |
rs150779008 | snp | A/G | 0.000181322 | 0.00951988 | missense | ASAP2 | GRCh38.p7 | 2:9368428 | TCATTTTTGCAGCTC[A/G]CCAAGAATATTGGGA | 8853 |
rs150783470 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286565 | TGCTCCATTGTTGTG[A/G]CACTGAAAACATGCA | 8853 |
rs150793221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324491 | GAGGGGCTGCATCTG[A/G]TGAGGACCTTCTTGC | 8853 |
rs150814250 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339859 | CTGTGTCCAGCCTGC[A/G]TCACATTCCACATTC | 8853 |
rs150866907 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271088 | GTGAGCCACCGCGCC[C/T]GGCCCTGTTTTCATT | 8853 |
rs150871096 | snp | C/T | 0.0003957 | 0.0140604 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374882 | AGAGATATTTTTGGA[C/T]TGCTCCAAGCTTATG | 8853 |
rs150888713 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ASAP2 | GRCh38.p7 | 2:9391821 | AACTCCTGACCTCAG[A/G]TGATCCACCTGCCTC | 8853 |
rs150890280 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9309316 | AACTACTGGTACACG[C/T]AACTACATGAATGAA | 8853 |
rs150919117 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303977 | GGTGCTGTATGGGGC[A/G/T]GTGACCTCTGGCAAC | 8853 |
rs150922083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382553 | ATCATTTTCTACAGC[A/G]TTTAATTCTCTCATC | 8853 |
rs150928429 | snp | C/G | 1.64947e-05 | 0.00287177 | missense | ASAP2 | GRCh38.p7 | 2:9388317 | CAACCGGCGGGAAGA[C/G]CGGCCCATCAGCTTC | 8853 |
rs150973280 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240159 | ATGTTCCAAGACCCT[C/T]GGTGGATGCCTGCAG | 8853 |
rs150975730 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307671 | ACTTAGAGCCTGAAA[G/T]ATCAGAGCTGTTGAC | 8853 |
rs150986114 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350397 | ATGCTAAGAAAAAAC[A/G]CTTTTAAGATCACCA | 8853 |
rs151046594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283891 | CACTTGACCTCATCT[A/G]AACCTAATTATTATG | 8853 |
rs151058650 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294896 | AAGCAGGACCATGGA[C/G]GTTGCGTTCCTGTTT | 8853 |
rs151062778 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9403192 | GCTCTATGTAATGCT[C/G]TTCAAAGTTTCCACC | 8853 |
rs151068403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227022 | CCAGTCCAGGTGTTC[A/G]GGTCCTGCTCCCTGG | 8853 |
rs151110830 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327230 | TCTGACAGCGGAGGG[A/G]ATGGGGACTCATGAA | 8853 |
rs151121116 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231540 | CCGGAGGCCAGCTCT[G/T]TTGTGTGTGCATGCC | 8853 |
rs151130463 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269888 | CACAGTGTGCACCGT[A/C]CCCACTGTCCCCACA | 8853 |
rs151136042 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341123 | CTCTTACTTTTTATG[G/T]TATTCTTCTCTCCAG | 8853 |
rs151183840 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272851 | CACATTTGTAAAAAA[C/T]GAGTTCACTGTAAAT | 8853 |
rs151207108 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312729 | ATTCACCCGAGGGGA[A/G]AGGCTGTCTGAGGAC | 8853 |
rs151256252 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9222080 | GGCGTGAGCCACCGC[A/G]CTGGCCTATTGCTTT | 8853 |
rs151259904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247845 | CTGCTGCTAAACTCA[A/G]CTGATCCAGGAAACT | 8853 |
rs151262133 | in-del | -/TTT/TTTACACATACATATTT | 0.506829 | 0.0867722 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279880 | TTTTACACATATATA[-/TTT/TTTACACATACATATTT]TTTACACATATATAT | 8853 |
rs151277744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259779 | TGAACTCATCTGAGG[C/G]CGACAGGCAAAGTAG | 8853 |
rs151320104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291461 | GCCACAAGTGAGGTC[A/G]GAAACAGGTGGCATG | 8853 |
rs151325668 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367151 | TTCTCCTGTCTCAGC[C/T]TCCTGAGTAGCTGGG | 8853 |
rs180671045 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321437 | TCCATTCAGCCCAGG[A/G]AGGCCCCCACCCAGG | 8853 |
rs180676928 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9277063 | GCAAAGCCTGGAGCC[A/G]GCCCAGATTCTGCGA | 8853 |
rs180677278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295706 | TTTGCTGAATCTGGT[C/T]TCAGAAATTCATTTA | 8853 |
rs180684094 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313165 | CACTGCTGAAATGAA[C/T]GAAGAACGAAAGCAA | 8853 |
rs180699207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331051 | CGTGCGTGTTTCCAC[A/G]TGTGGGAGCGCCTCT | 8853 |
rs180710190 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348656 | TTTTTTAATATGTAG[A/G]CACATTTATGTCTTC | 8853 |
rs180723888 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366454 | CTGGGGACAGTGTCC[C/T]GCTTGGATTGTATGC | 8853 |
rs180728219 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382335 | GTTTCTGCTGTTGTC[C/G]TCATTTTACAGATGA | 8853 |
rs180801522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210377 | GAGGGTTTAGGAAGA[C/T]AGTACATAGCACAGA | 8853 |
rs180804116 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398355 | TCTTTACAAAAAATT[G/T]TGAAAGTTAGCCAAG | 8853 |
rs180819717 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243546 | ATCTGCTTTCTGTAC[A/G]TCAGGCAGATGAATT | 8853 |
rs180820561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285411 | TGTCCCACGTGTATA[C/T]AAAACAGTAGTCTTC | 8853 |
rs180822197 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266231 | AGCCCACTGCAGCCT[C/T]GACTTCCCAGACTCA | 8853 |
rs180826763 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226371 | CCTATTGCAGGGAGC[C/G]GGGTCACCTCCCTGA | 8853 |
rs180828357 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302718 | GACCTCAAGTGATCC[A/G]CCCGCCTGGGTCTCC | 8853 |
rs180833328 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9259011 | GGCCTGCTCTTCGGC[C/T]TTTCTCTGTGGTGTC | 8853 |
rs180834054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233376 | TATGCTTTTTGTGCT[A/G]TTTTCCTTTATGGGC | 8853 |
rs180848390 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213065 | ATCACTGATAAACAG[A/T]CAGTTACGTAACAAC | 8853 |
rs180856448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216081 | CTTGTTTGTGTCACA[C/T]GGCATGTACTGCCTT | 8853 |
rs180860596 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9251135 | CGGGAGTGGAGCGTG[A/G]AGGGCTGGTAAACAG | 8853 |
rs180864834 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248106 | GCTGATGGAAGGGGG[G/T]CGGCTGACAGCAGCA | 8853 |
rs180878830 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230392 | GCAGTGCAGCCGTGA[C/G]TCTGGCAGGCGAGTT | 8853 |
rs180880424 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263607 | ATGAAAGCCATGGGG[C/T]GCTCCCACCGAAGCC | 8853 |
rs180890558 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221979 | TTTTTTTTTTGTATT[G/T]TTAGCAGAGATGGGG | 8853 |
rs180907709 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254663 | ACAGGTTTGAGCCAC[C/T]GTCCCCGGCCTATAA | 8853 |
rs180915806 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280535 | AATTTAACAGAAGAC[A/G]CACAGGAATCCTACA | 8853 |
rs180938005 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315622 | GGCGGGAACTGTGAC[A/G]GGAGTTTCATTCCTC | 8853 |
rs180948620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291475 | CGGAAACAGGTGGCA[C/T]GTACAGCCGACAGCC | 8853 |
rs180954041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309144 | TTTCTGACACTATTT[A/G]AAAGAGTCTCCATCC | 8853 |
rs180956454 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207020 | CGGCGGCAGCGGCGG[G/T]GTCCGAGCGGCGGTC | 8853 |
rs180958165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327413 | GAAATGTCTCAGGAC[A/G]AGAGACATGATGCCA | 8853 |
rs180960607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351648 | GTACTGTAGGAAGGC[A/G]GTGCTGTTCTCTGTG | 8853 |
rs180967186 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9238239 | TTCTGTTTTTAAAAC[C/G]TCAGCTCCTCTAGTC | 8853 |
rs180973459 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272231 | CATTTGTTATTGCCT[A/G]CCTTTTGCCTATAAA | 8853 |
rs180975004 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298703 | ACTGCATGGGCCCAG[A/G]GTAAAGATCCGTAGA | 8853 |
rs180981041 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334942 | GTGTGGCGTTCCCAC[A/G]CCTGTCCTCTGTCTT | 8853 |
rs180998444 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369507 | GTATTATGGCTCTTA[C/T]GTCTATAGGGGGACA | 8853 |
rs181146507 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396351 | GTGATCACGGTTCAC[C/T]GCAGCCTCGACCTCC | 8853 |
rs181167119 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210201 | TACTTTTCTTAATGC[C/T]GAATTCTCTAAATTA | 8853 |
rs181172002 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225784 | TAGGGGTCTGGATTA[A/G]GGCATAGGGAATACA | 8853 |
rs181174337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344341 | TCCTTCTCCAGCCTG[A/G]TAGATGGCATTTATC | 8853 |
rs181186648 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362453 | ACAACATGATGTTTT[A/G]GTATGTTGTATACAT | 8853 |
rs181194398 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378588 | GCCGGCCTAGCACAG[C/G/T]AGCCTCGGCGCAGCC | 8853 |
rs181290225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398054 | TGAGCCACTGCGCCC[A/G]GCCTCAAAAGGATAT | 8853 |
rs181311451 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367224 | TTTTAGTAGAGATGG[G/T]GTTTCACCTTGTTGC | 8853 |
rs181362563 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233957 | CTTTACTAAAAATAT[A/G]AAAATTAGCTGGTCG | 8853 |
rs181366384 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243148 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 8853 |
rs181376824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217326 | TGTTCTTCTTTCCTC[C/T]CCTCACTGCTCTGCT | 8853 |
rs181382704 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251903 | TTTAGGAATGAGAAG[C/G]CTGTGCCCACATTGC | 8853 |
rs181384884 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286665 | TCCATGCACAAAGAT[G/T]TTCACTTTGTTGTTG | 8853 |
rs181388300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330927 | GAGAGAGAGTGTGTA[C/T]GCTGCCTGCTCTTCA | 8853 |
rs181389904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312883 | ACATGATGAAACCCC[A/G]TCTCTACTAATAATA | 8853 |
rs181390754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267477 | AGAGGACATGATTTA[A/G]TTCTTTTTTATGGCT | 8853 |
rs181394184 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276253 | ACCTGCCACCCTATC[G/T]TGGAGGTGGCAAGGC | 8853 |
rs181400849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336283 | ATGAAGATGAAGCAG[A/G]TCCCTCCCTCCCTCC | 8853 |
rs181404157 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352809 | CAGGAAGGACTTGTA[C/G]CCTGTGATGCCCAGA | 8853 |
rs181405283 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348226 | GGTTCAAGCAGTTCT[C/T]CTGCCTCAGCCTCCC | 8853 |
rs181405322 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9303759 | TACATTTTGGTTGTG[G/T]CATAGCCACATAATA | 8853 |
rs181410974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370180 | CATGTCTTTGAGAAA[C/T]GGAGATTGCAGGACC | 8853 |
rs181422824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386988 | GGCGGGCGGATCACG[A/G]GGTCAGGAGATTGAG | 8853 |
rs181437675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307485 | GTTTTACCATCACCC[A/G]GTTTTAGAAGTAGTT | 8853 |
rs181438366 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340665 | CAAAAATGACTCCTC[A/G]ACAAGCTTGTCAATC | 8853 |
rs181459121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372986 | AAAATGCTGTTATTC[A/G]AGGGCCTGTTGTGCC | 8853 |
rs181474697 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404022 | AGGTTATATAAAACT[G/T]CATTTCCTGAATTTG | 8853 |
rs181476807 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264662 | TCCTGTCACCGTCTT[C/G]TCTCCTCATCTAGGT | 8853 |
rs181482436 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326892 | TTGTAAACTTTTGTG[G/T]TTATCTTCTTAGAAT | 8853 |
rs181483174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300046 | AGACCAGCCTGGGCA[A/G]CATGGGGAACCCCTG | 8853 |
rs181496095 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361950 | CTGAAGTCTTTTTAC[A/C]TCTTTATCTTATCTC | 8853 |
rs181521323 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258825 | TCTCTCGCTCTCTCT[A/C]CTCTTCACTTCTCAA | 8853 |
rs181532435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294780 | CCTGCTGGGCTTTGC[A/G]TTCATTGCCCAGCAC | 8853 |
rs181553644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221510 | GTTTTCAATGTACAA[A/G]TCTTACACTTCTTCT | 8853 |
rs181572146 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322291 | CTTGCCCTAATGACA[A/G]GGAGCCCTCTGGAAC | 8853 |
rs181574592 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9237855 | GTCTTGAGGAAAACC[A/G]GTGAGATGATCCCAT | 8853 |
rs181575649 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205768 | ACCATGCCACAAGTC[C/T]GGTGTAGAGTTATAG | 8853 |
rs181584324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254282 | GTATGCATATATATA[A/G]TATATTGTTATAATT | 8853 |
rs181592874 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9290753 | TGGGTCTGAGGCCCA[C/T]TGCGACTTGGAACAC | 8853 |
rs181599027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271544 | TTATATGGATATAAT[C/T]CTCAGTGCCAGCAGG | 8853 |
rs181613090 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313433 | TTCATGTTCATGTGT[A/G]TACTCCCGCTTCATG | 8853 |
rs181615058 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209506 | TTTAACAAATAAATA[A/C]AATTTGCAAGCTCTT | 8853 |
rs181617934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283157 | ATCTCGGCTCACTGC[A/G]GCCTCCGCCTCCTGG | 8853 |
rs181626323 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344144 | GAAAGCTGGTTTTGT[C/T]GTTTTGCTTGGAAAC | 8853 |
rs181633521 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317552 | CACAATCTCTCACAT[C/T]CACAATCACACTCTC | 8853 |
rs181685089 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395771 | CACCACCACGCCTGG[A/C]CAATTTTTTATATTT | 8853 |
rs181752731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251382 | TAGGGGACCTGCCCT[C/T]CCTGTGGGGGCCCAG | 8853 |
rs181787257 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9391840 | TCCACCTGCCTCAGC[C/T]TCCCAGAGTTCTGGG | 8853 |
rs181797455 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286357 | GAGCTGAAACTGCAC[C/T]ACTGCACTTCATCCT | 8853 |
rs181802582 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356509 | ATGAACTGTGCAGAC[C/T]GCGGCAGGGGAGAGG | 8853 |
rs181806675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321722 | AGAGTGCCTGAGAGA[A/G]TCATCTGGTTCTGAA | 8853 |
rs181808734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331596 | AACATGGTGAAACCT[C/G]GTCTCTACTAAAAAT | 8853 |
rs181808772 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372304 | ACACTGTGCTGGAGG[C/G]CCTAAGAGGAGAACC | 8853 |
rs181812298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348987 | TTGGAATCCTAGCTT[C/G]CCCGCTCCCTAGCTG | 8853 |
rs181835532 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205399 | CTTCAGACACCAAAA[C/G]GATCAAAAAACATAA | 8853 |
rs181838313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221099 | AGTGTGAGTCTTTCA[A/C]CTTTGTTTTTTTTTC | 8853 |
rs181865807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248992 | GTAAATTCCTCCCAA[C/T]CCGAATACATAGGAT | 8853 |
rs181969907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233632 | GACCTGGACTCAGAT[A/G]TAGGTTTTGCTAATT | 8853 |
rs181978873 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248478 | GGGCTTTGGAGTCGC[A/T]GTCCAGGGTGTGCCT | 8853 |
rs181984755 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213224 | TGCAGAGAGGAAGCC[A/T]GCCACAGAAGATGTG | 8853 |
rs181985296 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282372 | AGTCACCTGAGGAAA[C/T]GTGATACTTTCTCCT | 8853 |
rs181988274 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264139 | AGAGGTTGCAGTGAG[C/G]CAAGATCACACCACT | 8853 |
rs181992206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237766 | CAGGAGACTGAGTCT[C/T]TTCTTGCTCACCTGG | 8853 |
rs181997881 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299280 | CTTCCAGACAGCAGC[C/T]GGAGGATTCAGAATC | 8853 |
rs182003345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316084 | AGCACTTTGAGAGGC[C/T]GAGGAGGGCAGATTG | 8853 |
rs182005458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335711 | GTAATGACGTCTCTG[C/T]GTGCTAACACGTCAG | 8853 |
rs182017791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352179 | TCCAGCCTTGGTAAC[A/G]TAGCAAGACCCTAAC | 8853 |
rs182030280 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383233 | AGGATCAATTGGGGA[A/G]GTCACAAGTATCGTG | 8853 |
rs182034830 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266848 | CTGGGGAGAAAAGCC[C/T]GAGGCCTGAGCTGGC | 8853 |
rs182068818 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339714 | CCGTCCTCTGGCCCT[A/G]TGTCTTCATGGCTCT | 8853 |
rs182070164 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9400208 | CTCCTGCCCCCTCCC[C/T]TCCTGCCCCCTCCCC | 8853 |
rs182082289 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396567 | CAGGCATGAGGCACT[A/G]CGCCTCACCTCTTTT | 8853 |
rs182094418 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9228582 | GCTTGGCAGAGTGAG[C/T]GGCCCCCATCTTCCT | 8853 |
rs182102479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245215 | CACACAGGAGCTTCT[A/G]GTTTGAGAACCACAG | 8853 |
rs182115101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303981 | CTGTATGGGGCGGTG[A/G]CCTCTGGCAACTCCT | 8853 |
rs182116858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261993 | GGGAGTCAGAAACAC[C/T]TGAGCACACCAGGAA | 8853 |
rs182120305 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287188 | GTTGCTGGGGGCACA[C/T]GGTGGAGAAAACAAG | 8853 |
rs182126327 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403458 | GCCACTGCTCTGTTT[C/T]AAAAACTCAGAGGCA | 8853 |
rs182133188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278428 | TGAGGCAGGAGAATT[A/G]CTTGAACCCAGGAGG | 8853 |
rs182133232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322623 | CAAGATGAATGTAGA[A/G]AGGATAATTAAGCCG | 8853 |
rs182144171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357508 | AAAACCCGAAAATAC[A/G]TTTTTGGCAGGAGAT | 8853 |
rs182149608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374189 | AAAGGCCAGAAAGTA[C/G]AACACAAAGAGGACT | 8853 |
rs182197820 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9393924 | GCTGCTCACCCCCCA[G/T]GTGGTCTCTGTTTCT | 8853 |
rs182244754 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398701 | GTAATTCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 8853 |
rs182312689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366686 | GAGGTCCCAGAGCCA[A/G]GACTGAGCAAGGAGG | 8853 |
rs182343839 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231527 | TAGCTGCCACCTCCC[A/G]GAGGCCAGCTCTGTT | 8853 |
rs182355585 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214251 | TTTTCTTTTTTATTT[A/T]GTTTGAGGTGGAGTC | 8853 |
rs182359544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235189 | ATGGTAGAATTAATC[C/G]AGTTAGAGATGGGGC | 8853 |
rs182360836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265187 | AAAAATACAGTGTAA[A/C]AACTGTTTACATAGC | 8853 |
rs182368172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267689 | ATCACTTGAGGCCGG[A/G]AGTTCGAGACCAACC | 8853 |
rs182369093 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249685 | TGAGTGAGACTGGGC[G/T]CTGGGCTGAGATTGC | 8853 |
rs182374024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283628 | GACACTTAGATGGCT[C/T]GGGCTGCTATAACAA | 8853 |
rs182423518 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297850 | AAGGTAACCTGTAAT[A/C]AAAGCACAGAAATTA | 8853 |
rs182435301 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332614 | CGCTCTCACTCTCGC[C/T]CTCTGTCTGACCGTA | 8853 |
rs182473547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311387 | AAAAAAAGTTTGCCT[C/G]CTTGTTGGTCCAACG | 8853 |
rs182483334 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346584 | CCTTCTAAATACCTT[A/C]CAGATCTCAACACCT | 8853 |
rs182487655 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364479 | CACTGCTCTCCAGCC[C/T]GGGTGACAGAGTAAG | 8853 |
rs182492637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379924 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 8853 |
rs182505300 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230803 | TTAAGCAGACCAGAT[A/T]TATAAGGGTTTTGAT | 8853 |
rs182529776 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367005 | CTCCCAAAGCATGTT[C/T]GTTAACTCCTTTGCC | 8853 |
rs182538006 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384001 | GGGAACATCACAAAC[C/T]GGGGCCTGTCATGGG | 8853 |
rs182590601 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386765 | TGCTAGAAAAGCACT[C/T]GTCATATCCAGTGAA | 8853 |
rs182594352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362955 | CATGCTTTGACCAAC[A/G]TGCCCACCCCCAACC | 8853 |
rs182607963 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252489 | TACGGCAGGAGAATC[G/T]CTTAAACCCAGGAGG | 8853 |
rs182666851 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400372 | CATGCCTTCCTCCCC[C/T]GCCACCTGCCTTCCT | 8853 |
rs182667324 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314611 | TCACTAAGATGAACA[C/T]GAGAAGAGCCTGCCA | 8853 |
rs182692217 | snp | A/C | 0.00190635 | 0.0308147 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399997 | CCTCCGGTAGCAGTA[A/C]ATCTACTTTTTCCCT | 8853 |
rs182692457 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289028 | TTTCCCCATAGAGTG[C/T]TGTGTTTCCACCTCG | 8853 |
rs182694385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349424 | TGTAACCATGTTTCT[A/G]GAAATAGATCATTTG | 8853 |
rs182701646 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304855 | GATATTGGTGGAGGA[C/G]GTTGTAATAGTGGGG | 8853 |
rs182705191 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331700 | TTGAACCCAAGAGGC[A/G]GAGGTTGCAGTGAGC | 8853 |
rs182711083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384918 | CCTGCCTTGGGGCAG[A/G]AGAAGTTCAGAGAGA | 8853 |
rs182725961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222972 | GTCTATTTCCAGACC[C/T]TCCAAGGCCTGTGTT | 8853 |
rs182726200 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256248 | GAGTGCCAACCATGT[G/T]CCAGCTTGGGGTGAT | 8853 |
rs182742055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273894 | GCTAATTTATTAGTC[C/T]TGCAAAGGCTGTCTA | 8853 |
rs182745795 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310070 | CTCTTAATTGATACA[A/G]TGAGGTGTGAGGTCT | 8853 |
rs182752380 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329244 | TGGAAAAGCCTTAGG[A/G]ATGTGGATGGCCCCA | 8853 |
rs182831748 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217866 | TGAGGCACCCACCTC[A/G]GCTTCCCAAAGTGCT | 8853 |
rs182880570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318247 | AAATATTTTTTCTTC[A/G]CTGCAATGATTGTCT | 8853 |
rs182895497 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257771 | TCAAGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 8853 |
rs182907428 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9292663 | TTACCTGTCCTTGGA[G/T]CCCCAGTTCAATGTC | 8853 |
rs182914298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353351 | GGGAGGATTGCTTGA[A/G]GTCAGGAGTTCGAGA | 8853 |
rs182933665 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9218587 | AAAGGAAGGGAGAAT[A/G]TTGAGGCCTTGTACT | 8853 |
rs182934643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387351 | CTCAGCTCTGCCAGG[A/G]TGGCTCAAAAGCAGC | 8853 |
rs182936863 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259538 | TAGGTGGATGCTATC[A/G]GAGGGCACAGTTTTC | 8853 |
rs182937214 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354133 | TCCGCGAACCCCATA[A/G]GCACCCTGGGAGGGA | 8853 |
rs182942864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371255 | TCCATTCCTTCTCAA[C/T]TGAAATTACTTTCTT | 8853 |
rs182943180 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227429 | TTGTGTTCTTATTTC[C/T]TAAAACCGAACTGCA | 8853 |
rs182945867 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240122 | TTATCTAAATACTGA[A/T]GCCCCATTATCCCTG | 8853 |
rs182948274 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243942 | TTTTTATGAAATATG[C/T]ATATGAAGTTTTCTT | 8853 |
rs182951253 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277582 | GTTTTAGGTTCACAA[C/G]AAAATTGAATGGAAA | 8853 |
rs182964759 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9235479 | TCCAGCAGAGGCCGG[A/G]TGTGTAAATCATCCT | 8853 |
rs182970165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296062 | GGGGCTTTCAGGATC[G/T]GTCCCTTGGTGGAGG | 8853 |
rs183008773 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342387 | TGATTTATTTTTAAC[A/C]AGGGTGCCAAGGCAA | 8853 |
rs183038781 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375729 | AAAACCCATCTCCAG[A/G]TGGAGGAGAAGACAT | 8853 |
rs183107032 | snp | A/C | 0.0119091 | 0.0762411 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405932 | TGAATCCTGGTCTCC[A/C]GTCCACACCTCTGCC | 8853 |
rs183116403 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404553 | GATTCATAGTAGGAA[C/T]ATTGGAAATTTTGGC | 8853 |
rs183124998 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388988 | CTTACCCATGATCCC[C/T]ATAAAAGATATTGGG | 8853 |
rs183138711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211813 | ATTCTGAATGTTAGC[C/T]CTTTGTGACTTGTTT | 8853 |
rs183145793 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244497 | GAACAGAGAACCCTT[G/T]ATGAGAACACATGCG | 8853 |
rs183162099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278089 | AATAATGGACACTCA[A/G]TAGCAGTAGTTATTA | 8853 |
rs183179172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274600 | AGTGCTGGGATTACA[A/G]GCATGAGCCACCGCG | 8853 |
rs183181234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301094 | CCATTCTTCTTCCTG[G/T]TTTTGGTCACATCTG | 8853 |
rs183193486 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336797 | GAGGAGGAGGTAGTG[C/T]GAGGGCAGGAGCCAG | 8853 |
rs183205664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313867 | GAGCCATTAGTATCT[A/G]TGCAGTGTAAAATAT | 8853 |
rs183209920 | snp | C/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370783 | GAAAATGAGGTTCCT[C/T]TCCAGTTAAGTTTCA | 8853 |
rs183250079 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394106 | TAGACCCAGGTCAAG[C/G]TTAGCTGTTTGTCCA | 8853 |
rs183293127 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359230 | ACGTCTAAAGACAGG[A/G]AAGTACTTGTTTTCC | 8853 |
rs183308457 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363998 | ATTCTAAAGCAAACC[A/T]ACTTTGGGAAAAACT | 8853 |
rs183311693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338083 | CCACGTCGTCCATCC[A/G]ATGGTGTTCTGCCAG | 8853 |
rs183326921 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9374538 | GTGGGCTGAGAGAAC[A/C]TGGGGAGTTGTCCCC | 8853 |
rs183334131 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396826 | GGCCAACATGGCAAA[A/C]CCCTATCTCTACTAA | 8853 |
rs183370397 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207628 | TGAAGTGGACCGGCG[A/G]GGGCAGCTCCGCGCT | 8853 |
rs183374797 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354080 | CCATTGCCTGCAGAC[C/G]GACCCCACTCATAGC | 8853 |
rs183384504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222457 | TTTCCAAGCTGCTGT[C/T]TCTGCTGGTGAGTGT | 8853 |
rs183386905 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371109 | TGGAACCCTTCAGTA[A/T]GAACGTTCTGTCTGC | 8853 |
rs183392492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388135 | TTCACTCTTGCAGCT[C/G]TCACGCAACTTGTAG | 8853 |
rs183398105 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238452 | AAAGCATTGTCTTAC[C/G]AGCCTGTGCAGAATC | 8853 |
rs183410296 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231051 | GGCTGCTTTGCGGTT[C/G]TATGTCGGTCACTTT | 8853 |
rs183417085 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227766 | GTATTTGTGAGTACA[C/T]GTGCATATACAAAGA | 8853 |
rs183418377 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208275 | TGGGCCAGGATGTCA[A/G]GTTACAGTTTTAAAA | 8853 |
rs183425550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260879 | CCCTGCCCCTACTCT[A/C]TCTGCTTCTCCGCCA | 8853 |
rs183428673 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394466 | ACTGCACCAGGCCCC[A/C]GTTCGTGGCTCTTAA | 8853 |
rs183430482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296756 | GCTTCCTGGAGGAAG[C/T]ATGAGTCTGTAGGAT | 8853 |
rs183517881 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280566 | TCAACAAGTACAAAA[C/T]GCTGCTGACCAAAAT | 8853 |
rs183523674 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325181 | ATTTTTTTGTAAACA[C/T]ATATCATGTGTAGTG | 8853 |
rs183526645 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342835 | CTGGGTGCTGACCAC[A/G]TGACCGTGACCTCCC | 8853 |
rs183531507 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298956 | AGGGACACAACTATG[A/G]TAAGAAAATATAACA | 8853 |
rs183536616 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252894 | GCACTCCAGCCTCGC[C/G]ACAAAGCGAGACTCC | 8853 |
rs183541705 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346103 | ACTCCCCCTGCCCCC[A/G]CGACCCCAGGGCCAT | 8853 |
rs183543735 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284059 | TTGTGATGACATTGG[C/T]CTCATCCAGATAATC | 8853 |
rs183549129 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265627 | ATTATTTTCTTTCTG[A/T]ATCTTTATATACAGA | 8853 |
rs183549418 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301653 | CGGTCTGCAGAACCC[A/G]CTCCACATGAAGATC | 8853 |
rs183551742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379328 | GTCTTGCAGCTCTCA[C/T]GGATGCCAGGTGAAT | 8853 |
rs183557889 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319145 | GTTTGCTCATGAGCA[C/T]GCAGGCCAGGAGCTG | 8853 |
rs183692167 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9215526 | CCATGTGTTGCTTAC[A/G]TTTGTAATTGAAAGA | 8853 |
rs183711622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210970 | AAACCAGCCTGACCA[A/G]CATGGAGAAACCCTG | 8853 |
rs183714717 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360459 | CTGGGACACAAATTG[A/G]CATTTTAGTGGGTTG | 8853 |
rs183723508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376061 | CTCCTGACCTCAGGA[A/C]TGGGCTGGCTGCCTA | 8853 |
rs183759065 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269914 | CCACACACTGTCCCC[A/G]TCCCCTGTCCTGGCT | 8853 |
rs183777123 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288250 | TACCAAATCAACACG[A/T]TGACTTCATCTGTTT | 8853 |
rs183789560 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323972 | TGGAAACAGCTGCCA[A/C]CTCTGCCTGGGGTTA | 8853 |
rs183810840 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358153 | AGCTGTCTCTGCCAT[A/T]TAGTGAGATAAAAAT | 8853 |
rs183869853 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401909 | ATCTTTAAGCATTAG[A/T]GGGATCATCTGTGAC | 8853 |
rs183902887 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266022 | CAAGTGATCCACCCC[C/T]CCACCCCCTGCCTTG | 8853 |
rs183906708 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233126 | ACGGCTTTGAGACAG[A/T]TTGAGTCATCTAATT | 8853 |
rs183907827 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250907 | CTCGGGGCTTGCTCC[C/G/T]GGGGAACTTAAAACA | 8853 |
rs183911307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284807 | TCTTAGTGTAGGAGG[A/G]GTGAACTTACAATTT | 8853 |
rs183940960 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302268 | GCCTCTGCCTCTCGC[G/T]TTCAAGCGATCCTTC | 8853 |
rs183965209 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9400233 | CTCCCCTCCTGCCCC[C/T]TCCCCTCCTGCCCCC | 8853 |
rs183971999 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382252 | GCCTCCCAAAGTGCT[G/T]GGATTATAGGCGTGA | 8853 |
rs183978242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304590 | GGAGAGGCTGTAGTC[C/T]TGGGAGTATAGATAT | 8853 |
rs183993146 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341558 | GGCACGAACAGTGTT[A/G]GCGGTGTTGTCACAT | 8853 |
rs184025369 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214520 | GCTGGGATTATAGGC[A/G]TGAGCCGCTGCGCCC | 8853 |
rs184042469 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273231 | ATTTCTTACATCATC[G/T]TTTTATAGTTTTCGC | 8853 |
rs184053301 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250310 | TATTTAACCACAGAC[A/T]TCCTGCCTAGGCACC | 8853 |
rs184069492 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405438 | ACTAAGAGTAACTGT[A/G]TGATCTGTTAAGGGG | 8853 |
rs184074124 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309590 | TAGGAATATCCATGT[G/T]TCATAGCATATCAAG | 8853 |
rs184080718 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344400 | TTTTTGCTGTGTTGA[C/G]AAAGGGAAATTTCTC | 8853 |
rs184096083 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247653 | TCTGAAATTTGGGAA[A/T]GATACTCAGTCATTA | 8853 |
rs184125017 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236117 | AAGGCTTCAGGTGAT[G/T]GTGGACTTGGAGGGC | 8853 |
rs184126892 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212912 | TCGAGACGGAACCCC[A/G]GCTGCACACTGGAGT | 8853 |
rs184133747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219419 | GTGTATCTGGTCTGT[A/C]ACATGAGAGATTTGG | 8853 |
rs184138583 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253321 | GGTGCCCGCCACCAC[A/T]CCTGGCTAATTTTTG | 8853 |
rs184151382 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270774 | CAGTCTCCATGAGTT[C/G]AATTGTTTTCATTTT | 8853 |
rs184152101 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330943 | GCTGCCTGCTCTTCA[A/C]ATCAGTCAGGCAGCT | 8853 |
rs184157008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348480 | ATGGATAGAATTTTC[C/T]CCCATAAATTTTTCT | 8853 |
rs184157342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237486 | GCATGATCTCAGCTC[A/G]CTGCAGCCTCGACCT | 8853 |
rs184158465 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9398108 | GAGATTCACTTCAGC[A/C]CTCAGAAAATATTAT | 8853 |
rs184159919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366143 | TGGAGGGGTTCTCTA[C/T]GGGCTGAAACGTAAA | 8853 |
rs184173411 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214806 | AAAAAAAAGTGAACA[A/G]GACTAGCTCCTTCCT | 8853 |
rs184182688 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231667 | GCAGCGGGCCTGTCT[A/G]TCTGCCTGGCCCTTG | 8853 |
rs184190626 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255463 | TTACTTAAATTCTCC[C/T]ATGGAATTTTAAAAA | 8853 |
rs184197261 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291915 | GTCTTCAGCTCTTAG[A/C]TCTTATCTAGGCTAA | 8853 |
rs184204094 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351455 | TGTTTACTCAGCACC[C/G]CCTAAATTAAAGGGC | 8853 |
rs184218059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368874 | TAATCCTGAGCCACC[A/G]AGATGGCTGGTTGTG | 8853 |
rs184224577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385907 | TGCCTCCTCCTCCAG[C/T]TCCCTTCTTACCATC | 8853 |
rs184230206 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328994 | TTTGTTCCCTGATAC[A/C]GTCTCCAACAGCCAG | 8853 |
rs184283997 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253748 | ATCTTTAGACCACTC[A/C]TTTGCATTGCTGAAT | 8853 |
rs184287212 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9220332 | GGCTGCACCACTTGA[C/T]ATTCTTACCAGCCAT | 8853 |
rs184293838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402367 | GGGCGCGGTGGCTCA[C/T]GCCCATAATCCCAGC | 8853 |
rs184323556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289776 | TTGTATTTTAATAGC[A/G]CACACCTTGGCCTGA | 8853 |
rs184352927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315720 | TACTCATCAGCACGG[C/T]CTTCTGTTTGTCCTT | 8853 |
rs184389998 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258705 | CTTGTGGCTGTTGCA[A/C]CTTCTTTAGATCTCT | 8853 |
rs184400551 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243120 | TTTTGTTTTGTTTTG[C/T]TTTTTTGAGACGGAG | 8853 |
rs184403783 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276241 | GCTGAGATGAGTACC[C/T]GCCACCCTATCGTGG | 8853 |
rs184405638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402880 | TGCCACTTTAGGTGA[C/T]GTTGCAGCTCACAAA | 8853 |
rs184421461 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312339 | GAATCCCCCTCATTG[A/G]CCTGGCACCAGGCTT | 8853 |
rs184423070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293623 | GTAGGAAAATCTTCA[C/T]CTTGGGGTGATCTGC | 8853 |
rs184435737 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330789 | CGCCCCTTTATTTTG[A/C]CCAAACCAGTCAGTT | 8853 |
rs184443618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9223384 | GAACCTTCTTGGATC[C/G]TTCAAGCATCTGTAT | 8853 |
rs184456996 | snp | A/G | 1.6498e-05 | 0.00287206 | missense | ASAP2 | GRCh38.p7 | 2:9335097 | TGTTTTTAAAGATCA[A/G]ACAGGCCCAGGATGA | 8853 |
rs184479077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369557 | GTTGTGATGCAAAGT[A/G]AAACAGACGGAAGGA | 8853 |
rs184516275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395663 | CCCAGGCTGGAGTGC[A/G]GTGGCGCGATCTTGG | 8853 |
rs184534553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209154 | TTGCTTCATGCTGCC[A/G]TCTAAGCCCAAGAAT | 8853 |
rs184592637 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351797 | ATCACTCCACCTCAC[C/T]CACAATGGCTTGCTC | 8853 |
rs184614635 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386358 | GTCAAAGTGAGAAGA[A/G]TTGACTGATTTCATA | 8853 |
rs184644058 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365495 | TTTCCCTGCCCCACC[C/G]CAAACTCTCAAAACA | 8853 |
rs184702563 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321227 | TTTAAAAAAAAAATA[A/G]CTCAGGATATCTTTC | 8853 |
rs184713329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354559 | GGAAGATCGCTTGAG[C/T]CTGGGAGATTGAGGC | 8853 |
rs184725311 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302721 | CTCAAGTGATCCACC[C/T]GCCTGGGTCTCCCAA | 8853 |
rs184729496 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285690 | TTTTAGCTGTTTGAC[A/C/G]TATCAGTGGGTGGAA | 8853 |
rs184730962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321695 | CCAAGGGCAGAAAGG[C/G]CTTTCTGAAGAAGAG | 8853 |
rs184745644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339545 | TAATAAACTATCTTA[A/G]TAGTTCATTCAACAA | 8853 |
rs184748000 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390562 | CCAGAAATATGTTTG[C/T]GGGAGGGAGGGAGAG | 8853 |
rs184749833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355827 | CGGCGTCTTTTAAAA[C/T]TTGAATGAGGGAAAG | 8853 |
rs184759106 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9372047 | TAGGAGCTGCCTTCG[G/T]GGCCTCCAAGCCCTG | 8853 |
rs184794896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315506 | TCAAGCAAGTGAGGA[C/G]GGTGGGAGAGAGGGC | 8853 |
rs184829661 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279167 | CTCCCAGAAACAGGT[A/G]CCGAGGGACCTGGCA | 8853 |
rs184829880 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205406 | CACCAAAAGGATCAA[A/G]AAACATAAAAAGAAA | 8853 |
rs184832883 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237790 | CACCTGGTGGAGTAC[A/G]TTGTATACAGTAGGT | 8853 |
rs184836021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221116 | TTTGTTTTTTTTTCC[C/T]AAGATTGTTTTGGCT | 8853 |
rs184836261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262304 | CGTAATGACTGAGAC[A/G]GTCCTGGGGTAACAG | 8853 |
rs184843891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377984 | GTGATGCCTCTCCCT[C/T]CATGCACATTTTCAG | 8853 |
rs184845293 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254207 | CAGAGGGAGACTGTC[C/T]CAAAAAAAAAAAAAA | 8853 |
rs184846225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338619 | ACTCGTTTGTTGATT[A/C]ACACATCCAGCTACC | 8853 |
rs184851393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298045 | CAGCTCTGTGCTATC[C/T]TCGTGATGGGGACAA | 8853 |
rs184859774 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315229 | TCTTTATTAGGGACA[C/G]AACCCCAGACAAGCC | 8853 |
rs184861863 | snp | C/G | 0.000831601 | 0.0203742 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334018 | GCATTATTTCTCTCT[C/G]TCTCTGTCTCTGTCT | 8853 |
rs184874862 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350366 | TGTGAAATTACCTTC[A/G]CTGGAAGTGAGGTTT | 8853 |
rs184887713 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298609 | GCCTCAGCCCCATGC[C/T]CTGGACACTGGCAGG | 8853 |
rs184914195 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334528 | CTCAAATACTTAAGC[C/T]TATTGCATTTCCTTT | 8853 |
rs184914717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213075 | AACAGACAGTTACGT[A/C]ACAACCTTAGGCAGT | 8853 |
rs184948625 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230405 | GACTCTGGCAGGCGA[A/G]TTTCCCAAGCCGAGG | 8853 |
rs184954004 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247903 | TCCTCCTCTGCCCCC[A/C]ACACTGATAACCTCT | 8853 |
rs184956385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248267 | TCCCAACAATACTGA[G/T]TATTTAAGCCAAATT | 8853 |
rs185007548 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395864 | TGCCCTCCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 8853 |
rs185012898 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232428 | CTTTCGCAGCTGACT[A/G]TCCACATTATACTGT | 8853 |
rs185014821 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265723 | AATTTGTGTGTGTGT[A/G]TGTGTCTGTGCGTGT | 8853 |
rs185017113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209917 | AATCTGTTATTTCCA[A/G]TGTAGGTTCTATCTG | 8853 |
rs185036135 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227014 | GCTCAGATCCAGTCC[A/G]GGTGTTCGGGTCCTG | 8853 |
rs185043229 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302027 | ATGGGGTTTCACCAC[A/G]TTAGCCAGGATGGTC | 8853 |
rs185062615 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9224430 | AAATGTTTGTTGATT[A/G]TCAAGGTCCAGCTAA | 8853 |
rs185072185 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229869 | TAAATTGTGGGTGGG[C/T]CAGGCTGTTGGGGGC | 8853 |
rs185077309 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242200 | GGCATTCTTTGGACC[A/G]TGATCTTAGGGGCGC | 8853 |
rs185079450 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209302 | AAAGTTGTTCACTTT[C/G]TGAGGTAAATCAATG | 8853 |
rs185079941 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263497 | AGGACTTTTCTTCCC[C/G]CTAAATAAAAGTCAG | 8853 |
rs185097174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258562 | GTCTCCATGGTGCCC[A/C]CGCCGCCACACTCAT | 8853 |
rs185107316 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250525 | GTGTAAAAGTGTTTT[C/T]CCATTCCACAGAGGG | 8853 |
rs185111585 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225159 | CCAGAAGAAGATGCA[A/G]CAGAGACCGTGTATA | 8853 |
rs185142777 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284393 | TTTCTCAGTTAATTA[A/G]AAGCCCTTGAGGTGA | 8853 |
rs185154683 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320043 | AGAGTGTCATAACTG[C/G/T]GTGGCAGCACCTTGC | 8853 |
rs185209442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393995 | TCTGTGGTGTGAGGC[A/G]TGGATTTCCCACAAA | 8853 |
rs185252425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228882 | ATAGTGAAGTGTGTT[A/G]ATAGTCCTATTTCCT | 8853 |
rs185354695 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9396435 | CGCACCACCATGCCC[A/G]GTTAATTTATTTTTA | 8853 |
rs185380441 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212824 | GAAATGCAGAGCCCC[A/G]GGTTCCACCCAGGAC | 8853 |
rs185406407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381750 | TCCACAAAAACGTTT[C/T]GAATTAGCTGGGTGT | 8853 |
rs185433180 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327497 | GGGCAGGAGTGTGTT[A/T]GAGATGGTTAGAAAT | 8853 |
rs185445526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344348 | CCAGCCTGATAGATG[G/T]CATTTATCAGTTCCT | 8853 |
rs185460491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378649 | GGTTCACCCCGGTAG[C/T]GCACTGCCCCACCTT | 8853 |
rs185496496 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290279 | CAGTGGCACGATCTC[A/G]GCTCACTGCAACCTC | 8853 |
rs185524134 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326674 | ATAAGTAGATCTTTC[A/G]CTGCTGATGCTTTAT | 8853 |
rs185534529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361416 | TGTGGTCATGGTGTC[A/G]TGGCTCTAAACCTTA | 8853 |
rs185556371 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311690 | TCTCGGCCAGAACTC[C/G]AGGATGGCTCGTTCG | 8853 |
rs185557256 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370634 | ACAGAGGCATTGGGG[C/G]CATGAGCGGGATGAT | 8853 |
rs185576889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346829 | AGGTCTGGTAATCCT[C/T]TGCTGACAGCATAAA | 8853 |
rs185594911 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247277 | GAGGATGAACTCTTC[A/G]CTCCTCAATTAAGGA | 8853 |
rs185595614 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380557 | TACCTTCTGTATTTA[A/G]CTGTAGTTCTATACA | 8853 |
rs185616620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271495 | ATCCCTTGGACAGTA[A/G]TAAGGGCCTTCCTGC | 8853 |
rs185631981 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217709 | AAGCTCCGCCTCCTG[A/G]GTTCACGCCATTCTT | 8853 |
rs185640338 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234355 | TCAGTGAGAAAACCC[A/G]GGGAGAACATTTAGC | 8853 |
rs185647172 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307172 | TCGCCTGCGTGGCTT[G/T]TTAGACCACACCTGT | 8853 |
rs185657073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343480 | GAGACAAGGTCTCGC[G/T]CTGTCACTGAGGTTG | 8853 |
rs185662267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251923 | GCCCACATTGCTTTT[C/T]TTTTTCTTTCCTTAA | 8853 |
rs185672654 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286837 | AAATTTATGTACACC[A/G]TGTGTGATTAAAAAG | 8853 |
rs185677080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267505 | GCTGCGTCATATTCC[A/G]TGGTGTATATGTACC | 8853 |
rs185678622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377128 | TGAATTAAAGACAGA[A/G]AAAGGACTGCCAGGT | 8853 |
rs185678981 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303901 | TGGTGAGGCCTTGGG[C/T]GTGGGAGGGAGAACT | 8853 |
rs185694217 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266491 | TTGTGTTTTGTCCTC[A/C]GTGCTGTTCCTGTGC | 8853 |
rs185697790 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341309 | GATACTGAAGTAATT[C/T]GCACTAAAACAGTTT | 8853 |
rs185700336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330080 | GGCACGTATTTGCAG[C/T]AGTGAATTGCACTGT | 8853 |
rs185704517 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231221 | TTCCCTTCACTCCCT[C/T]CTGTAGCCAGGACCT | 8853 |
rs185709067 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254557 | TTTTTTTTTTTTAGT[A/G]GAGACGGGGTTTTAC | 8853 |
rs185718950 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364816 | TCAGTGGTCATTTAC[A/G]GAGGAACTGTTATGC | 8853 |
rs185719489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213923 | GGTCAATCAAGGAAA[C/G]ATTGAAGCATAGCTG | 8853 |
rs185721789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271836 | GTACGTGGCTTATTT[C/T]CCTTAACATAATAAC | 8853 |
rs185729729 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308054 | CAAAAACAAAAGTGG[C/T]CTAGATGATTGTATT | 8853 |
rs185735214 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291048 | ATGTCCTCCCTTTTT[A/T]AAACTTGGCTTTCTG | 8853 |
rs185739671 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9326923 | AAATTCCTGGGAGTA[G/T]AATTTCTAGGTCAAA | 8853 |
rs185744891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251198 | GCCAGAGCGTTGTCA[A/C]ATCAGGAGTTTAGTC | 8853 |
rs185745326 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216109 | CTTTGACTCTGCAGG[A/G]CAAGTTCCATTGTGA | 8853 |
rs185748981 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275787 | TCTGGTAGGCACTGG[C/G]GATACAATGAACAAA | 8853 |
rs185755021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344145 | AAAGCTGGTTTTGTC[A/G]TTTTGCTTGGAAACC | 8853 |
rs185765616 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404330 | TGAAATTGAATCTGT[C/T]CATCTGTTTATAATC | 8853 |
rs185827823 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207395 | CCCGCCTAGGTGGCT[C/T]GGAGGAGATGGGTGA | 8853 |
rs185836011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397535 | CTTGTGAAGGATGCT[A/G]TCCCTTCCCCACCAC | 8853 |
rs185837766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238241 | CTGTTTTTAAAACCT[C/G]AGCTCCTCTAGTCTT | 8853 |
rs185847970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273115 | TGATAGAGATTGCAT[C/T]GAATCTGTAAATCGT | 8853 |
rs185880492 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292817 | CTCACCCCAGCATAC[C/T]GTCACATCCCTGTTG | 8853 |
rs185885377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9237891 | CCCATGATTTTGAGA[A/G]TATGATCTCTGTCCC | 8853 |
rs185886087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233405 | GCTCTGGTAGTTCTT[G/T]AGTGTTTTATAATCT | 8853 |
rs185919440 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392406 | CGAGGTGCTCGTGAC[C/T]TCCTTAGAGTAAGTT | 8853 |
rs185944250 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222034 | ATCTCGTGATCTGCC[C/T]GCCTCGGCCTCCCAA | 8853 |
rs185952043 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233747 | CAGTAAGTGCTTAAC[A/C]CATGTTAAATGGATT | 8853 |
rs185962906 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277820 | CTTTGTATTGCAGCC[A/G]CTCTGTCAAATGTCT | 8853 |
rs185965879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216709 | CAAGTGATCCACCCA[C/T]CTTGGCCTCCCAAAG | 8853 |
rs185972569 | snp | A/G | 0.00557542 | 0.0525036 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404686 | ACTGCATTTGTTGTG[A/G]TGGTGCATTTGATTG | 8853 |
rs185973526 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259842 | ATGCTAAATGCCCCC[C/G]ATGTCTCCTCAGCTC | 8853 |
rs185982468 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9255137 | TGGAATCTTATTGTG[G/T]TTTAATTTATATTTC | 8853 |
rs185987817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296326 | GAATCACCTGTGTCC[C/G]CTCCCCCATTCCTAC | 8853 |
rs185994750 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313539 | TTATCACTGGATGGT[C/T]CTGGTGCCTTTGGCG | 8853 |
rs185997142 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331698 | ACTTGAACCCAAGAG[G/T]CGGAGGTTGCAGTGA | 8853 |
rs186003907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348991 | AATCCTAGCTTCCCC[A/G]CTCCCTAGCTGTATA | 8853 |
rs186013783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366694 | AGAGCCAGGACTGAG[C/T]AAGGAGGTGGAGTTG | 8853 |
rs186023991 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383394 | CGAGTAGCTGAGACT[A/G]CAGATGCATGCCACC | 8853 |
rs186064899 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369758 | AATGACACGAGTCTT[C/T]CCAAAGGACAGTGAG | 8853 |
rs186075134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386832 | CTCACAATCATACCT[A/G]GTTTAATGAAGCTGG | 8853 |
rs186115273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370838 | AGCTCTTCCTGGGCG[A/G]GCCTGAGGGTCCCGC | 8853 |
rs186160385 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357356 | TGGTAGTGCGCACAT[A/G]TAGTCCCAGCTACAT | 8853 |
rs186195652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291609 | TCTCCACCAGGCTGC[C/T]GCCATAGAGAACATA | 8853 |
rs186213095 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9282449 | CTGCTTTTAGTAGCA[C/T]GTTCTTTTGCATATA | 8853 |
rs186221207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299363 | CAATGCCATTAAAAT[C/T]GTGAGGAAACTAACT | 8853 |
rs186228441 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255811 | ATACTCTGATGTTTG[C/T]ATCACATAGCAGGGA | 8853 |
rs186234587 | snp | C/G/T | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316892 | GTTCCCTTTTATCTC[C/G/T]TTTGCCTAGCAACAC | 8853 |
rs186238127 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353472 | TGAGATGGGAGGATC[A/G]CTTGAGTTCAGGAGG | 8853 |
rs186240537 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336116 | ATACATATATATATT[C/T]CTTTTATATATTAAT | 8853 |
rs186242831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273407 | TGTATCCTGCAACTT[C/T]ACTGAATTTATCTAT | 8853 |
rs186251077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352626 | GCAGGGAGGATCAGT[A/G]GACGGCAAGTGTGCA | 8853 |
rs186257301 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387674 | CTCATAAGATAAATA[A/G]CTTATATTTTAAATC | 8853 |
rs186258429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243710 | AATGCATGTATAACC[A/G]GGGCATTCTGGTACG | 8853 |
rs186262343 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225823 | GACGTATTCCAGGGA[A/T]GTTAAGTGGCAACTC | 8853 |
rs186270254 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226807 | CTGGCCTAACATCAT[C/T]GGTGTGTGATCTCTC | 8853 |
rs186271700 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9259168 | CTCTTGTTCTGTTAG[A/C]TGGGGTTTCAAATTT | 8853 |
rs186295089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277329 | CGGCTGGAAGACTGG[A/G]GAGGAAAAGTGATGA | 8853 |
rs186306119 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258897 | CTCAGCATTTTAGAG[A/T]CTGTAGGTCCATGCT | 8853 |
rs186309271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295247 | GAATCAGAAAATTTG[A/G]GTTTGAATCCCAGCT | 8853 |
rs186317175 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373890 | AGTGAGCTGCTGTTT[C/G]GCTCTCCCTCTTGTA | 8853 |
rs186325234 | snp | C/T | 0.00130278 | 0.025489 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393677 | GCCAGCTCGGCCATC[C/T]GTGCTCCTGCCCTCT | 8853 |
rs186360894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249002 | CCCAACCCGAATACA[C/T]AGGATGCTAGAATTT | 8853 |
rs186392853 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283221 | TAGCTGGGATTACAG[G/T]TGTCTACCACCACAC | 8853 |
rs186403728 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318060 | TTGCAGCAGACAGAA[A/G]ACTCTGCCTTTGTTT | 8853 |
rs186416392 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210202 | ACTTTTCTTAATGCC[A/G/T]AATTCTCTAAATTAC | 8853 |
rs186438586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243403 | ATGAGCCACCGTGCC[C/T]GGCCTAAAGATTTTT | 8853 |
rs186441263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210541 | GAATGAAACACTACC[A/G]TGTATCTGTTAACCC | 8853 |
rs186447217 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352996 | AAAAGGTGCCTTCCT[A/T]TGAGTATCTGTAGTG | 8853 |
rs186455110 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276602 | GAGTGTAGCGGCACA[A/G]TCTTGGCTCACTGCA | 8853 |
rs186480035 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304019 | CAGGGGACACAGATG[A/C]TTTTATTAGAAGACA | 8853 |
rs186494885 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323323 | CTGTGGGAGCATCTC[A/T]CCGGTACCAGCGGCT | 8853 |
rs186496970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341486 | GTCTGATTCTGTTGA[A/G]AAGAATGTCCCTTAT | 8853 |
rs186507226 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312944 | TGTGCCTGTAATCCC[A/T]GCTACCTGGGAGGCT | 8853 |
rs186508383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357794 | ATGGATAACATTTTT[A/G]ATAACTTGAACATTT | 8853 |
rs186511160 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9374284 | GTCATAGTCCATGCC[C/G]CAAGGAGCTCATGGG | 8853 |
rs186520982 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221622 | CTAGTGTATAGAAAT[A/G]TGGTTACTTTTTGTA | 8853 |
rs186527838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395401 | AATCCCTTGAACCCA[G/T]GAGGCGGAGGTTGCA | 8853 |
rs186588630 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265037 | GCTACTCAGGACGCT[C/G]AGGCAAGAGGATCAC | 8853 |
rs186597559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211109 | GCGGTGAGTCGAGAT[C/T]GTGCCATTGCACTCC | 8853 |
rs186601139 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300125 | GTAGTCCCTGCTACT[C/T]GGGAGGCTGAGGCTG | 8853 |
rs186618951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362209 | TGCCATGCAGGGCCT[C/T]GGCTGACTTGCTTAT | 8853 |
rs186619317 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267056 | TTCTTTTCTTTAAAA[G/T]ATGCTTTAATTTTAC | 8853 |
rs186622022 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336472 | TTTTGAGTGTTGGTT[A/G]TGCCTTAAGTGCACA | 8853 |
rs186645464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244307 | TCTCAAAACAACAAC[A/G]ATAAAAAGAATTTGA | 8853 |
rs186657902 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397135 | CCACAGGCCATGCTT[C/G]TCTTGGCTTCTGGGC | 8853 |
rs186674852 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231569 | CCCATTGAGATGCCC[A/G]GGTGCCGCCACACCC | 8853 |
rs186685743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214301 | GGAGTGCAGTGGTGC[A/G]ATCTCGGTTCACTGC | 8853 |
rs186763265 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205809 | TATTTGACTGGTATC[C/T]TCAGAGCTTCTGGAT | 8853 |
rs186787900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398910 | GATCAGGCCTTCCCT[A/G]CGAGTGTTCTGTAGT | 8853 |
rs186807934 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346643 | TGTCCACTCGCTGTT[A/T]GTTTGAACTCCGATT | 8853 |
rs186810901 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364548 | AGGCATCAAGAGCAT[G/T]ACCAAATATTTACTG | 8853 |
rs186819301 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380477 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 8853 |
rs186834263 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270832 | GAGTCTCGCTCCGTC[A/G]CCCAGGCTGGAGTGC | 8853 |
rs186838813 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304917 | GGGTGTAGATGTTAG[C/T]GGAGAGGCTGGAGTA | 8853 |
rs186843739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289495 | ATGAATAAAAGTAAA[C/T]GCGGATACATTCTGT | 8853 |
rs186846335 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9324663 | TAATCCACTCATGCA[A/G]TGACCTCCCAAAGGT | 8853 |
rs186855604 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251440 | GCTCAGTGGGTCTGG[A/G]CGCAAAGCATGTGGA | 8853 |
rs186856130 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367111 | TCTCGGCTCACTGCA[A/G]TCTTCACCTCCTGGA | 8853 |
rs186861472 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227452 | GAACTGCAAACTCCT[A/G]AGGGCAGGATCTCTT | 8853 |
rs186863904 | snp | A/T | 0.109814 | 0.206997 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286429 | GAAAAGGATTTTTTT[A/T]AAAAAAGGAAAAAAA | 8853 |
rs186863989 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384378 | GTTCTTGTAAAGGCG[A/G]TTTCACAAGCAGCAG | 8853 |
rs186864118 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342445 | TTGTGCTGGGGCAGC[A/T]GGATAGCCACAAGCA | 8853 |
rs186869008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359523 | CTGGCCACCTAATAC[A/G]TGAGCTTTCATGACT | 8853 |
rs186880057 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303648 | CCCAAAAGACTTCAA[C/T]GCTAAGCTATGTTCT | 8853 |
rs186893263 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265294 | ATATGACAACATTCT[A/G]CATTACGAATTGAGC | 8853 |
rs186899387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339762 | CACTATCTGACTCAA[A/G]ATGCTGTCATACCCA | 8853 |
rs186900301 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249706 | CTGAGATTGCTGGCA[C/T]GGGTCTCCTGGAGCT | 8853 |
rs186904159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283910 | CTAATTATTATGCTT[C/T]CCGATGGCCCCATCT | 8853 |
rs186904840 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209236 | TTTAAGCAAATCTAC[A/T]TACATGCTATGATGA | 8853 |
rs186915737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372503 | TTACCCTATGCCAAT[C/T]GATGTAAACCAGAGT | 8853 |
rs186922098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301396 | AAAGGGAAAACCAGA[C/T]GGCTCCAGAAATGTG | 8853 |
rs186930139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318317 | TGTGAAATATATACA[G/T]ACCTAGACTTTTCAT | 8853 |
rs186963174 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400231 | CCCTCCCCTCCTGCC[C/T]CCTCCCCTCCTGCCC | 8853 |
rs186984977 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329040 | ACACAGTAGGTACTC[A/G]GCTGTTTCTTGAATG | 8853 |
rs186988726 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236763 | CTGCCTTTAAATTTG[A/G]AACTATAATTATTTG | 8853 |
rs186999889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363238 | TCTCGACTATTGTGA[A/G]TAGTGCTGCAGTAAA | 8853 |
rs187012484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253467 | CTGTGCCCGGCCAAA[A/G]TTCACGTTTTAAATG | 8853 |
rs187047085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256515 | AGGAGATATTAGATG[C/T]TGTTAGTGGTAGAGA | 8853 |
rs187065518 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274024 | GCCCAGGAATGAACA[A/G]GGACAGCTTGGAGGT | 8853 |
rs187075481 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232584 | TCCCCTTCTCCCCAT[C/T]AGATCATAAGCTTCC | 8853 |
rs187075814 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310325 | GGTAAGATCCTTTGG[C/T]CATATTGTATATTAC | 8853 |
rs187077357 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9292205 | GTGCTGCCCTGTGGC[A/G]ATTTTGAGAGTTGAG | 8853 |
rs187077822 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321835 | AAAACCCTAGAATTT[A/G]GGAGGAGGGAGCAGC | 8853 |
rs187080312 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250632 | CCACAAGTAACTATC[A/G]GACAAGGTTGGAAGC | 8853 |
rs187090217 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9329431 | CACGGACCCTGGGGT[C/T]TCATGGGGGAGGCAA | 8853 |
rs187091455 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346401 | ATATCACGCCACTGC[A/G]CTCCAGCCTGGGAGA | 8853 |
rs187104899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356547 | AGATGTTTGCCTGCC[A/G]GGCCCCAGAGCAGGA | 8853 |
rs187127857 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211845 | AAAAACAGTTCCTCC[A/T]AGTCCCCAGAACAGA | 8853 |
rs187141377 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230912 | GGCCAGGGGGTCCTG[C/T]GTGACCTTGGAGGTG | 8853 |
rs187152001 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264359 | GGGGGCCCGTGCTGG[C/T]GTCACCACTGTCCCC | 8853 |
rs187153222 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396568 | AGGCATGAGGCACTG[C/T]GCCTCACCTCTTTTA | 8853 |
rs187167051 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291941 | GCTAAGAGCTGAAGA[C/T]AGCGACAATGTCATT | 8853 |
rs187197065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345210 | CTTAGGAAGATTTCT[A/G]CTTTTCCATTAAGAG | 8853 |
rs187213759 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9379197 | GAAGGAGAACCTACC[A/G]CTAATGAGAAAGAGC | 8853 |
rs187217559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313416 | CCACTCACTCGTGTA[C/T]ATTCATGTTCATGTG | 8853 |
rs187272161 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348784 | CGAACACCTTTCCCC[A/G]TATCACAGGGAAAAA | 8853 |
rs187274007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218918 | ATTCCCTCCTTGGAG[A/G]TATCACTGGAGTTGA | 8853 |
rs187286990 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364069 | TAATGTAGAAGATCA[A/T]GATTTCAGCTTTGAT | 8853 |
rs187299390 | snp | A/C/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383103 | TGCATATCATCTCGG[A/C/G]GGGGCCACGGGACTG | 8853 |
rs187333467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248860 | GTCGACTCTGATGTG[A/C]GCTCAGTGTTAGGTG | 8853 |
rs187366997 | snp | C/T | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403594 | ATTTTAACTATTATA[C/T]ATAATCAAGATCCTG | 8853 |
rs187400497 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405940 | GGTCTCCAGTCCACA[A/C]CTCTGCCGGACAGAG | 8853 |
rs187434477 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295830 | CCCATTAGAACCCTC[C/T]AGTCCCCCAAATGCC | 8853 |
rs187439353 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331233 | AGGGCTCAGGTTTGG[C/T]TGTTGACCCTTGGAA | 8853 |
rs187462207 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389604 | TGGGTGTCTCACAGA[A/C]CCTCACACGGCTCTG | 8853 |
rs187465248 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9400213 | GCCCCCTCCCCTCCT[A/G]CCCCCTCCCCTCCTG | 8853 |
rs187478517 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235681 | CTCGGGGCCAGGAGT[G/T]GCTGACAGCTGAGGT | 8853 |
rs187480493 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253312 | GGGATTACAGGTGCC[C/T]GCCACCACACCTGGC | 8853 |
rs187499798 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366569 | TTAGCTTCCTGGTGC[A/T]TAGGTACCTGTCACC | 8853 |
rs187516180 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385480 | TGTAGCTTACTTTAT[A/G]CTTTCATTGATCTCA | 8853 |
rs187519858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349695 | ATCTGACTTTATCTG[A/G]CTTTCACTAGTCCAA | 8853 |
rs187535587 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384956 | TCCTGAGGCCTTAAC[A/G]CTCCATGTTATAACC | 8853 |
rs187587109 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398416 | CTCAGGAGGCTGAAG[C/T]GGGAGGATCACTTGA | 8853 |
rs187635981 | snp | C/T | 4.94214e-05 | 0.00497074 | synonymous-codon, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9279361 | CAAAATGAAGAAATC[C/T]GTGAAAGCAATCAAC | 8853 |
rs187642127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298149 | CCAGCTTTTCTTTCC[C/T]GTTTTTCTTCTCCAG | 8853 |
rs187657982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315397 | GGAATGTTGGAAGAC[A/G]GGTCTGCGTATGTAG | 8853 |
rs187661841 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334308 | CCCACCTTGGCCTCC[C/G]CAAGTCCCTCACCCT | 8853 |
rs187672284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350652 | AGGCCTCTGTAACTT[A/G]TCCCAGTCAAGCCTT | 8853 |
rs187674611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402085 | GCAAGTGGCACAGCT[C/T]CGCAACTGAGCTCAG | 8853 |
rs187677663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368202 | ACTCTATCCAGAGCG[C/T]GTTTTATGACAATGC | 8853 |
rs187688906 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301660 | CAGAACCCGCTCCAC[A/C]TGAAGATCAGCATCC | 8853 |
rs187697014 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241343 | TAGTTTTTGGTGAGA[A/G]GTTTTCTGGGAAGTC | 8853 |
rs187697883 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207813 | GGTGTGTGAGAGTCG[G/T]CGCTTCTGGGTCCAA | 8853 |
rs187700708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319258 | CACCACGGAAGGGAC[A/G]TGATTGTGGCTGCCT | 8853 |
rs187706714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274803 | CTTTATTTCTAATCT[A/G]TTTAACAGATTGTAG | 8853 |
rs187717499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337396 | TGGGGGTTCCATCTT[A/G]TATACCTCAAATTTG | 8853 |
rs187719958 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9238625 | TGCATGGGGAGGAGA[C/G]GCTGAGGCAACAGCC | 8853 |
rs187720781 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9354106 | ATAGCAAATTCAAGT[C/T]CTGAGCCATTATCCG | 8853 |
rs187729138 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9222496 | TTTTGGTTGCTTTCT[A/G]TCAACATTGCCTTGA | 8853 |
rs187731593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371183 | TACATCCCCCAACCC[C/T]GGGCTTTTTTCAAAA | 8853 |
rs187738376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311477 | GCCATTTTACATAAT[A/G]TATTTGTTAAAAGTG | 8853 |
rs187740270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388198 | CCAGGCCCAGCAGAG[C/T]TGGTGTCAGTGAGGT | 8853 |
rs187745759 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400493 | TCTGAGACCCCTGCT[A/C]CTGAGCAGCTCAGTC | 8853 |
rs187778017 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367568 | GAGTTCGAGACCAGC[C/G]TGGGCAACATGGTGA | 8853 |
rs187800265 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331976 | CCCATCAGCAGACAC[A/C]GCATTGGAATGTGGT | 8853 |
rs187834036 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405791 | TACTTTTAGCATGAG[C/T]GGTAATCTTTTAAGG | 8853 |
rs187915336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394739 | ACCACACCAGACTGA[C/T]AGACATGAGGCACAG | 8853 |
rs187924571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228583 | CTTGGCAGAGTGAGC[A/G]GCCCCCATCTTCCTG | 8853 |
rs187937651 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212498 | TAGGTAAATATTGAT[A/C]TACTCCTGAGGTGGT | 8853 |
rs187943434 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262079 | GACTCAAACTCCTGG[C/G]CTCAAGCGATCCTCC | 8853 |
rs187954126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246043 | GGTGGTGTGACCCCG[C/T]TGGGGGAAGGAGCTC | 8853 |
rs187954691 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9228066 | ATTATGAGTGTATCT[A/G]TAATTATAATTGAAA | 8853 |
rs187966194 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278499 | GCCTGGGTGACAGAG[C/T]GAGACCCCTTCTCAA | 8853 |
rs187971238 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296770 | GCATGAGTCTGTAGG[A/T]TGCAGAGGAGTTTGG | 8853 |
rs187976914 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314967 | AAAATATTGGAGGAT[C/G]TGGGGGAGGGAGGGA | 8853 |
rs187977166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297950 | GCCTCGGTTTTCAGC[C/T]GTGGGAATGCGGTGC | 8853 |
rs187989888 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9223797 | GCCAATGGGAGGGAG[A/G]GGAAGAGAGGAGTTA | 8853 |
rs188001860 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257776 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 8853 |
rs188005904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292701 | CATCTGAGTCCTCAG[C/T]GCCTAGCACATTGCC | 8853 |
rs188023888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329880 | CCAGCTTATGGATCA[C/T]TCCTGCTTTGCGATG | 8853 |
rs188025461 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9223066 | TTAGGCAGAGGCCTT[C/T]CTGCATCTCTCAAGT | 8853 |
rs188055268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282043 | AAAATAGCATTTGCC[A/G]CTTTATGAAAGAAAA | 8853 |
rs188064091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314331 | CAAAATAGGTGCTCA[A/G]TAAATCACTTGAATG | 8853 |
rs188066547 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284557 | AGCCTCAATTTCCTC[A/T]TGTGTAAAATGGGAA | 8853 |
rs188075539 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320589 | TTTTCAGGAAAGTTC[A/G]TTGAGGGAAGTTAAG | 8853 |
rs188076727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299163 | TTTCTAAAAATGGAA[C/T]GGAAGAGTCTCCAAG | 8853 |
rs188076897 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343203 | GCTTTAAGGAGCTCT[G/T]CACCTGGAGCAAACC | 8853 |
rs188079488 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360615 | GTAAATACTCCCACA[A/G]TGGCCAATTTCAAGC | 8853 |
rs188084513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349261 | TAGATATAGGAGTTA[C/T]TCCTATATCTAAGAC | 8853 |
rs188085455 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315774 | CCGCACCTTAAACTG[C/T]GCTTTTCAGCATTTA | 8853 |
rs188091402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335704 | TCTTTCTGTAATGAC[A/G]TCTCTGTGTGCTAAC | 8853 |
rs188091524 | snp | A/G | 0.00143371 | 0.0267358 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376872 | GAATTGAATGCTCCC[A/G]TTAGAATTCTGGAAT | 8853 |
rs188121615 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9375856 | CCCTGGAACCCACAC[C/T]CCACTGTGCTCCCCC | 8853 |
rs188229125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244710 | GCCAGTGACACTTAG[A/G]GACTCTTCCCTGAGC | 8853 |
rs188252266 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219679 | TTGTTGTTGCTTTTT[A/T]AAAAAAAAATTGAGA | 8853 |
rs188260085 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278130 | GCTGTAGGGCAGGGT[A/G]CTTCATTTAGTTTTC | 8853 |
rs188270336 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9208815 | TTATGGAATGATTGC[A/T]ACCAAAAAGGTAGCT | 8853 |
rs188281188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210327 | CAGCTTTAAAGTCTG[C/G]TTAATAATACCTATC | 8853 |
rs188285760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379863 | CGGGTATGGTGGCGC[A/G]CACCTGTAGGCCCAG | 8853 |
rs188287302 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226164 | ACAGCTGGCTGGCCA[C/T]GTAGACGATAATGCT | 8853 |
rs188295389 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251004 | GGCAGGCTCACCAAG[A/G]AGGTGGCATTTGGGT | 8853 |
rs188298636 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233281 | AAGGAATTGCGAAGC[C/T]GTACTATGTTGAGGT | 8853 |
rs188306578 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366319 | GAATTCTCCTCCTCC[A/C]ATCTCCCCACCCCCA | 8853 |
rs188308075 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284939 | GCTGGAAAACTGTGG[C/G]CAGACACCTGTGTTT | 8853 |
rs188311406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238976 | GTTCCCTGGGCCTCC[C/T]GCAGCCTGGAGGGGT | 8853 |
rs188312468 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266024 | AGTGATCCACCCCCC[C/G]ACCCCCTGCCTTGGC | 8853 |
rs188313052 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382263 | TGCTGGGATTATAGG[A/C]GTGAGCCACCACACC | 8853 |
rs188314511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302407 | TGAATTCCTGACCTC[A/G]TGATCTGCCCACCTC | 8853 |
rs188329999 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321383 | GGTGTACATTCATTC[A/G]GAAGCACAGGCAGAG | 8853 |
rs188330532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265731 | TGTGTGTGTGTGTCT[A/G]TGCGTGTAATGGATT | 8853 |
rs188334389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339056 | TAGTGACATGCACGT[A/G]TAGTCCCAGCTACCC | 8853 |
rs188343165 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9238687 | CCCTTTTTGGCCAGT[G/T]TTTTTTTGGTGGCAT | 8853 |
rs188357868 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302069 | ACCTCGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 8853 |
rs188364950 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229926 | TTCTGCAGCCCTGGC[A/G]GTTGTCAGTGTGGGC | 8853 |
rs188443017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398197 | GGCAGAGTTGAATAC[C/T]TGAAACAGAGATGCT | 8853 |
rs188491550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270137 | CTGAAGGTCAGCTTC[C/T]ACCTGGCCCCTGAGA | 8853 |
rs188505839 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9400249 | TCCCCTCCTGCCCCC[C/T]TCCCCTCCTGCCCTC | 8853 |
rs188506837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254628 | ATCTACCCACCTCAG[C/T]CTCCCAAAGTGCTGG | 8853 |
rs188524374 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304735 | TGGACTAGTGGGGTA[C/T]AGGTATTGGTGGAGG | 8853 |
rs188525084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212937 | TGGAGTTGCTTGGGC[A/G]TTTGTGAAGCAGAGC | 8853 |
rs188525618 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271867 | CTCTATTTCCATCCA[C/T]ATCATTGCAGCTGAC | 8853 |
rs188533850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308957 | GTTCTTTCAGATAAG[C/T]GGCCTTTAGAAAGAA | 8853 |
rs188535760 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291312 | AATATGTTTTCAGCC[A/G]TTTAGTTGGGATGAT | 8853 |
rs188536287 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341618 | TTTTTCTCCCCCAAA[A/T]CAATAGACGTATTTC | 8853 |
rs188544865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396881 | ATGGCACACACCTGT[A/G]ATCCCAGCTACTCGG | 8853 |
rs188552630 | snp | C/T | 0.000956291 | 0.0218456 | missense | ASAP2 | GRCh38.p7 | 2:9374820 | CAAGGAAGAAGCACG[C/T]GGATAACGCGGCGAA | 8853 |
rs188554059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327063 | CTTACAGTTTCACAG[C/T]AGCTTTCCACCTCCT | 8853 |
rs188554243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344304 | CCTTCAGCCAGTTTG[A/G]GAATATTGGTTTCCT | 8853 |
rs188560180 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9386033 | GCCCTGGCTCCTAGC[C/T]GCGACCCACTTCCAT | 8853 |
rs188564168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362316 | CTGGACAGGTTCTCT[C/G]ACAGGAGTAGCATCT | 8853 |
rs188574697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378525 | CTCCCGTGGGACAGG[A/G]TGGATGAGTCACACA | 8853 |
rs188577384 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9215060 | CCTAGAGTGCACTTA[A/C]ACACACCCAGATGGC | 8853 |
rs188584413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371335 | ACTTCATAGTATACT[C/T]AGGCATTTACATATA | 8853 |
rs188588267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402433 | TCAGGAGTTCGAGAC[C/T]AGCCTGGCCAACATG | 8853 |
rs188614505 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330506 | TAAAAGCCCTAAGTT[C/G]ACCACCAGGCCTATA | 8853 |
rs188638761 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365365 | GTCTCCTGAGCTCAG[C/T]GGTCAGGGAAGTCTG | 8853 |
rs188674094 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394191 | TTTTTTTGAGACTGA[A/G]TCTAGCTCTGTCACC | 8853 |
rs188699563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397552 | CCCTTCCCCACCACC[A/G]GTGATTTTGTCTCTG | 8853 |
rs188736610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231977 | AAGCTCCTGCTTCCA[C/T]CTCTCTTGATCTGGC | 8853 |
rs188764102 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276245 | AGATGAGTACCTGCC[A/C]CCCTATCGTGGAGGT | 8853 |
rs188764445 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207934 | GTTTTAGTAAAGTGC[C/T]CTCAAGGTGCAAAGT | 8853 |
rs188768805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265638 | TCTGTATCTTTATAT[A/G]CAGAGTTTTAAGTGT | 8853 |
rs188779062 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218286 | TCACTGAATGTGATT[A/G]CCTGGAGGTCATCAG | 8853 |
rs188784214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288328 | ACACGTATGTCATCT[C/T]CACAGTGTTCATGGT | 8853 |
rs188803029 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252552 | GCATTCCAGCCTGGG[C/G/T]GACAAAGTGAGACCC | 8853 |
rs188813564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324062 | ATAGCAGTGCAAACT[C/T]AGGTTTCAAATGTAC | 8853 |
rs188823525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358214 | GATTTGATACAAAAG[G/T]GCTCTGTGATTGCTG | 8853 |
rs188832254 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287211 | AAAACAAGCAGCAAC[C/G]TGGGGAACACCCTAC | 8853 |
rs188866275 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284066 | GACATTGGCCTCATC[C/T]AGATAATCCAGATAA | 8853 |
rs188910178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347108 | ATCGCCGCCTACATC[C/T]TGCAGGGGTGGTAGG | 8853 |
rs188924821 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380568 | TTTAGCTGTAGTTCT[A/C]TACAATTACAAGATA | 8853 |
rs188971052 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369979 | CCTGAGTAGCTGGGA[C/T]AGGCACATGCCACCA | 8853 |
rs188976831 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386933 | TGACCGGCCGAGCGC[C/G]GGGGCTCACGCCTGT | 8853 |
rs188984070 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293701 | GTCGTGGTGGGCACC[A/G]TGCTAGGTGTTAGAG | 8853 |
rs188993246 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312690 | TTGGTAGTTTACTTA[C/T]CTAAACATGGGGCGT | 8853 |
rs188994934 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330899 | AATCTTCCATTACTT[C/T]GTTTTTGGATATGAG | 8853 |
rs189001398 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348172 | GGAGTCTCGCTGTGT[C/T]GCCCAGGCTGGATGG | 8853 |
rs189009505 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214703 | TTCACTCATAAATGT[A/G]TATTGGGCCCCTACC | 8853 |
rs189010327 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365504 | CCCACCCCAAACTCT[C/G]AAAACAATGTCCAGA | 8853 |
rs189020551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381954 | GTCCTCTTTCTAAGC[A/G]CTGTACATCCACGAG | 8853 |
rs189035291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250347 | AGAGGGGAAAGAACA[C/T]GACATGTGAATACAC | 8853 |
rs189079553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325655 | GTTGCTTCCTGTGGT[A/G]TGCACCTTGCACTGG | 8853 |
rs189085233 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403940 | ATAACCTGTTGTGAA[C/G]AATCATACTTAACAA | 8853 |
rs189094168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235262 | CACAGATGGCTGGTC[A/G]TCCTGTGCACCAGTG | 8853 |
rs189096189 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267727 | CATGGTGAAACCCCC[A/G]TCTCTACTAAAAATA | 8853 |
rs189112980 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351863 | TGAATCTCTGGGGAG[A/G]GTTGAGCACTGTGAT | 8853 |
rs189132869 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9386631 | GTGCTTAGTTCTGCA[C/T]ACCTGAGCTGGGTTT | 8853 |
rs189155016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332776 | TCTATTTCACAAGAA[C/T]TTGAAATGATTAAGA | 8853 |
rs189177729 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371842 | AGAGGGAGGGCCGGG[C/T]GCGGTGGCTCACGCC | 8853 |
rs189181824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348567 | GCAAACAGTTATTAA[A/T]GTAAAACAGAACTGC | 8853 |
rs189191905 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321716 | TGAAGAAGAGTGCCT[A/G]AGAGAGTCATCTGGT | 8853 |
rs189193936 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339688 | ACATATCCCTTAGCC[G/T]CCTTGTTGGTCCGTC | 8853 |
rs189209188 | snp | C/T | 0.000236641 | 0.010875 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356361 | GTGACCCAGGGACCC[C/T]ACCCGACCCTGGGCT | 8853 |
rs189209780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237813 | CAGTAGGTGCCCATG[C/T]TTCTTCTTTTGATTT | 8853 |
rs189211901 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205475 | AATGATAAAAGCTAT[C/T]CACGAATACAGCGAT | 8853 |
rs189214584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372109 | AAAGGAAGTCCACTT[C/T]CTCTCTATCCCTTTC | 8853 |
rs189217746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221167 | CCATATGAATTTTAG[G/T]ATCAACTTTTCAATT | 8853 |
rs189225827 | snp | C/T | 0.34437 | 0.231505 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254254 | ATATATATATATATA[C/T]ACACGTGTGTGTGTA | 8853 |
rs189234820 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391341 | TGGCTCTTGTGCAGG[A/G]CTCTCAGCTCCCCCA | 8853 |
rs189241569 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271515 | GGCCTTCCTGCCGTT[A/T]CTCTGTTGAATTCTT | 8853 |
rs189272760 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258567 | CATGGTGCCCCCGCC[A/G]CCACACTCATCTTCT | 8853 |
rs189286759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293000 | CTACATGTGTGGCCC[A/G]TAGAGGGGGCGCAAA | 8853 |
rs189288087 | snp | C/T | 1.65921e-05 | 0.00288024 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9403315 | GTCATTTGTGCACTT[C/T]ATCGCTGACTGAATT | 8853 |
rs189294749 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276024 | AAGCAGTTCTGTGCA[C/T]GTAGTAAGTCCTGGG | 8853 |
rs189312466 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9215545 | GTAATTGAAAGATAC[A/G]ATAAATTTCAGTTAG | 8853 |
rs189328013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243427 | GATTTTTTTTATAAT[A/G]TGCATTTTTGTCCAT | 8853 |
rs189371756 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312946 | TGCCTGTAATCCCAG[C/T]TACCTGGGAGGCTGA | 8853 |
rs189384551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213155 | GTTCTGGAGATCAGG[A/G]AACCGAAATCAGGAA | 8853 |
rs189389824 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263559 | ACTGTCATCTGTTTC[C/G/T]GTTTCTCTAAGATAG | 8853 |
rs189401736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298653 | GTCTCATCACCAGGT[C/T]GGGAAAGAGTGGAGA | 8853 |
rs189406950 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369735 | TGGAATAAGCCTGAA[A/G]TAGAATTAATGACAC | 8853 |
rs189413480 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263820 | GGCCGTCTGGAGGTC[A/G]TCAGCTGAGGGCACA | 8853 |
rs189419856 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248358 | TTTTAGAAAACCCTT[C/T]GGTATCTTGGTGTCA | 8853 |
rs189422085 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334609 | ATATTTTAAGGTTCT[G/T]TTCATACAGTCTTTT | 8853 |
rs189440789 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369226 | GTTTCACCATGTTGG[C/T]CAGGCTGGACTCGAA | 8853 |
rs189444446 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9224625 | CCATCCCAATTAATA[A/T]CTGATTTCTTCTTTG | 8853 |
rs189456287 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242398 | CTCTAGTGATCTGCT[C/T]CTAGAAGCCTTTTCT | 8853 |
rs189458500 | snp | A/C | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209502 | CTCATTTAACAAATA[A/C]ATAAAATTTGCAAGC | 8853 |
rs189459567 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330955 | TCAAATCAGTCAGGC[A/C]GCTTTGACTTTCTCA | 8853 |
rs189468421 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390787 | CTTCAAATGATACTG[A/G]TATTTGATAAATAAA | 8853 |
rs189625928 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258992 | GGGCCAGACCAGGAC[C/G]CTGGGCCTGCTCTTC | 8853 |
rs189636758 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295405 | GAATAAGTGACGCCT[C/G]TTGCTGCTGTTACTT | 8853 |
rs189637521 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225618 | GGGGAAATATTAAGG[A/G]CTTTTGCGTAGGGGA | 8853 |
rs189651949 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354701 | TTGTAGAAAGTGGTC[A/G]GGCCAGAAGTCCAGG | 8853 |
rs189658355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247953 | CTCTCAGGCATAATT[A/G]TGCTCCACTTATCCA | 8853 |
rs189658891 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258819 | TTTATTTCTCTCGCT[C/G]TCTCTCCTCTTCACT | 8853 |
rs189666038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396456 | TTTATTTTTATATTT[A/T]GTAGAGGTGGGGGTC | 8853 |
rs189677386 | snp | A/C | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396009 | CTGGTATCCCCCATC[A/C]AGACACCGTCCGTTT | 8853 |
rs189683874 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9280361 | CTGCTCCCCCCCACC[A/G]CCCCCACCAGTTACA | 8853 |
rs189712777 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351505 | ATAAGATAAACCTTT[A/T]TTCCTAGGTAGTTCT | 8853 |
rs189778596 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250245 | AAAACTCCACAAACT[C/G]TAAGGAATGTTACAC | 8853 |
rs189790656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284034 | CTCCCTCTTCTACAT[A/G]TAAGGACCCTTGTGA | 8853 |
rs189795363 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265300 | CAACATTCTACATTA[C/G/T]GAATTGAGCATCCTT | 8853 |
rs189809423 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301434 | TGAAATTAAAGTGCT[C/T]ATGAAGTCAGCCTAG | 8853 |
rs189814115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318818 | TTGGCACAACAAAGT[C/T]GGTGAGGGGAGGAGA | 8853 |
rs189816093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362577 | GGTGTGGTGGCCGGC[A/G]CCTGTAATCCCAGTA | 8853 |
rs189818895 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392728 | TGTGTAGCTGAAGGC[C/G]TCATTCTTCCTGGCT | 8853 |
rs189820131 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337119 | GTTGTTTTTTGTTAA[C/T]CAGCCCATCTGCCCC | 8853 |
rs189824300 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378694 | AGCAACAACAGGGAT[A/G]CCCCCCTCCCCTTTT | 8853 |
rs189830644 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353936 | GCTGTGATTGTGCCA[C/G]TGCACTGTAGCCTGG | 8853 |
rs189836172 | snp | C/T | 0.498034 | 0.0312882 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400269 | CTCCTGCCCTCTTCC[C/T]CTCCTTCCTTCCCTC | 8853 |
rs189848442 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303919 | GGGAGGGAGAACTCA[A/C]AGAGACGAGGACTGG | 8853 |
rs189874925 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341354 | ACAGATTATATTCCT[A/C]TTTTTTACAAATGTG | 8853 |
rs189883375 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9357397 | GGCAGGAGAATCACT[C/T]GAATCCAGGTGGCAG | 8853 |
rs189902436 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395600 | GTTTTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 8853 |
rs189918618 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210143 | TCTGAAGTGGACTTT[A/G]AACTTGGCTCCTGCT | 8853 |
rs189919652 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321913 | TTTATTAATGTGGGA[G/T]ATTCATTTATCCCAA | 8853 |
rs189928609 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243124 | GTTTTGTTTTGTTTT[G/T]TTGAGACGGAGTCTT | 8853 |
rs189940951 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356735 | CCTACTTTGCAGAAC[C/T]TCTGAAGTAGCTTTA | 8853 |
rs190003461 | snp | A/G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9377504 | CCTTTAGAGATGTGC[A/G/T]CAGGCAGTTTACCAC | 8853 |
rs190026648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251986 | TGAATTTAGTTCATC[A/G]GTTATTTGAAATAAA | 8853 |
rs190038096 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286867 | GGAATAGATGATAAA[C/T]GATGATAAAGAATAT | 8853 |
rs190040132 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267635 | CGTGCAGTTTCTCAT[C/G]CCTGTAATCCCAGCA | 8853 |
rs190074662 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231361 | ACTTGCTCTAGGGCT[A/T]AAGTCAGGTCACATC | 8853 |
rs190084723 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397894 | CTCCTGAGTAGCTGG[A/G]ACTACAGGCGCCCGC | 8853 |
rs190090286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212886 | GCACGTGAGAGCTTG[C/T]GAAGCACTGTTCGAG | 8853 |
rs190092467 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214149 | CGTTCCGTGATATGA[A/T]CCTACCTCCTTTGCT | 8853 |
rs190107924 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249588 | GAAGGAAATGCCAGG[C/T]TGACCCATCACATAG | 8853 |
rs190118739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247459 | CTTATTACCTCATGC[G/T]CTGCTTTCGGTCCAT | 8853 |
rs190159232 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396957 | CAGTGAGCCAAGATC[A/T]CACCACTGCACTCCA | 8853 |
rs190161864 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9329320 | AGCTCTTGAAGAAAT[C/T]GAAGCAGAGGACCAT | 8853 |
rs190173584 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404543 | GCGAGGGTAAGATTC[A/G]TAGTAGGAATATTGG | 8853 |
rs190174815 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307276 | CACGCTGGCCTTGCT[G/T]GTCAGGAGCCACACT | 8853 |
rs190183175 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343798 | TGGATGCCAGACACT[G/T]GACTTGGGCCCTGGG | 8853 |
rs190189112 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233488 | ACTTACAAAAGTTGT[A/G]TGGTGGCTTGGGACC | 8853 |
rs190189826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340311 | CAGGCATGAGCCACC[A/G]CGCCCGGCCAGCCAT | 8853 |
rs190203978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372973 | TTAACATTATAACAA[A/G]ATGCTGTTATTCGAG | 8853 |
rs190215727 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266792 | TAGTTTAGTAAGATT[G/T]CCCAAAACCACCTCC | 8853 |
rs190217003 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346537 | TCACTGTCTTTAATA[A/T]TAGGAATGTTAGATT | 8853 |
rs190228993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364444 | CCCAGGAGGTTGGCT[A/G]TAGTGAACTGAGATT | 8853 |
rs190230174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302928 | GGGGCATCCTGGCTT[A/G]GCTGCATTGGTACTA | 8853 |
rs190234112 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305770 | TTGGTGGAGGGGCTG[G/T]AGTAGTGAGGTATAG | 8853 |
rs190237864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379866 | GTATGGTGGCGCGCA[C/T]CTGTAGGCCCAGCTA | 8853 |
rs190248820 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361507 | GCTTGGAAATTTCAA[C/G]GCTTCTTTCTTTCTT | 8853 |
rs190308203 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399159 | TTGAGGCCAGACAGG[G/T]TTCATTCCGAGCAGC | 8853 |
rs190326164 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233826 | TTAAAGAAGAGGGGA[A/G]TGGGCTGGGCATGGT | 8853 |
rs190342758 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216840 | CTGGACTCAAGTGAT[C/T]CTCCTGCCTTGCCCT | 8853 |
rs190347086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229143 | AAACATCTGTACAGA[A/T]GTGGAGCCCCCCCCG | 8853 |
rs190405317 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290719 | TATCTTTATAACCAG[C/G]AGAGGCTCAGGTGAG | 8853 |
rs190411762 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395669 | CTGGAGTGCGGTGGC[A/G]CGATCTTGGCTCACT | 8853 |
rs190438991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296487 | CTTTCAGGTGCTACT[C/T]TGAGGCCTAATGATA | 8853 |
rs190450179 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251260 | TCTAGTCACTTGTCT[C/T]ACAGAGAAGGGGACT | 8853 |
rs190450420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216507 | ACTCTGTCACCCAGG[C/G]TGGACTGCAGTGGTG | 8853 |
rs190453333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313563 | TTTGGCGCTGCCCCC[A/G]CCAGCTGCCGGACAG | 8853 |
rs190456399 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221091 | AATCAGGAAGTGTGA[C/G]TCTTTCAACTTTGTT | 8853 |
rs190457289 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331699 | CTTGAACCCAAGAGG[C/T]GGAGGTTGCAGTGAG | 8853 |
rs190460283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312071 | CCCATTTCAAGTGTA[A/C]ACATCAGTGATTTCC | 8853 |
rs190471919 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253871 | AATAGTACATACAAC[A/G]AGATATTTTGAGAAA | 8853 |
rs190474697 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349009 | CCCTAGCTGTATAAC[C/G]TCAACCAGATTATTT | 8853 |
rs190480645 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286177 | TGAGGCAGATGGATC[A/G]CTTGAGCTCAGGAGT | 8853 |
rs190481098 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366727 | TAATGTTTTATGCTT[G/T]GGGCCGCCTAGAAAA | 8853 |
rs190481729 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289949 | AAAGTGGAACAAGCC[C/T]GGGGTGTTGGAGAAG | 8853 |
rs190489019 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383475 | ATGTTGCCTGGGCTG[G/T]TCTCAAACTCCTGGC | 8853 |
rs190501840 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317022 | AACCACACTCACACA[A/G]CATGCAATCATTCCC | 8853 |
rs190506231 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273796 | TCTGCAAAATATCTC[A/C]AGTGCTGATATTATG | 8853 |
rs190514314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309760 | TTACTGAGTCTAGCA[A/G]GTCTCTAGCCACATG | 8853 |
rs190524445 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352630 | GGAGGATCAGTAGAC[A/G]GCAAGTGTGCATGCC | 8853 |
rs190541080 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267068 | AAAGATGCTTTAATT[G/T]TACTTGTATTCTTAA | 8853 |
rs190548163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251768 | GCCTTCAGGAATGAC[A/G]CAAGGGGAAGGTGGC | 8853 |
rs190648874 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208001 | TCCTGGGGAGAGGAA[C/G]ACGTAGGAACGAAGA | 8853 |
rs190671171 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9204995 | CAATGCAACACAGCT[A/T]TGCAATTTTATTTTT | 8853 |
rs190673554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238766 | TACAAATGTACAGTT[G/T]TGTAATCCCCACCAT | 8853 |
rs190686559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222826 | TCCTTCCATTGTCTA[C/T]ACTCCTGGTCCCACC | 8853 |
rs190688469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255897 | AGATCGTCTGATTTA[C/T]TTGTATGCGTATTGG | 8853 |
rs190703479 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210930 | GGAGGCCAAGGCGGG[C/G]AGATCACTTGGGGTC | 8853 |
rs190706018 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255319 | GGCTGTTCAGGAGAA[A/G]TGGACTATTTAAGTA | 8853 |
rs190706592 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237514 | CCTCCTAGGCTCCAG[C/T]AATCTTCCCATCTTA | 8853 |
rs190709867 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291821 | GTGCACCCTGCCTTC[A/G]TTCTGTTATGCTGGT | 8853 |
rs190716624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271348 | TACGAGGAACTGGCA[C/T]AATATATGTTCTTGC | 8853 |
rs190727438 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328167 | CACAGAGACAGAAAG[C/G]AGGTGAGTGATTGCC | 8853 |
rs190738023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227130 | GGCGTCTCCAGCCCT[C/G]CTGTGCTTGAGAAGT | 8853 |
rs190745327 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243828 | AGGACTCACAGTTTA[G/T]TTGTGAGGGACCGAT | 8853 |
rs190754912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277463 | CCACTTGGGAAAATA[C/T]GAGTTAACTCCATAT | 8853 |
rs190761238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313429 | TACATTCATGTTCAT[A/G]TGTGTACTCCCGCTT | 8853 |
rs190767022 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295957 | GGAACAAATGTTCCC[G/T]CGTTTTCCCACATTG | 8853 |
rs190782363 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388046 | TTACAATTCGAGGTG[A/C]GATTTGGGTGGGGAC | 8853 |
rs190816245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314428 | TCTGAAGCCCCTGTA[G/T]ATTCTGTCTTTCACA | 8853 |
rs190822381 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373972 | TGTTGACGCACATAC[A/C/G]TCTCATGGTGCTACT | 8853 |
rs190833955 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349332 | GTTGTGTCATCACAG[A/G]GAGGTAACAGAATAG | 8853 |
rs190931369 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217830 | TGTGTTAGCCAGGAT[A/G]GTCTTGATCTCCTGA | 8853 |
rs190938505 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238428 | GAGCTACAGCCACAT[C/T]CGCTTGAAAAAGCAT | 8853 |
rs190948871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273165 | TTAACAATATTGATT[C/G]TTCCAGTCCACAAAT | 8853 |
rs190967788 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207564 | CCCGCCGCCGCCCGC[C/T]GCCGCCCGGGGTCTT | 8853 |
rs190979538 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309252 | AGGTGTCTGGCTAGA[C/T]GGCAGTGTAGCCATA | 8853 |
rs190991153 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344365 | ATTTATCAGTTCCTA[C/G]AGCAGAATCTGATGT | 8853 |
rs191001192 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9206254 | CTGTCTCCTAGGCCT[A/G]CGACGATGCAATGAC | 8853 |
rs191017417 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9238145 | GCTGACCCGCTACCT[A/G]CTGATCTTCACACGG | 8853 |
rs191020696 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404849 | ACCTTTCAAAGTTCC[A/G]GGTAAAAATGTGTTA | 8853 |
rs191022444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370870 | TGGTGAAGGAAACGT[C/T]GTGAATCCAGCATGG | 8853 |
rs191036530 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265084 | GAGGCTGCAGTGAGC[C/T]GTGATCACACCACTG | 8853 |
rs191047535 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297707 | AAATGCATTCGTCTT[C/G]TTAAGGGCCTCTGAC | 8853 |
rs191063925 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300189 | AGTGAGCTGACATCA[C/T]GCCCCTGTACTCCAC | 8853 |
rs191068305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332548 | GCTGGAAACAGCATC[C/T]TGACGAGAAGTCTCT | 8853 |
rs191079163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336775 | AAAATAGTGGGCTAG[C/T]GGTAACGAGGAGGAG | 8853 |
rs191086819 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9367182 | ACTACAGGTGCACGC[C/T]GCCATGCCTGGCTAA | 8853 |
rs191100519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394104 | CTTAGACCCAGGTCA[A/G]GCTTAGCTGTTTGTC | 8853 |
rs191100826 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380542 | CATCTTTTAAAGTTT[C/T]ACCTTCTGTATTTAG | 8853 |
rs191102985 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339331 | GGCATTTGAATCCTG[A/G]GTCTCCCACTTCCTA | 8853 |
rs191117245 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371906 | CGGATCACGAGGTCA[A/G]GAGATCGAGACCATC | 8853 |
rs191135025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341522 | TCGTGAGACCTGAAA[A/G]TCGCTCTGATTAATA | 8853 |
rs191157368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374379 | CTGCATGGAGGGCAG[A/G]GGCAGGGCCTTCCTG | 8853 |
rs191173655 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393922 | TTGCTGCTCACCCCC[C/T]AGGTGGTCTCTGTTT | 8853 |
rs191187623 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234524 | TCACTTCCTGCTGGG[G/T]CAGCTGGGACATTGT | 8853 |
rs191231925 | snp | A/C | 0.136506 | 0.222754 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221920 | TGCCTCAGCCTCCCG[A/C]GTAGCTGGGACTACA | 8853 |
rs191257813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397328 | CCTTGTTCTCAGAAG[C/T]GTTCTAGCTGGCGGG | 8853 |
rs191293759 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370748 | TCACATCTGTACCCT[A/G]CATTGATTCCATACA | 8853 |
rs191298615 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283254 | AACTAATTTTTGTAA[A/T]TTTAGTGGAGATGGG | 8853 |
rs191308941 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318207 | ATTCTAGGCTTTCGA[C/T]GTAATTCTGTCATTG | 8853 |
rs191314318 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271016 | GCCAGGATAGTCTCG[A/G]TCTCGTGACCTCGTG | 8853 |
rs191320796 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9304937 | AGGCTGGAGTAGTGA[A/G]GTATAGATATTGGCG | 8853 |
rs191324578 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289775 | TTTGTATTTTAATAG[C/G/T]GCACACCTTGGCCTG | 8853 |
rs191337382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231581 | CCCGGGTGCCGCCAC[A/G]CCCCTAGCCTGCGCC | 8853 |
rs191341038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324963 | GTTATTTTACTTTTT[C/T]TTATGTCTGTCTCGT | 8853 |
rs191347296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342773 | TCCAGCCCGTCTTGT[C/T]CACCCCTGGGCCTTA | 8853 |
rs191351416 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360255 | CAGGCCACTTTATAT[A/G]TACTAGGCTCATTTG | 8853 |
rs191364018 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375980 | TACCAGCACCCAAGT[A/G]GGGTGGCATGTGTCC | 8853 |
rs191365298 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209256 | TGCTATGATGATGGT[A/C]TGTGTGAGCTTGGTT | 8853 |
rs191377421 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9223959 | GTGCGCTGGGATGCA[C/T]GTAATCCACTGAGGA | 8853 |
rs191495561 | snp | A/G | 0.030278 | 0.119257 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286456 | AAAAAAAATATATAT[A/G]TATATACTGTATCTG | 8853 |
rs191500623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227578 | GAGAAACAGCATCAC[A/G]GAGGTTTAACGGCTC | 8853 |
rs191516343 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259915 | TGGGCTAAGTGGAGC[C/T]GAGTATGGAACCCAG | 8853 |
rs191523291 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353185 | GGAGCATCTGTCTTC[A/T]CCCCTCTCAGATTCC | 8853 |
rs191538769 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9215447 | TGAATATAAACAATA[C/T]GAGATATTTCTAATA | 8853 |
rs191542474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387165 | CTTGCAGTGAGCTGG[G/T]ATTGCGCCACTGCAT | 8853 |
rs191565901 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266010 | AACTCCTGACCTCAA[A/G]TGATCCACCCCCCCA | 8853 |
rs191571278 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232601 | GATCATAAGCTTCCT[A/G]GGGGCAGGGATTTTT | 8853 |
rs191573615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250835 | CACAGGCCACCATGG[A/G]CCATCTGTGAGCAAA | 8853 |
rs191576759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292548 | ACAAAAGAAAAACAG[A/C]GAAAGTATTAACAGT | 8853 |
rs191597317 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228088 | TAATTGAAATGGAAT[A/G]GGGGTGAATCTTTTA | 8853 |
rs191607252 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244923 | CTTAGCCTTTCTGCG[G/T]AGAATAATTGCTTAT | 8853 |
rs191608717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212346 | CAGGTGGTCCCAGGG[C/T]GTGGGGCTGTGGTGA | 8853 |
rs191637802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379232 | CCCTGCCTGTTCCAC[A/G]AGGCCGCATTCACCA | 8853 |
rs191750385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211403 | TCTTCTTTTTTTTTC[A/G]TTTCTTCGAGCCTCT | 8853 |
rs191751720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213547 | CATGAAAGGAAAGAG[G/T]GAGACCAGTTGTGGG | 8853 |
rs191754791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248975 | GCTGTCCTTTAACTT[A/G]CGTAAATTCCTCCCA | 8853 |
rs191757931 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244364 | TACCTTAGCAAGGTA[C/T]ACTGAGATTAGGAAT | 8853 |
rs191768589 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277822 | TTGTATTGCAGCCAC[G/T]CTGTCAAATGTCTGG | 8853 |
rs191782742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282596 | GTAACTACAGTCATG[G/T]GCTCTGAAGGCAGCT | 8853 |
rs191789470 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284592 | ATAGGTCATAGGATT[A/G]CTAGTGAAGATTAAG | 8853 |
rs191791952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310912 | GTGACATTAGCATAA[C/T]GATTTTGTTCTTTAT | 8853 |
rs191795889 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329550 | TTCAGGAAGCTTCTC[A/G]GCTGTAACAAGATTA | 8853 |
rs191852029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269572 | TTGATGCTGAGCCCA[C/T]GGGGGAACCATGGCC | 8853 |
rs191865369 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9400218 | CTCCCCTCCTGCCCC[C/T]TCCCCTCCTGCCCCC | 8853 |
rs191868530 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244027 | AATATCAGCTGGGCA[C/T]GTTGGCTCATAACGA | 8853 |
rs191868857 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331279 | TTATTTTGCTTTTTC[A/T]TCTCGCTTTAAGTGT | 8853 |
rs191875643 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304431 | AATGGCTCTAGTGGG[A/G]ATGTAGATAGGGGGT | 8853 |
rs191903451 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329221 | GAGTGGCGTGAAACG[A/G]AACTGCATGGAAAAG | 8853 |
rs191921447 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363498 | AGGTGTGAGATGATC[A/G]TGGTTTTAATTTGCA | 8853 |
rs191960092 | snp | A/G/T | 0.000265566 | 0.0115202 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350934 | CGCCATAGAGACGTT[A/G/T]TCTTATGCTCTCCTC | 8853 |
rs191970752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368776 | TAGAGAGCCTCACTC[A/G]CCACTGGTGGGTGGA | 8853 |
rs191983724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385818 | TTTGGGATATTGAAG[A/C]CTCAAGAGAAAAGTT | 8853 |
rs191998716 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219189 | CTTCAAGAAAATACT[A/G]ATTTTCTTATATCCA | 8853 |
rs192018444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396750 | CTCACACCTACAATC[C/T]CAGCACTTTGGGAGG | 8853 |
rs192031052 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9398573 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCAGATCA | 8853 |
rs192033022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222118 | CTGATTGCTGGATCA[G/T]TTCTTAATCATCTTT | 8853 |
rs192035738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235859 | CTTCCCATGAATGGC[A/G]AGGGCAGTGGGCTTA | 8853 |
rs192038055 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253313 | GGATTACAGGTGCCC[A/G]CCACCACACCTGGCT | 8853 |
rs192046818 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9288684 | CTAATAGCTTGTACT[C/G]CCCATACAACAAATG | 8853 |
rs192052059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270715 | CCATCCCCACTTCCA[C/T]CCCACCTACCCTTCC | 8853 |
rs192060162 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230984 | CCAGCTTCTTGCTTC[C/T]TGGCAGCACAAACCC | 8853 |
rs192068705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264660 | TCTCCTGTCACCGTC[C/T]TCTCTCCTCATCTAG | 8853 |
rs192119057 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9218423 | CAAGGACTAGGAGCC[A/G]CCCAGACCCATAGAG | 8853 |
rs192120831 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402298 | CAGAGCTGGGTTCAC[C/T]GGTCTTTCCTGTGGC | 8853 |
rs192137604 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252605 | CCCAAAAAAAGCCTT[C/T]GGAAGACAGTTAAAG | 8853 |
rs192142492 | snp | C/G/T | 0.00279258 | 0.0372817 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364805 | GAAATTGACTATCAG[C/G/T]GGTCATTTACGGAGG | 8853 |
rs192145579 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315440 | GAATTTGTTGAGAAG[A/C/T]GTGCCGCACGGCTGG | 8853 |
rs192157810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225129 | TTATGGTTTTTAGGG[A/G]TTGTAAACAAAATCC | 8853 |
rs192172589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391252 | GTAGATCTGGATGGC[A/G]GGGGGTGCTCTCTGG | 8853 |
rs192172956 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287496 | CTCCTGGTTTCGGAA[C/G]GGGCAGGAGAGGGCG | 8853 |
rs192178677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348902 | GCAAGCAACCGCCTT[A/C]CATGGATACCCACGT | 8853 |
rs192183447 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9323871 | GCATTTCTCTGAGAT[C/G]AGAGACCATGGATTA | 8853 |
rs192184170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258643 | CCTTCCCGGGTCCTG[A/G]GGCAGTGTGGCTTGA | 8853 |
rs192190910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242907 | GCTCCTGCTTTGATA[C/T]AACTGAGGCCCAGTA | 8853 |
rs192204929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276188 | TGCTCACACCATTTT[A/G]TCCAATGAAATGCTA | 8853 |
rs192207348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337741 | TTGTTTTAGTGTGGA[A/G]CTTGTGCCGTTCTGG | 8853 |
rs192208904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312238 | CAATCTCTATTATAA[C/T]AATTTATTTTCTGAT | 8853 |
rs192215847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293300 | GAATTGAGAAGAAAC[A/G]AAGTCTTGTCCTAGC | 8853 |
rs192215980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354130 | TTATCCGCGAACCCC[A/G]TAGGCACCCTGGGAG | 8853 |
rs192231166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371248 | AGCTACTTCCATTCC[G/T]TCTCAACTGAAATTA | 8853 |
rs192233877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330718 | TTTAGGAAGTGGGTC[A/G]CTTCCTTGCTGATAT | 8853 |
rs192239995 | snp | A/G/T | 0.0111272 | 0.0738324 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388827 | GCCAACTGGGCTCCC[A/G/T]GGGCTGGGCCAAAAG | 8853 |
rs192272981 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405799 | GCATGAGCGGTAATC[C/T]TTTAAGGTTCTCTTA | 8853 |
rs192274176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258531 | TCACCTAAGGCCCCA[A/G]TCCGAGTAGGTGACA | 8853 |
rs192279463 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292720 | TAGCACATTGCCTGA[C/T]GCATTGTAAGTGATC | 8853 |
rs192312377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330048 | TTTTATATCTACAGT[A/G]TGTGGCACATTTACC | 8853 |
rs192336895 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219900 | TGGCAGTCACTCATC[C/T]ACTTTCTGTCTCTAT | 8853 |
rs192337156 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253495 | ATGTGCAGTTTAGTG[G/T]GTTTTGTGAAATCGT | 8853 |
rs192340825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278268 | CTTTTTACCCAGCAT[A/G]TTGGGAGGTTGAGGC | 8853 |
rs192411107 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383112 | TCTCGGGGGGGCCAC[C/G]GGACTGTTTGAGTCA | 8853 |
rs192419032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262116 | AGCCTCCTCAGTAGC[C/T]GGGAATGATAGGCGC | 8853 |
rs192426929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247199 | AGTCTGTCTGCTCGT[C/G]AGTTTTGACGGCACA | 8853 |
rs192431240 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278754 | CAACCCTGCAAAGTG[C/G]GTATTGTTCCTGCTG | 8853 |
rs192526015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395470 | ACAAGAATGAAACTC[C/T]ATCTCAAAAATAAAA | 8853 |
rs192557173 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9209074 | GTGCAGGAGATTACC[C/G]TAGAGCTCAGTTACT | 8853 |
rs192592062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239675 | CCATCTAAGGGGCAC[A/G]AAACCATTGTTTTTT | 8853 |
rs192596748 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274426 | CCCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 8853 |
rs192603261 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297961 | CAGCCGTGGGAATGC[A/G]GTGCTGGTGCCTGCT | 8853 |
rs192609330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315074 | CAGGGATAGGGAAGA[C/T]GTTTCCGTCGAATAG | 8853 |
rs192612916 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9333135 | GCTGAGTTTAAAAGA[A/C]GTAAACATCACCTCA | 8853 |
rs192631951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386047 | CCGCGACCCACTTCC[A/G]TCTGTCCTTCAGCAT | 8853 |
rs192654089 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214471 | TCTTGAACTCCTGAC[C/T]TCAGGTGATCCGCCC | 8853 |
rs192655482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360620 | TACTCCCACAATGGC[C/T]AATTTCAAGCTACCT | 8853 |
rs192663141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377108 | AACCTTCCCAGTTCT[A/G]AACATGAATTAAAGA | 8853 |
rs192670992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241399 | TAAACTGGTGCGATT[A/G]TGAGTTCCTTATCCA | 8853 |
rs192698800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275345 | AAAGCACTGGTATTA[C/T]AGTAGGTGTGAGCTA | 8853 |
rs192707597 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311633 | TGGAGCTGCCTGAGC[A/G]CAAGGGATATGTAAT | 8853 |
rs192711852 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346703 | ACTAAGTTCTAGTTC[A/G]TGCTTTTACAGCTCT | 8853 |
rs192715641 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261694 | CTTTAACAGTGTGGC[C/G]GAGTGTAGGAGGGAG | 8853 |
rs192722704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237311 | GGACATTTCTCATTT[A/G]CATTGTGACTTTTAG | 8853 |
rs192727720 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405958 | CTGCCGGACAGAGGT[C/T]CATGCCAGTGATACC | 8853 |
rs192765954 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302212 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGCGC | 8853 |
rs192769473 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394903 | TTGGCTGGGGGTTAC[A/C/G]GTCAGAGTCTCTTCA | 8853 |
rs192772946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338457 | GTCCACCACAGCCAT[A/G]ATTTTCTTCTGCCTC | 8853 |
rs192779945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371426 | GGTGAACCAGTGACT[A/C]TTTAATGAATCAGCG | 8853 |
rs192846323 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257717 | GTAGAGATGGGGTTT[C/G]ACCACGTTGGCTAGG | 8853 |
rs192848717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9223124 | TGACATTTAAAGTTG[A/G]CCTCCTTTCCTACCA | 8853 |
rs192855609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402436 | GGAGTTCGAGACCAG[C/T]CTGGCCAACATGGTT | 8853 |
rs192871752 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229324 | CTTTGCTCAGTGGTG[C/T]CCGCCACAGTGAGCC | 8853 |
rs192888170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263299 | TGTGGGTGTCAGGGA[A/G]CCCCAGGCCAGGCCC | 8853 |
rs192891904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298409 | GCACTCGGGCCCTTG[C/T]TCTTTCTCCCCGTCT | 8853 |
rs192892308 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324078 | AGGTTTCAAATGTAC[A/C]CAATGTGTGGGTGAT | 8853 |
rs192896775 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394289 | CCTGCCTGAGCCTCC[C/T]GAGTAGCTGGGACTA | 8853 |
rs192900905 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358612 | TAAATTGGTGGTAAT[C/T]ATGGACAAAGTTTCC | 8853 |
rs192904231 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250511 | TTAAGCCTTGGGAGG[G/T]GTAAAAGTGTTTTCC | 8853 |
rs192919500 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284179 | TCACAAGTTCCAGGG[A/G]TTAGGAGGTGGGCAT | 8853 |
rs192926988 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319640 | TTACCTGAGGCCATT[A/G]AAAAGCCAAAAAGTA | 8853 |
rs192943198 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347421 | GCTCCTGAGTGTGCT[C/T]GTTTACAGTCAGGAA | 8853 |
rs192950164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381301 | CCTGGCCTTGCCGGG[A/G]GCTCCCCAGCTTGGC | 8853 |
rs192971413 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321052 | GGCTTCAATTATTTT[A/C]AATACTGGAAAGATA | 8853 |
rs192983352 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354510 | GGTGCGGTGGCCCAC[A/G]CCTGTCATCTCAGTA | 8853 |
rs192991282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214704 | TCACTCATAAATGTA[C/T]ATTGGGCCCCTACCG | 8853 |
rs192991637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | ASAP2 | GRCh38.p7 | 2:9389803 | CTGGCTTGATGAGGA[C/T]GTCCCTGAGCACAGA | 8853 |
rs193013912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375526 | ATATCCATTACCTCA[C/G]AGGCTCATCCATTTT | 8853 |
rs193038796 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212610 | CTCAATTCTTCCCAT[A/G]CACCCCACGTTTCCA | 8853 |
rs193072485 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212898 | TTGCGAAGCACTGTT[C/G]GAGACGGAACCCCGG | 8853 |
rs193086849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247468 | TCATGCGCTGCTTTC[A/G]GTCCATCGTCTAGCT | 8853 |
rs193098732 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279504 | GACTCCTTTATCGGG[G/T]CATGCAGATCACAGA | 8853 |
rs193110146 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401674 | TCCTTCATTTTGAGG[A/T]CTTGAGTTTCTAGGT | 8853 |
rs193118228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304834 | GGGCTGGACGAGTGG[C/G]GTGTAGATATTGGTG | 8853 |
rs193125031 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271352 | AGGAACTGGCATAAT[A/G/T]TATGTTCTTGCACCT | 8853 |
rs193132721 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341655 | GTGCAGTTGAGTCTC[C/T]TGACAGGTTTATTTT | 8853 |
rs193134181 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306658 | GGGTTGATGAGCCCA[C/G]CCAGGAGTCAAGCCT | 8853 |
rs193135926 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367688 | GTCACCTGAGCCTGG[G/T]GAGGGCAAGGTTGCA | 8853 |
rs193138063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343313 | CCTCGGCCCTTTCCT[A/G]GTTGACCTGTGAACA | 8853 |
rs193157909 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232316 | GTCGCCCTGCTCTTC[A/G]TATCTCCCTGCCTGT | 8853 |
rs193159851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265641 | GTATCTTTATATACA[A/G]AGTTTTAAGTGTTTG | 8853 |
rs193175682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365433 | AGAGAAGAATGTCAC[A/G]GCAATTGTTGTCCTT | 8853 |
rs193228040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397661 | CTGCCTGTTTTTTAG[C/G]GCCATGAGCTAAGAA | 8853 |
rs193281880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290127 | AGGTATACTCAGTTC[C/T]GAAGGCTGTGTCCCT | 8853 |
rs193284820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349739 | AACCCAAATCCTTCA[C/T]GCTGCAAGGATGGGT | 8853 |
rs193285940 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326441 | CAGTATGTCAAATAG[A/G]TAGTACAGACCTTCT | 8853 |
rs193289828 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385007 | TGAGAGTTACGAGCC[A/G]GGAACTGTGGATGAA | 8853 |
rs199504138 | snp | A/G | 0.000148269 | 0.00860886 | missense, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9297350 | CTGGAGAAGTTTGGC[A/G]GCAACTGTGTATGCA | 8853 |
rs199505309 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369985 | TAGCTGGGACAGGCA[C/T]ATGCCACCACACCCA | 8853 |
rs199536600 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9259019 | CTTCGGCCTTTCTCT[C/G]TGGTGTCTGCAGGCC | 8853 |
rs199571916 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395609 | CTTTTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 8853 |
rs199579358 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9304889 | AGATATTGGTGGACA[A/G]GCTGGAGTAGTGGGG | 8853 |
rs199603726 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362268 | TTCATTAGGCCCCTT[A/C]GTGCCTTGTGAAAGG | 8853 |
rs199603891 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264201 | GTCTCAAAAAAATAA[-/T]AATAATAATAATAAT | 8853 |
rs199614997 | in-del | -/GA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232266 | CACTGCCCTGCGCCC[-/GA]TCCTTTTACACAGGT | 8853 |
rs199625106 | snp | A/G | 3.45913e-05 | 0.00415866 | missense | ASAP2 | GRCh38.p7 | 2:9379009 | GCTGCCTGACCGACA[A/G]TGCCGAGTGCCTCAA | 8853 |
rs199645553 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305437 | TGGAGAGGCTGTAGT[A/G]GTGGGGTATAGATAT | 8853 |
rs199689150 | snp | A/G | 3.57194e-05 | 0.00422592 | missense | ASAP2 | GRCh38.p7 | 2:9378970 | ATAAACAGACAGGGA[A/G]AGGCAGCACAGCCCT | 8853 |
rs199700755 | in-del | -/TGCAGTGGCAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9391933 | TCCCCCAGGCTGGAG[-/TGCAGTGGCAC]AATCATGGCTCACTG | 8853 |
rs199707219 | in-del | -/TTG | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205446 | TTTTTAAATTGTAAC[-/TTG]TTGTCTAGTGCAATG | 8853 |
rs199730021 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305382 | CAGTGAGGTATAGAT[-/A]ATTGGTGGAGGGGCT | 8853 |
rs199764191 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208398 | GAAGCAATGGCGTTA[-/T]TTTTTTTTTCTGGTT | 8853 |
rs199769382 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9306863 | GTGGGCAGGGTTTGT[A/G]CCATTGGTGCCCCAG | 8853 |
rs199776366 | in-del | -/GTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258332 | TGATAGTAATCAGTA[-/GTT]GTTTTTTTTTTTTTT | 8853 |
rs199777278 | snp | A/G | 0.00027204 | 0.0116596 | missense | ASAP2 | GRCh38.p7 | 2:9393586 | GGGATCTCACAGATC[A/G]GGCCCCCACCTCTGC | 8853 |
rs199779613 | in-del | -/CC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9316963 | ACACCCTCCCACACA[-/CC]CCCCCCGTCACACCC | 8853 |
rs199782056 | snp | C/T | 0.00204206 | 0.0318882 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376895 | TCTGGAATGCCTTTG[C/T]TTGGTTTTTCAGGAG | 8853 |
rs199818282 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254236 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 8853 |
rs199820452 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9252932 | AAAAAAAAAAAAAAA[C/T]AATTTAGGAACACAA | 8853 |
rs199852919 | snp | C/G | 0.000208601 | 0.0102106 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400873 | CTCTGCTCTAGCCAG[C/G]GGGGTGCAGGTGGTT | 8853 |
rs199888184 | in-del | -/CC | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392781 | GCGCCTTATGTGTTA[-/CC]CATCCTGAGGCCCAG | 8853 |
rs199918521 | in-del | -/AT/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286445 | AAAAAGGAAAAAAAA[-/AT/T]AAATATATATATATA | 8853 |
rs199921712 | in-del | -/GTTTTT | 0.0475351 | 0.146656 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380181 | GTGGCTGCTTCAACA[-/GTTTTT]GTTTTTGTTTTTGTT | 8853 |
rs199934195 | in-del | -/GT | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208336 | CCTGGGCTAGCAGGA[-/GT]GTGTGTGTGTGGGTG | 8853 |
rs199971591 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305740 | TGGAGAGGCTGTAGT[A/G]GTGGGGTATAGATAT | 8853 |
rs199972994 | snp | A/C/T | 0.000296523 | 0.0121728 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9334762 | GGATGGACTCAAAGC[A/C/T]GTGGAAAGCCTCAAA | 8853 |
rs199989550 | in-del | -/ATATA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397746 | TATATATATATATAT[-/ATATA]TTTTTTTTTTTTTTT | 8853 |
rs200039381 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9354662 | AAAAAAAAAAAAAAA[C/T]AAAAAGAAAAAGATG | 8853 |
rs200099142 | in-del | -/TTTACACATATATA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279867 | TACACATACATATTT[-/TTTACACATATATA]TTTACACATATATAT | 8853 |
rs200100248 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9334200 | TGTATTTTTGTATTT[-/G]GTTTTTTTTTTTTTT | 8853 |
rs200121461 | snp | C/T | 0.00563663 | 0.0527877 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380712 | TGGGTTTTGCCTTAA[C/T]GCCTCCTTTGCTCGC | 8853 |
rs200140240 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369030 | GCTTTTTTTTTTTTT[-/C]TCTGGGAGACGGAGT | 8853 |
rs200147493 | in-del | -/TGG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305854 | GTGGGGTATAGATAT[-/TGG]TGGTGTAGAGGCTGT | 8853 |
rs200163597 | in-del | -/T | 0.0232847 | 0.105357 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273194 | TATGGAATATCTTCA[-/T]TTTTTTTTGGTGTCC | 8853 |
rs200193103 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250592 | GGCAAATGCAGTGTG[G/T]TGTGCTCTTTCATTT | 8853 |
rs200225020 | snp | A/G | 0.000221641 | 0.0105248 | missense | ASAP2 | GRCh38.p7 | 2:9374768 | AGGAATGCAAGAAAG[A/G]ACTACATCACAGCCA | 8853 |
rs200241081 | in-del | -/TATTGG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305988 | GTAGTGGGGTATAGA[-/TATTGG]TGTAGAGGCTGTAGT | 8853 |
rs200319277 | snp | C/T | 3.31713e-05 | 0.00407242 | missense | ASAP2 | GRCh38.p7 | 2:9400757 | TGGATCTCTCTGCAA[C/T]GGAAGCTCTGGGTCC | 8853 |
rs200322386 | snp | C/T | 0.00171909 | 0.0292675 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401440 | CTGGGGGCTGAGCCA[C/T]GTCCCTGCCCACCTG | 8853 |
rs200342085 | in-del | -/AC/ACTC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317443 | CACATACTCACATTC[-/AC/ACTC]TCACACACACATGTG | 8853 |
rs200363543 | snp | C/G | 1.65108e-05 | 0.00287317 | missense | ASAP2 | GRCh38.p7 | 2:9350885 | GAAGAAGTGCTTTGA[C/G]CTCATTTCACGTAAG | 8853 |
rs200401085 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9344441 | TGTTGTTAAAAAAAA[A/C]ACACATTAGGCATAA | 8853 |
rs200408709 | in-del | -/TAG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9304693 | GAGGGGGTGTAATAG[-/TAG]TGGGGTATAGATATT | 8853 |
rs200448898 | in-del | -/AT/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239444 | GGGTAGAATGAAATC[-/AT/CA]ATGTGTGTGGTGATG | 8853 |
rs200451277 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9316162 | GTCTACAAAAACTAC[-/A]AAAAAAAAAATTAGC | 8853 |
rs200458713 | snp | A/G | 5.00571e-05 | 0.00500261 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9388521 | CACCAGCGCCCCCCC[A/G]CTTCCTCCACGGAAT | 8853 |
rs200471523 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9394215 | TGTCACCCAGGCTGG[A/G]GTGCAGTGGCGTGAT | 8853 |
rs200474324 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260426 | GATTGTAGAAAAATG[C/T]AAGGTTCATGCCTAG | 8853 |
rs200478985 | in-del | -/T | 0.021333 | 0.101051 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269770 | AAATTTGAATGAATC[-/T]TTATAGAAACATTCC | 8853 |
rs200485589 | snp | A/G | 0.00199798 | 0.0315436 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358752 | GCCCTGTTCTCTTTG[A/G]CAGATCCTACATGGC | 8853 |
rs200529548 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343446 | GCTACTGTTTGTTTT[G/T]TTTGGTTTTTGTTTT | 8853 |
rs200555388 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366935 | CAGACCTCTTGGGCT[C/G]TCCTTCAGTCAGTTC | 8853 |
rs200556334 | in-del | -/AT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264203 | CTCAAAAAAATAATA[-/AT]AATAATAATAATAAT | 8853 |
rs200560260 | in-del | -/AT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397728 | AAAAAAATCAAAAGG[-/AT]ATATATATATATATA | 8853 |
rs200563982 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327133 | GGGTACCCCTACCCC[-/A]CCCCCGCCCATCCTT | 8853 |
rs200566092 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387078 | GGGCTTGGTGGTGGG[-/T]GGGGGGGCGCCTGTA | 8853 |
rs200585825 | snp | C/T | 0.00075792 | 0.0194521 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378937 | CTCTGTTCCTGTTCT[C/T]GGGCAGTGGGAACCT | 8853 |
rs200610258 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317434 | CACACACCTACACAT[A/T]CTCACATTCTCACAC | 8853 |
rs200615640 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313065 | TGTGTCTTAAAAAAT[-/A]AAAAAAAAAAGCTGC | 8853 |
rs200635465 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9309495 | GGGGGTAAGGAGCTG[G/T]GGTTGCAAAAGGGGC | 8853 |
rs200655024 | in-del | -/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211393 | TCCTTTTTTTTCTTC[-/T]TTTTTTTTCGTTTCT | 8853 |
rs200656327 | in-del | -/CC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232269 | TGCCCTGCGCCCGAT[-/CC]TTTTACACAGGTGGT | 8853 |
rs200662484 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378675 | ACCTTGGCCCCACAT[A/G]CTCAGCAACAACAGG | 8853 |
rs200663168 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305753 | TAGTGGGGTATAGAT[-/A]ATTGGTGGAGGGGCT | 8853 |
rs200696845 | snp | C/G | 0.00291057 | 0.038037 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323275 | TGGTGAAGGCAGGTC[C/G]TACAGCCCAGGCTGT | 8853 |
rs200706880 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234112 | CGAAGCTATGTCTCA[A/G]AAAAAAAAAAAAAAA | 8853 |
rs200713419 | snp | A/C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247196 | AGCAGTCTGTCTGCT[A/C/T]GTGAGTTTTGACGGC | 8853 |
rs200731060 | snp | G/T | 0.000313095 | 0.012508 | missense | ASAP2 | GRCh38.p7 | 2:9388425 | GCAGAGGGCTTTCAT[G/T]CCCAGCATCTTGCAG | 8853 |
rs200734625 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9279388 | CAACAGCTCTGGGCT[A/G]GGTGAGTATACATCC | 8853 |
rs200768133 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301074 | CTTTTTTGGAATTTT[A/C]TGCACCATTCTTCTT | 8853 |
rs200773230 | in-del | -/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9316971 | CCACACACCCCCCGT[-/CA]CACACCCTCTCATGT | 8853 |
rs200790306 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9396667 | AACCAGAAGACTCCC[A/C]AAACTTTTTAAATGC | 8853 |
rs200795222 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305451 | TAGTGGGGTATAGAT[A/G]TTGGTGTAGAGGCTG | 8853 |
rs200824083 | in-del | -/TGTT | 0.498306 | 0.0290512 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348117 | TGACACTTTTTTGTC[-/TGTT]TGTTTGTTTGTTTGT | 8853 |
rs200824833 | snp | C/G | 0.493658 | 0.0559517 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305232 | TTGGTTGACAGGCTG[C/G]AGTAGTGGGGTATAC | 8853 |
rs200848294 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317340 | TCATATCTTCACTCA[A/C]ACACACCCTCACACA | 8853 |
rs200872410 | snp | A/G | 0.00295844 | 0.0383467 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9393612 | TCTGCCCCCACAGCC[A/G]CCCAGCCGCCTCCCG | 8853 |
rs200913453 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343409 | GGCACTGGTGGCCTC[C/T]TACTCTCAACTCAGA | 8853 |
rs200918891 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286449 | AAGGAAAAAAAAAAA[-/T]ATATATATATATACT | 8853 |
rs200930760 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380201 | TTGTTTTTGTTTTTG[-/T]TTTTTGTTTTTTTTG | 8853 |
rs200932221 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240412 | GCATGCACCACCATG[C/G]CAAGCTAATTTTTTG | 8853 |
rs200935497 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395489 | TCAAAAATAAAAAAA[-/T]AAAGAATTTGGAGAC | 8853 |
rs200968786 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256182 | AAAAAAAAAAAAAAA[A/G]AAAGCAAGTAATTCT | 8853 |
rs200991549 | snp | A/C | 0.00191439 | 0.0308793 | utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207059 | CTGCGGCAGTTGAGG[A/C]GGCGGCGCCCCTGCG | 8853 |
rs200991684 | in-del | -/CC/CCCCCA | 0.499992 | 0.00199679 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260040 | GGCAGGCTGGCCTCT[-/CC/CCCCCA]CCCCGAGTCAGGCAC | 8853 |
rs201037488 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320002 | CCAGGGCAGGGAGTA[A/G]GGCACAGGTGACACA | 8853 |
rs201038328 | snp | C/T | 9.98885e-05 | 0.00706642 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9388503 | GCCTGCAGCCCCCAG[C/T]ACCACCAGCGCCCCC | 8853 |
rs201066855 | in-del | -/A | 0.00953873 | 0.0683987 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251951 | TAATTTTTTTTTTTT[-/A]ATTATCATCTGTAGC | 8853 |
rs201073070 | in-del | -/ATA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397748 | TATATATATATATAT[-/ATA]TTTTTTTTTTTTTTT | 8853 |
rs201120621 | snp | C/T | 0.00359579 | 0.0422489 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344514 | AAGATTAAAAACACA[C/T]TCTTCACCATTTTTT | 8853 |
rs201130402 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333580 | AGAAACAGAATGCAG[A/G]GGGCCAGGGGCAGGA | 8853 |
rs201136535 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9360155 | CTATGGCAGTTGTTT[C/T]TTTTACTGATTTTCT | 8853 |
rs201158432 | snp | A/T | 0.0041127 | 0.0451601 | missense | ASAP2 | GRCh38.p7 | 2:9374849 | AAGCTTCACAGTCTT[A/T]GCGAGGCCGTCAAAA | 8853 |
rs201192378 | snp | C/T | 3.32762e-05 | 0.00407885 | missense | ASAP2 | GRCh38.p7 | 2:9385354 | ACATGGATGAGAAAT[C/T]GCAGGTCTGTGCCAG | 8853 |
rs201220993 | in-del | -/GA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305927 | GTATAGATATTGGTG[-/GA]GAGGGGCTGTAATAG | 8853 |
rs201225397 | snp | C/T | 0.00299554 | 0.0385849 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9388512 | CCCCAGCACCACCAG[C/T]GCCCCCCCGCTTCCT | 8853 |
rs201232207 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362353 | TTTTGGGTAAATAGA[A/C]CAGCCTCTGTTTCAG | 8853 |
rs201234579 | in-del | -/AATCTT | 0.0275645 | 0.114116 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274631 | TCCAGCCTAACACTC[-/AATCTT]AAACAATCATTCTAG | 8853 |
rs201252471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323767 | AGGCCCAGGTGGCCT[A/G]GGGAGCGCCTCTCTG | 8853 |
rs201264761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214483 | GACCTCAGGTGATCC[A/G]CCCACCTCGGCCTCA | 8853 |
rs201291876 | snp | A/G/T | 0.00014828 | 0.00860927 | missense | ASAP2 | GRCh38.p7 | 2:9388366 | CAGCTTCAGTCTAAC[A/G/T]CTGTATCTTTGGCCA | 8853 |
rs201296883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279285 | GGTCTCAGCACAGAC[A/G]CGGTTTAATGACTGT | 8853 |
rs201343119 | in-del | -/CAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317178 | CACTCTCACCACACT[-/CAA]CACACACCCCACGCA | 8853 |
rs201353291 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237178 | TAAAAAAAGAGAGTT[-/A]AAAAAAAAAGCCCTG | 8853 |
rs201380277 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9270421 | TCTAAGATTTCAGTA[-/T]TTTTTTTTTAAATTT | 8853 |
rs201414841 | in-del | -/CC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317890 | ATTCACTCACATACA[-/CC]CTCATGTGCATTCAC | 8853 |
rs201431993 | in-del | -/TTGT | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406034 | GCCTTCAGTGTGTGT[-/TTGT]CACTGAGTGGACCTC | 8853 |
rs201446686 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257059 | GCTCCAGGGTGTCTT[A/G]CCCTAACAGCCTGTC | 8853 |
rs201448983 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9309806 | AAATGTGGCTAGGGC[A/G]ACTGAGGAACTCAAT | 8853 |
rs201465009 | snp | A/G | 0.000107452 | 0.00732901 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378894 | GGGCAGTCCCTGGTC[A/G]TCCAGCCTGTGACAC | 8853 |
rs201498447 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380004 | TCAAAAAAAAAAAAA[-/T]AAATAAAGTATATAC | 8853 |
rs201505810 | snp | A/G/T | 0.000379879 | 0.0137769 | missense | ASAP2 | GRCh38.p7 | 2:9374804 | ATCGAGAGGAGATAC[A/G/T]CAAGGAAGAAGCACG | 8853 |
rs201559652 | in-del | -/CGAT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232265 | TCACTGCCCTGCGCC[-/CGAT]CCTTTTACACAGGTG | 8853 |
rs201573612 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317135 | ACAACCACACAACAC[A/T]CATCCCAATCACACC | 8853 |
rs201587172 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279880 | TTTTTACACATATAT[A/T]TTTACACATATATAT | 8853 |
rs201593883 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398183 | TTTCACACCACAGTG[C/T]CAGAGTTGAATACTT | 8853 |
rs201594475 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267923 | AAAAAAAAAAAAAAA[C/T]AATGATTATAAAGCC | 8853 |
rs201594484 | snp | A/G | 0.000665008 | 0.0182226 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379079 | GTGGGCCCGGGCCCC[A/G]GGGGTGGGCTCAGCT | 8853 |
rs201609622 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295713 | AATCTGGTCTCAGAA[A/T]TTCATTTAATTTATC | 8853 |
rs201623848 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9334197 | TTTTGTATTTTTGTA[-/T]TTTGTTTTTTTTTTT | 8853 |
rs201642234 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317341 | CATATCTTCACTCAC[A/T]CACACCCTCACACAA | 8853 |
rs201651583 | in-del | -/AGT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305405 | AGGGGCTGTAATAGT[-/AGT]GGGGTATAGATATTG | 8853 |
rs201661941 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250595 | AAATGCAGTGTGGTG[-/T]GCTCTTTCATTTAAG | 8853 |
rs201672265 | in-del | -/GCA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9235494 | TGTGTAAATCATCCT[-/GCA]GCAGCAGTTCTGTCT | 8853 |
rs201681173 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313150 | CCAGAGGTCACACTC[-/A]ACTGCTGAAATGAAC | 8853 |
rs201718470 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380307 | GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCT | 8853 |
rs201728061 | snp | A/G | 0.000494805 | 0.0157212 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318641 | GGCAGCTTTTACACC[A/G]TGTAGAGTCACAGTA | 8853 |
rs201729599 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305920 | TAGTGGGGTATAGAT[-/A]ATTGGTGGAGGGGCT | 8853 |
rs201750537 | snp | C/G | 1.68858e-05 | 0.00290561 | missense | ASAP2 | GRCh38.p7 | 2:9401385 | GACGGGGAGGAGGAC[C/G]AGGAGTGGTGGGTGA | 8853 |
rs201763614 | in-del | -/CA | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402235 | CATGTCTTCAGCCTC[-/CA]GAGGCGCTGTGAGCT | 8853 |
rs201765350 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9304595 | GGCTGTAGTCTTGGG[-/A]GTATAGATATTGGTG | 8853 |
rs201787601 | snp | A/G | 0.000182299 | 0.00954548 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400013 | ATCTACTTTTTCCCT[A/G]TCTTTGTAGGGCTGA | 8853 |
rs201835459 | in-del | -/ATATATA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397744 | TATATATATATATAT[-/ATATATA]TTTTTTTTTTTTTTT | 8853 |
rs201848669 | in-del | -/G | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269252 | GAGGAATTATTTTGC[-/G]GGGGGGGAGGGGGCG | 8853 |
rs201853311 | snp | C/T | 7.91484e-05 | 0.0062903 | missense | ASAP2 | GRCh38.p7 | 2:9393589 | ATCTCACAGATCAGG[C/T]CCCCACCTCTGCCCC | 8853 |
rs201862499 | snp | C/T | 1.6492e-05 | 0.00287154 | missense | ASAP2 | GRCh38.p7 | 2:9380782 | GACATTGCCAAGCGC[C/T]TCAAGCACGAGCACT | 8853 |
rs201880816 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279905 | ATATATTTTTTAAAC[A/C]CATGCAACTTTTGGC | 8853 |
rs201884874 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208265 | TAAATGTCTCTGGGC[A/C]AGGATGTCAGGTTAC | 8853 |
rs201907360 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395574 | GTTTTGTTTTGTTTT[-/G]TTTTTCTTGTGTTTT | 8853 |
rs201915080 | snp | G/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210427 | ACCAGATTATATAGT[G/T]AGTGAGTCCACAGGC | 8853 |
rs201955790 | in-del | -/C | 0.0189856 | 0.0955633 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245932 | TGCAAGAGGAGTGAG[-/C]CCCACATTTGATTAT | 8853 |
rs201960685 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230711 | GCAGATATGTGCAAG[A/G]CAAGGACGTTGTTTC | 8853 |
rs201963992 | snp | C/T | 3.29788e-05 | 0.00406058 | missense | ASAP2 | GRCh38.p7 | 2:9358867 | CCCTGACCTTAGATG[C/T]ACTGGGAACATCTGA | 8853 |
rs202021086 | snp | A/G | 0.000131794 | 0.00811661 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391119 | CTGTAAGTGTGGACG[A/G]TGGAAGCCGGCAGCG | 8853 |
rs202031367 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290876 | TAGAAAGCACTTGGC[C/G]TGGGACCTAGTATAT | 8853 |
rs202062554 | in-del | -/AATA | 0.0252325 | 0.109451 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339521 | TTTATTAATAATCTT[-/AATA]AATATTAATAAACTA | 8853 |
rs202130478 | in-del | -/TTTG/TTTGG/TTTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275085 | TTCATTTGTCTGTTT[-/TTTG/TTTGG/TTTT]TTTTTTTTTTTTTAA | 8853 |
rs202145090 | snp | C/G/T | 8.81764e-05 | 0.00663931 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374742 | TTTGCAAGGCAATTA[C/G/T]GTTTGGTTTCAGGAA | 8853 |
rs202213691 | in-del | -/TA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305996 | GTATAGATATTGGTG[-/TA]GAGGCTGTAGTAGTG | 8853 |
rs202225896 | in-del | -/CT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317240 | AATCACACAACCACA[-/CT]CATACACACCCCGTG | 8853 |
rs202226524 | snp | C/T | 1.67801e-05 | 0.00289651 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335043 | AACGTTTCACTGTAC[C/T]TCAGTCTTAATTTTC | 8853 |
rs202239754 | in-del | -/TTCC | 0.0356815 | 0.128715 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361546 | TTTTTCTTTCTTTCT[-/TTCC]TTCCTTCCTTTCTTT | 8853 |
rs207461514 | snp | A/C/G | 1.6513e-05 | 0.00287336 | ASAP2 | 2 | allele_origin=G(germline)/C(somatic) | 2:9323225 | TGGAAAAGGAGAGGC[A/C/G]CTTCTTCCAGCTACA | 8853 |
rs367556455 | in-del | -/ACA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317180 | CTCTCACCACACTCA[-/ACA]CACACCCCACGCAAT | 8853 |
rs367622738 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286449 | AAGGAAAAAAAAAAA[A/T]ATATATATATATACT | 8853 |
rs367632563 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9303964 | CTATCCATGCGCTGG[G/T]GCTGTATGGGGCGGT | 8853 |
rs367643851 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317971 | TCAGTCGTACACACT[C/T]ATTGACACACACTCT | 8853 |
rs367645105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218995 | GTTTGAGATTGGGCC[G/T]AATGAGGCCGTGTTG | 8853 |
rs367672474 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381466 | AGGCCAGGCACAGTG[A/G]CTCACGCCTTGTAAT | 8853 |
rs367679590 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, synonymous-codon | ASAP2 | GRCh38.p7 | 2:9389780 | CACATCCCAGACCGC[A/G]TCCATCCCTGGCTTG | 8853 |
rs367684286 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381773 | CTGGGTGTGGTGGCA[C/T]GCACCTGCAGTCCCA | 8853 |
rs367685758 | snp | A/G | 1.66123e-05 | 0.00288199 | missense | ASAP2 | GRCh38.p7 | 2:9374943 | CACTGGCCAACGGAC[A/G]TGTAAGAGTGTGGGT | 8853 |
rs367693141 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364950 | GCAGGATTTACATTC[C/G]AACTATCAGACTCCA | 8853 |
rs367714536 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355504 | CCTGGCAAAACACTT[A/G]TAAAACTGTGCTGAC | 8853 |
rs367723073 | snp | C/G/T | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377631 | TTTTGACTCCCTGAT[C/G/T]GTGGTTTGAGCCATG | 8853 |
rs367733277 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359828 | TCTAGGAATTCCTTT[A/T]TGGTCTTGAAAGACA | 8853 |
rs367784853 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395564 | TTGTTTTTTTGTTTT[G/T]TTTTGTTTTGTTTTT | 8853 |
rs367789969 | snp | A/T | 1.6476e-05 | 0.00287014 | missense | ASAP2 | GRCh38.p7 | 2:9358794 | CTGGGCATCCTGACC[A/T]GCATCGAGTGTTCCG | 8853 |
rs367798419 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364603 | TCTTCTATTTCTGTT[C/T]TCATACGGTTGTTAA | 8853 |
rs367807541 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9241671 | AACTAATTGCTTTAA[A/G]TAAATGTTCATGCCT | 8853 |
rs367813068 | snp | A/G | 0.000969529 | 0.021996 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368373 | TGGGTAATGTGTAGC[A/G]GTAGAATGTATTAAT | 8853 |
rs367832482 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271665 | GGTGGAAATGGTCTG[C/T]GGAAGACGGCGGGCA | 8853 |
rs367835217 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240948 | TAGCATGGACCTTGT[G/T]GTTCTGCCAGACAAA | 8853 |
rs367862531 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212562 | GTCACCTGGTCTCTA[A/G]AGGGCTGCTCAGACC | 8853 |
rs367866019 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278907 | CTCTATAGGGGGAAG[A/G/T]GGTGCAGGCACGATA | 8853 |
rs367871092 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9251887 | GCCACTGACAGGGAG[C/T]TTTAGGAATGAGAAG | 8853 |
rs367871926 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9303180 | GTATCATCTTTTTGG[A/G]AGGAAGATTTAAGTC | 8853 |
rs367878784 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9215812 | CCTAGGCCAGTGTTA[A/G]AATTATGAGGCGCTA | 8853 |
rs367886367 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378893 | CGGGCAGTCCCTGGT[C/T]GTCCAGCCTGTGACA | 8853 |
rs367888272 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373509 | GGACCCCAGGGTAGA[C/T]AGGATCTCTACTCCC | 8853 |
rs367889986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257477 | CTAATGAACCAGTAC[A/G]TGATGTCGGAAAGAA | 8853 |
rs367897917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269264 | TTGCGGGGGGGAGGG[A/G]GCGCGCATAACATTT | 8853 |
rs367905159 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355055 | TCCCCTAGCTTTCCC[C/T]TCTGTTAACATCTTA | 8853 |
rs367911320 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9308727 | GCTTCACTGTTCTAG[C/T]CAACTCCGCTGCTAA | 8853 |
rs367936275 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305300 | TTGGTGTAGAGGCTG[G/T]AGTAGTGGGGTATAG | 8853 |
rs367946138 | snp | C/T | 1.6628e-05 | 0.00288335 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399982 | GAAAGGGGCAGGTGC[C/T]CTCCGGTAGCAGTAA | 8853 |
rs367951028 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350140 | TTTTTGAAACTGTAA[C/T]AAAATAGCCATTTTT | 8853 |
rs367984765 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307300 | CCACACTGAGAACCA[C/T]TGCCCCAAGGACAGC | 8853 |
rs368014487 | snp | A/G | 3.30568e-05 | 0.00406538 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388282 | CGCCTCTGCCCCAAT[A/G]TTCTCCTGCAGCCCA | 8853 |
rs368017296 | in-del | -/TTAAAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365923 | TGGGTGATACAGAAC[-/TTAAAC]ACTCCCTCCTCTCCT | 8853 |
rs368018172 | snp | G/T | 1.64887e-05 | 0.00287125 | missense | ASAP2 | GRCh38.p7 | 2:9335108 | ATCAAACAGGCCCAG[G/T]ATGAAGAAAGAAGGC | 8853 |
rs368026338 | snp | A/G | 0.00275821 | 0.0370337 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297252 | AACCTGGTGGGGAGT[A/G]AGGGTGGCATGCCTG | 8853 |
rs368028773 | snp | A/G | 0.000717761 | 0.0189305 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400840 | CAGGCAGTAAGTGAC[A/G]AGCCCCCTTTCCTGC | 8853 |
rs368070565 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231621 | TTCCTCCTGTCAGAG[A/G]GCCCTGTTCTTGCTC | 8853 |
rs368078293 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9314072 | CACTGCAACCTCCGC[C/T]TCCTGGATTCAAGTG | 8853 |
rs368086842 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232579 | CTATCTCCCCTTCTC[C/G]CCATTAGATCATAAG | 8853 |
rs368092375 | snp | A/G | 1.64819e-05 | 0.00287066 | missense | ASAP2 | GRCh38.p7 | 2:9368431 | TTTTTGCAGCTCGCC[A/G]AGAATATTGGGAATG | 8853 |
rs368099657 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9389344 | GGGGGGCCCAGGAAG[A/G]ACAAGAGTCTGCACA | 8853 |
rs368126758 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380577 | AGTTCTATACAATTA[C/G/T]AAGATACATTCAGCC | 8853 |
rs368127886 | in-del | -/CTCT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338305 | GCTCTCTCTCTCTCT[-/CTCT]GTCTGTCTGTGTCTG | 8853 |
rs368165889 | in-del | -/GTGT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265725 | TTTGTGTGTGTGTGT[-/GTGT]CTGTGCGTGTAATGG | 8853 |
rs368180584 | in-del | -/TC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317134 | ACAACCACACAACAC[-/TC]ACATCCCAATCACAC | 8853 |
rs368222538 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343769 | ATTTGTTAAACACCA[A/G]TTGAGCCACCTGTTG | 8853 |
rs368227351 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279059 | AGACAGCTTGCATGC[C/T]GCAGGAGGAGGAGTT | 8853 |
rs368234575 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9324273 | AATGAGTTTTTATTC[A/C]CAGAGCAGACTCTTA | 8853 |
rs368235210 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241273 | TATTAAGTAATGCTG[A/C]AGAATTTTGGTTGAA | 8853 |
rs368236859 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294196 | TAGAGACAGCGTTTC[A/G]TCATGTTGGCCAGGC | 8853 |
rs368240459 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381538 | GGCCAGGAATTCGAG[A/G]TCAGCCTGGCAACAT | 8853 |
rs368241804 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264204 | TCAAAAAAATAATAA[-/T]AATAATAATAATAAT | 8853 |
rs368248643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262872 | TCAGTCTCTTTCACG[C/T]GGGGTTCAGAAAGAA | 8853 |
rs368261721 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9299679 | GACGGCTGACGACGT[A/G]GGAGACGGGTGGAGG | 8853 |
rs368266994 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9393696 | CTCCTGCCCTCTGAC[C/G]TCACCTGCCCAGGGC | 8853 |
rs368269772 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272783 | CATGGATATTTAGTC[C/T]TCCCAGCACAATTTA | 8853 |
rs368297520 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353881 | TTGGGAGGCTGAGGT[C/G]GGGGGATCACTTGAG | 8853 |
rs368300185 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369863 | TTTAGATTTTTTTTT[-/T]CCCCTTCAAGACCTC | 8853 |
rs368322740 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9312600 | CAGTCCTGGCTCCTC[C/T]GGTATCTAGGCTAGA | 8853 |
rs368342412 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317796 | CACCCATACACAATC[A/G]CATTCACACACTCAC | 8853 |
rs368349648 | snp | A/G | 0.000139164 | 0.00834043 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393461 | GCTGACCCTCTGCAC[A/G]TCTCTCCCTGTCCTC | 8853 |
rs368353093 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274319 | TTTCTAGCATTCAAT[C/T]TTTTTTTTTTTTTTT | 8853 |
rs368358711 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9385820 | TGGGATATTGAAGCC[C/T]CAAGAGAAAAGTTGA | 8853 |
rs368364738 | in-del | -/CT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258816 | TATTTATTTCTCTCG[-/CT]CTCTCTCTCCTCTTC | 8853 |
rs368370663 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276312 | GTGTGCACGGGCTGG[A/G]AAGACAGCAGGGGGA | 8853 |
rs368374125 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307937 | GGGAGTGTGTGCATA[C/T]GTGTGCTTGTCTGTG | 8853 |
rs368375254 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275880 | TTGTTGATATTTTCT[A/G]TAACCTAAGATGTCC | 8853 |
rs368375460 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258167 | CAGGGAAATGCAGTG[A/G]AATTCTTCATTAAAA | 8853 |
rs368377027 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9238877 | CTGGCATTTCTACAT[A/C]GATGATTTTGTCTTC | 8853 |
rs368378582 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9330857 | TGGCCTTTTATGGAC[A/G]TGATCCCAGTAACCT | 8853 |
rs368381046 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221603 | ATTTCTGGATTATTC[A/G]TTGCTAGTGTATAGA | 8853 |
rs368385327 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295969 | CCCTCGTTTTCCCAC[A/C]TTGTCAGGCCCAGCC | 8853 |
rs368390071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282953 | CACCCAGTCTGTAAA[C/T]GGACTCCCCCATCCC | 8853 |
rs368412391 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402395 | AGCACTTTGGGAGGC[C/G]GAGGCAGGCGGAACA | 8853 |
rs368412618 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9262268 | TCATTCTAAACATTA[C/T]CAGACCTGAAAAGTA | 8853 |
rs368426992 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222613 | GTTTTTGTTTTTTGG[C/T]AAATAGGAATGAGGT | 8853 |
rs368442615 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9209066 | TGTATGCTGTGCAGG[A/G]GATTACCCTAGAGCT | 8853 |
rs368447847 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306815 | CACCCCATATCAGTG[-/C]CCATATACTCCAGGT | 8853 |
rs368451993 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332267 | TGTAGTTAGGACTGT[C/T]ATAGGGACAGCAGCC | 8853 |
rs368477668 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365306 | CCTCCACCCTTCGGG[A/G]ATCCAAGGGGCCCAG | 8853 |
rs368539220 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313808 | GCCAGCTGGCCTGAC[C/T]ACCTAAAACCTAAGT | 8853 |
rs368547367 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9385271 | CTTATCTGGAAGATT[C/T]AATTCTCACGTTCAC | 8853 |
rs368550288 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400875 | CTGCTCTAGCCAGGG[A/G]GGTGCAGGTGGTTTC | 8853 |
rs368558120 | snp | C/T | 6.70578e-05 | 0.00579003 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401228 | TCTCTGCCCTGAGAG[C/T]TGAGGCCTGCAGCCA | 8853 |
rs368558485 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237443 | TTTTGACAGATTCTT[C/G]CTTTGTTGCCCAGGC | 8853 |
rs368559092 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398453 | GAGTTCCGAGGCTGC[A/G]GTGAACTGATTGCCG | 8853 |
rs368559837 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221211 | CAGCTGAGATTTTCA[C/T]TGAGGTTATGTTGAC | 8853 |
rs368561669 | snp | C/T | 0.000207322 | 0.0101793 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356388 | GGCTCTAGGACATTT[C/T]AATCCCATTCTGATT | 8853 |
rs368584943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226402 | GGCCATGCAGAACTC[A/G]GCATGGGTCTACTTT | 8853 |
rs368599933 | snp | A/G | 1.78563e-05 | 0.00298795 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350939 | TAGAGACGTTGTCTT[A/G]TGCTCTCCTCTGGGG | 8853 |
rs368636139 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208217 | TCAGAATAGGTTTAC[A/C]AGTCACACGTGTGGC | 8853 |
rs368641997 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317785 | ACACCCTCACACACC[C/G]ATACACAATCGCATT | 8853 |
rs368648732 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395585 | TTTTGTTTTTCTTGT[G/T]TTTTTTTTCTTTTTT | 8853 |
rs368666237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348156 | TTTTTCTTTTTGAGA[C/T]GGAGTCTCGCTGTGT | 8853 |
rs368675874 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228047 | AGAGGATAGTCTAGA[A/T]AACATTATGAGTGTA | 8853 |
rs368747081 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305649 | GAGTAGTGGGGTATA[C/G]ATATTGGTGGAGGGG | 8853 |
rs368758579 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361083 | ATTCTCCATTTCTGT[A/C]TCCCAGAGCCTCCAT | 8853 |
rs368800353 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350433 | TGAGCTGGGTGCCCA[A/C]GTTACCTGGCAAATC | 8853 |
rs368810649 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288110 | GCTGTTTTGGATGAT[A/C]CCTCCAGGAAAAGGT | 8853 |
rs368812682 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301854 | TTTGAGACGGAGTCT[C/T]GTTCTGTTGTCCAGG | 8853 |
rs368830223 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255213 | TTGATGTTATGTGTC[C/T]ATACTTGTACCATGT | 8853 |
rs368832419 | in-del | -/TATT | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252997 | ACCAAGCATCTTGAC[-/TATT]TAGTTGTTCACTGCA | 8853 |
rs368863473 | in-del | -/TGTT | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406031 | CAGGCCTTCAGTGTG[-/TGTT]TGTCACTGAGTGGAC | 8853 |
rs368863859 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359087 | TGTTGCAAAACTTTA[C/T]TCTTAAATGAATAAA | 8853 |
rs368865655 | snp | C/T | 8.44787e-05 | 0.00649863 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391200 | TGACATCTACCAGTA[C/T]GTTTTTTTCCTTTTT | 8853 |
rs368867823 | in-del | -/TTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279864 | ATTTACACATACATA[-/TTT]TTTACACATATATAT | 8853 |
rs368869357 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9296633 | AACTCTAAGCACATC[C/T]GATGTATGGGGAACA | 8853 |
rs368881769 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239045 | TCTCTGTCCCGTGGC[A/G]TTAGCAGCAAGCGCT | 8853 |
rs368884304 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341081 | TGGAGTCTCCAGGAA[C/T]TGGGGCAACATGGAC | 8853 |
rs368889305 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9269579 | TGAGCCCACGGGGGA[A/G]CCATGGCCAGGGCCT | 8853 |
rs368967861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235557 | GGAAAGCCCAGTACA[C/T]TAGGGAGTGAAGGGA | 8853 |
rs368997042 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291971 | TAGCAAATGAAGAAA[C/T]GGTTTTTGCTGTGGG | 8853 |
rs369015012 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305853 | TAGTGGGGTATAGAT[A/G]TTGGTGTAGAGGCTG | 8853 |
rs369047547 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265296 | ATGACAACATTCTAC[A/G]TTACGAATTGAGCAT | 8853 |
rs369069088 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276595 | CAGGCTGGAGTGTAG[C/G]GGCACAATCTTGGCT | 8853 |
rs369077105 | snp | C/G | 1.65124e-05 | 0.00287331 | missense | ASAP2 | GRCh38.p7 | 2:9388459 | GAGACTTACGGAGCC[C/G]TCCTGAGTGGCAGCC | 8853 |
rs369084550 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291252 | TAGATTTCTGGAAGT[G/T]GGATTATCCAGAAGA | 8853 |
rs369088120 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305274 | GGGGCTGTAATAGTG[A/G]GGTATAGATGTTGGT | 8853 |
rs369100209 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230402 | CGTGACTCTGGCAGG[C/T]GAGTTTCCCAAGCCG | 8853 |
rs369104120 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9259073 | GGAATTGCTCTGGGC[C/T]GTGGTCCAGCCCGTG | 8853 |
rs369109192 | snp | A/C | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214711 | TAAATGTATATTGGG[A/C]CCCTACCGTATGTTG | 8853 |
rs369109260 | snp | A/G | 0.000115545 | 0.00759994 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297474 | TGTATGAAATGCTGC[A/G]GTTACTTCAGTTGGG | 8853 |
rs369109334 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244633 | TGCCTCAGTGGCCTG[G/T]CACTTACTGGACTGA | 8853 |
rs369163445 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380598 | ACATTCAGCCTCGAC[G/T]AGGTCAAACTCACTG | 8853 |
rs369166206 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9324939 | ATTGATATGATTGGA[G/T]TTACTTCTGTTATTT | 8853 |
rs369176717 | snp | A/G | 0.000157987 | 0.00888644 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393655 | GCGCCGGGGTAAGCC[A/G]CCCCCAGCCAGCTCG | 8853 |
rs369188848 | snp | A/G | 4.94287e-05 | 0.00497111 | missense | ASAP2 | GRCh38.p7 | 2:9380752 | TTAGCAAACGAGTCA[A/G]GAGAGACTCCGCTGG | 8853 |
rs369207362 | snp | A/G | 4.94735e-05 | 0.00497336 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297285 | ACTCACAGCACCTCC[A/G]TCATTCTGTTGCAGC | 8853 |
rs369217184 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216973 | TTCTTTACATATATC[A/G]ATTATTAACTCATTT | 8853 |
rs369275807 | snp | G/T | 5.05259e-05 | 0.00502597 | missense | ASAP2 | GRCh38.p7 | 2:9374780 | AAGGACTACATCACA[G/T]CCAAGTACATCGAGA | 8853 |
rs369283099 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266657 | AGATGGGAATGGAAT[C/T]TCAGAAAGGAAGCCA | 8853 |
rs369288060 | in-del | -/TAT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9208937 | AGTTTGTCAGTTAAA[-/TAT]TATTAACACTGGCAG | 8853 |
rs369291652 | snp | C/T | 0.000317214 | 0.0125899 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9401366 | GGGGGATGTGATCAT[C/T]GTGGACGGGGAGGAG | 8853 |
rs369304402 | snp | A/C | 3.3315e-05 | 0.00408122 | missense | ASAP2 | GRCh38.p7 | 2:9388508 | CAGCCCCCAGCACCA[A/C]CAGCGCCCCCCCGCT | 8853 |
rs369315730 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219005 | GGGCCGAATGAGGCC[A/C/G]TGTTGTTTGCCATCT | 8853 |
rs369318253 | snp | A/G | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390580 | GAGGGAGGGAGAGAG[A/G]GCCCCTCCTCTAGTG | 8853 |
rs369345634 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284521 | AGCCTGTGACATTAG[G/T]ACGATTATTTTACCT | 8853 |
rs369356470 | in-del | -/AA | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211156 | GTGAAACTGCGTCTC[-/AA]AAAAAAAAAAAAAAG | 8853 |
rs369411828 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9388018 | GTCACCTCCTTCCCT[C/T]GACAAGTGAAGATTA | 8853 |
rs369416536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265864 | TGCAACCTCCACCTC[C/T]CCGGTTCAAGTGATT | 8853 |
rs369436276 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383266 | CTCTGGTGCAGTAAA[C/T]AATTTTTTTAAAAAA | 8853 |
rs369449557 | in-del | -/CAT | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405754 | AAAGTACACTATCAT[-/CAT]ACTGTACATGGGATC | 8853 |
rs369467344 | snp | A/G | 0.000593354 | 0.0172141 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344671 | AGAGTTTAAATGTAC[A/G]TTCGTTATCTTGTGT | 8853 |
rs369480232 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381498 | CCAAAGCTTTGGGAG[A/G]CTAAGGCAGGGGATG | 8853 |
rs369504408 | snp | G/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207800 | GAACTGCGGGCAAGG[G/T]GTGTGAGAGTCGGCG | 8853 |
rs369507378 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351492 | TGTCTAAAAGAAAAT[A/G]AGATAAACCTTTTTT | 8853 |
rs369508475 | in-del | -/CTCAAGATGCTTTTGAACT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353275 | AGATGCTTTTGAACT[-/CTCAAGATGCTTTTGAACT]GCCTGGGTGGGCCAG | 8853 |
rs369512597 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9401476 | AGAGACGGGCTTGCA[A/G]GTGAGGTTTTCTCAG | 8853 |
rs369514989 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254720 | TATAGAAAAAAAAAA[C/T]CCAGTATATACAGGA | 8853 |
rs369521220 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295224 | GTAGAGTAGGAGAGT[A/G]GACTTTGGAATCAGA | 8853 |
rs369526140 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287833 | GACTTGTGGAATCCT[A/G]TCCGCAGTGACCACT | 8853 |
rs369534882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9333480 | GAAGGCCTCACTAAC[C/T]GGGGATGTTTAACCT | 8853 |
rs369556927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401044 | AGAGTACCCTGCCCC[A/G]GCCGCTTCGTTTCCC | 8853 |
rs369575097 | snp | A/G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369266 | TCAGGTGATCCACTC[A/G/T]CTGCAGCCTCCCAAA | 8853 |
rs369577864 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315105 | AACAAATTGAGCACA[G/T]GCGTAGAATCAGGGA | 8853 |
rs369600575 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318901 | CTCCAGGGAGCAGGG[A/C]AACCTGTGGGAGGAG | 8853 |
rs369601941 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305435 | GGTGGAGAGGCTGTA[A/G]TAGTGGGGTATAGAT | 8853 |
rs369625337 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392957 | CCTCCTTGTCTGTAA[A/C]ACGTAGACACTAAGA | 8853 |
rs369660217 | snp | C/T | 3.60789e-05 | 0.00424714 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385201 | GTCCAGATGCATGGC[C/T]GAGTGTATGAGCAAC | 8853 |
rs369713021 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272612 | CTGTGCTTGTGGGGC[A/G]TTACTCAAGAATTCT | 8853 |
rs369737271 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381478 | GTGACTCACGCCTTG[C/T]AATCCCAAAGCTTTG | 8853 |
rs369754810 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378622 | GGGACGTGAGAAGGA[C/T]GCTGGGCTCTAGGTT | 8853 |
rs369755685 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233928 | CCAGCTTGGCCAACA[C/T]GGTGAAACCCCATCT | 8853 |
rs369759514 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9224877 | AAGCACAGTGGTCGT[A/G]CCCACAGCTGTCAGG | 8853 |
rs369806962 | snp | C/T | 6.59e-05 | 0.00573983 | synonymous-codon, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9297349 | TCTGGAGAAGTTTGG[C/T]GGCAACTGTGTATGC | 8853 |
rs369819965 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271717 | GCGACGGGGCCCAAG[C/G]GGGAGGCTGCTGAGT | 8853 |
rs369823992 | snp | C/T | 5.33604e-05 | 0.00516501 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401424 | TGGGCCTGGGAGGTT[C/T]CTGGGGGCTGAGCCA | 8853 |
rs369836728 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9401043 | CAGAGTACCCTGCCC[C/T]GGCCGCTTCGTTTCC | 8853 |
rs369839541 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259294 | AATGGCCTTTGCTGA[A/C]CCTAGCAGCACAGCC | 8853 |
rs369842584 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9392146 | AGGTGTGGGCCACCA[C/T]GCCCAGCCTGGCATG | 8853 |
rs369843930 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348575 | TTATTAATGTAAAAC[A/G]GAACTGCTGGTGATA | 8853 |
rs369860524 | snp | A/G/T | 0.000331449 | 0.0128694 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368561 | TTGCTGAGTAAAGGT[A/G/T]TGCCTTTGCCCGAGC | 8853 |
rs369881349 | in-del | -/GGA | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280160 | TTGGGTGACAGGGTG[-/GGA]GGAGGAGGGGCCTGG | 8853 |
rs369883371 | in-del | -/TGT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9297021 | TCGGAGAGGTGGAAA[-/TGT]TGTGTGTCCTTGGCC | 8853 |
rs369884764 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9269465 | ACCATTCAGCCTGTG[G/T]TGACACAGGATGGAG | 8853 |
rs369913605 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230038 | CAGCTTCATGAATTC[C/T]GCAAGAAGAGATGAT | 8853 |
rs369913849 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229028 | ACACCTGCCTTGTTA[A/C]CACGTAGGGATCTGG | 8853 |
rs369933015 | snp | A/G | 0.000153988 | 0.00877328 | missense | ASAP2 | GRCh38.p7 | 2:9356301 | TCATCTCAGAAGTGC[A/G]GAGGATGACGGGCAA | 8853 |
rs369963328 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281600 | TCTATAGCATTTTTT[-/C]ATCACCCTCTTTGAA | 8853 |
rs369984545 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336270 | CTGCTGTTCCTTTAT[-/G]AAGATGAAGCAGGTC | 8853 |
rs369988603 | snp | A/C | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403897 | TAATTTGTGAGGTTG[A/C]AGCTATCATTATATT | 8853 |
rs370001439 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383616 | TTAGCAGAATTCAGA[A/C]CCTTCCCATAATCCT | 8853 |
rs370001923 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371648 | GACGTGTAACTGGGG[C/G]AGGTGGAGCAGGGAA | 8853 |
rs370002539 | snp | A/C/G | 7.40924e-05 | 0.00608617 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356362 | TGACCCAGGGACCCC[A/C/G]CCCGACCCTGGGCTC | 8853 |
rs370006320 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9326498 | CTCTGTTGCTGATTG[A/T]AAAAATAGTATATAC | 8853 |
rs370036758 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380389 | TTTTAGTAGAGACGG[A/G]GTTTCACCATGTTGG | 8853 |
rs370048223 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359514 | AGGGTGCTTCTGGCC[A/C]CCTAATACATGAGCT | 8853 |
rs370050638 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391236 | CTTGCCCGTGGGCTT[A/T]GTAGATCTGGATGGC | 8853 |
rs370054861 | snp | A/G | 0.000153988 | 0.00877328 | missense | ASAP2 | GRCh38.p7 | 2:9374937 | AAATCCCACTGGCCA[A/G]CGGACATGTAAGAGT | 8853 |
rs370074868 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358302 | CTTATGTACATAGTA[C/T]GTTCTCTGTTATTAT | 8853 |
rs370085355 | snp | A/T | 6.61912e-05 | 0.0057525 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323109 | TTGATGTATCCTTGC[A/T]TTCACACGTAGAACC | 8853 |
rs370099908 | snp | A/C/T | 0.00045859 | 0.0151368 | missense | ASAP2 | GRCh38.p7 | 2:9393626 | CGCCCAGCCGCCTCC[A/C/T]GCAGAAGAAGCCTGC | 8853 |
rs370102368 | snp | C/T | 4.97244e-05 | 0.00498596 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400107 | CTGAGTTTGTTTCTG[C/T]TTGGTCCATGGGGGC | 8853 |
rs370108399 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248634 | CGCTGACGGTGAGGT[C/T]TTAGATACCCAGGCC | 8853 |
rs370139450 | snp | C/T | 4.94246e-05 | 0.0049709 | intron-variant, synonymous-codon, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391117 | CTCTGTAAGTGTGGA[C/T]GGTGGAAGCCGGCAG | 8853 |
rs370150424 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286436 | ATTTTTTTTAAAAAA[A/G]GAAAAAAAAAAATAT | 8853 |
rs370150464 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257668 | GGAGTACAAACTCAC[A/G]CCACCATGCCCGGCT | 8853 |
rs370159202 | snp | C/T | 1.65712e-05 | 0.00287843 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9403288 | TCCTGGTCGCAAAGG[C/T]GCATTCCCGGTGTCA | 8853 |
rs370160539 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317572 | ATCACACTCTCACAC[A/C]CCCACACACCCGTAC | 8853 |
rs370178699 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293169 | TAAACTCTGTATGTA[C/T]ACATGCATGCTGGCT | 8853 |
rs370186013 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9261952 | GAGCGCCTCACCCCA[C/T]CATTTGCCATGTGCC | 8853 |
rs370187197 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9344030 | GTGTGATCCTATTGA[A/G]TCCTTACTGTTTATT | 8853 |
rs370189117 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9372960 | ATTGATTTTTTTCTT[A/C]ACATTATAACAAAAT | 8853 |
rs370197094 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351219 | CCTAAAACTCCTTCA[C/G]TTGAAAAAGAGAGAA | 8853 |
rs370202378 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9388139 | CTCTTGCAGCTCTCA[C/T]GCAACTTGTAGCTCT | 8853 |
rs370206383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397688 | AGAACTAAGAATGGC[C/T]TTTATATTTGTAATT | 8853 |
rs370217929 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211755 | GACCCCTCCTAGCAG[C/T]AACAGTGGGAACCAG | 8853 |
rs370218710 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323372 | TGCTGGACTCCCTTT[-/T]GCCCCTGTGTTGACA | 8853 |
rs370228017 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366782 | GGGTTGAATTAGGAA[A/G]GCTCATCATCCAGCT | 8853 |
rs370229199 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247139 | CTGTGGCCAGCCTGT[C/T]CAGTAATATTTTTAA | 8853 |
rs370230137 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381512 | GGCTAAGGCAGGGGA[G/T]GATGGCTTGAGGCCA | 8853 |
rs370265481 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256875 | ACTGTCTCTTAGCCG[C/T]TTGTCCTGTCCACCC | 8853 |
rs370266251 | snp | C/T | 1.64942e-05 | 0.00287173 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376865 | GGACACAGAATTGAA[C/T]GCTCCCATTAGAATT | 8853 |
rs370281578 | in-del | -/TCAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9393236 | TGAGAAAATACTCAC[-/TCAC]AGGCTGATAGAAAAA | 8853 |
rs370286333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285219 | AGTATCAGAATACCC[C/T]GGGGTCTTGTTAAAA | 8853 |
rs370300651 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9252107 | TCGTGTCACAAAAGC[C/T]GTTAACACACACTGT | 8853 |
rs370327863 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9226171 | GCTGGCCACGTAGAC[A/G]ATAATGCTGTACACC | 8853 |
rs370338238 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207423 | TGATGGCCACCTTGG[C/G]CCTCTTTAAGACCTC | 8853 |
rs370368512 | in-del | -/CTCA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317454 | ATTCTCACACACACA[-/CTCA]TGTGCATTCACCTTA | 8853 |
rs370407285 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237780 | TTTTCTTGCTCACCT[C/G]GTGGAGTACATTGTA | 8853 |
rs370419649 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301820 | GTGTGTATCCATCAT[-/C]TTTTTTTTTTTTTTT | 8853 |
rs370429713 | snp | C/T | 0.000188126 | 0.00969677 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374988 | AAAAAAAAAAAAGGC[C/T]GGCCACGGTGGCTCA | 8853 |
rs370434002 | snp | C/T | 0.000146258 | 0.00855029 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356365 | CCCAGGGACCCCACC[C/T]GACCCTGGGCTCTAG | 8853 |
rs370438347 | snp | A/G | 0.000852463 | 0.0206278 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350920 | CCTCTGAGATGCCGC[A/G]CCATAGAGACGTTGT | 8853 |
rs370448288 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225427 | GACCTGCTGCTGGTA[C/G]AAGCAGCCTTTTCTT | 8853 |
rs370466661 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328028 | CTATAGTAAAGGGAA[C/T]GAGGTGCTGACTCAT | 8853 |
rs370470792 | in-del | -/CAAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9357490 | TTTAAAACAAACAAA[-/CAAA]AAACCCGAAAATACG | 8853 |
rs370476940 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236845 | CTGTGTTGGAGCAAA[A/G]GTGCTGTGTGTTGTC | 8853 |
rs370498209 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9334202 | GTATTTTTGTATTTG[G/T]TTTTTTTTTTTTTGT | 8853 |
rs370509173 | snp | C/T | 3.4303e-05 | 0.00414129 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388577 | TCATCCCTGTGAATA[C/T]ATAGAGGGTCTTGTT | 8853 |
rs370518116 | snp | A/G | 1.64841e-05 | 0.00287085 | missense | ASAP2 | GRCh38.p7 | 2:9374844 | CGGCGAAGCTTCACA[A/G]TCTTTGCGAGGCCGT | 8853 |
rs370528993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399178 | ATTCCGAGCAGCGAA[C/G]GGAGTGTCGACAGAC | 8853 |
rs370536562 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321733 | GAGAGTCATCTGGTT[C/T]TGAAAAGAAAAGGTT | 8853 |
rs370556434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352770 | CCAGTGTCTTTGCTG[C/T]AGCCTGATGCATTGA | 8853 |
rs370570366 | snp | C/T | 4.94262e-05 | 0.00497098 | missense | ASAP2 | GRCh38.p7 | 2:9334791 | AACCTTCCATTGAAA[C/T]GCTGTCTACGGATCT | 8853 |
rs370573140 | in-del | -/ATT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337438 | GATCATTTGGTCATT[-/ATT]GTTTAGGCCGTCATT | 8853 |
rs370585507 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9319303 | AATTCTTTGGATCTG[C/T]GCACGATTCCTGGGT | 8853 |
rs370588405 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349046 | TCCGGGCCAGTGTCT[G/T]TAGCTACAAAATTGG | 8853 |
rs370592546 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9314183 | GAGATGGGGTTTTGC[C/T]GTGTTGGTCAGGCTG | 8853 |
rs370594893 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9298597 | AGCCCTCGCCCTGCC[A/T]CAGCCCCATGCCCTG | 8853 |
rs370632027 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221465 | TGGCCTCATTTTCTT[A/G]TCTTTAATTTCTTTC | 8853 |
rs370634728 | snp | C/T | 6.6011e-05 | 0.00574466 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9385280 | AAGATTTAATTCTCA[C/T]GTTCACGTTGAATAT | 8853 |
rs370638854 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217763 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCGGC | 8853 |
rs370648228 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9339120 | GGAGGTGGAGGTTGC[A/G]GTGAGCCAAAATCGC | 8853 |
rs370722857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273915 | AGGCTGTCTAGTCCC[C/T]AGGCAGGAAGAGGGG | 8853 |
rs370737533 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257082 | AGCCTGTCACAGGGC[A/G]TTTGGTAGAAACTAA | 8853 |
rs370739220 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237272 | GAAAAGTTTAACAGG[A/G]CCTCAACTCCTGAGG | 8853 |
rs370779610 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240980 | GGAGGAGTCACGTCC[C/T]GCGTGGGAGGCAGGA | 8853 |
rs370784285 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221268 | ACATCTTAACAATCT[A/G]TCATAACCTCTTCTA | 8853 |
rs370799549 | snp | C/T | 0.000392602 | 0.0140052 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403369 | GTTATGTTCCTGTTT[C/T]GTTATTGGTACCAAA | 8853 |
rs370812978 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253076 | AGGCAACAAAGAAAC[A/G]AAAGTCGTTTTTTGT | 8853 |
rs370821937 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9282337 | CTTTATTTCGGAACA[A/G]GCGTTGTCTACTGCA | 8853 |
rs370822687 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9231471 | CGGTACCTGCTACCC[A/G]TTCGCTGAGATGCCA | 8853 |
rs370836601 | snp | A/C | 0.00319442 | 0.0398372 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207278 | GGTATCCCGCGCCCC[A/C]GCCCCGCCCGCCGCT | 8853 |
rs370841866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313657 | CATTGGCTCCCAGCC[A/G]GGCAGGGTTCAGGAC | 8853 |
rs370851313 | snp | G/T | 0.00020271 | 0.0100655 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320389 | TTTGGGATTTCAAAT[G/T]TAAACCAACCTCGTA | 8853 |
rs370873207 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9285404 | ATCTGCATGTCCCAC[A/G]TGTATACAAAACAGT | 8853 |
rs370889106 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9394259 | AAGCTCTGCCTCCAG[C/G]GTTCTTGCCATTCTC | 8853 |
rs370893673 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381539 | GCCAGGAATTCGAGA[C/T]CAGCCTGGCAACATA | 8853 |
rs370929803 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9241791 | TAAGTCAAGGAAAGC[A/G]AGGAGAAGGAAAGGG | 8853 |
rs370967927 | snp | A/G | 6.59337e-05 | 0.0057413 | missense | ASAP2 | GRCh38.p7 | 2:9374858 | AGTCTTTGCGAGGCC[A/G]TCAAAACGAGAGATA | 8853 |
rs370992889 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9273525 | AGTAATTCACGCAGA[C/G]CCAGCTGTGCAGGAA | 8853 |
rs370995133 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331768 | GCGATTTTTTTTTTT[C/T]AAAAAAAATACAACC | 8853 |
rs371006820 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343231 | ACCACTTATTTTCAT[A/T]GTGTCCCTGTTTCTC | 8853 |
rs371019520 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338004 | TACACAGTTAAACTC[A/G]TTGGCACTGCTCATC | 8853 |
rs371025140 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319440 | ACATTCCCCATCGAG[A/C]CTTCAGGGGCTTGGA | 8853 |
rs371071516 | snp | C/G | 0.000482943 | 0.0155318 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358710 | GATGTGACTCCTGAC[C/G]CTCTTTTTTACTGGA | 8853 |
rs371084673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246046 | GGTGTGACCCCGTTG[A/G]GGGAAGGAGCTCTGT | 8853 |
rs371094699 | in-del | -/GTTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348138 | TTTGTTTGTTTGTTT[-/GTTT]TTTTCTTTTTGAGAC | 8853 |
rs371111318 | in-del | -/CTGTCT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9334033 | TCTCTGTCTCTGTCT[-/CTGTCT]TTCTCCTTTTTTTTT | 8853 |
rs371169665 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381531 | GGCTTGAGGCCAGGA[A/G]TTCGAGATCAGCCTG | 8853 |
rs371176545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360293 | GTAACAACCTGATGA[C/T]CTTGGTATATTATCC | 8853 |
rs371176745 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313120 | CCCACTAGGCTGCGG[A/G]CCCTGTTCCCAGCAT | 8853 |
rs371177674 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9329689 | TGGCTTCGTGACAGC[A/G]GGAGTGGAAGGTGTG | 8853 |
rs371179006 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9231663 | CACAGCAGCGGGCCT[A/G]TCTGTCTGCCTGGCC | 8853 |
rs371190426 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302807 | CAGGTGTGAGCCACC[A/C]CGCCTGGTCAGAAGA | 8853 |
rs371196555 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271672 | ATGGTCTGCGGAAGA[C/T]GGCGGGCAGAGGGTA | 8853 |
rs371207125 | snp | G/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406118 | CTCTGTGACATCTCG[G/T]CTTCCTCAGGCCTTC | 8853 |
rs371214715 | snp | C/T | 2.09501e-05 | 0.00323645 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378909 | GTCCAGCCTGTGACA[C/T]ACTATGCTCTCTCTC | 8853 |
rs371237622 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317812 | CATTCACACACTCAC[A/T]CAATCACACCCTTAG | 8853 |
rs371247060 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358450 | TGGTGTGTTTTCACC[A/T]CCAGCCATTGAGGAG | 8853 |
rs371250546 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9242029 | AAGTTGGTTAGCTTC[C/T]TCGAGCACTAGTTTC | 8853 |
rs371266206 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270937 | AGCTGGGACTACAGG[C/T]GCCCGCCACTACGCC | 8853 |
rs371270544 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395569 | TTTTTGTTTTGTTTT[G/T]TTTTGTTTTTCTTGT | 8853 |
rs371278637 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9298481 | ACTGTTTCTCTGCTC[A/G]AGCTTTTCACTTAGA | 8853 |
rs371320739 | snp | A/G | 1.65803e-05 | 0.00287922 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400115 | GTTTCTGCTTGGTCC[A/G]TGGGGGCAATGTGGG | 8853 |
rs371358982 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295885 | TCCCCCATAGGATGG[A/G]TGAGCAGACCATTCA | 8853 |
rs371375146 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233479 | TTAAGTAACACTTAC[A/G]AAAGTTGTATGGTGG | 8853 |
rs371378701 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316167 | ACAAAAACTACAAAA[A/G]AAAAATTAGCCAAGC | 8853 |
rs371398535 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9228296 | CTTATGTCATCTGTC[A/T]TGGTGAGTATTCCAG | 8853 |
rs371406441 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256242 | TTTATTGAGTGCCAA[C/T]CATGTGCCAGCTTGG | 8853 |
rs371415354 | snp | A/G | | | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9215187 | AGTTACAGTATTTAT[A/G]TGTGGTATTTGTGTA | 8853 |
rs371415410 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9363637 | CGCCCAGGCTGGAGT[A/G]CAGTGGTGCCATCTC | 8853 |
rs371416165 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9216439 | CTACAGGTGTGCCCC[A/C]CCATGCCTGTTTAAT | 8853 |
rs371418559 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9396504 | CTGGTCTCGAACTCC[-/T]GGGCTCAAGCAGTCC | 8853 |
rs371438104 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9316913 | TAGCAACACCCCCCC[-/C]AACACACACCCCCTC | 8853 |
rs371443794 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336841 | GTGGCTGCTCCCCAG[C/T]GCACCGTTGGAAATG | 8853 |
rs371489784 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250390 | GGCTCCTGGAGTTCT[C/T]GCGGTGCCCCAGGTG | 8853 |
rs371494207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213370 | CGGGCAGAGGGGTGG[A/G]CAGTGCCAGGTCACA | 8853 |
rs371508378 | in-del | -/GT/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258335 | AGTAATCAGTAGTTG[-/GT/T]TTTTTTTTTTTTTTT | 8853 |
rs371545473 | snp | A/C | 1.66308e-05 | 0.00288359 | missense | ASAP2 | GRCh38.p7 | 2:9400825 | ATGCCTAGGAAGTCG[A/C]AGGCAGTAAGTGACG | 8853 |
rs371558207 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333868 | AATCACTTGTTATAG[G/T]TGACCTCACAGCATT | 8853 |
rs371572430 | snp | A/G | 6.75573e-05 | 0.00581155 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327926 | AGTAAGTTCTTCTCT[A/G]TTATGTTATCTTAAA | 8853 |
rs371588307 | snp | A/G/T | 3.29616e-05 | 0.00405954 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344648 | CGGGTACGTGAGGGG[A/G/T]TGTGGCTAGAGTTTA | 8853 |
rs371602206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9391668 | CAACCTCTGCCTCCC[A/G]GGTTCAAGAGATCGT | 8853 |
rs371603748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398749 | GGGTGGCAGAGGTTG[C/T]AGTGAGCCGAGATTG | 8853 |
rs371622428 | in-del | -/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9270784 | GAGTTCAATTGTTTT[-/CA]TTTTTTTTTTTTTTT | 8853 |
rs371629570 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9389452 | GTCCTTATGTGGTAG[A/C]TGCTAGCTGGGCAGG | 8853 |
rs371656952 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334024 | TTTCTCTCTCTCTCT[C/G]TCTCTGTCTTTCTCC | 8853 |
rs371658117 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305918 | GAGTAGTGGGGTATA[C/G]ATATTGGTGGAGGGG | 8853 |
rs371722162 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350774 | TCCTTCCACCCAACC[C/G]CAACCTTTTTTGTTG | 8853 |
rs371728421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253345 | ATTTTTGTATTTTTA[A/G]TAGAGACAGAGATTC | 8853 |
rs371752402 | in-del | -/TCT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300395 | AAAGGAATCCCTCCT[-/TCT]CCTTTATAAAATTTC | 8853 |
rs371812775 | snp | A/G | 2.51994e-05 | 0.00354952 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379092 | CCGGGGGTGGGCTCA[A/G]CTGCACCCTGGCCTC | 8853 |
rs371838484 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9296242 | TGTTTTATTATAGAC[C/T]GGCTGGTTTCCTTTG | 8853 |
rs371859515 | snp | A/C | 8.24205e-05 | 0.00641899 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9335117 | GCCCAGGATGAAGAA[A/C]GAAGGCAGTTGATAC | 8853 |
rs371884148 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294698 | TTCACTTAGAGCAAC[A/T]CTGAGGTCCAGTCCT | 8853 |
rs371966280 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332485 | AGATGAAATCTAAAT[C/T]TAAATCCAAATTCAT | 8853 |
rs371979863 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227464 | CCTGAGGGCAGGATC[C/T]CTTTTTTCTTTTTTT | 8853 |
rs371989716 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276427 | AGCAGGCAGAGCTCA[A/G]ATGATCAGATTTTTA | 8853 |
rs372037244 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310691 | CAGTGGCCAGAGAAC[A/G]GAGAGGGTGACCTGT | 8853 |
rs372051839 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331715 | GGAGGTTGCAGTGAG[C/T]TGAGATCATGCTGCT | 8853 |
rs372064434 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213160 | GGAGATCAGGAAACC[A/G]AAATCAGGAAAAGCC | 8853 |
rs372079133 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ASAP2 | GRCh38.p7 | 2:9403053 | AAGAGCTCCTTACAC[A/G]GGAGAGGCCTGCACT | 8853 |
rs372085807 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9386224 | GATAGGTCAGTAGGT[A/C]ACCAGATGGCATTTC | 8853 |
rs372104561 | snp | A/G | 6.59261e-05 | 0.00574097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279400 | GCTGGGTGAGTATAC[A/G]TCCTTCCCTAGAGGT | 8853 |
rs372107136 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9399895 | AAAAAGAGACAGCTA[A/C]GTGACAGTGGAGGAA | 8853 |
rs372111874 | snp | C/T | 3.7409e-05 | 0.00432471 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393444 | GAGTGGGAAGCCTGG[C/T]GGCTGACCCTCTGCA | 8853 |
rs372129549 | in-del | A/CC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370085 | CCTCGTGATCTGCCC[A/CC]CCTTGGCCTCCCAAA | 8853 |
rs372133174 | in-del | -/CCCCAGTGA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248526 | CTCCTTGCTAGTTGA[-/CCCCAGTGA]GAGTCAGCGTTTTGG | 8853 |
rs372146000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294085 | CCCACTGCAACCTCC[A/G]CTTTCTAGGTTCAAG | 8853 |
rs372161354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280137 | CCGTGCTCAGGTGCA[A/G]ATAGAGTTTGGGTGA | 8853 |
rs372161834 | snp | A/G | 6.64927e-05 | 0.00576558 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399987 | GGGCAGGTGCCCTCC[A/G]GTAGCAGTAAATCTA | 8853 |
rs372164164 | snp | A/G | 2.09606e-05 | 0.00323726 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378908 | CGTCCAGCCTGTGAC[A/G]CACTATGCTCTCTCT | 8853 |
rs372168675 | snp | A/T | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404158 | AGCAACTGTACACAG[A/T]AGAATTCTGTGGCGC | 8853 |
rs372176888 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9399193 | GGGAGTGTCGACAGA[C/T]GGGAGCGTACAGTGG | 8853 |
rs372210306 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9324348 | TTGAAAGTTAAGTCC[A/G]TTTTGTCTAATGTTA | 8853 |
rs372233696 | snp | C/G | 0.000153988 | 0.00877327 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400854 | CGAGCCCCCTTTCCT[C/G]CCTCTCTGCTCTAGC | 8853 |
rs372237689 | snp | C/T | 1.65037e-05 | 0.00287256 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297280 | CTGAGACTCACAGCA[C/T]CTCCGTCATTCTGTT | 8853 |
rs372243884 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308227 | TGCTCGGCTTCTGGG[A/C/G]AGGCCTCAGGAAACT | 8853 |
rs372252394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258928 | CCTGATTACAGACTG[A/G]GGTCTGCAGCCCTCC | 8853 |
rs372258428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314129 | GCTAGGATTACAGGC[A/G]TGCGCCACCTCGCCT | 8853 |
rs372261587 | in-del | -/GAG | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279070 | ATGCTGCAGGAGGAG[-/GAG]TTGGTTTTCAGTAAT | 8853 |
rs372272948 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264711 | CTTTGCCTCTTCCAG[A/G]GTTTTTTTCTCCCTG | 8853 |
rs372277363 | snp | C/T | 3.30142e-05 | 0.00406276 | missense | ASAP2 | GRCh38.p7 | 2:9388306 | CAGCCCAGTCCCAAC[C/T]GGCGGGAAGACCGGC | 8853 |
rs372311775 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9251349 | CTCCATCTGCTTGGT[A/G]CTCACGTGTAACAGC | 8853 |
rs372311906 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229858 | CCTGTCCCCTGTAAA[C/T]TGTGGGTGGGCCAGG | 8853 |
rs372347154 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365019 | CTGAACATTTTTTAA[A/G]CCACAAAGTCTATCA | 8853 |
rs372347602 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345230 | TCCATTAAGAGAAAA[A/G]AATGGGCAGGACTCT | 8853 |
rs372354978 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398010 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 8853 |
rs372358495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382095 | TTTAAGCAATTCTTC[C/T]GCCTCAGCCTCCTGA | 8853 |
rs372362702 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296922 | TGGGCTGCAGGCTAG[A/G]GAGGAATGGGGCATC | 8853 |
rs372364949 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381467 | GGCCAGGCACAGTGA[C/T]TCACGCCTTGTAATC | 8853 |
rs372401763 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239278 | AGCACAGATTTGGTG[A/T]CATCATGTTGGGATT | 8853 |
rs372412922 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249659 | GTCGTGTGGACAGAA[A/G]GTTCACAGCCTGAGT | 8853 |
rs372414037 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9223906 | ATTGATGTTAGGTTG[G/T]TCATTAAGAATAGTC | 8853 |
rs372414191 | snp | C/T | 4.94409e-05 | 0.00497172 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9388422 | GAAGCAGAGGGCTTT[C/T]ATGCCCAGCATCTTG | 8853 |
rs372432405 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209248 | TACATACATGCTATG[A/G]TGATGGTATGTGTGA | 8853 |
rs372447395 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9304307 | TTGTTTTTGTTTTTG[C/T]CATTGTGTGTTTTCT | 8853 |
rs372456769 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9216113 | GACTCTGCAGGGCAA[A/G]TTCCATTGTGAAGCA | 8853 |
rs372459236 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305670 | GGTGGAGGGGCTGTA[A/G]TAGTGGGGTATAGAT | 8853 |
rs372489626 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9323801 | CACTCCATTCCACCC[A/G]CAGCCTCAGCCCTTC | 8853 |
rs372489671 | in-del | -/TC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338348 | CTCTGTCTGTCTCTA[-/TC]TCTCTCTCTCTCTCT | 8853 |
rs372516505 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234097 | GCCTGGGTGACAGAG[C/T]GAAGCTATGTCTCAA | 8853 |
rs372519755 | snp | C/T | 0.00020598 | 0.0101463 | missense | ASAP2 | GRCh38.p7 | 2:9393644 | AGAAGAAGCCTGCGC[C/T]GGGGTAAGCCACCCC | 8853 |
rs372533245 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9401525 | AGTTCCTGGTGCCTC[C/T]GCCCCTTAGCATCCT | 8853 |
rs372542200 | in-del | -/AC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317394 | CACATCCACACACAC[-/AC]CCTCAAACACACACA | 8853 |
rs372555752 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279878 | ATTTTTTACACATAT[-/A]TATTTACACATATAT | 8853 |
rs372599269 | in-del | C/TT | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404744 | TGTGTAGAGTTTTTT[C/TT]TTTTTTGGCATTGTA | 8853 |
rs372600563 | in-del | -/CACA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317587 | ACCCACACACCCGTA[-/CACA]ATCACATTCACGCAC | 8853 |
rs372603966 | in-del | -/GT | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205672 | TATTGAATTTCCAGT[-/GT]CTCTCACACTTCCTC | 8853 |
rs372622862 | in-del | -/TC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317177 | ACACTCTCACCACAC[-/TC]AACACACACCCCACG | 8853 |
rs372627242 | snp | A/G | 1.65515e-05 | 0.00287671 | missense | ASAP2 | GRCh38.p7 | 2:9374795 | GCCAAGTACATCGAG[A/G]GGAGATACGCAAGGA | 8853 |
rs372652227 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9222629 | AAATAGGAATGAGGT[A/G]TGTTTACTACTGGAG | 8853 |
rs372684615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372985 | CAAAATGCTGTTATT[C/T]GAGGGCCTGTTGTGC | 8853 |
rs372688916 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395829 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 8853 |
rs372722732 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348898 | CCAGGCAAGCAACCG[C/T]CTTCCATGGATACCC | 8853 |
rs372728171 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9306162 | TAGACATGGGGTGGA[A/G]GGGCTCTAGGGGTGT | 8853 |
rs372748901 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9261282 | TGGGAGGGGGAGCAC[A/G]GCTCTGGAAGCTGCC | 8853 |
rs372760014 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9324323 | TCAGTCCCAGGAATC[A/C]GGGTGGCAGTTGAAA | 8853 |
rs372781516 | snp | C/T | 0.000284706 | 0.0119278 | missense | ASAP2 | GRCh38.p7 | 2:9393508 | CCCACGCCGCCCCCA[C/T]CCGTTGCCAAGACGC | 8853 |
rs372849106 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381507 | TGGGAGGCTAAGGCA[G/T]GGGATGATGGCTTGA | 8853 |
rs372857134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357796 | GGATAACATTTTTAA[C/T]AACTTGAACATTTAA | 8853 |
rs372859535 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327668 | CCCCAAAATAAAGAA[A/G]CGGTTACGGAATCCA | 8853 |
rs372889027 | snp | G/T | 1.74888e-05 | 0.00295704 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335230 | ACCCCATTCTTGGAG[G/T]CTTTGGGTCTGAAGA | 8853 |
rs372896780 | snp | A/G | 1.67542e-05 | 0.00289427 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401237 | TGAGAGCTGAGGCCT[A/G]CAGCCACACTAACCG | 8853 |
rs372906062 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317786 | CACCCTCACACACCC[A/G]TACACAATCGCATTC | 8853 |
rs372918640 | snp | A/G | 6.70736e-05 | 0.00579071 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323294 | AGCCCAGGCTGTGCC[A/G]GCTCTGCCCTCACCT | 8853 |
rs372919930 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290495 | GATTACAGGCGTGAG[C/T]CACTGCACCTGGCCT | 8853 |
rs372940878 | in-del | -/CC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362353 | TTTGGGTAAATAGAA[-/CC]CAGCCTCTGTTTCAG | 8853 |
rs372945449 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9255828 | TCACATAGCAGGGAG[A/G]TGATCTCACCAGAAC | 8853 |
rs372954102 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286438 | TTTTTTTAAAAAAGG[A/G]AAAAAAAAAATATAT | 8853 |
rs372957731 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214722 | TGGGCCCCTACCGTA[C/T]GTTGTCACTGCCAGG | 8853 |
rs372970440 | snp | A/G | 0.000153988 | 0.00877328 | missense | ASAP2 | GRCh38.p7 | 2:9400756 | GTGGATCTCTCTGCA[A/G]CGGAAGCTCTGGGTC | 8853 |
rs372974499 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243656 | AGCGTTTCCACTTAC[A/G]GAAGCTTGTTTTATC | 8853 |
rs372977657 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9340389 | GGCTCACACAGTGGC[A/G]TCAGAGCCAGGATTT | 8853 |
rs372985680 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260402 | CCTCTCCCATCACCT[C/T]ACTGCTTGGATTGTA | 8853 |
rs372989344 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240996 | GCGTGGGAGGCAGGA[C/T]GGTGTGAGATTTCAT | 8853 |
rs372989754 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9246486 | TTGTAGAGACGGAGT[A/G]TCACCATATTGCCCA | 8853 |
rs373003746 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9206408 | GGGCCGGCGCGGCCC[A/G]CCGTTCAAGTGGGGA | 8853 |
rs373023360 | snp | A/C | 4.97484e-05 | 0.00498715 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320276 | GCCTAATTTATTATT[A/C]TTTGTTTACAGGATC | 8853 |
rs373034353 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321287 | AGTGAGCCCCACACC[C/T]TTGATACTCCTTCTA | 8853 |
rs373037678 | snp | C/T | 0.000444968 | 0.0149093 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374851 | GCTTCACAGTCTTTG[C/T]GAGGCCGTCAAAACG | 8853 |
rs373040649 | snp | G/T | 0.000153988 | 0.00877328 | missense | ASAP2 | GRCh38.p7 | 2:9401373 | GTGATCATCGTGGAC[G/T]GGGAGGAGGACCAGG | 8853 |
rs373041234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334396 | CGCGGTCGCCTGTTG[C/T]GGCACATTCTTCAGT | 8853 |
rs373047260 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9356644 | GTACAGTGAGAGTGA[A/G]CTCAAGGTCATGTGG | 8853 |
rs373050910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383379 | CTCACCTCAGCCTCC[C/T]GAGTAGCTGAGACTA | 8853 |
rs373070738 | snp | C/T | 8.6485e-05 | 0.00657533 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350790 | CAACCTTTTTTGTTG[C/T]TTTTTGCTTTTAAAC | 8853 |
rs373092585 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276696 | GCACACCCACCAACA[C/T]GCCCGGCTAATTTTT | 8853 |
rs373096238 | snp | A/G | 1.71143e-05 | 0.00292521 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318612 | GGGTATGACATTGAC[A/G]CTGTGACACCAGGGG | 8853 |
rs373097155 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315564 | AGGAGAGCTGGCTGC[A/G]TACTTGGGGCTGCCT | 8853 |
rs373124564 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396503 | GCTGGTCTCGAACTC[C/T]TGGGCTCAAGCAGTC | 8853 |
rs373148674 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254908 | CAAGTCTTTGTGTAG[C/G]TAGACACGTTTTATA | 8853 |
rs373166672 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9388151 | TCACGCAACTTGTAG[C/T]TCTCAGGCAACAGTT | 8853 |
rs373169062 | snp | A/C | 1.66197e-05 | 0.00288263 | missense | ASAP2 | GRCh38.p7 | 2:9385255 | CTCAGCTGACCCAAG[A/C]CTTATCTGGAAGATT | 8853 |
rs373171418 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264169 | TGCACTCCACCCTGG[C/G]CAGTGAGTGAGACCC | 8853 |
rs373172372 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245654 | TGGGTGCTGGTGCTG[C/T]GTTTGTGAACAGAGC | 8853 |
rs373188977 | in-del | -/AAGA | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213959 | ACTGGGGCCCAGGGA[-/AAGA]GAGAAGCATGGCTGC | 8853 |
rs373197221 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381487 | GCCTTGTAATCCCAA[A/C]GCTTTGGGAGGCTAA | 8853 |
rs373199618 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397781 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 8853 |
rs373259980 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9312631 | AATAATGTGTTTTCC[C/T]TGAAGTTCCATGGTG | 8853 |
rs373287167 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336590 | GCGCTCATTTAGTAG[G/T]ATTTTGGTAAACATG | 8853 |
rs373290183 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9297770 | CTACTCTCCTTCTGG[A/T]AATTATAGTAGGCAT | 8853 |
rs373292592 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9238819 | GCTTCCCTCTTGCTA[-/A]CCTGACTGACTTGGT | 8853 |
rs373302237 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234730 | CTGTTGAATTGAGCT[-/G]GGGGCAGGTGGAATA | 8853 |
rs373319152 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211150 | ACAAGAGTGAAACTG[C/T]GTCTCAAAAAAAAAA | 8853 |
rs373372100 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326549 | TATAAGAAAATATAT[A/G]TAAAAGGAATTAAAA | 8853 |
rs373398768 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281137 | AAAGTATCTTGGAAG[A/T]TTTTTTTTTTTTTTA | 8853 |
rs373425778 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344442 | GTTGTTAAAAAAAAA[A/G]CACATTAGGCATAAG | 8853 |
rs373450589 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240142 | ATTATCCCTGGGGGG[-/G]TATGTTCCAAGACCC | 8853 |
rs373455860 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315182 | TAAGGATGGATTGTG[A/G]AGAGTGTGAAATGCA | 8853 |
rs373474924 | snp | A/G | 3.65564e-05 | 0.00427514 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356366 | CCAGGGACCCCACCC[A/G]ACCCTGGGCTCTAGG | 8853 |
rs373518661 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219947 | GTTGTTTCATATATG[G/T]AATCAAACAATATGT | 8853 |
rs373522266 | snp | G/T | 1.64751e-05 | 0.00287007 | missense, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9297387 | ACCCAGATTTAGGAA[G/T]TGCGTTCCTGAAGTT | 8853 |
rs373542574 | snp | C/T | 3.29582e-05 | 0.00405931 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9391027 | GCACGTGTATGTGTG[C/T]GTGCATGCGTCTGTG | 8853 |
rs373590047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328955 | AAGATTTAGGGTAGA[A/G]TTTTTTGTTTTTTGT | 8853 |
rs373599189 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295600 | TATTTACAGGTGGAC[A/G]TAGGACTGGAACCTA | 8853 |
rs373603134 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274511 | TATTTTTAGTAGAAT[C/T]GGAGTTTTACCATGT | 8853 |
rs373609916 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237781 | TTTCTTGCTCACCTG[A/G]TGGAGTACATTGTAT | 8853 |
rs373613557 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359581 | TCTCTCCTGGGATAG[C/T]TGGATGTTGACAGTA | 8853 |
rs373637097 | snp | A/G | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403408 | CAGATAACCAGTTTC[A/G]TGAACTGTTTGTATG | 8853 |
rs373641255 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305328 | TAGATGTTGGTGGAG[A/G]GGCTGTAGTAGTGGG | 8853 |
rs373665346 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243234 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 8853 |
rs373665400 | snp | A/G | 6.65945e-05 | 0.00576999 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9327906 | ATACTTTCATGCCCA[A/G]TGCAAGTAAGTTCTT | 8853 |
rs373682144 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9270862 | CAGTGGCGCGATCTC[A/G]GCTCACTGCAAGCCC | 8853 |
rs373693333 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342848 | ACGTGACCGTGACCT[C/T]CCTGTGTCTTCTGTG | 8853 |
rs373727546 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231762 | TGCCTTCCTTTGGAG[A/G]CTCTCCTCTCTGTGC | 8853 |
rs373727563 | in-del | -/TG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9285806 | CATTCTTATCGAGAG[-/TG]ATATTCCTACCCTCA | 8853 |
rs373747329 | snp | G/T | 0.000115368 | 0.00759412 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376899 | GAATGCCTTTGTTTG[G/T]TTTTTCAGGAGCCGG | 8853 |
rs373782547 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366804 | CATCCAGCTATTAGG[C/T]TACCCCACATAATTC | 8853 |
rs373850518 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217573 | ACCTCTTTCCCCAGC[A/T]TCTCAGAAGAAATCA | 8853 |
rs373865534 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9360526 | TCCTTCCCTATCACC[A/G]TCCCCAACAAATGTT | 8853 |
rs373874090 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9393758 | CTACTCCAGCGTGGG[C/T]GCCACATAACTAATT | 8853 |
rs373877125 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240268 | TTTTTTTTTTTTTTT[A/T]TTTGAGACAGGGTCT | 8853 |
rs373902492 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214398 | GTGACTGCCACCATG[C/T]CCGGCTGATTTTTGT | 8853 |
rs373906425 | in-del | -/TGT | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205450 | TAAATTGTAACTTGT[-/TGT]CTAGTGCAATGATAA | 8853 |
rs373909522 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9342819 | TATTTGTCTAGCTTC[C/T]CTGGGTGCTGACCAC | 8853 |
rs373911232 | snp | C/T | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404826 | ATGTTGTATAGCAAT[C/T]GCTTTTTACCTTTCA | 8853 |
rs373935498 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288532 | TGGGGTCATGGGGTA[A/T]GACGTGGCAAAAATG | 8853 |
rs373939606 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221699 | TATAGTTTTGTGTAT[A/T]TGTATGTGTATTCCT | 8853 |
rs373952094 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366921 | CAGTGTATCTAACCC[A/G]GACCTCTTGGGCTCT | 8853 |
rs373964574 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272902 | TCTCTATTCCATTAG[C/T]CTATGTGTCTGTTTT | 8853 |
rs373964971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287966 | TGCTATTTAATTTGG[C/T]TGGCTTTTATAGTCA | 8853 |
rs373975885 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395559 | TGTTTTTGTTTTTTT[G/T]TTTTGTTTTGTTTTG | 8853 |
rs373981932 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368900 | TTGTGGTAGATATGT[G/T]ATTATGTAGCGTCCT | 8853 |
rs373982694 | snp | A/G | | | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391308 | CGTGCCAAGTGCCCC[A/G]TGTTGTATGGCTCCC | 8853 |
rs373985638 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401842 | AGTGCCGGCCACCTA[A/G]GAATTCAGACTTGGC | 8853 |
rs374012052 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347236 | TCCCTATTTCCCTGC[A/G]TGCTCTGGAAGTCAG | 8853 |
rs374014789 | snp | A/G | 1.71006e-05 | 0.00292404 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327943 | TATGTTATCTTAAAT[A/G]TTTGTTCATGTGTGG | 8853 |
rs374044186 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9289822 | GCTAGCTGCCTGTGC[A/T]GAACACAACCAGACT | 8853 |
rs374047603 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359820 | CCAGTCTTTCTAGGA[A/G]TTCCTTTATGGTCTT | 8853 |
rs374060349 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9330571 | AAAAAATATAAAAAG[A/T]GAGCTCATCTCTACT | 8853 |
rs374070675 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302058 | TCGATCTCCTGACCT[C/T]GTGATCCACCCGCCT | 8853 |
rs374078193 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247510 | GTGCTTCTGTGGATT[A/T]GCTCGCTGCGTCTGT | 8853 |
rs374116513 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237747 | AGGCTAGATTCTGAG[C/T]GACCAGGAGACTGAG | 8853 |
rs374154872 | in-del | -/AAAG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9379648 | GAAGGACTGTTAAAT[-/AAAG]AGGAAAGAATAGAAA | 8853 |
rs374173287 | snp | A/G | 0.00262455 | 0.0361301 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279259 | CTCAACGTGGTGCTC[A/G]CTGCTAGCGTGGTCT | 8853 |
rs374175582 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9298966 | CTATGGTAAGAAAAT[A/G]TAACATTAAAAATCC | 8853 |
rs374175970 | snp | A/T | | | intron-variant, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9287064 | CACTGAGTAGTGATC[A/T]GCCAGTGTCATCTAG | 8853 |
rs374193314 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233320 | AAACATCCTCAGAAT[-/T]GGAAGGTCCAGATGA | 8853 |
rs374202514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232217 | TCCCTCCCACCCCAT[C/T]TCATCCATGCCTGTC | 8853 |
rs374229116 | snp | C/T | 5.34593e-05 | 0.00516979 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350936 | CCATAGAGACGTTGT[C/T]TTATGCTCTCCTCTG | 8853 |
rs374243385 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384645 | TGGTTTATTATAAAG[A/G]ATATTGCAAAGCATA | 8853 |
rs374255595 | snp | A/G | 6.58989e-05 | 0.00573978 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279310 | GACTGTATTCTCTAC[A/G]TTTTAGGCTTTGGAC | 8853 |
rs374280719 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227809 | AGAAACTTCTTTGAC[C/G]AGCCTCTTCATTTGA | 8853 |
rs374291754 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387497 | GGAGCTCCTGTTCAT[A/G]TGGGAGGAAAACATC | 8853 |
rs374314184 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345310 | AATCTTAACATATGG[C/T]GCCCAACTTTAAGGC | 8853 |
rs374323344 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359216 | AGATGTGGAATGCAA[C/T]GTCTAAAGACAGGAA | 8853 |
rs374330784 | snp | A/G | 3.29864e-05 | 0.00406105 | missense | ASAP2 | GRCh38.p7 | 2:9388319 | ACCGGCGGGAAGACC[A/G]GCCCATCAGCTTCTA | 8853 |
rs374377815 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338142 | TCCCAAAGCCTCATC[A/C]CTTGTGTGCAGGCTC | 8853 |
rs374406091 | snp | C/G | 1.66338e-05 | 0.00288386 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399978 | ATGAGAAAGGGGCAG[C/G]TGCCCTCCGGTAGCA | 8853 |
rs374417305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396810 | AGTTCAAGACCTGCA[C/T]GGCCAACATGGCAAA | 8853 |
rs374441140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302431 | CCACCTCGGCCTCCC[A/G]AAGTGCTAGGATTGC | 8853 |
rs374454994 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9398184 | TTCACACCACAGTGG[C/T]AGAGTTGAATACTTG | 8853 |
rs374459209 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382181 | TAGAGACGGGGTTTC[A/G]CCATATTGGTCAGGC | 8853 |
rs374468818 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236954 | GGTGTGGGTACCAGG[C/T]AGGGCTGGGGTACGG | 8853 |
rs374482724 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337496 | ACTTAGACAACTGAA[A/G]GTGTTAAGAGGATTT | 8853 |
rs374486924 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9226748 | AAGAACACGCCGTCC[A/G]TCCACTCAAAACATT | 8853 |
rs374500295 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311891 | CGTGTGTGCTGTGTG[C/G]ATTGCATACACCAAG | 8853 |
rs374538173 | snp | C/G | 0.00557542 | 0.0525036 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404410 | CACTTTTTACTGTTT[C/G]AGGCCATCATATCAT | 8853 |
rs374579538 | snp | A/G | 3.44679e-05 | 0.00415124 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350915 | GGCTCCCTCTGAGAT[A/G]CCGCGCCATAGAGAC | 8853 |
rs374590710 | in-del | -/AGAC | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213788 | GCCCCCTGAACAGAC[-/AGAC]CTTCCAGCATCCCCA | 8853 |
rs374602374 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9347901 | AAAGCCTGACAAATC[A/G]GGAAAAAATAGAACG | 8853 |
rs374611543 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381516 | AAGGCAGGGGATGAT[G/T]GCTTGAGGCCAGGAA | 8853 |
rs374621495 | snp | A/C/G | 0.000148457 | 0.00861448 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391157 | TCAGATCCGCCAGCT[A/C/G]TCCATCCACCGCTGC | 8853 |
rs374666019 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9241394 | CATGCTAAACTGGTG[C/T]GATTATGAGTTCCTT | 8853 |
rs374672166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247378 | CAGACGGTCCCCGGT[C/T]CTCATTTGCACGAGG | 8853 |
rs374674599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336847 | GCTCCCCAGCGCACC[A/G]TTGGAAATGATCGAG | 8853 |
rs374686138 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395574 | GTTTTGTTTTGTTTT[G/T]TTTTTCTTGTGTTTT | 8853 |
rs374692643 | snp | C/T | 3.40762e-05 | 0.00412758 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344498 | AAATTAGGACCTGGA[C/T]AAGATTAAAAACACA | 8853 |
rs374708871 | in-del | -/C | | | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214813 | GTGAACAGGACTAGC[-/C]TCCTTCCTTAGAAAG | 8853 |
rs374723061 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9339412 | TCCCCGTCTGTCAAA[C/T]AGGAATAATACAGCC | 8853 |
rs374724954 | snp | A/G | 1.69298e-05 | 0.0029094 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327929 | AAGTTCTTCTCTGTT[A/G]TGTTATCTTAAATGT | 8853 |
rs374727970 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9299673 | GCCCAGGACGGCTGA[C/T]GACGTAGGAGACGGG | 8853 |
rs374743691 | snp | A/G | 0.000133429 | 0.0081668 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320364 | CGTTTTTAAATTTAC[A/G]TATAGGTAATTTGGG | 8853 |
rs374752937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211886 | CTTCAGAAGGACATC[A/G]CCTTCTTGCCCAGAG | 8853 |
rs374770550 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317667 | ACTTACACAATCACT[C/G]ACATCCATAATCACA | 8853 |
rs374770551 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364137 | GGGTACTACTATCAT[A/G]ATCAATTTCACTATC | 8853 |
rs374814644 | in-del | -/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317625 | ATCCACAATCACACC[-/CA]CACACACCCATACAC | 8853 |
rs374849192 | snp | A/G | 1.66203e-05 | 0.00288268 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401268 | TTGTTCCCTCTCCTG[A/G]CCCAGACCAAGTTGA | 8853 |
rs374854043 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391118 | TCTGTAAGTGTGGAC[A/G]GTGGAAGCCGGCAGC | 8853 |
rs374860170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397611 | TCTTAGGGTAGGAGT[C/T]AGCAAACTATGGCTC | 8853 |
rs374864722 | snp | A/C/G | 0.000152215 | 0.00872272 | missense | ASAP2 | GRCh38.p7 | 2:9388483 | GGCAGCCCACCTCCC[A/C/G]CCCAGCCTGCAGCCC | 8853 |
rs374869948 | snp | A/T | 0.000148357 | 0.00861141 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344668 | GCTAGAGTTTAAATG[A/T]ACGTTCGTTATCTTG | 8853 |
rs374875425 | snp | C/T | 0.000307953 | 0.0124049 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403333 | CGCTGACTGAATTGC[C/T]ACTGAACAAAAGCAT | 8853 |
rs374878966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387171 | GTGAGCTGGGATTGC[A/G]CCACTGCATTCCAGC | 8853 |
rs374888567 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9268788 | CGAGGGGAGAGGAGA[C/T]AGGACGGGAGAGCGG | 8853 |
rs374916169 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264993 | ATTTGAAAATTAGCC[A/G]GGTGTGGTGGCATGT | 8853 |
rs374920804 | snp | C/T | 5.26931e-05 | 0.00513262 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374744 | TGCAAGGCAATTACG[C/T]TTGGTTTCAGGAATG | 8853 |
rs374930054 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248384 | TGTCATTTTTTTTTT[-/T]CTTCTGGGTAATTAG | 8853 |
rs374953608 | in-del | -/AACA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9326248 | ACAAACAAACAAACA[-/AACA]TGACTTTAAAATTAT | 8853 |
rs374963036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321627 | CACTTCACTCAGCCT[C/T]CCTTGCTGCCCGTCT | 8853 |
rs375002980 | snp | A/G | 0.000115332 | 0.00759293 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380726 | ACGCCTCCTTTGCTC[A/G]CCCTTGAATTTTAGC | 8853 |
rs375039940 | in-del | -/GTGG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305741 | GGAGAGGCTGTAGTA[-/GTGG]GGTATAGATATTGGT | 8853 |
rs375042900 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331815 | TGATGAATGTTGAAT[C/T]GACTTGTTCTTTGAG | 8853 |
rs375047975 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312389 | CTTCTGCTGACTCCT[C/T]GACTGCCACGGCTGG | 8853 |
rs375058373 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337100 | CAGAAGTTCTTTATA[A/G]TTTGTTGTTTTTTGT | 8853 |
rs375065022 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307263 | TCCTGTTCCTAGTCA[C/T]GCTGGCCTTGCTGGT | 8853 |
rs375066368 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240095 | AGATTTTCACAGTTG[A/G]TCTTCACAGACTTAT | 8853 |
rs375082691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360675 | GGAAAAAGATGTTCA[C/T]TATATAGTACATTCA | 8853 |
rs375110388 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362673 | GGGAGACCTCCATCT[C/G]TACAAATAATTTTTT | 8853 |
rs375129759 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9340971 | AGTGCCCACCTACCC[G/T]GCATACTCAGGCACA | 8853 |
rs375137493 | in-del | -/TCTG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249317 | CCCGTGGCCTGTCTG[-/TCTG]CCCCATTCTGCCCTC | 8853 |
rs375140981 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390407 | GTGCACAGCCTCCAA[C/T]ATGGGGTCACACCTA | 8853 |
rs375157989 | multinucleotide-polymorphism | CA/TG | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278437 | AGAATTGCTTGAACC[CA/TG]GGAGGCAGAGGCTGC | 8853 |
rs375170989 | in-del | -/GTCT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338341 | TATCTCTCTCTGTCT[-/GTCT]CTATCTCTCTCTCTC | 8853 |
rs375171879 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381534 | TTGAGGCCAGGAATT[C/T]GAGATCAGCCTGGCA | 8853 |
rs375189555 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209653 | TGGCTCACTGCATCC[C/T]CTGCCTCCCAGGTTC | 8853 |
rs375213211 | in-del | -/GTGT | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406079 | TTCCTCAGGCCTTCA[-/GTGT]GTGTTTGTCACTGAG | 8853 |
rs375215885 | snp | A/G | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403624 | GCCTCTACGGAATTA[A/G]CTAAACCTAAAAATG | 8853 |
rs375218676 | in-del | -/TCTTAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274633 | CAGCCTAACACTCAA[-/TCTTAA]ACAATCATTCTAGCT | 8853 |
rs375246163 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263365 | CCAGGCTGGCTGGGG[G/T]GGTCCTGCCCAGAGC | 8853 |
rs375255389 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351503 | AAATAAGATAAACCT[C/T]TTTTCCTAGGTAGTT | 8853 |
rs375283836 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397750 | TATATATATATATAT[-/A]TTTTTTTTTTTTTTT | 8853 |
rs375290888 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332332 | TTCTCCTGACGCCAG[A/G]GCTGACTGCACTTTG | 8853 |
rs375298686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385586 | GCTAATTATGTACTT[A/G]TAGGCAGCCTTTTGC | 8853 |
rs375306615 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248490 | CGCAGTCCAGGGTGT[A/G]CCTCTTGTTTATTCT | 8853 |
rs375311012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228685 | GGTGCCTCTGGATCA[C/T]TGAATTTCTCAGACT | 8853 |
rs375332819 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373313 | CGGGCACCCTGGGGC[A/G]TGATTTCCTCTCCAG | 8853 |
rs375349415 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222062 | CAAAGTGCTGGGATT[A/C]GAGGCGTGAGCCACC | 8853 |
rs375351258 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395503 | ATAAAGAATTTGGAG[A/G]CTAGGCACCATGGCC | 8853 |
rs375352768 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381471 | AGGCACAGTGACTCA[C/T]GCCTTGTAATCCCAA | 8853 |
rs375366988 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362344 | CTCTCCTCTTTTGGG[-/A]TAAATAGAACAGCCT | 8853 |
rs375367455 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370825 | CTCAAGGTGAAGGAG[C/T]TCTTCCTGGGCGAGC | 8853 |
rs375386878 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317710 | CACACGCCCACACAC[A/G]CCCATACACAATCAC | 8853 |
rs375396031 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9283874 | ATCAGGAGGGCCTCA[A/C]CCACTTGACCTCATC | 8853 |
rs375415297 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257070 | TCTTTCCCTAACAGC[C/T]TGTCACAGGGCGTTT | 8853 |
rs375418456 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381488 | CCTTGTAATCCCAAA[A/G]CTTTGGGAGGCTAAG | 8853 |
rs375420769 | snp | C/T | 0.00100103 | 0.0223497 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400839 | GCAGGCAGTAAGTGA[C/T]GAGCCCCCTTTCCTG | 8853 |
rs375421035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263814 | GTTGACGGCCGTCTG[A/G]AGGTCATCAGCTGAG | 8853 |
rs375430614 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271707 | AAGTAGGGAAGCGAC[A/G]GGGCCCAAGGGGGAG | 8853 |
rs375434864 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244702 | AGCCCAGTGCCAGTG[A/G]CACTTAGGGACTCTT | 8853 |
rs375436568 | snp | C/G | 3.29571e-05 | 0.00405924 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334821 | TTCACACGGTGAGTA[C/G]CTTCCCTCCCACTGT | 8853 |
rs375449899 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234243 | TCTTCTTGACGCTAT[G/T]TGTGCTGCCTCTCAG | 8853 |
rs375456459 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317891 | TTCACTCACATACAC[A/C]CTCATGTGCATTCAC | 8853 |
rs375460705 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377635 | GACTCCCTGATCGTG[G/T]TTTGAGCCATGTGTG | 8853 |
rs375481405 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265794 | TTTATTTTTTTGAGA[C/T]GGAGTTTCACTCTTG | 8853 |
rs375498259 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9226205 | AATCAACATTATAAT[A/G]AAACTCTTAAAAATC | 8853 |
rs375498949 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373138 | GAGCATGTGCCGGGG[C/G]ACGTTGAGGCACCCG | 8853 |
rs375556846 | in-del | -/TTTG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302490 | TTTTTTGTTTGTTTG[-/TTTG]AAACAGAGTCTCACT | 8853 |
rs375560832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262132 | GGGAATGATAGGCGC[A/G]TGCCATCATGCCTGT | 8853 |
rs375570723 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349488 | ATTGGTAACAATCCA[C/T]GATCAGTGGTGCTTT | 8853 |
rs375571122 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381011 | GGACCCACCCCTCGC[A/G]GTGAGACTTGGGGTG | 8853 |
rs375585046 | snp | A/C/G | 0.000481819 | 0.0155141 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399988 | GGCAGGTGCCCTCCG[A/C/G]TAGCAGTAAATCTAC | 8853 |
rs375599593 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9340061 | AGAATCTCCCTCTGT[C/T]GTCTAGGCTGGAGTG | 8853 |
rs375624483 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9340254 | TCTCGAGCTCCTGAC[A/C]TCGTGATCTGCCCGC | 8853 |
rs375645991 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294868 | TGGCTCAGAAAGCAG[C/T]GAGCGAGGGAGTAAG | 8853 |
rs375658377 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272081 | TATGTACACAGCAGT[A/G]GAATTGCTGGATCAT | 8853 |
rs375658594 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230991 | CTTGCTTCCTGGCAG[C/T]ACAAACCCCTGCCTG | 8853 |
rs375672013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358568 | GAAGAAGAGGGAGAG[C/T]AGATGTGTGCATATT | 8853 |
rs375674458 | snp | A/T | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404999 | TTGCACAGTGCACTT[A/T]TGTCTATTTTAACAA | 8853 |
rs375679866 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9386575 | CAGCAGACAGCAGCC[A/G]TGGGCTTTGCAATTT | 8853 |
rs375681606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231511 | CGCTGGTCATGTTAC[A/G]TAGCTGCCACCTCCC | 8853 |
rs375691674 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344858 | GAGGTTGGTGTTGGA[A/C/G]GACTTTCTGAAGTTA | 8853 |
rs375750693 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219198 | AATACTGATTTTCTT[A/G]TATCCAGCGAGCTTC | 8853 |
rs375756515 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392930 | AGAGCTCTTCCCCTC[C/T]GTGGGCCTCAGCCTC | 8853 |
rs375764510 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322929 | AAATACTTGTTGAGT[-/T]AAGTGGGAAGACCCG | 8853 |
rs375789125 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9323284 | CAGGTCCTACAGCCC[A/G]GGCTGTGCCGGCTCT | 8853 |
rs375793564 | snp | C/T | 0.000181586 | 0.00952679 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297473 | GTGTATGAAATGCTG[C/T]GGTTACTTCAGTTGG | 8853 |
rs375796721 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294130 | CAGCCTCCCGAGTAG[C/G]TGGAATTACAGGCAT | 8853 |
rs375814958 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359155 | TGAGATTCTACAGAA[A/G]TGGAGTAAGATGGTG | 8853 |
rs375828907 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331769 | CGATTTTTTTTTTTC[A/C/T]AAAAAAATACAACCA | 8853 |
rs375829366 | snp | A/T | 1.65853e-05 | 0.00287964 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320275 | TGCCTAATTTATTAT[A/T]CTTTGTTTACAGGAT | 8853 |
rs375868345 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396292 | TCAACTAGGTTGACT[G/T]TGATTTATCTTTCAC | 8853 |
rs375868643 | snp | A/G | 0.00597247 | 0.0543191 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405949 | TCCACACCTCTGCCG[A/G]ACAGAGGTCCATGCC | 8853 |
rs375874873 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9344866 | TGTTGGAGGACTTTC[C/T]GAAGTTAGAGGGCAG | 8853 |
rs375889850 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213006 | TCTGGGTGGGGCTTC[A/G]AGCCTTGGCATTTTT | 8853 |
rs375892619 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317566 | TCCACAATCACACTC[A/T]CACACACCCACACAC | 8853 |
rs375934864 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259607 | CTGCATCTCTTTGGC[C/T]CTCGCCTCTGTCTCC | 8853 |
rs375935098 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9262187 | TTGATGGAAAAAAAA[-/A]TGTATTAGTGGAAAT | 8853 |
rs375938605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309103 | CTCCTTTGCGCTCTG[C/T]TCCAAGACCACCTTA | 8853 |
rs375940305 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9309740 | GGGAATAGTGTGTAT[C/T]TGCTTTACTGAGTCT | 8853 |
rs375950540 | in-del | -/GG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9289873 | CCACAAAGACTGGCT[-/GG]GTTTCTTGAGGAATC | 8853 |
rs375951958 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9216002 | ACATTGGACCTTCTG[A/T]GTCCTGTAATTAGGA | 8853 |
rs375960088 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9377953 | GGGGTTTCGTAAACA[C/T]TTGGTTGATAGCTGC | 8853 |
rs375964737 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294648 | AGCCACCTAGTAGGC[A/G]TTGACCTTTATACGA | 8853 |
rs375965733 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389526 | CAGGGCTGAGCAGAC[A/G]GCTGCAGCTTTGTGC | 8853 |
rs375978845 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348971 | GAGCCAGCCTGACTT[G/T]TTGGAATCCTAGCTT | 8853 |
rs375988003 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306174 | GGAGGGGCTCTAGGG[A/G]TGTAGAGAGGGAGTG | 8853 |
rs375998977 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264328 | TGCTTCTGCAGGCAT[A/G]TCTTCCAGAGACTGG | 8853 |
rs376005370 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292632 | TGTGATCTGCTCCTT[A/C]TCTACTCGACAAGTC | 8853 |
rs376020880 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278442 | TGCTTGAACCCAGGA[A/G]GCAGAGGCTGCAGTG | 8853 |
rs376025539 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260705 | CCTGCTTCCCATTCT[A/G]CCATAGGGGAATGGG | 8853 |
rs376045581 | snp | G/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208350 | GAGTGTGTGTGTGGG[G/T]GGGGGGGTGGGTGTC | 8853 |
rs376046856 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248288 | AAGCCAAATTATATT[C/T]AGCATTTGTTAATAA | 8853 |
rs376063524 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401611 | GGGTGGCTTCCTCCC[-/CT]GTTAGGGTGCAGTTT | 8853 |
rs376094101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294525 | CCTACCAACTCTATG[A/G]TCTGGGGCAGGTGAC | 8853 |
rs376102794 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9330760 | GAAGAAGCTATTCTG[C/G]GATTTCCTTCCCCCG | 8853 |
rs376111263 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258242 | AGAGCGATACTTCAT[C/T]TCAAAAAAAAAAAAA | 8853 |
rs376115048 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328183 | AGGTGAGTGATTGCC[A/G]CAGCTTGGAGGAAGA | 8853 |
rs376116627 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279701 | GCCTGGCTGATGGGG[A/G]CCTGGATTCATTCCT | 8853 |
rs376176576 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9335060 | CAGTCTTAATTTTCT[G/T]ATTGGTTCTGTTGTG | 8853 |
rs376193798 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346952 | TGGCAGATAGTACGG[C/T]TATAACCGGCATTAC | 8853 |
rs376201548 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9400779 | TCTGGGTCCTCTGTC[C/T]AATGCTATGGTCCTG | 8853 |
rs376208691 | snp | C/G | 6.89738e-05 | 0.00587215 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327796 | GTATTCTGCTTACTT[C/G]CATGACATTTCCTTT | 8853 |
rs376211023 | snp | C/T | 1.68783e-05 | 0.00290498 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320388 | ATTTGGGATTTCAAA[C/T]TTAAACCAACCTCGT | 8853 |
rs376216551 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380840 | AAGGACGGGGTGGGG[C/T]ACCTGTCACGGGACA | 8853 |
rs376225033 | snp | A/G | 3.30038e-05 | 0.00406212 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9380793 | GCGCCTCAAGCACGA[A/G]CACTGTGAGGAGCTG | 8853 |
rs376259305 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383426 | CGCCTGGCTAAAAAA[C/G]TTTTTAAATTTTTTG | 8853 |
rs376268191 | snp | G/T | 1.68567e-05 | 0.00290312 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358939 | AAATGAGCTGTAAGC[G/T]AAATTTTACTTTTGG | 8853 |
rs376279895 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225287 | TCTCACAGATCTACT[C/G]TGTCCCAGAGTCTGT | 8853 |
rs376283643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237051 | AAGGGGAGGGGAAGG[A/C]AGGAACAGCTTGGAG | 8853 |
rs376289923 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9215482 | TAATGTAATGTTCAT[A/G]TCTTTTATTGCAAGT | 8853 |
rs376291601 | snp | A/G | 4.97199e-05 | 0.00498573 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320344 | AACAAAAATGTGAGT[A/G]TTCTCGTTTTTAAAT | 8853 |
rs376296754 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271029 | CGATCTCGTGACCTC[A/G]TGATCCACCTGCCTC | 8853 |
rs376297062 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9241961 | TTTGTTATCAGGCGG[A/G]CACATGTGAATTTCA | 8853 |
rs376301112 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374857 | CAGTCTTTGCGAGGC[C/T]GTCAAAACGAGAGAT | 8853 |
rs376308531 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9252871 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 8853 |
rs376309204 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9289557 | ACATAAAAAAAAATA[C/T]GCAGTAGCCCAGTCT | 8853 |
rs376314081 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338256 | AGTGCTGAAACCACC[A/G]TGGTTTTCCACTCTG | 8853 |
rs376327302 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337222 | CAAGACCTAACTCAA[C/T]AGTCTCCTAGTTGTG | 8853 |
rs376358778 | snp | C/G/T | 0.000115531 | 0.00759948 | utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207086 | TGCGGCTGTGCGCCA[C/G/T]CGCCCTCGCGCCGAG | 8853 |
rs376382602 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266068 | GGGATTACAGGTGTG[A/C]GCCACCACACCCAGC | 8853 |
rs376412211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364157 | ATTTCACTATCATAC[A/G]TGAAGTTAATAAAGG | 8853 |
rs376422553 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221129 | CCCAAGATTGTTTTG[A/G]CTATTGAGGCTCCCT | 8853 |
rs376503789 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357059 | TCCCCTTTTCATTCC[-/T]CTAATTCTATGACAA | 8853 |
rs376512954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251697 | TTTCCTGGGGACCTT[C/T]GGTTTTGTGATGAGG | 8853 |
rs376545698 | in-del | -/TCATGT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313425 | CGTGTACATTCATGT[-/TCATGT]GTGTACTCCCGCTTC | 8853 |
rs376547614 | in-del | -/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9401933 | CTGTGACAGGGAGGT[-/CA]CACACACACAGTCTG | 8853 |
rs376564245 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9223366 | TTTGCTCTTTTAATT[G/T]ATGAACCTTCTTGGA | 8853 |
rs376570439 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315084 | GAAGACGTTTCCGTC[C/G]AATAGAACAAATTGA | 8853 |
rs376571843 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9287803 | GCTAACAACAATGAT[C/T]GGAATTTAGATGGTG | 8853 |
rs376574722 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221321 | TCATTTTCTTTTCTT[C/T]TCTTTTTTTTTTTTT | 8853 |
rs376585923 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387619 | TGTTTGGGAAGGGGA[A/G]CTTCAGGGAAAATGC | 8853 |
rs376591339 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405871 | ACACTTCTGAAAATC[C/T]GCTTTGTGTGTCTTA | 8853 |
rs376601465 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361857 | GGTGTGAGCCACTGC[A/G]CTTGGCCTCAAGCCT | 8853 |
rs376641455 | in-del | -/GAT | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212591 | CCAAGAATTTGGGGT[-/GAT]CCTCAATTCTTCCCA | 8853 |
rs376662845 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205855 | AGAATTTCCTTAAGA[A/G]CTGTAAATAAAAATC | 8853 |
rs376668354 | in-del | -/TCTGGC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9238074 | GGGAGGAGCCATGGC[-/TCTGGC]CTCCGACTGCTGGGG | 8853 |
rs376684276 | in-del | -/CAAT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317354 | ACACACACCCTCACA[-/CAAT]CATTCACATTCACCC | 8853 |
rs376697505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345827 | GGGGTCCAGAGAAAC[A/G]GCCCTGAGGTTCATA | 8853 |
rs376707608 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366493 | TATAAACCAGGCGCT[C/G]TGACATTGGGGTTCA | 8853 |
rs376715709 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386579 | AGACAGCAGCCGTGG[G/T]CTTTGCAATTTAGAA | 8853 |
rs376734786 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253379 | ATGTTGGCCAGGCTG[G/T]TCTCCAACTCCTGAC | 8853 |
rs376736268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324384 | TCTACTTATCTTAGC[C/T]TGTTTTCTGTTGCTA | 8853 |
rs376739108 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234237 | CATTTTTCTTCTTGA[C/T]GCTATTTGTGCTGCC | 8853 |
rs376740755 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371032 | ACCAGGGGTACCTAA[C/T]GAAAGCAGGGCATTT | 8853 |
rs376740776 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300833 | CCTTCTTGACTGATC[A/G]TAAGGGTTCAAGTTT | 8853 |
rs376749131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233575 | CCTCTCGTTATAGCT[C/T]AGCCTATGTAGTGAT | 8853 |
rs376756150 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266024 | GTGATCCACCCCCCC[-/C]ACCCCCTGCCTTGGC | 8853 |
rs376769255 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371175 | AAGAAATTTACATCC[C/T]CCAACCCCGGGCTTT | 8853 |
rs376780814 | snp | C/T | 3.30677e-05 | 0.00406605 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374914 | TGATGGTGTGGATCT[C/T]ACGGAAAAAATCCCA | 8853 |
rs376797241 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272602 | CTTTGGTTGCCTGTG[C/T]TTGTGGGGCATTACT | 8853 |
rs376799423 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9273578 | AATCAGTCTCCTGGA[A/G]CATTCGGGGATCAGA | 8853 |
rs376816649 | snp | A/C/G | 5.0252e-05 | 0.00501237 | missense | ASAP2 | GRCh38.p7 | 2:9388513 | CCCAGCACCACCAGC[A/C/G]CCCCCCCGCTTCCTC | 8853 |
rs376837545 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343072 | GGATGGTGAGCTGCT[C/G]AGTGGCAATGATGAG | 8853 |
rs376841220 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302999 | AGTGTGAGCTGATTG[A/T]CCATATTAGTAAGGC | 8853 |
rs376861732 | snp | A/G | 3.31851e-05 | 0.00407326 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400124 | TGGTCCATGGGGGCA[A/G]TGTGGGGGATGTTTC | 8853 |
rs376867714 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361378 | CCCACGGCTCCCCCA[A/G]TCCATTTTTTGTATG | 8853 |
rs376887717 | snp | A/G | 1.65869e-05 | 0.00287979 | missense | ASAP2 | GRCh38.p7 | 2:9400781 | TGGGTCCTCTGTCCA[A/G]TGCTATGGTCCTGCA | 8853 |
rs376922630 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373083 | AAGTCAGCCAGCACC[A/G]CAGTGAGCTCAGTGC | 8853 |
rs376932865 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9231687 | CCTGGCCCTTGGGTG[A/T]CCCTGGCATCTGCAT | 8853 |
rs376947580 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264198 | CCTGTCTCAAAAAAA[-/T]AATAATAATAATAAT | 8853 |
rs376949638 | in-del | -/CTCTCT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338364 | TCTCTCTCTCTCTCT[-/CTCTCT]TTCTCTTGCTCCCTC | 8853 |
rs376961986 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317811 | GCATTCACACACTCA[A/C]ACAATCACACCCTTA | 8853 |
rs376964304 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214737 | TGTTGTCACTGCCAG[A/G]TGCCAGGGATGTAAA | 8853 |
rs376985677 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9215350 | AAAATTTTTACCATG[-/C]CTCATAATGCTTCTT | 8853 |
rs376987956 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316989 | CACCCTCTCATGTCC[A/G]CTCTCATACACTCTC | 8853 |
rs377003709 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214008 | GGGATCTGCTCATGC[A/G]ACCCTCTGCTGTTTC | 8853 |
rs377005133 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242945 | ATTTTTGCTCAAAAA[A/G]AGAGGCATAAGCAGC | 8853 |
rs377011905 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256125 | CGTTCAGACATTCAT[A/T]GAAATGGCAGGAGAA | 8853 |
rs377047010 | snp | C/T | 3.4929e-05 | 0.00417891 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393460 | GGCTGACCCTCTGCA[C/T]GTCTCTCCCTGTCCT | 8853 |
rs377080194 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221446 | AGGCATGAGCCACTG[C/T]ACCTGGCCTCATTTT | 8853 |
rs377081497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391307 | ACGTGCCAAGTGCCC[C/T]GTGTTGTATGGCTCC | 8853 |
rs377086521 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337241 | CTCCTAGTTGTGGGC[-/G]TGTTGTGTTTTCTGT | 8853 |
rs377095422 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381509 | GGAGGCTAAGGCAGG[A/G]GATGATGGCTTGAGG | 8853 |
rs377096338 | snp | C/T | 3.30049e-05 | 0.00406219 | missense | ASAP2 | GRCh38.p7 | 2:9374816 | TACGCAAGGAAGAAG[C/T]ACGCGGATAACGCGG | 8853 |
rs377099778 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266311 | ACCACCACACCCGGC[C/T]AATTTTTTTACTTTT | 8853 |
rs377103805 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306715 | TCAGCGAATTGATAG[A/C]AATTCAGCATGTGCT | 8853 |
rs377103929 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227291 | GGGACTTGGGGTTGT[A/G]CGCCCCTGTGCCCTG | 8853 |
rs377105478 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9368454 | TGGGAATGCAGGCTT[C/T]AATGAGATCATGGAA | 8853 |
rs377107800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281837 | ATCACCCCACTGTGA[A/G]CCTCAGGTGAGTAAA | 8853 |
rs377163614 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207415 | GAGATGGGTGATGGC[A/C]ACCTTGGGCCTCTTT | 8853 |
rs377201237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240353 | CCATTTCCTGGGCCC[A/G]GGTGATCCTCCCACA | 8853 |
rs377202646 | snp | A/G/T | 4.94249e-05 | 0.00497096 | synonymous-codon, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9297391 | AGATTTAGGAAGTGC[A/G/T]TTCCTGAAGTTCTCA | 8853 |
rs377210326 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318859 | AAAGAAAACTGCTAT[A/T]TTGGAAAAAGTAAAG | 8853 |
rs377301065 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9367622 | AAAAATCAGCTGGGC[A/G]TGGTGGCGTGTGCCT | 8853 |
rs377305971 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401721 | TGGATTAGTGGAATC[C/G]GGTGTCTGGAGAGAG | 8853 |
rs377365765 | snp | C/T | 0.000153988 | 0.00877328 | missense | ASAP2 | GRCh38.p7 | 2:9350895 | TTTGACCTCATTTCA[C/T]GTAAGGCTCCCTCTG | 8853 |
rs377375537 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295662 | TGCGGGTGTGTGTGT[A/G]TGCACATGTATGTTT | 8853 |
rs377379521 | snp | A/G | 1.64741e-05 | 0.00286998 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391067 | GTGGGTTCAGTTCAG[A/G]CAGCCTCCTCTGCTA | 8853 |
rs377390154 | snp | A/C/G/T | 6.76918e-05 | 0.00581742 | synonymous-codon, missense | ASAP2 | GRCh38.p7 | 2:9401387 | CGGGGAGGAGGACCA[A/C/G/T]GAGTGGTGGGTGAGT | 8853 |
rs377394039 | snp | C/T | 1.73558e-05 | 0.00294578 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350919 | CCCTCTGAGATGCCG[C/T]GCCATAGAGACGTTG | 8853 |
rs377423224 | snp | C/T | 4.97228e-05 | 0.00498587 | missense | ASAP2 | GRCh38.p7 | 2:9385260 | CTGACCCAAGCCTTA[C/T]CTGGAAGATTTAATT | 8853 |
rs377447754 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9231283 | TTGACTCCTCACCAG[A/G]TTTTCAGGCTCTGCC | 8853 |
rs377452852 | snp | C/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211742 | GTCCATGGGACCAGA[C/G]CCCTCCTAGCAGCAA | 8853 |
rs377472537 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9270613 | ATTTTTAAATGTACA[A/G]TAAATTATTGTTGAC | 8853 |
rs377472546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297821 | AAATATGTTTCAGGC[C/T]CATCTTACACAGCAA | 8853 |
rs377481923 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212263 | GAATCCTGTAAACAA[A/G]TCAGTGCAGTAAAAT | 8853 |
rs377496975 | snp | G/T | 0.000151534 | 0.00870311 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380860 | GTCACGGGACAGGGA[G/T]CCAAGCCTGTCCTCC | 8853 |
rs377512134 | snp | C/G | 1.68818e-05 | 0.00290527 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403359 | AGCATTAACAGTTAT[C/G]TTCCTGTTTCGTTAT | 8853 |
rs377545255 | in-del | -/TTCT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352378 | CAGGGTTTTAGGCCT[-/TTCT]GTTTTCTGAACTAGT | 8853 |
rs377546737 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254926 | GACACGTTTTATATT[G/T]TGACTTCGGGAAATA | 8853 |
rs377549631 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235275 | TCGTCCTGTGCACCA[G/T]TGTGGCAGGGATGGA | 8853 |
rs377580412 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9269893 | TGTGCACCGTCCCCA[C/T]TGTCCCCACACACTG | 8853 |
rs377613521 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9354236 | GACCTTCCAGGTCCA[C/T]ATGGCAGGTTAGCGG | 8853 |
rs377616051 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402113 | CAGAGCAGACAGTTC[A/G]GCTGGGAACTCACAG | 8853 |
rs377621642 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355433 | GAGCAGCACAGAATG[A/C]TGCTGCCACATCCCA | 8853 |
rs377625467 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325874 | TTCACAGTTGAGTGA[C/G]AGCTGTACTATATGC | 8853 |
rs377690823 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285358 | AGAACCCCCCATCCC[C/T]ACTTCAAACACTGAA | 8853 |
rs377691011 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298421 | TTGCTCTTTCTCCCC[A/G]TCTTCACTTATGAAC | 8853 |
rs377699675 | snp | C/T | | | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391323 | GTGTTGTATGGCTCC[C/T]TGTGGCTCTTGTGCA | 8853 |
rs377706530 | snp | A/G | 0.000132677 | 0.00814375 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9400758 | GGATCTCTCTGCAAC[A/G]GAAGCTCTGGGTCCT | 8853 |
rs377730857 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309761 | TACTGAGTCTAGCAA[G/T]TCTCTAGCCACATGT | 8853 |
rs377738222 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381519 | GCAGGGGATGATGGC[A/T]TGAGGCCAGGAATTC | 8853 |
rs377741658 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247467 | CTCATGCGCTGCTTT[C/T]GGTCCATCGTCTAGC | 8853 |
rs386389500 | in-del | -/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281150 | GATTTTTTTTTTTTT[-/TT]TACTGCGTTCACTTG | 8853 |
rs386642980 | multinucleotide-polymorphism | AAG/CAA | | | upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9204862 | GGCTTATGCAGTAGG[AAG/CAA]GTTAGATTTCTAAGG | 8853 |
rs386642981 | multinucleotide-polymorphism | CA/GG | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210930 | GGAGGCCAAGGCGGG[CA/GG]GATCACTTGGGGTCA | 8853 |
rs386642982 | in-del | GATCC/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232266 | CACTGCCCTGCGCCC[GATCC/T]TTTTACACAGGTGGT | 8853 |
rs386642983 | multinucleotide-polymorphism | ACA/GCT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256385 | GGCAGTGTCAACTGT[ACA/GCT]TAAAGAAATTAGCGT | 8853 |
rs386642984 | in-del | AA/TGT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267638 | GCAGTTTCTCATGCC[AA/TGT]AATCCCAGCACTTTG | 8853 |
rs386642985 | multinucleotide-polymorphism | CAT/TAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9270947 | ACAGGTGCCCGCCAC[CAT/TAC]GCCCGGCTAATTTTT | 8853 |
rs386642986 | in-del | AACCACACAACA/TCACAACCACACAACACT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317122 | ACCCCACGCAATCAC[lengthTooLong]CACATCCCAATCACA | 8853 |
rs386642987 | multinucleotide-polymorphism | AT/CG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317550 | CACACAATCTCTCAC[AT/CG]CCACAATCACACTCT | 8853 |
rs386642988 | multinucleotide-polymorphism | CT/TC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318245 | TGAAATATTTTTTCT[CT/TC]ACTGCAATGATTGTC | 8853 |
rs386642989 | in-del | ACATGATTTTGTGGCTCTTTT/CCACGA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322513 | AGCCCACCTTAGCAG[ACATGATTTTGTGGCTCTTTT/CCACGA]TTACCCTGGTGGCTC | 8853 |
rs386642990 | in-del | AGGGTTTCACCATATT/TAAAAATCTCTACTAAATCAGCCA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348306 | ATTTTTAGTAGAGAC[lengthTooLong]GGTCAGGCTGATCTG | 8853 |
rs386642991 | multinucleotide-polymorphism | AT/TC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9360888 | TTTAACAGTTGACTC[AT/TC]ATGAGCTGGTAGGAG | 8853 |
rs386642992 | in-del | -/G/GT/TGGG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387077 | CGGGCTTGGTGGTGG[-/G/GT/TGGG]GGGGGGGCGCCTGTA | 8853 |
rs386642993 | in-del | GGC/TG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387078 | GGGCTTGGTGGTGGG[GGC/TG]GGGGGGCGCCTGTAG | 8853 |
rs386642994 | multinucleotide-polymorphism | GGC/TGG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387078 | GGGCTTGGTGGTGGG[GGC/TGG]GGGGGCGCCTGTAGT | 8853 |
rs397699205 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258259 | AAAAAAAAAAAAAAA[-/A]TTTCTATGATTACCA | 8853 |
rs397711666 | in-del | -/C | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9209002 | TAAAATTGGCATACC[-/C]TTTCTCTGATTAATT | 8853 |
rs397727073 | in-del | -/TA/TC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343408 | GGCACTGGTGGCCTC[-/TA/TC]CTACTCTCAACTCAG | 8853 |
rs397755709 | in-del | -/GTG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9289993 | AGGAAGAAGCCGGTG[-/GTG]AGAGGCATCCTTCCA | 8853 |
rs397756780 | in-del | -/AAAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9344439 | GTTGTTGTTAAAAAA[-/AAAA]CACATTAGGCATAAG | 8853 |
rs397770902 | in-del | -/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274340 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAT | 8853 |
rs397771522 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260423 | TGGATTGTAGAAAAA[-/A]TGAAAGGTTCATGCC | 8853 |
rs397868670 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353566 | TCTAAAAAAAAAAAA[-/A]GACATTTGGGCAGTT | 8853 |
rs397869342 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9391593 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC | 8853 |
rs397870173 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217926 | GCTTTTTTTTTTTTT[-/T]ACATGAAAAAATAAT | 8853 |
rs397873056 | in-del | -/TAGT | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210427 | ACCAGATTATATAGT[-/TAGT]GAGTCCACAGGCCCC | 8853 |
rs397976704 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311047 | AGTGAACTCGGGGGG[-/G]AAAAGCTAAGACAGG | 8853 |
rs397983827 | in-del | -/A | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234131 | AAAAAAAAAAAAAAA[-/A]GGAAGAGGGGAGTGG | 8853 |
rs397983830 | in-del | -/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345003 | ATGTTTTTTTTTTTT[-/T]AATTTTAATTTTAAT | 8853 |
rs398071238 | in-del | -/GGG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257296 | AGTCTGAAAGCAGGG[-/GGG]ACTGTTTTATAGTAG | 8853 |
rs398080019 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9209001 | TTAAAATTGGCATAC[-/C]CTTTCTCTGATTAAT | 8853 |
rs398090132 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9306528 | GAAGGGTTCCTAGGG[-/G]TGAGAGGGGCTTGAG | 8853 |
rs527236485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306284 | GGGATAGAGATACCG[A/G]GTGGGAGGGCTGTAG | 8853 |
rs527262483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395797 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGGGT | 8853 |
rs527265414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261392 | CTTAAACTCTTTGAG[A/T]CAGTTTCTTCTCCTT | 8853 |
rs527284393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343713 | TGGTCTCCCCAGATG[C/T]TGGGATTACAGGCAT | 8853 |
rs527314250 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286258 | CAAAAATTAGCTGGG[C/T]ATGATGGTGTATGCC | 8853 |
rs527334451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273520 | GGAAGAGTAATTCAC[A/G]CAGAGCCAGCTGTGC | 8853 |
rs527334508 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267638 | GCAGTTTCTCATGCC[C/T]GTAATCCCAGCACTT | 8853 |
rs527348133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356605 | CAAAGTTTGAAATGC[C/T]TTTTGAGAAATGAAA | 8853 |
rs527363706 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228577 | GTTATGCTTGGCAGA[C/G]TGAGCGGCCCCCATC | 8853 |
rs527365797 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9220081 | TCTATCAAATGTGTA[A/T]GATACATTTTGTTTA | 8853 |
rs527392401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313440 | TCATGTGTGTACTCC[C/T]GCTTCATGAAAAACC | 8853 |
rs527403398 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284022 | TGACTCTTCTGCCTC[C/T]CTCTTCTACATATAA | 8853 |
rs527410569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350203 | CTTGGTGTCGTGTGT[A/G]GGGGAGAGGGTTTGG | 8853 |
rs527443856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377133 | TAAAGACAGAAAAAG[G/T]ACTGCCAGGTGTGAG | 8853 |
rs527458325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211600 | TAATCTACTTCCTTC[C/T]GGGGCCATAATTCTC | 8853 |
rs527480369 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249930 | GGAACATTGGGCCAC[C/T]GTCTCCTGCCCATCA | 8853 |
rs527518421 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377641 | CTGATCGTGGTTTGA[G/T]CCATGTGTGTACTGG | 8853 |
rs527519023 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243515 | GTAACTGTTAAAATA[A/C]AACTTTGCTTACAAT | 8853 |
rs527537037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337844 | GAGAATACTACTCTT[C/T]GGTATTTCCATTATT | 8853 |
rs527539749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207979 | GCTAAGCAGTACGCT[C/T]TCCAGGTCCTGGGGA | 8853 |
rs527565485 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262049 | AGACAGGGTGTTGCT[A/T]CGTTGCCCAGGCTGG | 8853 |
rs527582899 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382574 | TTCTCTCATCCTGGT[G/T]GAAAAGGCTGGGTTT | 8853 |
rs527598583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338437 | GTGCCACCCAGGCAG[C/T]CAAGGTCCACCACAG | 8853 |
rs527602528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255600 | TCGGCAGATGGTGTC[A/G]TCAGAGATTATGGAG | 8853 |
rs527645800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237775 | GAGTCTTTTCTTGCT[C/T]ACCTGGTGGAGTACA | 8853 |
rs527650022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319554 | GGCTCAGTGCTGCAT[A/G]TCAGGCTGCCAGGGT | 8853 |
rs527651806 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, missense | ASAP2 | GRCh38.p7 | 2:9389801 | CCCTGGCTTGATGAG[G/T]ACGTCCCTGAGCACA | 8853 |
rs527661687 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233212 | GATGTCTGTGTGACA[A/G]TTATAATGAAGGCTG | 8853 |
rs527662347 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9231160 | TGGGGGAAAGGCAGT[A/G]GCTGGGTGTTTCTCT | 8853 |
rs527688573 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387193 | CATTCCAGCCTGGGC[A/G]ACAGAGAGAGACTCT | 8853 |
rs527697244 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275047 | TTGAAGTTTACCACC[A/G]CTTCCAGTCCCATGT | 8853 |
rs527729905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402404 | GGAGGCCGAGGCAGG[C/T]GGAACACTTGAGGTC | 8853 |
rs527772405 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288864 | AGGAGGGAAGCAGCT[C/T]TCTGGTTAAGGAGAG | 8853 |
rs527783974 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387081 | CTTGGTGGTGGGTGG[C/G]GGGGCGCCTGTAGTC | 8853 |
rs527786164 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326203 | CTGGGCAACATGGTG[A/T]GACCTTGTCTCTACA | 8853 |
rs527803631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244166 | AAAAATTTGGTGGCA[C/T]GCACCTGTGGTCTGA | 8853 |
rs527828200 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366066 | CCCCTTGGTTTCTGC[C/G]TGCCTGTCCTGCTGG | 8853 |
rs527841812 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9329948 | TGCCACCACACCGTC[C/T]GCTTGTCTCCATGAT | 8853 |
rs527848388 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266358 | CACTGTGTTGCCTAG[C/G]CCTGTCTGAAATGCT | 8853 |
rs527851623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390902 | TATCTTCCACATGCC[A/G]GAGACAGGAGTAAAA | 8853 |
rs527856827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9215322 | TATTGAAATTCAGTT[A/G]GGAGAATATTTTAAA | 8853 |
rs527859473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263704 | CTCTCGTTGTTCATG[C/T]GTCGTTTTTTCATAG | 8853 |
rs527860245 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301500 | GAGAATCCTGGAAAG[A/T]CTCCAAGGGCCACCT | 8853 |
rs527870424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257025 | CTGTCACTTTCTTCA[A/G]GATGTGCCTGTGTTA | 8853 |
rs527872740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345789 | GCTTTTCTGGCCCCT[A/G]TAGAAATGTCATCAC | 8853 |
rs527892316 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216080 | TCTTGTTTGTGTCAC[A/T]CGGCATGTACTGCCT | 8853 |
rs527892872 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269009 | AGGGGCCGCTGGTGC[C/T]GTGGGAGGGGCATTT | 8853 |
rs527915130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383985 | ACTTGGACACAGGGC[A/G]GGGAACATCACAAAC | 8853 |
rs527917770 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302074 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 8853 |
rs527917832 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327254 | TCATGAAGTCCTTCT[A/G]TTTCCTGACACTGGT | 8853 |
rs527925101 | in-del | -/AAT | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287797 | CTGCTGGCTAACAAC[-/AAT]GATTGGAATTTAGAT | 8853 |
rs527930252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209817 | CAGGTGATCCACCTG[C/T]CTCAGCCTCCCACAG | 8853 |
rs527951209 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351575 | CTCCCCTTTGAAGAG[G/T]CAGTCACTAGGGATT | 8853 |
rs527971500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222622 | TTTTGGCAAATAGGA[A/G]TGAGGTGTGTTTACT | 8853 |
rs527985471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396954 | TTGCAGTGAGCCAAG[A/G]TCACACCACTGCACT | 8853 |
rs528003113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315291 | GCAGAGACTAGGAAG[A/C]GGCAGCAGGGAGCAG | 8853 |
rs528018212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345160 | CAGCAAACTGCTCCC[C/T]CAGCTCTCTTTGTCT | 8853 |
rs528029050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263096 | GCATCGCCACGGCTG[A/G]AGGGCCTGGCCCAGG | 8853 |
rs528050533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372856 | ACACAGCAGTTAGCC[A/G]AACGTGCACAGCTTT | 8853 |
rs528065278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326998 | ATCAAAAAGAAAGAG[A/G]GAAAGAAGGACCTAT | 8853 |
rs528077723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290405 | ATTAAAGATTGGGTT[C/T]CGCCCTGTTGGCCAG | 8853 |
rs528092503 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283037 | AGCTCTCTTTGACTT[C/T]AGCGTAGCCCTCTTT | 8853 |
rs528147514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257644 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGAGTAC | 8853 |
rs528150828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295950 | CCCTCCAGGAACAAA[C/T]GTTCCCTCGTTTTCC | 8853 |
rs528170955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384786 | CGAGAACCAGTCCTC[C/T]TTGATTTTTATGGAA | 8853 |
rs528187929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378638 | GCTGGGCTCTAGGTT[C/G]ACCCCGGTAGTGCAC | 8853 |
rs528199100 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245693 | ATCTGGGCCTGGGGG[C/T]GCTTGCAGGATTCTG | 8853 |
rs528202695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9333000 | AGAGTTCATGCCCCA[C/T]GGCCTGTGTGTCCCT | 8853 |
rs528205778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251179 | TTTTGAAAGGAGGAA[C/T]GTGGCCAGAGCGTTG | 8853 |
rs528212090 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340233 | TCACCATGTTGGCCA[A/G]GCTGGTCTCGAGCTC | 8853 |
rs528244481 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9296499 | ACTTTGAGGCCTAAT[A/G]ATAGTAAAATGCCAT | 8853 |
rs528271560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397651 | ATCCAGCCTGCTGCC[C/T]GTTTTTTAGGGCCAT | 8853 |
rs528286976 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367903 | ATCAACCCAGAAGTA[C/T]AGGTATCATCCCATT | 8853 |
rs528296020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316800 | CAATTTAATCCATGC[A/G]GACGGTGTGTGTCCC | 8853 |
rs528313225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270856 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 8853 |
rs528315857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398053 | GTGAGCCACTGCGCC[C/T]GGCCTCAAAAGGATA | 8853 |
rs528328995 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317506 | ACACACCCACTTACA[C/G]CCCCACAATCACACC | 8853 |
rs528335513 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348990 | GAATCCTAGCTTCCC[C/T]GCTCCCTAGCTGTAT | 8853 |
rs528366758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283687 | AGAAATTTATTTTCT[C/T]ACAGGCCTGGGGGCT | 8853 |
rs528377896 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301273 | TTATAAAGCAGTTGG[A/C]AGATCTCCAGAGAAA | 8853 |
rs528382429 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367336 | CCATGCCTGGCCTGC[A/C]TGCATAATCAATAGA | 8853 |
rs528420626 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349822 | TGTAAGTGCTTGAGG[G/T]TTTCACAGGTCTGTC | 8853 |
rs528456399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341219 | GGTTTTCTCTGTCAG[A/G]CCTTCACCTGGTCAG | 8853 |
rs528459008 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385870 | CTATTTAGAGGCAGG[C/T]TTGGGACTGCACGAA | 8853 |
rs528474774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348128 | TGTCTGTTTGTTTGT[C/T]TGTTTGTTTGTTTTT | 8853 |
rs528483798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211693 | GCAGGGGTGGGGTGA[A/G]CATCTGGGCCTGCAG | 8853 |
rs528501815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230284 | CAGGGCTTGTTTGCT[A/C]AGGGTCTGGCCAGGG | 8853 |
rs528523300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379862 | CCGGGTATGGTGGCG[C/T]GCACCTGTAGGCCCA | 8853 |
rs528542831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372601 | TTCTAATATTAAACA[C/T]TGAAATATGAGCGAT | 8853 |
rs528547857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271059 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 8853 |
rs528548786 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217126 | TTCTTTTAGCAGCCA[A/C]CAGCCTCTGTAGAGC | 8853 |
rs528549854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264695 | GCGCTATAACTAAGT[C/T]CTTTGCCTCTTCCAG | 8853 |
rs528552589 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309940 | CAATGCCTGCCTCAC[A/T]CACATGTTGTAGGCC | 8853 |
rs528552827 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353042 | GGGGTATGTGGGTTT[A/G]GGTTGAAAACTGGCC | 8853 |
rs528581090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392699 | TTCATGTTTCCCCAC[A/G]CCAGTTTCCTCTCTG | 8853 |
rs528629388 | snp | A/C/T | 4.97583e-05 | 0.00498765 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374791 | CACAGCCAAGTACAT[A/C/T]GAGAGGAGATACGCA | 8853 |
rs528638211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265303 | CATTCTACATTACGA[A/G]TTGAGCATCCTTGGA | 8853 |
rs528657698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329042 | ACAGTAGGTACTCGG[C/T]TGTTTCTTGAATGAG | 8853 |
rs528692191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368925 | CGTCCTTCTTGCCAA[C/T]GTCCTTGCCTCCTTG | 8853 |
rs528692664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240589 | ATAACTAAGCACTTG[C/G]CACGCACCACGGCCG | 8853 |
rs528707609 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375101 | ATAGGGAGGCCCCAT[A/C]TCTACAAAAAAAAAA | 8853 |
rs528711160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341597 | CACTTACTTTGTGCA[A/G]GGCTTTTTTTCTCCC | 8853 |
rs528718260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285116 | CCCTCATGATGGGGT[C/T]AGTGCCCTGCTTAAA | 8853 |
rs528721104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322612 | CAGGTTAGGCACAAG[A/G]TGAATGTAGAAAGGA | 8853 |
rs528754158 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212254 | AGAGGAACAGAATCC[A/T]GTAAACAAATCAGTG | 8853 |
rs528754526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259250 | GCCCTTCCTTGGGGA[A/G]AAACATTCATCCCTC | 8853 |
rs528783995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380305 | CAGGTTCAAGCGATT[C/T]TTCTGCCTCAGCCTC | 8853 |
rs528790114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266716 | TCTTATGTTTGCTGC[C/T]GTCAAAGTTGCTACT | 8853 |
rs528793772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291451 | GAGATCATGCGCCAC[A/G]AGTGAGGTCGGAAAC | 8853 |
rs528828924 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312084 | TACACATCAGTGATT[A/T]CCAGTAACTTTACCA | 8853 |
rs528828969 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291810 | CCATAAGGCTGGTGC[A/T]CCCTGCCTTCGTTCT | 8853 |
rs528838325 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234026 | TGAGGCATGAGAATT[A/G]CTTGAACCCGGGAGG | 8853 |
rs528845414 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226501 | ATGACTTCAAGGGCA[C/G]CTTCCAGCTTGGGGA | 8853 |
rs528845887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214272 | AGGTGGAGTCTTGCT[C/T]GGTTACCCAGGCTGG | 8853 |
rs528859456 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317697 | ATCCTGAAACCCTCA[C/G]ACGCCCACACACACC | 8853 |
rs528860231 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355373 | TTAATTTGGATTTCT[C/G]TAGTGTTTTCTCATG | 8853 |
rs528861537 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402738 | CCTTTTATTTGCCTA[C/T]ATCATTTACACTCTT | 8853 |
rs528862077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399457 | CGAGATGAGGGACCC[C/T]TCTCTGCCAGCCCTG | 8853 |
rs528867010 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245213 | CCCACACAGGAGCTT[A/C]TGGTTTGAGAACCAC | 8853 |
rs528924194 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400153 | TCCTGCCAGGTGGTC[A/G]GGACTGAGGGAGGGC | 8853 |
rs528939818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278290 | GGTTGAGGCAGGTGG[A/G]TCCCCTGAGGTCAGG | 8853 |
rs528949305 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404866 | GTAAAAATGTGTTAT[A/G]TCTGTAGTTTTTTGT | 8853 |
rs528957202 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9242640 | CACCTTTCAAAGGAA[C/T]GCAGTCCAGAGGCCT | 8853 |
rs528969702 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369603 | GGGCCAGTTAACAGA[A/G]CACCTGCATTTGAGT | 8853 |
rs528979930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241259 | AGATATTTTGTCAGT[A/G]TTAAGTAATGCTGCA | 8853 |
rs528989575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285882 | AAATGCTGATTTTCC[C/T]TCAAATCCTTACCAT | 8853 |
rs528993407 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9268545 | TCACAGTGCAAGTCT[A/G]CGCTTCCCAAAAGGC | 8853 |
rs528996143 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233407 | TCTGGTAGTTCTTTA[C/G]TGTTTTATAATCTCT | 8853 |
rs529000272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271594 | CTTGCATCAGCAAAG[A/G]AGTTTAAATAGTGGA | 8853 |
rs529000509 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277427 | GTATCTTGAAGGAAG[A/G]TAGGAATGGATCAGA | 8853 |
rs529013768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278793 | AGAAGAAATCTGAGG[C/T]TCGGGAAGCAATAGG | 8853 |
rs529033722 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9344350 | AGCCTGATAGATGGC[A/G]TTTATCAGTTCCTAG | 8853 |
rs529070986 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212823 | TGAAATGCAGAGCCC[C/T]GGGTTCCACCCAGGA | 8853 |
rs529071096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219858 | ACCCATTAGGAGTCA[C/T]TCCCTAGTCACCTGT | 8853 |
rs529097705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299296 | GGAGGATTCAGAATC[A/G]GAATGGTGGTGAACT | 8853 |
rs529109356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213081 | CAGTTACGTAACAAC[C/T]TTAGGCAGTTGATAC | 8853 |
rs529112680 | in-del | -/ACTC | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393230 | TCTAGCTGAGAAAAT[-/ACTC]ACTCACAGGCTGATA | 8853 |
rs529116444 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355813 | TCAGTTTTTAGAAGC[C/G]GCGTCTTTTAAAACT | 8853 |
rs529118849 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205933 | TGGCTGCTGTAGCAC[G/T]TTCTCCCCCTCCTCC | 8853 |
rs529127355 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341778 | TCTAAATTTTGGTGC[C/T]GATGTTCCGCCCTTC | 8853 |
rs529140901 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348919 | ATGGATACCCACGTC[A/G]AGGACAGGGAGGGTG | 8853 |
rs529155953 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387148 | AAACCCGGGAGGCGG[A/G]GCTTGCAGTGAGCTG | 8853 |
rs529160882 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304632 | CTGGAGTAGTGGAGT[A/G]TAGATATTGGTGGAG | 8853 |
rs529194018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394471 | ACCAGGCCCCAGTTC[A/G]TGGCTCTTAATCTGG | 8853 |
rs529195413 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259939 | AACCCAGGTCTAAAA[C/T]TGGGAATGGCTGTCC | 8853 |
rs529197803 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217092 | TCAAATCAAGCATTT[C/T]GACACCAGAGTCTGC | 8853 |
rs529212152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349403 | TACTTGGTTGCATAC[A/G]TGTTTTGTAACCATG | 8853 |
rs529224904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370255 | GAGCCAGAACATTGC[A/G]AGGGAGTGAACAGGG | 8853 |
rs529239316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376607 | TGCTTGCAGGCAGGG[A/G]TCTGCCTTGTGGTGC | 8853 |
rs529259446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276700 | ACCCACCAACACGCC[C/T]GGCTAATTTTTGTAT | 8853 |
rs529269882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287405 | TTTAGTTGTAAGAGC[A/G]GCATTTAAAGAAGAA | 8853 |
rs529280323 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315541 | TAGGAAGGAAGAGCA[C/T]TGGAGGAAGGAGAGC | 8853 |
rs529285931 | snp | A/G/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331061 | TCCACGTGTGGGAGC[A/G/T]CCTCTCATTCCCCCA | 8853 |
rs529301677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370665 | GGGGTCAGACATGTG[A/G]TGCTTAGTTTTAGTG | 8853 |
rs529312935 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331002 | GTACAACGTGGAGCT[C/T]GAGCAACTCAGCTGC | 8853 |
rs529335371 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381881 | TGCGCACCAGCCTGG[A/G]GGAGAAAAAAAAGAA | 8853 |
rs529343660 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207225 | ACTGTGGCGGCCATC[A/G]AGGAGGTGAGGCGGC | 8853 |
rs529348942 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366090 | CTGCTGGCACCTGCA[A/G]CCTCCATTTGCAAAT | 8853 |
rs529354755 | in-del | -/TTTG | 0.0263992 | 0.111815 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348110 | AACTGATGACACTTT[-/TTTG]TTTGTCTGTTTGTTT | 8853 |
rs529357037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376092 | TCAGCAAGGATGCCT[C/T]ACGGCTGCAGCATCT | 8853 |
rs529391574 | in-del | -/AT | 0.0107246 | 0.0724382 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317271 | GCATCACACACACTC[-/AT]ATCCACACCCTCACA | 8853 |
rs529422709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330702 | TTCTTATGTCAGGCA[A/G]TTTAGGAAGTGGGTC | 8853 |
rs529473615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313926 | CATTCTTGGTGTGTA[C/T]GTACATAATTCTTCC | 8853 |
rs529475984 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350370 | AAATTACCTTCACTG[G/T]AAGTGAGGTTTATGC | 8853 |
rs529491063 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306472 | GACCACAGGTGTTCA[C/G]TGTTCTAAGAAGGGT | 8853 |
rs529493509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268361 | TTAAGATAATACCAA[A/G]ACACGCCCTTCTCAT | 8853 |
rs529511161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229359 | CCCCACCTCTGTTGT[C/T]TTCACCCTTTGACCT | 8853 |
rs529523151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357609 | TGTTTCATACGCTTT[A/G]ATAAAGAACTCAAAG | 8853 |
rs529530220 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395836 | ATGGTCTCAATCTCC[A/T]GACCTCGTGATCTGC | 8853 |
rs529587227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364914 | AAAAAAAGACCAGAG[A/C]GGTTAAGAAACTTAC | 8853 |
rs529594668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318406 | CACAGTACATGCACC[A/G]GCCAGGTTTTAGGTG | 8853 |
rs529615127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214519 | TGCTGGGATTATAGG[C/T]GTGAGCCGCTGCGCC | 8853 |
rs529626114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390203 | CCTTACCTGCCATCT[C/T]CACCATTCTCTGTGT | 8853 |
rs529634314 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210282 | GCTGAGTGAACTTGA[A/G]TGAGATGCCTAACAT | 8853 |
rs529635662 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9310341 | CATATTGTATATTAC[A/G]TGGTAACAAAATGGC | 8853 |
rs529638562 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338482 | TGCCTCTGGGTTCGC[A/G]TATCTTACATGCCCA | 8853 |
rs529646436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344969 | CTCCGTCTTGATTTG[A/G]TGCACCTGCAGCCTG | 8853 |
rs529651938 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365311 | ACCCTTCGGGGATCC[A/T]AGGGGCCCAGTTAAC | 8853 |
rs529663474 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300663 | CTCTTGGCAGCTGTG[A/C]AGGATAGTTTGTATC | 8853 |
rs529686014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255804 | AAGATTTATACTCTG[A/G]TGTTTGCATCACATA | 8853 |
rs529704579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294588 | AAATAGGGATAATAA[C/T]AGCCAACTCTTAGTG | 8853 |
rs529726409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214158 | ATATGAACCTACCTC[C/T]TTTGCTTACGCCTTT | 8853 |
rs529738265 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319174 | TGTTTCGGGGGCAGC[A/C/G]GACAGGGCTAGAGGC | 8853 |
rs529739429 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221951 | GGTGCCCGCCACCAC[G/T]CCTGGCTAATTTTTT | 8853 |
rs529740679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383141 | CATGAGTCAGGTTCA[A/G]TGGAGTCAGTTGGTC | 8853 |
rs529751219 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219579 | AGTCCTGAAAAGACA[A/G]CATCATTGCTGAATC | 8853 |
rs529769960 | snp | A/G | 0.000714167 | 0.0188832 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350923 | CTGAGATGCCGCGCC[A/G]TAGAGACGTTGTCTT | 8853 |
rs529782736 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261526 | TTGGAGTTGGGCCCT[A/G]GGTGTGATTTTAGAG | 8853 |
rs529819797 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262087 | CTCCTGGGCTCAAGC[A/G]ATCCTCCTGCCTCAG | 8853 |
rs529834879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244252 | AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG | 8853 |
rs529871237 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315609 | ATGTGGCCCTGGAGG[C/T]GGGAACTGTGACGGG | 8853 |
rs529877459 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326286 | TTTCCCCAAACTGAA[A/G]TTCTCAAGCTTTAAG | 8853 |
rs529879003 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326868 | GTGTATCTTCTTTTC[A/T]GTTCATCTTTGTAAA | 8853 |
rs529891147 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339071 | GTAGTCCCAGCTACC[C/T]GGGAGGCTGAGGTGA | 8853 |
rs529892905 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209675 | CCCAGGTTCAAGCGA[G/T]TCTCCTGCCTCAGCC | 8853 |
rs529892943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331943 | CAGAGGAGGGAGGGG[C/T]GGGTGTCACAGACAG | 8853 |
rs529904436 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9280755 | GGTGGCCATCCGTCT[C/G]TAGCTTTTTTACCTG | 8853 |
rs529908230 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284077 | CATCCAGATAATCCA[C/G]ATAATCTCCCCATCT | 8853 |
rs529915307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256817 | TTCCTCTGTGTGACA[A/G]AGGAGTTGGGTTTTA | 8853 |
rs529928623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303310 | TATTATTAGGTGTCC[A/G]TTTCTGACATTTGCT | 8853 |
rs529945048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295182 | TGACAAGGTAAACTT[C/T]TTAACGATGAAAACA | 8853 |
rs529953321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250531 | AAGTGTTTTCCCATT[C/T]CACAGAGGGTACAAA | 8853 |
rs529962956 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302081 | ACCCGCCTTGGCCTC[C/T]CAAAGTGCAGGGATT | 8853 |
rs529972150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249963 | AGGCTACATGCCATG[C/T]GGAAGGAAGGCAGGG | 8853 |
rs530004668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377890 | TCGTGGTGGAAGCTG[C/T]CCTGATGCCCCATCT | 8853 |
rs530026141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270277 | AGTTGCTTTTCCCCC[A/G]CTCTGAGCTGGAGTG | 8853 |
rs530051475 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9293219 | CAGAGTCTCTCAGTT[C/T]ATCCTTTTGCAGGGA | 8853 |
rs530056241 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247902 | CTCCTCCTCTGCCCC[C/G]CACACTGATAACCTC | 8853 |
rs530084564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315360 | GCGCAGCCAAGGCAG[G/T]GGACGTGAGAATGGC | 8853 |
rs530095351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396984 | TCCAGCCTGGGCAAC[A/G]GAGCCAGACTCCGTC | 8853 |
rs530115244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366733 | TTTATGCTTTGGGCC[A/G]CCTAGAAAAAGCTTT | 8853 |
rs530146679 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390953 | AAGGGTCATACTGAC[C/G]GTTTCATAAGGGGGA | 8853 |
rs530149426 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294204 | GCGTTTCATCATGTT[A/G]GCCAGGCTGGTCTCA | 8853 |
rs530155217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397551 | TCCCTTCCCCACCAC[C/T]GGTGATTTTGTCTCT | 8853 |
rs530161512 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308605 | GCAGCATGTGCCCAG[A/C]CTCAGCTTAGCTTAG | 8853 |
rs530167968 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402069 | CCACCACACAGTAGA[C/T]GCAAGTGGCACAGCT | 8853 |
rs530178411 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275711 | GGCACTTGAGCCCCT[C/G]CATTTTGGGCTCATC | 8853 |
rs530219558 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9224172 | CATTGCTGAGCAGTG[C/T]GAGGGAAGGGAGGAT | 8853 |
rs530222837 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314872 | GAAAGCAGAGGTTGC[A/G]GTGAGCCGAGATCAC | 8853 |
rs530225087 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258016 | CACTTTTAGAAGTGC[A/T]GTGCAGTTGGAAGCC | 8853 |
rs530229815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340298 | AGTGCTGGGATTACA[A/G]GCATGAGCCACCGCG | 8853 |
rs530230892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402437 | GAGTTCGAGACCAGC[C/T]TGGCCAACATGGTTC | 8853 |
rs530238056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296660 | AACACATTTGCCAGA[C/G]TATTTCAATATAACA | 8853 |
rs530278352 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395642 | AGATGGAGTCTTGCT[C/T]TGTCGCCCAGGCTGG | 8853 |
rs530290640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210476 | AGTGAGGATGGGATT[C/T]ACATGGGGGGAAGTG | 8853 |
rs530295211 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278898 | TTGTTAGGGCTCTAT[-/A]GGGGGAAGGGGTGCA | 8853 |
rs530303013 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250713 | GAGCTCTGAATCAGA[A/G]CCAGGGTGGAGCGGA | 8853 |
rs530309156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251214 | ATCAGGAGTTTAGTC[C/T]GCAAGTAGAGGTGGG | 8853 |
rs530328689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391389 | TGCAAACCCCTGCCT[A/G]TCCCCACACTGCACC | 8853 |
rs530337345 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276054 | GCTCCTGTTTTCATC[A/G]TTAATTTGTGTTTCT | 8853 |
rs530379845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373984 | TACGTCTCATGGTGC[C/T]ACTGTGAGGATGTAT | 8853 |
rs530383241 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349733 | TTTATTAACCCAAAT[C/T]CTTCACGCTGCAAGG | 8853 |
rs530400257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309224 | ACTGGAAACAACTCA[A/G]ATGTCCATCAGCAGG | 8853 |
rs530402312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216144 | CCAGAAGATTCATGG[G/T]CACCACCTACCCAGA | 8853 |
rs530404586 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302095 | CCCAAAGTGCAGGGA[C/T]TACAGGCGTGAGCCA | 8853 |
rs530406879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9224541 | AATCAAGGTTGTCGT[C/G]TCATCCTTTGAAACA | 8853 |
rs530414861 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358392 | GGTCTCATTGTTTTC[C/T]TCTTGCTCCATTCTG | 8853 |
rs530425967 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284984 | TAAGAATGGTTTCTT[-/A]ACCATCGTTACCTGC | 8853 |
rs530459952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339971 | TACAAGTGTGGCCAA[C/T]GATCCTTACAAGCCA | 8853 |
rs530468965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321873 | AAACTTGAAGTAATT[A/G]TAGGATAAATAAAGG | 8853 |
rs530478348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367407 | CATGGAAATGAAAAT[A/G]TGTTTTCTCAAAGCA | 8853 |
rs530480585 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246635 | ATAAAGTTGCATCCT[A/G]CATTCAGAATAAAGA | 8853 |
rs530502677 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328182 | CAGGTGAGTGATTGC[A/C/T]GCAGCTTGGAGGAAG | 8853 |
rs530513049 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373301 | GCTCAGGTGGAACGG[G/T]CACCCTGGGGCGTGA | 8853 |
rs530514897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379761 | AAGAAATTATAGGCC[A/G]GGTGCAGTGGCTCAC | 8853 |
rs530515213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290461 | GAGATCTGCCCATCT[C/T]GGCCTCCCAAAGTGC | 8853 |
rs530556094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283797 | CCTTCTCCCTGTACC[C/T]TCACATGGCAGCGAG | 8853 |
rs530562373 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232107 | TAAAGATTTGCTCTT[C/T]AGCTTCTCAGCTGAA | 8853 |
rs530562431 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239702 | TTTTGTTGTTGTCGT[A/T]GTTGTTGAAACCACT | 8853 |
rs530576132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310003 | TTCCAGCACTGGAAG[A/G]CTGTTTCACACTCTG | 8853 |
rs530579156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334190 | TAGTAGCTTTTTGTA[C/T]TTTTGTATTTGTTTT | 8853 |
rs530580010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225755 | GCATTGGCCACTGCC[A/G]TGGGAAGTGGTTGTA | 8853 |
rs530594835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398681 | GTGCGTGGTGGTGCA[C/T]ACCTGTAATTCCAGC | 8853 |
rs530613039 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378067 | CAAAAGTGGGGGAGA[A/C]TTCTGAAAATGAAAC | 8853 |
rs530643555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334550 | ATTTCCTTTTCTGTT[C/T]GCTCCTGCTAATTTT | 8853 |
rs530662551 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310946 | TAATAGCTCTATGTG[C/G]TGCCTGCCCCACTGA | 8853 |
rs530662643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303309 | CTATTATTAGGTGTC[C/T]GTTTCTGACATTTGC | 8853 |
rs530674142 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210122 | ATTTGCCAAAGGTTA[C/T]AGAGCTCTGAAGTGG | 8853 |
rs530699616 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317192 | TCAACACACACCCCA[A/C]GCAATCACACCCACT | 8853 |
rs530709068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265425 | CCTTTGACACATTTT[G/T]GTGCTCAGAGTTAAA | 8853 |
rs530727452 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404720 | CAGCTTGTCTTTATT[A/G]TGCAAGACTGTGTAG | 8853 |
rs530736229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354499 | GAAATTGGCCAGGTG[C/T]GGTGGCCCACGCCTG | 8853 |
rs530763176 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321215 | TTCATTAGATTGTTT[-/A]AAAAAAAAATAGCTC | 8853 |
rs530782968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304440 | AGTGGGGATGTAGAT[A/G]GGGGGTGGAAGGGCT | 8853 |
rs530784102 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297971 | AATGCGGTGCTGGTG[C/T]CTGCTGCCTGTGGCT | 8853 |
rs530788732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212345 | GCAGGTGGTCCCAGG[A/G]CGTGGGGCTGTGGTG | 8853 |
rs530806212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335721 | CTCTGTGTGCTAACA[C/T]GTCAGCAGGGACAGT | 8853 |
rs530892338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380418 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 8853 |
rs530912661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386862 | GCATTTGAAATAGAA[A/G]TTAGGTCTAAGTTAC | 8853 |
rs530919579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252928 | TCAAAAAAAAAAAAA[A/G]AAAGAATTTAGGAAC | 8853 |
rs530919826 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259794 | CCGACAGGCAAAGTA[G/T]CCCTGCACATCTGGG | 8853 |
rs530928576 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9293062 | ATTTTTGCTGAAACA[A/G]TTTGCACTGGGCCTT | 8853 |
rs530932678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342411 | AAGGCAATGGAGAAG[A/G]AGTAGTCTTTTCAAC | 8853 |
rs530943455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298588 | CAGCAGTGGAGCCCT[C/T]GCCCTGCCTCAGCCC | 8853 |
rs530953703 | snp | A/G/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252733 | ATCCTGGCTAACACG[A/G/T]TGAAACCCTGTCTCT | 8853 |
rs530961302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369648 | AGCGTGTCCTGGCAG[G/T]ACAGAGAAAAATGAA | 8853 |
rs530990740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323312 | TCTGCCCTCACCTGT[A/G]GGAGCATCTCACCGG | 8853 |
rs530992531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330512 | CCCTAAGTTGACCAC[C/T]AGGCCTATAACAAAA | 8853 |
rs531021269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218609 | CCTTGTACTGTATTC[C/T]CCTGATAGCCTGAAT | 8853 |
rs531066086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329213 | AAAAAGGAGAGTGGC[A/G]TGAAACGAAACTGCA | 8853 |
rs531085291 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387121 | CAGGAGGCTGAGGCA[A/G]GAGAATGGCGTAAAC | 8853 |
rs531107916 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248749 | CCTTACACCATTTGA[A/C]ATGTAGGTTGTATAT | 8853 |
rs531128587 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240642 | GAAGGCAAAGCTAGC[A/T]TGAGTTTATTTTTTT | 8853 |
rs531142325 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9261733 | GTTCCTTCTGGCTGG[A/C]CTGCCACATGCAGGG | 8853 |
rs531194009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336414 | TGAGTTCACAGAGCA[C/T]ATCCTGTTTGAATGC | 8853 |
rs531201903 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245763 | GTGCCATGCATTAGT[C/T]GGTTCGTCGTCTGCC | 8853 |
rs531224863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375198 | GGGGTGAGAGGAATC[A/G]GTTGAGCCCAGAAAT | 8853 |
rs531226931 | snp | G/T | | | intron-variant, missense | ASAP2 | GRCh38.p7 | 2:9390163 | CCCTAGCATCATTTC[G/T]TCTTCCAGTAATGTA | 8853 |
rs531228910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285220 | GTATCAGAATACCCC[A/G]GGGTCTTGTTAAAAT | 8853 |
rs531239535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306004 | ATTGGTGTAGAGGCT[A/G]TAGTAGTGGGGTGGT | 8853 |
rs531254414 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248056 | GAGCTCAGCTGTCCT[C/G]GAGTCTGGGACAGAC | 8853 |
rs531256215 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9222526 | ATTTGGTCCCCACAG[A/G]AGACTGCTCACTTCT | 8853 |
rs531267466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271991 | TGTTTCCAAATCTTG[A/G]CCATTGTGAACAGTG | 8853 |
rs531278888 | in-del | -/C | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236925 | GAGTGTCAGAAAGAT[-/C]CCCCCCCGAGGCTGG | 8853 |
rs531283904 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235099 | GTGTTTCACTGTCCC[C/T]GCCCGACATATGCCA | 8853 |
rs531326438 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303845 | ATACGGTAACCCCCA[C/T]ACAGAGAAAGTGGGA | 8853 |
rs531337965 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368911 | ATGTGATTATGTAGC[A/G]TCCTTCTTGCCAACG | 8853 |
rs531338602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219955 | ATATATGGAATCAAA[C/G]AATATGTGGCCTTTT | 8853 |
rs531353176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267013 | TTTCATTTTGGCAAC[A/G]TTTTCTGGTTCTTTC | 8853 |
rs531394093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254893 | ATGAACATTTGACTA[C/T]AAGTCTTTGTGTAGG | 8853 |
rs531432600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376674 | TAGAAATGAAACTCC[C/T]GAACTTCTCATTTAT | 8853 |
rs531445666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400198 | TTCCACAGCCCTCCT[A/G]CCCCCTCCCCTCCTG | 8853 |
rs531455161 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327095 | CTTGGGCTGCAGAGA[A/G]ACCTCAGCCAGCAAC | 8853 |
rs531467096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260542 | GGCCAGGCTCTAAAA[C/G]GCACATGACCTTGTT | 8853 |
rs531476730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343067 | TCCAAGGATGGTGAG[C/G]TGCTCAGTGGCAATG | 8853 |
rs531478883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267968 | ACTCCAAGCGCGCCC[C/T]GCAGGCCTGTCCCAT | 8853 |
rs531481453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272955 | GGCTACTATAGCTCT[A/G]TAGTATAATTTAAGT | 8853 |
rs531495301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221132 | AAGATTGTTTTGGCT[A/G]TTGAGGCTCCCTTGC | 8853 |
rs531503798 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254401 | TCTGTTGCCTAGGCT[A/G]GAGTGCAGTGGCATC | 8853 |
rs531518809 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9237990 | CTCCAGTGTGTGGAT[A/C]CGTGGGCTGGCGTGT | 8853 |
rs531520057 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260430 | GTAGAAAAATGAAAG[A/G]TTCATGCCTAGAGAT | 8853 |
rs531521481 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9396365 | CCGCAGCCTCGACCT[C/T]CTGGGCCCAGGTGAT | 8853 |
rs531533469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337753 | GGAGCTTGTGCCGTT[C/T]TGGTCCCGGTGACCT | 8853 |
rs531553154 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219296 | TTCACATTTGCCCTG[C/T]GATTCGGTTGTGTTT | 8853 |
rs531554140 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371206 | TTTCAAAATGAGGGC[A/C/G]GATGACCCGTGTGAT | 8853 |
rs531561723 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243442 | GTGCATTTTTGTCCA[G/T]AGATTACAATCACTG | 8853 |
rs531563156 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249449 | CACTTGGGCTTGTTC[A/T]TTGCTCTGATGGGGA | 8853 |
rs531563570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364974 | GACTCCAGAGCCTGT[A/G]TTTTAGCCTTTTTTT | 8853 |
rs531574704 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207955 | GGTGCAAAGTCATCA[A/C]GCCTAGCTGCTAAGC | 8853 |
rs531607282 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263242 | TCCATTTTCTACCTC[C/G]AGTCTGCTCTCCTGC | 8853 |
rs531642610 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401568 | CCTCCATGGACACCC[C/G]CTTCTGAGCAGGCCT | 8853 |
rs531662769 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207309 | CCCGCATCCGCATCC[C/G]GAGAAAACTTTCTTT | 8853 |
rs531674041 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338245 | TCACAGGTCTGAGTG[A/C]TGAAACCACCATGGT | 8853 |
rs531679613 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290014 | CATCCTTCCAGTTGC[-/T]CATCCTGCACGGGAG | 8853 |
rs531684648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377109 | ACCTTCCCAGTTCTA[A/C]ACATGAATTAAAGAC | 8853 |
rs531708098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294510 | AAGTGCACCGATCCT[C/T]CTACCAACTCTATGG | 8853 |
rs531713074 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257071 | CTTTCCCTAACAGCC[G/T]GTCACAGGGCGTTTG | 8853 |
rs531726669 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280383 | CCAGTTACAATAGGG[C/T]GGGCACAAGCTCCAG | 8853 |
rs531746459 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288167 | TTTGGGATGCCCATA[A/C]CCCCATAAACCTGTC | 8853 |
rs531749418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365366 | TCTCCTGAGCTCAGC[A/G]GTCAGGGAAGTCTGG | 8853 |
rs531771529 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9324887 | CAATCTCTGCCTTTC[G/T]ATTGGATTGTTTAAT | 8853 |
rs531777876 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319107 | GAGCTGTTTAAGGGG[G/T]CAGCAGACGGGGCTG | 8853 |
rs531778525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236932 | CAGAAAGATCCCCCC[C/T]GAGGCTGGTGTGGGT | 8853 |
rs531812800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222584 | GGTTTTCTTCTCACC[C/T]TGTAAATTCTCTTGT | 8853 |
rs531828815 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307883 | AGGGACGGGCTGGGC[A/G]CATCTGTTCAGGAGG | 8853 |
rs531839868 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306525 | TGGGAAGGGTTCCTA[-/G]GGGTGAGAGGGGCTT | 8853 |
rs531844845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274317 | TGTTTCTAGCATTCA[A/G]TCTTTTTTTTTTTTT | 8853 |
rs531850444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243161 | TCGCCCAGGCTGGAG[C/T]GCAGTGGCACAACCT | 8853 |
rs531862163 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324701 | CTCAACACTGCTGCA[C/T]TGGGGACCCAGTTTC | 8853 |
rs531891254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365993 | GCCCACAAATTCCTT[A/C]TGGGTGCCAGTGAGA | 8853 |
rs531893496 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361176 | GCCTGCTTAATCAAT[G/T]TCTGCAGATATTTTC | 8853 |
rs531894923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395843 | CAATCTCCTGACCTC[A/G]TGATCTGCCCTCCTC | 8853 |
rs531899661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222003 | GATGGGGTTTCACCA[C/T]GGTCTTGATCTCCTG | 8853 |
rs531928476 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230375 | CTGTGTTACAAGACT[A/G]AGCAGTGCAGCCGTG | 8853 |
rs531928536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274901 | AAGATTCCATATGGT[A/G]ACCTATTTTTTCAAG | 8853 |
rs531935559 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214644 | TGGGCTGTATTTTTA[G/T]GATGATGGTCATTTC | 8853 |
rs531949117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302044 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 8853 |
rs531957674 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358235 | GTGATTGCTGAAGCT[C/G]TTAACAACACAAACT | 8853 |
rs531965636 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9303710 | CACATTGTTTGATCG[-/A]GACAATGAACAAATA | 8853 |
rs531968229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390347 | GGCTTCCTCTGGACC[C/T]AGTGGCCTGGCCCAT | 8853 |
rs531992931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210266 | GCTCTACAGCTTGCC[A/G]GCTGAGTGAACTTGA | 8853 |
rs532006148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339853 | ACCTCTCTGTGTCCA[A/G]CCTGCGTCACATTCC | 8853 |
rs532014058 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357785 | TTTTCCAACATGGAT[A/G]ACATTTTTAATAACT | 8853 |
rs532016324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295738 | TTTATCTAGAACTCT[C/T]AGGCTCTTTACTGGA | 8853 |
rs532025568 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387031 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAA | 8853 |
rs532039577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313951 | TCTTCCTCTGAAAGG[G/T]CAGGCATCGTGTTTC | 8853 |
rs532058881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301470 | GGGGTTCTTTTCCTC[C/T]TCCCCAATGGATGTG | 8853 |
rs532080871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268906 | CACCCCTGCTGGTTC[G/T]CATTGAGAACTCAGG | 8853 |
rs532081981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262926 | CTCCCCTGTTTATTT[C/G]ACTAAAGTGAAGTTC | 8853 |
rs532100192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357848 | ACTGACTAAAGTTGC[A/G]ATATTTACCTGCCGT | 8853 |
rs532104226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377937 | CTCCTAGAACGCAGC[A/G]GGGGTTTCGTAAACA | 8853 |
rs532135038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250568 | CAGGGCACATTGCAC[A/G]GCCCCCAGGGCAAAT | 8853 |
rs532135085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257604 | ATTCACGTCAACCTT[C/T]GTTTCCCAGGTTCAA | 8853 |
rs532138400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289155 | GCAGATCTCTTAGAA[A/G]CCTTTTGGCTGCTCT | 8853 |
rs532158101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238407 | CAAATTGTCCACAGC[G/T]TTGCTGAGCTACAGC | 8853 |
rs532160676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320456 | GAAAAGAATGTTTAT[C/T]AGCCATGTTGCTGTG | 8853 |
rs532171836 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251130 | GTGGACGGGAGTGGA[A/G]CGTGGAGGGCTGGTA | 8853 |
rs532220556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321106 | ATCTCTGTGTCTTGG[A/G]GTGCTCTGAATGGAA | 8853 |
rs532269221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332836 | TAAAATACAAGAATT[A/G]GATGAGTTCAGAAAC | 8853 |
rs532318199 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402676 | AACCACAGCACCCCC[A/C/G]ACCCACTCCACAAAA | 8853 |
rs532318884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244953 | TTTGACAGGGTGACA[C/T]GATGGTGTGTGAGCT | 8853 |
rs532336493 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9224875 | GGAAGCACAGTGGTC[A/G]TGCCCACAGCTGTCA | 8853 |
rs532341768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359341 | CCATGGGGGGAGATA[C/T]TGGTCTTCATTTTTA | 8853 |
rs532365837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367253 | GCCCAGGCTAGTCTC[A/G]AACTCCTGAGCTCAG | 8853 |
rs532383815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315432 | AAGACCTGGAATTTG[C/T]TGAGAAGCGTGCCGC | 8853 |
rs532399242 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276486 | ACCAGGAAGCCTTAT[-/A]AGTGCCTGGGCTGGG | 8853 |
rs532404558 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217050 | ACCAAGTTCATGGAG[A/C]TTGGAGGTGATGAAG | 8853 |
rs532445693 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231899 | GACCCAGCGGACACT[G/T]TGGGAAGTGGCAACC | 8853 |
rs532449818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9223595 | TAGCTGGAATAACCT[A/G]GCAGCCATAGGGCGT | 8853 |
rs532481308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366770 | GTGTCAAGGGCCGGG[C/T]TGAATTAGGAAAGCT | 8853 |
rs532485889 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274246 | TTATTTCTTTCTCTT[A/G]TCTAATCTCTAGCTA | 8853 |
rs532508604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260764 | CTGAGAAGTTGAAGA[C/T]GGAGAAATGAAAGAC | 8853 |
rs532508857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316046 | AATTTAGTCCAGGCG[C/T]GGTGGCTCATGCCTG | 8853 |
rs532516400 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9299712 | CGGGTTCTGCTTCTC[A/G]CTCCCAGACTGCCCT | 8853 |
rs532524362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391523 | GTGATTTTCAATATT[C/T]TGGGGACAGTCACTT | 8853 |
rs532529633 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9354372 | GAAGCTCTGGAAGCC[A/G]TCCGCTTATTTGTAG | 8853 |
rs532530066 | in-del | -/TGTT | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278622 | CGTTGAACAGATAAC[-/TGTT]TGAGCGCCTCCTATG | 8853 |
rs532542655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352912 | CTCATCCCTCCTCCT[C/T]CCCTGCTTGTCTTCC | 8853 |
rs532546814 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270829 | ACGGAGTCTCGCTCC[C/G]TCGCCCAGGCTGGAG | 8853 |
rs532548761 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9220078 | TATTCTATCAAATGT[G/T]TATGATACATTTTGT | 8853 |
rs532552598 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9363247 | TTGTGAATAGTGCTG[C/T]AGTAAACAAGATGGT | 8853 |
rs532554361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379828 | GAAACCCTGTCTCCA[C/T]TAAAAATACAAAAAT | 8853 |
rs532589543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374108 | AACTCAGGCTTCTTT[A/G]GCCCCCTTTTGTTCC | 8853 |
rs532590127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270418 | TTGCTCTAAGATTTC[A/G]GTATTTTTTTTTAAA | 8853 |
rs532596035 | in-del | -/AG | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369208 | ATTTTTAGTAGAGAC[-/AG]AGTTTCACCATGTTG | 8853 |
rs532612194 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276327 | GAAGACAGCAGGGGG[A/C]GGGGGAGCCACAGGT | 8853 |
rs532624797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246754 | AAATGGTTTAATCCA[C/T]TGTGGCTCGATGTGG | 8853 |
rs532629753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258104 | TTGGGGTAGGATATA[C/T]GGACATACACATTTC | 8853 |
rs532645207 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383285 | TTTTTTAAAAAAAGA[C/T]AGTGTCTCTCTGTTG | 8853 |
rs532670057 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253564 | ACGCAGAACTCCCCT[C/G]TTCAGTTGGTTCCCC | 8853 |
rs532685241 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210942 | GGGCAGATCACTTGG[G/T]GTCAGGAGTTCGAAA | 8853 |
rs532689371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385673 | TCTCTTGCTATGGAG[C/T]CATGTCATAAAGAGC | 8853 |
rs532748753 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240186 | GCAGCCAGCTAATAT[C/T]GAACTAGTTTGCCTT | 8853 |
rs532763340 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397089 | AATGGGCTTTCCAGT[A/G]CTAATTATTTCTGCC | 8853 |
rs532773892 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267984 | GCAGGCCTGTCCCAT[C/T]GTAACGCCCTCAGAA | 8853 |
rs532773912 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404848 | TACCTTTCAAAGTTC[C/T]GGGTAAAAATGTGTT | 8853 |
rs532791503 | in-del | -/TCTATCATAACCTCT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221265 | TAGACATCTTAACAA[-/TCTATCATAACCTCT]TCTATCTATGAACTT | 8853 |
rs532830985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217760 | GCTGGGACTACAGGC[A/G]CCTGCCACCACGCCC | 8853 |
rs532835436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296778 | CTGTAGGATGCAGAG[A/G]AGTTTGGGAGGGAAG | 8853 |
rs532841356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258635 | AATGCAAACCTTCCC[A/G]GGTCCTGGGGCAGTG | 8853 |
rs532844854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374579 | CCCAGGAGGTCGCAG[C/T]GAAGACCAGTGCAGC | 8853 |
rs532846871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368092 | GAGGATGTGAAATAG[A/G]TTCACTTTGGTTGAG | 8853 |
rs532867672 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211644 | TTGGTTACCTTGGCA[A/G]TCCCATTGCTGTCAT | 8853 |
rs532874073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284160 | GCCAAGTAGCATAAC[A/G]TACTCACAAGTTCCA | 8853 |
rs532877190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247350 | TCCCAGTCCGCAGAT[A/G]CCTAGGGAGTCCCAG | 8853 |
rs532889437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277477 | ACGAGTTAACTCCAT[A/G]TAAGAAATCTTGATT | 8853 |
rs532890924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240474 | TGGTCTCAAACTCCT[A/G]GACTGGAGCGATTCA | 8853 |
rs532900411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239882 | CAGGTGCACACCACC[A/G]TGCCCCAGTAATTTT | 8853 |
rs532910286 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232619 | GGCAGGGATTTTTGA[C/G]TCTTACTTAGTGATG | 8853 |
rs532923384 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338932 | GCTATAGTCCCAGCA[C/G]TTTGGGAGGCCAAGG | 8853 |
rs532931765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393990 | GACCCTCTGTGGTGT[A/G]AGGCGTGGATTTCCC | 8853 |
rs532941800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322537 | CCCTGGTGGCTCTTC[C/T]TTGGATGTGCTCATT | 8853 |
rs532949074 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218694 | TGCGTCATTTGTAAC[A/C]TGGAGGGTTGGATGC | 8853 |
rs532960164 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396912 | GAGGCAGAGGCAGGA[A/G]AATCACTTGAACCCA | 8853 |
rs532968996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259356 | TCCCCTCCCTTCTGC[A/G]CCATCCTGCAGTGGC | 8853 |
rs532986361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233275 | ATAGTGAAGGAATTG[C/T]GAAGCCGTACTATGT | 8853 |
rs532991806 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387112 | CCAGCTACTCAGGAG[C/G]CTGAGGCAGGAGAAT | 8853 |
rs533005789 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335461 | GCTCTCAGTGGCTTC[A/G]TCACAGAGACCATGT | 8853 |
rs533006614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317276 | ACACACACTCATATC[C/T]ACACCCTCACACCCT | 8853 |
rs533016456 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265466 | CCCTGCTTGATGGGA[A/G]GAGAAGAGAAAAGGG | 8853 |
rs533026496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213479 | GGAATAACATGGTCC[A/G]ATATCCATTTTAAAG | 8853 |
rs533046560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354551 | CTGAGGTGGGAAGAT[C/T]GCTTGAGCCTGGGAG | 8853 |
rs533072090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329021 | CCAGCACACAGTGCC[C/G]GGAACACAGTAGGTA | 8853 |
rs533074270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284990 | ATGGTTTCTTACCAT[C/T]GTTACCTGCACAATA | 8853 |
rs533078063 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9269520 | CAAGAAGAGGTAGAG[A/G]AGCCCCCACATGGAG | 8853 |
rs533090914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311340 | CTGTGCTCCATCCTG[A/G]GTGAGAGGCACTCTC | 8853 |
rs533095667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271802 | CAAATAATTGAAAAC[A/G]TGGAGTGTTTGTCTT | 8853 |
rs533101284 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311886 | CCAGGCGTGTGTGCT[G/T]TGTGGATTGCATACA | 8853 |
rs533101680 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212367 | GCTGTGGTGAGGGAG[A/G]GCCTTATATGATGTC | 8853 |
rs533119671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292467 | AGGTTGCAGTGAGCC[A/G]AGATTGCACCACTGC | 8853 |
rs533123750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299190 | CAAGTTGAGAGGCTC[A/G]CAAGTACCCAGCGCA | 8853 |
rs533161430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292954 | CTTCCTCACTGTGCT[A/G]TGGGCCACACTGACC | 8853 |
rs533193564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304588 | GTGGAGAGGCTGTAG[C/T]CTTGGGAGTATAGAT | 8853 |
rs533205197 | snp | C/G | 2.0922e-05 | 0.00323428 | utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207095 | GCGCCAGCGCCCTCG[C/G]GCCGAGGCGATGCCG | 8853 |
rs533219019 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361658 | CTGCAACCTCTGCCT[C/T]CTGGGTTCAAGCAAT | 8853 |
rs533239901 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9400347 | TCCTCTCCCCCTCCC[C/T]CCCCCATCTCATGCC | 8853 |
rs533240729 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324914 | TAATCCATTAACGTT[A/G]AATGTTACTATTGAT | 8853 |
rs533245422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226413 | ACTCGGCATGGGTCT[A/G]CTTTCCGCCCCTCTT | 8853 |
rs533251171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387557 | TGGAGATTGAGTGCA[A/G]CGGGCTGGCCAGAGC | 8853 |
rs533254352 | snp | C/T | | | intron-variant, missense | ASAP2 | GRCh38.p7 | 2:9390057 | TGTTCCACTGGGTCA[C/T]GGAGGGGTAAACTCT | 8853 |
rs533265354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399342 | AGCCACTGGCACTGG[C/T]CCTTAGCTCTGGAGT | 8853 |
rs533265925 | snp | A/G | 5.03309e-05 | 0.00501627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380852 | GGGCACCTGTCACGG[A/G]ACAGGGAGCCAAGCC | 8853 |
rs533276420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358133 | CTCGAGCCTGAGCAT[C/T]GCAAAGCTGTCTCTG | 8853 |
rs533282001 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336648 | CAAGGTTATATTTAG[C/T]GCTAGAAAGGACCTA | 8853 |
rs533315345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381228 | TCAATACCATCTTTT[A/C]CTGTTCTGGAAGAAA | 8853 |
rs533321362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365840 | ATGCCTCATGCCCAG[C/T]ACAGACGAGGGGCTC | 8853 |
rs533337201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317989 | TGACACACACTCTCC[A/G]TCCCCAACACACACA | 8853 |
rs533352351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253993 | TGGGTGGATCACAAG[A/G]TTGGGAGTTCGAGAC | 8853 |
rs533363006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248102 | GGTGGCTGATGGAAG[A/G]GGGGCGGCTGACAGC | 8853 |
rs533365723 | snp | C/T | 0.00111953 | 0.0236328 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356104 | GTCAAATGTAAGTTA[C/T]ATGGTGGTGGGACTT | 8853 |
rs533470885 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234375 | GAACATTTAGCCAGA[C/G]CCTGTCGCATGGCTG | 8853 |
rs533521893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235167 | GTGTGTGGCTACAGA[A/G]TGACTAATGGTAGAA | 8853 |
rs533536804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337309 | AGCAAGTTGGACAAT[C/T]TTTGAACACAGTTGC | 8853 |
rs533539793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254486 | GCCTCCCAAGTAGCT[A/G]GGATTACAGGCATGC | 8853 |
rs533564575 | in-del | -/CA | 0.00755907 | 0.0610114 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309936 | CTTCAATGCCTGCCT[-/CA]CACACACATGTTGTA | 8853 |
rs533574805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364847 | TCCAGGCATTGTTGT[A/G]GGTGTTCTACGTACA | 8853 |
rs533596763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207430 | CACCTTGGGCCTCTT[G/T]AAGACCTCCCCTCTC | 8853 |
rs533602109 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307916 | CCTGTGTGAGAGTGC[A/G]TAGACGGGAGTGTGT | 8853 |
rs533619678 | snp | A/G | 1.66374e-05 | 0.00288417 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9400827 | GCCTAGGAAGTCGCA[A/G]GCAGTAAGTGACGAG | 8853 |
rs533636617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330607 | GAAAAGACCTTGCAA[C/T]TATATAGTTTTCAAG | 8853 |
rs533639202 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294190 | TTTTAGTAGAGACAG[C/T]GTTTCATCATGTTGG | 8853 |
rs533665158 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305840 | GGAGGGGCTGTAATA[A/G]TGGGGTATAGATATT | 8853 |
rs533671089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343272 | ATGAACTGGATAGGC[A/G]TTCTCATTAAACACC | 8853 |
rs533698043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260671 | TCTTCTCCCTTCCCT[A/G]TTCTGGGTTTTTCTC | 8853 |
rs533701478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364651 | AAGCGGGTCAACACA[C/T]AGTCTGATCTGAAAG | 8853 |
rs533701562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370849 | GGCGAGCCTGAGGGT[A/C]CCGCTTGGTGAAGGA | 8853 |
rs533705476 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331492 | CCATGGTTTGGCAAG[C/G]CATGGTGGCTCATGC | 8853 |
rs533713015 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307023 | CTTGAGCAGCACTGC[A/C]CTGGAGCAGAGGTCC | 8853 |
rs533722044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299651 | CAGGGGGCCTAGAAA[A/G]CAGCCAGCCCAGGAC | 8853 |
rs533727288 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236488 | ATATCTTACTTTTAT[A/G]AAGATTAATAAAATT | 8853 |
rs533750927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280446 | GTGCAAGCCACAATC[A/G]GGAAGAATCTAGCAG | 8853 |
rs533754215 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381618 | GAGCATGCCTGTAGC[C/G]CCAGTTACCCAGGAG | 8853 |
rs533764330 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9206343 | CAGGGTGCCCGCCGG[C/T]GGAGCGCATCCTCCG | 8853 |
rs533819694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376257 | AGCAGGCAGGGCAGG[C/T]GGCCTGGGAAGCACC | 8853 |
rs533835194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370426 | GTTTTACATACCAGG[C/T]ATGAGGTTGACAATG | 8853 |
rs533842165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376695 | TCTCATTTATTTCCC[A/G]TGGAGTCAGGAGAAA | 8853 |
rs533845041 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260041 | GGCAGGCTGGCCTCT[A/C]CCCGAGTCAGGCACC | 8853 |
rs533857369 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331225 | CAGATTCCAGGGCTC[A/C]GGTTTGGCTGTTGAC | 8853 |
rs533866216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212904 | AGCACTGTTCGAGAC[A/G]GAACCCCGGCTGCAC | 8853 |
rs533868150 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397994 | CGATCTCCTGACCTC[A/G]TGATCCGCCCGCCTC | 8853 |
rs533888032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298957 | GGGACACAACTATGG[C/T]AAGAAAATATAACAT | 8853 |
rs533912243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389163 | GCAAACCAAAGCTCT[C/T]AGAAGTTAAGTAATT | 8853 |
rs533918979 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395920 | CCCATCCCTGAAGTT[G/T]TTTAGGAGTAGAGAA | 8853 |
rs533947909 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268938 | TGCTGGGGACAAACC[A/G]GTGCTGTGCTGCCTG | 8853 |
rs533973416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, splice-acceptor-variant | ASAP2 | GRCh38.p7 | 2:9389724 | GCAGACCTTCCCCCA[A/G]GCAGGCCCAGAAGCC | 8853 |
rs533985316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235551 | CTGATTGGAAAGCCC[A/G]GTACATTAGGGAGTG | 8853 |
rs533985878 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307348 | GACTCTCACCCTTGG[C/T]GAGATGGAGACTTCA | 8853 |
rs534009295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228206 | CCTTGAAGAAGTAAT[A/G]ATCTTGAATTATTTA | 8853 |
rs534052152 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401601 | TTATTCCCCAGGGTG[G/T]CTTCCTCCCCTGTTA | 8853 |
rs534072196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357801 | ACATTTTTAATAACT[C/T]GAACATTTAAAAAAT | 8853 |
rs534100989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294792 | TGCATTCATTGCCCA[A/G]CACCGTGAAGGAGGA | 8853 |
rs534105632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242810 | ATGATGCTGGGGAAG[C/T]AGGTTTTGATTGTCC | 8853 |
rs534107661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324168 | CAACAAAGCTAATCC[A/G]GAAGGCACTTTCTGA | 8853 |
rs534111575 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209253 | ACATGCTATGATGAT[A/G]GTATGTGTGAGCTTG | 8853 |
rs534146283 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314119 | CTCCCGAGTAGCTAG[G/T]ATTACAGGCGTGCGC | 8853 |
rs534158059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306687 | CTCTGCTCCTGGCTC[A/G]CTGAGGGAATTGTCA | 8853 |
rs534165251 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279954 | TCACCTGTAGCATAC[C/T]TTCCCTTGTACAAAT | 8853 |
rs534173734 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377923 | GAGTGCCAGCCCGGC[C/T]CCTAGAACGCAGCAG | 8853 |
rs534181348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262370 | ACACCTAGCCTCTCC[A/G]AGAACTGGAGGACAC | 8853 |
rs534184712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344049 | TTACTGTTTATTGGC[C/T]TTACTGGGTATTCTT | 8853 |
rs534203727 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302715 | CCTGACCTCAAGTGA[C/T]CCACCCGCCTGGGTC | 8853 |
rs534212363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301010 | GGAAGGCCCAGTGGC[A/G]GCTCCTGCAAAGCTG | 8853 |
rs534224810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382836 | TTGTAGTCGCCTGAC[A/T]GGTTCTTCTTGCCTG | 8853 |
rs534242503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214215 | TTGCTAGGGCCCTTC[C/T]AGGTACTTTTTTTCT | 8853 |
rs534248390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300334 | ATGGAATCCGGACGA[A/G]ACTAACTTGTCTCAG | 8853 |
rs534255034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401129 | GGCTCCTGAGCTGCA[C/G]TGACCTGCCCCACCT | 8853 |
rs534269809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256073 | GTAGAATGACCAGTG[C/T]GTCACTATATTTTCC | 8853 |
rs534275565 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352939 | TTCCAGTGGGTAAAA[C/T]GAATTCCAGTCCTGC | 8853 |
rs534277156 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356875 | AAATAAGATTTTATT[G/T]TTACATTTTGATAAA | 8853 |
rs534288835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282383 | GAAACGTGATACTTT[C/T]TCCTGTCATGTTGAT | 8853 |
rs534289722 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313626 | TCTTGCACGTGCCTT[G/T]TTCTAGACCGCACAG | 8853 |
rs534296498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319928 | CTTTCTTTTAGAGAG[A/G]CATCCTGAAGTATTT | 8853 |
rs534314001 | in-del | -/C | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343947 | TTGGTCAGGGTCAGA[-/C]CCCCCCTTACTCAAG | 8853 |
rs534323051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, splice-donor-variant | ASAP2 | GRCh38.p7 | 2:9237926 | CAGAAGAGCCCTGAG[C/G]TGAGGTAAAGATGTT | 8853 |
rs534353618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230925 | TGTGTGACCTTGGAG[A/G]TGTGTGAGGGAGGCC | 8853 |
rs534354948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320570 | TAGTGGTTATAGGAT[A/G]TTATTTTCAGGAAAG | 8853 |
rs534367873 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377492 | GATTAGAAATGGCCT[A/T]TAGAGATGTGCACAG | 8853 |
rs534380175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339329 | TTGGCATTTGAATCC[C/T]GGGTCTCCCACTTCC | 8853 |
rs534383932 | in-del | -/CA | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317559 | TCTCACATCCACAAT[-/CA]CACTCTCACACACCC | 8853 |
rs534397987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331995 | TTGGAATGTGGTGGC[A/G]TGAAGGCTGCAGGAG | 8853 |
rs534405699 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225286 | GTCTCACAGATCTAC[C/T]CTGTCCCAGAGTCTG | 8853 |
rs534431617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371481 | GTGCCTGCTTAAATA[A/G]GCTAGTATTTTACTT | 8853 |
rs534442236 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9304042 | AGAAGACATGTGCCG[G/T]GACAGCCACTGGCAG | 8853 |
rs534465082 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271503 | GACAGTAGTAAGGGC[C/T]TTCCTGCCGTTTCTC | 8853 |
rs534466848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9223876 | GGTCTCACTAAGCCA[C/T]AGCAGAGCATGTTTA | 8853 |
rs534468866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9215742 | TATATTTCATAATTA[C/T]TATACTGTCCTTGCC | 8853 |
rs534477492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214765 | AAAAGTGGACAGGAT[G/T]GCCTGGACGTCTAAA | 8853 |
rs534482987 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325179 | ACATTTTTTTGTAAA[C/G]ACATATCATGTGTAG | 8853 |
rs534521080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346287 | CAAAAATTAGCCAGG[C/T]ATGGTGGTGCATGCC | 8853 |
rs534522394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338674 | CAGCACTCCACAAAC[A/G]CAACAGAACAAGATG | 8853 |
rs534553104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216556 | ATCTCTGCCTCCCAG[A/G]TTCAAGTGATTCTTG | 8853 |
rs534562963 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302255 | TTGGCTCACTGCAGC[C/T]TCTGCCTCTCGCGTT | 8853 |
rs534592089 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9316257 | GCTCAAGAAGTTGAG[-/A]GCTGAAGTGCCCTCC | 8853 |
rs534600597 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295886 | CCCCCATAGGATGGG[A/T]GAGCAGACCATTCAT | 8853 |
rs534603982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402241 | TTCAGCCTCCAGAGG[C/T]GCTGTGAGCTCTCAG | 8853 |
rs534614804 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358594 | ATATTTGGGTATTGC[A/T]TGTAAATTGGTGGTA | 8853 |
rs534623568 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222953 | CTTGACTTTCATTGC[C/G]TTGGTCTATTTCCAG | 8853 |
rs534627952 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366818 | GCTACCCCACATAAT[G/T]CTTCTGTTTTTAAAA | 8853 |
rs534630969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397137 | ACAGGCCATGCTTCT[C/T]TTGGCTTCTGGGCTC | 8853 |
rs534637067 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229536 | GGAGAGGCCCAGCAT[A/G]TGTCTAGGGAGGAGC | 8853 |
rs534648189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352428 | TGCGTTAAAATGCCC[A/G]TCCTTAACTCATAAG | 8853 |
rs534665875 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9288642 | TTCCTCCATTAAAGG[A/T]TGTGAATATAATTGG | 8853 |
rs534668641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325826 | GGTCCTGGCTCTGCA[A/G]AGCTGGCACTTGGAG | 8853 |
rs534674741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243782 | CTTATTTACTATGCT[A/G]GTTGCTGAGGATTCT | 8853 |
rs534675022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379194 | AGAGAAGGAGAACCT[A/G]CCGCTAATGAGAAAG | 8853 |
rs534690133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334349 | GCATGAGCCACAGCA[C/T]CCGGCCTCTGCATTC | 8853 |
rs534693859 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373298 | CCTGCTCAGGTGGAA[C/T]GGGCACCCTGGGGCG | 8853 |
rs534714941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244413 | TTGGAAGATTAAGTG[A/G]ATGTTAATCTAAGCA | 8853 |
rs534734340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373637 | TCCAGCAGCCATGGC[C/T]CCTTGCCATAGTCAG | 8853 |
rs534758897 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340149 | TGTCTCAGCCTCCCA[A/G]TTAGCTGGGATTACA | 8853 |
rs534785789 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9333536 | AGCCAGGTGAAGCAG[A/G]CACACCTTAGGAGAA | 8853 |
rs534819952 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9333631 | AAGGGAGAAAAGGCC[A/G]GTATGTCTGGAACTG | 8853 |
rs534830047 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263924 | AGGCCAGGTGCCGTG[A/T]CTCACACCTGTAATC | 8853 |
rs534850422 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360813 | CATAATTATGAGTTT[A/T]TATAGCATAATTTTT | 8853 |
rs534861525 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9391580 | CTTTTCTTTTTCTTT[C/T]TTTTTTTTTTTTTGA | 8853 |
rs534882282 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240006 | TTCCCTGTCCTGCTA[C/G/T]TTTTGGGGTGGTTTA | 8853 |
rs534891642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359466 | GTGGCTTTCAAGAGT[A/G]TCGAGACTGTAGTCC | 8853 |
rs534907952 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270950 | GGTGCCCGCCACTAC[A/G]CCCGGCTAATTTTTT | 8853 |
rs534909079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269886 | CCCACAGTGTGCACC[A/G]TCCCCACTGTCCCCA | 8853 |
rs534939522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308372 | AGGGGCATGATGCCA[A/C]ACCAGTCGTGAGAAC | 8853 |
rs534943025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225440 | TAGAAGCAGCCTTTT[C/T]TTCCCCAGGAAATGT | 8853 |
rs534963124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327714 | CGATCATGCACTCTA[C/T]GCATTGTAAAAGATG | 8853 |
rs534974154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367628 | CAGCTGGGCGTGGTG[C/G]CGTGTGCCTATAGTC | 8853 |
rs534985814 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211958 | GCCACCTTTTAAACT[C/G]TGTTCTGAAATTTGA | 8853 |
rs534988068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296857 | AGACCACTGCTGTTG[C/T]TGTATTAAAAGGAGA | 8853 |
rs535023470 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321535 | GATTCCTGCTTTGCA[C/G]AGGGAAAACCAAGAG | 8853 |
rs535041106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276855 | TCTTTCTTCTTTATT[C/T]GTGAGGTGTTTTCTC | 8853 |
rs535063573 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386354 | CACTGTCAAAGTGAG[A/G]AGAGTTGACTGATTT | 8853 |
rs535065066 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303419 | TCACGATGCTGCGAG[C/T]TGAAGAGCAAGGTGA | 8853 |
rs535083593 | in-del | -/GATTTTTTTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254526 | CCCAGCTAATTTTTG[-/GATTTTTTTT]TTTTTTTTTTTTTTT | 8853 |
rs535095943 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9308531 | TTGTATGTACCTGAC[A/G]GGCTGCTCTGTGTAA | 8853 |
rs535098891 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266099 | CCATAAGCTTGTAAT[A/T]TTCTATTTCTGAAAT | 8853 |
rs535102401 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302569 | AGCCTCCGCCTCCCG[G/T]GTTCCAGCTATTCTT | 8853 |
rs535109595 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339793 | GCTCTAGGCTTCTCC[A/T]CTTACTCCTGACCCA | 8853 |
rs535123194 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386937 | CGGCCGAGCGCGGGG[C/G/T]CTCACGCCTGTAATC | 8853 |
rs535136380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271296 | GCATTTAAACCCCAT[A/G]AATCTTCAGCTGATC | 8853 |
rs535164631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258232 | GCTGGGTGACAGAGC[A/G]ATACTTCATCTCAAA | 8853 |
rs535187684 | snp | C/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210791 | TGGTCTAGATCTCCT[C/G]ACCTTGTGATCCGCC | 8853 |
rs535204665 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371066 | TGTTCTGGGGCTAGG[C/T]GATTCTAAAAAATGA | 8853 |
rs535210558 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392966 | CTGTAAAACGTAGAC[A/G]CTAAGAAAGCTCTTC | 8853 |
rs535224163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291554 | TCGTGTCGTGACACA[C/T]ATTTGAGTAGTAATC | 8853 |
rs535237478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380914 | AGTGTCCTGAGCAGA[G/T]CTCAGTGTTTCTGAT | 8853 |
rs535247230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291980 | AAGAAACGGTTTTTG[C/T]TGTGGGAGGAAGAGC | 8853 |
rs535259662 | snp | A/G | 3.3211e-05 | 0.00407485 | missense | ASAP2 | GRCh38.p7 | 2:9374939 | ATCCCACTGGCCAAC[A/G]GACATGTAAGAGTGT | 8853 |
rs535260938 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240602 | TGCCACGCACCACGG[C/T]CGTAGCTTTTGCAGT | 8853 |
rs535283370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329365 | GTGATCTGCCAGGCG[C/T]TATTAGGGGTTTTGG | 8853 |
rs535317997 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369385 | CTTGCCCATCTTATC[A/G]GAGTGTCAGTGGCCA | 8853 |
rs535332448 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313417 | CACTCACTCGTGTAC[A/G]TTCATGTTCATGTGT | 8853 |
rs535344717 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328463 | TCATTTGACCTATTC[C/T]GCAACTCTCAGATGT | 8853 |
rs535355610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252690 | GGAGGTTGAGGCGGG[A/C]AGATCACGAGGTCAG | 8853 |
rs535357411 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266015 | CTGACCTCAAGTGAT[A/C]CACCCCCCCACCCCC | 8853 |
rs535367880 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403722 | AATTATTATTTTAGG[C/T]GGCCAGTGAACTGCT | 8853 |
rs535397768 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9335474 | TCGTCACAGAGACCA[C/T]GTGTCATTTGTGCTA | 8853 |
rs535411025 | snp | C/T | 0.000399281 | 0.0141238 | missense | ASAP2 | GRCh38.p7 | 2:9393625 | CCGCCCAGCCGCCTC[C/T]CGCAGAAGAAGCCTG | 8853 |
rs535434322 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348416 | AGGCGTGAGCTACTG[C/T]GCCCAGGTGACACTG | 8853 |
rs535437477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317737 | TCACATTCACACTCA[C/T]ATCCACACTCACACT | 8853 |
rs535445634 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399711 | AGGCAGGGAAGGGGC[A/T]GAGCAGACTCGGGGC | 8853 |
rs535448091 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370625 | TTCCCCCTCACAGAG[A/G]CATTGGGGGCATGAG | 8853 |
rs535488318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312311 | CCAAAGAGAAAAACC[A/G]TGAATGAAACCAGAA | 8853 |
rs535503410 | in-del | -/TCCT | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387486 | AGGAATCTCAGGAGC[-/TCCT]TCCTGTTCATATGGG | 8853 |
rs535568675 | snp | G/T | | | intron-variant, utr-variant-5-prime, missense | ASAP2 | GRCh38.p7 | 2:9237918 | TCCCAATTCAGAAGA[G/T]CCCTGAGGTGAGGTA | 8853 |
rs535572851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278630 | AGATAACTGTTTGAG[C/T]GCCTCCTATGTGCTG | 8853 |
rs535579632 | snp | A/G | 0.0150606 | 0.0854603 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406101 | TTTGTCACTGAGTGG[A/G]CCTCTGTGACATCTC | 8853 |
rs535586719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233700 | TCATTTGTGTTTAAC[A/G]AACACTTATATTGCA | 8853 |
rs535611826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305984 | TGTAGTAGTGGGGTA[C/T]AGATATTGGTGTAGA | 8853 |
rs535613578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9220148 | ACTTTTAGGCTATTA[C/T]GAATAATCCTGTGAA | 8853 |
rs535627764 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247697 | GCGTTTAGAAAGCGC[A/C]TAGGCTGGTGCCAGA | 8853 |
rs535697238 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259562 | AGTTTTCAGCCCAAA[A/C]CCTTAAGGAACAAAA | 8853 |
rs535698373 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213366 | GAGACGGGCAGAGGG[G/T]TGGGCAGTGCCAGGT | 8853 |
rs535708636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388944 | CTTCTGCCTTCATCT[A/G]GTCCAGCTCATGGCC | 8853 |
rs535720442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311679 | GTTTCCGTCCCTCTC[A/G]GCCAGAACTCGAGGA | 8853 |
rs535728122 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394358 | TCTAGTAGAGACGAG[C/G]TTTCGCCGTGTTAGC | 8853 |
rs535730524 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273090 | TCTGTGAAGAAAAGC[A/G]TTGGTATTTTGATAG | 8853 |
rs535732690 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9372211 | CTAACTGCCTGTCAG[A/G]AGAGGCATTTACATC | 8853 |
rs535777628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335938 | AGCATAAAGTTCCCT[A/G]TTGGCAGTTTGGTGA | 8853 |
rs535785673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253069 | AATCCCGAGGCAACA[A/G]AGAAACGAAAGTCGT | 8853 |
rs535796195 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341269 | AAAGGCTATTGTTAC[A/G]GGGTCGCCTGGGAGT | 8853 |
rs535797636 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228035 | CAGCGAGATCGGAGA[C/G]GATAGTCTAGATAAC | 8853 |
rs535837063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242912 | TGCTTTGATATAACT[C/G]AGGCCCAGTAACAAC | 8853 |
rs535839733 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234456 | CAAGGTAATGGCGGC[C/G]CGTGGCCTTGCAGGG | 8853 |
rs535842729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294061 | TAGAGTGCAGTGGTG[C/T]GATCTCTGCCCACTG | 8853 |
rs535862298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249656 | ACTGTCGTGTGGACA[C/G]AAAGTTCACAGCCTG | 8853 |
rs535872775 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243329 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 8853 |
rs535877417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227477 | TCTCTTTTTTCTTTT[C/T]TTAAAATAAGCTCTC | 8853 |
rs535904918 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329945 | TGTTGCCACCACACC[A/G]TCTGCTTGTCTCCAT | 8853 |
rs535935502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369854 | AGGGAGAGAATTTAG[A/G]TTTTTTTTTCCCCTT | 8853 |
rs535940349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343739 | GGCATAAGCCACTGC[A/G]CCCAGCCTGATATCA | 8853 |
rs535944358 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9309138 | AAGGCCTTTCTGACA[C/T]TATTTGAAAGAGTCT | 8853 |
rs535963216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323472 | TCTTAAAAGTAGAGA[A/G]AAACCACTAAATGTC | 8853 |
rs535969967 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255106 | GGCATTATCAGCCAT[G/T]TTACTGGGTGTGTAA | 8853 |
rs535977157 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337919 | GTGCAGTGACCACCC[A/G]TAGTGCAATATTATA | 8853 |
rs536023609 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388236 | CCTGTGTTGAATGTT[A/G]TCACCAGGAGCAGTT | 8853 |
rs536037549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260836 | GAAGAGCCCCGGATT[A/G]TGTAACCTGGACACA | 8853 |
rs536056393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343414 | TGGTGGCCTCCTACT[C/T]TCAACTCAGAGTGTC | 8853 |
rs536064854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268517 | TGCTCTGGCTTTAAA[C/T]GGAGCCCACAGGTCA | 8853 |
rs536072904 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263866 | CTATAATAGGTTAAG[C/T]ATTTTTTTCTCCATT | 8853 |
rs536077751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274514 | TTTTAGTAGAATCGG[A/T]GTTTTACCATGTTGT | 8853 |
rs536090916 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299678 | GGACGGCTGACGACG[C/T]AGGAGACGGGTGGAG | 8853 |
rs536092293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229876 | TGGGTGGGCCAGGCT[A/G]TTGGGGGCATTTGTG | 8853 |
rs536205442 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300328 | CACACCATGGAATCC[A/G]GACGAAACTAACTTG | 8853 |
rs536224763 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382920 | TTTAATTATGGCAAG[C/G]TGGCTGAGCGGTGGG | 8853 |
rs536229404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390431 | ACACCTAGCACCTGG[A/G]CCCTGTGCACCTGAG | 8853 |
rs536248390 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214140 | GAGAGGTGACGTTCC[A/G]TGATATGAACCTACC | 8853 |
rs536260799 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402070 | CACCACACAGTAGAC[A/G]CAAGTGGCACAGCTC | 8853 |
rs536266127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287669 | GGAAGGTTCCTGCAG[C/T]GGGTGGACGGCCTCT | 8853 |
rs536310045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207490 | GGCCTGGTCTTTTCC[C/G]CGCAGCGCGGCCAAC | 8853 |
rs536332401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351289 | TGATGTTAGAAATGC[C/T]AAAATGAGGGTCTTC | 8853 |
rs536335741 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293411 | TTAGAGTTTAAGATA[A/C]ATTTGAACAAGGGGG | 8853 |
rs536358508 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382173 | ATTTTTAATAGAGAC[A/G]GGGTTTCACCATATT | 8853 |
rs536371461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222077 | AGAGGCGTGAGCCAC[C/T]GCGCTGGCCTATTGC | 8853 |
rs536398737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228945 | AGCACCCCTCACGGG[C/T]CAACTCCCCAGAGGT | 8853 |
rs536409862 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345906 | TGTGTTCCTCTGGGG[A/C/G]TGCCTTTGTTTTTGC | 8853 |
rs536433090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313686 | ACCAAATTGACCTGC[A/G]CCGGTGACTCTGATT | 8853 |
rs536449257 | snp | G/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212639 | CAGGCACCGGTGCCT[G/T]CCTTTGTGGAGCATA | 8853 |
rs536450291 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378365 | AACTTTTGAAAATCT[C/T]AAGATTCCCCTTTAG | 8853 |
rs536456767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289858 | CATCCTGGGGTACCA[C/T]CCACAAAGACTGGCT | 8853 |
rs536458941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282494 | CTAAGGATAGATTAA[A/G]TTTTTTTAGAACTAG | 8853 |
rs536485541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221704 | TTTTGTGTATTTGTA[G/T]GTGTATTCCTTAGGA | 8853 |
rs536494695 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314204 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 8853 |
rs536505869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324934 | TTACTATTGATATGA[C/T]TGGATTTACTTCTGT | 8853 |
rs536514771 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257178 | ACTGGTGCTGGAGAT[A/T]CAAAAATCAGAAGGT | 8853 |
rs536519721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339422 | TCAAATAGGAATAAT[A/G]CAGCCAACCTCAGAG | 8853 |
rs536548384 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250731 | AGGGTGGAGCGGAGG[A/T]GTCTCAGCCCCTGAG | 8853 |
rs536551806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378030 | AGGTCCCAGTTTCTT[G/T]TTTTCCAGAGTGGAA | 8853 |
rs536561442 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249746 | CATGCCCGGGCTGGC[A/G]GGGGAGCTGCATGCA | 8853 |
rs536573972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401176 | CTCAGGCCTAGGTAC[A/G]GGACTCCTGAGACCG | 8853 |
rs536575213 | snp | C/T | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404402 | AAACATCCCACTTTT[C/T]ACTGTTTCAGGCCAT | 8853 |
rs536581748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281607 | CATTTTTTCATCACC[A/C]TCTTTGAAGTTCGTG | 8853 |
rs536611700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214913 | CTTTGACACTCTGGC[A/G]AAGGTGATCTGCCTC | 8853 |
rs536636279 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403425 | GAACTGTTTGTATGG[C/T]AGCCCATGTTCTCTA | 8853 |
rs536661342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338781 | GAGCACTCGTGGACA[G/T]CAGCTCCAGGAAGCA | 8853 |
rs536662146 | in-del | -/CTAT | 0.0115144 | 0.0749975 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332758 | GAGATCTCTGTCCTC[-/CTAT]CTATTTCACAAGAAT | 8853 |
rs536670362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270558 | ACCTCAAAGCATTTA[A/G]CCTTCTTTTGTGTTA | 8853 |
rs536677363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308956 | CGTTCTTTCAGATAA[A/G]CGGCCTTTAGAAAGA | 8853 |
rs536694346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9215454 | AAACAATACGAGATA[C/T]TTCTAATAAAGATAA | 8853 |
rs536732260 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9342881 | CTATCCACTTTGCCT[G/T]GAAGATCCTACCCTG | 8853 |
rs536762962 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307495 | CACCCGGTTTTAGAA[G/T]TAGTTTTGGGTGCCT | 8853 |
rs536801863 | snp | A/G | 1.7117e-05 | 0.00292544 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344495 | TAAAAATTAGGACCT[A/G]GACAAGATTAAAAAC | 8853 |
rs536813753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210674 | ATTCTCCTGCCTCAG[C/T]CTCCCGAGTAGCTGG | 8853 |
rs536816427 | snp | A/G | 3.61919e-05 | 0.00425378 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385194 | TCAGTGGGTCCAGAT[A/G]CATGGCCGAGTGTAT | 8853 |
rs536817329 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9316710 | CGCATCTTGAGTTGA[C/G]TCGCATTTGAACTGC | 8853 |
rs536817540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247093 | CTGCCTGCCTTAGCC[C/T]CTAAAATGCTGGGAT | 8853 |
rs536833670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326521 | GTATATACTTTTAAA[A/G]AAAATTGGTTAATAT | 8853 |
rs536835158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9333051 | CTGCATTAAAGGCCA[C/T]GCTGCAGTGTTTTCA | 8853 |
rs536848427 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211095 | AAGAGGTAGAGGTTG[C/T]GGTGAGTCGAGATCG | 8853 |
rs536852518 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9283552 | TTCCTTAGCTCACGG[C/T]TCCCTTCCATCTTCA | 8853 |
rs536877797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238083 | CATGGCTCTGGCCTC[C/T]GACTGCTGGGGTTTG | 8853 |
rs536878644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245160 | TAGAGATTCCAGGAA[C/T]TTGTAGCTTGATTTT | 8853 |
rs536910183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209976 | GCTGTTTTGATTTGC[A/C]TACTTGTTGCTGGAA | 8853 |
rs536939835 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9285353 | ACCTCAGAACCCCCC[A/G]TCCCCACTTCAAACA | 8853 |
rs536966111 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309408 | GCGGGATGATTCCAG[A/C]TACCGTATATAAAAT | 8853 |
rs537042673 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328574 | ATGACTGTGATGAGC[A/T]AAGGAAGATGTTAGT | 8853 |
rs537077484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240155 | GGGTATGTTCCAAGA[C/T]CCTCGGTGGATGCCT | 8853 |
rs537081048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368345 | GGCCATTAAATAAAT[C/T]ATCAGATGGGGATGG | 8853 |
rs537098660 | snp | C/T | 0.00010784 | 0.00734223 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391244 | TGGGCTTTGTAGATC[C/T]GGATGGCGGGGGGTG | 8853 |
rs537122771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334382 | TTTCTTTTCCATGTC[A/G]CGGTCGCCTGTTGCG | 8853 |
rs537127486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290736 | GAGGCTCAGGTGAGC[G/T]CTGGGTCTGAGGCCC | 8853 |
rs537149922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246080 | GACTGGCAGGAGCCC[G/T]GGTTTGGGAGTGTTG | 8853 |
rs537157019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230987 | GCTTCTTGCTTCCTG[A/G]CAGCACAAACCCCTG | 8853 |
rs537199127 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226140 | AGAAGGTCAGTTGTT[A/T]GAAGTCCCACAGCTG | 8853 |
rs537206532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354283 | CCTGGCCACAAGCTG[C/T]CCTTCACTGGCCACC | 8853 |
rs537217349 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9376258 | GCAGGCAGGGCAGGC[A/G]GCCTGGGAAGCACCT | 8853 |
rs537220028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258288 | CAGCTATTTATTTGT[A/G]AAGTTGAAATAAATG | 8853 |
rs537267210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354839 | TCAGGAGTAAACACC[A/G]CTACAGAGAGGTGGC | 8853 |
rs537271475 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265729 | TGTGTGTGTGTGTGT[C/G]TGTGCGTGTAATGGA | 8853 |
rs537276881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379276 | CTTTGGGCGCGTTTA[C/T]AGGCATTTTACAGAT | 8853 |
rs537285852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218367 | CCTTGACCAATTGGC[C/G]TCCTTAGAGCTGAGG | 8853 |
rs537312012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270869 | GCGATCTCGGCTCAC[G/T]GCAAGCCCCGCCTCC | 8853 |
rs537326099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353219 | TCTACTTCCTCACCA[A/G]CCTCATGGGATGAGT | 8853 |
rs537328878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225216 | ATCATCTGCTCCTTT[A/G]TAGAAAAAGTTGTCC | 8853 |
rs537334643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346393 | GTGAGCCGATATCAC[A/G]CCACTGCACTCCAGC | 8853 |
rs537360547 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232908 | AGAGGGGCTGCCTTG[A/C]CCTTCTGGAAGAAGG | 8853 |
rs537370380 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322662 | GAAAGGTGGTTGGTC[A/G]TCTTCTACAGTGATG | 8853 |
rs537373833 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271649 | CCAATTTCTTTTTCT[C/T]GGTGGAAATGGTCTG | 8853 |
rs537398971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298183 | CTCCTAAAGGTCAGG[A/G]AAGGCCAGGTCAAGA | 8853 |
rs537406290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219290 | GTGATTTTCACATTT[A/G]CCCTGTGATTCGGTT | 8853 |
rs537410742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374357 | TTGGAACAGAGGTTG[A/G]CCAGGGCTGCATGGA | 8853 |
rs537418228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380636 | CATTAACCAGGCCCA[A/G]TTTAATTTAGTGCTG | 8853 |
rs537424269 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253225 | CTGGAGTGCAATGGC[A/G]CGATATTGGCTCACT | 8853 |
rs537445956 | in-del | -/TAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264222 | TAATAATAATAATAA[-/TAA]ACACAAGTACTGCTG | 8853 |
rs537479327 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9255021 | CCATTTTCCAAAGTG[G/T]CTGCATCATTTTTCA | 8853 |
rs537485798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292135 | CAGGATCCATGGAAT[A/G]AAAGGACTCAGCAGT | 8853 |
rs537527021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341275 | TATTGTTACGGGGTC[A/G]CCTGGGAGTCACCTA | 8853 |
rs537555184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386970 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 8853 |
rs537577328 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9289162 | TCTTAGAAGCCTTTT[G/T]GCTGCTCTCCGTTAC | 8853 |
rs537608549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376156 | TGAGCTGGTCCCACT[C/T]TCTCCCCATCCCCAG | 8853 |
rs537609869 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325871 | TGTTTCACAGTTGAG[A/T]GAGAGCTGTACTATA | 8853 |
rs537615203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286411 | TCCAAAACAGAAAAA[A/C]AGGAAAAGGATTTTT | 8853 |
rs537622626 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9340257 | CGAGCTCCTGACCTC[A/G]TGATCTGCCCGCCTC | 8853 |
rs537624075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214088 | ATGCTATCCCCATTT[C/T]AGCTCCCCAAACACT | 8853 |
rs537625128 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217683 | GCGGTGGCACAATCT[C/T]GGCTCACTGCAAGCT | 8853 |
rs537626991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398945 | GATGACTGCCGGCCA[C/G]GGGGTCAGCCAGGTC | 8853 |
rs537632376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248846 | GAAGTCTTCCTGATG[C/T]CGACTCTGATGTGAG | 8853 |
rs537634834 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317495 | CTTACACCCTTACAC[A/C]CCCACTTACACCCCC | 8853 |
rs537650657 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359560 | CCTAGAAAGCAGTTC[C/T]TGAATTCTCTCCTGG | 8853 |
rs537690720 | snp | A/C/G | 0.000474862 | 0.0154028 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393678 | CCAGCTCGGCCATCC[A/C/G]TGCTCCTGCCCTCTG | 8853 |
rs537711591 | snp | C/T | | | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9215079 | CACCCAGATGGCATG[C/T]AGGCACCTAGGCTAT | 8853 |
rs537713793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253604 | CTCCTGTCATCTCTG[C/T]GCTGCTTTCTGTCCT | 8853 |
rs537733852 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207491 | GCCTGGTCTTTTCCC[C/T]GCAGCGCGGCCAACT | 8853 |
rs537735187 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9392881 | TGGACTCACAGCCTC[C/T]CTCCAGGTCTTACCA | 8853 |
rs537739821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277792 | AATGTATAATGACAT[A/G]ATTATAACTTCTCTT | 8853 |
rs537740923 | snp | C/G | | | missense | ASAP2 | GRCh38.p7 | 2:9388339 | ATCAGCTTCTACCAG[C/G]TGGGCTCCAACCAGC | 8853 |
rs537750057 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243359 | GTGATCCACCCACCT[C/T]GGCCTCGCAAAGTGC | 8853 |
rs537772217 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9405020 | ATTTTAACAATCCTC[C/G]TGCATCTGTATTTTA | 8853 |
rs537775040 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278399 | ACCCCTGTAATCCCA[A/G]CTACTTGGGAGGCTG | 8853 |
rs537818317 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352121 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGTAGG | 8853 |
rs537834642 | snp | C/T | 3.40686e-05 | 0.00412713 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318605 | GTGAAAGGGGTATGA[C/T]ATTGACACTGTGACA | 8853 |
rs537841249 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212887 | CACGTGAGAGCTTGC[A/G]AAGCACTGTTCGAGA | 8853 |
rs537872894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273758 | TGATCTGGGTGGTGT[C/T]AGCTGATCCAGTGAA | 8853 |
rs537876811 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306037 | ATATGGGATGGAGGG[C/G]CTGTGGGAGAGTATC | 8853 |
rs537880529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380960 | TCAGCCTGCCTTGGA[A/G]AAGGTATGCTAGGGA | 8853 |
rs537921781 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225360 | CACTTGTCTAGTGGT[C/G]TGTAGGACGCATGGC | 8853 |
rs537923538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218797 | CACCCTTGCTTTTTT[C/T]GGCTGTCGTCTCTGT | 8853 |
rs537938389 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279461 | CTGGTACCGTAATAT[C/T]GATGACCATTAACAA | 8853 |
rs537941013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272377 | AGATATGTCTATTTA[C/T]ATCTTTTGCCCTTTT | 8853 |
rs537949614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394238 | GGCGTGATCTCGGCT[C/T]ACTGCAAGCTCTGCC | 8853 |
rs537959505 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222040 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 8853 |
rs537969511 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400454 | TCCCTCCTCCCTCCT[G/T]CCATCCTCCCTCCTC | 8853 |
rs537973947 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9292175 | AGCCCTGAGGAGGTG[A/G]GGACAATGAGACCTG | 8853 |
rs538004593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300327 | CCACACCATGGAATC[C/T]GGACGAAACTAACTT | 8853 |
rs538008762 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302466 | ATGAGCCACCATGCC[C/T]GGCCAACTTTTTTTG | 8853 |
rs538013410 | in-del | -/CCT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362206 | GCATGCCATGCAGGG[-/CCT]CGGCTGACTTGCTTA | 8853 |
rs538014467 | in-del | -/AAAC | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357479 | ACGAGACTGTATTTA[-/AAAC]AAACAAACAAAAAAC | 8853 |
rs538024600 | snp | G/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208213 | CGGCTCAGAATAGGT[G/T]TACAAGTCACACGTG | 8853 |
rs538033855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241906 | TGCACATGTTAGGGT[C/T]CCAATAAGTTTAGGG | 8853 |
rs538067878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234619 | CACTATCCCCATTGT[A/G]TGGATCCAGAAGCTG | 8853 |
rs538088399 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382805 | TGTGGGGTTCTCCCC[C/G]GACCCCATACACCAA | 8853 |
rs538091090 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300857 | CAAGTTTCAACTTGC[A/C]CTTTATGGAAGTCGG | 8853 |
rs538097260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208188 | TGTGTGAAGTGCTTA[A/G]CACTCTGCTCGGCTC | 8853 |
rs538119068 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268445 | GATCTTAATTCTTAG[C/T]GACACCTGCTATTCT | 8853 |
rs538149449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232079 | GCTCCCACTGAGGTC[A/G]TGGTGATTGTCTTAA | 8853 |
rs538194698 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261629 | AGTAGGCCTTTCTTT[A/C]CCTGGGAGCACTTTG | 8853 |
rs538223592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288420 | AGGCTCCAGGATCTC[A/G]TGAAACCACAGGAGT | 8853 |
rs538251985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267679 | AGGTGGGTGGATCAC[C/T]TGAGGCCGGGAGTTC | 8853 |
rs538281198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228720 | AGGGACAGCAGAATG[C/T]GTATGTGAACTGGCA | 8853 |
rs538284522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237243 | TGACTTTTGCTTTTC[A/G]AAAAGTGAAAATGGA | 8853 |
rs538319390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364467 | CTGAGATTGTGCCAC[C/T]GCTCTCCAGCCTGGG | 8853 |
rs538330006 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9379818 | CCAACATGGTGAAAC[C/T]CTGTCTCCACTAAAA | 8853 |
rs538358436 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328550 | TTTATATATTATCCT[C/G]TGGAGCCAATGACTG | 8853 |
rs538358540 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318117 | CTGGGGCCTGGGGCC[A/C]AGAGCACCAACCCCA | 8853 |
rs538360851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227526 | CTATTTTCAAACGCT[A/G]TTCGGGTGGGACAGG | 8853 |
rs538360917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235380 | CAGCCCTGGTGGGTG[A/G]CACCCCAGCCCTTCC | 8853 |
rs538381915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324976 | TTTTTATGTCTGTCT[C/T]GTGTCTTTTGCTCCT | 8853 |
rs538407933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257961 | CCTGTGTTACCAACT[G/T]CCCAGGTTGGAGAGT | 8853 |
rs538418101 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255218 | GTTATGTGTCTATAC[C/T]TGTACCATGTAAGTT | 8853 |
rs538451631 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351761 | ATGTGATTCAGCGCT[C/G]CCAGCAAACTGCGGG | 8853 |
rs538468626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269636 | CGCCCTCAGGCGGTA[C/T]AGTGGGGCCCATGAA | 8853 |
rs538508104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326394 | TTAAAGCTATGGAGC[C/T]CTTTCTTCAAAATTC | 8853 |
rs538521491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350422 | TCACCAGAAATTGAG[C/G]TGGGTGCCCAAGTTA | 8853 |
rs538522131 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384307 | AGGGAGGACAGCCAG[C/G]CTGTGAGGCCAGAAG | 8853 |
rs538561961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229967 | ATGTGTGTTTGTGTA[C/T]GGAGCAAGGAAGGTC | 8853 |
rs538568052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319841 | CTAGGAGGATGTGGC[A/G]GCCTTTCTATTTCTG | 8853 |
rs538583879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343934 | ATGATTAAGCTCCCT[C/T]GGTCAGGGTCAGACC | 8853 |
rs538587785 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254664 | CAGGTTTGAGCCACC[A/G]TCCCCGGCCTATAAA | 8853 |
rs538589207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351353 | GTTTTTCTTCCTCAC[C/T]ACAGGAATAGTCTTT | 8853 |
rs538598893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358471 | CATTGAGGAGCCCTT[A/G]GTCACTGGAGTGTGT | 8853 |
rs538602213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280750 | CAGAAGGTGGCCATC[C/T]GTCTCTAGCTTTTTT | 8853 |
rs538618217 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217546 | TCTAGCCAGGCAGTC[A/G]GGATTGTCGGGACCT | 8853 |
rs538621155 | in-del | -/TCAC | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317662 | TACACACTTACACAA[-/TCAC]TCACATCCATAATCA | 8853 |
rs538632093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384132 | CAAATCTGCACGTTG[G/T]GCACATGTACCCTAG | 8853 |
rs538632770 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253080 | AACAAAGAAACGAAA[A/G]TCGTTTTTTGTTGTT | 8853 |
rs538639079 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281767 | ATTGTGAGTGGTTAT[C/T]GTTCTTAACCCTTTC | 8853 |
rs538640355 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210109 | GAGAGGTTAAGTAAT[A/T]TGCCAAAGGTTATAG | 8853 |
rs538649471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365647 | TGCCCACACACAGAC[A/G]ACTCCCCCGTATGGT | 8853 |
rs538657454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372023 | AACAGACCTGTGCCC[A/G]TGTTTGTGTAGGAGC | 8853 |
rs538658566 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286047 | TTATCAATTAGAACA[-/G]GGCAGTTCAGAACAA | 8853 |
rs538663772 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302225 | TCGCCCAGGCTGGAG[C/T]GCAGTGGTGCAGTCT | 8853 |
rs538678194 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249540 | AGATTGCCCTGTAGG[A/G]GGAATTGCTGATGTC | 8853 |
rs538698378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331432 | GATCCTGTACTCTAG[C/T]GGAATCTAGAAGTAG | 8853 |
rs538713007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345401 | AGCTTATGAAAAGCC[A/G]GTCAGGATAAAGTTC | 8853 |
rs538717739 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318127 | GGGCCCAGAGCACCA[A/G]CCCCAGTACAGTCCA | 8853 |
rs538730664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243366 | ACCCACCTCGGCCTC[A/G]CAAAGTGCTGGGATT | 8853 |
rs538731750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377358 | CAGTGTCCTGAGCAG[C/T]AGGGAGGTAGCAGGC | 8853 |
rs538733732 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371027 | CAAGCACCAGGGGTA[C/G]CTAACGAAAGCAGGG | 8853 |
rs538740131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249986 | AGGCAGGGCTTGGGG[C/T]CAAATCTGGGTATAC | 8853 |
rs538764865 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9246547 | TCAGCCTTGGCCTCC[A/C]ATGCCAGGATTACAG | 8853 |
rs538800238 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387515 | GGAGGAAAACATCGA[C/T]CTCTGCTGAATGAGC | 8853 |
rs538807160 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9355933 | TTATACAAATCAGTA[A/G]TTTCGTAACAGAGAG | 8853 |
rs538808061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367014 | CATGTTTGTTAACTC[C/T]TTTGCCTGCATAATT | 8853 |
rs538816770 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307630 | ATTCTAGTGGAGAAG[C/G]GGGCAGAGGGCCCAG | 8853 |
rs538855005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238606 | TTAAGTACAGTGTTT[C/T]GTTTGCATGGGGAGG | 8853 |
rs538882698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401793 | AAACAAGCTGTGGCC[A/G]CCCAGGCGTCCAGCA | 8853 |
rs538894124 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317760 | CTCACACTCACATCC[A/G]TACACAATCACACCC | 8853 |
rs538905604 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9228254 | CCTTTTGAGAGAATC[A/G]TATCTTCCTTCAGTG | 8853 |
rs538916386 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9333433 | AAGTATAAGAAGGCC[C/T]CTTATAGGGGAATAA | 8853 |
rs538920790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251377 | AGCCTTAGGGGACCT[A/G]CCCTCCCTGTGGGGG | 8853 |
rs538923384 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274574 | GTAATCCGGCCATCT[C/T]GGCCTCCCAAAGTGC | 8853 |
rs538923800 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282335 | ATCTTTATTTCGGAA[C/G]AAGCGTTGTCTACTG | 8853 |
rs538933873 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346621 | CTGTGGTTTGCTTTC[A/G]AATTGGTGTCCACTC | 8853 |
rs538938229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9237881 | CCCATCTCTTCCCAT[G/T]ATTTTGAGAGTATGA | 8853 |
rs538938929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289965 | GGGGTGTTGGAGAAG[G/T]CGGAGGAAGTGGCAG | 8853 |
rs538941639 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226419 | CATGGGTCTACTTTC[A/C/T]GCCCCTCTTGAGCTT | 8853 |
rs538945804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373054 | AACCCACTGAGACCA[C/T]GTATCTCACACACAA | 8853 |
rs538955804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396219 | GGACACTTCAGGACT[A/G]CAGATAGGAGCATTT | 8853 |
rs538973711 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245247 | TAGCAATGGCTTTGT[G/T]GAGGAGGGTGTTGGT | 8853 |
rs538984466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295587 | AAGGTCATACAGATA[C/T]TTACAGGTGGACATA | 8853 |
rs538989716 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216422 | CTCCTGTGTAGCTGG[G/T]ACTACAGGTGTGCCC | 8853 |
rs538997559 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378342 | CTGGTCTTGTGATAT[A/G]TTGGAAGAACTTTTG | 8853 |
rs539029648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210742 | TGTATTTTTAGTAGA[G/T]ATGGGGTTTCACCGT | 8853 |
rs539029825 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392222 | GTAAAGAAGCGGGAG[A/G]AGGTTTTTAGGAAGA | 8853 |
rs539034299 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9377149 | ACTGCCAGGTGTGAG[C/G]TACTCCATGGCAATC | 8853 |
rs539051249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309443 | GAAAGTGCAGTGTTC[C/T]CTGGCAAAGAAGCAG | 8853 |
rs539054797 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218764 | GCTGCTGTCTGCAAC[A/T]CTTCCCCTGCCTCTT | 8853 |
rs539062295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271165 | GTCCAAGTTAAAAGC[A/G]GACCCCAAATGGTTA | 8853 |
rs539092615 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392940 | CCCTCCGTGGGCCTC[A/T]GCCTCCTTGTCTGTA | 8853 |
rs539115360 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238483 | CAGATCACTTTCATC[A/C/T]ACCTTCCCATGGGGG | 8853 |
rs539118946 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403648 | AAAAATGTTTGCATT[A/G]ATGAATAAATTCTTC | 8853 |
rs539137399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308669 | TGCCAGCAGGAGTTT[C/T]AGTCCAGCCGTCTTT | 8853 |
rs539138756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360629 | AATGGCCAATTTCAA[A/G]CTACCTAAGTGAATT | 8853 |
rs539150135 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301790 | TAGAGGAAATGGAAA[G/T]CTCTACCAAGCAACG | 8853 |
rs539161501 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263863 | CTTCTATAATAGGTT[A/C]AGTATTTTTTTCTCC | 8853 |
rs539173145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270944 | ACTACAGGTGCCCGC[C/T]ACTACGCCCGGCTAA | 8853 |
rs539180242 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9297713 | ATTCGTCTTCTTAAG[A/G]GCCTCTGACTTGAAT | 8853 |
rs539199999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297515 | AGTAGAGGATAGTTA[C/T]GGTTTGTTTGATAAA | 8853 |
rs539204255 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325049 | TAGAGATATTCACTA[G/T]ATGAAAAACAAGCAA | 8853 |
rs539211394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320815 | CCTTCAGATTCATCT[C/G]CCAAAAAATAACCTG | 8853 |
rs539212642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245798 | CTAGAGTGTCATGGA[G/T]GCTCCTGGGGGACAG | 8853 |
rs539220110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386928 | GCACATGACCGGCCG[A/G]GCGCGGGGGCTCACG | 8853 |
rs539229222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379940 | GAGGTTGCAGTGAGC[C/T]GAGATTGCACCATTG | 8853 |
rs539245542 | snp | A/G | 3.2987e-05 | 0.00406108 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9335158 | TATTTTGAAATCCGC[A/G]TTGCAGGTTGAACAG | 8853 |
rs539248559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239153 | TCAGATGCTTTTTCC[A/G]CACTGACTGAGATGA | 8853 |
rs539286748 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298069 | GGGACAACATTTTGA[A/G]GAAGTGGGCAGCCCA | 8853 |
rs539295335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291546 | CACAACATTCGTGTC[A/G]TGACACACATTTGAG | 8853 |
rs539306776 | in-del | -/CTGT | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249310 | CAGCCTGCCCGTGGC[-/CTGT]CTGTCTGCCCCATTC | 8853 |
rs539329517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291653 | ACGCTCCCTTCGCCG[A/G]GCTGTCTGCATGGAA | 8853 |
rs539329803 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332173 | CAACAAAATTTGATT[C/G]GGTAATGTTGATGGT | 8853 |
rs539354914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327187 | ATCAGCAGCTTTTCC[A/G]GGGGACATTCCATTT | 8853 |
rs539362189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386248 | GCATTTCTGAAACCT[G/T]TTGGACTGTCTGCTC | 8853 |
rs539393341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225354 | TAAAGACACTTGTCT[A/C]GTGGTCTGTAGGACG | 8853 |
rs539404217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398408 | CCCAACTACTCAGGA[A/G]GCTGAAGCGGGAGGA | 8853 |
rs539406306 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316950 | ACACCCTCACTCTCA[A/C]ACCCTCCCACACACC | 8853 |
rs539412595 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9375576 | AATCGACTCAGTTTT[A/G]AAATAGACGCTATGT | 8853 |
rs539422324 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354123 | TGAGCCATTATCCGC[A/G]AACCCCATAGGCACC | 8853 |
rs539426450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395210 | AGGCGCCATGGCTCA[C/T]GCCTGTAATCCCAGT | 8853 |
rs539441887 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405181 | AGTCTACAATTTGGT[A/G]CTATTGTGCAGTAAC | 8853 |
rs539475871 | in-del | -/A | 0.339203 | 0.233544 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398809 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 8853 |
rs539514425 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9222537 | ACAGGAGACTGCTCA[C/G]TTCTTGACAAAAGGT | 8853 |
rs539525173 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341268 | CAAAGGCTATTGTTA[C/T]GGGGTCGCCTGGGAG | 8853 |
rs539555202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232213 | TGCCTCCCTCCCACC[C/G]CATCTCATCCATGCC | 8853 |
rs539562272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361672 | TCCTGGGTTCAAGCA[A/G]TCCTCCCACCTCAGC | 8853 |
rs539628196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252633 | AAGAATTTAGGAACA[C/T]GGCCGGGTGCAGTGG | 8853 |
rs539639527 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9261197 | AGCAGGGGTAATGCC[C/G]GGTGGTTATTTTCCC | 8853 |
rs539656423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380509 | GGCCAGTTTTAGTTT[C/T]TTGATTAGTTCAAAC | 8853 |
rs539674116 | in-del | -/GTC | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293686 | GGAGGGATGGCTGTT[-/GTC]GTGGTGGGCACCGTG | 8853 |
rs539678984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374385 | GGAGGGCAGGGGCAG[C/G]GCCTTCCTGGGGGAG | 8853 |
rs539721288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354964 | TTCCCCTGCCCCTGC[C/T]TTTCTTTATTAAATA | 8853 |
rs539744791 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317729 | ATACACAATCACATT[A/C]ACACTCACATCCACA | 8853 |
rs539762734 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9282402 | TGTCATGTTGATGAC[A/G]TCATTCACAGTGTCT | 8853 |
rs539765160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226757 | CCGTCCGTCCACTCA[A/G]AACATTGGCAATCTA | 8853 |
rs539766539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234357 | AGTGAGAAAACCCGG[A/G]GAGAACATTTAGCCA | 8853 |
rs539772756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266425 | GTGTTGGGGTTACAA[A/G]CATGAGCCACTGTGC | 8853 |
rs539804511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369263 | ACCTCAGGTGATCCA[C/G]TCGCTGCAGCCTCCC | 8853 |
rs539816536 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9360232 | TTTATTTTGTACTAT[-/G]TATTTTGCAGGCCAC | 8853 |
rs539836142 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330284 | ATAGGGATAGAACTG[A/T]AAGTCATTATCTTAA | 8853 |
rs539850840 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405803 | GAGCGGTAATCTTTT[A/C]AGGTTCTCTTAACTC | 8853 |
rs539874000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335762 | GGGACTTGTTTTTAA[A/G]AAGCCATTAAAAAGT | 8853 |
rs539878800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363192 | TTTTAAAATCCATTC[A/G]TCCATTGGTGGCATT | 8853 |
rs539891170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325531 | AGACATCTATTTACC[C/T]AAACACTTTAAGACT | 8853 |
rs539898315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247364 | TGCCTAGGGAGTCCC[A/C]GACGGTCCCCGGTCC | 8853 |
rs539913377 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247171 | TGAGGAGAAAGGTCT[A/C/T]CTTCCTGACAGCAGT | 8853 |
rs539915543 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252972 | GCGTGGGCCCAATCA[C/G]TGGTCCTACACCAAG | 8853 |
rs539925346 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359159 | ATTCTACAGAAATGG[A/C]GTAAGATGGTGACAT | 8853 |
rs539938494 | snp | C/G/T | 1.65231e-05 | 0.00287424 | missense | ASAP2 | GRCh38.p7 | 2:9385270 | CCTTATCTGGAAGAT[C/G/T]TAATTCTCACGTTCA | 8853 |
rs539949250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247553 | GTTTTTAAGGCAGCC[A/G]TGTGGATGGGCAGTG | 8853 |
rs539971707 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302567 | GCAGCCTCCGCCTCC[C/T]GGGTTCCAGCTATTC | 8853 |
rs539985071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312256 | TTTATTTTCTGATTA[A/G]AAAAGTAATAGTTTC | 8853 |
rs540006780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272788 | ATATTTAGTCTTCCC[A/C]GCACAATTTATTGAA | 8853 |
rs540025674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349057 | GTCTTTAGCTACAAA[A/G]TTGGTGTAGTTCCTA | 8853 |
rs540031327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394443 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 8853 |
rs540043394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267429 | TGTTGATTTGCTTAG[C/G]ATTAGGGCCTGCAGC | 8853 |
rs540046089 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400566 | CACTGGGGGACACTC[A/G]CTGCCACACAAGCTC | 8853 |
rs540084110 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394850 | CTTCGCTGAAAGGAC[C/T]CGAAGCCTGGGGGTG | 8853 |
rs540096024 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9389455 | CTTATGTGGTAGCTG[C/G]TAGCTGGGCAGGCTG | 8853 |
rs540128220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271676 | TCTGCGGAAGACGGC[A/G]GGCAGAGGGTACGGA | 8853 |
rs540130977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242032 | TTGGTTAGCTTCTTC[A/G]AGCACTAGTTTCCTC | 8853 |
rs540134911 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322070 | TGTCAGCGACACCTT[A/G]GAGTTGTATAATTCT | 8853 |
rs540135283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279241 | GAGGCAATCAGAGTG[A/G]CACTCAACGTGGTGC | 8853 |
rs540135787 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363896 | TCTTTTCCAATGGAA[A/T]GGAAGTTGCATAATT | 8853 |
rs540142941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399614 | ATGGACAGCGCTGAC[C/T]CAGAGTGCTCGGACC | 8853 |
rs540163499 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234699 | GATGGATTTACTCAG[G/T]GTTCAGTTGGTTGGA | 8853 |
rs540166095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272179 | ACATTCCCACCAATA[A/G]TGTACAGGGGTTCCC | 8853 |
rs540197443 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285746 | CAACAGAAGATTTTC[A/C]TTTTCACTTCTCTAG | 8853 |
rs540221353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213548 | ATGAAAGGAAAGAGG[C/G]AGACCAGTTGTGGGG | 8853 |
rs540271643 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9299189 | CCAAGTTGAGAGGCT[C/T]ACAAGTACCCAGCGC | 8853 |
rs540273371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207724 | CATCCCGGGCTGCCC[C/G]GGAAGGCGTGCCCGC | 8853 |
rs540280043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293688 | AGGGATGGCTGTTGT[C/T]GTGGTGGGCACCGTG | 8853 |
rs540322546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267771 | GGCGTAGTAGTGCAC[A/G]CCTGTAGTTCCAGCT | 8853 |
rs540325137 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395111 | ACTGCTCAGTTACAA[A/G]CTCAGACACAGTCGG | 8853 |
rs540338593 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229559 | GGAGGAGCGGAGCGG[C/T]TGTGGCCAGCATTGA | 8853 |
rs540351778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299242 | GAGGCATCCCTGTGT[C/G]AACTTGCAAAAGATC | 8853 |
rs540373324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355797 | TTTTCATTGAATAGC[C/T]TCAGTTTTTAGAAGC | 8853 |
rs540393165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306108 | GTAGGGGCTGTGAGG[G/T]GTGTATATATTGGTG | 8853 |
rs540404402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261027 | TAGTGTGCTGGGAGC[C/T]GTATGACAGCCCCTT | 8853 |
rs540420243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312482 | CCCCCACCTCACGAT[A/G]CCCCATCTTTTGAAG | 8853 |
rs540427044 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227360 | AGTGTCGTTCAGCAG[C/T]GAGCCTCCTCTAAAG | 8853 |
rs540456920 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305242 | GGCTGCAGTAGTGGG[A/G]TATACATATTGGTGG | 8853 |
rs540466352 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219680 | TGTTGTTGCTTTTTT[A/T]AAAAAAAATTGAGAT | 8853 |
rs540478148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280901 | ACAAATGAGTAACCT[A/G]CAAATCAGAGAGTTC | 8853 |
rs540486673 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317677 | TCACTCACATCCATA[A/C]TCACATCCTGAAACC | 8853 |
rs540495840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234003 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAT | 8853 |
rs540498156 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9287324 | CGTGGCACATGCCCC[A/G]AAGGTGAGCCACACA | 8853 |
rs540545769 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227036 | CGGGTCCTGCTCCCT[A/G]GCGAGAAGGAAGTAT | 8853 |
rs540549435 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9312914 | CAAAAATTAGCTGGG[C/T]ATGGCATGGTGGCGT | 8853 |
rs540556164 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9251739 | CTGGAGGACATCAGC[A/G]TGGCAAATGGAATGC | 8853 |
rs540573495 | snp | C/T | 3.29511e-05 | 0.00405887 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9376946 | CCTTGCAGTCAGATC[C/T]GTGGATCGAACCTCT | 8853 |
rs540583343 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265332 | GATTTTGGAATTCAA[A/C]GGAATCCCGGAATTA | 8853 |
rs540585267 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217793 | CTAATTTTTGGTATT[G/T]TTAGTAGAGACGGGG | 8853 |
rs540597243 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381780 | TGGTGGCACGCACCT[C/G]CAGTCCCAGCTACTG | 8853 |
rs540600232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331620 | TAAAAATACAAAAAT[C/T]AGCCGGATGCGGTAG | 8853 |
rs540603575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314403 | AGGTGTTAATAGAAC[C/T]AACATTTTATCTGAA | 8853 |
rs540612355 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367020 | GTTAACTCCTTTGCC[-/T]TGCATAATTTTTTTT | 8853 |
rs540622037 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221927 | GCCTCCCGAGTAGCT[A/G]GGACTACAGGTGCCC | 8853 |
rs540628266 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9289498 | AATAAAAGTAAATGC[A/G]GATACATTCTGTACT | 8853 |
rs540658937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396353 | GATCACGGTTCACCG[C/T]AGCCTCGACCTCCTG | 8853 |
rs540660184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222413 | AGGCTTAGAGCCAGG[A/C]CTCGTGTGTTCTCTG | 8853 |
rs540664521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293299 | AGAATTGAGAAGAAA[C/T]GAAGTCTTGTCCTAG | 8853 |
rs540678497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318907 | GGAGCAGGGAAACCT[A/G]TGGGAGGAGTCGGGC | 8853 |
rs540703964 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307708 | AGAAGCAGCATTAAG[A/T]GCAGAAACCAGGTCA | 8853 |
rs540708314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342981 | CAGTTCCTGAGTGCT[C/T]TTGTTCTCAGCTTCC | 8853 |
rs540744162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319320 | CACGATTCCTGGGTC[C/G]CATCGGGGATGACTG | 8853 |
rs540753537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254076 | CCGGGCGTGGTGGCA[C/T]GTTCCTGTAGTCCCA | 8853 |
rs540771165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343511 | GAGTGCAGTGGTGCT[A/G]TCATGACTCACTGCA | 8853 |
rs540780090 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345990 | GGGATTCTCGGTGAC[C/T]TCTGGTCTAGGGGTT | 8853 |
rs540780727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229204 | AACCCAACAGATTTA[A/G]AGATAGTAGGGCATA | 8853 |
rs540790381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280236 | TGTCCCCTCACCCTC[A/G]TGGTGTCTTTCTTTA | 8853 |
rs540794989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401813 | GGCGTCCAGCAGGGT[A/G]TGGGAGCAAGATGAG | 8853 |
rs540806835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235838 | GGTGGATGCAGCCGG[C/T]AATGCCTTCCCATGA | 8853 |
rs540812146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243400 | GGCATGAGCCACCGT[G/T]CCCGGCCTAAAGATT | 8853 |
rs540855129 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365219 | GCTTTGGAGGCAGCA[C/G]TTTGGTCAAGCCCCT | 8853 |
rs540858778 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9242031 | GTTGGTTAGCTTCTT[C/T]GAGCACTAGTTTCCT | 8853 |
rs540887898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249247 | AGCTTTAGCCTCAAA[C/T]TCCACCTTGAATGTG | 8853 |
rs540907311 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378496 | TAATGATAGAGAAAA[C/G]CTCAGCCTCCGTCCT | 8853 |
rs540924132 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9226859 | CAGAAAGGCGGGAGG[A/T]CTGGAGAGAGATTGC | 8853 |
rs540934633 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9367204 | CCTGGCTAATTTCTT[C/T]TGTATTTTAGTAGAG | 8853 |
rs540948681 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267726 | ACATGGTGAAACCCC[C/T]GTCTCTACTAAAAAT | 8853 |
rs540948881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9215018 | TGACGAACATGCATC[G/T]TTAAGATTTCTTCAT | 8853 |
rs540952400 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344901 | TGTTCTCCGTGTGTG[A/T]TGGTATTAAGGATGT | 8853 |
rs540973408 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339054 | TGTAGTGACATGCAC[A/G]TGTAGTCCCAGCTAC | 8853 |
rs540984281 | snp | A/G | 0.000190934 | 0.00976886 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350918 | TCCCTCTGAGATGCC[A/G]CGCCATAGAGACGTT | 8853 |
rs541020992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230192 | CAGCTGATTACCATA[C/T]GGTGTGATAAATGTG | 8853 |
rs541047354 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269268 | GGGGGGGAGGGGGCG[C/T]GCATAACATTTATCT | 8853 |
rs541061267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359033 | AGAAACTCATTGATA[A/G]TTCTTCATTTTTAGC | 8853 |
rs541070167 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249809 | GGGATACTGCAGAGG[A/T]TGACCGAGGGGCATG | 8853 |
rs541074621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275615 | ATGCACTTCCTGCCT[A/G]CCCTGATCCATTACC | 8853 |
rs541086489 | snp | C/T | 0.000116317 | 0.00762528 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9401345 | CGATGAGCTCACCTT[C/T]TCCGAGGGGGATGTG | 8853 |
rs541107095 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9309825 | AGGAACTCAATTTTT[-/A]AACTTCATTTAAGTT | 8853 |
rs541109581 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233217 | CTGTGTGACAATTAT[A/G]ATGAAGGCTGGTATT | 8853 |
rs541173450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244832 | AGGCAAACCCTTTTC[A/G]TTAGATCCTTTCTGA | 8853 |
rs541184307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295147 | GGATTTTAAAAATCT[A/G]AAAATTAGATACTTT | 8853 |
rs541195997 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326723 | AGTATGTTGATGTCC[A/G]TGTCAGAAATTTTGG | 8853 |
rs541200881 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377695 | GCCACAGAAATTGCT[C/G]CAAAGGAAATGGAAA | 8853 |
rs541213514 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213334 | TGGGGAGGAGTGGGC[A/G]AGGAAGAGAAGGATG | 8853 |
rs541246201 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264448 | TGTTCTCATTATGAG[A/T]CCCCAGCTCTGACGG | 8853 |
rs541293523 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210852 | AGGTGACCCATGTGT[A/G]TTTTTTAAAAGTTTG | 8853 |
rs541296619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238751 | CACTTTGATGAATCT[C/T]ACAAATGTACAGTTG | 8853 |
rs541305560 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300295 | GTCCTTGCCTAGGCA[G/T]GCCCACTTGGAGCAC | 8853 |
rs541321183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270256 | TTACACATAAGTTCC[C/T]GTGAAAGTTGCTTTT | 8853 |
rs541325016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360228 | ATTGTTTATTTTGTA[C/T]TATGTATTTTGCAGG | 8853 |
rs541354954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390614 | GATTTGCACTCTGCC[C/T]CCAACCTGTGCCAGC | 8853 |
rs541355001 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383108 | ATCATCTCGGGGGGG[A/C]CACGGGACTGTTTGA | 8853 |
rs541380655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373119 | TTAGCGCTGTGTGGA[C/T]GGGGAGCATGTGCCG | 8853 |
rs541389018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397514 | GGAACACACCGGTAC[A/G]CCCTCCTTGTGAAGG | 8853 |
rs541392429 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286145 | CTCACGCCTGTAATC[C/T]TAGCACTTTGGGAGG | 8853 |
rs541406353 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379628 | CCTCAGGAGGAAGTA[C/T]TTTTGAAGGACTGTT | 8853 |
rs541416438 | in-del | -/TGTC | 0.0185938 | 0.0946107 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348113 | CTGATGACACTTTTT[-/TGTC]TGTTTGTTTGTTTGT | 8853 |
rs541423354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283330 | TGATCCACCAGCCTC[A/G]GCCTCCCTGTAATAG | 8853 |
rs541424891 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307436 | AATACATTTGAAAAA[C/G]TACTTTCATTTCTGG | 8853 |
rs541453659 | snp | C/T | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403616 | AAGATCCTGCCTCTA[C/T]GGAATTAGCTAAACC | 8853 |
rs541467685 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380014 | AAAAATAAATAAAGT[A/G]TATACTTTCAGGGTT | 8853 |
rs541469713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290951 | AGTTTTCCCCACCAC[C/T]GTTAGCATTTTGATG | 8853 |
rs541472513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250944 | TATGAAACGAGGCGT[A/G]GTGAAAGTCAATTTC | 8853 |
rs541516307 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9285211 | CTGGAGAGAGTATCA[G/T]AATACCCCGGGGTCT | 8853 |
rs541542221 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256523 | TTAGATGTTGTTAGT[A/G]GTAGAGAGTTGAAAC | 8853 |
rs541583427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210808 | CCTTGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA | 8853 |
rs541584437 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294485 | CTGGAGGCAGCCTGC[A/G]TGGTCCATAAAGTGC | 8853 |
rs541634668 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9277226 | TGTGGTCTAAGCTTC[C/G]CGAACTGGTGTTTCT | 8853 |
rs541649070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232505 | AAGTGCAGAGAACTT[A/G]TCTGATTTGTTTAAC | 8853 |
rs541654713 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368214 | GCGCGTTTTATGACA[A/G]TGCGTCTCTGTAATA | 8853 |
rs541656797 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9330650 | ATGGAGACTCAAAAT[A/T]CTTACTTTGTGATGA | 8853 |
rs541666456 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320885 | CTACAAGAAGTAGAA[A/T]TGGTTTCCTGACCCG | 8853 |
rs541697559 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9287479 | ATCTGAAGGACGCGG[A/G]GCTCCTGGTTTCGGA | 8853 |
rs541730018 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328078 | TTGAGAACACGTTCA[A/G]TGAAGGAAGCCAGAC | 8853 |
rs541743866 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365708 | GGGACTGCTCTGCTC[A/G]TCTGGGCCTGGTGCC | 8853 |
rs541771977 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298785 | TCCCCGCACCTGGGT[C/G]GATAAGCCCTTTCCA | 8853 |
rs541773279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218559 | GTTAACAGAGGACTT[C/T]GGAGAGGTTTTGAAA | 8853 |
rs541790197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252187 | GACACCAGCTGCTAG[A/G]ACTGCATTGGAGTGA | 8853 |
rs541807112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211413 | TTTTCGTTTCTTCGA[A/G]CCTCTGGGCACTTTG | 8853 |
rs541859043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212324 | GTCCTGTGGATGTGC[A/G]AGGGTGCAGGTGGTC | 8853 |
rs541861551 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392392 | GAGAATTCTAGAGCC[A/G]AGGTGCTCGTGACTT | 8853 |
rs541883804 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405242 | ATTAACGACCCTGCT[A/G]ATATCCTTTCTTAGT | 8853 |
rs541894378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347214 | GAGTGTTCCTTTTCT[C/T]ACCTTTTCCCTATTT | 8853 |
rs541896772 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9329646 | CAGCTCCTGTCCCTG[C/T]GCAGACCAGAGATGA | 8853 |
rs541931201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302809 | GGTGTGAGCCACCAC[A/G]CCTGGTCAGAAGACA | 8853 |
rs541932037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340271 | CGTGATCTGCCCGCC[C/T]CCGCCTCCCAAAGTG | 8853 |
rs541935519 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364867 | TTCTACGTACACTGT[A/G]TTATCTAACCTAAAT | 8853 |
rs541951507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258533 | ACCTAAGGCCCCAAT[C/T]CGAGTAGGTGACAGT | 8853 |
rs541959903 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239907 | AATTTTTTTGTAGAG[A/T]TGAGTTTTTGTCATG | 8853 |
rs541968555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217640 | TTTTTTTGAGACGGA[A/G]TCTTCGCTCTGCCAC | 8853 |
rs541974255 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368689 | TTTTGGGTGACCAAA[G/T]AGAAATTTTTTTAGG | 8853 |
rs541981348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393429 | CCAGTGAGGAGGCCT[C/G]AGTGGGAAGCCTGGC | 8853 |
rs541991640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271689 | GCGGGCAGAGGGTAC[A/G]GAAAGTAGGGAAGCG | 8853 |
rs542002922 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322443 | TTTTTTGAGTGCTTT[C/G]TGTTGGTTTTGTTTA | 8853 |
rs542006633 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9209036 | GTTTACAGTGTATAA[C/T]TCCAAAGCTCTTTTT | 8853 |
rs542016333 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299116 | TTTAGAAAGAGAGAA[C/G]GTTGTCATCAATGCA | 8853 |
rs542024895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329706 | GAGTGGAAGGTGTGG[A/G]CTGACAAGAAATCTT | 8853 |
rs542026712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336932 | AAATAAGGCAGAGCA[A/G]CTGCTGGGGCCAAAT | 8853 |
rs542035484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233123 | GATACGGCTTTGAGA[C/T]AGTTTGAGTCATCTA | 8853 |
rs542036162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240322 | GCAGTGGCGCCATCA[C/T]GGCTCACTGCAGCCA | 8853 |
rs542036600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375195 | GCTGGGGTGAGAGGA[A/G]TCGGTTGAGCCCAGA | 8853 |
rs542043851 | in-del | -/TA | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271012 | TTAGCCAGGATAGTC[-/TA]TCGATCTCGTGACCT | 8853 |
rs542045042 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205652 | GGAGACGGCTTTGTC[C/T]GACATATTGAATTTC | 8853 |
rs542045851 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264956 | CCAGCCTGGGCAACA[C/T]AGGGAGACGTCTCTG | 8853 |
rs542059113 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9206580 | GCGGCGCGCGGGGCC[C/T]GGAACGCCGAGACAA | 8853 |
rs542073225 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361367 | GTGGACATCTCCCCA[C/T]GGCTCCCCCAATCCA | 8853 |
rs542077768 | in-del | -/GT | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285805 | ACATTCTTATCGAGA[-/GT]GATATTCCTACCCTC | 8853 |
rs542079212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362198 | TCAGAGTTGCATGCC[A/G]TGCAGGGCCTCGGCT | 8853 |
rs542083765 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236091 | CCTGATGTTGAGAAA[C/T]GCTGGGTCAAAAGGC | 8853 |
rs542094897 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219499 | TTGTATTCATATATA[C/T]TGGATGTGAAAAGTC | 8853 |
rs542111643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246481 | ATTTTTTGTAGAGAC[A/G]GAGTATCACCATATT | 8853 |
rs542117644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335286 | CTCACAGTTCACTCG[C/G]GCTGTGTCAGGCACC | 8853 |
rs542160115 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9259509 | AGTCCTCCTCTTGTA[C/T]TCCTGCTCCCTGGTA | 8853 |
rs542196778 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393839 | AAATGTCTTACAAAT[A/G]TACATTTTAAGTCCA | 8853 |
rs542204342 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235016 | GGTGCAAGGAGTAGA[C/T]GGCCCAGCCTTCTGC | 8853 |
rs542208538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342850 | GTGACCGTGACCTCC[C/G]TGTGTCTTCTGTGTA | 8853 |
rs542213009 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248036 | AGTCAACAGAAAAGG[C/T]CTTGGAGCTCAGCTG | 8853 |
rs542225032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370504 | ACCCAAACCTAGAGA[A/G]GCAGTAGGGACATAG | 8853 |
rs542232629 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348755 | AGAAATCTATCTTTG[A/G]TAGTAGTTAAGAACG | 8853 |
rs542242561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235613 | GAGAACTGGAGCTGG[A/G]GCACGTGAGCTGCTG | 8853 |
rs542244579 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364729 | TTACAACTGTCTTCT[A/C/G]AGTTCACCTAGGACT | 8853 |
rs542248635 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355814 | CAGTTTTTAGAAGCG[G/T]CGTCTTTTAAAACTT | 8853 |
rs542266282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266526 | GGTGGGCGTCTGCAT[A/G]TACACAGGCCAGCTT | 8853 |
rs542285206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330375 | AAGAAAGGCATACCC[A/G]TGGATGTAGAGAGTA | 8853 |
rs542306609 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271466 | CTGGTTTCTTTTTGG[G/T]GTAATCATCAGCGAT | 8853 |
rs542322934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226325 | CACACTGTATGGCTG[C/T]GTACCCTTATGCACA | 8853 |
rs542338300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354472 | TGTGCAGTTTTTACA[C/T]GTCAGAATGCAGAAA | 8853 |
rs542340184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363081 | TGGCTTATTTCACTT[A/C]GTATAATGTCCTTCA | 8853 |
rs542408952 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221122 | TTTTTTTCCCAAGAT[G/T]GTTTTGGCTATTGAG | 8853 |
rs542421720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381026 | AGTGAGACTTGGGGT[A/G]TGAGTCAGTGTTTGC | 8853 |
rs542428479 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261110 | TGAAGGGGTGGACAG[A/C]ACTCTTGGTGTGGAA | 8853 |
rs542443682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395674 | GTGCGGTGGCGCGAT[C/T]TTGGCTCACTGCAAG | 8853 |
rs542460956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381906 | AAAGAACTATTAATA[A/G]TAAATGCTATACAAG | 8853 |
rs542493563 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387070 | AATTAGCCGGGCTTG[A/G]TGGTGGGTGGGGGGG | 8853 |
rs542495408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259755 | TGTTTTAGCGCAGAG[A/C]TCTTCAGATGAACTC | 8853 |
rs542504915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389231 | TGAAGGCAGGTCCGG[C/T]GAGTGACCCACTCAG | 8853 |
rs542510452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267537 | CATTTTCTTTATCCA[A/G]TCCACTGTTGATGGG | 8853 |
rs542513386 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318246 | GAAATATTTTTTCTT[C/T]ACTGCAATGATTGTC | 8853 |
rs542522998 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233089 | GGACCAAAGTAGTTT[C/T]GTGGTAGAGAGATAC | 8853 |
rs542549152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267880 | TCCAGCCTGAGCAAC[A/G]GAGCAAGACTCTATC | 8853 |
rs542554250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387323 | AAAGCGTCACAGTCC[A/G]TGTTAACAATTACTC | 8853 |
rs542554868 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273439 | AGTGTAACCACCCAA[G/T]GGGTTCACCTTGCCC | 8853 |
rs542556113 | snp | A/G | 0.000263687 | 0.0114793 | missense | ASAP2 | GRCh38.p7 | 2:9380770 | GAGACTCCGCTGGAC[A/G]TTGCCAAGCGCCTCA | 8853 |
rs542573043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228321 | TTCCAGTTACAATGC[A/G]TATTTCTTTTTTTCA | 8853 |
rs542573316 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219408 | GCCAGTTAACTGTGT[A/T]TCTGGTCTGTAACAT | 8853 |
rs542582351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377060 | GGGAAGGAATCGGAC[A/G]CTGCCTCATCGCTTC | 8853 |
rs542635788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227621 | TAATTGGTAAGTAGT[A/G]GCCCTGAGACTTTAA | 8853 |
rs542645053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400188 | CTGTCTGCCATTCCA[C/T]AGCCCTCCTGCCCCC | 8853 |
rs542648336 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245489 | CTGTTGGTCATTTCT[C/G]AAAGTGATGACGTTA | 8853 |
rs542653891 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377608 | ACTTCAAGACCCCTC[A/T]ACGTGTATTTTGACT | 8853 |
rs542665907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261841 | GATGGGTGGACACCC[A/C]GGTGGCCACTCCTAC | 8853 |
rs542684201 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345466 | GATCACAGACACAGC[C/T]CTGCACACCACACTG | 8853 |
rs542713235 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352856 | AGTTGGGGGCAGTGT[C/T]GTGAGTTTGCTAGAG | 8853 |
rs542713425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370047 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCTTGAA | 8853 |
rs542721414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382353 | ATTTTACAGATGAGG[A/G]CACAGGCACAGGAAA | 8853 |
rs542721649 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9280478 | AAATCCCAGGTGCAG[G/T]ATAATGTTACAGTTG | 8853 |
rs542725001 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295008 | TGCCCATGTCTTGAC[A/C]GCTAATTTTGAGATA | 8853 |
rs542742085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323763 | CCGAAGGCCCAGGTG[A/G]CCTGGGGAGCGCCTC | 8853 |
rs542766602 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349937 | AGTGGGGCCCAAGAA[C/T]GATGGAAGTTTAAGA | 8853 |
rs542771568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300456 | TGCATGTTACAGCTG[A/G]TACATTGCTCACCAC | 8853 |
rs542793203 | snp | C/G | 1.67534e-05 | 0.0028942 | missense | ASAP2 | GRCh38.p7 | 2:9388546 | CGGAATGTTGGCAAA[C/G]GTATGAAGCTGTCCG | 8853 |
rs542793905 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255512 | TGTTACTATGGAATG[G/T]TTGATTTGATGTAAA | 8853 |
rs542828022 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343556 | GGCTCAAGCAGTCCT[C/G]CTGCTTCAGCCTCCC | 8853 |
rs542848902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319430 | CTGTTCAGACACATT[C/T]CCCATCGAGCCTTCA | 8853 |
rs542882252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213820 | GGTGAAGCTGTTGCT[A/G]TCTAGAGCTACTTAG | 8853 |
rs542897233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288654 | AGGATGTGAATATAA[C/T]TGGGAGTAAAATTTC | 8853 |
rs542899063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281017 | CACTCTGTTTCAAAG[C/G]CACCATGCCTTCAGT | 8853 |
rs542941915 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9374272 | TACAAAAAAGAGGTC[A/G]TAGTCCATGCCCCAA | 8853 |
rs542957224 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371540 | GCTTTATTTCAGAAC[A/C]GCACACCATCTGCAG | 8853 |
rs542963789 | snp | A/G/T | 0.00239393 | 0.0345281 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313411 | TTTTCCCACTCACTC[A/G/T]TGTACATTCATGTTC | 8853 |
rs543005593 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308424 | TCTCCCACCAGGCCC[C/T]AGCTCCAACACTGGG | 8853 |
rs543010634 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9270301 | TGGAGTGGAGTTTTC[A/G]TTTGGGGAGCATGGT | 8853 |
rs543024004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209681 | TTCAAGCGATTCTCC[C/T]GCCTCAGCCTCCCAA | 8853 |
rs543031351 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208412 | ATTTTTTTTTTCTGG[G/T]TTTTTTTTTTTTTTC | 8853 |
rs543037191 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390684 | ACAGCCCATGGGAAG[G/T]AGTCGGTGGGAGGGT | 8853 |
rs543049325 | in-del | -/AA | 0.299971 | 0.244955 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278513 | GCGAGACCCCTTCTC[-/AA]AAAAAAAAAAAAAAG | 8853 |
rs543054389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9215823 | GTTAGAATTATGAGG[C/T]GCTAAAGGTGTTTAG | 8853 |
rs543055921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331653 | CACACCTGTAGTCCC[A/G]GCTACTCGGGAGACT | 8853 |
rs543059225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254872 | GCTATTATGGATAAA[A/G]CTTCTATGAACATTT | 8853 |
rs543070397 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213118 | TAAAGGAAAGTCATG[C/T]ATAACATGGGGATAG | 8853 |
rs543072030 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345575 | GACAGCTTTGGTAAC[A/G]TCTCAAGGCCGAGGT | 8853 |
rs543076722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396400 | CCACCTCAGCCTCCG[C/T]ATAGCTGGGACCACA | 8853 |
rs543122632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293795 | ATCTAAAAATCCCCA[A/G]CTAGGCCAGTGCACA | 8853 |
rs543125209 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337749 | GTGTGGAGCTTGTGC[A/C]GTTCTGGTCCCGGTG | 8853 |
rs543137840 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396840 | AACCCTATCTCTACT[A/T]AAATTACAAAAATTA | 8853 |
rs543159043 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211410 | TTTTTTTCGTTTCTT[C/T]GAGCCTCTGGGCACT | 8853 |
rs543180461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274190 | TCACATCATCTGCAA[A/T]CAAGGCTAATTCAAC | 8853 |
rs543187792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338147 | AAGCCTCATCACTTG[C/T]GTGCAGGCTCTCTCT | 8853 |
rs543194950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229407 | AGGGATTTCCCCTGT[C/T]GATGAACCAACCTGA | 8853 |
rs543212170 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9292590 | GGACTCCCTGGTATT[A/C]CCCTGGGGCTAATGC | 8853 |
rs543224293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9333979 | ACAGTGTGGCCACCA[A/G]AGCTGCTTGGTTGGT | 8853 |
rs543227446 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244858 | TCTGAGGCATCATAA[A/C]AATCATGGTTTTATG | 8853 |
rs543231004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237565 | TACAGGTACATGCCA[C/T]CATGCCTGGCTAATT | 8853 |
rs543275649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358179 | AAAATCCCTGCCCTG[A/G]TCATCTCATGGAACT | 8853 |
rs543291085 | snp | A/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214794 | AAAAAAAAAAAAAAA[A/T]AAAAGTGAACAGGAC | 8853 |
rs543306495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243425 | AAGATTTTTTTTATA[A/C]TGTGCATTTTTGTCC | 8853 |
rs543311943 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365361 | TGGGGTCTCCTGAGC[G/T]CAGCGGTCAGGGAAG | 8853 |
rs543312465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332042 | TGTGGGGCCCAGAGA[A/G]GAAAGGAGCTACTCT | 8853 |
rs543334294 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338122 | CTGTTGGGGTGCTGG[C/T]GGAGTCCCAAAGCCT | 8853 |
rs543344121 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9289644 | CACAGGGAGGTCATT[-/G]GGGGTGACGTTTAGT | 8853 |
rs543349409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243892 | CCAGCAATTTTTGTT[C/T]CCTCCCCAGAATAAA | 8853 |
rs543365513 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345012 | TTTTTTTAATTTTAA[C/T]TTTAATTTTTATTTT | 8853 |
rs543368286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295721 | CTCAGAAATTCATTT[A/G]ATTTATCTAGAACTC | 8853 |
rs543375302 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325927 | TTATCTAACAGTAAA[C/T]TCACAGTTTTCACAG | 8853 |
rs543392761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251018 | GGAGGTGGCATTTGG[A/G]TGGATCTTGAAAGGT | 8853 |
rs543398168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301427 | ACATGTGTGAAATTA[A/G]AGTGCTTATGAAGTC | 8853 |
rs543429836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352843 | GTTTGCTGAGCCCAG[C/T]TGGGGGCAGTGTCGT | 8853 |
rs543442294 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232286 | TTTTACACAGGTGGT[C/T]CCTCTGTTTGTAGAG | 8853 |
rs543450018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315977 | GGCTGTGGATGCAGA[C/T]GTTATTATACACCTT | 8853 |
rs543455389 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378154 | TTGAAAATGTAATTG[C/G]TTTCCTTCTCATGGA | 8853 |
rs543475084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238298 | GGGCAACTTAGTTCC[G/T]CTTTCTGGAGCCTCA | 8853 |
rs543485418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327335 | TCCAAGTTAAAAATA[A/G]CTTTAATTCATTTCA | 8853 |
rs543506882 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9394233 | GCAGTGGCGTGATCT[A/C]GGCTCACTGCAAGCT | 8853 |
rs543528494 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390265 | CATGCAGATAAATAG[C/G]AAATGGAGTTGACAG | 8853 |
rs543545673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367222 | TATTTTAGTAGAGAT[A/G]GGGTTTCACCTTGTT | 8853 |
rs543557262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296345 | CCCCATTCCTACCCA[C/T]GGTTTAAATCAGAGG | 8853 |
rs543588495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320990 | CTAGAGTAGAGAGAG[C/T]CGAGCTACAGGGAAT | 8853 |
rs543597133 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289614 | CCAAGTGTACTCCTA[C/T]AAGCAGTAGGAGCTT | 8853 |
rs543635193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385627 | AGGTGTGTGTGGCGG[A/G]GGGGTTGATTCCAGT | 8853 |
rs543636628 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247125 | ATAGGTGTGAGCCAC[A/T]GTGGCCAGCCTGTCC | 8853 |
rs543654234 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379791 | CGAGGTCAAGAGATC[A/G]AGACCATCTGGCCAA | 8853 |
rs543675993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341037 | AGTTTAGGTTGTCTT[C/T]GTCTCTCTTAGGAAA | 8853 |
rs543682239 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282919 | GTGCCAGCTGTACTT[A/C]TGTGTCTTTGCACAG | 8853 |
rs543684273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297191 | GCTTGACTTTTCTCA[C/G]ATTTTTCTTCTGCTG | 8853 |
rs543690305 | in-del | -/AC | 0.311524 | 0.242311 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317997 | CTCTCCGTCCCCAAC[-/AC]ACACACACGTCTTTT | 8853 |
rs543696148 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402326 | GGCCTCGTTTGCCCT[A/T]AATGGATTGAAAGTG | 8853 |
rs543696615 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264619 | TATCCTTGTGGTAAA[A/G]TTTTCAGGTGATAGC | 8853 |
rs543702244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353691 | TTCCTCATCTGGTCA[G/T]TTCATCTTGGAATCT | 8853 |
rs543737265 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9398940 | TTAGGGATGACTGCC[A/G]GCCAGGGGGTCAGCC | 8853 |
rs543749014 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378548 | GTCACACAGGCATCC[A/C]GAGGCCCTGCATCCA | 8853 |
rs543750230 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236632 | TAAAAACTTGATAAA[A/C]TTTAAAAAATTAAAA | 8853 |
rs543753725 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371636 | GGGGGTGTCAGGGAC[A/G]TGTAACTGGGGGAGG | 8853 |
rs543756213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367732 | ATGCCACTGCACTTC[A/G]GCCTGGGCAACAGAG | 8853 |
rs543777415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374461 | TGGAGGTGACGAGGG[C/T]GACAGTGAGGTCAGA | 8853 |
rs543803290 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276295 | TCTCAGGAGAGAGGA[C/G]TGTGTGCACGGGCTG | 8853 |
rs543821789 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9382552 | GATCATTTTCTACAG[C/T]GTTTAATTCTCTCAT | 8853 |
rs543835095 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403865 | AATTTACACATTAGC[A/C]TTGTACTTTCTAGCC | 8853 |
rs543835421 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210981 | ACCAACATGGAGAAA[A/C]CCTGTCTCTACTAAA | 8853 |
rs543839571 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276953 | GAGCCTGACAGGCTG[A/T]CATGGGTGTCTTCCA | 8853 |
rs543840143 | snp | A/G | 0.00017267 | 0.00929006 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374995 | AAAAAGGCCGGCCAC[A/G]GTGGCTCATGCCTGG | 8853 |
rs543854305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259035 | TGGTGTCTGCAGGCC[C/T]GACTGTCCCCTTAGC | 8853 |
rs543856089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252335 | CCTGTAATCCCAGCA[C/T]TTTGAGAGGTCGAGA | 8853 |
rs543860955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245388 | CCTGGCCACTTCTTC[G/T]GCTCTGTGCTTACTT | 8853 |
rs543873495 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239761 | TTAGATGAGGCCTCA[C/T]TGTGTCGCCCAGGCT | 8853 |
rs543873551 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209626 | CCAGGCTGGAGTGCA[A/G]TGGCACAATCTTGGC | 8853 |
rs543908848 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380089 | TGCATGGAAATAGGT[C/G]AGCAGTGCTTTTCGT | 8853 |
rs543912529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283434 | GGCCATGGGAAACCC[A/G]ACATGGGTCTCACTG | 8853 |
rs543947425 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217715 | CGCCTCCTGGGTTCA[C/T]GCCATTCTTCTGTCT | 8853 |
rs543956741 | snp | A/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237463 | GTTGCCCAGGCTGGG[A/T]TGCAGTGGCATGATC | 8853 |
rs543968588 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278714 | TGCTGAATATTATAT[A/T]TGAGAGTACCTCTAT | 8853 |
rs543983852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393134 | AGGCCCTGCTTCCCC[A/G]GGCAGAGCTGAGGGC | 8853 |
rs543991072 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291194 | CACTCTTTATAAATG[A/T]TCTGTACACACATCT | 8853 |
rs543993977 | in-del | -/ACAC | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317245 | CACAACCACACTCAT[-/ACAC]ACCCCGTGCATCACA | 8853 |
rs543998428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399241 | CCTTCCCCTTCCCTT[C/T]CTCCCTGGTCTTCCT | 8853 |
rs544015273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246667 | AACCGTGAGAGGTCT[C/T]CAATTTAGTCATCTT | 8853 |
rs544022410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302918 | ACCTGGCAGAGGGGC[A/G]TCCTGGCTTGGCTGC | 8853 |
rs544039498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386548 | ACTCATCCACGCTGC[C/T]CACCTGATTCTCAGC | 8853 |
rs544058792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303567 | AGTCGCTTTGGGCCC[C/T]TAGAAACCTCTGCCA | 8853 |
rs544076165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278095 | GGACACTCAATAGCA[A/G]TAGTTATTATGTGCC | 8853 |
rs544082639 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271014 | TAGCCAGGATAGTCT[C/T]GATCTCGTGACCTCG | 8853 |
rs544112371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225519 | TTTACCTCTGAGGTC[A/G]TGAGTAAGTCCAGGT | 8853 |
rs544119059 | in-del | -/AGG | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9333545 | AAGCAGACACACCTT[-/AGG]AGAAGGCTTTAGAGA | 8853 |
rs544132670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265165 | ATAATGAAAAATACA[A/G]ATTTTTAAAAATACA | 8853 |
rs544150506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291648 | CTTAAACGCTCCCTT[C/T]GCCGAGCTGTCTGCA | 8853 |
rs544164553 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295756 | GCTCTTTACTGGAAT[G/T]TTAAAAAAGAAAAAG | 8853 |
rs544173079 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247336 | TGTCTTGGAACTGCT[C/T]CCAGTCCGCAGATGC | 8853 |
rs544181595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241060 | TATGAATTGCTTATT[C/T]CTGGACTTTTCTGTG | 8853 |
rs544189127 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305152 | AGTGGGGTATAGATA[C/T]TGGTGGAGGGGCTGG | 8853 |
rs544208660 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205688 | TCTCTCACACTTCCT[C/T]CTTTTCAGATGCACA | 8853 |
rs544215629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317240 | AATCACACAACCACA[C/T]TCATACACACCCCGT | 8853 |
rs544237637 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352461 | ATAATAGTGAACCTA[C/T]CACCTGGAGGTGGGT | 8853 |
rs544302669 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211992 | TCAGAAAATTTTGAA[A/T]CACTTAAGGAAGCAG | 8853 |
rs544318166 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253208 | CACTCTTGTCACCCA[-/G]GCTGGAGTGCAATGG | 8853 |
rs544319817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394400 | CGATCTCCTGACCTC[A/G]TGATCCACCTGCCTC | 8853 |
rs544337553 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9223340 | GGAAATCTCTTAAGG[A/G]CCCTGTTTTATTTGC | 8853 |
rs544342496 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335392 | GCATTTACTACATGC[A/T]TGGCCTTAATGGCGG | 8853 |
rs544349332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363149 | TTTTTCAGGTCGAAT[A/G]GTATTCCATTATGTA | 8853 |
rs544371631 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343737 | CAGGCATAAGCCACT[A/G]CGCCCAGCCTGATAT | 8853 |
rs544393380 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317618 | CACTCACATCCACAA[C/T]CACACCCACACACAC | 8853 |
rs544399840 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387083 | TGGTGGTGGGTGGGG[C/G]GGCGCCTGTAGTCCC | 8853 |
rs544410063 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9377239 | GGTACTCAGGGAGAC[A/C]CCAAGTAGATATGGC | 8853 |
rs544411420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330989 | CACATTCTGGAGGGT[A/G]CAACGTGGAGCTCGA | 8853 |
rs544428417 | in-del | -/GTTGAAAGTCTTC | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392183 | TAATATCAACATGTG[-/GTTGAAAGTCTTC]GTTGAAAGTCCTGAA | 8853 |
rs544431032 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250458 | ATGCCAGACATGTGG[-/C]CCTTGGGTGGGAATT | 8853 |
rs544438021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355197 | ACCAGTTTTCCCCCA[A/G]ATGTCCTTTTTTCTG | 8853 |
rs544445564 | snp | A/G | | | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214938 | TGCCTCTTCAGAAAA[A/G]TGTTTTAATGCAGAG | 8853 |
rs544455726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249149 | TGTGGTGGAGCTAGG[C/T]TGGCCCTCTTGGGGC | 8853 |
rs544460151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240456 | TCTCCATGTTTCCCA[A/G]GCTGGTCTCAAACTC | 8853 |
rs544479606 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380989 | GAGTCTACAGGGAAA[C/T]CTAGGGGGACCCACC | 8853 |
rs544486675 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9356952 | ATTCTAATTGAGACA[C/T]AATGGTGGGGAGTGG | 8853 |
rs544516897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287248 | CCTGGCTGAGCCATC[A/G]TAGTCCTTCTGAAAA | 8853 |
rs544522207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233195 | CTTTGGTGATAGTGA[C/T]CGATGTCTGTGTGAC | 8853 |
rs544527886 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405506 | GATGTATGATATTCA[A/G]TTCATTCACCTGATT | 8853 |
rs544530853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330514 | CTAAGTTGACCACCA[C/G]GCCTATAACAAAACT | 8853 |
rs544552650 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323044 | CTCGCCAGGCTGGGT[A/C]CTGGGGTGGCTTCAA | 8853 |
rs544576694 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387461 | GCCACTGTTTGCTAA[A/C]CCTAATTTGGAGGAA | 8853 |
rs544599145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342932 | TTCATGTTTAAAACT[C/T]GCTTTTTCCTGTGCT | 8853 |
rs544620898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350160 | TAGCCATTTTTCATA[C/T]ACCTCTGATGAAAGT | 8853 |
rs544625321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337475 | TTGGTTGGATTTTCT[C/T]CTGTGACTTAGACAA | 8853 |
rs544632981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229063 | TGAAGGCTAGGGGCG[C/G]AAAGTGGACAATCAG | 8853 |
rs544637507 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365161 | TAAAGACATCATATG[G/T]AAACTTTTTCCCTGC | 8853 |
rs544642345 | snp | C/G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322958 | CGGTTTGACATCTTC[C/G/T]TGAGGACACCCATTT | 8853 |
rs544642418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253460 | TGAACCACTGTGCCC[A/G]GCCAAAATTCACGTT | 8853 |
rs544642474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260274 | TGTAGCAGTGACTCC[C/T]GCAGTAAGCCTGGGT | 8853 |
rs544644185 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381215 | TCATGTGGGTTGCTC[A/C]ATACCATCTTTTCCT | 8853 |
rs544658297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311805 | CGCGTCTGGCCCCCA[C/T]GCACTTGTTCTCTGG | 8853 |
rs544681161 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266705 | AGAAGTGTTTCTCTT[A/G]TGTTTGCTGCCGTCA | 8853 |
rs544706743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235724 | AGGGCAGAGTGAGCC[A/G]CATGGCCTGGCAGCT | 8853 |
rs544748242 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286581 | CACTGAAAACATGCA[C/T]GCAGAGTTTCTGGAA | 8853 |
rs544775736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242216 | TGATCTTAGGGGCGC[A/G]TGCTTTGGCGGTTTA | 8853 |
rs544851515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377112 | TTCCCAGTTCTAAAC[A/G]TGAATTAAAGACAGA | 8853 |
rs544854443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336989 | GTGTTTGCTTTGCCT[C/G]TGCAGAATTAGGAGG | 8853 |
rs544862734 | snp | A/G | 1.64768e-05 | 0.00287021 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279288 | CTCAGCACAGACACG[A/G]TTTAATGACTGTATT | 8853 |
rs544881231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253929 | CAGTATATTGTTGGC[C/T]GGGCACGGTGGCTCA | 8853 |
rs544895078 | snp | A/G | | | synonymous-codon, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9297424 | GTTTACAAAGGAGTT[A/G]ACAGCACTTTTCAAA | 8853 |
rs544899819 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9357442 | TGAGATCACGCCACT[A/G]CACTCCAGCCTGGGC | 8853 |
rs544901915 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292875 | TTGAGATGAAAAAGG[A/G]GGTGATTGAAGGTGA | 8853 |
rs544931415 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397515 | GAACACACCGGTACG[C/T]CCTCCTTGTGAAGGA | 8853 |
rs544933259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375946 | GTGGGCATCCAGCTG[A/G]AGTGGGTTTGCAGTA | 8853 |
rs544963747 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384815 | AAGCTTCTTGGTGTC[A/G]GCATCTCTTCCCCCA | 8853 |
rs544964475 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268723 | TTTTGTTTTGTCTAC[C/T]GTCTTTCAGAAATGT | 8853 |
rs544974025 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371731 | GGACCATTATACACA[C/T]CCTGTCCTTGAGAAG | 8853 |
rs544984764 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273511 | TGCAGTAGAGGAAGA[C/G]TAATTCACGCAGAGC | 8853 |
rs544993196 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221876 | TCGGCTCACTGCAAG[C/G]TCTGCCTCCCAGGTT | 8853 |
rs545009366 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380355 | GGCATGTGCCACCAC[A/G]CCTGGCTAATCTTTA | 8853 |
rs545012652 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341372 | TTTTACAAATGTGAA[A/G]TTTAATAGGCCAGCT | 8853 |
rs545018196 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346551 | ATTAGGAATGTTAGA[-/T]TAGATGAGACTAGGC | 8853 |
rs545025497 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288812 | CCACCACCTCCAACC[C/G]CCTTCTCCTTCCCTG | 8853 |
rs545059666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244066 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGCCTAT | 8853 |
rs545061302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256401 | CATAAAGAAATTAGC[A/G]TTTAACATGCTGTGC | 8853 |
rs545061415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249827 | ACCGAGGGGCATGAT[C/T]AGAGAGAGGCTACCC | 8853 |
rs545118780 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9394611 | AACTTGGAAATATAC[A/G]CACATGTACATGGAT | 8853 |
rs545139246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338833 | GGCAGGTGCCATCAG[A/G]GATGACTTCCCAAAG | 8853 |
rs545145231 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248548 | GAGAGTCAGCGTTTT[G/T]GGTCTCGGTTTCTTC | 8853 |
rs545148362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250392 | CTCCTGGAGTTCTCG[C/T]GGTGCCCCAGGTGCC | 8853 |
rs545167892 | snp | A/G | 3.29881e-05 | 0.00406115 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374821 | AAGGAAGAAGCACGC[A/G]GATAACGCGGCGAAG | 8853 |
rs545198712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332118 | GATAGAAATACACCC[C/T]TTCTAGCCTGGTGAG | 8853 |
rs545201620 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270089 | CTCTCTGGTTTTTGT[C/G]ATAAGTTCACTCTGT | 8853 |
rs545251350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301259 | GCGTGAAAGAATGTT[C/T]ATAAAGCAGTTGGAA | 8853 |
rs545282151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395765 | GGTGCCCACCACCAC[A/G]CCTGGCCAATTTTTT | 8853 |
rs545285056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261313 | TTCCGTCCTCCCTCC[A/G]TTGGCTGGAGCTCTC | 8853 |
rs545286206 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306243 | TGTAGTACTGGGGGT[A/G]GAGATATGGCCTGGT | 8853 |
rs545286692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352009 | CCACAGATTCTCATC[A/G]AAGCTTGCCTTTCAT | 8853 |
rs545291506 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211349 | AATAAGCAGTTGTGG[C/T]AGAAATTTGAAAAGT | 8853 |
rs545309239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308503 | ATCAGTGATTTTCCT[A/G]TTTAGAGTTTCCTTG | 8853 |
rs545341864 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311118 | TTGCCTGGGCTGGGT[A/G]TGGTGGCTCATGCCT | 8853 |
rs545343642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389385 | CCAGGCATTGTGGCC[G/T]CTGTGAGCCGCTGAT | 8853 |
rs545348252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237658 | CTCCTGGGCTCAAGA[C/G]ATCCTCCTGCCTCGG | 8853 |
rs545361081 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315405 | GGAAGACGGGTCTGC[A/G]TATGTAGGGTTAAGA | 8853 |
rs545365536 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305847 | CTGTAATAGTGGGGT[A/G]TAGATATTGGTGTAG | 8853 |
rs545382262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302355 | TTTTTATATTTTTAG[C/T]AGAGACGGAGTTTGA | 8853 |
rs545410785 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326118 | GGGCAGGGTGGCTCA[A/C]ACCTGCAATCCCAGC | 8853 |
rs545439171 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210324 | CCTCAGCTTTAAAGT[C/G]TGGTTAATAATACCT | 8853 |
rs545446338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390866 | CCTTGGAGCCTCTTC[G/T]GTTTCGCGAGTATCA | 8853 |
rs545466031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384638 | TGTTTACTGGTTTAT[C/T]ATAAAGGATATTGCA | 8853 |
rs545497809 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288189 | AAACCTGTCCGCAAA[C/G]CCAACCTACCAAGCA | 8853 |
rs545517106 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302067 | TGACCTCGTGATCCA[C/T]CCGCCTTGGCCTCCC | 8853 |
rs545531812 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294981 | CCCTTCCTGAACCCA[A/G]TGAAACTAAACTGCC | 8853 |
rs545613800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231057 | TTTGCGGTTCTATGT[C/T]GGTCACTTTCCCCAG | 8853 |
rs545652732 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402004 | CAGACAGTGAGGGCG[C/G]TGGATGAACCGGCTT | 8853 |
rs545657015 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244679 | ACCTGGGCTTTTACT[A/G]CCATTGCAGCCCAGT | 8853 |
rs545667526 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238900 | TTGTCTTCTGTGAAC[C/G]CTGTTTGCCTCCTTC | 8853 |
rs545668887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326568 | AAGGAATTAAAAATC[A/G]CCCCCAAATTTTACT | 8853 |
rs545693883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238159 | TACTGATCTTCACAC[A/G]GATGAGCTTATTGAT | 8853 |
rs545707227 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296992 | TGTGCCATCATTTGG[C/T]GAAGGAAGAGTCCTC | 8853 |
rs545724113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230371 | GAGCCTGTGTTACAA[A/G]ACTGAGCAGTGCAGC | 8853 |
rs545729963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320174 | CGTGGGATTACATAC[A/G]TCATTTATTGCAGAA | 8853 |
rs545741516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334066 | TTTTTTTTTTTTTTT[A/G]GGAGACAGTCTCACT | 8853 |
rs545763240 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389328 | ACTTTGATGCGGGGC[-/G]GGGGGGCCCAGGAAG | 8853 |
rs545768348 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317046 | CATTCCCAATCACTC[A/G]CATCCACACTCCACA | 8853 |
rs545786789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225582 | TGAGCATGTCAGTTG[A/G]AAATTGATTCAGAAG | 8853 |
rs545794455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290344 | CCTCCTGAGGAGCTG[A/G]GATTACAGACACCTG | 8853 |
rs545806276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257926 | TGAGTGTTACTTTCT[A/G]TGTTGTTGCAATAAT | 8853 |
rs545826796 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210754 | AGAGATGGGGTTTCA[A/C]CGTGTTAGCCAGGAT | 8853 |
rs545863258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352619 | GCAGGCAGCAGGGAG[A/G]ATCAGTAGACGGCAA | 8853 |
rs545874073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232961 | CAGCTGCAGTTTTGT[C/T]CTGTATCTATTGCCA | 8853 |
rs545877734 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9360809 | GTAACATAATTATGA[A/G]TTTATATAGCATAAT | 8853 |
rs545892005 | snp | A/C/G | 0.00874735 | 0.0655527 | upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9204864 | CTTATGCAGTAGGCA[A/C/G]GTTAGATTTCTAAGG | 8853 |
rs545907728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316751 | ACTTGCTTGCTCCTC[A/G]TGTACCTGTTGGTTA | 8853 |
rs545911154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217767 | CTACAGGCGCCTGCC[A/G]CCACGCCCGGCTAAT | 8853 |
rs545916528 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9389199 | ATTCCTGAAGAGCAG[C/G]TGGCTACGGTGCTTC | 8853 |
rs545927307 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278636 | CTGTTTGAGCGCCTC[C/T]TATGTGCTGGACATT | 8853 |
rs545931802 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9224317 | GTTCTTAGTTTTCCT[C/G]TGAAACCCCCACACC | 8853 |
rs545943613 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403987 | TGACAACGTAGGGTA[A/G]CTACAGTTCATTCTG | 8853 |
rs545958444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339858 | TCTGTGTCCAGCCTG[C/T]GTCACATTCCACATT | 8853 |
rs545966971 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328053 | ACTCATGCGACAACA[C/T]GGGTAAACATTGAGA | 8853 |
rs545982202 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232762 | CTGTTGCCGGAGCTC[C/T]GGTGTCATTGGTTCA | 8853 |
rs545988024 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342227 | CCTGAAAAAGAAGAA[C/T]AAAGTTGGAGGATTC | 8853 |
rs545995313 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373863 | ATTGTAAAATGCATG[A/T]ACTCTGTGACCAGTG | 8853 |
rs546000497 | in-del | -/TTTG | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302478 | GCCTGGCCAACTTTT[-/TTTG]TTTGTTTGTTTGAAA | 8853 |
rs546007624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246336 | GTCTTGCTCTGTTAC[C/T]TAGACTGGAGTGCAG | 8853 |
rs546008564 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252870 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 8853 |
rs546011303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398038 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC | 8853 |
rs546020499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283973 | AATATATGAATCTGG[A/G]GGAAGGGACGCAATT | 8853 |
rs546041877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304055 | CGGGACAGCCACTGG[C/T]AGCCTGCGGAGCCCT | 8853 |
rs546058160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380158 | AGTTTGGATGTGGAT[C/T]TTAATTAGGTGGCTG | 8853 |
rs546080623 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251507 | GATGTCCGTCGGGTG[G/T]GTTTTGTATGCTTAA | 8853 |
rs546101663 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259654 | CTCTCAGGCCCCCTG[A/C]CCCGAGGCTGGACCG | 8853 |
rs546104272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334388 | TTCCATGTCGCGGTC[A/G]CCTGTTGCGGCACAT | 8853 |
rs546108540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218489 | CTGCCACTGAAGGGT[A/G]AATCATGGATGTGGC | 8853 |
rs546131050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373176 | CTAGGCCCTGTAGAG[C/T]GGGCAGAACTGGAGC | 8853 |
rs546140897 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9280227 | TCTATACTGTGTCCC[C/T]TCACCCTCGTGGTGT | 8853 |
rs546158199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271182 | ACCCCAAATGGTTAC[A/G]TTATACAAGCTGTGA | 8853 |
rs546162540 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362517 | TGTCACCTCACATGC[A/T]TATGTTTTGTGGTGA | 8853 |
rs546165553 | snp | C/G | 0.000314692 | 0.0125398 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391175 | CATCCACCGCTGCCC[C/G]CTCTTCGCGTGACAT | 8853 |
rs546166142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252128 | CACACACTGTGAGGT[A/G]CCTTGGAGAGAGGTC | 8853 |
rs546168122 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245433 | TGCTAGGTGTGGAGG[A/G]TTCTATAAAAACAAA | 8853 |
rs546169618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398478 | TTGCCGCACTGCACT[C/T]GAGCTTGGGTAATAG | 8853 |
rs546188232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277842 | CAAATGTCTGGTGCC[G/T]TGTGATCATTTTTCC | 8853 |
rs546195127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271590 | CTTACTTGCATCAGC[A/G]AAGGAGTTTAAATAG | 8853 |
rs546223100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271441 | CAGGCAAACTTCTTA[A/G]ACGCCTTCACTGGTT | 8853 |
rs546250361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278200 | AAATGTTGTCTCCCT[C/G]CAGTCACAAGTCACC | 8853 |
rs546252536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354127 | CCATTATCCGCGAAC[C/T]CCATAGGCACCCTGG | 8853 |
rs546290296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368820 | TTCACCTGTGCTGTC[C/T]GTTCTGTTGAGTCAC | 8853 |
rs546298687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9277077 | CGGCCCAGATTCTGC[A/G]AGAGTGCTAGGCTGC | 8853 |
rs546300373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361709 | AGTAGCTGAGACTAC[A/G]GGCAAGTGCTACCAC | 8853 |
rs546309854 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404623 | TTTAACAAAAGTAAA[A/G]GAATAAATTTGCATA | 8853 |
rs546326725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350417 | TAAGATCACCAGAAA[C/T]TGAGCTGGGTGCCCA | 8853 |
rs546356376 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404337 | GAATCTGTCCATCTG[A/T]TTATAATCAAGAACA | 8853 |
rs546376541 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9261765 | AGAGGCCCCGCTGGT[A/G]GTGTCCCAGGTGGGA | 8853 |
rs546376957 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9319205 | GCGTTTGCCAGGCAG[C/T]GCGCTGCCCCTGCGC | 8853 |
rs546378757 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297886 | AATATTTAAAGGCCT[G/T]TTGTGCTCCCAAGTG | 8853 |
rs546384234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298077 | ATTTTGAAGAAGTGG[A/G]CAGCCCAAGAGGGCT | 8853 |
rs546398798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386989 | GCGGGCGGATCACGA[A/G]GTCAGGAGATTGAGA | 8853 |
rs546418211 | snp | C/T | 0.00029654 | 0.012173 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380725 | AACGCCTCCTTTGCT[C/T]GCCCTTGAATTTTAG | 8853 |
rs546453649 | snp | C/T | 8.21052e-05 | 0.0064067 | missense | ASAP2 | GRCh38.p7 | 2:9393596 | AGATCAGGCCCCCAC[C/T]TCTGCCCCCACAGCC | 8853 |
rs546467589 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265819 | CTCTTGTTGCCAAAG[C/G]TGGAGTGCAATGGCA | 8853 |
rs546468350 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291806 | GTAGCCATAAGGCTG[G/T]TGCACCCTGCCTTCG | 8853 |
rs546468351 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307611 | ATGTCCAAGCTTATC[C/T]TTTATTCTAGTGGAG | 8853 |
rs546474445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393188 | TTGAGTGGAGAGCAG[A/G]AAACTGCTGGCTTTC | 8853 |
rs546495735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259898 | GTGTCCTGCATAGTC[C/T]TTGGGCTAAGTGGAG | 8853 |
rs546510239 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259211 | ATGGAAAACAAACAA[A/G]GAAAGTAAAACTAAT | 8853 |
rs546512022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212721 | AGCTCTCAGCCGCCA[C/T]ATTGCAAGTACTCAG | 8853 |
rs546518261 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284167 | AGCATAACGTACTCA[A/C]AAGTTCCAGGGATTA | 8853 |
rs546536119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393721 | CAGGGCTCTGCAGGA[A/G]TGTTTGCAATCCCCA | 8853 |
rs546538085 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333409 | AGCAAAATACAAAAT[G/T]CTCTGAGAAAGTATA | 8853 |
rs546549067 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302109 | ATTACAGGCGTGAGC[C/T]ACCGCGCCCGGCCTT | 8853 |
rs546551890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292961 | ACTGTGCTGTGGGCC[A/G]CACTGACCTGTCAAG | 8853 |
rs546577851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398800 | GGTGACAGTGCAAGA[C/T]TCCATCTCAAAAAAA | 8853 |
rs546587504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311899 | CTGTGTGGATTGCAT[A/G]CACCAAGCATGGAAA | 8853 |
rs546595914 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333731 | CTTTCTCCTTAGCTC[A/G]TGGAAATGCCCGTTC | 8853 |
rs546605606 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226058 | TAAGCTCCTTGAAGG[C/T]GGAGGTTGTGTCCTG | 8853 |
rs546611374 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317321 | CCCACATCCACTCAC[A/T]CAATCATATCTTCAC | 8853 |
rs546628647 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234330 | CCTAGAGACAGGCTG[G/T]TGTGAGAATTCAGTG | 8853 |
rs546634194 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387691 | TTATATTTTAAATCC[A/C]TCACAGAATGGAGAA | 8853 |
rs546644817 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249387 | ATGTTCATTTCTCTG[A/C]TGATTGTAGTGTCTA | 8853 |
rs546653047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375984 | AGCACCCAAGTGGGG[C/T]GGCATGTGTCCAGAT | 8853 |
rs546681726 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330680 | AGCATGCAAATTACT[A/T]CTACAGTTCTTATGT | 8853 |
rs546713379 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292483 | AGATTGCACCACTGC[A/C]CTCTAGTCTGGGTGA | 8853 |
rs546722301 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286643 | ACAATCTTTTTGTGG[A/T]AGGAGATCCATGCAC | 8853 |
rs546722539 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257215 | CCCCATCCTGAAGGA[A/G]TGACAGTTTGTCCTT | 8853 |
rs546729318 | snp | A/G | 8.2573e-05 | 0.00642493 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368538 | AGTATGGGACTGGCT[A/G]TTCTCATTTGCTGAG | 8853 |
rs546733227 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253509 | GGGTTTTGTGAAATC[A/G]TCTAAGCACCCTACA | 8853 |
rs546746075 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322545 | GCTCTTCTTTGGATG[A/T]GCTCATTGGTCAGTT | 8853 |
rs546747789 | snp | A/C | 0.0053908 | 0.0516366 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316969 | CTCCCACACACCCCC[A/C]GTCACACCCTCTCAT | 8853 |
rs546776430 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257874 | AGGTGGCATTTTGGT[G/T]TATCCTTACCTATGT | 8853 |
rs546789185 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9204782 | ATTTATTGGAAGCTA[C/T]TCATTCTTATATTAA | 8853 |
rs546791830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381250 | TGGAAGAAAAGACAA[C/T]GTAGACAGTAGAAAG | 8853 |
rs546806280 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205853 | CGAGAATTTCCTTAA[A/G]AGCTGTAAATAAAAA | 8853 |
rs546833939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253059 | AGCCCAAGCCAATCC[C/T]GAGGCAACAAAGAAA | 8853 |
rs546837946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335814 | TATATTTTCACTACA[A/G]TGTGGGTATCATAAT | 8853 |
rs546839818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342679 | ATTAAAATTAAAAAG[C/T]TTTGTGCTTCAGAAT | 8853 |
rs546862579 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243457 | TAGATTACAATCACT[A/G]TTGTTTAGGAACTCA | 8853 |
rs546862626 | in-del | -/TTTTTTTTTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254528 | CAGCTAATTTTTGGA[-/TTTTTTTTTT]TTTTTTTTTTTTTTT | 8853 |
rs546871105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348298 | ATTTTTGTATTTTTA[G/T]TAGAGACTAAAAATC | 8853 |
rs546881265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303902 | GGTGAGGCCTTGGGC[G/T]TGGGAGGGAGAACTC | 8853 |
rs546903922 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259402 | CCTTGCGTCTGCCCC[C/T]GCTTCCTGCGCCCTG | 8853 |
rs546927665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218700 | ATTTGTAACATGGAG[A/G]GTTGGATGCGATGAG | 8853 |
rs546959371 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221817 | TTTGTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 8853 |
rs546977540 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323361 | AAACACCACATGCAT[C/T]GCTGGACTCCCTTTG | 8853 |
rs546980504 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369506 | AGTATTATGGCTCTT[A/T]TGTCTATAGGGGGAC | 8853 |
rs546982040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291272 | TATCCAGAAGAATGA[C/T]ACACATTAGTAAATT | 8853 |
rs546993849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369765 | CGAGTCTTCCCAAAG[A/G]ACAGTGAGCAACAGT | 8853 |
rs547011772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269032 | GGGCATTTTGCATGG[A/G]TCCTTGAGGCCAGGG | 8853 |
rs547065203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9220087 | AAATGTGTATGATAC[A/C]TTTTGTTTATTCATT | 8853 |
rs547074145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300115 | GCTCACGGCTGTAGT[C/T]CCTGCTACTCGGGAG | 8853 |
rs547093904 | snp | C/T | 1.67281e-05 | 0.00289202 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401244 | TGAGGCCTGCAGCCA[C/T]ACTAACCGTTGTTCC | 8853 |
rs547096258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255005 | ATCAAATGCTGCCAT[C/T]CCATTTTCCAAAGTG | 8853 |
rs547156557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337030 | CGGGCTGTTGTGAGA[A/G]AACTGGTTATTTACA | 8853 |
rs547176127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350221 | GGAGAGGGTTTGGGG[A/G]TTACAGATGTGAATG | 8853 |
rs547179430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364866 | GTTCTACGTACACTG[C/T]ATTATCTAACCTAAA | 8853 |
rs547184379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306371 | AAGAGCAGCCGTGTC[A/G]GCTTGGGTGCCTGCG | 8853 |
rs547187381 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273041 | TCTGGGTCTTTTGTG[C/G]TTCTATATAAATCTT | 8853 |
rs547205385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261402 | TTGAGTCAGTTTCTT[C/G]TCCTTTAAGCTGGGG | 8853 |
rs547206838 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349673 | AGAGTCTAGTACAAC[A/C]CTGTTTATCTGACTT | 8853 |
rs547210504 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369534 | GACATGGGTGGTTTA[C/T]CTGTTTTGTTGTGAT | 8853 |
rs547214817 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9224368 | TGGGACTAGGTATTA[A/C]TTCTCTTTGAATCCC | 8853 |
rs547224059 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267639 | CAGTTTCTCATGCCT[A/G]TAATCCCAGCACTTT | 8853 |
rs547224369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273551 | AGGAAACTGGAATTT[C/T]ATTATTATTCGAATC | 8853 |
rs547242963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249603 | CTGACCCATCACATA[A/G]ACTGCATAGCCATGA | 8853 |
rs547244567 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358567 | GGAAGAAGAGGGAGA[A/G]TAGATGTGTGCATAT | 8853 |
rs547253665 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250942 | ACTATGAAACGAGGC[A/G]TGGTGAAAGTCAATT | 8853 |
rs547273535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242422 | CTTTTCTTCTGGTAG[A/G]GTCACACCTAGAGGA | 8853 |
rs547282640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325522 | TAGTAAAGTAGACAT[C/T]TATTTACCTAAACAC | 8853 |
rs547297514 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327989 | CTATAGATAGCTCAT[A/G]GGAAATAAACACCAC | 8853 |
rs547309536 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211726 | TCCCAGGGGCCCTGC[C/T]GTCCATGGGACCAGA | 8853 |
rs547309929 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400235 | CCCCTCCTGCCCCCT[C/T]CCCTCCTGCCCCCTT | 8853 |
rs547329864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243291 | TTTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTC | 8853 |
rs547332677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396856 | AAATTACAAAAATTA[A/G]CCGGGCATGATGGCA | 8853 |
rs547358723 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358314 | GTACGTTCTCTGTTA[C/T]TATCAGCATCTGTAG | 8853 |
rs547360477 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268944 | GGACAAACCGGTGCT[C/G]TGCTGCCTGCAGTGT | 8853 |
rs547431446 | in-del | -/T | | | upstream-variant-2KB, intron-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205924 | AGGTTGGCTGGCTGC[-/T]TGTAGCACGTTCTCC | 8853 |
rs547438781 | snp | G/T | 0.0345262 | 0.126772 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305844 | GGGCTGTAATAGTGG[G/T]GTATAGATATTGGTG | 8853 |
rs547447733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293953 | GATCACCTTGGGGTT[A/G]CTGGGGATCAATACA | 8853 |
rs547489040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366119 | ATGCTTTGCTTTTGT[C/T]GATGGGTCTGGAGGG | 8853 |
rs547495041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357810 | ATAACTTGAACATTT[A/G]AAAAATAACTTCATG | 8853 |
rs547509601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351625 | TGCAGAGGACCACGC[C/T]GGACTGTGTACTGTA | 8853 |
rs547510594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268064 | GCCAACAAGGTGTAT[A/G]TCCCTAAACATAAAC | 8853 |
rs547536178 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393317 | ACTCCCTGCTTCCTC[-/T]CCTGTGAATGGTTTT | 8853 |
rs547538745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237083 | AATAGGCAAGAGGGA[C/T]AAGTCTCTGACCTCT | 8853 |
rs547560295 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274468 | GCTGGGATTATGGGC[A/C]TGCACCACCATGCCC | 8853 |
rs547580107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295354 | TAATACATGTCTTAC[A/G]AAGTTTAGAAAAAAT | 8853 |
rs547611590 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371845 | GGGAGGGCCGGGCGC[C/G]GTGGCTCACGCCTGT | 8853 |
rs547614511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402048 | ACAGAAAGCCCCAGG[C/T]TGAGCCCACCACACA | 8853 |
rs547625485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209889 | ACTAATTTTAAACTG[A/G]TTAACCTTTTTGAAT | 8853 |
rs547625995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255610 | GTGTCGTCAGAGATT[A/G]TGGAGTTCAAGCCAC | 8853 |
rs547641724 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405207 | GTAACTAATAGTACT[C/T]TTACCAGAGGAGAAA | 8853 |
rs547666946 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382591 | AAAAGGCTGGGTTTA[C/G/T]AGTGAATGAGCACAT | 8853 |
rs547681610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263128 | CGTGGCTGCATGCTG[A/G]CTTTCCACTGTCTCG | 8853 |
rs547690721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250710 | CAGGAGCTCTGAATC[A/G]GAGCCAGGGTGGAGC | 8853 |
rs547711873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383405 | GACTACAGATGCATG[C/T]CACCACGCCTGGCTA | 8853 |
rs547714214 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395016 | GGCTTCCTCATATCA[C/T]GGTGGCTGGGTCCAC | 8853 |
rs547717896 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263761 | TTCTTTTCTCACTTA[C/T]CTGTTCATACCGCAT | 8853 |
rs547733552 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294531 | AACTCTATGGTCTGG[G/T]GCAGGTGACATGACT | 8853 |
rs547737796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287567 | TATTTGTTCCTCTCT[A/G]GAGGAGGCTTTCACA | 8853 |
rs547740659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275059 | ACCGCTTCCAGTCCC[A/G]TGTTTTGTTTTTTCA | 8853 |
rs547756436 | in-del | -/TC/TCTCTC | 0.0763268 | 0.181341 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338347 | CTCTGTCTGTCTCTA[-/TC/TCTCTC]TCTCTCTCTCTCTCT | 8853 |
rs547772466 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359524 | TGGCCACCTAATACA[C/T]GAGCTTTCATGACTG | 8853 |
rs547782721 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301517 | TCCAAGGGCCACCTC[A/T]GTGCTGAGAAGTGGC | 8853 |
rs547803257 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257126 | ATGGTTTCATTCATT[A/C]CATGTTCGTGGAGTG | 8853 |
rs547806219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314824 | TAATCCCAGCAACTC[A/G]GGAGGCTGAGGCGGG | 8853 |
rs547807208 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325368 | TTGTTTTTCTCAATC[C/T]TGCTTCTGTAAGGGT | 8853 |
rs547834122 | snp | C/T | | | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9358880 | TGTACTGGGAACATC[C/T]GAGCTGCTGGTAATT | 8853 |
rs547837168 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283074 | CTTGTAATAGATTCT[C/T]TTTTTTTTCCTCTCT | 8853 |
rs547839605 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326208 | CAACATGGTGAGACC[G/T]TGTCTCTACAAAAAA | 8853 |
rs547843556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401606 | CCCCAGGGTGGCTTC[C/T]TCCCCTGTTAGGGTG | 8853 |
rs547856015 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282158 | GCTCATGTCCTTTTT[C/G]AGGCCCCGCACATAA | 8853 |
rs547875038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281797 | CCCAATTCATCTGTC[A/G]ATGAAACTGTCACTG | 8853 |
rs547882757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319129 | ACGGGGCTGGAGGGG[C/T]GTTTGCTCATGAGCA | 8853 |
rs547897677 | snp | A/G | 1.85503e-05 | 0.00304546 | missense | ASAP2 | GRCh38.p7 | 2:9379053 | GGGAAGGCCTCCATC[A/G]AGATAGGTGAGTGGG | 8853 |
rs547963469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309357 | ATGCGCAGTCCCAAA[A/G]TCATGATGCAAGAAG | 8853 |
rs547965133 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302075 | TGATCCACCCGCCTT[A/G]GCCTCCCAAAGTGCA | 8853 |
rs547975066 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316846 | TTGCTTCAGGGAGAA[G/T]AATGGGGGCACCAAG | 8853 |
rs547986742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257679 | TCACGCCACCATGCC[C/T]GGCTAATTTTTTTGT | 8853 |
rs548006881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210387 | GAAGATAGTACATAG[C/T]ACAGAAGCTGCCAGA | 8853 |
rs548024808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327053 | CAATTTGTAGCTTAC[A/G]GTTTCACAGCAGCTT | 8853 |
rs548034636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339941 | TACCTCACTTTTCAG[A/G]TTTTCCAGGCACTTT | 8853 |
rs548043683 | snp | A/G | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390396 | CCCTACAGGCCGTGC[A/G]CAGCCTCCAACATGG | 8853 |
rs548075728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308567 | AACAGGAGGGCTTTT[C/T]GATGGAGACAGCATC | 8853 |
rs548081951 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9391615 | GAGTCTCACTCCATC[A/G]CCCAGGCTGGATGCA | 8853 |
rs548094243 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271064 | TCCCAAAGTGCTGGG[A/C]TTACAGGCGTGAGCC | 8853 |
rs548096162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390918 | GAGACAGGAGTAAAA[A/G]CATTGAGGGTTCTAG | 8853 |
rs548108753 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327301 | GCTTTCTGATAGCTT[C/T]GTGGTCACTAATGAA | 8853 |
rs548116379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346960 | AGTACGGTTATAACC[A/G]GCATTACTGGGATGC | 8853 |
rs548121226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9215363 | ATGCTCATAATGCTT[C/T]TTTACTAAAGCATTT | 8853 |
rs548136104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260521 | GCTGGAGAGGGGCAC[A/G]GGGCTGGCCAGGCTC | 8853 |
rs548144931 | in-del | -/CTTTTC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361563 | TCCTTCCTTTCTTTT[-/CTTTTC]CTTTTCCTTTTCTTT | 8853 |
rs548146412 | in-del | -/GAGGTGGGGG | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353876 | GCTACTTGGGAGGCT[-/GAGGTGGGGG]GATCACTTGAGTCCA | 8853 |
rs548177646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327447 | ATCTCAGCTACAATA[C/T]GTTAGCAGTTATTGT | 8853 |
rs548187421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245643 | AAAATACCTACTGGG[C/T]GCTGGTGCTGCGTTT | 8853 |
rs548187668 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366927 | ATCTAACCCAGACCT[C/G]TTGGGCTCTCCTTCA | 8853 |
rs548216764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283731 | TCAGGGTGTCAGTGT[A/G]GATGGGTTCTGGTGA | 8853 |
rs548218910 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227743 | AGTTAAAAAAATATG[C/T]GGGTAAGGTATTTGT | 8853 |
rs548222663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251191 | GAACGTGGCCAGAGC[A/G]TTGTCACATCAGGAG | 8853 |
rs548242065 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230767 | AAACGCCTGCATTTT[C/T]TAATCACTGGAGAAG | 8853 |
rs548245177 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309955 | ACACATGTTGTAGGC[C/T]GTGAGCTCTGGCTCC | 8853 |
rs548289342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217849 | TTGATCTCCTGACCT[C/T]GTGAGGCACCCACCT | 8853 |
rs548289360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211023 | AGCTGGGTGTGGTGG[C/T]GCATGCCTGTAATCC | 8853 |
rs548326475 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297951 | CCTCGGTTTTCAGCC[A/G]TGGGAATGCGGTGCT | 8853 |
rs548338617 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374269 | GCCTACAAAAAAGAG[G/T]TCATAGTCCATGCCC | 8853 |
rs548355473 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240592 | ACTAAGCACTTGCCA[A/C]GCACCACGGCCGTAG | 8853 |
rs548358544 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210207 | TCTTAATGCCGAATT[C/G]TCTAAATTACTCCTT | 8853 |
rs548361429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302595 | TTCTTGTGCCTCAGC[C/T]TCCCAAGTAGCTGGG | 8853 |
rs548377226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270857 | GAGTGCAGTGGCGCG[A/C]TCTCGGCTCACTGCA | 8853 |
rs548415799 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264767 | GGGTTTTGCATCCTC[A/G]TGTTCAGTCACATAG | 8853 |
rs548417608 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362694 | ATAATTTTTTAAAAC[C/T]AGCTGGGAGTGGTGG | 8853 |
rs548467491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231980 | CTCCTGCTTCCATCT[C/G]TCTTGATCTGGCCCC | 8853 |
rs548471287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238964 | TTGCTGTACTGTGTT[A/C]CCTGGGCCTCCCGCA | 8853 |
rs548508113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240039 | GAAAGAAATTAAGTC[A/G]GGGTGAAAAAACTAG | 8853 |
rs548519867 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341220 | GTTTTCTCTGTCAGG[C/G]CTTCACCTGGTCAGG | 8853 |
rs548539848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355376 | ATTTGGATTTCTCTA[G/T]TGTTTTCTCATGAGT | 8853 |
rs548543537 | snp | C/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369631 | AGTGGTGAGGCTGGG[C/T]CAGCGTGTCCTGGCA | 8853 |
rs548544373 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266148 | GATTGCCTTTTTATC[C/T]TTTTTTTTTTTTTTT | 8853 |
rs548555308 | snp | A/G | 0.000181206 | 0.00951683 | missense, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9297357 | AGTTTGGCGGCAACT[A/G]TGTATGCAGAGATGA | 8853 |
rs548578517 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252553 | CATTCCAGCCTGGGC[A/G]ACAAAGTGAGACCCT | 8853 |
rs548578969 | in-del | -/CTTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383643 | TCCTAATCTTGAGGC[-/CTTT]CATTAGTCTTCCAAA | 8853 |
rs548608658 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274079 | GTCAGATCTCTTTCA[A/C]TGTAATAATTATCTC | 8853 |
rs548639260 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9355280 | GGTCTCTTGCAGTCT[C/G]TATCGGTTCTGTAGT | 8853 |
rs548643524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247395 | TCATTTGCACGAGGC[A/G]AATCAGTTTAGCAAT | 8853 |
rs548667827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303215 | TTTTAGACATAAACT[A/G]ATGAACTATGCTGAA | 8853 |
rs548669370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234076 | AGATCGCACCACTGC[A/G]CTCCAGCCTGGGTGA | 8853 |
rs548690450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258761 | TCAGCTTCAGAGCAG[A/G]CAGCATTCTGGCTGA | 8853 |
rs548699352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265372 | GGAGACCGAGGGACT[A/G]CAGTTTTGAGTATTT | 8853 |
rs548738446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294288 | ACAGGTGTGAGCCAC[C/T]GTGTCCGGCCACTAA | 8853 |
rs548750608 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381367 | TCTACAGTGCAGTCA[C/G]TTATACCAGTATATA | 8853 |
rs548779231 | in-del | -/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9324958 | CTTCTGTTATTTTAC[-/TT]TTTTTTATGTCTGTC | 8853 |
rs548807649 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221180 | AGGATCAACTTTTCA[A/G]TTCCTGCAAAAAAGC | 8853 |
rs548809606 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404943 | TTTCTGTTTGAACCC[G/T]TCATTTAATTTTCTC | 8853 |
rs548813972 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358490 | ACTGGAGTGTGTCCT[A/G]TTTATTTTTGCACAC | 8853 |
rs548838754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317699 | CCTGAAACCCTCACA[C/T]GCCCACACACACCCA | 8853 |
rs548853891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259961 | TGGCTGTCCAGTGTC[G/T]GCGCATCGCCCCCTC | 8853 |
rs548854337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380354 | AGGCATGTGCCACCA[C/T]GCCTGGCTAATCTTT | 8853 |
rs548884634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380939 | TCTGATGGGATGAGC[C/T]GAGAATCAGCCTGCC | 8853 |
rs548915092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284300 | GCTACAAATTAAAGG[A/G]TACCTAACATGCAGG | 8853 |
rs548917904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287427 | AAAGAAGAACCTGAA[A/C]ACCTTAGGGATGGAG | 8853 |
rs548918207 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217102 | CATTTTGACACCAGA[A/G]TCTGCTATTTCTTTT | 8853 |
rs548937658 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387133 | GCAGGAGAATGGCGT[A/G]AACCCGGGAGGCGGA | 8853 |
rs548958675 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9344252 | AGGGGGTTAAGGCTC[A/G]TAATGAAATAAAACC | 8853 |
rs548963217 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394132 | GTCCAAATAATGCCC[A/C]TTGTTGCAGATGGGT | 8853 |
rs548965956 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394525 | CTTTTAGTGGAAATG[A/G/T]TATTTAGAGGCCAAG | 8853 |
rs548997666 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348952 | AGTTGAGCCCCGAGC[A/C]CTGGAGCCAGCCTGA | 8853 |
rs549004643 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341836 | CTCATCCCATGAATG[C/T]GTGTGTGCCCTAGTT | 8853 |
rs549005542 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280355 | TTCCACCTGCTCCCC[A/C]CCACCGCCCCCACCA | 8853 |
rs549026457 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233437 | TTTTCAGAGAAAGCT[G/T]TTTGTAAATTCTTCA | 8853 |
rs549031091 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387977 | CTATCCCAAGAACAG[C/G]AGAGGGGAACCGCTG | 8853 |
rs549034525 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317486 | ACTCAGTCACTTACA[C/T]CCTTACACACCCACT | 8853 |
rs549060394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401467 | CCTGGCTGGAGAGAC[A/G]GGCTTGCAGGTGAGG | 8853 |
rs549063924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226569 | GTGGTAAAGGGGGAG[C/T]TGGGAGGAAGCCTCA | 8853 |
rs549073255 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376641 | TGCAGGGATGGGGAC[A/G]GGTCGATTGAGAGGA | 8853 |
rs549077683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370729 | TTCCTGTGGGTGACA[A/G]AAGTCACATCTGTAC | 8853 |
rs549133952 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399460 | GATGAGGGACCCCTC[G/T]CTGCCAGCCCTGAGA | 8853 |
rs549140207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311402 | GCTTGTTGGTCCAAC[A/G]TTAATAGCAGTGATT | 8853 |
rs549140953 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364952 | AGGATTTACATTCCA[A/C/G]CTATCAGACTCCAGA | 8853 |
rs549143414 | in-del | -/TCAA | 0.0103295 | 0.0711199 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317528 | AATCACACCCCACAC[-/TCAA]ATCCACACAATCTCT | 8853 |
rs549144350 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306495 | AGAAGGGTTGATAAC[A/G]GAAGAGGAAAGCAGG | 8853 |
rs549150327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213097 | TTAGGCAGTTGATAC[A/G]TGCTGTAAAGGAAAG | 8853 |
rs549158039 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9206109 | TGGGACTTTTAGTAG[A/G]GGCCCCTCACCGCTC | 8853 |
rs549160301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336752 | GAAAAAAAACTTGGC[A/G]TAAGGAGAAAATAGT | 8853 |
rs549162858 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313930 | CTTGGTGTGTATGTA[C/G]ATAATTCTTCCTCTG | 8853 |
rs549193800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214168 | ACCTCCTTTGCTTAC[A/G]CCTTTTCTGTGTAAT | 8853 |
rs549209682 | snp | C/T | 0.000345036 | 0.0131301 | intron-variant, missense, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207255 | CCTGCGCGGCGGCTC[C/T]GGCCGCAGGTATCCC | 8853 |
rs549220303 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380218 | TTTTGTTTTTTTTGA[A/G]GCAGAGTCTCGCTCT | 8853 |
rs549236581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400978 | GACTGCTTGGATCTG[A/G]GCAGCTGGTGGGTTT | 8853 |
rs549255867 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342701 | CTTCAGAATCTTTTT[C/T]CAAACTCAGAAATCC | 8853 |
rs549264762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304679 | GTATAGATATTGGTG[A/G]AGGGGGTGTAATAGT | 8853 |
rs549273788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268375 | AAACACGCCCTTCTC[A/G]TCTGTCCTTAGGCAC | 8853 |
rs549284686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253561 | GTCACGCAGAACTCC[C/T]CTCTTCAGTTGGTTC | 8853 |
rs549310581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395840 | TCTCAATCTCCTGAC[C/T]TCGTGATCTGCCCTC | 8853 |
rs549363298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9208785 | GGTGTTTTGAGAATA[C/T]ACCATTAATAATGTT | 8853 |
rs549373046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243152 | CTTGCTCTGTCGCCC[A/G]GGCTGGAGTGCAGTG | 8853 |
rs549374336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308396 | TGAGAACTTCACCCC[C/T]GTGATTGAGTCATCT | 8853 |
rs549384409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318461 | TCTCTAATGTCCTTG[C/T]TGTCCTTACTTTAGA | 8853 |
rs549387402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331944 | AGAGGAGGGAGGGGC[A/G]GGTGTCACAGACAGA | 8853 |
rs549388230 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273638 | CCAGTGAGTTGGGAG[G/T]GCTGATTGGTTGGGT | 8853 |
rs549403866 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240190 | CCAGCTAATATTGAA[C/G]TAGTTTGCCTTCAAT | 8853 |
rs549432114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307156 | CTGGAGTGCATCAGC[A/G]TCGCCTGCGTGGCTT | 8853 |
rs549462608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370317 | GTATCTCAGGTGAGC[A/G]ATTTAGTTGTTGTTG | 8853 |
rs549469814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338545 | GGGCCACCTGCCTGC[C/T]TCTCCTGCCAAGCTG | 8853 |
rs549484596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330709 | GTCAGGCAATTTAGG[A/G]AGTGGGTCGCTTCCT | 8853 |
rs549499730 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208127 | GTCCTCCTTTTCCTT[A/T]CCCATCAAACGGGAT | 8853 |
rs549504213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294647 | AAGCCACCTAGTAGG[C/T]GTTGACCTTTATACG | 8853 |
rs549524984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249971 | TGCCATGTGGAAGGA[A/G]GGCAGGGCTTGGGGT | 8853 |
rs549537505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242609 | AACTGCTGGGGCTGA[C/T]AGCTGGTCGCGGGAT | 8853 |
rs549549559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331068 | GTGGGAGCGCCTCTC[A/G]TTCCCCCACCACACA | 8853 |
rs549565941 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9268624 | AGAGTCGAATGCGTG[G/T]TGAGACAAAGCTGCC | 8853 |
rs549568209 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357659 | AAATGCCAAGACAGT[A/G]TGGGTAATATAAAAA | 8853 |
rs549580944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221968 | CTGGCTAATTTTTTT[C/T]TTTTTGTATTTTTAG | 8853 |
rs549593864 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358374 | TACAAGTAGACTTTG[G/T]CTGGTCTCATTGTTT | 8853 |
rs549602797 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265897 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 8853 |
rs549606609 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344342 | CCTTCTCCAGCCTGA[C/T]AGATGGCATTTATCA | 8853 |
rs549650818 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325582 | TTTGACATTCAAGTA[A/G]TATGTGAAGGTCATA | 8853 |
rs549650919 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332305 | AAGGAATAGTGTTCC[G/T]TTTCTTGAAGCTTCT | 8853 |
rs549689632 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213606 | AGAGGTCTTGGATGA[A/G]GAGGTAGCAGGGGGG | 8853 |
rs549692709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356778 | GCTCTGTGACCCTGG[A/G]AGAGCCACTTGCTTT | 8853 |
rs549712246 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326305 | TCAAGCTTTAAGTGC[A/T]TGCTGTTGTTTAGGT | 8853 |
rs549715215 | in-del | -/G | | | intron-variant, frameshift-variant | ASAP2 | GRCh38.p7 | 2:9389915 | TGCGGCTTTCTCCCC[-/G]CCTCTCCCAGATCCT | 8853 |
rs549728716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263279 | CAGGGGCCACAGCTC[A/G]GTAATGTGGGTGTCA | 8853 |
rs549747946 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275152 | GTGGCGCAATCATGG[G/T]TCGCTGCAGCCTCCA | 8853 |
rs549762433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243665 | ACTTACAGAAGCTTG[C/T]TTTATCTTACCTAGA | 8853 |
rs549779207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295187 | AGGTAAACTTTTTAA[C/T]GATGAAAACAAACAT | 8853 |
rs549793553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371376 | GAATTACTTCTTACT[C/G]ATTTTGGTTTTTCCC | 8853 |
rs549815747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371891 | GGAGGCCGAGGTGGG[C/T]GGATCACGAGGTCAG | 8853 |
rs549853866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351692 | GAGTGGGAGATGGCT[A/G]CCTTTTCAAATGTCA | 8853 |
rs549868154 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231404 | CCAGTTTTAGCATCT[G/T]GTATGGAGGCAACAG | 8853 |
rs549902140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255152 | GTTTAATTTATATTT[C/T]CCTGGTAACTAATGA | 8853 |
rs549903191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390954 | AGGGTCATACTGACC[A/G]TTTCATAAGGGGGAG | 8853 |
rs549922587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382751 | GGTTACACTGTTGTC[A/G]CAACAAGCAATACAG | 8853 |
rs549923795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346009 | GGTCTAGGGGTTTGA[A/G]TGTGTCTCTGAACTT | 8853 |
rs549949671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379088 | GGCCCCGGGGGTGGG[C/T]TCAGCTGCACCCTGG | 8853 |
rs549953499 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282224 | TTTTGTCATCCTTTA[G/T]CCATCTATTATGTCA | 8853 |
rs550000772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250534 | TGTTTTCCCATTCCA[C/T]AGAGGGTACAAAAGG | 8853 |
rs550010513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373350 | CAGCCAGCCTCACGC[C/T]GCGGCGTGTCCAGGA | 8853 |
rs550013564 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222800 | GGCCGTTCACCTTTT[C/T]CCATCTTCCTTCCTT | 8853 |
rs550089020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244253 | GTGAGCCAAGATCGC[C/G]CCACTGCACTCCAGC | 8853 |
rs550096019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289874 | CCACAAAGACTGGCT[A/G]TTTCTTGAGGAATCA | 8853 |
rs550098578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258036 | AGTTGGAAGCCTGTT[A/G]TTACTGCTACCCCCA | 8853 |
rs550111054 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284116 | GCTGATTAGCAACTG[C/T]ATTTCATCCACAATT | 8853 |
rs550115121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276686 | GGGATTACAGGCACA[C/T]CCACCAACACGCCCG | 8853 |
rs550117778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289072 | ACAGTGGATTGTTTT[C/T]GCATGTTTATCTTTG | 8853 |
rs550169560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384107 | ACATGGCACATTTGT[A/G]CGTATGTAACAAATC | 8853 |
rs550172644 | in-del | -/TTAT | 0.00359567 | 0.0422482 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290193 | AGACATATTCTAATG[-/TTAT]TTATTTATTTATTTA | 8853 |
rs550175384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308609 | CATGTGCCCAGCCTC[A/G]GCTTAGCTTAGCCTG | 8853 |
rs550176933 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216245 | CAAGAGTGTGTTGGG[C/G]ATATCCAGAGTGTGG | 8853 |
rs550186091 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339986 | CGATCCTTACAAGCC[A/T]CTTTACAGGGTAGGC | 8853 |
rs550198954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277414 | CAAGTCCCCTTTTGT[A/G]TCTTGAAGGAAGGTA | 8853 |
rs550203118 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361820 | TCCTCCTGCTTTGGC[C/T]TCCCAAAATGCTGGG | 8853 |
rs550216383 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327608 | TTATTAGGAGTTTTT[-/G]GCACTTCAATATTTA | 8853 |
rs550226010 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275726 | GCATTTTGGGCTCAT[C/G]ATCCTTTCCTGAGCT | 8853 |
rs550269416 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402602 | GCCATGTGGAAAATA[A/C]CTGCTCATTTCCAAA | 8853 |
rs550270078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374013 | ATTGTGTGCATTTTC[A/G]CAAGTCAGACTTACA | 8853 |
rs550271087 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396729 | ATGCAGGGCTGGGCA[A/C]AGTGGCTCACACCTA | 8853 |
rs550286045 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315362 | GCAGCCAAGGCAGTG[A/G]ACGTGAGAATGGCAT | 8853 |
rs550290459 | snp | A/C | | | intron-variant, missense | ASAP2 | GRCh38.p7 | 2:9390092 | CTCCTGGTTTCCCGA[A/C]GTCTTGGAATTCAAG | 8853 |
rs550314679 | snp | A/G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263725 | TTTTTCATAGTGTGT[A/G/T]TGGGTTTAGAGCTAC | 8853 |
rs550321872 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207957 | TGCAAAGTCATCACG[C/T]CTAGCTGCTAAGCAG | 8853 |
rs550352348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210894 | GGTGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 8853 |
rs550355233 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345585 | GTAACATCTCAAGGC[C/T]GAGGTCGTTGCCTTT | 8853 |
rs550356402 | snp | C/T | 3.6489e-05 | 0.0042712 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9393576 | TGCCCCGCCTGGGAT[C/T]TCACAGATCAGGCCC | 8853 |
rs550373958 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251820 | GCTGCCAGGAAGGAA[G/T]ACTGAATGTGAGTTT | 8853 |
rs550406653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391447 | CTGTCTTCCAAAGCA[C/T]TTCAGCAACATTTCC | 8853 |
rs550414340 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367491 | CCTGGCCAGGCGCAG[C/T]GGCTCACGCCTGTAA | 8853 |
rs550431768 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398244 | GCTGGGTGCAGTGGC[G/T]CACACCTATAATCCC | 8853 |
rs550443203 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378223 | CCACTTTGTGCAGGG[A/G]CACAAAGCTCACTGC | 8853 |
rs550462256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302112 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGCCTTTTT | 8853 |
rs550467346 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9251939 | TTTTTCTTTCCTTAA[-/T]TTTTTTTTTTTAATT | 8853 |
rs550486667 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307921 | GTGAGAGTGCATAGA[C/T]GGGAGTGTGTGCATA | 8853 |
rs550491091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340310 | ACAGGCATGAGCCAC[C/T]GCGCCCGGCCAGCCA | 8853 |
rs550495685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392914 | TCTGCCACCCTTGAC[A/G]AGAGCTCTTCCCCTC | 8853 |
rs550504198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265977 | CGGGGTTTCACCATG[C/T]TAGCCAGGCTGGTCT | 8853 |
rs550511237 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210500 | GGAAGTGTCAGGGAA[A/G]TGGATGAATGGCTGA | 8853 |
rs550520638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341283 | CGGGGTCGCCTGGGA[A/G]TCACCTAGAGGATAC | 8853 |
rs550525227 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9306733 | TTCAGCATGTGCTTG[C/T]TTGCATTCCTCCTTC | 8853 |
rs550535284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9333071 | CAGTGTTTTCACGGC[A/G]CCTTCTGTGTGTGAC | 8853 |
rs550564583 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349752 | CACGCTGCAAGGATG[A/G]GTTCAACTCTCCCAC | 8853 |
rs550571774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225244 | TCCCAAGCCTGGTTA[C/G]AGCTCTGAGTGAGTG | 8853 |
rs550578582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232143 | GTTGGTGGCTTCCCT[G/T]ACCTTTTGGAAAGTA | 8853 |
rs550606880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321874 | AACTTGAAGTAATTG[C/T]AGGATAAATAAAGGA | 8853 |
rs550631918 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373249 | AGTTCACCAGGTGCC[C/T]CTGGAAGTCCTTCCT | 8853 |
rs550648887 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291359 | TGAAAATGGTTCTCT[C/T]TCACGAGATGTCCAC | 8853 |
rs550663447 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297994 | CTGTGGCTGCTGCTT[C/G]GTGCTGTGGGTGAAT | 8853 |
rs550701947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336493 | TAAGTGCACAGATGG[C/G]TTTTCACCAGCTGGA | 8853 |
rs550724248 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292412 | AGTCTCAGCTACTCG[A/G]GAGGCTGAGGCAGGA | 8853 |
rs550742071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239040 | GCCCCTCTCTGTCCC[A/G]TGGCGTTAGCAGCAA | 8853 |
rs550743522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217877 | CCTCGGCTTCCCAAA[A/G]TGCTGGGATTACAGG | 8853 |
rs550743774 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328223 | GAAATGGCTGCTAAC[G/T]GGTATAGGGTTTCTT | 8853 |
rs550745196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234354 | TTCAGTGAGAAAACC[C/T]GGGGAGAACATTTAG | 8853 |
rs550750204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347757 | CCTCTTTGCCAGATT[C/T]GCAGGATTGCCACAC | 8853 |
rs550762710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297499 | GTTGGGAAAGTGGCT[C/T]AGTAGAGGATAGTTA | 8853 |
rs550801208 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301984 | GCCCACCGCCATGCC[C/T]GGCTAGTTTTTGGTA | 8853 |
rs550811998 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279460 | CCTGGTACCGTAATA[C/T]TGATGACCATTAACA | 8853 |
rs550826790 | snp | C/T | 0.000506209 | 0.0159012 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403358 | AAGCATTAACAGTTA[C/T]GTTCCTGTTTCGTTA | 8853 |
rs550828047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271089 | TGAGCCACCGCGCCC[A/G]GCCCTGTTTTCATTT | 8853 |
rs550828640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322680 | TTCTACAGTGATGAG[C/T]GGTGTTGTAGGTCAA | 8853 |
rs550888046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323317 | CCTCACCTGTGGGAG[C/G]ATCTCACCGGTACCA | 8853 |
rs550903681 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9316695 | TCCTGACTGAAGTTT[C/T]GCATCTTGAGTTGAC | 8853 |
rs550906694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233500 | TGTATGGTGGCTTGG[A/G]ACCAATACACTTTGC | 8853 |
rs550914604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349554 | AGCTTGGTATCTTCT[A/G]ATACTGATTTCTGAC | 8853 |
rs550917079 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395808 | GAGATGGGGTTTCAC[C/T]GGGTTAGCCAGGATG | 8853 |
rs550928425 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364110 | ATATGAAAAACAGTA[G/T]CACTGGTACTAGGGT | 8853 |
rs550933011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260002 | GAAACTCTGTGGTTG[A/G]GGAACCCCACTTACA | 8853 |
rs550952680 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9268932 | TCAGGGTGCTGGGGA[C/G]AAACCGGTGCTGTGC | 8853 |
rs550952986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248057 | AGCTCAGCTGTCCTC[A/G]AGTCTGGGACAGACG | 8853 |
rs550969561 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245772 | ATTAGTCGGTTCGTC[A/G]TCTGCCTCCACTAGA | 8853 |
rs550975935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343095 | ATGATGAGAGTGGCC[C/G]TAGACTCTGAGGATG | 8853 |
rs551008389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286050 | TCAATTAGAACAGGG[A/C]AGTTCAGAACAAATA | 8853 |
rs551013868 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386863 | CATTTGAAATAGAAG[A/T]TAGGTCTAAGTTACC | 8853 |
rs551023657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285245 | TAAAATAGGGATTGA[A/G]TTTCTGGTTCAGCAG | 8853 |
rs551034166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341726 | TCCACATTCCTTCCA[C/T]AGCATTGTTCTCAGC | 8853 |
rs551044048 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375200 | GGTGAGAGGAATCGG[C/T]TGAGCCCAGAAATTT | 8853 |
rs551055427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267628 | AAGGCCACGTGCAGT[G/T]TCTCATGCCTGTAAT | 8853 |
rs551070033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227719 | AGGTCCTCAGTAACC[A/G]TTTTATTGAGTTAAA | 8853 |
rs551076963 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380464 | CTGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 8853 |
rs551093352 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335722 | TCTGTGTGCTAACAC[A/G]TCAGCAGGGACAGTT | 8853 |
rs551098296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260563 | TGACCTTGTTTGCAT[C/T]GTCACACTCCTTTTT | 8853 |
rs551129899 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252948 | AATTTAGGAACACAA[A/G]CAGATAGTGCGTGGG | 8853 |
rs551132216 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376538 | AGGAGCAGGTAAAGA[G/T]ATTGGATTGTAGGTG | 8853 |
rs551142803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317721 | ACACACCCATACACA[A/G]TCACATTCACACTCA | 8853 |
rs551145873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376675 | AGAAATGAAACTCCT[C/G]AACTTCTCATTTATT | 8853 |
rs551146307 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221588 | TGTTTTCTTAATTTC[A/T]TTTCTGGATTATTCA | 8853 |
rs551147222 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9376129 | TGGTAACAGGCATGT[C/T]CGTGCAGGCTCTGAG | 8853 |
rs551152103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278910 | TATAGGGGGAAGGGG[C/T]GCAGGCACGATAGGA | 8853 |
rs551184260 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355425 | TTTGGCAAGAGCAGC[A/G]CAGAATGATGCTGCC | 8853 |
rs551185220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249487 | GAGGGACTCTCATGA[C/T]GCCATGCCTGCTCCA | 8853 |
rs551194499 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248779 | TTTCAATTAGATGGC[A/G]GTTCTTTATGGCCAG | 8853 |
rs551201852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399536 | GCTGGCCCAGAGGTT[C/T]ATGGATGGGGCTTGA | 8853 |
rs551217023 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262179 | TTTAAATGTTGATGG[-/A]AAAAAAAATGTATTA | 8853 |
rs551217158 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240678 | TTACCATTTCATGAA[G/T]AGAAGACCCACTTTT | 8853 |
rs551231110 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9403016 | GCCATCCCCACGAGC[A/G]AACATCTGGGACATG | 8853 |
rs551233631 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9273448 | ACCCAATGGGTTCAC[C/T]TTGCCCGCTGCTGCC | 8853 |
rs551242161 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343659 | GCTATGTTGCCTAAG[C/T]TGGTCTTGAACTCCT | 8853 |
rs551276898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376191 | AACTCATGCCCACCA[A/G]TGCAGTGTGGAGGGT | 8853 |
rs551286361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331199 | CAGGGTGAAGAGGCC[A/G]CTGTGTAAACCAGAT | 8853 |
rs551288016 | in-del | -/CAAGATGCTTTTGAACTCT | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353239 | TGGGATGAGTATCAC[-/CAAGATGCTTTTGAACTCT]CAAGATGCTTTTGAA | 8853 |
rs551297622 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254960 | GAGAGTGCAATTGCC[A/G/T]TGTTGTGTGCTAAGT | 8853 |
rs551299130 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405955 | CCTCTGCCGGACAGA[A/G]GTCCATGCCAGTGAT | 8853 |
rs551312197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278406 | TAATCCCAGCTACTT[C/G]GGAGGCTGAGGCAGG | 8853 |
rs551313192 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9238495 | ATCCACCTTCCCATG[G/T]GGGCTGCTCCATCCC | 8853 |
rs551314963 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287488 | ACGCGGGGCTCCTGG[C/T]TTCGGAAGGGGCAGG | 8853 |
rs551345431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388752 | CTCTTATTCTGGGCA[A/G]AGTTGTGGCATCTGC | 8853 |
rs551369782 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274147 | ATAGTTTTTATGATG[A/G]CATCTTTAGGTTTTT | 8853 |
rs551392044 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397790 | TTGAGACGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 8853 |
rs551408801 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381957 | CTCTTTCTAAGCACT[G/T]TACATCCACGAGCTC | 8853 |
rs551416658 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9342735 | AGGCTGCCTGTGCCT[G/T]GGGATGCAGTCGAAA | 8853 |
rs551427187 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317409 | ACCCTCAAACACACA[-/C]ATGCTCCCTCACACA | 8853 |
rs551435927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267028 | ATTTTCTGGTTCTTT[C/T]GCCAACTCTAATTTC | 8853 |
rs551462602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219298 | CACATTTGCCCTGTG[A/G]TTCGGTTGTGTTTAT | 8853 |
rs551469086 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400223 | CTCCTGCCCCCTCCC[C/T]TCCTGCCCCCTCCCC | 8853 |
rs551471717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371232 | GTGATGGCGAAACAT[C/T]AGCTACTTCCATTCC | 8853 |
rs551477594 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280414 | TTGCCGCTCTTGATT[C/T]TCCCCCCATGAGAGC | 8853 |
rs551479607 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358614 | AATTGGTGGTAATTA[C/T]GGACAAAGTTTCCAG | 8853 |
rs551481274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272972 | AGTATAATTTAAGTA[A/G]GGTAATGTGGTTCCT | 8853 |
rs551488422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401591 | GCAGGCCTGATTATT[C/T]CCCAGGGTGGCTTCC | 8853 |
rs551490705 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312926 | GGGCATGGCATGGTG[A/G]CGTGTGCCTGTAATC | 8853 |
rs551491897 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9334490 | GAAACTCAAGGCCTC[A/G]TTTTATATGGGTCGA | 8853 |
rs551513443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9287060 | GAGGCACTGAGTAGT[A/G]ATCTGCCAGTGTCAT | 8853 |
rs551513969 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304738 | ACTAGTGGGGTATAG[A/G]TATTGGTGGAGGGGG | 8853 |
rs551517612 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338421 | TGTGATAGAACAGTT[-/TG]TGCCACCCAGGCAGC | 8853 |
rs551527785 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299802 | TAATACCATACCTGA[C/T]TGTGTGGATAGATTA | 8853 |
rs551530411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394809 | GTACTGTGGGGTCTT[C/T]GTCTTTTCTCCACAG | 8853 |
rs551547194 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243183 | GCACAACCTCAGCTC[A/G]CTGCAAGCTCCGCCT | 8853 |
rs551551947 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390390 | CCTTTGCCCTACAGG[C/T]CGTGCACAGCCTCCA | 8853 |
rs551554603 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311370 | CTCAAAAAAAAAAAG[-/A]AAAAAAAAGTTTGCC | 8853 |
rs551556211 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300946 | AAAATTAGCACTCAC[A/C]ATGCCTGGTTTTCCA | 8853 |
rs551576672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242782 | ATGGAGGAAAATTGC[C/T]GTCTGGGGAAGCATG | 8853 |
rs551595575 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207956 | GTGCAAAGTCATCAC[C/G]CCTAGCTGCTAAGCA | 8853 |
rs551596707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301477 | TTTTCCTCTTCCCCA[A/G]TGGATGTGAGAATCC | 8853 |
rs551604518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381472 | GGCACAGTGACTCAC[A/G]CCTTGTAATCCCAAA | 8853 |
rs551626883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395859 | TGATCTGCCCTCCTC[A/G]GCCTCCCAAAGTGCT | 8853 |
rs551627263 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9347637 | ATTGAGGATAACATC[C/T]GGGAGATTCGTTCAA | 8853 |
rs551627568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236045 | GACTGCACCCACCAC[A/G]AAGAAGTACCTTGTC | 8853 |
rs551628071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337198 | CTGTCTGCCCAGTTG[A/G]CTCCTTGTCAAGACC | 8853 |
rs551646801 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301937 | CATGCCATTCTCCTG[C/T]CTCAGCCTCACATGT | 8853 |
rs551676225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293247 | GGATTGATGGGTTTC[A/G]TGCAGTGAGGTGGGG | 8853 |
rs551678613 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214685 | TTTGACTGATTTAGT[G/T]TCTTCACTCATAAAT | 8853 |
rs551703648 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300059 | CAACATGGGGAACCC[C/G]TGTTTCTACAAAAAA | 8853 |
rs551715564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356838 | TGAAGGGACAGGACC[C/T]TTTCAGCTGACACAT | 8853 |
rs551730805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207333 | TTTCTTTGCTCCGAA[A/G]CCGGACGCGGCCGGG | 8853 |
rs551734659 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9316312 | GTTTCAAAAAAAAAG[-/A]AAAAAAAAATTAGTA | 8853 |
rs551738660 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314015 | TGAGACAAAAGTCTC[A/G/T]CTCTGTTACCTAGGC | 8853 |
rs551742008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313604 | CCTCCCTGTAGGCTG[C/T]CTTCTTTCTTGCACG | 8853 |
rs551761664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326402 | ATGGAGCCCTTTCTT[A/C]AAAATTCATTTAATA | 8853 |
rs551782016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228772 | TGGTGATACCTAATA[C/T]ATGTAAATGTATGCT | 8853 |
rs551789976 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319115 | TAAGGGGGCAGCAGA[C/T]GGGGCTGGAGGGGCG | 8853 |
rs551795072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268446 | ATCTTAATTCTTAGC[A/G]ACACCTGCTATTCTT | 8853 |
rs551797754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307203 | TGGACTTCCCCTAGA[A/G]TTTCTGATTCCGCAG | 8853 |
rs551835959 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284533 | TAGGACGATTATTTT[A/C]CCTTTCTGAGCCTCA | 8853 |
rs551846277 | in-del | -/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9391592 | TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTCTCAC | 8853 |
rs551863398 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324793 | CTATTTGCACCCTTT[C/T]ACATTCAACCTGTGA | 8853 |
rs551865084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365035 | CCACAAAGTCTATCA[C/G]AAAAAATTGAGCACC | 8853 |
rs551882034 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322185 | TGTTTATTTTTCACT[A/C]ATTCACTCCTTCAAA | 8853 |
rs551888902 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279297 | GACACGGTTTAATGA[C/G]TGTATTCTCTACATT | 8853 |
rs551893505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401052 | CTGCCCCGGCCGCTT[C/T]GTTTCCCAGCCCTTG | 8853 |
rs551905309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244312 | AAACAACAACAATAA[A/G]AAGAATTTGAATATG | 8853 |
rs551911993 | snp | G/T | | | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214814 | GTGAACAGGACTAGC[G/T]CCTTCCTTAGAAAGC | 8853 |
rs551929669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325365 | TTTTTGTTTTTCTCA[A/G]TCCTGCTTCTGTAAG | 8853 |
rs551949183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307922 | TGAGAGTGCATAGAC[A/G]GGAGTGTGTGCATAC | 8853 |
rs551957892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344396 | CCCTTTTTTGCTGTG[C/T]TGAGAAAGGGAAATT | 8853 |
rs551962333 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245726 | TGCTTTCCTTCCTCC[C/T]GTCTCTGCAGTCTGA | 8853 |
rs551962642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339204 | ACAAAAAACTGGGGA[C/T]GGGGCAGGAGTTAGC | 8853 |
rs551965281 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338607 | CCTCAGTGGAGGACT[C/T]GTTTGTTGATTCACA | 8853 |
rs551977045 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302461 | CAGGCATGAGCCACC[A/G]TGCCTGGCCAACTTT | 8853 |
rs551983631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9215261 | TGAGAGGTCGTCTGT[A/G]TGGTTCATTGTTGAC | 8853 |
rs551986032 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9329809 | TACAGAATTGTTTCT[C/T]TTCCTAGAAGGCCTC | 8853 |
rs552020938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326966 | TTAAAAATTTGATAC[A/G]TTACCAAATATTTAA | 8853 |
rs552028253 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332389 | CCTCAAGGAGGGTAC[A/G]GGAAGGTCAGCACTT | 8853 |
rs552052156 | in-del | -/TTTTG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243099 | TGAGCCTTGAAGATT[-/TTTTG]TTTTGTTTTGTTTTG | 8853 |
rs552060951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359410 | GGTAACACTTAAGCC[A/G]TGTGATAGAGATAGG | 8853 |
rs552062147 | in-del | -/CT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233051 | TGCTGCCAGTCTGTG[-/CT]CTGTGTTTTTTTTGC | 8853 |
rs552072554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229543 | CCCAGCATGTGTCTA[A/G]GGAGGAGCGGAGCGG | 8853 |
rs552074575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221401 | ATCTTGGCTCACTGC[A/G]ACATTGGCCTCCCAA | 8853 |
rs552091040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350942 | AGACGTTGTCTTATG[C/G]TCTCCTCTGGGGCGT | 8853 |
rs552113893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352375 | ACTCAGGGTTTTAGG[C/T]CTTTCTGTTTTCTGA | 8853 |
rs552123180 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281628 | GAAGTTCGTGGAAGT[C/T]AGTTCCAGAGCATGG | 8853 |
rs552149665 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9391822 | ACTCCTGACCTCAGG[C/T]GATCCACCTGCCTCA | 8853 |
rs552222719 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231915 | TGGGAAGTGGCAACC[A/T]TAAGTCTGCCTGGCT | 8853 |
rs552228411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402701 | ACAAAAAGCCCACCA[C/T]TCATATTTTGGCTGT | 8853 |
rs552240235 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366293 | AGGGAAGCAGCTCTT[C/T]GATTCCTGGGGAATT | 8853 |
rs552240454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372824 | CGTCCACACTCAGTC[A/G]CAGTGGGGCCTTTGA | 8853 |
rs552241062 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249638 | GCAGGGTGGAGCACC[C/T]ACACTGTCGTGTGGA | 8853 |
rs552258968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257767 | GACCTCAAGTGATCC[A/G]CCCGCCTCGGCCTCC | 8853 |
rs552278780 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209775 | GGTTTCACCATGTTG[A/G]TCAGGCTGGTCTCGA | 8853 |
rs552294986 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250193 | TAGCATTTAACACGC[C/T]GCCTGACACAAAGTG | 8853 |
rs552329208 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288994 | CTTTTCTGTTACCAG[-/C]CCCCAGAAAATGTAC | 8853 |
rs552335568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250585 | CCCCCAGGGCAAATG[C/T]AGTGTGGTGTGCTCT | 8853 |
rs552362514 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234452 | AGAACAAGGTAATGG[C/T]GGCGCGTGGCCTTGC | 8853 |
rs552370763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275904 | GATGTCCACAATATT[G/T]TTTTAACGTGGCACT | 8853 |
rs552374931 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360478 | TTTAGTGGGTTGTCT[G/T]GCTAGATGATAAACA | 8853 |
rs552398351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216501 | TGTCTCACTCTGTCA[C/T]CCAGGCTGGACTGCA | 8853 |
rs552405753 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245062 | TGGTTGTGAACTTTT[A/T]CCTCTTACTGGTAGT | 8853 |
rs552408966 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351097 | GTTTGACTTTGAGGG[A/C]TGGCCCTGCTCCTTG | 8853 |
rs552442689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276404 | ATATGAGGAGCTGAT[A/G]CCAGAGAAGCAGGCA | 8853 |
rs552453556 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283830 | AAAGCAAGATGTCCA[A/C]TTTCTCCTCTTATAA | 8853 |
rs552466632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373503 | TTCAAGGGACCCCAG[A/G]GTAGACAGGATCTCT | 8853 |
rs552482999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252476 | CTACTCAGGAGGCTA[C/T]GGCAGGAGAATCGCT | 8853 |
rs552483855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275230 | GCATGTTCCCATGCC[C/T]GGCTAACTTATTTTT | 8853 |
rs552512235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264675 | TTCTCTCCTCATCTA[A/G]GTGCGCGCTATAACT | 8853 |
rs552515506 | in-del | -/CT | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317102 | ACACACTCAACCACA[-/CT]CATACCCCACGCAAT | 8853 |
rs552538177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217099 | AAGCATTTTGACACC[A/G]GAGTCTGCTATTTCT | 8853 |
rs552554345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385483 | AGCTTACTTTATGCT[C/T]TCATTGATCTCAGTA | 8853 |
rs552603826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302513 | AGAGTCTCACTGTGT[C/T]GCCCAAGCTAGAGTG | 8853 |
rs552608515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397620 | AGGAGTCAGCAAACT[A/G]TGGCTCACAGGCCAC | 8853 |
rs552611225 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260878 | ACCCTGCCCCTACTC[C/T]ATCTGCTTCTCCGCC | 8853 |
rs552614946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211665 | TTGCTGTCATAAGCA[C/T]AGGGTTCTAACTGCA | 8853 |
rs552629965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352914 | CATCCCTCCTCCTTC[C/T]CTGCTTGTCTTCCAG | 8853 |
rs552641619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296850 | GCTGCAAAGACCACT[A/G]CTGTTGCTGTATTAA | 8853 |
rs552641648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209354 | CTTTCCCAGGTGTCT[A/G]ATGTTCGTGTCTATT | 8853 |
rs552650402 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309305 | AAAAAGAAGTGAACT[A/G]CTGGTACACGCAACT | 8853 |
rs552672398 | snp | A/C/G | 0.000148274 | 0.008609 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9391036 | TGTGTGCGTGCATGC[A/C/G]TCTGTGTGCATGCGT | 8853 |
rs552686512 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249857 | CTGAAAACACTCTGC[C/T]AGGCTTCCAGATTTT | 8853 |
rs552689918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392326 | TCTCCTGCTGCAGCA[G/T]CCCTGGAGTGGGGAG | 8853 |
rs552716000 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374151 | CTCTTTGGATGGGGC[A/G]GAGTCTGAGCATGTT | 8853 |
rs552741166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328343 | TATGGCTTTATGGCT[C/T]AGGGATTATATCTTA | 8853 |
rs552755280 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9354765 | TGCAGCTTAGCCTCT[C/G]TAGGCTTCAGCCCTC | 8853 |
rs552792195 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383358 | CTCCTGAGCTCAAGC[A/G]ATCCTCTCACCTCAG | 8853 |
rs552816086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386254 | CTGAAACCTGTTGGA[C/T]TGTCTGCTCATGGAG | 8853 |
rs552847452 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379848 | AATACAAAAATTAGC[C/T]GGGTATGGTGGCGCG | 8853 |
rs552854910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297676 | TAAATGTACACAGCT[A/G]TGGGACAAAATGGGT | 8853 |
rs552888937 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9293658 | GTGGGTCAGTCAGTG[C/T]CATGTTAATCATGGA | 8853 |
rs552904129 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264998 | AAAATTAGCCGGGTG[C/T]GGTGGCATGTGCCTG | 8853 |
rs552923816 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9224629 | CCCAATTAATATCTG[A/C]TTTCTTCTTTGAAAA | 8853 |
rs552958207 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379550 | GTCCCTCCCTCTCTC[A/G]AGGACCCCGACATGC | 8853 |
rs552963530 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9298284 | AACAAGTGAAAAACA[C/T]AGCTCATTCCTGAGA | 8853 |
rs552964097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303415 | TGTTTCACGATGCTG[C/T]GAGCTGAAGAGCAAG | 8853 |
rs552973198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277529 | ACTCTTTAGTATGGC[A/G]GGAAAGAATGCCTTT | 8853 |
rs552994218 | snp | A/C | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214154 | CGTGATATGAACCTA[A/C]CTCCTTTGCTTACGC | 8853 |
rs553010332 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397812 | CGCCCAGGCTGGAGT[G/T]CAGTGGCTCGATCTC | 8853 |
rs553011932 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275447 | CATCTGTGGGAGTAT[C/T]AGAGGCAGGAGGGCT | 8853 |
rs553031372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322367 | TACTTGGGTCTTCTG[A/G]TGTCTACTTCAGGCT | 8853 |
rs553038204 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348165 | TTGAGACGGAGTCTC[A/G]CTGTGTTGCCCAGGC | 8853 |
rs553040513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340734 | CAAAATGTCAGTTTT[C/T]AAGCTATCCTAGAGT | 8853 |
rs553069560 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317740 | CATTCACACTCACAT[A/C/T]CACACTCACACTCAC | 8853 |
rs553070567 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233633 | ACCTGGACTCAGATA[C/T]AGGTTTTGCTAATTG | 8853 |
rs553075943 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309481 | GTTGCCAGAGACTTG[C/G]GGGTAAGGAGCTGGG | 8853 |
rs553096447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317079 | ACCACACAAAATCAC[A/G]TCCACACACACACTC | 8853 |
rs553100716 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405225 | ACCAGAGGAGAAATT[A/G]TATTAACGACCCTGC | 8853 |
rs553124502 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374387 | AGGGCAGGGGCAGGG[C/T]CTTCCTGGGGGAGGA | 8853 |
rs553146291 | snp | C/T | 6.61737e-05 | 0.00575174 | missense | ASAP2 | GRCh38.p7 | 2:9374916 | ATGGTGTGGATCTTA[C/T]GGAAAAAATCCCACT | 8853 |
rs553150950 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225379 | AGGACGCATGGCCCT[A/G]TTTAGACATTCTGCT | 8853 |
rs553152830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216836 | ACTCCTGGACTCAAG[C/T]GATCCTCCTGCCTTG | 8853 |
rs553155168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328798 | GAGACACAGTGATGT[A/G]CAGTGCTGGCATAGT | 8853 |
rs553174394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346450 | CAAAAAAAAAAAAAA[A/G]AGCCATTCTTTCCAT | 8853 |
rs553174928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329271 | CCCAGACATCTTGCA[A/G]AAGTTTTTAGATTTT | 8853 |
rs553185777 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9382054 | AGTGACATGATCTCT[C/G]TTCACTGCAACCTCC | 8853 |
rs553188434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342840 | TGCTGACCACGTGAC[C/T]GTGACCTCCCTGTGT | 8853 |
rs553206466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211402 | TTCTTCTTTTTTTTT[C/T]GTTTCTTCGAGCCTC | 8853 |
rs553213895 | in-del | -/TTTG/TTTTG | 0.193653 | 0.243567 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275084 | TTTCATTTGTCTGTT[-/TTTG/TTTTG]TTTTTTTTTTTTTTA | 8853 |
rs553215232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226767 | ACTCAAAACATTGGC[A/G]ATCTAGCAAACGGTG | 8853 |
rs553219388 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317732 | CACAATCACATTCAC[A/C]CTCACATCCACACTC | 8853 |
rs553232196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240720 | TAGCAACCTCAGCAT[A/G]GGAATTTTTCCTTAA | 8853 |
rs553258357 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253326 | CCGCCACCACACCTG[A/G]CTAATTTTTGTATTT | 8853 |
rs553259990 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211103 | GAGGTTGCGGTGAGT[C/T]GAGATCGTGCCATTG | 8853 |
rs553263075 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9382176 | TTTAATAGAGACGGG[G/T]TTTCACCATATTGGT | 8853 |
rs553263621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379997 | CTCCATCTCAAAAAA[A/G]AAAAAATAAATAAAG | 8853 |
rs553264832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349061 | TTAGCTACAAAATTG[A/G]TGTAGTTCCTACCTC | 8853 |
rs553277360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218066 | TAGTGACATGCCTCC[A/G]GGTTCCACATCCCAC | 8853 |
rs553287879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252454 | GGGCATGGTGGCACA[C/T]GCCCAGCTACTCAGG | 8853 |
rs553295248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260081 | GCCTGATGGCTCTGC[C/T]ATGGAGGTGGGAGGG | 8853 |
rs553296757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312304 | AATAATTCCAAAGAG[A/G]AAAACCGTGAATGAA | 8853 |
rs553297183 | snp | A/G | 1.65116e-05 | 0.00287324 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377024 | TTAAGGGAGGCACTC[A/G]TTTTCTCCTTGGTAT | 8853 |
rs553309864 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9316767 | TGTACCTGTTGGTTA[A/G]GAGGCTTCCATTCCA | 8853 |
rs553334712 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246442 | CAGGTGTGCGCTAAC[A/T]TGCCTGGCTAATTTT | 8853 |
rs553334821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252653 | GGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 8853 |
rs553344121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370031 | CTTTAGTAGAGATGG[A/G]GTTTCACCATGTTGG | 8853 |
rs553362937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271444 | GCAAACTTCTTAAAC[A/G]CCTTCACTGGTTTCT | 8853 |
rs553370447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242090 | CATGTACCTCACAGG[C/T]GTTCGTTGTGTTTGC | 8853 |
rs553376317 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245948 | CCCACATTTGATTAT[A/G]TAATAATTAAAACCT | 8853 |
rs553378111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355037 | AGAATATCCATATAT[C/T]CCTCCCCTAGCTTTC | 8853 |
rs553387362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363014 | TCTATGAGTTCAGCT[C/T]TTTTAGATTTTGCAT | 8853 |
rs553445669 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212486 | GCCTCCCTGCCTTAG[A/G]TAAATATTGATCTAC | 8853 |
rs553445932 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336844 | GCTGCTCCCCAGCGC[A/G]CCGTTGGAAATGATC | 8853 |
rs553452671 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271687 | CGGCGGGCAGAGGGT[A/C]CGGAAAGTAGGGAAG | 8853 |
rs553457714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277868 | TTTCCATTTAAAATT[A/G]CCAGCACTAATCATG | 8853 |
rs553458714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247555 | TTTTAAGGCAGCCAT[A/G]TGGATGGGCAGTGGG | 8853 |
rs553458796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368580 | CTTTGCCCGAGCCCC[A/G]GGAGGCAGGGGAATA | 8853 |
rs553469884 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9392001 | TCCTCCTGCCTTAGC[C/T]TCCTGAGTAGCTGGG | 8853 |
rs553481055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248416 | GTATGTGTAGCTCTT[C/T]ATTTTTCAAGCATGG | 8853 |
rs553513497 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273426 | GAATTTATCTATCAG[G/T]GTAACCACCCAATGG | 8853 |
rs553520149 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369287 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCGTGA | 8853 |
rs553524520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362062 | ATAAAGTATTAGTTA[C/T]CATTGTTATCTCCTT | 8853 |
rs553530115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365067 | AAGCATGTACTTACT[C/T]ACATATGATGTACCT | 8853 |
rs553561614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212905 | GCACTGTTCGAGACG[A/G]AACCCCGGCTGCACA | 8853 |
rs553578096 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253756 | ACCACTCCTTTGCAT[G/T]GCTGAATAATGTTCT | 8853 |
rs553583663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298307 | TCCTGAGATGGTGAT[C/G]ACAGTGGTTTTGGGA | 8853 |
rs553585054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360007 | CATGTAATAATGCAC[A/G]TAACCTACAGCTTAG | 8853 |
rs553586756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311705 | GAGGATGGCTCGTTC[A/G]GCTGCGGGCCTGAGG | 8853 |
rs553599459 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267820 | TGAGAATCGCTTGAA[A/C]CCAGGAGGCAGAGGT | 8853 |
rs553623127 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9206395 | CCGCTTTCCTCATGG[C/G]CCGGCGCGGCCCGCC | 8853 |
rs553667559 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364680 | AGAGAGCATGTGGAG[A/G]GGAAAGCTCCTCAAA | 8853 |
rs553676439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393752 | GGGCTCCTACTCCAG[C/T]GTGGGCGCCACATAA | 8853 |
rs553680094 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207439 | CCTCTTTAAGACCTC[C/T]CCTCTCTCGGCCTCG | 8853 |
rs553686656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272183 | TCCCACCAATAGTGT[A/C]CAGGGGTTCCCTTTT | 8853 |
rs553688688 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266480 | AGCTGCCTTACTTGT[A/G]TTTTGTCCTCAGTGC | 8853 |
rs553695765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401142 | CACTGACCTGCCCCA[C/T]CTTGGCATCTGCAGG | 8853 |
rs553695899 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9363418 | CAGTGTGCAAGCCTT[C/G]CCTTTTCTCCACATC | 8853 |
rs553737798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387010 | GAGATTGAGACCATC[C/T]TGGCTAACACGGTGA | 8853 |
rs553738668 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370441 | CATGAGGTTGACAAT[C/G]TGATCATCCTCTCTT | 8853 |
rs553759524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262404 | TAATCACTATTAGAT[A/G]TTGAGTGCTGACTGT | 8853 |
rs553764860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324195 | CTGATTTTGGAATGT[A/G]TGTTTGTTAATTGTA | 8853 |
rs553774473 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294376 | AGGAGGGATGATAAG[A/G]AGTGCTTTTGTATTT | 8853 |
rs553798773 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9388841 | CGGGGCTGGGCCAAA[A/G]GACACACTCCTTCAG | 8853 |
rs553816956 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232621 | CAGGGATTTTTGACT[C/G]TTACTTAGTGATGCA | 8853 |
rs553823047 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387809 | TAGTTTATAAAAGAA[-/AG]AGGTCTAATTCACTC | 8853 |
rs553835016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268486 | CTTTATTCCCACAAG[C/G]GGGGAGGTTCGTTAT | 8853 |
rs553839819 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299658 | CCTAGAAAGCAGCCA[A/G]CCCAGGACGGCTGAC | 8853 |
rs553844952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261695 | TTTAACAGTGTGGCC[A/G]AGTGTAGGAGGGAGG | 8853 |
rs553850659 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344098 | GGAACTGAGGCTGAG[A/C]GCTTATGTGATGGTT | 8853 |
rs553860315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375588 | TTTGAAATAGACGCT[A/G]TGTAGTCTTACCTGG | 8853 |
rs553861075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300367 | AACAAAAGGGCAGCT[A/G]CATAGTTAAATAAAA | 8853 |
rs553868780 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381005 | CTAGGGGGACCCACC[C/G]CTCGCAGTGAGACTT | 8853 |
rs553873074 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299040 | CAAAAAGACCAAAAA[A/G/T]TGGGAAATAGATAAA | 8853 |
rs553884884 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219031 | CATCTGTCTTGCCTC[A/C]GAGCAGTATTTTTTG | 8853 |
rs553894281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280460 | CGGGAAGAATCTAGC[A/G]GGAAATCCCAGGTGC | 8853 |
rs553902885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208374 | GGGTGTCACCAAAGA[G/T]CTTTAAATGAAGCAA | 8853 |
rs553908765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236092 | CTGATGTTGAGAAAC[A/G]CTGGGTCAAAAGGCT | 8853 |
rs553913785 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292722 | GCACATTGCCTGATG[A/C]ATTGTAAGTGATCAG | 8853 |
rs553922051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222162 | TTTGCACAGAATAGG[C/T]GCTCAGTAACTTTAT | 8853 |
rs553944871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395124 | AAGCTCAGACACAGT[C/T]GGGGCAGAGAGGACT | 8853 |
rs553957599 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256763 | TGATGGTATGCATTT[C/G]AGCAATTTGTATTCC | 8853 |
rs553977491 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349912 | CTTGAAGTGACCGGT[G/T]GCCAAGGGAAGTGGG | 8853 |
rs553979852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273907 | TCCTGCAAAGGCTGT[C/T]TAGTCCCCAGGCAGG | 8853 |
rs553982903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350549 | CCTCAAAGCTGGCAT[C/T]GCTTGTCCTCTTGTC | 8853 |
rs554010331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294421 | ATAAAGTCTACTATC[A/C]GTGAGAAGGCCGGCT | 8853 |
rs554015996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318681 | GCCGGGCAGCAGCCA[C/T]GCCAGTACGTTCTCA | 8853 |
rs554034673 | in-del | -/T | 0.290977 | 0.246619 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334201 | GTATTTTTGTATTTG[-/T]TTTTTTTTTTTTTTG | 8853 |
rs554048898 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294813 | TGAAGGAGGACACCA[C/T]GGCCCAGCTCCCCTC | 8853 |
rs554051554 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370851 | CGAGCCTGAGGGTCC[C/T]GCTTGGTGAAGGAAA | 8853 |
rs554054448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371494 | TAAGCTAGTATTTTA[C/T]TTCCAGATGAAAAGG | 8853 |
rs554069846 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344237 | CCTCATGTCACTGTC[-/A]GGGGGTTAAGGCTCG | 8853 |
rs554082278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324886 | ACAATCTCTGCCTTT[C/T]GATTGGATTGTTTAA | 8853 |
rs554082467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400578 | CTCGCTGCCACACAA[A/G]CTCTCCAAGGTCTGC | 8853 |
rs554107036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351055 | TTCCATTAGTAACTG[C/T]TGGCTTGCCAGCCTT | 8853 |
rs554117221 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307379 | GGTGCCCCAGGTCCT[C/G]TGGAGGTCAGAGCTA | 8853 |
rs554150170 | in-del | -/TTAT | 0.00444802 | 0.0469492 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290197 | ATATTCTAATGTTAT[-/TTAT]TTATTTATTTATTTA | 8853 |
rs554153145 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315091 | TTTCCGTCGAATAGA[A/C]CAAATTGAGCACATG | 8853 |
rs554155964 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322874 | CTGTGCAGACTTCCT[A/G]CCTCCTCTGACCCAT | 8853 |
rs554163295 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9304355 | AGGGACAACTGCCAC[A/G]ATGTAGGTGACCTCA | 8853 |
rs554227025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401832 | GAGCAAGATGAGTGC[C/T]GGCCACCTAAGAATT | 8853 |
rs554233970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214799 | AAAAAAAAAAAAAAA[C/G]TGAACAGGACTAGCT | 8853 |
rs554234449 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232246 | TCCTCTGTGTCAACA[C/T]GCCTCACTGCCCTGC | 8853 |
rs554257205 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322042 | TCTGGACGGTCTCTT[G/T]CCTGTGAAGGAGTGT | 8853 |
rs554273622 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258474 | TTTTAAAGGTGGTAC[A/T]TTCATAGAATTTTGT | 8853 |
rs554273916 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279871 | CATACATATTTTTTA[C/G]ACATATATATTTACA | 8853 |
rs554307876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221639 | GGTTACTTTTTGTAT[A/G]TTGATCTTATGGCCT | 8853 |
rs554314130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351816 | AATGGCTTGCTCTTA[C/T]CCTCCCTGTTCCCCT | 8853 |
rs554333269 | snp | C/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216621 | GCCAACCACCACACC[C/T]AGCTAATTTTTGTAT | 8853 |
rs554350749 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353007 | TCCTATGAGTATCTG[C/T]AGTGAAAATGGTTTG | 8853 |
rs554367876 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362676 | AGACCTCCATCTCTA[C/T]AAATAATTTTTTAAA | 8853 |
rs554369004 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332001 | TGTGGTGGCGTGAAG[G/T]CTGCAGGAGGGGCCC | 8853 |
rs554381812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274632 | CCAGCCTAACACTCA[A/G]TCTTAAACAATCATT | 8853 |
rs554396680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308380 | GATGCCAAACCAGTC[A/G]TGAGAACTTCACCCC | 8853 |
rs554410480 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230255 | CCAAATCAGTCATAA[A/C]CTTCAGGAGTGAACA | 8853 |
rs554413537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301046 | ATGGGGAGCGGATTA[C/T]GGCGGAAGTCTCCTT | 8853 |
rs554420009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243846 | GTGAGGGACCGATAT[A/G]AGTAATTAGGAAATA | 8853 |
rs554436074 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256119 | TTTGCACGTTCAGAC[A/T]TTCATAGAAATGGCA | 8853 |
rs554445863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9215782 | TTCTAAGAGTCTAGC[C/T]GAGAAGAGTTGCACC | 8853 |
rs554463640 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213655 | ATTGAGGTCCATTGT[A/G]CAAGAAGAGGGGTCC | 8853 |
rs554492566 | snp | C/T | 0.000164756 | 0.00907472 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9388365 | CCAGCTTCAGTCTAA[C/T]GCTGTATCTTTGGCC | 8853 |
rs554493738 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249733 | AGCTGCAGGCAGGCA[G/T]GCCCGGGCTGGCGGG | 8853 |
rs554504930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334379 | CCTTTTCTTTTCCAT[A/G]TCGCGGTCGCCTGTT | 8853 |
rs554525729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230961 | CTGGTTCCATGGCAG[A/G]GCACAGTCCAGCTTC | 8853 |
rs554541474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390657 | GTTCCTCTTCACATG[G/T]TGGTGACTCCCACAG | 8853 |
rs554558014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238754 | TTTGATGAATCTTAC[A/G]AATGTACAGTTGTGT | 8853 |
rs554575848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345498 | TCTTTCCATGGCAGC[A/G]TTATACATACTATTG | 8853 |
rs554605495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372132 | TCCCTTTCCTGTGGA[A/G]GTCGCAGTAATGATT | 8853 |
rs554608840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301896 | TGGCACAATCTCAGC[G/T]CTCTGCAAGCTCTGC | 8853 |
rs554627056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327302 | CTTTCTGATAGCTTC[A/G]TGGTCACTAATGAAT | 8853 |
rs554632003 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326453 | TAGGTAGTACAGACC[C/T]TCTGTGAGCGGAGAA | 8853 |
rs554639620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340439 | TCAAACTGGTTCTCC[A/G]GAGTCTTTTAAAAAT | 8853 |
rs554640330 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9255905 | TGATTTATTTGTATG[A/C]GTATTGGTAGGTAGC | 8853 |
rs554641885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9333864 | CCTGAATCACTTGTT[A/T]TAGGTGACCTCACAG | 8853 |
rs554722413 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328689 | GTCTCTGACCTGGCT[C/T]CTGCTCCTCGACCCC | 8853 |
rs554726708 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9347741 | AACTCTAATTAGATA[C/T]CCTCTTTGCCAGATT | 8853 |
rs554747847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9237929 | AAGAGCCCTGAGGTG[A/G]GGTAAAGATGTTAGA | 8853 |
rs554750672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257790 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGATGT | 8853 |
rs554756550 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302548 | GGCACGATCTTGGCT[C/T]ACTGCAGCCTCCGCC | 8853 |
rs554771236 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9326183 | CCCAGGAGTTCAAGA[C/G]CAGCCTGGGCAACAT | 8853 |
rs554778398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263955 | CCAGCACTTTAGGAG[C/G]CCAAGGCGGGCGGAT | 8853 |
rs554780798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265061 | GGATCACTTGAGCCC[A/G]GGAGGTGGAGGCTGC | 8853 |
rs554783916 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240978 | AGGGAGGAGTCACGT[C/T]CCGCGTGGGAGGCAG | 8853 |
rs554792378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251955 | TTTTTTTTTTTAATT[A/G]TCATCTGTAGCTCAT | 8853 |
rs554885506 | snp | A/T | 3.41886e-05 | 0.00413438 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391208 | ACCAGTACGTTTTTT[A/T]CCTTTTTCCTTTCTT | 8853 |
rs554890824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270510 | AGGCATGCAGTGCAT[A/G]ATAATCACATTAGGG | 8853 |
rs554911404 | in-del | -/AAAG | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332804 | AGAAAATAGTTACAT[-/AAAG]AAAAACACGTAAATA | 8853 |
rs554931500 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373685 | GGTCAGGAGGGAACC[A/G]TGCGGGGACTCCAGC | 8853 |
rs554944232 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259564 | TTTTCAGCCCAAAAC[C/G]TTAAGGAACAAAAAT | 8853 |
rs554972187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327751 | AAGTAGAAGAAATCA[C/T]CTCAGTCCTCAGAAG | 8853 |
rs554979087 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402417 | GGCGGAACACTTGAG[C/G]TCAGGAGTTCGAGAC | 8853 |
rs554990651 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9228734 | GCGTATGTGAACTGG[C/T]ATACCCAAATGCAAA | 8853 |
rs554991424 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283351 | CCTGTAATAGTTTCT[G/T]ATTGCTGTTGTAACA | 8853 |
rs554993049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367638 | TGGTGGCGTGTGCCT[A/G]TAGTCCCCGCTGCTT | 8853 |
rs555010594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322119 | GTCACACTCCTTTCC[A/G]GATGCATAGACTCAT | 8853 |
rs555019649 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265668 | TTTGATATATCACTT[G/T]TCTATCCTCTTTTAT | 8853 |
rs555020237 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366568 | ATTAGCTTCCTGGTG[C/T]ATAGGTACCTGTCAC | 8853 |
rs555034753 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348430 | GCGCCCAGGTGACAC[C/T]GTATTTTTCCAAATT | 8853 |
rs555035203 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251445 | GTGGGTCTGGGCGCA[A/G]AGCATGTGGAGAAAT | 8853 |
rs555043084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303926 | AGAACTCACAGAGAC[A/G]AGGACTGGGCACCTG | 8853 |
rs555056854 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370887 | TGAATCCAGCATGGC[A/G]AGGTCATCTCCTGCT | 8853 |
rs555068012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386943 | AGCGCGGGGGCTCAC[A/G]CCTGTAATCCCAGCA | 8853 |
rs555094469 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9335786 | AAAAAGTAAGTTTTA[A/C]AGATAATTTTACTAT | 8853 |
rs555102893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342007 | TTTTTTGGTTTTTCT[C/T]TTTTGGCAGAGTTTA | 8853 |
rs555122357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379225 | AGCCTCTCCCTGCCT[C/G]TTCCACGAGGCCGCA | 8853 |
rs555124682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375478 | TTTTGATCTATGTTT[A/G]CATCATGGAATGATT | 8853 |
rs555125757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225452 | TTTCTTCCCCAGGAA[A/G]TGTATACTAAATGAA | 8853 |
rs555130897 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285597 | ATTTATTTTAAACTC[C/T]TACTTGTCTAAAATT | 8853 |
rs555137439 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226092 | GCTGCCTCATGCGAG[A/C]TAGTCTCACCCTGGG | 8853 |
rs555149008 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9379860 | AGCCGGGTATGGTGG[C/T]GCGCACCTGTAGGCC | 8853 |
rs555151374 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291616 | CAGGCTGCTGCCATA[A/G]AGAACATATGTCTCT | 8853 |
rs555152479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398444 | TGACCCCAGGAGTTC[C/T]GAGGCTGCGGTGAAC | 8853 |
rs555163507 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405278 | GCTCCTTGCAAATTA[A/G]AAAAGCAACTAAGAG | 8853 |
rs555169590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286362 | GAAACTGCACCACTG[C/T]ACTTCATCCTGGGTG | 8853 |
rs555200378 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380591 | ACAAGATACATTCAG[A/C]CTCGACTAGGTCAAA | 8853 |
rs555212021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317008 | TCATACACTCTCACA[A/G]CCACACTCACACAAC | 8853 |
rs555237345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289459 | GAAATATTCTTGACC[C/T]GTAATGGAAGCACAC | 8853 |
rs555247698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291997 | GTGGGAGGAAGAGCA[C/T]TGGACTCAGAGTCAG | 8853 |
rs555258795 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276893 | ACTTGCTGGCCCATG[G/T]AAGGTGCTTAGTAAG | 8853 |
rs555288003 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221456 | CACTGCACCTGGCCT[C/T]ATTTTCTTGTCTTTA | 8853 |
rs555347291 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404443 | TTAAGCTACTTGGGG[A/T]GGTAGTAGAGGATTA | 8853 |
rs555350857 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297050 | GCCATCTCATCTGAT[-/A]ATGCTGAGGACCACT | 8853 |
rs555350975 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316360 | AAATCGGATGCCATA[A/T]TGCTTTAAAAGTGGT | 8853 |
rs555352899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252691 | GAGGTTGAGGCGGGC[A/G]GATCACGAGGTCAGG | 8853 |
rs555356042 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312326 | GTGAATGAAACCAGA[A/T]TCCCCCTCATTGACC | 8853 |
rs555393874 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211947 | GGTCAAACAGGGCCA[C/G/T]CTTTTAAACTGTGTT | 8853 |
rs555400966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247716 | GCTGGTGCCAGACGC[A/G]GAGTAGGTGTTCAGT | 8853 |
rs555401847 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332603 | TCATGCTCACGCGCT[C/G]TCACTCTCGCTCTCT | 8853 |
rs555410011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392983 | TAAGAAAGCTCTTCA[C/T]CCACCCACTCCGGAG | 8853 |
rs555411050 | snp | A/C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311710 | TGGCTCGTTCGGCTG[A/C/T]GGGCCTGAGGCTGCT | 8853 |
rs555421960 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212459 | GCTGGTTCATTCTGG[C/T]CTTCTGTACCTGCCT | 8853 |
rs555427526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272299 | TGATTTGCATTGCTC[A/G]GATGATCAATGATGT | 8853 |
rs555437022 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335303 | CTGTGTCAGGCACCA[C/G]TAAAACATTTAATGT | 8853 |
rs555455341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310247 | CAAAGCGTCTTTTCT[A/C]CCTCTCAAGTTTCTC | 8853 |
rs555469593 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217703 | CACTGCAAGCTCCGC[A/C]TCCTGGGTTCACGCC | 8853 |
rs555485356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399830 | TTTTAGGATCAGAAA[C/T]GTTGAATTTAGCACT | 8853 |
rs555497995 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9206589 | GGGGCCCGGAACGCC[A/G]AGACAATGCGGCGCG | 8853 |
rs555508203 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210804 | CTGACCTTGTGATCC[A/G]CCCGCCTTGGCCTCC | 8853 |
rs555522079 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369408 | AGTGGCCATGTCACA[C/G]TAGTCTTCGAGAAGA | 8853 |
rs555548944 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368051 | TACCAGAACTACCTC[A/T]TAGCTGGCATAAGTA | 8853 |
rs555557613 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337837 | CTGTAAGGAGAATAC[C/T]ACTCTTTGGTATTTC | 8853 |
rs555560817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323021 | TGAAACGTGTGGTGA[A/G]CGTTGGTCTCGCCAG | 8853 |
rs555562622 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278632 | ATAACTGTTTGAGCG[A/C]CTCCTATGTGCTGGA | 8853 |
rs555592858 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279063 | AGCTTGCATGCTGCA[A/G]GAGGAGGAGTTGGTT | 8853 |
rs555594424 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341288 | TCGCCTGGGAGTCAC[C/G]TAGAGGATACTGAAG | 8853 |
rs555615521 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327700 | GCGATACTAAGTGTC[A/G]ATCATGCACTCTACG | 8853 |
rs555633837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343435 | TCAGAGTGTCTGCTA[C/T]TGTTTGTTTTGTTTG | 8853 |
rs555658064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299696 | GAGACGGGTGGAGGC[C/T]CGGGTTCTGCTTCTC | 8853 |
rs555686559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238957 | CTTTCTCTTGCTGTA[C/T]TGTGTTCCCTGGGCC | 8853 |
rs555694659 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254639 | TCAGCCTCCCAAAGT[G/T]CTGGGATTACAGGTT | 8853 |
rs555739112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394378 | GCCGTGTTAGCCAGG[A/G]TGGTCTCGATCTCCT | 8853 |
rs555742005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324947 | GATTGGATTTACTTC[C/T]GTTATTTTACTTTTT | 8853 |
rs555753797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394973 | CTCAGCTGGGCTGTG[A/G]CCAGAACACCTACAT | 8853 |
rs555765089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355539 | GCAGTATGTAAGTGT[A/G]GGATTTTATATTCGA | 8853 |
rs555778748 | snp | A/G/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210756 | AGATGGGGTTTCACC[A/G/T]TGTTAGCCAGGATGG | 8853 |
rs555806198 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9285043 | CCACAGTGTGATGGT[C/T]TCTGGAGATGGGGCC | 8853 |
rs555816757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317602 | CACAATCACATTCAC[A/G]CACTCACATCCACAA | 8853 |
rs555832901 | in-del | -/GCTACAGGTGTGC | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246423 | TCCCAAGTAGCTGGA[-/GCTACAGGTGTGC]GCTAACATGCCTGGC | 8853 |
rs555836870 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267143 | CAATGAGATTTTTTT[A/T]AAAAATTCAACTTTT | 8853 |
rs555850695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241806 | GAGGAGAAGGAAAGG[A/G]ATGGCATTTTGATCT | 8853 |
rs555852764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233709 | TTTAACAAACACTTA[C/T]ATTGCACTTACTGTG | 8853 |
rs555867284 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236167 | GGATGTCCTTGGCAC[C/T]TGGACTGCTTTGGGG | 8853 |
rs555870494 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226867 | CGGGAGGTCTGGAGA[C/G]AGATTGCAGGTGGCT | 8853 |
rs555871835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371015 | TGTCGTTTCTTCCAA[A/G]CACCAGGGGTACCTA | 8853 |
rs555880851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331310 | TCTTAAAGAATACTT[C/G]GTGTTCTTTTATTTT | 8853 |
rs555895734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306890 | CCAGGGGCCCTGGCC[A/G]GACATCCACAGAGCA | 8853 |
rs555905780 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357882 | TTTCTCAGGGCAACA[A/T]ACAGTTCTGAAGAGA | 8853 |
rs555907601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350657 | TCTGTAACTTGTCCC[A/G]GTCAAGCCTTCCTCT | 8853 |
rs555917409 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378575 | TCCAGCACAGCTGGC[C/T]GGCCTAGCACAGCAG | 8853 |
rs555923169 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9222714 | TTGCATACTTTTGAT[C/T]TGGAAGAGGTGCCGG | 8853 |
rs555933039 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365148 | TTAAAGGGTCAGGTA[A/G]AGACATCATATGTAA | 8853 |
rs555949706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293468 | AGAACAGCTTTCACA[A/G]TTCTGTAAATAAAAG | 8853 |
rs555995904 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381723 | GCCTGGGCAACAGAG[A/C]AACACGCCATCTCCA | 8853 |
rs556001398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267646 | TCATGCCTGTAATCC[C/T]AGCACTTTGGGAGGT | 8853 |
rs556017412 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342873 | TCTGTGTACTATCCA[C/G]TTTGCCTTGAAGATC | 8853 |
rs556029665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9220322 | TTGCCAAAGAGGCTG[C/T]ACCACTTGACATTCT | 8853 |
rs556037486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268546 | CACAGTGCAAGTCTA[C/T]GCTTCCCAAAAGGCT | 8853 |
rs556042760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357196 | AAAAAAAAAGAATAC[C/T]GACTGGGTGCAGTGA | 8853 |
rs556062937 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299157 | AGGCAATTTCTAAAA[A/C]TGGAACGGAAGAGTC | 8853 |
rs556081896 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260217 | AGGTGATCAAGTAAT[G/T]TGTGTGTGGAGATGT | 8853 |
rs556087973 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263879 | GTATTTTTTTCTCCA[-/T]TTTTTTTCCCTTTTA | 8853 |
rs556088241 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349735 | TATTAACCCAAATCC[G/T]TCACGCTGCAAGGAT | 8853 |
rs556136149 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377615 | GACCCCTCAACGTGT[A/T]TTTTGACTCCCTGAT | 8853 |
rs556170557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318806 | CTGGCCGTCCTGTTG[G/T]CACAACAAAGTTGGT | 8853 |
rs556196685 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263426 | TGTGCAGTGGTGATC[A/T]TGCCAAAATGTGGCT | 8853 |
rs556202137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337981 | TGATTTTTGGAGAAG[A/G]TCCTATTTACACAGT | 8853 |
rs556217590 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262643 | AGCACTGGGTTTTCT[A/C]ATTTTTAATGCATCC | 8853 |
rs556223455 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332244 | CTTAAGAAAATTTTC[A/T]GGGGCTATGTAGTTA | 8853 |
rs556224568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294084 | GCCCACTGCAACCTC[C/T]GCTTTCTAGGTTCAA | 8853 |
rs556226443 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9393085 | GTGGGTAGGGCCTCA[G/T]CCCTTTGGCCACAGG | 8853 |
rs556247479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370523 | GTAGGGACATAGATA[C/T]CTCAGTCCTTATCTG | 8853 |
rs556255339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376334 | GGTTCTCTCACCCAC[C/T]CACCTGCTGAAACAA | 8853 |
rs556274288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274525 | TCGGAGTTTTACCAT[A/G]TTGTGCAGGCTGGTC | 8853 |
rs556301683 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9235889 | AGGCAGATGGAGCTG[C/T]TCCACCTGGCAGTTT | 8853 |
rs556318316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376796 | AAGAGATAAGTTTCT[A/C]GAAGGGAAAGATAAA | 8853 |
rs556328495 | in-del | -/GTTGACA | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359587 | CTGGGATAGCTGGAT[-/GTTGACA]GTAAACAGTAAGTAG | 8853 |
rs556335441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314236 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 8853 |
rs556342298 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232841 | TGGTTCGAAAGTTGA[A/C]TTAGTGAGTGTAAAT | 8853 |
rs556356873 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402331 | CGTTTGCCCTTAATG[C/G]ATTGAAAGTGTCTGT | 8853 |
rs556362021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269047 | ATCCTTGAGGCCAGG[A/G]CTCAGCAAACCTTTT | 8853 |
rs556365703 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387041 | AACCCCGTCTCTACT[-/A]AAAAATACAAAAAAA | 8853 |
rs556369023 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283164 | CTCACTGCAGCCTCC[A/G]CCTCCTGGGTTCAAG | 8853 |
rs556400101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378086 | TGAAAATGAAACACA[C/T]CCCCCGCTCCCCATG | 8853 |
rs556401680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396054 | ATAGAAGCTTCCTGT[A/C]CTTAGTAGGTTGGGC | 8853 |
rs556430089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365562 | GTGGGCCCTGCTCAG[A/G]TAGGTGCTAAGGACG | 8853 |
rs556460788 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372345 | AAATGGGTCTTCCCT[G/T]GTAGGCCCACCAGCT | 8853 |
rs556465744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366489 | TGGCTATAAACCAGG[C/T]GCTCTGACATTGGGG | 8853 |
rs556476561 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345296 | GATTTTATTATTGAA[A/C]TCTTAACATATGGTG | 8853 |
rs556479530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401190 | CGGGACTCCTGAGAC[C/T]GGGGAAGGCAGGGTG | 8853 |
rs556480210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320160 | GGTTCTTTATTTTTC[A/G]TGGGATTACATACGT | 8853 |
rs556532988 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333481 | AAGGCCTCACTAACC[A/G]GGGATGTTTAACCTA | 8853 |
rs556543014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395693 | GCTCACTGCAAGTTC[C/T]GCTTCCCAGGTTCAC | 8853 |
rs556543544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288711 | AATGTTGAATTCACC[C/T]CTTGGCTTTGAACCC | 8853 |
rs556544226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397711 | TTGTAATTGGTTGGG[A/G]AAAAAAAATCAAAAG | 8853 |
rs556569707 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284652 | GTTCTGGACATACAC[A/G]TGGTAAGTGTGACAG | 8853 |
rs556578056 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243967 | TTTCTTTTGGGAATT[A/C]GTGGGAACATGATAT | 8853 |
rs556611574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332088 | TAATTGCCTCTAAGT[A/G]GGTGTATTTTAAAGG | 8853 |
rs556616748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209989 | GCATACTTGTTGCTG[C/G]AATATTATTATAGTA | 8853 |
rs556618726 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402963 | GAAGTAGTGGTCAGA[C/G]AGCTGACCTGTGTGC | 8853 |
rs556623543 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214924 | TGGCGAAGGTGATCT[G/T]CCTCTTCAGAAAAAT | 8853 |
rs556655871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275964 | GTGCTGGTAGCTGCT[C/G]TAGTGGATGGCTGTG | 8853 |
rs556680194 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397371 | TTCCTCTGGAACACA[A/G]TTTTACCTGGTTTCA | 8853 |
rs556732541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301191 | TCTGGCTAAGACTCA[C/T]AGTGCTACCTCTTGT | 8853 |
rs556741770 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219233 | ATTTTGTGGGGAACC[A/G]GTGTTCTCATCATTG | 8853 |
rs556811200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302293 | TCCTTCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG | 8853 |
rs556813542 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250751 | CAGCCCCTGAGATGT[A/T]GCAGTCTTCCTGTTA | 8853 |
rs556818514 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238138 | ACTGTTAGCTGACCC[A/G]CTACCTACTGATCTT | 8853 |
rs556843917 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210695 | GAGTAGCTGGGACTA[A/C]AGGTGCCCGCCACCA | 8853 |
rs556850636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244580 | ACACAAACTTAAATA[C/T]CAAACTTAGTTCAGA | 8853 |
rs556873309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332597 | CGGGGCTCATGCTCA[C/T]GCGCTCTCACTCTCG | 8853 |
rs556876283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302655 | AAGTTTTGTATTTTT[A/C]GTACAGACGGGGTTT | 8853 |
rs556899695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9224248 | CTCTGAATACTCTGG[C/T]GCTTCCTTTTTGGGG | 8853 |
rs556939705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322243 | ACACAGAGAAATCAC[A/G]TTTCTTGCCTCTTCT | 8853 |
rs556956098 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232299 | GTCCCTCTGTTTGTA[A/G]AGTCGCCCTGCTCTT | 8853 |
rs556961237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352597 | GCCTCCACCTTTTTA[C/T]AACACAGCAGGCAGC | 8853 |
rs556963804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340177 | ACAGGTACGCGCCAC[C/T]ACGCCTGGCTAATTT | 8853 |
rs556967760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247455 | GGACCTTATTACCTC[A/C]TGCGCTGCTTTCGGT | 8853 |
rs556978805 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286438 | TTTTTTTAAAAAAGG[-/A]AAAAAAAAAATATAT | 8853 |
rs556993786 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339945 | TCACTTTTCAGGTTT[G/T]CCAGGCACTTTACAA | 8853 |
rs557004851 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271679 | GCGGAAGACGGCGGG[C/T]AGAGGGTACGGAAAG | 8853 |
rs557011414 | snp | A/G | 3.31713e-05 | 0.00407242 | missense | ASAP2 | GRCh38.p7 | 2:9327893 | AGAATCTGATCAAAT[A/G]CTTTCATGCCCAATG | 8853 |
rs557023957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353329 | AAGCACTTTGGGAGG[C/T]CAAGGTGGGAGGATT | 8853 |
rs557045105 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315668 | TGCCAGGACTGTCAA[G/T]GACAGTGGAAATCTA | 8853 |
rs557055814 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343229 | AAACCACTTATTTTC[A/C]TTGTGTCCCTGTTTC | 8853 |
rs557058409 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9289173 | TTTTGGCTGCTCTCC[A/G]TTACCTGGGATGAAG | 8853 |
rs557070701 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328673 | CTTCAGTCTGACCCA[C/T]GTCTCTGACCTGGCT | 8853 |
rs557099838 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300103 | CCAGGCGTGGTGGCT[C/T]ACGGCTGTAGTCCCT | 8853 |
rs557123389 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249707 | TGAGATTGCTGGCAC[A/G]GGTCTCCTGGAGCTG | 8853 |
rs557132675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314880 | AGGTTGCGGTGAGCC[A/G]AGATCACGCCACTGC | 8853 |
rs557158376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348516 | CTTTACTGTTTGCTA[A/G]TACTTAATCTATGTA | 8853 |
rs557177146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259075 | AATTGCTCTGGGCCG[C/T]GGTCCAGCCCGTGGG | 8853 |
rs557177951 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291491 | GTACAGCCGACAGCC[A/G]GAGGAAATGGTCTCC | 8853 |
rs557189379 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232931 | GAAGAAGGAATTCCA[C/T]GTTAGACGTGTTCCC | 8853 |
rs557210636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247126 | TAGGTGTGAGCCACT[A/G]TGGCCAGCCTGTCCA | 8853 |
rs557232193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354314 | AGCACCTGAGTGCTC[C/T]GATCGCCCCCTCTGT | 8853 |
rs557232398 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402029 | CGGCTTGAATGGGGC[A/G]TGGACAGAAAGCCCC | 8853 |
rs557267323 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406045 | TGTGTCACTGAGTGG[A/G]CCTCTGTGACATCTC | 8853 |
rs557296770 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313438 | GTTCATGTGTGTACT[C/T]CCGCTTCATGAAAAA | 8853 |
rs557301799 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253265 | GCTTCCTGGGTTCAA[A/G]CGATTCTCGTGCGTC | 8853 |
rs557318242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375000 | GGCCGGCCACGGTGG[C/T]TCATGCCTGGGATCC | 8853 |
rs557338697 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253605 | TCCTGTCATCTCTGC[A/G]CTGCTTTCTGTCCTT | 8853 |
rs557342701 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398866 | TCTGCCTCTTTAAAG[-/A]AAAAAGTCTGCTCAC | 8853 |
rs557350166 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9405023 | TTAACAATCCTCCTG[C/T]ATCTGTATTTTATAG | 8853 |
rs557372553 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362851 | TGTCTCAAAACAAAA[A/T]TTTTAAGTATACAGT | 8853 |
rs557392909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290758 | CTGAGGCCCACTGCG[A/G]CTTGGAACACAGCTC | 8853 |
rs557396708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317523 | CCCACAATCACACCC[A/C]ACACTCAAATCCACA | 8853 |
rs557414645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259610 | CATCTCTTTGGCCCT[C/T]GCCTCTGTCTCCACC | 8853 |
rs557451127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379916 | AGAATCACTTGAACC[C/T]GGGAGGCGGAGGTTG | 8853 |
rs557452793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373745 | GATTGTAGGCAGTGC[C/T]GTGTTACAAATGGAT | 8853 |
rs557488180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279179 | GGTGCCGAGGGACCT[A/G]GCAGAGGAGGCTTGT | 8853 |
rs557514368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374363 | CAGAGGTTGGCCAGG[C/G]CTGCATGGAGGGCAG | 8853 |
rs557515667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218434 | AGCCACCCAGACCCA[C/T]AGAGTATTCCCTTCG | 8853 |
rs557516699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370390 | TGGTGTCGCATTTCC[C/T]TGAGAATTGGATAAC | 8853 |
rs557521835 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310016 | AGGCTGTTTCACACT[A/C]TGATACCCTTGTTAA | 8853 |
rs557547246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399970 | AAAAGGGGATGAGAA[A/G]GGGGCAGGTGCCCTC | 8853 |
rs557583652 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375527 | TATCCATTACCTCAC[A/T]GGCTCATCCATTTTT | 8853 |
rs557591640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393691 | CCGTGCTCCTGCCCT[C/G]TGACCTCACCTGCCC | 8853 |
rs557597044 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317025 | CACACTCACACAACA[A/C/T]GCAATCATTCCCAAT | 8853 |
rs557635783 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371792 | ATGTATCATTATGTT[A/T]ATTGTTTTTCTGCAA | 8853 |
rs557691082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336177 | ACCTTTCATTGTTGT[A/G]GACTTTATTAAAGGC | 8853 |
rs557717277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364581 | TCAGCTTTCTGTTTC[C/T]TGACTTTCTTCTATT | 8853 |
rs557730326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399034 | CTAGACTGGTCAAAT[A/G]GGAGGGGTCTTTGTT | 8853 |
rs557736836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395648 | AGTCTTGCTCTGTCG[A/C]CCAGGCTGGAGTGCG | 8853 |
rs557736859 | snp | G/T | 1.64792e-05 | 0.00287042 | missense | ASAP2 | GRCh38.p7 | 2:9388416 | CAAGGAGAAGCAGAG[G/T]GCTTTCATGCCCAGC | 8853 |
rs557741549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247883 | TTTGGCCCTATTTCC[C/T]GCTCTCCTCCTCTGC | 8853 |
rs557766424 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9269913 | CCCACACACTGTCCC[C/T]GTCCCCTGTCCTGGC | 8853 |
rs557784945 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9235078 | AGCTGAATTTCTCCA[A/G]GTGCCGTGTTTCACT | 8853 |
rs557786842 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311923 | ATGGAAAGGCAGAGG[C/G]AAGCAGGCTGATGTC | 8853 |
rs557799275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241920 | TCCCAATAAGTTTAG[A/G]GGAGCATGTTAGACA | 8853 |
rs557801032 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386975 | TTTGGGAGGCTGAGG[C/T]GGGCGGATCACGAGG | 8853 |
rs557801603 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9292054 | GCTGCAAACTCACTG[G/T]GTGACCTTGAGCAAG | 8853 |
rs557805077 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212086 | TTCTTAGGCTCAAGA[C/G]TAGAAGTACTGATGC | 8853 |
rs557805826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329519 | GAGAGAGACAGTGGT[A/G]TTGGTTAGAAGCAGC | 8853 |
rs557850346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9220547 | TTCAAATCCTTTGCC[A/G]TGTTTATATTGGATT | 8853 |
rs557873841 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395031 | CGGTGGCTGGGTCCA[C/T]GGACAGGTCCCCAGA | 8853 |
rs557876647 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373358 | CTCACGCTGCGGCGT[A/G]TCCAGGAGCCACATG | 8853 |
rs557884423 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208206 | CTCTGCTCGGCTCAG[A/T]ATAGGTTTACAAGTC | 8853 |
rs557895859 | snp | A/C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376110 | GGCTGCAGCATCTTT[A/C/T]TCTTGGTAACAGGCA | 8853 |
rs557895969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298206 | GGTCAAGAACTCAGT[A/G]ATGCTTTCTCTGTAG | 8853 |
rs557909423 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260984 | TGGTGAACTTTAGAT[A/T]CTTGTGCCCCTGGTG | 8853 |
rs557909795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363837 | CCTCGGCTTCCCAAA[A/G]TGCTGGGATTATAGG | 8853 |
rs557969541 | in-del | -/TT | 0.356811 | 0.226034 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293997 | GTATAAGGACAAGAA[-/TT]TTTTTTTTTTTTTTT | 8853 |
rs557981439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355733 | AATTACTTTTTGGGG[A/G]CCAACTCTGTAGTGA | 8853 |
rs557985835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324083 | TCAAATGTACACAAT[A/G]TGTGGGTGATGTTTG | 8853 |
rs557997228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389006 | AAAAGATATTGGGGA[A/G]CGATGCTCGGCCTAA | 8853 |
rs558002983 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9308650 | TGTAAACCATCTTGC[C/T]CTGTGCCAGCAGGAG | 8853 |
rs558012251 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229625 | CGAGCCTGGAAGGAC[A/G]TGCAGGTGTTAGGGA | 8853 |
rs558020379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338008 | CAGTTAAACTCGTTG[G/T]CACTGCTCATCTTTG | 8853 |
rs558048793 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371196 | CCCGGGCTTTTTTCA[A/G]AATGAGGGCGGATGA | 8853 |
rs558064071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330162 | TGCATTTCTAAAGCA[C/T]TTGAGGTCAGGCGGC | 8853 |
rs558070786 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207658 | TCCGAGCTCCCCGCC[G/T]CAGCCCCCGAGCGCC | 8853 |
rs558085571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331459 | GTAGGGCATTATAAC[A/G]TTATAAAATAAAGAC | 8853 |
rs558104153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287722 | GAGGTGAGGACGTGG[A/G]CTCGAAGGCCCTGGA | 8853 |
rs558147877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349877 | TATCTGGATTAATCC[C/T]AAATTCAGGTTTTTT | 8853 |
rs558152499 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229068 | GCTAGGGGCGGAAAG[C/T]GGACAATCAGGATAG | 8853 |
rs558192923 | snp | C/G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264341 | ATGTCTTCCAGAGAC[C/G/T]GGGGGGGCCCGTGCT | 8853 |
rs558193862 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382276 | GGCGTGAGCCACCAC[A/G]CCTGACCTGTCTCAT | 8853 |
rs558209161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350443 | GCCCAAGTTACCTGG[A/C]AAATCAACTGTGTTG | 8853 |
rs558209555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324997 | TTTTGCTCCTTGATT[C/T]CTCCTTTACCGCCTT | 8853 |
rs558214336 | in-del | -/CA | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317747 | ACTCACATCCACACT[-/CA]CACTCACATCCGTAC | 8853 |
rs558273316 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318875 | TTGGAAAAAGTAAAG[A/C]GTTTCGGTCTCTCCA | 8853 |
rs558280081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219463 | TGACCATCCTCCCTG[A/G]CCTAAAAATTCCATA | 8853 |
rs558302890 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345506 | GGCAGCGTTATACAT[-/A]ACTATTGCCTCACCT | 8853 |
rs558318417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358038 | GGTCATGTTAGTGAG[C/T]AGCCGAGCTGTGAGG | 8853 |
rs558327998 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228096 | ATGGAATGGGGGTGA[A/G]TCTTTTAATATGAGG | 8853 |
rs558328477 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9293539 | CCAAGCTATTTATTT[C/T]AGGTTCCTGTTTTAA | 8853 |
rs558336246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256425 | GCTGTGCCAATGATG[A/G]TGCTGTCCATGGGCT | 8853 |
rs558365417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243397 | ACAGGCATGAGCCAC[C/T]GTGCCCGGCCTAAAG | 8853 |
rs558392303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230054 | GCAAGAAGAGATGAT[A/G]ATGTTTGCTTCTTTT | 8853 |
rs558392706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249684 | CTGAGTGAGACTGGG[C/T]GCTGGGCTGAGATTG | 8853 |
rs558393106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381757 | AAACGTTTCGAATTA[C/G]CTGGGTGTGGTGGCA | 8853 |
rs558404136 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236329 | TGAATATATTAAGTT[C/T]GTCGACATCTTCAAA | 8853 |
rs558418578 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9342362 | AGAAATAAATCCTTA[C/T]ATTTAGAGATGATTT | 8853 |
rs558436849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262848 | CCATGGCCTCAGGAA[C/T]CAAAGTCCTCAGTCT | 8853 |
rs558437980 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279592 | CAGGTGTGGGATTTC[A/G]TCCCCTGTCATCCCC | 8853 |
rs558439618 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247367 | CTAGGGAGTCCCAGA[C/T]GGTCCCCGGTCCTCA | 8853 |
rs558457249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214956 | TTTTAATGCAGAGAA[C/T]AAAATAAGATTCCGA | 8853 |
rs558480115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344033 | TGATCCTATTGAGTC[C/T]TTACTGTTTATTGGC | 8853 |
rs558509725 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343721 | CCAGATGTTGGGATT[A/G]CAGGCATAAGCCACT | 8853 |
rs558530331 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267635 | CGTGCAGTTTCTCAT[-/G]CCTGTAATCCCAGCA | 8853 |
rs558539299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314337 | AGGTGCTCAATAAAT[C/G]ACTTGAATGAATGAA | 8853 |
rs558550243 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226641 | TCCTTTCAGGCTGCC[G/T]TGGGGAGGACTGTCC | 8853 |
rs558575159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377402 | CACATTAGCCATGGT[C/T]TGAGCCAGAGATTAG | 8853 |
rs558576666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222024 | TGATCTCCTGATCTC[A/G]TGATCTGCCCGCCTC | 8853 |
rs558589200 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351355 | TTTTCTTCCTCACCA[A/C]AGGAATAGTCTTTCT | 8853 |
rs558609003 | snp | A/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277686 | AGTGGTATGCTGGTG[A/T]CCCTCAGTGAACCGA | 8853 |
rs558624447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339663 | GATACTGCTGCTGTC[A/G]TTGTGTGTGACATAT | 8853 |
rs558638072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332626 | CGCTCTCTGTCTGAC[C/T]GTAGGGAGAATTGCC | 8853 |
rs558638502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371065 | TTGTTCTGGGGCTAG[A/G]CGATTCTAAAAAATG | 8853 |
rs558645819 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300818 | CATGGCCTCTTGTCA[C/G]CTTCTTGACTGATCA | 8853 |
rs558651611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243724 | CAGGGCATTCTGGTA[C/T]GTAGTCACTCATTCA | 8853 |
rs558676944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210615 | GCTGGAGTGCAGTGG[C/T]TCGATCCCCACTCAC | 8853 |
rs558697938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371416 | TGTTGCTTCTGGTGA[A/G]CCAGTGACTATTTAA | 8853 |
rs558699778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365179 | ACTTTTTCCCTGCAC[A/G]CCAGAGTGTCCTTTT | 8853 |
rs558700964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326645 | TCCCTATGTATACAT[G/T]CAAAAAAAATCGTAT | 8853 |
rs558702203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308344 | TTTTAAACTCACTTG[C/T]TACACAGTACCAAGG | 8853 |
rs558703337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367603 | CCATCTCTACAAACA[A/G]TACAAAAATCAGCTG | 8853 |
rs558705664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280839 | TACTGTGTATCTTGT[A/G]CTTTCTGTACATTGT | 8853 |
rs558741868 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361463 | TTAAGCAGTACGTAG[A/G]GTGTCAGGTGTTAGT | 8853 |
rs558769251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301260 | CGTGAAAGAATGTTT[A/G]TAAAGCAGTTGGAAG | 8853 |
rs558770742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276834 | CATGAGCCACTGCGC[A/G]TGGTCTCTTTCTTCT | 8853 |
rs558771013 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270656 | GTTTCTATCAAATAC[A/T]AGATCTTATTCATTC | 8853 |
rs558780789 | in-del | -/AC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317995 | CACTCTCCGTCCCCA[-/AC]ACACACACACGTCTT | 8853 |
rs558782230 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384210 | GAGTCAGTTTTAGGG[A/C]GGGACTATTACCATC | 8853 |
rs558785558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390595 | AGCCCCTCCTCTAGT[A/G]TCTGATTTGCACTCT | 8853 |
rs558814999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378347 | CTTGTGATATGTTGG[A/G]AGAACTTTTGAAAAT | 8853 |
rs558820722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245267 | AGGGTGTTGGTGTGA[C/T]TATCGAATTGTCAGT | 8853 |
rs558826071 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358493 | GGAGTGTGTCCTGTT[G/T]ATTTTTGCACACACA | 8853 |
rs558835390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9403055 | GAGCTCCTTACACGG[A/G]AGAGGCCTGCACTAT | 8853 |
rs558841812 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315020 | AGTAGAGAAGGTGGC[A/G]TTTGAGTAACTCCTG | 8853 |
rs558877735 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9228479 | TTGGTATTTGGTCTT[-/A]TGGTCTCTTTCTTTG | 8853 |
rs558900350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378785 | CATGTAGGCAGGGAC[A/G]GTGCCAGGTCCCACC | 8853 |
rs558900848 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397474 | GAGCCATGTCGTCAG[C/T]GCCCAGTGGAGTTCT | 8853 |
rs558905923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296584 | ATATTTCAGGCACAC[A/G]ACTTCGTCGAAGATG | 8853 |
rs558925133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253578 | TCTTCAGTTGGTTCC[C/G]CCATTCCTGCCTCCT | 8853 |
rs558931575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396769 | CACTTTGGGAGGCCA[A/G]GGTGGGTGGATCACT | 8853 |
rs558990636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296161 | GTTGTGCCTGTAAAT[A/C]GTTGTGTTATATTTC | 8853 |
rs559002331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383952 | CTCACTCATAGGTGG[A/G]AACTGAACAGTGAGA | 8853 |
rs559003189 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257404 | GCAAAATTAAAATAG[C/T]TTTATTTTCTTGGTT | 8853 |
rs559035405 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384171 | GTATAATAAAAAAAT[A/T]AATTAATTAAAAAGA | 8853 |
rs559049167 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210118 | AGTAATTTGCCAAAG[C/G]TTATAGAGCTCTGAA | 8853 |
rs559052763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257928 | AGTGTTACTTTCTAT[A/G]TTGTTGCAATAATAT | 8853 |
rs559055150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332918 | AATAAAGAATGATGT[A/G]TCTGTCTAAAGGTGA | 8853 |
rs559063859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384782 | AGCTCGAGAACCAGT[C/T]CTCTTTGATTTTTAT | 8853 |
rs559065262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301804 | AGCTCTACCAAGCAA[C/T]GTGTGTATCCATCAT | 8853 |
rs559068109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295850 | CCCCAAATGCCACTG[A/G]AGGTCAAAGACATGG | 8853 |
rs559115882 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402866 | CCAACTTATACCTTT[A/G]CCACTTTAGGTGACG | 8853 |
rs559117677 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9310633 | GCAGCTCCCTGGGGT[A/G]GGGCTGCACCTCCAC | 8853 |
rs559128864 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231706 | TGGCATCTGCATGCT[C/G]TGTTCCCATGGTCCT | 8853 |
rs559153695 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9280803 | GGAGCAATAATGATA[A/G]TTTTGATTTTTTTGA | 8853 |
rs559182869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327189 | CAGCAGCTTTTCCAG[A/G]GGACATTCCATTTCA | 8853 |
rs559193413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290359 | GGATTACAGACACCT[A/G]CCACCACTCCTGGCT | 8853 |
rs559200627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315736 | CTTCTGTTTGTCCTT[G/T]TTCCTTCCAGTCGTT | 8853 |
rs559223687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378611 | GCGCAGCCAGTGGGA[C/T]GTGAGAAGGACGCTG | 8853 |
rs559228121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302361 | TATTTTTAGCAGAGA[C/T]GGAGTTTGACTGTAT | 8853 |
rs559235965 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238635 | GGAGAGGCTGAGGCA[A/C]CAGCCTGTGAGTTCA | 8853 |
rs559266881 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317429 | TCCCTCACACACCTA[C/T]ACATACTCACATTCT | 8853 |
rs559270721 | in-del | -/C | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208474 | TGCTTGAAAAAAAAT[-/C]CAGAATGTTTTCCCT | 8853 |
rs559281216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283996 | ACGCAATTCAGTCCC[A/G]TAGCAAACACTGACT | 8853 |
rs559366003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341192 | TCAGAACCTTGGTCA[C/T]GTGAAAGGGCCGGTT | 8853 |
rs559377529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257643 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGAGTA | 8853 |
rs559392197 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371993 | TCACAAAACCAGGGG[A/G]CATGTGTGGAGTTAA | 8853 |
rs559399216 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248107 | CTGATGGAAGGGGGG[C/T]GGCTGACAGCAGCAA | 8853 |
rs559403955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218720 | GATGCGATGAGTCCA[A/G]TCTTTCCAGCTCTTG | 8853 |
rs559428964 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9399769 | CTCCAGACCCTGGCC[A/T]TCGGTGGCAGGCTCA | 8853 |
rs559461464 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225585 | GCATGTCAGTTGGAA[A/C/G]TTGATTCAGAAGGTT | 8853 |
rs559470158 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338203 | TTGTGTGCTTCTATG[A/G]GGAGGATCAGGCTCT | 8853 |
rs559485187 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272802 | CAGCACAATTTATTG[A/G]AAAAATTGTCCTTTC | 8853 |
rs559501684 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346491 | GAGGGTATGAGTTCT[A/G]TAGACCAAGGGAAGC | 8853 |
rs559514053 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231961 | TCTTGTCCTGTGAGT[A/G]AAGCTCCTGCTTCCA | 8853 |
rs559522760 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247365 | GCCTAGGGAGTCCCA[G/T]ACGGTCCCCGGTCCT | 8853 |
rs559557926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336217 | TGCATAAATATTAGG[C/G]AAGTGGACATTTTCT | 8853 |
rs559563519 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244921 | TACTTAGCCTTTCTG[C/T]GGAGAATAATTGCTT | 8853 |
rs559570813 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9375725 | AAAGAAAACCCATCT[C/T]CAGGTGGAGGAGAAG | 8853 |
rs559581057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367794 | AATTTAATGTTTAAC[A/G]TGTCAGAAGATTGAT | 8853 |
rs559582038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218504 | GAATCATGGATGTGG[C/T]GTGTCTAGGCAGACT | 8853 |
rs559583078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360502 | ATAAACATTTAAACA[C/T]CTCTACTGTCCTTCC | 8853 |
rs559585210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276455 | TTAAAGCTTGCTAAA[G/T]ATGTTATTCTGAGAA | 8853 |
rs559645994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342348 | AGAGCTGAGAGTCCA[A/G]AAATAAATCCTTACA | 8853 |
rs559655743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252892 | CTGCACTCCAGCCTC[A/G]CGACAAAGCGAGACT | 8853 |
rs559656538 | snp | C/G/T | 1.7164e-05 | 0.00292945 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344487 | TGCTTTTCTAAAAAT[C/G/T]AGGACCTGGACAAGA | 8853 |
rs559678320 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245436 | TAGGTGTGGAGGGTT[C/G]TATAAAAACAAACCC | 8853 |
rs559681706 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347482 | GTGGAAGTCTAAGAG[C/T]AGAGCCTGGCACATA | 8853 |
rs559738027 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258670 | TTGAGCAGGCGAAAC[C/G]CCCGGAAGCTGCTGA | 8853 |
rs559752114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271847 | ATTTCCCTTAACATA[A/G]TAACCTCTATTTCCA | 8853 |
rs559773657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259249 | AGCCCTTCCTTGGGG[A/G]GAAACATTCATCCCT | 8853 |
rs559797159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393247 | TCACTCACAGGCTGA[C/T]AGAAAAATTGTCATC | 8853 |
rs559819663 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353879 | ACTTGGGAGGCTGAG[A/G]TGGGGGGATCACTTG | 8853 |
rs559827440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309871 | TGAAGAGGGGCATGT[A/G]GCTATTATCTGTCCT | 8853 |
rs559833693 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265845 | TGGCACGATCTTGAC[C/T]CACTGCAACCTCCAC | 8853 |
rs559843672 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361268 | TTATCAGGAAAAGTA[C/G]AGACAGCAGTGAATT | 8853 |
rs559845552 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369586 | GAAGGAGAGAGGCTA[A/C]TGGGCCAGTTAACAG | 8853 |
rs559845639 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241232 | CTTTCTTAATTTAGC[A/G]TGTGTGCTGGAAGAT | 8853 |
rs559846573 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364983 | GCCTGTGTTTTAGCC[-/T]TTTTTTTTAAAGCCA | 8853 |
rs559852560 | snp | A/G | 1.65743e-05 | 0.00287869 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323253 | ACAGATGTGCGAGGT[A/G]AGGCGGTGGTGAAGG | 8853 |
rs559905368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234004 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCATG | 8853 |
rs559920694 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205426 | ATAAAAAGAAACAGA[C/T]ACAATTTTTAAATTG | 8853 |
rs559927288 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387598 | GTGGGGTAGCATAAG[A/T]AGGCATGTTTGGGAA | 8853 |
rs559961193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211674 | TAAGCACAGGGTTCT[A/G]ACTGCAGGGGTGGGG | 8853 |
rs559964981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291809 | GCCATAAGGCTGGTG[C/T]ACCCTGCCTTCGTTC | 8853 |
rs559970360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363958 | ATCTTAACTACTTTA[A/G]CACACACCAGCTTAA | 8853 |
rs559990557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329614 | CAAGGGTGGATGTGG[G/T]CAATTGCTTGTGTAC | 8853 |
rs560000793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285801 | TAGAACATTCTTATC[A/G]AGAGTGATATTCCTA | 8853 |
rs560027436 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380181 | GGTGGCTGCTTCAAC[A/T]GTTTTTGTTTTTGTT | 8853 |
rs560040024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272801 | CCAGCACAATTTATT[A/G]AAAAAATTGTCCTTT | 8853 |
rs560040095 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266824 | AGAGTTAGTGGGAAG[C/T]GCCTGATGCTGGGGA | 8853 |
rs560040830 | snp | C/T | 1.64825e-05 | 0.00287071 | synonymous-codon, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9297304 | TTCTGTTGCAGCTCA[C/T]GTGGAAAATGAAGAG | 8853 |
rs560060796 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9326590 | AATTTTACTTATCCA[A/G]AGATAACCACTTTGA | 8853 |
rs560071375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349376 | ATGGGTGGGTGTACA[A/C]CCGTGTTAAAGTACT | 8853 |
rs560104734 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305257 | GTATACATATTGGTG[G/T]AGGGGCTGTAATAGT | 8853 |
rs560118083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399443 | CCAGGTGGCAGGTTC[A/G]AGATGAGGGACCCCT | 8853 |
rs560127113 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260399 | CCCCCTCTCCCATCA[A/C]CTCACTGCTTGGATT | 8853 |
rs560130222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297896 | GGCCTTTTGTGCTCC[C/T]AAGTGTAGAACCTAA | 8853 |
rs560130414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279258 | ACTCAACGTGGTGCT[C/T]GCTGCTAGCGTGGTC | 8853 |
rs560135895 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276479 | CTGAGAACACCAGGA[A/T]GCCTTATAGTGCCTG | 8853 |
rs560173303 | snp | G/T | 0.000399281 | 0.0141238 | missense | ASAP2 | GRCh38.p7 | 2:9400055 | CACTGACCAACAAAG[G/T]CCAACCGAGAGGACC | 8853 |
rs560182607 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359732 | CTCTCAAGGGGCCAT[C/G]AGTCTTATTGATGAC | 8853 |
rs560182921 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381278 | AAGAGCCCACCAGGC[C/G]AGGCAGCCCTGGCCT | 8853 |
rs560190533 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322578 | TACCCTGAACTGCAC[A/C]CTCGACATTTAGGTA | 8853 |
rs560211773 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317686 | TCCATAATCACATCC[C/T]GAAACCCTCACACGC | 8853 |
rs560216839 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9223272 | TATGGTCAAAGCGAA[A/G]TAAAGGAGATTTGAT | 8853 |
rs560224573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233380 | CTTTTTGTGCTATTT[A/T]CCTTTATGGGCTCTG | 8853 |
rs560247375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381868 | ATGATTATGCCAATG[C/T]GCACCAGCCTGGGGG | 8853 |
rs560282849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376599 | AAGATTCTTGCTTGC[A/G]GGCAGGGATCTGCCT | 8853 |
rs560337132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313518 | CTTTCTTCCCCACAA[C/T]CCACCTTATCACTGG | 8853 |
rs560344878 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234748 | GGCAGGTGGAATAAA[G/T]TCTGGTCAGCCACTC | 8853 |
rs560348540 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281157 | TTTTTTTTTTACTGC[A/G]TTCACTTGGACTTTT | 8853 |
rs560367932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212808 | CACCTGGAAACTTGC[C/T]GAAATGCAGAGCCCC | 8853 |
rs560378061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287393 | GTTGTTTCATTATTT[A/C]GTTGTAAGAGCAGCA | 8853 |
rs560388982 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9385618 | ACAAAGGAAAGGTGT[G/T]TGTGGCGGGGGGGTT | 8853 |
rs560416457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348916 | TCCATGGATACCCAC[A/G]TCGAGGACAGGGAGG | 8853 |
rs560426345 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304592 | AGAGGCTGTAGTCTT[G/T]GGAGTATAGATATTG | 8853 |
rs560435558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343015 | ACACTGATTTTCCTG[C/T]GTTAGTTCTTTCATC | 8853 |
rs560438584 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9303647 | ACCCAAAAGACTTCA[A/G]CGCTAAGCTATGTTC | 8853 |
rs560449566 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278374 | AAAAATTAGCTGGGC[A/G]TGGTGGCATACCCCT | 8853 |
rs560454440 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229571 | CGGTTGTGGCCAGCA[C/T]TGAGCTGGCTGCTTT | 8853 |
rs560461778 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317808 | ATCGCATTCACACAC[A/T]CACACAATCACACCC | 8853 |
rs560472793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312487 | ACCTCACGATGCCCC[A/G]TCTTTTGAAGGTCTG | 8853 |
rs560490829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242515 | AGGGATGGGCACTTG[C/T]GGTGCCCTCAGCCTG | 8853 |
rs560499482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207731 | GGCTGCCCGGGAAGG[C/T]GTGCCCGCCTCAGCC | 8853 |
rs560509939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330685 | GCAAATTACTTCTAC[A/G]GTTCTTATGTCAGGC | 8853 |
rs560525731 | snp | C/T | 0 | 0 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214491 | GTGATCCGCCCACCT[C/T]GGCCTCACAAAGTGC | 8853 |
rs560538028 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228607 | CTTCCTGAGCAGAGT[G/T]CATGTGTGATATACA | 8853 |
rs560568456 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294680 | GTCCCTTCCCTTTGG[C/G]TGTTCACTTAGAGCA | 8853 |
rs560571313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213766 | ACAGCCAAGCTCAGT[C/T]CATCCAAGCCCCCTG | 8853 |
rs560580742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370660 | ATGATGGGGTCAGAC[A/G]TGTGGTGCTTAGTTT | 8853 |
rs560587885 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306144 | GCTGGCGTAGTGGGG[G/T]TGTAGACATGGGGTG | 8853 |
rs560610612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261055 | CTTGGGGTGGCAGGA[A/G]CTGGCTTGTGTGGAG | 8853 |
rs560622921 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324550 | AGTGCAGGACATCAC[A/C/G]TGGTGGGGGCCTCAC | 8853 |
rs560625142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280276 | GTGATTGGAACAGGA[A/G]GACAGGGAGTGCCTT | 8853 |
rs560681787 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318359 | TCATTTGTAAGATGA[A/C]ATTGTTACAAAGAAT | 8853 |
rs560691508 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221942 | GGGACTACAGGTGCC[C/T]GCCACCACGCCTGGC | 8853 |
rs560722268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332282 | CATAGGGACAGCAGC[C/G]AGCGGAGAAGGAATA | 8853 |
rs560736117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300654 | CATTTATTCCTCTTG[A/G]CAGCTGTGCAGGATA | 8853 |
rs560747590 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227398 | ACCATTTACACGGTG[A/G]ACTTGTTTCCTGTGT | 8853 |
rs560750475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244251 | CAGTGAGCCAAGATC[A/G]CGCCACTGCACTCCA | 8853 |
rs560755162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236599 | AAGAGGATTTTTTAC[C/T]GGAGAGGCAAAGGGA | 8853 |
rs560786818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364908 | ATTTTTAAAAAAAGA[C/G]CAGAGAGGTTAAGAA | 8853 |
rs560796165 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349836 | GGTTTCACAGGTCTG[C/T]CCAGGTGTAGATGCA | 8853 |
rs560817002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269275 | AGGGGGCGCGCATAA[C/T]ATTTATCTTAATTAA | 8853 |
rs560838676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331631 | AAATTAGCCGGATGC[A/G]GTAGTGCACACCTGT | 8853 |
rs560849992 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253277 | CAAGCGATTCTCGTG[C/T]GTCAGCCTCCTGAGT | 8853 |
rs560861070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371114 | CCCTTCAGTATGAAC[C/G]TTCTGTCTGCACTGT | 8853 |
rs560907202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295717 | TGGTCTCAGAAATTC[A/G]TTTAATTTATCTAGA | 8853 |
rs560921715 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371852 | CCGGGCGCGGTGGCT[C/G]ACGCCTGTAATCCCA | 8853 |
rs560922407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351424 | GAATCCCCACAGAAC[C/T]ATCCATTGTGGTGAA | 8853 |
rs560924588 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353824 | CTCATGAAGGTGGAA[C/T]TGGGGCCAGGGGCAG | 8853 |
rs560925407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250998 | GGAGTGGGCAGGCTC[A/C]CCAAGGAGGTGGCAT | 8853 |
rs560925899 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359111 | GAATAAAGGGGAGTG[A/C]AACCAAAACAGGAGC | 8853 |
rs560960664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326223 | TTGTCTCTACAAAAA[A/C]ACAAAAACAAACAAA | 8853 |
rs560974309 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270273 | TGAAAGTTGCTTTTC[A/C]CCCGCTCTGAGCTGG | 8853 |
rs560977532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268839 | GTGCTGCAGGCCTCT[C/G]CTCTCCCCAGGGCAG | 8853 |
rs560984042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344946 | CCCTGTCAGAAACGC[C/T]TGCTGGCCTCCGTCT | 8853 |
rs561009995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389554 | TGCTGCACGTACACT[C/T]GGCTGTGCTGCTGGG | 8853 |
rs561045128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288952 | TCAATGAGGAAATTC[A/C]TCTAAATGTCATCTG | 8853 |
rs561074963 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9357253 | GAAGACTGAGGCGGG[C/T]GGATCACTTGAGGTC | 8853 |
rs561090498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303274 | TACGTGGGAATATCC[A/G]CCCTTGGATTAGTCC | 8853 |
rs561098189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264597 | CCATGCAAGTCATAC[G/T]TGAATATATCCTTGT | 8853 |
rs561108186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367179 | GGGACTACAGGTGCA[C/T]GCCGCCATGCCTGGC | 8853 |
rs561148808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320919 | TCAACCAATAGACAA[A/G]ACTCTGTTGGTTGAC | 8853 |
rs561167137 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352163 | AGCTCAGGAGTAGAC[A/G]TCCAGCCTTGGTAAC | 8853 |
rs561188020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282166 | CCTTTTTGAGGCCCC[A/G]CACATAACAGCCTGG | 8853 |
rs561199632 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377733 | AATGCAAAAGCCATG[C/G]GATAGTTTGCATTTT | 8853 |
rs561209735 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295159 | TCTAAAAATTAGATA[A/C]TTTTGTTTGACAAGG | 8853 |
rs561244692 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362471 | ATGTTGTATACATTG[A/G]GTGTGACTAAATCAA | 8853 |
rs561322871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275644 | CCCTCCCTGTGGCCT[A/G]AGTAACCTTCAAGCA | 8853 |
rs561351917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347235 | TTCCCTATTTCCCTG[C/T]GTGCTCTGGAAGTCA | 8853 |
rs561378366 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231808 | CCTTGAGGTTTTAGC[A/T]CTGTCACCTGGCAGC | 8853 |
rs561391915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372649 | ATTCTGGCTACTAAG[C/T]GGGATAAAGAAAGAT | 8853 |
rs561393925 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317122 | ACCCCACGCAATCAC[A/C]ACCACACAACACACA | 8853 |
rs561407361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390941 | GGTTCTAGGTAGAAG[C/G]GTCATACTGACCGTT | 8853 |
rs561417888 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249325 | CTGTCTGTCTGCCCC[A/G]TTCTGCCCTCACGTC | 8853 |
rs561420811 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385592 | TATGTACTTATAGGC[A/G]GCCTTTTGCTACAAA | 8853 |
rs561433356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258554 | AGGTGACAGTCTCCA[C/T]GGTGCCCCCGCCGCC | 8853 |
rs561434873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282825 | TTTCCTGATTTGTCA[C/T]AGATTGGCCCCATTT | 8853 |
rs561435818 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270773 | TCAGTCTCCATGAGT[C/T]CAATTGTTTTCATTT | 8853 |
rs561451393 | snp | C/G | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390483 | AGAAGGGCTTGTGAC[C/G]TGGAAAATGCCATCT | 8853 |
rs561468504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9224539 | AAAATCAAGGTTGTC[A/G]TGTCATCCTTTGAAA | 8853 |
rs561502710 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404700 | GATGGTGCATTTGAT[C/T]GAAGCAGCTTGTCTT | 8853 |
rs561505260 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9400584 | CCACACAAGCTCTCC[-/A]AAGGTCTGCATCCAA | 8853 |
rs561540324 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9396737 | CTGGGCACAGTGGCT[C/T]ACACCTACAATCCCA | 8853 |
rs561550335 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315926 | AGTTTATTTCTGAAA[A/T]GACAGTCATTAATTG | 8853 |
rs561554181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308582 | CGATGGAGACAGCAT[C/T]TAGGATGGCAGCATG | 8853 |
rs561567316 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398676 | TTGCTGTGCGTGGTG[G/T]TGCACACCTGTAATT | 8853 |
rs561578781 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219773 | GAGGTTTTTAGTGTA[C/T]TCACAAAGTTGTGTA | 8853 |
rs561581870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9223368 | TGCTCTTTTAATTTA[C/T]GAACCTTCTTGGATC | 8853 |
rs561590584 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307449 | AAGTACTTTCATTTC[C/T]GGTTGATGGCTTCAG | 8853 |
rs561618811 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340940 | AATTTCATGAAAGCC[G/T]TTTGAGGTTCCACCA | 8853 |
rs561641867 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404230 | AGTGTACCACTGCCT[A/T]CCCTTCTAGCCCAGG | 8853 |
rs561648334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284628 | TAACATGAAAAAGTG[C/G]CATGCATGGTTCTGG | 8853 |
rs561669399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391383 | CACAGCTGCAAACCC[C/T]TGCCTGTCCCCACAC | 8853 |
rs561670305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297132 | CTGTTGCCGGCACCA[C/T]GGGTTGTTGTTGGGA | 8853 |
rs561703050 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211422 | CTTCGAGCCTCTGGG[C/T]ACTTTGAAATATTCT | 8853 |
rs561721801 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277938 | AGAACCAGGGCTTAC[A/G]ATTCTGCTATTGAAA | 8853 |
rs561756162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334172 | GTGCCTCAGCCTCCC[A/G]AGTAGTAGCTTTTTG | 8853 |
rs561760655 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271479 | GGTGTAATCATCAGC[A/G]ATCCCTTGGACAGTA | 8853 |
rs561770340 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211548 | ATTGATGTAGTTTTA[A/C]AAATAAATTTGATGT | 8853 |
rs561773484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296640 | AGCACATCCGATGTA[C/T]GGGGAACACATTTGC | 8853 |
rs561793117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374445 | CTGAATAAGAAGGGT[A/G]TGGAGGTGACGAGGG | 8853 |
rs561809985 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251698 | TTCCTGGGGACCTTC[A/G]GTTTTGTGATGAGGA | 8853 |
rs561829436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399210 | GGAGCGTACAGTGGA[A/G]AGAATCCCATCCTTG | 8853 |
rs561843556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362207 | CATGCCATGCAGGGC[C/T]TCGGCTGACTTGCTT | 8853 |
rs561856052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368691 | TTGGGTGACCAAATA[G/T]AAATTTTTTTAGGAA | 8853 |
rs561872960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311793 | CCTGCCGAGAAGCGC[A/G]TCTGGCCCCCACGCA | 8853 |
rs561873097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303811 | CTGTTTCTTTTTGGG[A/G]TTGGGAGGGAATGCT | 8853 |
rs561906674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389584 | GCCCATCTTCCCTGC[C/T]GTCCTGGGTGTCTCA | 8853 |
rs561912675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271073 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 8853 |
rs561939162 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225651 | GACATGAGCATAGCT[G/T]GGCTTAGGAAGTCTG | 8853 |
rs561946628 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387075 | GCCGGGCTTGGTGGT[C/G]GGTGGGGGGGCGCCT | 8853 |
rs561988274 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9209082 | GATTACCCTAGAGCT[C/T]AGTTACTGAGCAGAT | 8853 |
rs561995696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226370 | GCCTATTGCAGGGAG[C/T]GGGGTCACCTCCCTG | 8853 |
rs562012594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212576 | AGAGGGCTGCTCAGA[C/T]CAAGAATTTGGGGTG | 8853 |
rs562014974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266697 | AAAATGAAAGAAGTG[C/T]TTCTCTTATGTTTGC | 8853 |
rs562015355 | in-del | -/AA | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338248 | CAGGTCTGAGTGCTG[-/AA]ACCACCATGGTTTTC | 8853 |
rs562026780 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205659 | GCTTTGTCTGACATA[C/T]TGAATTTCCAGTGTC | 8853 |
rs562033091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336337 | ATTCTACACATCTCT[C/G]TAGTCCCTCTGAAGC | 8853 |
rs562069789 | in-del | -/CA | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317260 | ACACACCCCGTGCAT[-/CA]CACACACTCATATCC | 8853 |
rs562090031 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205643 | GCAGTGTCAGGAGAC[C/G]GCTTTGTCTGACATA | 8853 |
rs562094880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219004 | TGGGCCGAATGAGGC[C/T]GTGTTGTTTGCCATC | 8853 |
rs562120985 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305973 | GGTGGAGGGGCTGTA[A/G]TAGTGGGGTATAGAT | 8853 |
rs562138557 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295233 | GAGAGTGGACTTTGG[A/G]ATCAGAAAATTTGGG | 8853 |
rs562156758 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347982 | TAAAGCTGTTGCATC[-/T]TTTTTTTTACCATTC | 8853 |
rs562159844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252910 | ACAAAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 8853 |
rs562197524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280534 | AAATTTAACAGAAGA[C/T]GCACAGGAATCCTAC | 8853 |
rs562239405 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234098 | CCTGGGTGACAGAGC[A/G]AAGCTATGTCTCAAA | 8853 |
rs562241577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242213 | CCGTGATCTTAGGGG[C/T]GCATGCTTTGGCGGT | 8853 |
rs562245123 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9324138 | GCCAGCTCTTAATTC[C/G]CTCTGAGCAATCAAC | 8853 |
rs562245733 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349446 | GATCATTTGCTGTAT[G/T]GGTTCCTGGATAAGT | 8853 |
rs562246224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285912 | TCTCCCACATACAAA[A/G]GAAAATGAGAATACA | 8853 |
rs562250185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365101 | CTTACTAAGAAATAC[A/G]TACTTTGTAAACTAC | 8853 |
rs562266565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375813 | TGAGCTTCATGCTAA[C/T]GAGAGAAGCTCTCTG | 8853 |
rs562284373 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292391 | GAAGTGGTGGTGTGC[A/G]CCTGTAGTCTCAGCT | 8853 |
rs562284791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292835 | CACATCCCTGTTGCC[A/G]GGCTGGAAATAGTAA | 8853 |
rs562291123 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327175 | GCCAGGGCATGAATC[A/G]GCAGCTTTTCCAGGG | 8853 |
rs562307398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369635 | GTGAGGCTGGGTCAG[C/T]GTGTCCTGGCAGGAC | 8853 |
rs562336383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272852 | ACATTTGTAAAAAAT[A/G]AGTTCACTGTAAATG | 8853 |
rs562339656 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361438 | TAAACCTTATTCCTT[A/C]GCCCTTCAGTTAAGC | 8853 |
rs562339790 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9393324 | TGCTTCCTCCCTGTG[A/C]ATGGTTTTCTGAAAA | 8853 |
rs562345287 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381948 | TAACAGGTCCTCTTT[C/T]TAAGCACTGTACATC | 8853 |
rs562372661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313718 | TGGTTTTGTATGATC[A/G]TGTAGATGAGTGGGC | 8853 |
rs562373368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267580 | TTCCATGTCTTTGCT[A/G]TTGATACAAATGACA | 8853 |
rs562377813 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9389585 | CCCATCTTCCCTGCC[A/G]TCCTGGGTGTCTCAC | 8853 |
rs562388774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254878 | ATGGATAAAGCTTCT[A/G]TGAACATTTGACTAC | 8853 |
rs562402134 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375197 | TGGGGTGAGAGGAAT[C/T]GGTTGAGCCCAGAAA | 8853 |
rs562404462 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370073 | TTGAACTCCTGACCT[C/G]GTGATCTGCCCACCT | 8853 |
rs562482305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317927 | TACTCAAGCACAGTC[A/G]CACCTTTACACACCC | 8853 |
rs562485771 | snp | C/T | 0.000132681 | 0.00814389 | missense | ASAP2 | GRCh38.p7 | 2:9400772 | CGGAAGCTCTGGGTC[C/T]TCTGTCCAATGCTAT | 8853 |
rs562489457 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364746 | GTTCACCTAGGACTG[A/C]AATGTGCCACCCAGA | 8853 |
rs562491838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312704 | ACCTAAACATGGGGC[A/G]TGTCTCCCCATTCAC | 8853 |
rs562519181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394726 | GTTCTAGTAACAAAC[C/T]ACACCAGACTGACAG | 8853 |
rs562526029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357759 | AAGTGCAGACACAGA[C/T]GCCAAGAAGGTTTTC | 8853 |
rs562533182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273455 | GGGTTCACCTTGCCC[A/G]CTGCTGCCTAGACCA | 8853 |
rs562536638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278865 | TTTTTCCAAATCCAG[A/G]GTGGGGTTGCCTCCA | 8853 |
rs562536915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286553 | TAACTAGTACTCTGC[C/T]CCATTGTTGTGGCAC | 8853 |
rs562567428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337750 | TGTGGAGCTTGTGCC[A/G]TTCTGGTCCCGGTGA | 8853 |
rs562607434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376645 | GGGATGGGGACAGGT[C/T]GATTGAGAGGACTTA | 8853 |
rs562680992 | snp | A/G | 5.08936e-05 | 0.00504423 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388561 | GGTATGAAGCTGTCC[A/G]TCATCCCTGTGAATA | 8853 |
rs562697091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401994 | GCGGCAGCTGCAGAC[A/G]GTGAGGGCGGTGGAT | 8853 |
rs562707046 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205084 | AGTTGTATATAAAGA[C/G]AGAACAGAGAATACC | 8853 |
rs562709492 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243160 | GTCGCCCAGGCTGGA[C/G]TGCAGTGGCACAACC | 8853 |
rs562712610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389315 | AGGAGGCTGCTGAGA[C/G]TTTGATGCGGGGCGG | 8853 |
rs562734573 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305390 | GTATAGATATTGGTG[A/G]AGGGGCTGTAATAGT | 8853 |
rs562760978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228358 | GCCTACTCACTTGGT[A/G]TTATCCTTGAGAAGA | 8853 |
rs562762052 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396426 | CCACAGGCACGCACC[A/C]CCATGCCCGGTTAAT | 8853 |
rs562778046 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9223656 | CCCAATGAAGTAGAA[A/C]GTAAGCTACTATAAA | 8853 |
rs562810924 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381220 | TGGGTTGCTCAATAC[C/T]ATCTTTTCCTGTTCT | 8853 |
rs562817801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267964 | CAGCACTCCAAGCGC[A/G]CCCCGCAGGCCTGTC | 8853 |
rs562819560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306208 | GCGCTGCAGGAGGGT[A/G]TATATACCACGTGGA | 8853 |
rs562824445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249428 | TTCTGATGAACTTGA[C/G]CCCCTCACTTGGGCT | 8853 |
rs562846403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221130 | CCAAGATTGTTTTGG[C/T]TATTGAGGCTCCCTT | 8853 |
rs562871247 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227542 | TTCGGGTGGGACAGG[G/T]CTCATGCACATTTTA | 8853 |
rs562874604 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249775 | CACTGCCACCCCCAG[A/G]GGAGGGCAGGGCCGT | 8853 |
rs562884288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325256 | ACCACCTTCCTGGCC[C/T]ACCTCATAGAGTGGC | 8853 |
rs562911113 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209734 | GCCACCATGCACAGC[G/T]AATTTTTTGTATTTA | 8853 |
rs562929668 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9389207 | AGAGCAGCTGGCTAC[A/G]GTGCTTCTTGAAGGC | 8853 |
rs562933990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268892 | AGCCAGCCTCTTCCC[A/G]CCCCTGCTGGTTCGC | 8853 |
rs562951411 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207872 | CCTGGGTCTCACCTG[C/G]TTGAACCCGGAATGC | 8853 |
rs562973178 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382450 | CTGAGACACCCATAG[A/T]GTGTAACGAATTAAC | 8853 |
rs562993155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338178 | GCTGTTTGATGTGGA[A/G]AACCCAGACTTGTGT | 8853 |
rs563004997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307876 | TGCTGCCAGGGACGG[A/G]CTGGGCGCATCTGTT | 8853 |
rs563014206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9208494 | ATGTTTTCCCTTAAT[A/G]GAAAAATTTTTTCTT | 8853 |
rs563018053 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319067 | TGTTTAGGACATGCC[C/T]AGCCACCATAAGCAC | 8853 |
rs563064935 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256936 | CCTGCTGCAGCCAAG[A/G]GCTGGGAGGGGGCAG | 8853 |
rs563078520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313939 | TATGTACATAATTCT[C/T]CCTCTGAAAGGGCAG | 8853 |
rs563086230 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358186 | CTGCCCTGGTCATCT[C/T]ATGGAACTCTTAGAT | 8853 |
rs563091495 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308451 | TGGGGACTGCAATTG[C/G]ACATGAGGTTTGAGC | 8853 |
rs563102478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339174 | GCAGAGCATGACCTC[A/G]TCTCCAAAACAAAAA | 8853 |
rs563113176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351473 | TAAATTAAAGGGCCC[A/G]TGATGTCTAAAAGAA | 8853 |
rs563119020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9215852 | AGAAGCGCTCTTGGC[A/G]GGGAGCCATCCACTG | 8853 |
rs563124815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295195 | TTTTTAACGATGAAA[A/G]CAAACATCGTGTAGT | 8853 |
rs563128501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269411 | CGTGTGTGCCCACCC[C/T]GAGCCAGGTCATCTC | 8853 |
rs563155722 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9242563 | TGTATTGGGCGGTGT[G/T]TGGGCTCTGTTCCCT | 8853 |
rs563160425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327361 | TTTCAATTAAACTTT[A/G]TTTTTTTCCAACAAT | 8853 |
rs563180285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250556 | TACAAAAGGATACAG[A/G]GCACATTGCACGGCC | 8853 |
rs563224891 | in-del | -/A | 0.284517 | 0.247606 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278514 | CGAGACCCCTTCTCA[-/A]AAAAAAAAAAAAAAG | 8853 |
rs563236465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319436 | AGACACATTCCCCAT[C/T]GAGCCTTCAGGGGCT | 8853 |
rs563238059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345617 | TGTTGCTAGAGAGAT[C/G]CTGAGGGTTGTTTGC | 8853 |
rs563278645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383246 | GAAGTCACAAGTATC[A/G]TGGCCTCTGGTGCAG | 8853 |
rs563298158 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383911 | AGCAAATTATTGCAA[G/T]GACAGAAAACCAAAC | 8853 |
rs563300721 | in-del | -/A | 0.269809 | 0.249214 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357176 | GGCCTTGGATCCATT[-/A]AAAAAAAAAAAAAGA | 8853 |
rs563319058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257585 | GTGCAGTGGCACGAT[C/T]TCCATTCACGTCAAC | 8853 |
rs563322523 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341622 | TCTCCCCCAAATCAA[C/T]AGACGTATTTCTTGG | 8853 |
rs563326610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366767 | CACGTGTCAAGGGCC[A/G]GGTTGAATTAGGAAA | 8853 |
rs563365679 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257264 | AATGAAAAGTCTCAA[C/T]TGCCTTGGGAAATTT | 8853 |
rs563374630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351835 | CCCTGTTCCCCTTCT[C/T]ATACCCTCTGTGTGA | 8853 |
rs563381541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353758 | TGGTTGCAGTTACTT[C/T]CTACAAGATGTTCCT | 8853 |
rs563440751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231475 | ACCTGCTACCCGTTC[A/G]CTGAGATGCCAGTGA | 8853 |
rs563443384 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9215219 | CTAAACATAGAAAAG[A/G]CAGTAAAAATCCCTC | 8853 |
rs563460624 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377306 | ACAGGGGCCGTCCTC[A/G]CCTCATCCTGTGAGC | 8853 |
rs563497103 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258626 | CCCACAACAAATGCA[A/G]ACCTTCCCGGGTCCT | 8853 |
rs563508005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283503 | GCTTCAGGGGAAATC[A/G]GTGTCCTTTTCCTGC | 8853 |
rs563540421 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378566 | GGCCCTGCATCCAGC[A/C]CAGCTGGCCGGCCTA | 8853 |
rs563563785 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271015 | AGCCAGGATAGTCTC[C/G]ATCTCGTGACCTCGT | 8853 |
rs563571444 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295730 | TCATTTAATTTATCT[A/G]GAACTCTCAGGCTCT | 8853 |
rs563585584 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402579 | GCGCCAACCTGACCA[C/G]AGGCTTAGCCATGTG | 8853 |
rs563592018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332816 | CATAAAGAAAAACAC[A/G]TAAATAAAATACAAG | 8853 |
rs563610346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289618 | GTGTACTCCTACAAG[C/G]AGTAGGAGCTTCACA | 8853 |
rs563620295 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258093 | GTACCCTGACTTTGG[G/T]GTAGGATATACGGAC | 8853 |
rs563625786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397568 | GTGATTTTGTCTCTG[A/G]GATAAATGTGAATTT | 8853 |
rs563676366 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211034 | GTGGCGCATGCCTGT[A/G]ATCCCAGCTACTTGG | 8853 |
rs563714727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211635 | TTGTTGTCCTTGGTT[A/G]CCTTGGCAATCCCAT | 8853 |
rs563718607 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221258 | GGGAGTATAGACATC[A/T]TAACAATCTATCATA | 8853 |
rs563724652 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9224696 | AACACTCCTCATTTA[G/T]CAGAACAAATTTCTG | 8853 |
rs563760928 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9334997 | GAGGGAGGCAGTTGT[C/T]GCATTGTGTGGAAAT | 8853 |
rs563764171 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239787 | AGGCTGGTCAGTGGA[A/G]TGGTCACGGCTCACT | 8853 |
rs563770943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278111 | TAGTTATTATGTGCC[A/G]GTAGCTGTAGGGCAG | 8853 |
rs563777419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365961 | ATCCAGTCTGGCTCA[A/G]TTTCTGCCTCAGTGC | 8853 |
rs563793380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276302 | AGAGAGGAGTGTGTG[C/T]ACGGGCTGGGAAGAC | 8853 |
rs563801443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237573 | CATGCCACCATGCCT[A/G]GCTAATTACTTTTAT | 8853 |
rs563819557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252735 | CCTGGCTAACACGGT[A/G]AAACCCTGTCTCTAC | 8853 |
rs563829389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360440 | ACTTAAACCTTTGAC[A/G]AGCCTGGGACACAAA | 8853 |
rs563845249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316039 | AATGTAAAATTTAGT[C/T]CAGGCGTGGTGGCTC | 8853 |
rs563859631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297210 | TTTCTTCTGCTGATG[C/T]GTTCAGTGTTATTCA | 8853 |
rs563866495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374521 | ACAAGGCAGAGAGGC[A/G]GGTGGGCTGAGAGAA | 8853 |
rs563875015 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333954 | ACCCACGGTTTCCTA[C/T]CCCGCAGACACAGTG | 8853 |
rs563895249 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271737 | GGCTGCTGAGTCCTC[C/G]GCAGTGGCTCAGTGA | 8853 |
rs563897697 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247344 | AACTGCTCCCAGTCC[G/T]CAGATGCCTAGGGAG | 8853 |
rs563921601 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284827 | ACTTACAATTTTAGA[C/T]GTAAGTGGTGTGTGT | 8853 |
rs563931485 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9310209 | TGAGCAGCATTTGCT[C/T]GAATTAAAATCTCCC | 8853 |
rs563935104 | snp | C/T | 1.68556e-05 | 0.00290302 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334697 | CAAAATTATTTTTTC[C/T]TTTGTGAAATGTCAT | 8853 |
rs563952074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392471 | GTGCCATGTGTGCAC[A/G]TGCCGGCAGCAGAGC | 8853 |
rs563953154 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393977 | TTTTGAACACATAGA[A/C]CCTCTGTGGTGTGAG | 8853 |
rs563967305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217038 | TTAGGCCACGGTACC[A/G]AGTTCATGGAGCTTG | 8853 |
rs563976991 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9287914 | CTTAACTAACGTCCA[A/G]GTGTTGGCATGAATC | 8853 |
rs563989019 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380123 | AGGTTTATGATGAAT[C/T]GCTTTATTCAATGAG | 8853 |
rs563990319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369480 | GCTCGCCTTAGACTT[C/T]AGCTCTGTTTAGTAT | 8853 |
rs564017793 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335460 | AGCTCTCAGTGGCTT[C/T]GTCACAGAGACCATG | 8853 |
rs564026963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398702 | TAATTCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 8853 |
rs564045622 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260689 | CTGGGTTTTTCTCCT[-/C]CCTGCTTCCCATTCT | 8853 |
rs564047096 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385645 | GGTTGATTCCAGTGG[A/G]TTTAGAGGAAGGTCT | 8853 |
rs564061574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271518 | CTTCCTGCCGTTTCT[C/T]TGTTGAATTCTTATA | 8853 |
rs564065905 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267829 | CTTGAACCCAGGAGG[C/T]AGAGGTTGTAGTGAG | 8853 |
rs564081453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239872 | GCTTGGACTCCAGGT[A/G]CACACCACCATGCCC | 8853 |
rs564126711 | in-del | -/AGA | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213341 | GAGTGGGCGAGGAAG[-/AGA]AGGATGAGAGACGGG | 8853 |
rs564134420 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404783 | TTTTTGTTATAAAGG[A/G]AGACAGAACAAACTG | 8853 |
rs564145795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297852 | GGTAACCTGTAATCA[A/G]AGCACAGAAATTACC | 8853 |
rs564147030 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311810 | CTGGCCCCCACGCAC[G/T]TGTTCTCTGGCCCAG | 8853 |
rs564162350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328247 | GTTTCTTTGTGGGAT[A/G]TTGAAAATATTCCAG | 8853 |
rs564182890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291269 | GATTATCCAGAAGAA[C/T]GATACACATTAGTAA | 8853 |
rs564191178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246727 | ATGCTCTTGATCTTT[C/T]TTGTCACATCTAAAT | 8853 |
rs564214089 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405691 | GGACATGGTTTTATT[C/T]TTAATGTTTTTAATC | 8853 |
rs564247172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363150 | TTTTCAGGTCGAATA[C/G]TATTCCATTATGTAT | 8853 |
rs564265581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317624 | CATCCACAATCACAC[C/T]CACACACACCCATAC | 8853 |
rs564281285 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9216172 | AGAATTTTAAGGGAG[A/T]CTTTGCAGTGTGTGT | 8853 |
rs564286933 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305157 | GGTATAGATATTGGT[A/G]GAGGGGCTGGAGTAG | 8853 |
rs564298068 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209347 | TAATGCTCTTTCCCA[C/G]GTGTCTAATGTTCGT | 8853 |
rs564356608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324508 | GAGGACCTTCTTGCT[C/G]GTGGGCGCTCTGCAG | 8853 |
rs564357597 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337006 | GCAGAATTAGGAGGT[A/T]TGGGAAAACGGGCTG | 8853 |
rs564369969 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233196 | TTTGGTGATAGTGAT[C/T]GATGTCTGTGTGACA | 8853 |
rs564384986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219105 | GTGCTTTGCTTCTCT[A/G]GTGAAAAGCAGGTTG | 8853 |
rs564385786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317243 | CACACAACCACACTC[A/G]TACACACCCCGTGCA | 8853 |
rs564409677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233844 | GGCTGGGCATGGTGG[C/T]TCACGCCTGTAATCC | 8853 |
rs564416991 | snp | A/G | 2.11138e-05 | 0.00324907 | utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207094 | TGCGCCAGCGCCCTC[A/G]CGCCGAGGCGATGCC | 8853 |
rs564438178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311290 | GTGGTCCCAGCTACT[C/T]GGGAGGCAGAGGTGG | 8853 |
rs564459552 | in-del | -/GG | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336799 | GAGGAGGTAGTGCGA[-/GG]GGGCAGGAGCCAGAA | 8853 |
rs564470219 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212612 | CAATTCTTCCCATGC[A/C]CCCCACGTTTCCAGG | 8853 |
rs564477451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336603 | AGGATTTTGGTAAAC[A/G]TGGGTCAACTAAGTG | 8853 |
rs564478418 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253973 | AGCACTTTGGGAGGG[C/T]GAGGTGGGTGGATCA | 8853 |
rs564484718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236974 | CTGGGGTACGGAGAC[A/G]GGCAGGCGGACCAGG | 8853 |
rs564491708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212958 | GAAGCAGAGCTGCCT[A/G]GCTCCACTCCCTAAA | 8853 |
rs564496414 | in-del | -/TGG | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305186 | GTGAGGTATAGATAT[-/TGG]TGGAGGGTCTGGAGT | 8853 |
rs564540444 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235132 | TGGAGCTTTTCCTGT[C/G]CTGTTGTAGGCGGGG | 8853 |
rs564580735 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387087 | GGTGGGTGGGGGGGC[A/G]CCTGTAGTCCCAGCT | 8853 |
rs564587607 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343662 | ATGTTGCCTAAGCTG[C/G]TCTTGAACTCCTGGG | 8853 |
rs564605890 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260184 | GCCCGCATTTTAAGG[A/G]TAGGAACACTGAGGC | 8853 |
rs564621089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330519 | TTGACCACCAGGCCT[A/G]TAACAAAACTGCACT | 8853 |
rs564655422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242226 | GGCGCATGCTTTGGC[A/G]GTTTACAGATAGAGA | 8853 |
rs564660814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308535 | ATGTACCTGACGGGC[C/T]GCTCTGTGTAAAAGG | 8853 |
rs564674363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228543 | AACCCATTTGGGAGC[C/T]GATAGTTGATGTATT | 8853 |
rs564682169 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307882 | CAGGGACGGGCTGGG[C/T]GCATCTGTTCAGGAG | 8853 |
rs564692489 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364122 | GTATCACTGGTACTA[C/G]GGTACTACTATCATG | 8853 |
rs564696471 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287254 | TGAGCCATCGTAGTC[C/G]TTCTGAAAAATTCCA | 8853 |
rs564704890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255590 | TGCCGTGGATTCGGC[A/G]GATGGTGTCGTCAGA | 8853 |
rs564712507 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243099 | GTGAGCCTTGAAGAT[G/T]TTTTGTTTTGTTTTG | 8853 |
rs564714843 | in-del | -/CACACTCA | 0.0441095 | 0.141807 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317214 | ACACCCACTCACATC[-/CACACTCA]CACAATCACACAACC | 8853 |
rs564736432 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375948 | GGGCATCCAGCTGGA[G/T]TGGGTTTGCAGTAAC | 8853 |
rs564738184 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368238 | TGTAATAGGCATGCC[A/G]CTTCTTATCTTTAAT | 8853 |
rs564743489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249903 | CTGCTCAGGATCTGT[A/G]AGAAGTATGTAGGAA | 8853 |
rs564746114 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306269 | CTGGTGGGGCTGTAG[A/G]GGATAGAGATACCGG | 8853 |
rs564753997 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9377981 | TGCGTGATGCCTCTC[C/T]CTCCATGCACATTTT | 8853 |
rs564770249 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261380 | TTGGACAAGTCACTT[A/T]AACTCTTTGAGTCAG | 8853 |
rs564771034 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264832 | CAATAAAAACTAATA[C/G]AGCAATTTAAAAAAT | 8853 |
rs564773156 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365750 | AGTGTTCAGGATGAA[A/C]TTCTTTTCCAGGGCT | 8853 |
rs564773847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338941 | CCAGCACTTTGGGAG[A/G]CCAAGGCAGGTGGAT | 8853 |
rs564795670 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376499 | AAACTTTAAGCCTGC[G/T]TAAGAAACATATGTT | 8853 |
rs564799467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370132 | CATGAGCCACTGTAC[C/G]TGGCCTAGATTTTTT | 8853 |
rs564810668 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9215824 | TTAGAATTATGAGGC[A/G]CTAAAGGTGTTTAGA | 8853 |
rs564821520 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395308 | CAAAACCCCACCTCT[A/T]CTAAAAATACAAAAA | 8853 |
rs564873216 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315222 | AGTTTAGTCTTTATT[A/G]GGGACACAACCCCAG | 8853 |
rs564875234 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9223222 | TCTATAGCAATGTTG[A/G]AAGGAGCTTAATTTT | 8853 |
rs564887179 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380370 | GCCTGGCTAATCTTT[A/C]TATTTTTAGTAGAGA | 8853 |
rs564887710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388798 | TGGGAACTCCCCCAG[A/G]GCAGCCTGAGGTGGC | 8853 |
rs564897159 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281638 | GAAGTCAGTTCCAGA[A/G]CATGGGAGAGAGAAG | 8853 |
rs564901383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313771 | AACTGGGACAGTTAC[C/T]CTTCCTTCTTCCCAA | 8853 |
rs564909989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283879 | GAGGGCCTCACCCAC[C/T]TGACCTCATCTAAAC | 8853 |
rs564941388 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268774 | TTTCGTCCGTGGAAC[C/G]AGGGGAGAGGAGATA | 8853 |
rs564974845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274967 | CCCATGACATAATAT[A/G]GGAGGAAATTTGTCA | 8853 |
rs564989817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235752 | GCTGTGATGGGAACA[C/T]GTAAGAAGTGGTCAG | 8853 |
rs564994107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273519 | AGGAAGAGTAATTCA[C/T]GCAGAGCCAGCTGTG | 8853 |
rs564997033 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353339 | GGAGGCCAAGGTGGG[A/C]GGATTGCTTGAGGTC | 8853 |
rs565006134 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341508 | GTCCCTTATCCTGTT[C/T]GTGAGACCTGAAAAT | 8853 |
rs565049884 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321209 | AAGTATTTCATTAGA[C/T]TGTTTAAAAAAAAAA | 8853 |
rs565050002 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343027 | CTGCGTTAGTTCTTT[C/G]ATCGTTTGGGGATGT | 8853 |
rs565054707 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9208577 | GAATCCTGTTAATAT[A/C]ACTTGGGTAGCCTTC | 8853 |
rs565057899 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294519 | GATCCTCCTACCAAC[C/T]CTATGGTCTGGGGCA | 8853 |
rs565067175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371769 | AGAGCCCCTCCTCTG[A/C]ACACCAAATGTATCA | 8853 |
rs565094404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383101 | ACTGCATATCATCTC[A/G]GGGGGGCCACGGGAC | 8853 |
rs565146688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390888 | CGAGTATCAGTGTCT[A/G]TCTTCCACATGCCGG | 8853 |
rs565153366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389488 | TCGGTGCGTGAGGGT[A/G]GCTGAGGCCGGGAGA | 8853 |
rs565166458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262039 | ATGTTTTTAGAGACA[A/G]GGTGTTGCTACGTTG | 8853 |
rs565223700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396508 | TCTCGAACTCCTGGG[C/T]TCAAGCAGTCCTCCC | 8853 |
rs565238167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326132 | ACACCTGCAATCCCA[A/G]CACTTTGGGAGGCTG | 8853 |
rs565247051 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281318 | GTGTAGCTGCTGCTC[A/C/G]TCTGGAGGAGAGACT | 8853 |
rs565260115 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269481 | TGACACAGGATGGAG[G/T]CCCTGTAGGGTTCTG | 8853 |
rs565261685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236982 | CGGAGACGGGCAGGC[A/G]GACCAGGCAGGGGCT | 8853 |
rs565280737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282107 | AGTCACAAAGCTCTA[C/T]AGTGACAGGGCTGGG | 8853 |
rs565295383 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9357354 | CGTGGTAGTGCGCAC[A/G]TGTAGTCCCAGCTAC | 8853 |
rs565296345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263070 | CCAGACTCTGAGCTC[A/G]GCTGCCTTCTGCATC | 8853 |
rs565327439 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229326 | TTGCTCAGTGGTGCC[C/T]GCCACAGTGAGCCTC | 8853 |
rs565366215 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234689 | GGTGAAGGAAGATGG[A/T]TTTACTCAGGGTTCA | 8853 |
rs565372371 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319898 | GTGATGAGATTCATC[A/T]ATCAATTAGAGTTCC | 8853 |
rs565383190 | snp | A/G | 3.29641e-05 | 0.00405968 | missense | ASAP2 | GRCh38.p7 | 2:9374852 | CTTCACAGTCTTTGC[A/G]AGGCCGTCAAAACGA | 8853 |
rs565407334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244116 | ACCAGTCTGGGCAAC[A/G]TGGTGAAACCCCTTC | 8853 |
rs565421065 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314720 | AGGTGGATCACTTGA[A/G]GTCAGGAGTTTGAGA | 8853 |
rs565455647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9223155 | CTCTGACTCCCCTCA[A/G]TTTTCTAGAACTGGG | 8853 |
rs565476983 | in-del | -/T | 0.332106 | 0.236133 | intron-variant | ASAP2 | GRCh38.p7 | 2:9391577 | TTTCTTTTCTTTTTC[-/T]TTTTTTTTTTTTTTT | 8853 |
rs565479292 | snp | G/T | | | intron-variant, missense | ASAP2 | GRCh38.p7 | 2:9390045 | AAGATTTTATTTTGT[G/T]CCACTGGGTCATGGA | 8853 |
rs565488314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272990 | TAATGTGGTTCCTCC[A/T]GTTTTGTTCTTTTTG | 8853 |
rs565514870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211741 | CGTCCATGGGACCAG[A/G]CCCCTCCTAGCAGCA | 8853 |
rs565520601 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263697 | CTGCAGCCTCTCGTT[G/T]TTCATGCGTCGTTTT | 8853 |
rs565524642 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295544 | TTATGTAGCTGACGC[C/T]GCAGGCCCAGCGTCA | 8853 |
rs565551858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9223814 | GAAGAGAGGAGTTAG[A/G]CCAGCTTAGAAGGGT | 8853 |
rs565618030 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231073 | GGTCACTTTCCCCAG[G/T]CCACTTCCTTCCTTT | 8853 |
rs565625908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209789 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 8853 |
rs565633233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320488 | TTCATTTTGATGACA[A/G]ATGTGTTTGGTGATG | 8853 |
rs565634962 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315046 | TCCTGATGGATGAGA[A/T]GGCTTTGAACAGCAG | 8853 |
rs565662020 | in-del | -/TGTGAAT | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393318 | CTCCCTGCTTCCTCC[-/TGTGAAT]CTGTGAATGGTTTTC | 8853 |
rs565668058 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222857 | TTTTCCTTGGGGACT[A/G]GGATGCTTATGCTGG | 8853 |
rs565670761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, missense | ASAP2 | GRCh38.p7 | 2:9237925 | TCAGAAGAGCCCTGA[G/T]GTGAGGTAAAGATGT | 8853 |
rs565671163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340139 | GTGATTCTTCTGTCT[C/T]AGCCTCCCAATTAGC | 8853 |
rs565673395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366294 | GGGAAGCAGCTCTTC[A/G]ATTCCTGGGGAATTC | 8853 |
rs565688599 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251431 | AGTCTGGCTGCTCAG[G/T]GGGTCTGGGCGCAAA | 8853 |
rs565721171 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340380 | CCCTTGCTGGGCTCA[C/T]ACAGTGGCATCAGAG | 8853 |
rs565756828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243725 | AGGGCATTCTGGTAC[A/G]TAGTCACTCATTCAT | 8853 |
rs565758550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250604 | GTGGTGTGCTCTTTC[A/G]TTTAAGCCGAGGCCA | 8853 |
rs565761346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397624 | GTCAGCAAACTATGG[C/G]TCACAGGCCACATCC | 8853 |
rs565765873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214452 | ACCATGTTGGCCAGG[C/T]TGGTCTTGAACTCCT | 8853 |
rs565774463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251908 | GAATGAGAAGCCTGT[C/G]CCCACATTGCTTTTT | 8853 |
rs565780100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332486 | GATGAAATCTAAATC[C/T]AAATCCAAATTCATA | 8853 |
rs565786147 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9401526 | GTTCCTGGTGCCTCC[A/G]CCCCTTAGCATCCTC | 8853 |
rs565795908 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301236 | AATTACCACCTACCT[A/G]CTTGGAGGCGTGAAA | 8853 |
rs565797301 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370889 | AATCCAGCATGGCGA[A/G]GTCATCTCCTGCTGT | 8853 |
rs565802684 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9242762 | TTTCTTTTCTCACCT[A/C]CTTTATGGAGGAAAA | 8853 |
rs565808835 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289249 | CTCTGGACACACCAA[A/G]CGCCTTGAATTCCCC | 8853 |
rs565856964 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346908 | GGAGGCTTAGTTGTC[A/T]TTAAATTTGGATGGG | 8853 |
rs565863244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352393 | TTCTGTTTTCTGAAC[C/T]AGTAACACACAAGAA | 8853 |
rs565869812 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308811 | TGCAAAATGGGGGTC[A/C]CGGCACATACTTCTC | 8853 |
rs565886500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258169 | GGGAAATGCAGTGGA[A/G]TTCTTCATTAAAAAT | 8853 |
rs565887975 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9298774 | GCTGCCTGCTCTCCC[C/T]GCACCTGGGTGGATA | 8853 |
rs565903865 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263921 | AGAAGGCCAGGTGCC[A/G]TGTCTCACACCTGTA | 8853 |
rs565906590 | snp | C/T | 1.64738e-05 | 0.00286995 | intron-variant, synonymous-codon, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391088 | TCCTCTGCTAACACC[C/T]TGTGGAAGACAAACT | 8853 |
rs565961807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402838 | CACAAGTACTTAACT[C/T]ATTGAAATGGGGCCA | 8853 |
rs565980222 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269885 | ACCCACAGTGTGCAC[A/C/T]GTCCCCACTGTCCCC | 8853 |
rs565984146 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9342389 | ATTTATTTTTAACAA[C/G]GGTGCCAAGGCAATG | 8853 |
rs566010679 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245977 | CTTAAAAACAAGCAT[A/G]CGATGGGGATGGCTA | 8853 |
rs566011688 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9308530 | CTTGTATGTACCTGA[C/T]GGGCTGCTCTGTGTA | 8853 |
rs566064661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286591 | ATGCACGCAGAGTTT[C/T]TGGAAAGCAGTTTGG | 8853 |
rs566065301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264682 | CTCATCTAGGTGCGC[A/G]CTATAACTAAGTCCT | 8853 |
rs566065654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367621 | CAAAAATCAGCTGGG[C/T]GTGGTGGCGTGTGCC | 8853 |
rs566069563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302560 | GCTCACTGCAGCCTC[C/T]GCCTCCCGGGTTCCA | 8853 |
rs566090116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392964 | GTCTGTAAAACGTAG[A/G]CACTAAGAAAGCTCT | 8853 |
rs566095887 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9398300 | GGATTGCTTGAGACT[A/G]GGAGTTCGAGACCAG | 8853 |
rs566143530 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239917 | TAGAGATGAGTTTTT[A/G]TCATGTTTAAGTGAC | 8853 |
rs566156336 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302239 | GCGCAGTGGTGCAGT[C/G]TTGGCTCACTGCAGC | 8853 |
rs566157101 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266073 | TACAGGTGTGAGCCA[C/T]CACACCCAGCCCATA | 8853 |
rs566160832 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384181 | AAAATAAATTAATTA[A/T]AAAGAAAAGAACAGA | 8853 |
rs566164946 | snp | A/G | 0 | 0 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391541 | GGGACAGTCACTTGG[A/G]TTAGAATCTGGCTTT | 8853 |
rs566185887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361835 | CTCCCAAAATGCTGG[A/G]ATTACAGGTGTGAGC | 8853 |
rs566196209 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321612 | AGGAAGCAGCTTTCC[A/C]ACTTCACTCAGCCTC | 8853 |
rs566205165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210617 | TGGAGTGCAGTGGCT[C/T]GATCCCCACTCACTG | 8853 |
rs566213192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379861 | GCCGGGTATGGTGGC[A/G]CGCACCTGTAGGCCC | 8853 |
rs566222346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385001 | GGGATTTGAGAGTTA[C/T]GAGCCGGGAACTGTG | 8853 |
rs566227978 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239174 | ACTGAGATGACCATA[C/T]GGTTTCCCTTTTTTA | 8853 |
rs566229078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271192 | GTTACATTATACAAG[C/G]TGTGAGGTTTTTAAA | 8853 |
rs566239471 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276847 | GCATGGTCTCTTTCT[A/T]CTTTATTCGTGAGGT | 8853 |
rs566252249 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321489 | TTTATTTGTGTGCCA[A/G]TTGGGTGAAATAAAT | 8853 |
rs566267565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232261 | CGCCTCACTGCCCTG[C/T]GCCCGATCCTTTTAC | 8853 |
rs566302505 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398802 | TGACAGTGCAAGACT[A/C]CATCTCAAAAAAAAA | 8853 |
rs566311442 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404391 | GTAATACTCCCAAAC[A/T]TCCCACTTTTTACTG | 8853 |
rs566311706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322062 | TGAAGGAGTGTCAGC[A/G]ACACCTTGGAGTTGT | 8853 |
rs566324796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354596 | GAGCTGTGCACTGCA[C/T]GTTTGCACCACTCCA | 8853 |
rs566334727 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373608 | AGGGCAGGTACAGAA[A/C]AGTCAACAACTGCTC | 8853 |
rs566336250 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265937 | GCCACCATGCCCAGC[C/T]AATTTTTTGTATTTT | 8853 |
rs566337443 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380902 | TTGCTGTGAACCAGT[G/T]TCCTGAGCAGAGCTC | 8853 |
rs566401906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283853 | TCTTATAAGGACCCT[A/G]ATGCCATCAGGAGGG | 8853 |
rs566416880 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386935 | ACCGGCCGAGCGCGG[G/T]GGCTCACGCCTGTAA | 8853 |
rs566423932 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9288598 | ATTCTGTAATGTAGC[A/G]AGTCAGATTGCTTTG | 8853 |
rs566428523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310090 | GTGTGAGGTCTTTCT[A/G]CAACTGCCCACCCTT | 8853 |
rs566434499 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317395 | ACATCCACACACACA[C/T]CCTCAAACACACACA | 8853 |
rs566437611 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232689 | TGTTTAATATGTGTT[G/T]GTTGAATGAATAAAA | 8853 |
rs566442757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347920 | AAAAATAGAACGGCA[C/T]GATTAGAATGGAGAA | 8853 |
rs566455835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298108 | GTTTGGGACCCTGCC[C/T]GGGTGGAATGGACCC | 8853 |
rs566465564 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303416 | GTTTCACGATGCTGC[C/G]AGCTGAAGAGCAAGG | 8853 |
rs566478449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387138 | AGAATGGCGTAAACC[C/T]GGGAGGCGGAGCTTG | 8853 |
rs566484954 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397838 | ATCTCTGCTCATTGC[A/C]AGCTCCGCCTCCCGG | 8853 |
rs566490483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218077 | CTCCAGGTTCCACAT[C/T]CCACAACCAGCATTT | 8853 |
rs566492498 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226441 | CTTGAGCTTTTATTT[C/T]CCCAAATACCTTTGC | 8853 |
rs566499079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258956 | TCCAGTGATATTCCT[C/T]GGATTGCAGCCAGTT | 8853 |
rs566509881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253060 | GCCCAAGCCAATCCC[A/G]AGGCAACAAAGAAAC | 8853 |
rs566551311 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249459 | TGTTCTTTGCTCTGA[G/T]GGGGAGTAATTTGAG | 8853 |
rs566556475 | snp | A/G/T | 0.00159649 | 0.0282165 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398417 | TCAGGAGGCTGAAGC[A/G/T]GGAGGATCACTTGAC | 8853 |
rs566565338 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317734 | CAATCACATTCACAC[A/T]CACATCCACACTCAC | 8853 |
rs566568728 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404865 | GGTAAAAATGTGTTA[C/T]ATCTGTAGTTTTTTG | 8853 |
rs566577500 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9246219 | TTAAAACAGGTGGAC[A/G]GAACCAACTTTTCAT | 8853 |
rs566591537 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9220057 | TTTCTTTTTATGGCT[A/G]AATAATATTCTATCA | 8853 |
rs566603159 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226060 | AGCTCCTTGAAGGCG[G/T]AGGTTGTGTCCTGTG | 8853 |
rs566603827 | in-del | -/GGCAAGTAG | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329442 | GGGTCTCATGGGGGA[-/GGCAAGTAG]GAAACACGAGCCAAT | 8853 |
rs566618594 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9354361 | CCCTCACGGCTGAAG[C/T]TCTGGAAGCCGTCCG | 8853 |
rs566636836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335821 | TCACTACAATGTGGG[A/T]ATCATAATGTGAATT | 8853 |
rs566673691 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9228103 | GGGGGTGAATCTTTT[A/G]ATATGAGGTTTTAAG | 8853 |
rs566676080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298734 | TGCTGCCATGGAGGG[C/T]GTCTCCTGGTAGAAA | 8853 |
rs566686263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329363 | CTGTGATCTGCCAGG[C/T]GCTATTAGGGGTTTT | 8853 |
rs566686810 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258066 | ACAACCAGTGCTGGT[A/T]TCATCACATTTGTAC | 8853 |
rs566696602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253533 | CCCTACAGATGTAAC[A/G]TAGCAGAGTGCCGTC | 8853 |
rs566716873 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350582 | GGTGGGTTTGTGTAG[A/T]CCACCAAGGTGCCCT | 8853 |
rs566719969 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336668 | GAAAGGACCTACAAC[A/G]TGGTGACTTCCTCCT | 8853 |
rs566721716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247566 | CCATGTGGATGGGCA[A/G]TGGGTTCCAGGGTTC | 8853 |
rs566726277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218702 | TTGTAACATGGAGGG[C/T]TGGATGCGATGAGTC | 8853 |
rs566726685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323452 | TTACTTTAACACCAA[C/T]ATTTTCTTAAAAGTA | 8853 |
rs566740340 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210494 | ATGGGGGGAAGTGTC[A/G]GGGAAATGGATGAAT | 8853 |
rs566776924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341855 | TGTGCCCTAGTTTAT[C/T]CAGAGGCTCAAGTGC | 8853 |
rs566781964 | in-del | -/AA | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354645 | GTGAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 8853 |
rs566790501 | in-del | -/CTC | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376312 | TCTGTATCTGTCCTT[-/CTC]CTCTGGTTCTCTCAC | 8853 |
rs566838313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241636 | CTGGAGTCTCAAACC[A/G]GGCTCAAACAACAAC | 8853 |
rs566868887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363635 | GTCGCCCAGGCTGGA[A/G]TGCAGTGGTGCCATC | 8853 |
rs566884179 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248995 | AATTCCTCCCAACCC[A/G]AATACATAGGATGCT | 8853 |
rs566885135 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369821 | ACAAATAGGTGGTAG[A/T]GTATGGACCCTTTGT | 8853 |
rs566889890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337915 | AATTGTGCAGTGACC[A/G]CCCATAGTGCAATAT | 8853 |
rs566890517 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399685 | CCCTGCCCTTTCATG[G/T]GATGGGACCAAGGCA | 8853 |
rs566910812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394919 | GTCAGAGTCTCTTCA[C/T]GCCCCCCGTGGTAGC | 8853 |
rs566948342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248108 | TGATGGAAGGGGGGC[A/G]GCTGACAGCAGCAAG | 8853 |
rs566953250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305980 | GGGCTGTAGTAGTGG[A/G]GTATAGATATTGGTG | 8853 |
rs566963989 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343795 | TGTTGGATGCCAGAC[-/A]CTGGACTTGGGCCCT | 8853 |
rs566976458 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221263 | TATAGACATCTTAAC[A/G]ATCTATCATAACCTC | 8853 |
rs566977960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213300 | GATCATGGAAGGACT[A/G]AAGGAAGGTCAGGGT | 8853 |
rs567046776 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400253 | CTCCTGCCCCCTTCC[C/T]CTCCTGCCCTCTTCC | 8853 |
rs567051086 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9224901 | TGTCAGGCTCCTTGC[A/G]TGCTGGGCTGTGGTC | 8853 |
rs567056868 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321157 | CTATCTGTTAAACTA[A/G]AAGGTGTTATGAGGA | 8853 |
rs567060495 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267640 | AGTTTCTCATGCCTG[A/T]AATCCCAGCACTTTG | 8853 |
rs567105418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260805 | AGGGTTTTAATTTTC[C/T]CTCTGAAAAGCCCAG | 8853 |
rs567127821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364234 | CTTATGAGACCAGGC[A/G]CAGTGGTTCACACCT | 8853 |
rs567132847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237095 | GGACAAGTCTCTGAC[C/T]TCTTGGCTGTGCGGG | 8853 |
rs567173824 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267121 | CACATAGCATTAAAA[A/T]TTTTTTCAATGAGAT | 8853 |
rs567182372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228023 | ACCAGATAATAGCAG[C/T]GAGATCGGAGAGGAT | 8853 |
rs567190697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221918 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 8853 |
rs567209813 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243296 | TGTATTTTTAGTAGA[A/G]ATGGGGTTTCACTGT | 8853 |
rs567213908 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331933 | CAGAAGCTTGCAGAG[A/G]AGGGAGGGGCGGGTG | 8853 |
rs567215226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255042 | TCATTTTTCATTTCC[A/G]CTAACCACGTATGAG | 8853 |
rs567240154 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299666 | GCAGCCAGCCCAGGA[C/T]GGCTGACGACGTAGG | 8853 |
rs567258262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207489 | CGGCCTGGTCTTTTC[C/T]CCGCAGCGCGGCCAA | 8853 |
rs567284143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293967 | TGCTGGGGATCAATA[C/T]ATCGTTTAGAAGATG | 8853 |
rs567301056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249608 | CCATCACATAGACTG[C/T]ATAGCCATGACTTAG | 8853 |
rs567311938 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269596 | CATGGCCAGGGCCTC[C/T]GGGTGACCCCAGAGG | 8853 |
rs567312284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262481 | TTATTCCCAATTTAT[A/G]GATGAAGAAACAGAA | 8853 |
rs567323950 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317637 | ACCCACACACACCCA[C/T]ACACACATTTACACA | 8853 |
rs567344386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306434 | AAAGGCAGAAGAGCG[C/G]CTGCTGCAGGTGGAG | 8853 |
rs567349644 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263135 | GCATGCTGGCTTTCC[A/G]CTGTCTCGGTGTCCC | 8853 |
rs567351178 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388855 | AAGACACACTCCTTC[A/C]GGTCTCCCCTCTGCA | 8853 |
rs567362590 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345723 | CCGTCTTTCCTGCCC[C/T]TTGTCCCTCCAGTCC | 8853 |
rs567393749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261415 | TTCTCCTTTAAGCTG[A/G]GGAAAGAGGTGGTGA | 8853 |
rs567396129 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293358 | TTCCAAAGTCCCTCC[C/G]AGGTCAGTGATTATT | 8853 |
rs567416654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382137 | TACAGGCACCTGCCA[C/T]CACGCCCAGCTAATT | 8853 |
rs567433906 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249949 | TCCTGCCCATCAAAA[A/G]GCTACATGCCATGTG | 8853 |
rs567474607 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9252059 | TTAGCCTGTACAAAA[C/T]CTTCCCTCTGGGAAA | 8853 |
rs567498729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401660 | GCCTGAAATGACACT[C/T]CTTCATTTTGAGGTC | 8853 |
rs567511528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | ASAP2 | GRCh38.p7 | 2:9389784 | TCCCAGACCGCGTCC[A/G]TCCCTGGCTTGATGA | 8853 |
rs567525137 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9277248 | GGTGTTTCTGGCACA[G/T]CCCTGAGCACAACCT | 8853 |
rs567526083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377212 | AATTGCAGGGTCCAA[C/T]TTCTAGTGTCTGGTA | 8853 |
rs567533726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344446 | TTAAAAAAAAAACAC[A/G]TTAGGCATAAGTTTC | 8853 |
rs567570045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222685 | TTGGTTTGCCTTGGT[C/T]GCAGCCTGCCAGGTT | 8853 |
rs567574092 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244034 | GCTGGGCACGTTGGC[G/T]CATAACGATAATCCC | 8853 |
rs567588235 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256178 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGCAAGTAA | 8853 |
rs567603968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288298 | TGCAGAGTTGTAAGG[A/G]TGAAAGATATTTCTA | 8853 |
rs567604789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383465 | GGGTCTCGCTATGTT[A/G]CCTGGGCTGGTCTCA | 8853 |
rs567614434 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275212 | CAGCCTGGGATTACA[A/G]GTGCATGTTCCCATG | 8853 |
rs567626858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314837 | TCGGGAGGCTGAGGC[A/G]GGAGGATCACTTGAA | 8853 |
rs567656329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275070 | TCCCATGTTTTGTTT[C/T]TTCATTTGTCTGTTT | 8853 |
rs567664355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308172 | GTTTAATTGGCTTAC[A/G]GTTCCACAGGCTGTA | 8853 |
rs567666480 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378008 | TTTTCAGGGGGCAGG[A/C]GAGGGAAGGTCCCAG | 8853 |
rs567668102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384069 | CTTAATGTAAATGAT[A/G]AGTTAATGGGTGCAG | 8853 |
rs567684709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402881 | GCCACTTTAGGTGAC[A/G]TTGCAGCTCACAAAC | 8853 |
rs567701205 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364378 | TGAGTATGGTAGTAC[A/C]TGCCTGTGGTCCTAG | 8853 |
rs567716514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274487 | ACCACCATGCCCAGC[C/T]AATTTTTGTATTTTT | 8853 |
rs567718564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257687 | CCATGCCCGGCTAAT[C/T]TTTTTGTATTTTTGG | 8853 |
rs567738197 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314198 | CGTGTTGGTCAGGCT[G/T]GTCTCGAACTCCTGA | 8853 |
rs567741462 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260658 | TCCTTCCTGCCTTTC[C/T]TCTCCCTTCCCTATT | 8853 |
rs567749515 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403407 | CCAGATAACCAGTTT[C/T]ATGAACTGTTTGTAT | 8853 |
rs567753089 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343290 | CTCATTAAACACCTA[C/T]GAGCAGCCCTCGGCC | 8853 |
rs567758556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402061 | GGCTGAGCCCACCAC[A/G]CAGTAGACGCAAGTG | 8853 |
rs567770634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282448 | ACTGCTTTTAGTAGC[A/G]CGTTCTTTTGCATAT | 8853 |
rs567788077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326462 | CAGACCTTCTGTGAG[C/T]GGAGAAGGCGTGAGA | 8853 |
rs567798128 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248374 | GGTATCTTGGTGTCA[-/T]TTTTTTTTTTCTTCT | 8853 |
rs567807875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250728 | GCCAGGGTGGAGCGG[A/C]GGTGTCTCAGCCCCT | 8853 |
rs567864378 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281878 | CACCAGATGAGTTCC[A/G]AGCTCTTGTGCATTG | 8853 |
rs567865640 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221644 | CTTTTTGTATATTGA[G/T]CTTATGGCCTACAAT | 8853 |
rs567884203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9333040 | CCTTGGAGTTGCTGC[A/G]TTAAAGGCCACGCTG | 8853 |
rs567889239 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302090 | GGCCTCCCAAAGTGC[A/T]GGGATTACAGGCGTG | 8853 |
rs567936266 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301549 | TTCTAATGAAAGGCT[G/T]CATTTCAGGGCAGGT | 8853 |
rs567939472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309956 | CACATGTTGTAGGCC[A/G]TGAGCTCTGGCTCCT | 8853 |
rs567973251 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322928 | GAAATACTTGTTGAG[-/T]TAAGTGGGAAGACCC | 8853 |
rs567976140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321330 | TTACATTTCCATACC[C/T]GAGGTTGCTTGGCCC | 8853 |
rs567980916 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245805 | GTCATGGATGCTCCT[A/G]GGGGACAGAGCCTTT | 8853 |
rs567990693 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316091 | TGAGAGGCCGAGGAG[A/G]GCAGATTGCTTAAGT | 8853 |
rs567992340 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397208 | CCATGCTGCTGTTTT[C/T]CGAGAGAAACAAATC | 8853 |
rs568026229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275958 | AGACACGTGCTGGTA[G/T]CTGCTGTAGTGGATG | 8853 |
rs568097659 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373263 | CCCTGGAAGTCCTTC[A/C]TGGGCTGTGAAGCAT | 8853 |
rs568109015 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258669 | CTTGAGCAGGCGAAA[C/T]CCCCGGAAGCTGCTG | 8853 |
rs568122974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372873 | ACGTGCACAGCTTTG[A/G]GATGTGGGGGAAACC | 8853 |
rs568142408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328505 | GAAATGATACGATGT[G/T]AATGCAGTGTTTTAA | 8853 |
rs568149438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245142 | GAATAATATTGTTAT[G/T]AATAGAGATTCCAGG | 8853 |
rs568173214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211077 | GGAGAATCACTTGAA[C/T]CCAAGAGGTAGAGGT | 8853 |
rs568173269 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217858 | TGACCTCGTGAGGCA[C/G]CCACCTCGGCTTCCC | 8853 |
rs568183990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366984 | GATTTCAGGCTGCAG[C/T]AGCCTCTCCCAAAGC | 8853 |
rs568201804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347679 | AATTTCCTTCTTAGC[C/T]AAGTCTGTTTTCTGG | 8853 |
rs568221177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334381 | TTTTCTTTTCCATGT[C/T]GCGGTCGCCTGTTGC | 8853 |
rs568221749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346976 | GCATTACTGGGATGC[C/T]GAGAACTCAGCTTGT | 8853 |
rs568237991 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328149 | GTCAGGAATAAGTAC[A/C]TCCACAGAGACAGAA | 8853 |
rs568259827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211730 | AGGGGCCCTGCCGTC[C/T]ATGGGACCAGACCCC | 8853 |
rs568267381 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270861 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAAGCC | 8853 |
rs568276141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385081 | TGAGTTTCAAGGTTA[C/T]GCTGTGAAGTAGGCA | 8853 |
rs568283214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340449 | TCTCCGGAGTCTTTT[A/T]AAAATTACCCTTAAA | 8853 |
rs568284414 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232884 | AAAAATATGTTTGTG[A/C]CCTTGTACAGAGGGG | 8853 |
rs568294414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258265 | AAAAAAAAAATTTCT[A/G]TGATTACCAGCTATT | 8853 |
rs568306946 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336226 | ATTAGGGAAGTGGAC[A/G]TTTTCTGGGTTTACA | 8853 |
rs568311194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270553 | CCATCACCTCAAAGC[A/G]TTTAGCCTTCTTTTG | 8853 |
rs568311822 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368615 | GTTTTGGGTGCATCC[A/G]TCGTTGCTTCTTTAG | 8853 |
rs568312935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360581 | GAACCCTGGTTTGCA[A/C]CCTGCCTGTTCTCAT | 8853 |
rs568321823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252585 | TTCCCCTAACACCCC[C/T]GCCCCCCAAAAAAAG | 8853 |
rs568322479 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233486 | ACACTTACAAAAGTT[C/G]TATGGTGGCTTGGGA | 8853 |
rs568341213 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9223949 | CTCTGATTTGGTGCG[C/T]TGGGATGCACGTAAT | 8853 |
rs568348229 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9270918 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 8853 |
rs568385256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302622 | TGGGATTATAGGCGC[A/G]AGCCACCACACCCAG | 8853 |
rs568443515 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374321 | GGGCAGTGAGGCAGG[C/T]AGGCCTTCATGTAGA | 8853 |
rs568457403 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227786 | ATATACAAAGATTCT[A/G]TGTGCTTAGAAACTT | 8853 |
rs568508233 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259567 | TCAGCCCAAAACCTT[A/C]AGGAACAAAAATGAA | 8853 |
rs568509831 | snp | A/C | 1.64751e-05 | 0.00287007 | missense, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9297390 | CAGATTTAGGAAGTG[A/C]GTTCCTGAAGTTCTC | 8853 |
rs568540571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278341 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 8853 |
rs568545242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259969 | CAGTGTCTGCGCATC[A/G]CCCCCTCCCCTATCT | 8853 |
rs568563355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354753 | ATGCTTGTTTTTTGC[A/G]GCTTAGCCTCTCTAG | 8853 |
rs568574459 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225626 | ATTAAGGGCTTTTGC[A/G]TAGGGGAGTGACATG | 8853 |
rs568576739 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317490 | AGTCACTTACACCCT[C/T]ACACACCCACTTACA | 8853 |
rs568586571 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237178 | TAAAAAAAGAGAGTT[A/T]AAAAAAAAAGCCCTG | 8853 |
rs568590141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258777 | CAGCATTCTGGCTGA[A/G]AAACAGATGATCTTC | 8853 |
rs568613779 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302462 | AGGCATGAGCCACCA[C/T]GCCTGGCCAACTTTT | 8853 |
rs568615844 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266181 | ACACAGGATCTCACT[C/T]TGTTGCCCAGGCTAG | 8853 |
rs568624504 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355382 | ATTTCTCTAGTGTTT[A/T]CTCATGAGTGGATTG | 8853 |
rs568629411 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325129 | TAATTAAACTTAAAG[C/G]GTTCTTATAGACAGG | 8853 |
rs568636060 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9405014 | ATGTCTATTTTAACA[A/G]TCCTCCTGCATCTGT | 8853 |
rs568690003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291839 | CTGTTATGCTGGTGA[A/C]AGCACTTGGTGTTCA | 8853 |
rs568696971 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278527 | CAAAAAAAAAAAAAA[-/AA]GAAAAAGAACAAAGG | 8853 |
rs568699625 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405948 | GTCCACACCTCTGCC[A/G]GACAGAGGTCCATGC | 8853 |
rs568710506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368218 | GTTTTATGACAATGC[A/G]TCTCTGTAATAGGCA | 8853 |
rs568724066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284348 | ATATTGCTCCTGATT[A/G]TTCTCTAGTAGTTTT | 8853 |
rs568726439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322160 | CATCCCTCCCAAAGG[A/G]TCTCCTGTGTGTTTA | 8853 |
rs568744068 | snp | A/G | 0.000164883 | 0.00907824 | missense | ASAP2 | GRCh38.p7 | 2:9374828 | AAGCACGCGGATAAC[A/G]CGGCGAAGCTTCACA | 8853 |
rs568777219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277758 | GGGCTCACTCTTGTA[C/T]ATTCCATGGGCTTGG | 8853 |
rs568788554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380940 | CTGATGGGATGAGCC[A/G]AGAATCAGCCTGCCT | 8853 |
rs568814194 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254858 | CTTTCCAGTTTTTGG[C/T]TATTATGGATAAAGC | 8853 |
rs568840567 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359191 | GACCAGCTCACCCCA[C/T]CCATTAGACAGATGT | 8853 |
rs568849664 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9374458 | GTGTGGAGGTGACGA[A/G]GGCGACAGTGAGGTC | 8853 |
rs568852123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381433 | GCAGTTGACACACAG[A/C]GCTCAGTAAATAGAT | 8853 |
rs568855156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226636 | AAAGGTCCTTTCAGG[C/T]TGCCGTGGGGAGGAC | 8853 |
rs568876772 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400390 | CACCTGCCTTCCTCC[A/C]CCCCTCCCTTCCCCT | 8853 |
rs568885694 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363270 | AAGATGGTGAAGACG[A/T]GTCTTCAACAAACTG | 8853 |
rs568894019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218777 | ACACTTCCCCTGCCT[C/T]TTGCCACCCTTGCTT | 8853 |
rs568907073 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280374 | CCGCCCCCACCAGTT[A/T]CAATAGGGCGGGCAC | 8853 |
rs568916559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248209 | TCCCACGCTAACCAC[A/G]GAGGCCACGCAGGCC | 8853 |
rs568926904 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225204 | TCTAAAATATTTATC[A/G]TCTGCTCCTTTATAG | 8853 |
rs568937285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401028 | CACAATGGGCCCACT[C/T]AGAGTACCCTGCCCC | 8853 |
rs568948067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348468 | GGAAGGATTTTAATG[A/G]ATAGAATTTTCTCCC | 8853 |
rs568963445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399490 | AACTACTTCCTCACT[C/T]ATGTGTTTCTACCTT | 8853 |
rs568970033 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279974 | CTTGTACAAATCCTA[C/T]GAGTGATACAAAATA | 8853 |
rs568971360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311411 | TCCAACGTTAATAGC[A/G]GTGATTAAGATTAAT | 8853 |
rs568981893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286938 | AATAAATACTCATGA[A/G]GTATTTGTTAGAATA | 8853 |
rs569008083 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303974 | GCTGGTGCTGTATGG[G/T]GCGGTGACCTCTGGC | 8853 |
rs569016023 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298809 | CTTTCCATGCACACA[C/G]AGCTGCCTGTTAGCT | 8853 |
rs569031428 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359278 | CTGACAAGGCTGTGG[A/T]GACAACTTGCCTCAA | 8853 |
rs569031884 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252401 | GGCTGGGCAACATAG[A/C]AAAACCCCATCTTTA | 8853 |
rs569040899 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207296 | CCCGCCCGCCGCTCC[C/T]GCATCCGCATCCCGA | 8853 |
rs569062601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336764 | GGCGTAAGGAGAAAA[C/T]AGTGGGCTAGCGGTA | 8853 |
rs569065143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395842 | TCAATCTCCTGACCT[C/T]GTGATCTGCCCTCCT | 8853 |
rs569098260 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322187 | TTTATTTTTCACTCA[A/T]TCACTCCTTCAAATT | 8853 |
rs569113312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387988 | ACAGCAGAGGGGAAC[C/T]GCTGCCATGATCCAG | 8853 |
rs569129278 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9231701 | GTCCCTGGCATCTGC[A/G]TGCTGTGTTCCCATG | 8853 |
rs569133110 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9396160 | TAATTCTTCTGCATA[C/T]TACCTTGCCTTTCTC | 8853 |
rs569152706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273129 | TTGAATCTGTAAATC[A/G]TTCTGGGTAGTATGG | 8853 |
rs569178712 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9206137 | CTCTGAAGCACTCAC[A/T]CTTGAGTCAGGGAAC | 8853 |
rs569180371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299334 | AGCAGCACTGGAAAC[A/G]TTATGGCATGGAGCA | 8853 |
rs569189002 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267670 | GGGAGGTCAAGGTGG[G/T]TGGATCACTTGAGGC | 8853 |
rs569217646 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370320 | TCTCAGGTGAGCGAT[G/T]TAGTTGTTGTTGGAT | 8853 |
rs569230002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324662 | TTAATCCACTCATGC[A/G]GTGACCTCCCAAAGG | 8853 |
rs569235370 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381325 | GCTTGGCTTGGGAAG[G/T]AAACTCTCTTAGGCT | 8853 |
rs569267543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273729 | GGGCCACAGGACCAG[A/G]TGAGCCAGTTTATTG | 8853 |
rs569277081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331948 | GAGGGAGGGGCGGGT[A/G]TCACAGACAGACCCC | 8853 |
rs569286660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9235972 | ACTGGGGACTGGGGT[A/G]CTGGTGGCATCTGGT | 8853 |
rs569295984 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9277089 | TGCGAGAGTGCTAGG[C/G]TGCACGGTCACAGAT | 8853 |
rs569316913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242641 | ACCTTTCAAAGGAAC[A/G]CAGTCCAGAGGCCTT | 8853 |
rs569340153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332355 | GCACTTTGAAGGGGC[A/G]TCTGGGTGCCAAGAC | 8853 |
rs569355710 | in-del | -/C | 0.00217111 | 0.0328762 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400843 | GCAGTAAGTGACGAG[-/C]CCCCTTTCCTGCCTC | 8853 |
rs569372008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300812 | AGGAACCATGGCCTC[C/T]TGTCACCTTCTTGAC | 8853 |
rs569415978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9208840 | GTAGCTGAATATTTC[C/T]TAAGGGAAGGAAGCA | 8853 |
rs569441762 | in-del | -/TC | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262682 | AGCCTCTGTTCACAG[-/TC]TCACAAGGTGTACTT | 8853 |
rs569455367 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214176 | TGCTTACGCCTTTTC[A/T]GTGTAATGTGGCCTC | 8853 |
rs569464272 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383563 | TCCACTGGATGGTAA[A/G]CAATTACATTAATAG | 8853 |
rs569467953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261625 | GCACAGTAGGCCTTT[C/T]TTTCCCTGGGAGCAC | 8853 |
rs569484691 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9237868 | CCAGTGAGATGATCC[C/T]ATCTCTTCCCATGAT | 8853 |
rs569485155 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229947 | CAGTGTGGGCTGGGG[G/T]AGAGATGTGTGTTTG | 8853 |
rs569532358 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260892 | CTATCTGCTTCTCCG[C/G]CACCCTGGCCCTTCA | 8853 |
rs569534329 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356807 | TTGTTAAACATCGAT[A/T]TTCCTGTCTGTAAAG | 8853 |
rs569545688 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351398 | TTTTCCTTTTTGTGG[C/T]GTTCACAAAAGAATC | 8853 |
rs569548279 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370384 | TGTTTGTGGTGTCGC[A/G]TTTCCTTGAGAATTG | 8853 |
rs569589996 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311678 | GGTTTCCGTCCCTCT[C/T]GGCCAGAACTCGAGG | 8853 |
rs569592784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249982 | AGGAAGGCAGGGCTT[A/G]GGGTCAAATCTGGGT | 8853 |
rs569600787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237212 | TGTACACATTTTGAT[A/G]GTTAATGTTGCTTTC | 8853 |
rs569670787 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257306 | GCAGGGACTGTTTTA[A/T]AGTAGTCTCAAACAG | 8853 |
rs569671510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249667 | GACAGAAAGTTCACA[A/G]CCTGAGTGAGACTGG | 8853 |
rs569692505 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9228470 | TTGCTATGTTTTGGT[A/C]TTTGGTCTTTGGTCT | 8853 |
rs569710025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382765 | CACAACAAGCAATAC[A/G]GAAGCAGACTGCTGT | 8853 |
rs569734796 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338568 | CCAAGCTGCTAGGTA[G/T]CCTGGCTCTGGCCTC | 8853 |
rs569758826 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257741 | GGCTAGGCTGGTCTT[C/G]ATCTCCTTGTGACCT | 8853 |
rs569773804 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265863 | CTGCAACCTCCACCT[C/T]CCCGGTTCAAGTGAT | 8853 |
rs569776707 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351708 | CCTTTTCAAATGTCA[C/G]TTGACCTGTATTATT | 8853 |
rs569785942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319807 | TCCTGAATTGCACAC[A/G]GAAGAGCAGTAAGAG | 8853 |
rs569788289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255886 | TGGGGGGCACAAGAT[C/T]GTCTGATTTATTTGT | 8853 |
rs569815525 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365646 | ATGCCCACACACAGA[C/T]GACTCCCCCGTATGG | 8853 |
rs569834037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244255 | GAGCCAAGATCGCGC[C/T]ACTGCACTCCAGCCT | 8853 |
rs569838294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345376 | AGAAAAAACGGAGCC[C/T]TCTATGTTGAGCTTA | 8853 |
rs569839098 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331625 | ATACAAAAATTAGCC[A/G]GATGCGGTAGTGCAC | 8853 |
rs569849339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314887 | GGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 8853 |
rs569862627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275154 | GGCGCAATCATGGTT[C/T]GCTGCAGCCTCCAAC | 8853 |
rs569863943 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9335304 | TGTGTCAGGCACCAG[C/T]AAAACATTTAATGTA | 8853 |
rs569865376 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269630 | TGGCACCGCCCTCAG[C/G]CGGTACAGTGGGGCC | 8853 |
rs569902055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283213 | CTCCCAAGTAGCTGG[A/G]ATTACAGGTGTCTAC | 8853 |
rs569908366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263828 | GGAGGTCATCAGCTG[A/G]GGGCACAGTTTGCCT | 8853 |
rs569929884 | in-del | -/AT | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317435 | CACACCTACACATAC[-/AT]TCACATTCTCACACA | 8853 |
rs569959344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366158 | TGGGCTGAAACGTAA[A/G]CTGGAACTTGGCAGA | 8853 |
rs569972967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274531 | TTTTACCATGTTGTG[C/T]AGGCTGGTCTGGAAC | 8853 |
rs569973062 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282245 | TATTATGTCATGCCA[A/G]GTTTGAGTTATTCTA | 8853 |
rs569973974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216334 | CTCTGTTGCCCAGGC[C/T]TGAGTGCAGTGGTGT | 8853 |
rs569983776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390979 | GGGGAGGATCAATAA[C/T]GCAGTGTTCTGTTTC | 8853 |
rs569994559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251360 | TGGTACTCACGTGTA[A/C]CAGCCTTAGGGGACC | 8853 |
rs570014055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359324 | CTACCCCAGATTGTC[C/T]CCCATGGGGGGAGAT | 8853 |
rs570019266 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9330917 | TTTTGGATATGAGAG[A/T]GAGTGTGTACGCTGC | 8853 |
rs570049785 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384127 | TGTAACAAATCTGCA[C/T]GTTGTGCACATGTAC | 8853 |
rs570052054 | in-del | -/CTT | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306745 | TTGTTTGCATTCCTC[-/CTT]CTTTGGGAACTTTCA | 8853 |
rs570070965 | snp | C/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270333 | GTTGAGAGCCTGGGT[C/T]TGGTTAGAATTCTCA | 8853 |
rs570116885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334295 | CTCTAGTGATCCTCC[C/T]ACCTTGGCCTCCCCA | 8853 |
rs570137442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290489 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 8853 |
rs570152715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397034 | ATATGCATATCTGTG[C/T]CCTCCTAGTCTTAAA | 8853 |
rs570159846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308308 | GGCAGGGGCAAGAAT[G/T]AGGCGGGAGGTGCCA | 8853 |
rs570163372 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263642 | AGGCACAGACCTCCC[A/G]GGAGTGCCTGTGGGC | 8853 |
rs570166839 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9215566 | TTTCAGTTAGACCCT[A/G]ATGAAAATACAGATA | 8853 |
rs570196923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308631 | CTTAGCCTGGCCTGG[C/G]AGGTGTAAACCATCT | 8853 |
rs570199132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245221 | GGAGCTTCTGGTTTG[A/G]GAACCACAGCTAGCA | 8853 |
rs570199864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245771 | CATTAGTCGGTTCGT[C/T]GTCTGCCTCCACTAG | 8853 |
rs570220666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276697 | CACACCCACCAACAC[A/G]CCCGGCTAATTTTTG | 8853 |
rs570234582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384928 | GGCAGGAGAAGTTCA[A/G]AGAGATTCTGTCTCC | 8853 |
rs570241558 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368076 | TAAGTAAAGGTTGTT[G/T]GAGGATGTGAAATAG | 8853 |
rs570288114 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332286 | GGGACAGCAGCCAGC[A/G]GAGAAGGAATAGTGT | 8853 |
rs570291684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327617 | GTTTTTGGCACTTCA[A/G]TATTTAATTATCTGA | 8853 |
rs570292174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379124 | GCCTCCTGTCTGCCA[G/T]CCAAGCGCTGCTCTT | 8853 |
rs570301430 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9334910 | CCTGTGTTTTCATGC[C/T]GTGCCGCCCACGTGG | 8853 |
rs570304738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395198 | GAATTTGGGGCCAGG[C/T]GCCATGGCTCACGCC | 8853 |
rs570314492 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404320 | CACACTGTCTTGAAA[C/T]TGAATCTGTCCATCT | 8853 |
rs570333705 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297506 | AAGTGGCTCAGTAGA[G/T]GATAGTTATGGTTTG | 8853 |
rs570333771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303895 | ATAGCATGGTGAGGC[C/T]TTGGGCGTGGGAGGG | 8853 |
rs570351400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361654 | CTCACTGCAACCTCT[A/G]CCTCCTGGGTTCAAG | 8853 |
rs570353954 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233058 | AGTCTGTGCTCTGTG[-/T]TTTTTTTGCTCAGTG | 8853 |
rs570424048 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270941 | GGGACTACAGGTGCC[C/T]GCCACTACGCCCGGC | 8853 |
rs570434378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232183 | TGGGTCCTTCTCCTT[C/T]GTTGACCTGGCCCCT | 8853 |
rs570443810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303377 | TTTTCCTGCTGTCAG[C/T]GCTTGGGTGCCTCTA | 8853 |
rs570455817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293548 | TTATTTTAGGTTCCT[A/G]TTTTAAGGTTGTTTT | 8853 |
rs570462272 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264928 | GGAATCACTTGAGCC[C/G]AGGAGTTTGAGACCA | 8853 |
rs570473170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225345 | GAGGAACCTTAAAGA[C/T]ACTTGTCTAGTGGTC | 8853 |
rs570489196 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266876 | GGCCGACCTGCATTC[A/T]GTTTCCTCTGTCTCT | 8853 |
rs570493109 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367535 | GGAGGCTGAGGTGGC[C/G/T]GGATTGCATGAGCCC | 8853 |
rs570571008 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386877 | GTTAGGTCTAAGTTA[A/C]CTGAGTCATCATTCC | 8853 |
rs570578847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211777 | GGGAACCAGGGCTAC[A/G]TGCTTTTTGGCAAGA | 8853 |
rs570580151 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386231 | CAGTAGGTAACCAGA[G/T]GGCATTTCTGAAACC | 8853 |
rs570628973 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364955 | ATTTACATTCCAACT[A/C/G]TCAGACTCCAGAGCC | 8853 |
rs570645704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348243 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGACTGCA | 8853 |
rs570668439 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317728 | CATACACAATCACAT[C/T]CACACTCACATCCAC | 8853 |
rs570670869 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366959 | TCAGTTCCCTACAAG[A/G]GATAGACCCGATTTC | 8853 |
rs570692703 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217979 | TTCTCTGAGCTTTAA[G/T]TCTGTATTAAGGACT | 8853 |
rs570700274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252606 | CCAAAAAAAGCCTTC[A/G]GAAGACAGTTAAAGA | 8853 |
rs570709578 | in-del | -/TC | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382049 | AGTGCAGTGACATGA[-/TC]TCTGTTCACTGCAAC | 8853 |
rs570723126 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247504 | ATTTGAGTGCTTCTG[C/T]GGATTTGCTCGCTGC | 8853 |
rs570743376 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285257 | TGAGTTTCTGGTTCA[G/T]CAGGTCAGGGTTGGA | 8853 |
rs570757213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225953 | GCTCCATACCAGGCC[A/G]TGGGTTCTGCGGAGT | 8853 |
rs570834883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210893 | AGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 8853 |
rs570837857 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226728 | ACAGGGAGCCTGGAA[A/T]AACAAAGAACACGCC | 8853 |
rs570851314 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361579 | TTTTCCTTTTCCTTT[C/T]CTTTTTTTGACAGGG | 8853 |
rs570853160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325450 | ATTAAGTAGTAGTGT[C/T]TTACAAAGAATGAAT | 8853 |
rs570863351 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253718 | TAGTGCCCTGGAGAT[A/T]ACAATGTTACATGTA | 8853 |
rs570864222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335739 | CAGCAGGGACAGTTT[A/G]TGTTGTGGGGACTTG | 8853 |
rs570872105 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387389 | AGTATCTAAATGACA[A/G]GACATGGCTATGTTC | 8853 |
rs570885202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212347 | AGGTGGTCCCAGGGC[A/G]TGGGGCTGTGGTGAG | 8853 |
rs570885551 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359019 | TGGTTTGGATAATTA[C/G]AAACTCATTGATAAT | 8853 |
rs570896477 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343145 | GGTGTAATGGAAGGA[G/T]CCTCAGAGTGGAAGG | 8853 |
rs570938763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252958 | CACAAGCAGATAGTG[C/T]GTGGGCCCAATCACT | 8853 |
rs570951539 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254454 | GTCTCCCGGGTTCAA[A/G]CAATTCTCCTGCCTC | 8853 |
rs570962339 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312240 | ATCTCTATTATAATA[A/G]TTTATTTTCTGATTA | 8853 |
rs570967741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349034 | TTATTTGGTCTGTCC[A/G]GGCCAGTGTCTTTAG | 8853 |
rs570983710 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9231575 | GAGATGCCCGGGTGC[C/T]GCCACACCCCTAGCC | 8853 |
rs571046035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9220074 | ATAATATTCTATCAA[A/G]TGTGTATGATACATT | 8853 |
rs571046112 | in-del | -/TAAAAGG | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245011 | AGTCCTCCCGTCATA[-/TAAAAGG]TAAAAGTCTGAATCA | 8853 |
rs571050786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400230 | CCCCTCCCCTCCTGC[C/T]CCCTCCCCTCCTGCC | 8853 |
rs571055134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272020 | TGCTGCAGTAAACAC[A/G]GGAGAGCAGGTACCT | 8853 |
rs571077994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249491 | GACTCTCATGACGCC[A/G]TGCCTGCTCCAGACA | 8853 |
rs571096160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362862 | AAAATTTTTAAGTAT[A/G]CAGTACGTTATTATT | 8853 |
rs571116013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241502 | CCAGCACACTGGGAG[A/G]CCAAAGAAGCAGGAG | 8853 |
rs571122586 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225408 | CTTGGTATGGTGACC[C/T]AGGGACCTGCTGCTG | 8853 |
rs571129539 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304439 | TAGTGGGGATGTAGA[C/T]AGGGGGTGGAAGGGC | 8853 |
rs571170882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381597 | AAAAACTAGCAACGC[A/G]TGGTGGAGCATGCCT | 8853 |
rs571172065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271673 | TGGTCTGCGGAAGAC[A/G]GCGGGCAGAGGGTAC | 8853 |
rs571172361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278912 | TAGGGGGAAGGGGTG[C/T]AGGCACGATAGGAGT | 8853 |
rs571175544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260664 | CTGCCTTTCTTCTCC[C/T]TTCCCTATTCTGGGT | 8853 |
rs571214268 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388051 | ATTCGAGGTGAGATT[A/T]GGGTGGGGACACAAA | 8853 |
rs571237563 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9206262 | TAGGCCTGCGACGAT[A/G]CAATGACTGCACGCA | 8853 |
rs571246213 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213199 | GAGGTGACATTTGAG[C/T]AGGCTGGAATGCAGA | 8853 |
rs571269836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260027 | CTTACAAGGCCCCAG[G/T]CAGGCTGGCCTCTCC | 8853 |
rs571281163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355875 | TTAGAATGCCACCGT[C/T]GGTGAAGGCAGACAT | 8853 |
rs571286019 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9316464 | ACATAAGGTCCCAAG[C/T]CCCTCTTCTCGTCCT | 8853 |
rs571291962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212903 | AAGCACTGTTCGAGA[C/T]GGAACCCCGGCTGCA | 8853 |
rs571306576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268474 | CTTCAGGCCTGGCTT[C/T]ATTCCCACAAGGGGG | 8853 |
rs571306800 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274404 | CTCCGCTCACTGCAA[A/C]CTTTGTCCCCCAGGT | 8853 |
rs571341597 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268937 | GTGCTGGGGACAAAC[C/T]GGTGCTGTGCTGCCT | 8853 |
rs571349951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387243 | CCATATAACCTTCAG[A/G]GGGGAGCAGGGGTGG | 8853 |
rs571354182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235531 | GCCGGAGGCTCCTTG[A/G]TGGGCTGATTGGAAA | 8853 |
rs571370168 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9312948 | CCTGTAATCCCAGCT[A/G]CCTGGGAGGCTGAGG | 8853 |
rs571375946 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365054 | AAATTGAGCACCAAA[A/G]CATGTACTTACTTAC | 8853 |
rs571394388 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217627 | TGTTTTTTGTTTTTT[G/T]TTTTGAGACGGAGTC | 8853 |
rs571401059 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274776 | AAAAATTACCTCTTC[C/G]ACCTACCTCACCTTT | 8853 |
rs571425119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243209 | CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 8853 |
rs571430048 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376230 | CTGAGCTGTGCTGCC[A/G]CCAGAGGGCCCAGCA | 8853 |
rs571436430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365397 | TTTCTCTCACTTGCC[C/T]GTTCTCTCCTGGGGT | 8853 |
rs571437049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324154 | CTCTGAGCAATCAAC[A/G]ACAAAGCTAATCCAG | 8853 |
rs571486469 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9296668 | TGCCAGACTATTTCA[A/G]TATAACATGCTGAGT | 8853 |
rs571497997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324829 | AAGTGTATCACTTAT[A/G]GATAATATATATAGC | 8853 |
rs571506825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207381 | AGAAGCCCTTTGTTC[C/T]CGCCTAGGTGGCTCG | 8853 |
rs571509477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313616 | CTGCCTTCTTTCTTG[C/T]ACGTGCCTTGTTCTA | 8853 |
rs571526681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293263 | TGCAGTGAGGTGGGG[G/T]AGATAAAGGGGTGAT | 8853 |
rs571531845 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266034 | CCCCCCACCCCCTGC[A/C]TTGGCCTCCCAAAGT | 8853 |
rs571579904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401598 | TGATTATTCCCCAGG[A/G]TGGCTTCCTCCCCTG | 8853 |
rs571594760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389693 | AGTCATACCCCGAAG[A/C]ACAAACCTGCTGAGA | 8853 |
rs571635995 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314089 | CCTGGATTCAAGTGA[A/T]TCTCCTGCCTCAGCC | 8853 |
rs571647864 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401104 | GGGAGCTCTTCCCTT[C/T]TCTCTCCCTGGCTCC | 8853 |
rs571655086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390391 | CTTTGCCCTACAGGC[C/T]GTGCACAGCCTCCAA | 8853 |
rs571682551 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356870 | CTGTGAAATAAGATT[G/T]TATTTTTACATTTTG | 8853 |
rs571703522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236054 | CACCACAAAGAAGTA[A/C]CTTGTCCCAAGTGTG | 8853 |
rs571714335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230189 | AAACAGCTGATTACC[A/G]TATGGTGTGATAAAT | 8853 |
rs571743610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314352 | CACTTGAATGAATGA[A/G]TTCACACATGCATTT | 8853 |
rs571765644 | snp | C/T | 0.000178543 | 0.00944667 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318650 | TACACCATGTAGAGT[C/T]ACAGTAGCTTGGCCT | 8853 |
rs571766289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256055 | CTGTGTAGACTTAAA[A/G]TTGTAGAATGACCAG | 8853 |
rs571770566 | in-del | -/TAGAGATATTCAC | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325034 | CATTGAGAGAATGTT[-/TAGAGATATTCAC]TAGATGAAAAACAAG | 8853 |
rs571785593 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9401892 | TGGGGCAGGTTGCTT[G/T]TATCTTTAAGCATTA | 8853 |
rs571787712 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256979 | ACTCATTCCAAGTCC[G/T]TGGCTGGAGTGCCTC | 8853 |
rs571851580 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345157 | GAACAGCAAACTGCT[C/G]CCCCAGCTCTCTTTG | 8853 |
rs571870031 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350995 | TTCGGAAGAATTGGT[G/T]TTTGAAGAGACATAC | 8853 |
rs571888209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338960 | AGGCAGGTGGATTGC[C/T]TGAGTCCAGGAGTTC | 8853 |
rs571893029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382823 | CCCCATACACCAATT[A/G]TAGTCGCCTGACAGG | 8853 |
rs571894410 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263860 | GTTCTTCTATAATAG[G/T]TTAAGTATTTTTTTC | 8853 |
rs571907958 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250223 | GGTCATGTAACATTT[A/G]TTGGATAAAACTCCA | 8853 |
rs571914186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339269 | GCTTCTGACTAGGAC[A/G]GGGTTGCCTGGGGAG | 8853 |
rs571919813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313842 | TGTTTTCTCACCTTT[C/T]ATCAATGAGGAGCCA | 8853 |
rs571926788 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9215639 | GACAGAGAATTCCAG[A/G]CTTGATGGTAAGATT | 8853 |
rs571947192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250437 | AGATGGGAGTGGGGA[C/T]GCAGGATGCCAGACA | 8853 |
rs571978750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401810 | CCAGGCGTCCAGCAG[A/G]GTGTGGGAGCAAGAT | 8853 |
rs572000539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222225 | TGTAAGCTGCAGTTT[C/T]TTGTATTTAATTTGT | 8853 |
rs572008162 | in-del | -/AG | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246865 | TGTTTTGTTTGAGAC[-/AG]AGTCTTGCTCCATCA | 8853 |
rs572048993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274604 | CTGGGATTACAGGCA[C/T]GAGCCACCGCGTCCA | 8853 |
rs572058636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325682 | CTGGTTACTACTTCT[C/T]TTCTGTATCCAGGTG | 8853 |
rs572060156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280886 | ACTGATTCTCCTTAT[A/G]CAAATGAGTAACCTG | 8853 |
rs572065038 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332646 | GGAGAATTGCCAGGT[C/T]GCAAAGATTCTTGGA | 8853 |
rs572084968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281789 | AACCCTTTCCCAATT[A/C]ATCTGTCGATGAAAC | 8853 |
rs572098930 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9335881 | AGGAATGTATCTAAA[C/T]ATATATCTAGTGATT | 8853 |
rs572112371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308359 | CTACACAGTACCAAG[A/G]GGCATGATGCCAAAC | 8853 |
rs572146691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245271 | TGTTGGTGTGACTAT[C/G]GAATTGTCAGTGCCA | 8853 |
rs572183219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257466 | CCTTGAACAAACTAA[C/T]GAACCAGTACATGAT | 8853 |
rs572196254 | in-del | -/CTTA | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273006 | GTTTTGTTCTTTTTG[-/CTTA]GAATAGCTTTGGCTA | 8853 |
rs572204266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365745 | CTCATAGTGTTCAGG[A/G]TGAACTTCTTTTCCA | 8853 |
rs572231133 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280733 | TTTTCTAAAACTGAT[-/A]ACAGAAGGTGGCCAT | 8853 |
rs572239108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209592 | TTATTTATTTGTTAC[A/G]GAGTTTTGCTCTTGT | 8853 |
rs572246222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396809 | GAGTTCAAGACCTGC[A/G]TGGCCAACATGGCAA | 8853 |
rs572259347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351368 | CACAGGAATAGTCTT[C/T]CTGCTTCTCTGTGCT | 8853 |
rs572283424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307685 | AGATCAGAGCTGTTG[A/G]CTGCCAGAGAAGCAG | 8853 |
rs572296686 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360777 | TGATGAGTTTTGAGT[A/T]TATACTTGTTATTAA | 8853 |
rs572332857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214963 | GCAGAGAACAAAATA[A/G]GATTCCGAAGGAAAC | 8853 |
rs572337505 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391330 | ATGGCTCCCTGTGGC[G/T]CTTGTGCAGGGCTCT | 8853 |
rs572358094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373109 | AGTGCACGGGTTAGC[A/G]CTGTGTGGACGGGGA | 8853 |
rs572376433 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367136 | CCTGGATTCAAGCAA[A/T]TCTCCTGTCTCAGCC | 8853 |
rs572387051 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302087 | TTGGCCTCCCAAAGT[-/A]GCAGGGATTACAGGC | 8853 |
rs572428930 | in-del | -/ACA | 0.0130921 | 0.0798413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317120 | ATACCCCACGCAATC[-/ACA]ACCACACAACACACA | 8853 |
rs572435330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360193 | ATGGAAAGTGTTAAG[C/T]GATTCAAGATGATGT | 8853 |
rs572444700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210127 | CCAAAGGTTATAGAG[C/T]TCTGAAGTGGACTTT | 8853 |
rs572457691 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9262260 | TTTTTTTCTCATTCT[A/G]AACATTATCAGACCT | 8853 |
rs572485304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378451 | GGCTTTGGGAAAGTG[A/G]CTTTTCCCTTTCCTG | 8853 |
rs572487949 | snp | A/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236189 | GCTTTGGGGCCCCTG[A/T]TTCCTGCTCTTGGTG | 8853 |
rs572491920 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290016 | TCCTTCCAGTTGCTC[A/C]TCCTGCACGGGAGCT | 8853 |
rs572505168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297051 | GCCATCTCATCTGAT[A/G]TGCTGAGGACCACTG | 8853 |
rs572517590 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403689 | TGGCCCAGTTCTGGA[G/T]TTGGTGACCTTTATC | 8853 |
rs572522577 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320225 | TAGTACAGGGATAAG[G/T]AAGTTTATCTTGCAC | 8853 |
rs572524470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332627 | GCTCTCTGTCTGACC[A/G]TAGGGAGAATTGCCA | 8853 |
rs572529591 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386280 | TGGAGTTAACATCCA[C/T]ACTTAACTGCTTCTT | 8853 |
rs572546575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372613 | ACATTGAAATATGAG[C/T]GATGCATACATTTAA | 8853 |
rs572568468 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270949 | AGGTGCCCGCCACTA[C/T]GCCCGGCTAATTTTT | 8853 |
rs572571420 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397488 | GCGCCCAGTGGAGTT[A/C]TGACTGTAAAGGAAC | 8853 |
rs572575727 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9282954 | ACCCAGTCTGTAAAC[A/G]GACTCCCCCATCCCA | 8853 |
rs572599326 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392391 | TGAGAATTCTAGAGC[C/T]GAGGTGCTCGTGACT | 8853 |
rs572601851 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283308 | ATCTCGAGCTTCTGA[C/T]CTCAAGTGATCCACC | 8853 |
rs572605739 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265034 | CCAGCTACTCAGGAC[A/G]CTGAGGCAAGAGGAT | 8853 |
rs572614112 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9209092 | GAGCTCAGTTACTGA[A/G]CAGATTACAAAGAGA | 8853 |
rs572628690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238727 | ACAATGAAATTTACC[C/T]TAAGAGTACACTTTG | 8853 |
rs572637863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309096 | GCCCCGCCTCCTTTG[C/T]GCTCTGCTCCAAGAC | 8853 |
rs572678070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231147 | CCAGCAGGATGGATG[A/G]GGGAAAGGCAGTGGC | 8853 |
rs572680916 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9224478 | TTCATACCTTTTTCT[G/T]TCAAAGGATTGCTGT | 8853 |
rs572713976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316244 | GGAGGATCGCCTGAG[A/C]TCAAGAAGTTGAGGC | 8853 |
rs572719992 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365190 | GCACACCAGAGTGTC[A/C]TTTTGTGCTCTTTGC | 8853 |
rs572787889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252184 | CCTGACACCAGCTGC[C/T]AGGACTGCATTGGAG | 8853 |
rs572789044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320864 | CTTGGATGTGAACTA[C/T]GGTTTCTACAAGAAG | 8853 |
rs572789736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290908 | ACAGCCTTGCATATG[A/G]CAGTTTATTGACTGC | 8853 |
rs572820672 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379558 | CTCTCTCGAGGACCC[C/T]GACATGCCAACAGCC | 8853 |
rs572852070 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9297670 | GCAATTTAAATGTAC[A/G]CAGCTATGGGACAAA | 8853 |
rs572854313 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249931 | GAACATTGGGCCACC[A/G]TCTCCTGCCCATCAA | 8853 |
rs572856286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340777 | AGACAGCTCAAGGAT[C/T]CTACTGGTCATCTGG | 8853 |
rs572877207 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317551 | ACACAATCTCTCACA[G/T]CCACAATCACACTCT | 8853 |
rs572889774 | snp | A/C | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214463 | CAGGCTGGTCTTGAA[A/C]TCCTGACCTCAGGTG | 8853 |
rs572905242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257958 | TTGCCTGTGTTACCA[A/G]CTGCCCAGGTTGGAG | 8853 |
rs572909995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218505 | AATCATGGATGTGGC[A/G]TGTCTAGGCAGACTT | 8853 |
rs572916553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328803 | ACAGTGATGTACAGT[G/T]CTGGCATAGTTCCTA | 8853 |
rs572976077 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272917 | TCTATGTGTCTGTTT[C/T]TATGCCAGTACCATA | 8853 |
rs572979708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322386 | CTACTTCAGGCTCTA[C/G]AGAAAGAGCTGCTTC | 8853 |
rs572993808 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9382136 | TTACAGGCACCTGCC[A/G]CCACGCCCAGCTAAT | 8853 |
rs573027241 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353034 | TTTGTGCAGGGGTAT[G/T]TGGGTTTGGGTTGAA | 8853 |
rs573039891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244552 | CACAGTTAATGTCCA[C/T]GGGAAGAGCTTGACA | 8853 |
rs573067292 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380300 | CCTCCCAGGTTCAAG[C/T]GATTCTTCTGCCTCA | 8853 |
rs573076741 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336278 | CCTTTATGAAGATGA[A/T]GCAGGTCCCTCCCTC | 8853 |
rs573084337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368612 | GAAGTTTTGGGTGCA[C/T]CCATCGTTGCTTCTT | 8853 |
rs573106362 | snp | C/T | | | intron-variant, synonymous-codon | ASAP2 | GRCh38.p7 | 2:9390020 | GCTGACTGTGTGTGT[C/T]ACGGGAGGAAAGATT | 8853 |
rs573115765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252686 | TTAGGGAGGTTGAGG[C/T]GGGCAGATCACGAGG | 8853 |
rs573121779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284030 | CTGCCTCCCTCTTCT[A/G]CATATAAGGACCCTT | 8853 |
rs573137438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247943 | ATCCTCCCAGCTCTC[A/G]GGCATAATTATGCTC | 8853 |
rs573151798 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211332 | TTGGAAATAATGGAA[A/G]AAATAAGCAGTTGTG | 8853 |
rs573162607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233663 | GATACCTGTGTGGCC[A/G]TGGGCAAATATGCTC | 8853 |
rs573177400 | snp | A/C | 1.74278e-05 | 0.00295188 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335228 | TCACCCCATTCTTGG[A/C]GGCTTTGGGTCTGAA | 8853 |
rs573194062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218990 | TGCTGGTTTGAGATT[A/G]GGCCGAATGAGGCCG | 8853 |
rs573195113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226779 | GGCAATCTAGCAAAC[A/G]GTGTGCTCTTCCCTG | 8853 |
rs573196966 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404659 | TTGGAAAGTGAGGCA[A/G]CAATGCTGTTAACTG | 8853 |
rs573197760 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246445 | GTGTGCGCTAACATG[C/G]CTGGCTAATTTTTTA | 8853 |
rs573211261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277907 | TAGCATCCAATAAAA[C/T]TATCATTGTGGCATT | 8853 |
rs573218916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342336 | GACCAATGAAATAGA[A/G]CTGAGAGTCCAGAAA | 8853 |
rs573251096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271688 | GGCGGGCAGAGGGTA[C/T]GGAAAGTAGGGAAGC | 8853 |
rs573291377 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398623 | GACCAGCCTGGCCCA[C/T]ATGGTGAAACCCCGT | 8853 |
rs573294539 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213157 | TCTGGAGATCAGGAA[A/G]CCGAAATCAGGAAAA | 8853 |
rs573313291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363982 | AGCTTAATATCTTTA[A/G]ATTCTAAAGCAAACC | 8853 |
rs573330065 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278607 | CCAGGTGTGATTAGT[C/G]GTTGAACAGATAACT | 8853 |
rs573331480 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245019 | CGTCATATAAAAGGT[A/G]AAAGTCTGAATCATG | 8853 |
rs573339110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362109 | GAAAAATGGTCCCCA[C/T]GTGCTAGCATGTGAA | 8853 |
rs573347604 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369321 | ACCGTGCCTGGCCAG[C/T]GGAGAAGCTTTTGTG | 8853 |
rs573349159 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317744 | CACACTCACATCCAC[A/G]CTCACACTCACATCC | 8853 |
rs573373442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343030 | CGTTAGTTCTTTCAT[C/T]GTTTGGGGATGTGCT | 8853 |
rs573383272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260160 | TCACTGTATTGAGTA[A/G]CTATTACTGCCCGCA | 8853 |
rs573389826 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205466 | GTCTAGTGCAATGAT[A/C]AAAGCTATCCACGAA | 8853 |
rs573412576 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348734 | TTTGTGGTATGCTGC[A/G]AAGTGAGAAATCTAT | 8853 |
rs573415755 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271457 | ACGCCTTCACTGGTT[C/T]CTTTTTGGTGTAATC | 8853 |
rs573418298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253797 | TACAGAGTAAGTTCC[C/T]CCTTAGCTGCATTTT | 8853 |
rs573427096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248459 | CGTAGAGAGGATAGA[A/G]CACGGGCTTTGGAGT | 8853 |
rs573433864 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387318 | GGCCTAAAGCGTCAC[A/C]GTCCATGTTAACAAT | 8853 |
rs573434892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304336 | CTTAATTGCTGGCTA[C/T]TAAAGGGACAACTGC | 8853 |
rs573435760 | snp | C/G | 0.000399281 | 0.0141238 | missense | ASAP2 | GRCh38.p7 | 2:9380761 | GAGTCAGGAGAGACT[C/G]CGCTGGACATTGCCA | 8853 |
rs573467723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259743 | GCCTTGTGTGTGTGT[C/T]TTAGCGCAGAGATCT | 8853 |
rs573471723 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315365 | GCCAAGGCAGTGGAC[A/G]TGAGAATGGCATGGA | 8853 |
rs573477438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394355 | ATTTCTAGTAGAGAC[A/G]AGGTTTCGCCGTGTT | 8853 |
rs573480530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267858 | AGTCGAGAATGCACC[A/G]CTGTACTCCAGCCTG | 8853 |
rs573499274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349093 | AAGGGCAGTTAGGAA[A/G]ATTAAATGAATTATT | 8853 |
rs573521554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323731 | CTCACCTGCTCAGGC[A/G]GGGGCACTCATCTAG | 8853 |
rs573529193 | snp | C/G/T | 3.33985e-05 | 0.00408633 | missense | ASAP2 | GRCh38.p7 | 2:9388531 | CCCCCGCTTCCTCCA[C/G/T]GGAATGTTGGCAAAG | 8853 |
rs573563498 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345291 | TCAGTGATTTTATTA[C/T]TGAAATCTTAACATA | 8853 |
rs573571880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279262 | AACGTGGTGCTCGCT[A/G]CTAGCGTGGTCTCAG | 8853 |
rs573573222 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364717 | GAACTTAACGACTTA[A/C]AACTGTCTTCTAAGT | 8853 |
rs573574881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387021 | CATCTTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 8853 |
rs573591062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370492 | ATCTATATTTTTACC[C/G]AAACCTAGAGAGGCA | 8853 |
rs573599952 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234771 | AGCCACTCTGGGGCC[A/G]ATGCACAGGGGCCCA | 8853 |
rs573608927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324214 | TTGTTAATTGTAGCA[A/G]GAGCTTAACCCTTAT | 8853 |
rs573625885 | snp | A/G | 1.79738e-05 | 0.00299776 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356355 | CGCCAGGTGACCCAG[A/G]GACCCCACCCGACCC | 8853 |
rs573640136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375689 | TTTATTCTTACACCA[A/C]AAATGTAATGCCAGC | 8853 |
rs573651271 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382337 | TTCTGCTGTTGTCCT[C/T]ATTTTACAGATGAGG | 8853 |
rs573654758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330343 | ATATCGCATGTTCCC[A/G]CTCCTAAGTGGGTGC | 8853 |
rs573666562 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271723 | GGGCCCAAGGGGGAG[G/T]CTGCTGAGTCCTCGG | 8853 |
rs573675907 | snp | G/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9206531 | CAGCGGGTCGGAGTC[G/T]GGGCCTCGGGCCGGC | 8853 |
rs573701525 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9310238 | CCCACATTTCAAAGC[A/G]TCTTTTCTACCTCTC | 8853 |
rs573703915 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370041 | GATGGGGTTTCACCA[G/T]GTTGGTCAGGCTGGT | 8853 |
rs573751581 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228310 | CATGGTGAGTATTCC[A/G]GTTACAATGCATATT | 8853 |
rs573766544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306157 | GGGTGTAGACATGGG[G/T]TGGAGGGGCTCTAGG | 8853 |
rs573767213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261077 | TGTGTGGAGGAGAGC[C/T]ACTGGCAGCTTTCTT | 8853 |
rs573774553 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9316313 | GTTTCAAAAAAAAAG[-/A]AAAAAAAATTAGTAC | 8853 |
rs573805734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261741 | TGGCTGGACTGCCAC[A/G]TGCAGGGGAGAGGCC | 8853 |
rs573809067 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395671 | GGAGTGCGGTGGCGC[A/G]ATCTTGGCTCACTGC | 8853 |
rs573809515 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272845 | TCTTGGCACATTTGT[A/G]AAAAATGAGTTCACT | 8853 |
rs573810370 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286450 | AGGAAAAAAAAAAAT[A/T]TATATATATATACTG | 8853 |
rs573815403 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249737 | GCAGGCAGGCATGCC[C/T]GGGCTGGCGGGGGAG | 8853 |
rs573835501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279635 | TGCTGTCTGTCCCAC[A/G]TTGCACTTCCTGTTT | 8853 |
rs573835873 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227611 | TAAAATAAGATAATT[G/T]GTAAGTAGTAGCCCT | 8853 |
rs573839571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219301 | ATTTGCCCTGTGATT[C/T]GGTTGTGTTTATGTT | 8853 |
rs573853618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313332 | TAAATAACGAATAAT[C/T]TCAAAATAGATGGAT | 8853 |
rs573862699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235573 | TAGGGAGTGAAGGGA[A/G]TGAAGTAAAGAGAAA | 8853 |
rs573879462 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9280353 | CATTCCACCTGCTCC[C/T]CCCCACCGCCCCCAC | 8853 |
rs573894703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313683 | AGGACCAAATTGACC[C/T]GCGCCGGTGACTCTG | 8853 |
rs573916760 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9283298 | GGCTAGGCTGATCTC[A/G]AGCTTCTGACCTCAA | 8853 |
rs573919297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273438 | CAGTGTAACCACCCA[A/G]TGGGTTCACCTTGCC | 8853 |
rs573951065 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244762 | TGTTTGTAGGAAGAA[C/T]AGGAGATGGATTTAA | 8853 |
rs573971068 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318245 | TGAAATATTTTTTCT[C/T]CACTGCAATGATTGT | 8853 |
rs573990000 | snp | G/T | 9.98851e-05 | 0.0070663 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400709 | GGCTGTGATTGATGG[G/T]ATGTCTTAAGCTGCT | 8853 |
rs574000762 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343544 | CTCGATCTCCCAGGC[G/T]CAAGCAGTCCTCCTG | 8853 |
rs574009334 | snp | G/T | 0.0260105 | 0.111035 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208411 | TATTTTTTTTTTCTG[G/T]TTTTTTTTTTTTTTT | 8853 |
rs574011310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249738 | CAGGCAGGCATGCCC[A/G]GGCTGGCGGGGGAGC | 8853 |
rs574037831 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9241454 | ATACATGAAAATCAA[A/G]CTGGCTGGGTGTGGT | 8853 |
rs574051101 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357339 | CCATAATTAGCCCGG[C/T]GTGGTAGTGCGCACA | 8853 |
rs574070662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389181 | AAGTTAAGTAATTTG[C/T]TCATTCCTGAAGAGC | 8853 |
rs574093151 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344116 | TTATGTGATGGTTCT[G/T]TAGTAAGGGACAGAA | 8853 |
rs574096635 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239859 | AGCCTCTTGAGTAGC[C/T]TGGACTCCAGGTGCA | 8853 |
rs574104267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9215185 | ACAGTTACAGTATTT[A/G]TGTGTGGTATTTGTG | 8853 |
rs574115103 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300404 | CCTCCTTCTCCTTTA[C/T]AAAATTTCCTGCAAA | 8853 |
rs574123363 | in-del | -/ATGTC | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267343 | ATTGTTTGTTTCTTT[-/ATGTC]ATGAGTACTCAACAT | 8853 |
rs574176312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213779 | GTTCATCCAAGCCCC[C/T]TGAACAGACCTTCCA | 8853 |
rs574176313 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221685 | TGTTTATTGGCTTTT[A/T]TAGTTTTGTGTATTT | 8853 |
rs574182754 | in-del | -/TTTTGTGGCTCTTTT | 0.040671 | 0.13668 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322518 | CCTTAGCAGCCACGA[-/TTTTGTGGCTCTTTT]TTACCCTGGTGGCTC | 8853 |
rs574185265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314448 | TGTCTTTCACATATT[C/T]GATGCCCAAAAAAAT | 8853 |
rs574217559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214260 | TTATTTTGTTTGAGG[C/T]GGAGTCTTGCTCGGT | 8853 |
rs574248268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236693 | TGTGTAGGTGGTTGT[A/G]TGTATGTATGAGAGA | 8853 |
rs574271589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332727 | ATATTTTTCCTACTC[C/T]TTATCTTAGATCTTA | 8853 |
rs574271782 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351315 | TCTTCAACAGGTCCC[C/T]TGAAACTTCAGTGTT | 8853 |
rs574283471 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9379395 | CCCTGAGTCTACTCA[C/T]CCCCACCTGAGGCCA | 8853 |
rs574299845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281008 | TGAGTGGCCCACTCT[G/T]TTTCAAAGCCACCAT | 8853 |
rs574311978 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210638 | CCACTCACTGCAAGC[C/T]CCGCCTCCCAGGTTC | 8853 |
rs574324901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371514 | AGATGAAAAGGAATA[C/T]ACTGCTTCTAGCTTT | 8853 |
rs574334276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9333883 | GTGACCTCACAGCAT[G/T]GAGTTCTCAGCCTTA | 8853 |
rs574345630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222417 | TTAGAGCCAGGCCTC[A/G]TGTGTTCTCTGCAAC | 8853 |
rs574367690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298768 | CAGTTGGCTGCCTGC[C/T]CTCCCCGCACCTGGG | 8853 |
rs574386182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332015 | GGCTGCAGGAGGGGC[C/T]CTGGCACGGTGTGTG | 8853 |
rs574408519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210172 | CTGTTTTCAGAAACC[A/G]TGCTGCTTCCTGTTA | 8853 |
rs574409147 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229117 | AAGCGGAGTTTTAGT[A/G]CAGATGTACTAAACA | 8853 |
rs574410285 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359727 | TGTTCCTCTCAAGGG[G/T]CCATCAGTCTTATTG | 8853 |
rs574419923 | snp | A/G | | | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9215295 | AATGTCACTATGTGG[A/G]GCACGACTGTATATT | 8853 |
rs574424538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216634 | CCCAGCTAATTTTTG[C/T]ATTTTTAGTAGAGAC | 8853 |
rs574459954 | snp | A/G | 1.71666e-05 | 0.00292968 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327798 | ATTCTGCTTACTTCC[A/G]TGACATTTCCTTTTC | 8853 |
rs574466498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262873 | CAGTCTCTTTCACGC[A/G]GGGTTCAGAAAGAAA | 8853 |
rs574472963 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351833 | CTCCCTGTTCCCCTT[C/G]TCATACCCTCTGTGT | 8853 |
rs574489961 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275362 | GTAGGTGTGAGCTAC[C/T]GCATCCAGCCTAGTC | 8853 |
rs574512220 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9252455 | GGCATGGTGGCACAC[A/G]CCCAGCTACTCAGGA | 8853 |
rs574522809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340172 | GGATTACAGGTACGC[A/G]CCACCACGCCTGGCT | 8853 |
rs574537527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239346 | ACATTCAGTTATTGA[C/T]AGCAGCTAGGCTGTG | 8853 |
rs574538224 | snp | C/T | | | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214989 | GAAACTAATCACAGT[C/T]ATGCATTGCTTAATG | 8853 |
rs574541636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231833 | GGCAGCCTGGCCCTT[A/C]CCTGCAGCAGGTGAG | 8853 |
rs574580095 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251488 | AGCAGAACAGCTAAT[C/G]CCTGATGTCCGTCGG | 8853 |
rs574587846 | in-del | -/A | 0.00993419 | 0.0697739 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387241 | AACCATATAACCTTC[-/A]GGGGGGAGCAGGGGT | 8853 |
rs574614282 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258676 | AGGCGAAACCCCCGG[-/A]AGCTGCTGACTCTCT | 8853 |
rs574621027 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270960 | ACTACGCCCGGCTAA[-/T]TTTTTTGTATTTTTA | 8853 |
rs574628037 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269294 | TATCTTAATTAATTT[G/T]GGTTCAGTTGGTCTT | 8853 |
rs574636516 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384377 | TGTTCTTGTAAAGGC[A/G]GTTTCACAAGCAGCA | 8853 |
rs574637131 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391241 | CCGTGGGCTTTGTAG[A/C]TCTGGATGGCGGGGG | 8853 |
rs574657164 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346392 | GGTGAGCCGATATCA[C/T]GCCACTGCACTCCAG | 8853 |
rs574679973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302285 | TCAAGCGATCCTTCT[A/G]CCTCAGCCTCCCGAG | 8853 |
rs574681194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257813 | ACAGATGTGAGCCAC[A/G]GTGCCTGGCCTGAAA | 8853 |
rs574692517 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323727 | AGACCTCACCTGCTC[A/G]GGCGGGGGCACTCAT | 8853 |
rs574699626 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378872 | CCCGTAGCCCAGGCT[C/G]CCTGCCGGGCAGTCC | 8853 |
rs574722495 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322043 | CTGGACGGTCTCTTG[C/T]CTGTGAAGGAGTGTC | 8853 |
rs574751989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263561 | TGTCATCTGTTTCCG[C/T]TTCTCTAAGATAGGG | 8853 |
rs574754612 | in-del | -/T | 0.13446 | 0.221699 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404738 | CAAGACTGTGTAGAG[-/T]TTTTTTTTTTTTTGG | 8853 |
rs574759606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276288 | GAGGCCTTCTCAGGA[A/G]AGAGGAGTGTGTGCA | 8853 |
rs574769223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321594 | GAGTAATTGAGCCAG[A/G]CCAGGAAGCAGCTTT | 8853 |
rs574774097 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383815 | TGGCACATATACACC[A/G]TGCAATACTGTGCAG | 8853 |
rs574779101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232283 | TCCTTTTACACAGGT[A/G]GTCCCTCTGTTTGTA | 8853 |
rs574788759 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264136 | AAGAGAGGTTGCAGT[A/G]AGCCAAGATCACACC | 8853 |
rs574792576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257516 | GAGAATGTGAAAGTG[C/T]GGTTGTTTTGTTTTG | 8853 |
rs574797672 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212525 | TGGTGGCCAGCTCGG[C/T]GTCTGCGGTAGGATT | 8853 |
rs574801600 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301243 | ACCTACCTGCTTGGA[A/G]GCGTGAAAGAATGTT | 8853 |
rs574805850 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315971 | AGAATTGGCTGTGGA[G/T]GCAGACGTTATTATA | 8853 |
rs574809610 | in-del | -/CAGCT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318140 | AACCCCAGTACAGTC[-/CAGCT]CAGCTTATGGGTGGA | 8853 |
rs574829622 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353628 | GCAGTGAGGGTGATA[C/T]TTTCTGTGTGCATCT | 8853 |
rs574845640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380077 | GTTATATTGCAGTGC[A/G]TGGAAATAGGTGAGC | 8853 |
rs574855487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245360 | GGGGGCTGCCTGACA[C/T]GGAGCCAGCCTGCCT | 8853 |
rs574897289 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9347919 | AAAAAATAGAACGGC[A/G]CGATTAGAATGGAGA | 8853 |
rs574906928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380616 | GTCAAACTCACTGTG[G/T]ATTTCATTAACCAGG | 8853 |
rs574908878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225466 | AATGTATACTAAATG[A/G]AAGCAAGTACTTTCA | 8853 |
rs574908957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374455 | AGGGTGTGGAGGTGA[C/T]GAGGGCGACAGTGAG | 8853 |
rs574926353 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403752 | TGCTTCAGAAGTCCA[C/T]AGCCCAGCTCTGAAC | 8853 |
rs574929494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317018 | TCACAACCACACTCA[C/T]ACAACATGCAATCAT | 8853 |
rs574939745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392400 | TAGAGCCGAGGTGCT[C/T]GTGACTTCCTTAGAG | 8853 |
rs574947058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290239 | TTGAGATGGAGTCTC[A/G]CTGTGTCACCCAGGC | 8853 |
rs574962833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265682 | TGTCTATCCTCTTTT[A/G]TAAGTATTTTTTTCT | 8853 |
rs574963977 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393043 | CCCATCTCTCCTCAG[A/C]TCCACCCTGCCCAGC | 8853 |
rs574964201 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253388 | AGGCTGGTCTCCAAC[C/T]CCTGACCTCAGGTGA | 8853 |
rs574984741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226099 | CATGCGAGCTAGTCT[C/T]ACCCTGGGGCACGTA | 8853 |
rs575002671 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259008 | CTGGGCCTGCTCTTC[A/G]GCCTTTCTCTGTGGT | 8853 |
rs575032433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283433 | CGGCCATGGGAAACC[C/G]GACATGGGTCTCACT | 8853 |
rs575058862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309675 | GCTTAAAACTTTTCA[A/G]AAGCCATTTGTCCAA | 8853 |
rs575063326 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402678 | CCACAGCACCCCCCA[C/G]CCACTCCACAAAAAG | 8853 |
rs575071417 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405365 | AGCTGCAGGATTCTG[A/G]CATTTTGCATGCCAT | 8853 |
rs575083891 | in-del | -/ACT | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245782 | TCGTCGTCTGCCTCC[-/ACT]AGAGTGTCATGGATG | 8853 |
rs575094865 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310319 | GCCTCAGGTAAGATC[C/T]TTTGGCCATATTGTA | 8853 |
rs575126046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252718 | CAGGAGATCGAGACC[A/G]TCCTGGCTAACACGG | 8853 |
rs575153155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342067 | GGGTTGGAAGACTTA[C/T]TGTGAAGATAACAGT | 8853 |
rs575156490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291640 | TGTCTCTCCTTAAAC[A/G]CTCCCTTCGCCGAGC | 8853 |
rs575164591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247285 | ACTCTTCGCTCCTCA[A/G]TTAAGGAGACTGACT | 8853 |
rs575192103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285619 | TCTAAAATTTCCCAA[G/T]CTCTGGCTCAGCCCA | 8853 |
rs575220299 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298181 | TTCTCCTAAAGGTCA[A/G]GGAAGGCCAGGTCAA | 8853 |
rs575233152 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316970 | TCCCACACACCCCCC[A/G]TCACACCCTCTCATG | 8853 |
rs575236462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386448 | AAGCGGTCAGATGCC[A/G]CATTCCCATTTGATG | 8853 |
rs575243284 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305092 | ATAGATACTGGTGAG[A/G]GGCTGTAATAGTGGG | 8853 |
rs575258784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340969 | CAAGTGCCCACCTAC[C/T]CTGCATACTCAGGCA | 8853 |
rs575261940 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394992 | GAACACCTACATGTC[C/T]CTGGCATGGGCTTCC | 8853 |
rs575277742 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318269 | TGATTGTCTCTTTAC[A/G]AACTTTCTAGCATAA | 8853 |
rs575291309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335316 | CAGTAAAACATTTAA[C/T]GTATTCTTGCAATTT | 8853 |
rs575291862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277750 | TCACCTTAGGGCTCA[C/G]TCTTGTACATTCCAT | 8853 |
rs575292587 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297141 | GCACCACGGGTTGTT[A/G/T]TTGGGATAACGAAGC | 8853 |
rs575294367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218320 | CTAACTCCTGGGGAG[A/G]CACTTAACATCAGAA | 8853 |
rs575305776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279124 | TGCCATTTGGAAACC[A/G]GTCTTCCACACCACA | 8853 |
rs575317792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311797 | CCGAGAAGCGCGTCT[C/G]GCCCCCACGCACTTG | 8853 |
rs575336644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399857 | CACTTTCCTCAGGGC[C/T]TCTCATTCTTCCTTT | 8853 |
rs575353084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336095 | TTGCATGTTTTATTC[A/G]TGAACATACATATAT | 8853 |
rs575353154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328947 | TTTAGATAAAGATTT[A/G]GGGTAGAGTTTTTTG | 8853 |
rs575360194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363128 | CACAAATGACAGAAT[A/G]TCCTTTTTTTCAGGT | 8853 |
rs575361630 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302552 | CGATCTTGGCTCACT[G/T]CAGCCTCCGCCTCCC | 8853 |
rs575378899 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317617 | GCACTCACATCCACA[A/C]TCACACCCACACACA | 8853 |
rs575408339 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211561 | TAAAAATAAATTTGA[G/T]GTTGACTTGTAAGTA | 8853 |
rs575408466 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303448 | GACTTGGCTTGTTAG[A/T]CTTGGGTGCAAATTA | 8853 |
rs575416813 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300971 | TTTCCAGGCCAGCGC[C/T]GGTGTGGAAGCTGCA | 8853 |
rs575452113 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340173 | GATTACAGGTACGCG[C/T]CACCACGCCTGGCTA | 8853 |
rs575456928 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292077 | TGAGCAAGTCATCAC[C/T]CTCTCTGAGCTTTGG | 8853 |
rs575459693 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207568 | CCGCCGCCCGCCGCC[C/G]CCCGGGGTCTTTGGT | 8853 |
rs575467923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241034 | CATAGAACAGCAAGC[A/G]ATTTAAAAGTTATGA | 8853 |
rs575470952 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384783 | GCTCGAGAACCAGTC[A/C]TCTTTGATTTTTATG | 8853 |
rs575489500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369463 | CGGGCAGTGGGTGTC[C/T]GGCTCGCCTTAGACT | 8853 |
rs575500714 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322488 | AGAATAAAAACTCAC[A/G]GCTATTTCAAGCCCA | 8853 |
rs575515892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247818 | AAACTTCATGTGCCT[C/T]GGGTTTAAAATCTGC | 8853 |
rs575527194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306022 | GTAGTGGGGTGGTAG[A/G]TATGGGATGGAGGGG | 8853 |
rs575547799 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207042 | GCGGCGGTCGGAGCC[C/T]GCTGCGGCAGTTGAG | 8853 |
rs575557282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233772 | TGGATTTAATCCTTA[C/T]AACAACCCTGTGGCT | 8853 |
rs575566541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213393 | AGGTCACAGAGGGCC[G/T]TGTCCATCTTGGGGA | 8853 |
rs575568920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227522 | TTGGCTATTTTCAAA[C/T]GCTATTCGGGTGGGA | 8853 |
rs575575986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387443 | ACAGGTGGTAGTCCA[C/T]AGGCCACTGTTTGCT | 8853 |
rs575586348 | in-del | -/TAAA | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379643 | TTTTTGAAGGACTGT[-/TAAA]TAAAGAGGAAAGAAT | 8853 |
rs575603707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219428 | GTCTGTAACATGAGA[A/G]ATTTGGACTAGATGT | 8853 |
rs575630853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240452 | GGTTTCTCCATGTTT[C/T]CCAGGCTGGTCTCAA | 8853 |
rs575632184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343722 | CAGATGTTGGGATTA[C/T]AGGCATAAGCCACTG | 8853 |
rs575633466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226904 | GTCAGTCAGGAGGCA[C/T]TCCCTTCTCCTGCAT | 8853 |
rs575633975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228363 | CTCACTTGGTGTTAT[C/T]CTTGAGAAGAGAAAG | 8853 |
rs575657017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363695 | CTCATGCAATCCTTC[A/T]GGGTAGCTGGGACTA | 8853 |
rs575657902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9266699 | AATGAAAGAAGTGTT[C/T]CTCTTATGTTTGCTG | 8853 |
rs575684911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317759 | ACTCACACTCACATC[C/T]GTACACAATCACACC | 8853 |
rs575695283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393905 | AGGCTTCTGGGTTCT[A/G]TTTGCTGCTCACCCC | 8853 |
rs575699331 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272308 | TTGCTCGGATGATCA[A/T]TGATGTTGAACACCT | 8853 |
rs575715579 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9377211 | TAATTGCAGGGTCCA[A/G]CTTCTAGTGTCTGGT | 8853 |
rs575735215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331373 | CCTCTTTCCTGGAAT[A/G]TCTTGAAAACTTGTC | 8853 |
rs575741021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324449 | AAAAGAAATTTCCCA[G/T]TTCTGGAGGCTGCCA | 8853 |
rs575763720 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9209001 | ATTAAAATTGGCATA[C/T]CTTTCTCTGATTAAT | 8853 |
rs575779311 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337450 | ATTATTGTTTAGGCC[A/G]TCATTCCCTTTGGTT | 8853 |
rs575780993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355162 | TTGATGCTATTAACT[A/G]AAAATCTTACTCAGA | 8853 |
rs575808213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342906 | ACCCTGATTCTGTGC[C/T]AGTTCTTGCCTTCAT | 8853 |
rs575815051 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9289228 | ACTCTCCAGCCCTTC[C/G]CCATGCTCTGGACAC | 8853 |
rs575816515 | snp | C/G | | | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214838 | AGAAAGCACTTAATA[C/G]TCTCATGTTTTATGT | 8853 |
rs575823448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261948 | ACCAGAGCGCCTCAC[C/T]CCACCATTTGCCATG | 8853 |
rs575829604 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351342 | TGTTTGAAATTGTTT[C/T]TCTTCCTCACCACAG | 8853 |
rs575837771 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294453 | CTCTCTCCTACCAAG[A/G]GCTGGAGGACCAAGG | 8853 |
rs575842671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299161 | AATTTCTAAAAATGG[A/G]ACGGAAGAGTCTCCA | 8853 |
rs575846134 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348776 | GTTAAGAACGAACAC[C/G]TTTCCCCGTATCACA | 8853 |
rs575863997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375858 | CTGGAACCCACACCC[C/T]ACTGTGCTCCCCCTC | 8853 |
rs575869271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336956 | GCCAAATGGCCCTCT[A/G]GGCACAGTGCAAAGG | 8853 |
rs575881462 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292847 | GCCGGGCTGGAAATA[C/G]TAAGTTTTATGTTTG | 8853 |
rs575907486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243365 | CACCCACCTCGGCCT[C/T]GCAAAGTGCTGGGAT | 8853 |
rs575916585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343453 | TTTGTTTTGTTTGGT[G/T]TTTGTTTTTTTGAGA | 8853 |
rs575916918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229031 | CCTGCCTTGTTACCA[C/T]GTAGGGATCTGGCAG | 8853 |
rs575926831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376430 | ATCCCCAGTATGAGT[C/T]GGAGACAGTGCAGTT | 8853 |
rs575985223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332254 | TTTTCTGGGGCTATG[C/T]AGTTAGGACTGTCAT | 8853 |
rs575990651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365158 | AGGTAAAGACATCAT[A/G]TGTAAACTTTTTCCC | 8853 |
rs576021084 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9367499 | GGCGCAGCGGCTCAC[A/G]CCTGTAATCCCAGCA | 8853 |
rs576025760 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260915 | GCCCTTCAGAAGATT[C/G]TGAAACAAGGAATTG | 8853 |
rs576035109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370606 | TAAAAAAAGGGAGAT[A/G]ACGTTCCCCCTCACA | 8853 |
rs576046621 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371719 | CCCTGTGACTTGGGA[C/T]CATTATACACACCCT | 8853 |
rs576070192 | in-del | -/T | 0.143284 | 0.226079 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331756 | TGGGCGACAGAGCGA[-/T]TTTTTTTTTTTCAAA | 8853 |
rs576071358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250831 | TCAGCACAGGCCACC[A/G]TGGGCCATCTGTGAG | 8853 |
rs576077902 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364369 | AAAGTTAGCTGAGTA[C/T]GGTAGTACATGCCTG | 8853 |
rs576081021 | snp | C/T | 4.97583e-05 | 0.00498765 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9400774 | GAAGCTCTGGGTCCT[C/T]TGTCCAATGCTATGG | 8853 |
rs576089336 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280712 | CAGCAGCGGAAATTG[A/C]CAGGCCTTTTCTAAA | 8853 |
rs576089706 | snp | C/T | 3.29582e-05 | 0.00405931 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9344633 | CTACAAGAAGAGTGA[C/T]GGGTACGTGAGGGGG | 8853 |
rs576099972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287701 | TCTCTGAGGAAGTTA[C/T]AGAGGGAGGTGAGGA | 8853 |
rs576122209 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389324 | CTGAGACTTTGATGC[A/G]GGGCGGGGGGCCCAG | 8853 |
rs576144458 | snp | C/G/T | 0.000100225 | 0.00707845 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401251 | TGCAGCCACACTAAC[C/G/T]GTTGTTCCCTCTCCT | 8853 |
rs576153211 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269066 | AGCAAACCTTTTCTG[G/T]GAGGGGCCAGAGATA | 8853 |
rs576159764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221874 | TCTCGGCTCACTGCA[A/G]GCTCTGCCTCCCAGG | 8853 |
rs576168735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287233 | ACACCCTACGTGCCA[C/T]CTGGCTGAGCCATCG | 8853 |
rs576169376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222161 | ATTTGCACAGAATAG[A/G]TGCTCAGTAACTTTA | 8853 |
rs576198422 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214386 | CTGGGATTACAGGTG[A/T]CTGCCACCATGCCCG | 8853 |
rs576212652 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, synonymous-codon | ASAP2 | GRCh38.p7 | 2:9389807 | CTTGATGAGGACGTC[A/C]CTGAGCACAGAAGGC | 8853 |
rs576245230 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371024 | TTCCAAGCACCAGGG[G/T]TACCTAACGAAAGCA | 8853 |
rs576253641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280066 | GCAGGGCTAGGAACT[A/G]TGAGGAGTCCCTGAG | 8853 |
rs576257277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273942 | GGGGTTTATTTTGGG[A/T]AAGGGCCATTGTCAT | 8853 |
rs576259108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357277 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 8853 |
rs576264231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396859 | TTACAAAAATTAGCC[A/G]GGCATGATGGCACAC | 8853 |
rs576270048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396077 | GGTTGGGCAGGGCAG[C/T]GGCTAAGGCTACTCA | 8853 |
rs576289040 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282038 | TGCTTAAAATAGCAT[A/T]TGCCACTTTATGAAA | 8853 |
rs576293715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357995 | TCAAGCATTTTGTGG[G/T]TCCCTATCATCTGCT | 8853 |
rs576295793 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268621 | TGAAGAGTCGAATGC[A/G]TGGTGAGACAAAGCT | 8853 |
rs576311440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307539 | TCCAGTGCTGCCCTC[C/T]GGCTCCCAGAACCGG | 8853 |
rs576326617 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213919 | CCAGGGTCAATCAAG[A/G]AAAGATTGAAGCATA | 8853 |
rs576367619 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332090 | ATTGCCTCTAAGTGG[C/G]TGTATTTTAAAGGAT | 8853 |
rs576378120 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282572 | GACCACAGTTGGCTT[C/T]GGTGCACTGTAACTA | 8853 |
rs576380656 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9363574 | ATATACCTGTTGGTC[A/G]TTTGTAGGTCTTCTC | 8853 |
rs576380857 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9326646 | CCCTATGTATACATT[C/G]AAAAAAAATCGTATA | 8853 |
rs576403943 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288737 | AACCCCAGACACCTT[G/T]GGGTAGCCTGTCTCC | 8853 |
rs576405205 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401729 | TGGAATCGGGTGTCT[G/T]GAGAGAGCTGACCTA | 8853 |
rs576425855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244049 | TCATAACGATAATCC[C/T]AGCACTTTGGGAGGC | 8853 |
rs576434634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302345 | GCCCAGCTAATTTTT[A/G]TATTTTTAGCAGAGA | 8853 |
rs576438100 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230269 | ACCTTCAGGAGTGAA[A/C]AGGGCTTGTTTGCTC | 8853 |
rs576447251 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217541 | AGGATTCTAGCCAGG[C/T]AGTCAGGATTGTCGG | 8853 |
rs576452425 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9280380 | CCACCAGTTACAATA[A/G]GGCGGGCACAAGCTC | 8853 |
rs576458181 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214949 | AAAAATGTTTTAATG[C/G]AGAGAACAAAATAAG | 8853 |
rs576472970 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382979 | CCCACAAAGGCTCAG[A/C]GGTTAGGGTTTTTCA | 8853 |
rs576505359 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338804 | AGGAAGCAGTGTCTG[C/T]CCAGTGCGGGCTGGG | 8853 |
rs576527539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238141 | GTTAGCTGACCCGCT[A/G]CCTACTGATCTTCAC | 8853 |
rs576529033 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397448 | CTACCCGGGACAGAC[A/G]GGGATGGACGGAGCC | 8853 |
rs576550029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326103 | TCATGTTAAAAGGCC[A/G]GGCAGGGTGGCTCAC | 8853 |
rs576554543 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402357 | TCTGTGGCCTGGGCG[A/C]GGTGGCTCACGCCCA | 8853 |
rs576555802 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9208495 | TGTTTTCCCTTAATG[C/G]AAAAATTTTTTCTTT | 8853 |
rs576564302 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367013 | GCATGTTTGTTAACT[C/G]CTTTGCCTGCATAAT | 8853 |
rs576569480 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232649 | GCATCCTCAGCACCC[A/G]GAATTGCACTGGACA | 8853 |
rs576605979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301254 | TGGAGGCGTGAAAGA[A/G]TGTTTATAAAGCAGT | 8853 |
rs576621711 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325708 | AGGTGAATTGATCCT[G/T]TGAACTGACTAAGTC | 8853 |
rs576623743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209489 | TGACATAAAGTTACT[C/T]ATTTAACAAATAAAT | 8853 |
rs576651864 | in-del | -/AC | 0.0117932 | 0.0758783 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317996 | CACTCTCCGTCCCCA[-/AC]ACACACACGTCTTTT | 8853 |
rs576668048 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9393152 | CAGAGCTGAGGGCCC[C/T]GGCCTCCTGCTGTTG | 8853 |
rs576671305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327969 | TGTGGCAACTTCTGG[C/T]AGATCTATAGATAGC | 8853 |
rs576678437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320168 | ATTTTTCGTGGGATT[A/G]CATACGTCATTTATT | 8853 |
rs576681340 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248782 | CAATTAGATGGCAGT[C/T]CTTTATGGCCAGGGA | 8853 |
rs576708364 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9259324 | CAAGGGCCGCCATCC[C/T]TGCCTGTTGCTGCAC | 8853 |
rs576720368 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302675 | AGACGGGGTTTCTCC[A/C]TGTTGGCCAGGCTGG | 8853 |
rs576743534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320658 | TTTTAAACACTTTGT[C/T]CATTCCGTTACTGTT | 8853 |
rs576756019 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9389238 | AGGTCCGGCGAGTGA[C/T]CCACTCAGCTCTGGG | 8853 |
rs576759673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296983 | CTGGTGAGTTGTGCC[A/G]TCATTTGGTGAAGGA | 8853 |
rs576777161 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9216735 | CAAAGTGCTGGGATT[C/G]CAAGTGTGAGCCACC | 8853 |
rs576786584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237600 | TTATTTTTATTTTTT[G/T]TAGAGATGAGGGTCT | 8853 |
rs576793455 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384586 | TTGGGTTTGAATAAT[G/T]TGCTGGAGTGGCTCA | 8853 |
rs576817117 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9204815 | TCAGAAAGGCATTAG[C/T]TATGTTTTGCTCTGG | 8853 |
rs576818092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326567 | AAAGGAATTAAAAAT[C/T]GCCCCCAAATTTTAC | 8853 |
rs576827204 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232959 | CCCAGCTGCAGTTTT[G/T]TTCTGTATCTATTGC | 8853 |
rs576843778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270038 | AAAGTGGTTTGAAAC[A/G]GTAGTTTTCCTCAGA | 8853 |
rs576862169 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9223069 | GGCAGAGGCCTTCCT[C/G]CATCTCTCAAGTCAC | 8853 |
rs576918160 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379441 | TTGGCTCTGGGTTTA[C/G]ACGGATTACAGGGGG | 8853 |
rs576944479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334387 | TTTCCATGTCGCGGT[C/T]GCCTGTTGCGGCACA | 8853 |
rs576954461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285472 | CCCAGTCTTCAAAAT[A/G]ATGGCAACCCAGCCA | 8853 |
rs576985768 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290794 | CTTAGAAGTTGCAGG[A/G]TCCTGGGCTTGTTCA | 8853 |
rs576991280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307077 | CTGCACCAGCAGCAC[C/T]GGAATTGTTAGAAAT | 8853 |
rs577005942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246268 | AACCACTTATTACAC[G/T]GAGCAAACTAGTGTG | 8853 |
rs577050431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252784 | AGCCAGGCGTGGTGG[C/T]GGGCGCCTGTAATCC | 8853 |
rs577067021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252102 | AGCCTTCGTGTCACA[A/G]AAGCCGTTAACACAC | 8853 |
rs577088480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340607 | AAGATGGGGGAATGA[A/G]TTGGACATCACAGCC | 8853 |
rs577089330 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9391738 | GCCACCATGCTCAGC[-/T]TATTTTTTTTTTTTT | 8853 |
rs577105431 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211215 | ATACCTGTATTTTAT[A/C]ATTTTTCACTTGACC | 8853 |
rs577137137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240169 | ACCCTCGGTGGATGC[C/T]TGCAGCCAGCTAATA | 8853 |
rs577141570 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404593 | ATAAATAGGCATATG[A/G]TACCCACTTGGACTT | 8853 |
rs577152806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348103 | TCTCAATTAACTGAT[A/G]ACACTTTTTTGTCTG | 8853 |
rs577169148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247896 | CCCGCTCTCCTCCTC[C/T]GCCCCCCACACTGAT | 8853 |
rs577170041 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347068 | AATCTCCACTTCCAG[A/C]GGTCTCCTCCTGCCT | 8853 |
rs577175992 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361976 | ATCTCTTTCTCTGCG[C/T]GTGTGTGTGTGTGTG | 8853 |
rs577194763 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301374 | TTCTCTGCGGTGATG[C/G]AGGATGAAAGGGAAA | 8853 |
rs577247540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239477 | GGGGTGGTGGTGGGG[A/G]GAGATAATAACAAAC | 8853 |
rs577258040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9248337 | CTGTTTTATAACCAA[A/G]ATGGTTTTTAGAAAA | 8853 |
rs577278748 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403977 | TGATGGTTTATGACA[A/G]CGTAGGGTAACTACA | 8853 |
rs577311574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361105 | AGCCTCCATCTGCAT[C/T]CTTGTAGGAGTTTAA | 8853 |
rs577315683 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284448 | CATTTAGGATAAAGA[A/C]GACGTAGGTATTAGA | 8853 |
rs577325751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386559 | CTGCTCACCTGATTC[G/T]CAGCAGACAGCAGCC | 8853 |
rs577335922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311599 | GAGCATGAAAATGTC[A/G]TTACTCATAAATTGA | 8853 |
rs577347785 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398467 | CGGTGAACTGATTGC[C/T]GCACTGCACTCGAGC | 8853 |
rs577355387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259208 | TGGATGGAAAACAAA[C/G]AAAGAAAGTAAAACT | 8853 |
rs577362033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375002 | CCGGCCACGGTGGCT[C/T]ATGCCTGGGATCCAG | 8853 |
rs577392790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367786 | AATGTGTTAATTTAA[C/T]GTTTAACATGTCAGA | 8853 |
rs577393575 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272577 | ATATGATCCCATTTA[C/T]CTGTTTTTGCTTTGG | 8853 |
rs577397253 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9216616 | CAGGTGCCAACCACC[A/G]CACCCAGCTAATTTT | 8853 |
rs577397263 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247037 | GTAGAGATGGGGTCT[C/G]TGTTGTCCAGGATGG | 8853 |
rs577428762 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9320623 | AATTTCTCTTAGGAG[A/G]TATTTCTTTCTGTTT | 8853 |
rs577430777 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9355729 | GAACAATTACTTTTT[-/G]GGGGCCAACTCTGTA | 8853 |
rs577434761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354319 | CTGAGTGCTCCGATC[G/T]CCCCCTCTGTCTCCT | 8853 |
rs577451580 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394416 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 8853 |
rs577454048 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9367703 | GGAGGGCAAGGTTGC[A/G]TTAAGCCATGATCAT | 8853 |
rs577456546 | snp | A/G | 3.29685e-05 | 0.00405995 | missense | ASAP2 | GRCh38.p7 | 2:9368515 | CCCAACCCAGGCAGC[A/G]ACATGTAAGTATGGG | 8853 |
rs577466082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399121 | GTGATGTTTTCTCTC[C/T]CTTCATTCTGGGACT | 8853 |
rs577473031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393711 | CTCACCTGCCCAGGG[C/T]TCTGCAGGAATGTTT | 8853 |
rs577473478 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9280159 | TTTGGGTGACAGGGT[A/G]GGAGGAGGAGGGGCC | 8853 |
rs577479213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303664 | GCTAAGCTATGTTCT[A/G]TACTCACAAATCTCT | 8853 |
rs577479359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265737 | TGTGTGTCTGTGCGT[A/G]TAATGGATTTAATAA | 8853 |
rs577482323 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244835 | CAAACCCTTTTCATT[A/G]GATCCTTTCTGAGGC | 8853 |
rs577484340 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370012 | CCCAGCTAATTTTTT[G/T]TATCTTTAGTAGAGA | 8853 |
rs577493426 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371215 | GAGGGCGGATGACCC[A/G]TGTGATGGCGAAACA | 8853 |
rs577500300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354960 | TGGATTCCCCTGCCC[C/T]TGCTTTTCTTTATTA | 8853 |
rs577516536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297859 | TGTAATCAAAGCACA[A/G]AAATTACCATGAATA | 8853 |
rs577554882 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279213 | CCAGAAACAGGTGCC[G/T]AGGGACCTGGCAGAG | 8853 |
rs577577298 | snp | C/T | 1.66515e-05 | 0.00288539 | missense | ASAP2 | GRCh38.p7 | 2:9388499 | CCCAGCCTGCAGCCC[C/T]CAGCACCACCAGCGC | 8853 |
rs577587442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271395 | CTGAATTACTTCTCC[A/T]TATTCTGGATGCTCA | 8853 |
rs577604419 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241126 | AAAATGAAACTGTGG[A/T]TAAGAGGGTAGTACT | 8853 |
rs577611384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393156 | GCTGAGGGCCCCGGC[C/T]TCCTGCTGTTGGGTC | 8853 |
rs577616758 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330174 | GCACTTGAGGTCAGG[C/T]GGCAAAGGAGGATGT | 8853 |
rs577628575 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384027 | ATGGGGTGGGGAGAC[A/G]GGGGAGGGATAGCAT | 8853 |
rs577637960 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328923 | AAAGAATATAATACA[A/G]GGACCTGATTTAGAT | 8853 |
rs577638925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389014 | TTGGGGAACGATGCT[C/T]GGCCTAATTGTAAAA | 8853 |
rs577689377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336188 | TTGTAGACTTTATTA[A/G]AGGCTGAAGAGTTTG | 8853 |
rs577693763 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292274 | GGCTGGGCGTGGTGG[C/T]TTTGGGAGGCTGAGG | 8853 |
rs577706611 | in-del | -/CTCT | 0.0667028 | 0.170006 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338291 | TCTCAAGTATGGTTG[-/CTCT]CTCTCTCTCTCTCTG | 8853 |
rs577714999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395093 | TGACTTCCGCCATAC[A/G]TCACTGCTCAGTTAC | 8853 |
rs577738829 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271277 | AAACTACAGTGAGCC[A/G]CAAGCATTTAAACCC | 8853 |
rs577753515 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227217 | CTACATTTTCAGGGC[A/G]CTTGGCCTCTGCTGT | 8853 |
rs577782478 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9303976 | TGGTGCTGTATGGGG[C/T]GGTGACCTCTGGCAA | 8853 |
rs577803863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400518 | TCAGTCCTGGGGCCC[C/G]TCACCTGTCCCCTCC | 8853 |
rs577822897 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9312116 | GTGGTGCAACCATCA[C/G]CTCAAATCCGTTTTA | 8853 |
rs577841581 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233972 | AAAAATTAGCTGGTC[A/G]TGGTGACAGGCACCT | 8853 |
rs577844809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241958 | AACTTTGTTATCAGG[C/T]GGACACATGTGAATT | 8853 |
rs577917054 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227544 | CGGGTGGGACAGGGC[G/T]CATGCACATTTTACA | 8853 |
rs577958773 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261002 | TGTGCCCCTGGTGAA[C/G]TTCAAATGCTAGTGT | 8853 |
rs577988002 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244472 | GTTTTTGAGTTTCAC[A/G]GTGTGAACAGAACAG | 8853 |
rs578014672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267304 | TCTCCACATCTCTCC[A/G]CTCTCTAGTAGTCCC | 8853 |
rs578023026 | snp | C/T | 6.59217e-05 | 0.00574078 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356173 | GCGTTGCTCTTGTTT[C/T]TCTAGATGGATGTCT | 8853 |
rs578033475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313169 | GCTGAAATGAACGAA[A/G]AACGAAAGCAAGCCG | 8853 |
rs578058499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267694 | TTGAGGCCGGGAGTT[C/T]GAGACCAACCTGCCT | 8853 |
rs578066416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343481 | AGACAAGGTCTCGCT[C/T]TGTCACTGAGGTTGG | 8853 |
rs578089526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254728 | AAAAAAACCCAGTAT[A/G]TACAGGATTTGGTAC | 8853 |
rs578120310 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264348 | CCAGAGACTGGGGGG[G/T]CCCGTGCTGGCGTCA | 8853 |
rs578147520 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9262860 | GAATCAAAGTCCTCA[G/T]TCTCTTTCACGCGGG | 8853 |
rs578151679 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371394 | TTTGGTTTTTCCCAC[C/T]GTAATATGTTGCTTC | 8853 |
rs578152742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337576 | TAGAAATTAAGTAAC[A/G]TGCCCCAAAGAAACT | 8853 |
rs578153466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243399 | AGGCATGAGCCACCG[C/T]GCCCGGCCTAAAGAT | 8853 |
rs578157367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325007 | TGATTCCTCCTTTAC[C/T]GCCTTGTTTTTCATT | 8853 |
rs578174191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376508 | GCCTGCTTAAGAAAC[A/T]TATGTTTCTACTCAA | 8853 |
rs578183138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382278 | CGTGAGCCACCACAC[C/G]TGACCTGTCTCATTT | 8853 |
rs578195044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207690 | CAGGGCCCCCACCCT[C/T]GGGTCCGCGGGTCCG | 8853 |
rs578197162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255258 | ATCATACAATGCATC[A/G]TGAGAGTAGAGATTC | 8853 |
rs578204754 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331038 | AAGAGCTCGCAGCCG[G/T]GCGTGTTTCCACGTG | 8853 |
rs578205113 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368364 | AGATGGGGATGGGTA[A/G]TGTGTAGCAGTAGAA | 8853 |
rs578215076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398508 | GGGCAGGACCCTGAC[C/T]CAAAAAACAAACACA | 8853 |
rs578238391 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212702 | GGCAGCCTAAGACAA[A/G]TCCAGCTCTCAGCCG | 8853 |
rs578239646 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344041 | TTGAGTCCTTACTGT[G/T]TATTGGCCTTACTGG | 8853 |
rs578255164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338058 | AGCCTCGCCTCCTGC[C/T]TTCCCCATCCCACGT | 8853 |
rs745324167 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225945 | GAGCAACTGCTCCAT[A/T]CCAGGCCGTGGGTTC | 8853 |
rs745327326 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9288364 | CTATCTGAGGCTTTA[A/G]AGACCATGTACTTTC | 8853 |
rs745331937 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317970 | CTCAGTCGTACACAC[C/T]CATTGACACACACTC | 8853 |
rs745359862 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358971 | ATTCTAATCCATTTT[C/G]GTAAGCTAGTGGTTG | 8853 |
rs745360760 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234307 | GGGAGGCAGCAATAA[C/T]CAGACTGCCTAGAGA | 8853 |
rs745383009 | in-del | -/TA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336186 | TGTTGTAGACTTTAT[-/TA]AAGGCTGAAGAGTTT | 8853 |
rs745425709 | snp | A/G | 1.66665e-05 | 0.00288669 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403334 | GCTGACTGAATTGCT[A/G]CTGAACAAAAGCATT | 8853 |
rs745428651 | snp | A/G | 1.64773e-05 | 0.00287026 | missense | ASAP2 | GRCh38.p7 | 2:9376968 | CGAACCTCTCTTCAC[A/G]TTGTAGACTTTTTAG | 8853 |
rs745433736 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356145 | TCAGCCGTTGTTTGT[A/G]GAATTTAACACAGCG | 8853 |
rs745435010 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9246343 | TCTGTTACCTAGACT[A/G]GAGTGCAGATCATGG | 8853 |
rs745444278 | snp | C/G/T | 6.07132e-05 | 0.00550941 | missense | ASAP2 | GRCh38.p7 | 2:9393485 | TGTCCTCCGCAGATC[C/G/T]CCTGACCCCCACGCC | 8853 |
rs745454944 | in-del | -/T | 0.000106479 | 0.00729577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388599 | GGTCTTGTTTTGTGG[-/T]TTGGGAAGTTTGCAG | 8853 |
rs745466090 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9386436 | TGCCTCTTCATCAAG[C/T]GGTCAGATGCCACAT | 8853 |
rs745475636 | snp | C/T | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403580 | TGAACTGAAAAGTTA[C/T]TTTAACTATTATACA | 8853 |
rs745481491 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9235738 | CGCATGGCCTGGCAG[C/G]TGTGATGGGAACATG | 8853 |
rs745489573 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278673 | GCCATAGACAACTGC[C/T]GTGTAGTAGCTGGTC | 8853 |
rs745503956 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307415 | TAAACCTGGATTCTT[A/G]GAGGTAATACATTTG | 8853 |
rs745513919 | snp | A/G | 1.66413e-05 | 0.0028845 | missense | ASAP2 | GRCh38.p7 | 2:9356280 | TCCAAGAACTGACAA[A/G]GGAGATCATCTCAGA | 8853 |
rs745515368 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9252347 | GCACTTTGAGAGGTC[A/G]AGATGGGTGGATCAC | 8853 |
rs745518413 | in-del | -/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213716 | CTAGTGGCATAGAGG[-/T]TAGACCCAATAGAAC | 8853 |
rs745520035 | snp | G/T | | | missense | ASAP2 | GRCh38.p7 | 2:9400744 | TTTTGCCCTACAGTG[G/T]ATCTCTCTGCAACGG | 8853 |
rs745527001 | in-del | -/TG | | | intron-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211957 | GGCCACCTTTTAAAC[-/TG]TGTTCTGAAATTTGA | 8853 |
rs745587121 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346981 | ACTGGGATGCTGAGA[A/T]CTCAGCTTGTCACAC | 8853 |
rs745591869 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294998 | GAAACTAAACTGCCC[A/G]TGTCTTGACCGCTAA | 8853 |
rs745592918 | snp | C/T | 2.16603e-05 | 0.00329084 | utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207091 | CTGTGCGCCAGCGCC[C/T]TCGCGCCGAGGCGAT | 8853 |
rs745615799 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336859 | ACCGTTGGAAATGAT[C/T]GAGAACTGCCTTTGT | 8853 |
rs745635247 | snp | A/G | 1.70874e-05 | 0.00292291 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327941 | GTTATGTTATCTTAA[A/G]TGTTTGTTCATGTGT | 8853 |
rs745642830 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9208540 | TCAATAAAAGGGAGT[C/T]AAAAGTAACATTCAG | 8853 |
rs745646222 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365952 | CTCTCCTCCATCCAG[C/T]CTGGCTCAATTTCTG | 8853 |
rs745648078 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370033 | TTAGTAGAGATGGGG[-/T]TTCACCATGTTGGTC | 8853 |
rs745659419 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305518 | TAGTGGGGTATAGAT[-/A]ATTGGTGGAGGGGCT | 8853 |
rs745667223 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9335827 | CAATGTGGGTATCAT[A/C]ATGTGAATTTAGTAT | 8853 |
rs745673299 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221462 | ACCTGGCCTCATTTT[C/G]TTGTCTTTAATTTCT | 8853 |
rs745680992 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9354663 | AAAAAAAAAAAAAAG[A/G]AAAAGAAAAAGATGC | 8853 |
rs745692334 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9376372 | TCATCTCTTCTCCCC[C/G]ACCTGCCAGGTGTAC | 8853 |
rs745731867 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366787 | GAATTAGGAAAGCTC[A/C]TCATCCAGCTATTAG | 8853 |
rs745775486 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284673 | AGTGTGACAGCTGTG[A/G]CATACCTCCTGTGTG | 8853 |
rs745776377 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9394851 | TTCGCTGAAAGGACT[C/T]GAAGCCTGGGGGTGG | 8853 |
rs745783935 | snp | C/G | 3.40443e-05 | 0.00412565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385385 | GTTGCTAACCATTAA[C/G]AGTTTTGATCAGCTT | 8853 |
rs745794509 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264799 | GTCTCAAGGGGAAAA[C/T]ATTCAAGAAAAAATA | 8853 |
rs745807023 | snp | C/T | 2.29524e-05 | 0.00338757 | missense, utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207204 | CGCACGGCGCAGTGC[C/T]GGAACACTGTGGCGG | 8853 |
rs745807252 | snp | A/G | 1.69407e-05 | 0.00291034 | missense | ASAP2 | GRCh38.p7 | 2:9374774 | GCAAGAAAGGACTAC[A/G]TCACAGCCAAGTACA | 8853 |
rs745812154 | snp | C/T | 1.64849e-05 | 0.00287092 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344713 | AAACTCTTATTGTTT[C/T]TCCCACTTATCCACA | 8853 |
rs745819905 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254690 | ATAAACTAAACTTTA[C/T]CAGAGGTATGTGTGT | 8853 |
rs745834857 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9283766 | TCTCCTCTCCTTCCT[A/G]GCTTGCAGACAGCTG | 8853 |
rs745844465 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352071 | GGCCAGAGTTTAAAA[C/T]GTGATTGCAAGCCAG | 8853 |
rs745848185 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295867 | GGTCAAAGACATGGT[A/G]CTTCCCCCATAGGAT | 8853 |
rs745858280 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9324572 | GGGCCTCACAAGAGA[C/G]AGCCAAACTGGCTTT | 8853 |
rs745869812 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315133 | GGAAGGAGAGAGTTC[A/G]GTTTGGAGAAATATG | 8853 |
rs745879084 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301246 | TACCTGCTTGGAGGC[A/G]TGAAAGAATGTTTAT | 8853 |
rs745892569 | snp | A/G | 4.97847e-05 | 0.00498897 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323074 | AGGCTGTCCCGTTGA[A/G]TTCTGTGCCAACAGG | 8853 |
rs745905125 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9342263 | TCCTGATTTCTGAAC[C/T]TACCACAAAGCTGTA | 8853 |
rs745946863 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383063 | GAGTGAAATCATAAG[A/T]GTATGAGAAACAGCC | 8853 |
rs745952057 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9339423 | CAAATAGGAATAATA[-/C]AGCCAACCTCAGAGT | 8853 |
rs745954196 | in-del | -/CT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317268 | CGTGCATCACACACA[-/CT]CATATCCACACCCTC | 8853 |
rs745969211 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9339931 | ATTTCCTGTTTACCT[C/T]ACTTTTCAGGTTTTC | 8853 |
rs745971215 | snp | C/G | 2.30391e-05 | 0.00339397 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379081 | GGGCCCGGGCCCCGG[C/G]GGTGGGCTCAGCTGC | 8853 |
rs745982648 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371261 | CCTTCTCAACTGAAA[C/T]TACTTTCTTGGCTCT | 8853 |
rs745984762 | snp | A/G | 4.99189e-05 | 0.00499569 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391184 | CTGCCCCCTCTTCGC[A/G]TGACATCTACCAGTA | 8853 |
rs746017364 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229021 | GAAAGCCACACCTGC[C/G]TTGTTACCACGTAGG | 8853 |
rs746025033 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9216580 | ATTCTTGTGCCTCAG[C/G]CTCCTGAGTAGCTGG | 8853 |
rs746035961 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373100 | AGTGAGCTCAGTGCA[C/T]GGGTTAGCGCTGTGT | 8853 |
rs746036241 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383762 | AGACTTGGAACCAAC[C/G]CAAATGTCTGTCAGT | 8853 |
rs746054934 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291203 | TAAATGTTCTGTACA[C/T]ACATCTCTGATCACC | 8853 |
rs746056070 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263340 | CTGTGGCTCTCCCCA[A/C]AGCAGGGCACCAGGC | 8853 |
rs746083115 | in-del | -/CT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317565 | ATCCACAATCACACT[-/CT]CACACACCCACACAC | 8853 |
rs746084799 | snp | C/T | 1.64751e-05 | 0.00287007 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380737 | GCTCGCCCTTGAATT[C/T]TAGCAAACGAGTCAG | 8853 |
rs746097486 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275363 | TAGGTGTGAGCTACC[A/G]CATCCAGCCTAGTCC | 8853 |
rs746106045 | snp | C/G | 1.65332e-05 | 0.00287512 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368410 | GTATCCTGAAATAGA[C/G]TTTCATTTTTGCAGC | 8853 |
rs746110785 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212874 | CGTACACCACAGGCA[C/T]GTGAGAGCTTGCGAA | 8853 |
rs746144023 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331371 | TACCTCTTTCCTGGA[A/G]TATCTTGAAAACTTG | 8853 |
rs746182795 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294649 | GCCACCTAGTAGGCG[C/T]TGACCTTTATACGAA | 8853 |
rs746195756 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9320789 | TTAGAAAGAGGGTTC[A/G]ATACCTGTCTCCTTC | 8853 |
rs746218113 | snp | C/G | 1.66095e-05 | 0.00288175 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399991 | AGGTGCCCTCCGGTA[C/G]CAGTAAATCTACTTT | 8853 |
rs746223828 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349602 | AGATATCTACAGATT[A/G]TGGAGAATATCTGAC | 8853 |
rs746257035 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332285 | AGGGACAGCAGCCAG[C/T]GGAGAAGGAATAGTG | 8853 |
rs746275355 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362398 | ACAGCAAAGGATTTT[A/T]TTTTTTTAATTAATT | 8853 |
rs746282174 | snp | C/T | 1.65671e-05 | 0.00287807 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400085 | CTGGTAATTATTTAA[C/T]TTGGGACTGAGTTTG | 8853 |
rs746301574 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279985 | CCTACGAGTGATACA[A/G]AATATTTTTTAAAAG | 8853 |
rs746303296 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9306627 | AGCTGTGGAGATCCT[-/G]TGCCCCTTTGTCCTC | 8853 |
rs746317455 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275177 | CCTCCAACTTCTGGA[-/T]TTAAGTGATCCTCCC | 8853 |
rs746319568 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9308018 | GCAATTCTGTGGCCC[-/A]GGGGATCTGTTCACT | 8853 |
rs746320644 | snp | A/T | 1.64863e-05 | 0.00287104 | missense | ASAP2 | GRCh38.p7 | 2:9388439 | TGCCCAGCATCTTGC[A/T]GAATGAGACTTACGG | 8853 |
rs746342296 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | ASAP2 | GRCh38.p7 | 2:9344574 | TATAGCTTACATCAG[C/T]CTCAGGGAAACAAGG | 8853 |
rs746353773 | snp | A/G | 0.000115667 | 0.00760396 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297492 | TACTTCAGTTGGGAA[A/G]GTGGCTCAGTAGAGG | 8853 |
rs746374721 | snp | C/T | 1.6522e-05 | 0.00287414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279435 | GTGTGGAAAATGTCG[C/T]ATTTGAAGTCCTGGT | 8853 |
rs746385363 | in-del | -/CCGTGG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239037 | CAGCCCCTCTCTGTC[-/CCGTGG]CCGTGGCGTTAGCAG | 8853 |
rs746407542 | in-del | -/TC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276538 | GTGTCATCTTTTTTT[-/TC]TCTTTTTTTTCTTTT | 8853 |
rs746408558 | snp | G/T | 1.6498e-05 | 0.00287206 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376862 | GTTGGACACAGAATT[G/T]AATGCTCCCATTAGA | 8853 |
rs746414062 | snp | C/T | 1.66371e-05 | 0.00288414 | missense | ASAP2 | GRCh38.p7 | 2:9388498 | GCCCAGCCTGCAGCC[C/T]CCAGCACCACCAGCG | 8853 |
rs746427113 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321721 | AAGAGTGCCTGAGAG[A/T]GTCATCTGGTTCTGA | 8853 |
rs746429383 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350315 | TCTGTCACCACTTCA[A/G]ACAGTAGGAAAATAA | 8853 |
rs746434783 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383851 | AAAAAGGATGAGTTC[A/G]TGTCCTTTGTAGGGA | 8853 |
rs746508837 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369632 | GTGGTGAGGCTGGGT[C/G]AGCGTGTCCTGGCAG | 8853 |
rs746510356 | in-del | -/AAAAG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325214 | AGAGGTTGCATTCTC[-/AAAAG]AAAAGCACATACCAT | 8853 |
rs746513141 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212228 | TCTTTGGAGGGACCT[A/G]CAGTCCAGCAAGAGG | 8853 |
rs746522288 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212619 | TCCCATGCACCCCAC[A/G]TTTCCAGGCACCGGT | 8853 |
rs746542797 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350955 | TGCTCTCCTCTGGGG[C/T]GTCCTTCACATTTCA | 8853 |
rs746557811 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257886 | GGTTTATCCTTACCT[A/G]TGTGGCCTTGGAAAA | 8853 |
rs746588714 | snp | C/T | 8.52806e-05 | 0.0065294 | missense | ASAP2 | GRCh38.p7 | 2:9393601 | AGGCCCCCACCTCTG[C/T]CCCCACAGCCGCCCA | 8853 |
rs746594301 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9246042 | GGGTGGTGTGACCCC[A/G]TTGGGGGAAGGAGCT | 8853 |
rs746597674 | snp | C/G | 1.65102e-05 | 0.00287312 | missense | ASAP2 | GRCh38.p7 | 2:9385276 | CTGGAAGATTTAATT[C/G]TCACGTTCACGTTGA | 8853 |
rs746598783 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9357896 | AAACAGTTCTGAAGA[C/G]AATTGTATTTATGGG | 8853 |
rs746600217 | snp | A/G | 3.00332e-05 | 0.00387501 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9393531 | CAAGACGCCCAGCGT[A/G]ATGGAAGCCTTGAGC | 8853 |
rs746601382 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9398538 | AAAGGCCAGGCACAG[A/T]GGCTCACACCCGTAA | 8853 |
rs746629349 | snp | C/T | 1.7161e-05 | 0.0029292 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327948 | TATCTTAAATGTTTG[C/T]TCATGTGTGGCAACT | 8853 |
rs746657294 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9246982 | TGTAGCTGGGGCCAC[A/G]GTATATACTACCACA | 8853 |
rs746680633 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9259092 | GTCCAGCCCGTGGGA[C/T]GGAGGTTCAGCCTCT | 8853 |
rs746687539 | snp | A/G | 5.2493e-05 | 0.00512286 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385409 | TCAGCTTCATCCAGA[A/G]CAGTGTGGGTCCTAA | 8853 |
rs746693166 | snp | C/T | 5.36596e-05 | 0.00517947 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207221 | GAACACTGTGGCGGC[C/T]ATCGAGGAGGTGAGG | 8853 |
rs746719101 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9334813 | TACGGATCTTCACAC[A/G]GTGAGTAGCTTCCCT | 8853 |
rs746748253 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9220064 | TTATGGCTGAATAAT[A/G]TTCTATCAAATGTGT | 8853 |
rs746786215 | in-del | -/GCCGG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9292832 | CGTCACATCCCTGTT[-/GCCGG]GCTGGAAATAGTAAG | 8853 |
rs746797916 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9375202 | TGAGAGGAATCGGTT[A/G]AGCCCAGAAATTTGA | 8853 |
rs746804718 | in-del | -/GCGGCGGCGCCCCTGCGGCTGT | 2.96375e-05 | 0.0038494 | utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207058 | GCTGCGGCAGTTGAG[-/GCGGCGGCGCCCCTGCGGCTGT]GCGCCAGCGCCCTCG | 8853 |
rs746819885 | in-del | -/T | 1.78131e-05 | 0.00298433 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350779 | CACCCAACCCCAACC[-/T]TTTTTTGTTGTTTTT | 8853 |
rs746831456 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358697 | ATGCAGGAAGAAAGA[C/T]GTGACTCCTGACCCT | 8853 |
rs746834399 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233923 | TGAGACCAGCTTGGC[C/T]AACACGGTGAAACCC | 8853 |
rs746841256 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348651 | TGTCATTTTTTAATA[C/T]GTAGGCACATTTATG | 8853 |
rs746850972 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9385006 | TTGAGAGTTACGAGC[C/T]GGGAACTGTGGATGA | 8853 |
rs746863587 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277456 | GAGATAACCACTTGG[A/G]AAAATACGAGTTAAC | 8853 |
rs746865148 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264560 | CAGAGCTGTCTTCTC[A/G]CTCATCATTTATTAA | 8853 |
rs746884992 | snp | A/G | 1.65869e-05 | 0.00287979 | missense | ASAP2 | GRCh38.p7 | 2:9401308 | GGGTGAAAGCGCTCT[A/G]TAACTGTGTGGCTGA | 8853 |
rs746893842 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205477 | TGATAAAAGCTATCC[A/C]CGAATACAGCGATTT | 8853 |
rs746897454 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9262335 | CGTCTTCTTAACGGC[C/T]ACTTTAATTGGCGTA | 8853 |
rs746909056 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365056 | ATTGAGCACCAAAGC[A/G]TGTACTTACTTACAT | 8853 |
rs746915310 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294873 | CAGAAAGCAGCGAGC[A/G]AGGGAGTAAGCAGGA | 8853 |
rs746930282 | snp | C/T | 1.74464e-05 | 0.00295345 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350924 | TGAGATGCCGCGCCA[C/T]AGAGACGTTGTCTTA | 8853 |
rs746938965 | snp | A/T | 1.6489e-05 | 0.00287128 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374881 | GAGAGATATTTTTGG[A/T]TTGCTCCAAGCTTAT | 8853 |
rs746939292 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9287747 | CCTGGAGATGTCTTC[C/T]AGTTGTGAGACTCTG | 8853 |
rs746953062 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265536 | CGAAAAAATTATCAA[A/C]TAATGTATTCATGTT | 8853 |
rs746960471 | snp | C/T | 3.32552e-05 | 0.00407756 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9350813 | TTTTAAACAGGCTAA[C/T]CGGCCTCCTGCAAAG | 8853 |
rs746966262 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391110 | AGACAAACTCTGTAA[A/G]TGTGGACGGTGGAAG | 8853 |
rs746974069 | snp | G/T | 3.53888e-05 | 0.00420632 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401421 | GGGTGGGCCTGGGAG[G/T]TTCCTGGGGGCTGAG | 8853 |
rs747012985 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311599 | AGCATGAAAATGTCA[-/T]TTACTCATAAATTGA | 8853 |
rs747040685 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353410 | AAAAAATTTAAAAAT[A/G]GTGCAGTATGGTGAC | 8853 |
rs747041311 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9312647 | TGAAGTTCCATGGTG[G/T]CTCATTCCTGGCTCT | 8853 |
rs747069224 | in-del | -/AT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254237 | AAAAAAAAAAAAAAA[-/AT]ATATATATATATATA | 8853 |
rs747091069 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366644 | TGCAACGCAGCCTCT[A/T]GGCTTTTGCCTCCTG | 8853 |
rs747093974 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365845 | TCATGCCCAGCACAG[A/T]CGAGGGGCTCAGAGT | 8853 |
rs747139980 | snp | C/T | 1.65732e-05 | 0.00287859 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380821 | CTGGTGAGTCTCCCA[C/T]CACAAGGACGGGGTG | 8853 |
rs747141739 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9393154 | GAGCTGAGGGCCCCG[A/G]CCTCCTGCTGTTGGG | 8853 |
rs747144150 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395073 | CCCTGGAAGCTGGCA[C/T]GGAATGACTTCCGCC | 8853 |
rs747145838 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9283629 | ACACTTAGATGGCTC[A/G]GGCTGCTATAACAAA | 8853 |
rs747174823 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240976 | AAAGGGAGGAGTCAC[A/G]TCCCGCGTGGGAGGC | 8853 |
rs747205822 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381686 | AAGCTACAGTGAGCC[A/G]TAATGGTGTCACTGC | 8853 |
rs747236741 | in-del | -/TGTT | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406140 | CAGGCCTTCAGTGTG[-/TGTT]TGTCACTGAGTGGAC | 8853 |
rs747238535 | snp | G/T | 2.49367e-05 | 0.00353097 | utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207080 | CGCCCCTGCGGCTGT[G/T]CGCCAGCGCCCTCGC | 8853 |
rs747239453 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278319 | GGAGTTTGAGACCAT[A/C/T]CTGTCTAACATGGTG | 8853 |
rs747259935 | snp | A/C | 1.65872e-05 | 0.00287981 | missense | ASAP2 | GRCh38.p7 | 2:9400784 | GTCCTCTGTCCAATG[A/C]TATGGTCCTGCAGCC | 8853 |
rs747265572 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322079 | CACCTTGGAGTTGTA[C/T]AATTCTAGTCCCAGG | 8853 |
rs747266776 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | ASAP2 | GRCh38.p7 | 2:9344604 | GAACATGGGACCGAG[C/T]GGAACGGCAGCCTCT | 8853 |
rs747286891 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9342643 | CAAGTGACAAATGAA[A/G]CAGTAGGTAAATGGG | 8853 |
rs747290099 | snp | A/C/T | 3.29773e-05 | 0.00406051 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344670 | TAGAGTTTAAATGTA[A/C/T]GTTCGTTATCTTGTG | 8853 |
rs747322711 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373031 | AAAACTCATGGCACT[A/G]TTGAGGGAACCCACT | 8853 |
rs747324413 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9354728 | CAGGAACCAAGTTCT[A/G]CTGCTGGCTATGCTT | 8853 |
rs747358128 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249488 | AGGGACTCTCATGAC[A/G]CCATGCCTGCTCCAG | 8853 |
rs747377048 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343388 | GGAAATAGAATTTCC[C/T]GCACTGGCACTGGTG | 8853 |
rs747386655 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9399953 | TCAGAAGGTTCTCTG[A/G]TAAAAGGGGATGAGA | 8853 |
rs747387012 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214584 | GTTTTTATCATGTCA[A/G]CAATGTCTTGGAATA | 8853 |
rs747413657 | in-del | -/TGTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258334 | ATAGTAATCAGTAGT[-/TGTT]TTTTTTTTTTTTTTT | 8853 |
rs747424730 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9388098 | GTGTGTTTCCTTCAC[A/G]AGACACAAGGAGGAG | 8853 |
rs747447489 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279785 | CTCTTTTACCCAGTC[G/T]TGCCTTTTCTAGTAT | 8853 |
rs747456061 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9308596 | TCTAGGATGGCAGCA[C/T]GTGCCCAGCCTCAGC | 8853 |
rs747456668 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362139 | ACCCCCAGGGAGGCC[A/T]TGCATGGTCTGTCTG | 8853 |
rs747457549 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9376979 | TCACATTGTAGACTT[C/T]TTAGTTCAGAACAGG | 8853 |
rs747477982 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9401801 | TGTGGCCGCCCAGGC[A/G]TCCAGCAGGGTGTGG | 8853 |
rs747482640 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237201 | AAGCCCTGTTTTGTA[C/T]ACATTTTGATGGTTA | 8853 |
rs747492776 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341802 | GCCCTTCTGAGAAAA[C/T]GTGGAAGCTGGGACC | 8853 |
rs747498756 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9290837 | CTGTTTCCTTGTCCA[C/T]TCAGAGGAGAATAAA | 8853 |
rs747501724 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402566 | CCATCCGGAAGGGGC[A/G]CCAACCTGACCACAG | 8853 |
rs747506762 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9319526 | GAAAGGCGCAGGTGC[A/G]CACAGGGAGCAGGGC | 8853 |
rs747514583 | snp | A/G | 1.67992e-05 | 0.00289816 | missense | ASAP2 | GRCh38.p7 | 2:9356294 | AAGGAGATCATCTCA[A/G]AAGTGCAGAGGATGA | 8853 |
rs747536564 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225627 | TTAAGGGCTTTTGCG[C/T]AGGGGAGTGACATGA | 8853 |
rs747542996 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278918 | GAAGGGGTGCAGGCA[C/T]GATAGGAGTCCCTGG | 8853 |
rs747543278 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328357 | TTAGGGATTATATCT[G/T]AATTAAAAATAAAAG | 8853 |
rs747562762 | in-del | -/AG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234955 | TTTGGGGAAGTGATA[-/AG]AGAGGAATTTGAGAA | 8853 |
rs747596392 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9292181 | GAGGAGGTGGGGACA[A/G]TGAGACCTGTGCTGC | 8853 |
rs747624248 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9309736 | TGATGGGAATAGTGT[G/T]TATCTGCTTTACTGA | 8853 |
rs747643025 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378612 | CGCAGCCAGTGGGAC[A/G]TGAGAAGGACGCTGG | 8853 |
rs747659431 | in-del | -/TC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9319847 | GGATGTGGCGGCCTT[-/TC]TATTTCTGTCGTTGG | 8853 |
rs747660435 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397857 | TCCGCCTCCCGGGTT[C/T]ACGCCATTCTCCTGC | 8853 |
rs747673569 | in-del | -/TT/TTT/TTTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266147 | GATTGCCTTTTTATC[-/TT/TTT/TTTT]TTTTTTTTTTTTTTT | 8853 |
rs747678172 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9238372 | GCTTGATATTTGACA[A/G]TACTCCAGGCTTTTG | 8853 |
rs747697797 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243860 | TAAGTAATTAGGAAA[C/T]AGTGTAGTAAAAATA | 8853 |
rs747715454 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325609 | CATAGCCATGACTTG[A/G]GGAGTAATTGGTTCC | 8853 |
rs747730338 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368775 | GTAGAGAGCCTCACT[C/T]GCCACTGGTGGGTGG | 8853 |
rs747734064 | snp | C/T | 3.30874e-05 | 0.00406726 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388267 | CATATTTGTCTCACA[C/T]GCCTCTGCCCCAATG | 8853 |
rs747756983 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257858 | AAAAAAGAGAATACA[A/G]AGGTGGCATTTTGGT | 8853 |
rs747771023 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243983 | GTGGGAACATGATAT[A/G]TATATAAACTCATCA | 8853 |
rs747774488 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9285818 | GAGTGATATTCCTAC[C/G]CTCAATCAGAATATC | 8853 |
rs747805201 | snp | A/G | 1.65102e-05 | 0.00287312 | missense | ASAP2 | GRCh38.p7 | 2:9374900 | CTCCAAGCTTATGCT[A/G]ATGGTGTGGATCTTA | 8853 |
rs747837031 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9386308 | CTTAGAATACAGAAT[A/G]AGAAATTACTTCACT | 8853 |
rs747838649 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9355643 | ATTTCTCATACTAAT[A/C]TTTTTCTGAGAAAGC | 8853 |
rs747844423 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9292448 | ACTTGAACCCAGGAG[C/T]TGGAGGTTGCAGTGA | 8853 |
rs747876261 | snp | C/T | 1.66029e-05 | 0.00288117 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9401333 | GGCTGACAACCCCGA[C/T]GAGCTCACCTTCTCC | 8853 |
rs747885168 | snp | A/G | | | intron-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212053 | CCTGCCCCCTGGTGA[A/G]TGCTGAATTCAGTTT | 8853 |
rs747897589 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325788 | ACTTGAGCCATCTTT[C/T]GAGCAGTCCTCAGGT | 8853 |
rs747900466 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212524 | GTGGTGGCCAGCTCG[A/G]CGTCTGCGGTAGGAT | 8853 |
rs747908895 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327380 | TTTTCCAACAATCAC[A/G]TTATTTTCCTTGTAA | 8853 |
rs747916242 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346348 | GCTTGAGGCAGGAGA[A/G]TTGCTTAAACGCAGG | 8853 |
rs747928952 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9356413 | CTGATTCACAGAATC[C/T]GTTCATTGATTTTCA | 8853 |
rs747944797 | in-del | -/CT | 6.20854e-05 | 0.00557125 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378916 | CTGTGACACACTATG[-/CT]CTCTCTCTGTTCCTG | 8853 |
rs747950048 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275635 | GATCCATTACCCTCC[C/G]TGTGGCCTGAGTAAC | 8853 |
rs747950855 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383979 | GAGAACACTTGGACA[C/G]AGGGCGGGGAACATC | 8853 |
rs747952808 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9398468 | GGTGAACTGATTGCC[A/G]CACTGCACTCGAGCT | 8853 |
rs747957388 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9357655 | TTTAAAATGCCAAGA[C/T]AGTGTGGGTAATATA | 8853 |
rs748007840 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9396805 | CCAAGAGTTCAAGAC[C/T]TGCATGGCCAACATG | 8853 |
rs748008024 | snp | C/T | 3.53676e-05 | 0.00420506 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350933 | GCGCCATAGAGACGT[C/T]GTCTTATGCTCTCCT | 8853 |
rs748043170 | snp | G/T | 0.000322361 | 0.0126916 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401430 | TGGGAGGTTCCTGGG[G/T]GCTGAGCCACGTCCC | 8853 |
rs748050759 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9218682 | TCCTGCCTCAGTTGC[A/G]TCATTTGTAACATGG | 8853 |
rs748051503 | in-del | -/T | 1.6473e-05 | 0.00286988 | splice-donor-variant | ASAP2 | GRCh38.p7 | 2:9356096 | CAGGAATGTCAAATG[-/T]TAAGTTACATGGTGG | 8853 |
rs748052568 | snp | C/T | 1.64852e-05 | 0.00287094 | missense | ASAP2 | GRCh38.p7 | 2:9323173 | CTCCATGGGATGATT[C/T]GGACTGAAATAAGCG | 8853 |
rs748059608 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373963 | CTGCAGGTGTGTTGA[C/T]GCACATACGTCTCAT | 8853 |
rs748070244 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9304401 | TGTTTGCCAAATCTA[C/T]AAGGTACTGTGTGGA | 8853 |
rs748073717 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233172 | TGGGAGGTTAACCCT[G/T]GTGGTTGCTTTGGTG | 8853 |
rs748090747 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9246538 | CTCAAACAATCAGCC[G/T]TGGCCTCCCATGCCA | 8853 |
rs748095534 | snp | A/G | 4.94173e-05 | 0.00497053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356105 | TCAAATGTAAGTTAC[A/G]TGGTGGTGGGACTTT | 8853 |
rs748114794 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9292616 | AATGCCTGTCTGTTT[C/T]TGTGATCTGCTCCTT | 8853 |
rs748115424 | snp | C/G/T | 0.000158847 | 0.00891082 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393477 | TCTCTCCCTGTCCTC[C/G/T]GCAGATCCCCTGACC | 8853 |
rs748116751 | snp | C/T | 3.31857e-05 | 0.00407329 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323083 | CGTTGAGTTCTGTGC[C/T]AACAGGCATCTTGAT | 8853 |
rs748123874 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9293689 | GGGATGGCTGTTGTC[A/G]TGGTGGGCACCGTGC | 8853 |
rs748185996 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9335435 | GTGCTCTGTCAGTTG[C/G]TAGATAAGGAGCTCT | 8853 |
rs748205150 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239828 | CCTTTCTGGGCTCAA[A/G]TGATCCACCCACCTC | 8853 |
rs748225995 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209234 | ACTTTAAGCAAATCT[A/G]CATACATGCTATGAT | 8853 |
rs748226896 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362709 | TAGCTGGGAGTGGTG[A/G]CAAGTACCTGTGGTC | 8853 |
rs748233938 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279500 | GCTAGACTCCTTTAT[C/T]GGGGCATGCAGATCA | 8853 |
rs748238509 | snp | C/T | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404149 | CACACAGAAAGCAAC[C/T]GTACACAGTAGAATT | 8853 |
rs748240939 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333539 | CAGGTGAAGCAGACA[C/T]ACCTTAGGAGAAGGC | 8853 |
rs748243468 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9392667 | ATGATAAAAAGAAAG[A/G]TCATAAGCTGGATCC | 8853 |
rs748244965 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219807 | ATCACCACTATTTAA[G/T]TCCAGATCATTTTCA | 8853 |
rs748276692 | snp | A/T | 1.72862e-05 | 0.00293987 | missense | ASAP2 | GRCh38.p7 | 2:9374758 | GTTTGGTTTCAGGAA[A/T]GCAAGAAAGGACTAC | 8853 |
rs748314154 | in-del | -/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9223082 | CTGCATCTCTCAAGT[-/CA]CACTTGCAAGCGACT | 8853 |
rs748322781 | snp | A/C | 1.67711e-05 | 0.00289573 | missense | ASAP2 | GRCh38.p7 | 2:9388514 | CCAGCACCACCAGCG[A/C]CCCCCCGCTTCCTCC | 8853 |
rs748333729 | snp | A/T | 1.69902e-05 | 0.00291458 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400864 | TTCCTGCCTCTCTGC[A/T]CTAGCCAGGGGGGTG | 8853 |
rs748337706 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365656 | ACAGACGACTCCCCC[A/G]TATGGTGAGTGCCAA | 8853 |
rs748355791 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9392700 | TCATGTTTCCCCACG[C/T]CAGTTTCCTCTCTGT | 8853 |
rs748359656 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272638 | ATTCTTTGCCCAGAC[C/T]AGTGTCCTGCAGTTT | 8853 |
rs748368782 | snp | C/T | 1.64868e-05 | 0.00287109 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344673 | AGTTTAAATGTACGT[C/T]CGTTATCTTGTGTCC | 8853 |
rs748377124 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405558 | TATATATTGTATAAC[C/T]GAAATTGATTATTTT | 8853 |
rs748383099 | snp | C/T | 5.51476e-05 | 0.00525079 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350761 | TATGATTTTCCATTC[C/T]TTCCACCCAACCCCA | 8853 |
rs748403640 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9246408 | CCTCCTGCCTTGTTC[-/T]CCCAAGTAGCTGGAG | 8853 |
rs748403945 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311763 | GCCTGCCCGCCACTC[A/G]GGCTGCAGGGCACAC | 8853 |
rs748404445 | snp | C/T | 0.000692738 | 0.0185981 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9391015 | TTGTTCGTGTGTGCA[C/T]GTGTATGTGTGCGTG | 8853 |
rs748420875 | snp | A/C | 0.000116089 | 0.00761781 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323085 | TTGAGTTCTGTGCCA[A/C]CAGGCATCTTGATGT | 8853 |
rs748422604 | snp | A/G | 1.66882e-05 | 0.00288857 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320248 | TCTTGCACAGAAGTG[A/G]ATGATTAGTCTTGCC | 8853 |
rs748432016 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351557 | GGGGAAGAAAGGGCC[A/G]GTCTCCCCTTTGAAG | 8853 |
rs748445127 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381530 | TGGCTTGAGGCCAGG[A/G]ATTCGAGATCAGCCT | 8853 |
rs748480745 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9299946 | TTTGAAGAGCTAATA[C/T]CTGGCCCGGCACAGT | 8853 |
rs748485366 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9342481 | GGAACTTGGTCCCTT[A/T]CCTCACACCATAATC | 8853 |
rs748502055 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9252777 | AAAAATTAGCCAGGC[C/G]TGGTGGCGGGCGCCT | 8853 |
rs748505004 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9375175 | TAGTCCCAGCTACTC[A/G]GGAGGCTGGGGTGAG | 8853 |
rs748510623 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370815 | TGGAGAGTTACTCAA[C/G]GTGAAGGAGCTCTTC | 8853 |
rs748538343 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353121 | TGATTTGATGAACAT[C/T]CTGAGAAGGTGAGGG | 8853 |
rs748590454 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9259457 | GGGGTGCCCCTCTCT[G/T]CAGGCTCCCACCCCT | 8853 |
rs748592272 | snp | C/T | 1.83165e-05 | 0.00302621 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356368 | AGGGACCCCACCCGA[C/T]CCTGGGCTCTAGGAC | 8853 |
rs748598473 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371826 | CCTGTCATTAAAAAA[A/G]AGAGGGAGGGCCGGG | 8853 |
rs748651944 | snp | A/G | 1.91727e-05 | 0.00309612 | splice-donor-variant | ASAP2 | GRCh38.p7 | 2:9379060 | CCTCCATCGAGATAG[A/G]TGAGTGGGCCCGGGC | 8853 |
rs748653584 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214532 | GGCGTGAGCCGCTGC[A/G]CCCGGCTGCCTTTCC | 8853 |
rs748663101 | snp | G/T | 1.64868e-05 | 0.00287109 | missense | ASAP2 | GRCh38.p7 | 2:9334738 | TCTTTTTCCTGCTAG[G/T]TTTTTTCAGGATGGA | 8853 |
rs748667534 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9329959 | CGTCTGCTTGTCTCC[A/G]TGATGACATCTTCCT | 8853 |
rs748676800 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250567 | ACAGGGCACATTGCA[C/T]GGCCCCCAGGGCAAA | 8853 |
rs748678400 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260564 | GACCTTGTTTGCATC[A/G]TCACACTCCTTTTTT | 8853 |
rs748679566 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9288551 | GTGGCAAAAATGAAG[G/T]GCTGAAAGCTGCTTA | 8853 |
rs748711733 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211046 | TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGGCA | 8853 |
rs748713553 | snp | C/T | 4.84015e-05 | 0.00491919 | missense | ASAP2 | GRCh38.p7 | 2:9393619 | CCACAGCCGCCCAGC[C/T]GCCTCCCGCAGAAGA | 8853 |
rs748766520 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307519 | GGTGCCTGAGTCCTG[G/T]GTTCTCCAGTGCTGC | 8853 |
rs748767448 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221658 | ATCTTATGGCCTACA[A/G]TTTGCTGAATTTGTT | 8853 |
rs748770214 | in-del | -/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9216288 | TCAGTTCATATTTTT[-/TT]TTTTTTTTTTTTTCT | 8853 |
rs748772681 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361875 | TGGCCTCAAGCCTTT[C/T]AAAAGTATCCAGATT | 8853 |
rs748801559 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236775 | TTGGAACTATAATTA[C/T]TTGTCAGCACAGTTA | 8853 |
rs748808013 | in-del | -/CCC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9356830 | TGTAAAGTGAAGGGA[-/CCC]CAGGACCCTTTCAGC | 8853 |
rs748839001 | snp | C/T | 1.64811e-05 | 0.00287059 | missense | ASAP2 | GRCh38.p7 | 2:9388424 | AGCAGAGGGCTTTCA[C/T]GCCCAGCATCTTGCA | 8853 |
rs748841789 | in-del | -/GTGAGGAGCTG | 1.65081e-05 | 0.00287293 | frameshift-variant | ASAP2 | GRCh38.p7 | 2:9380798 | TCAAGCACGAGCACT[-/GTGAGGAGCTG]GTGAGTCTCCCACCA | 8853 |
rs748845336 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9268830 | GCTGCCTGAGTGCTG[C/T]AGGCCTCTGCTCTCC | 8853 |
rs748848964 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9401754 | GACCTAGAGCGCAGA[A/G]CCCCAGGCCTGAGTC | 8853 |
rs748882499 | snp | A/G | 5.71162e-05 | 0.00534367 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374993 | AAAAAAAGGCCGGCC[A/G]CGGTGGCTCATGCCT | 8853 |
rs748898474 | snp | A/G | 1.6473e-05 | 0.00286988 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356121 | TGGTGGTGGGACTTT[A/G]GGCTGGACTCAGCCG | 8853 |
rs748912000 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254798 | TTCCCTGAAGATAAG[C/T]GGTACTACTTGTTAT | 8853 |
rs748947013 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279722 | ATTCATTCCTGCCTC[C/T]GTCATTTGGTTTTTG | 8853 |
rs748956901 | in-del | -/AC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302145 | TTTTTTTTTTCCCAA[-/AC]ACAGATGATGTGAGT | 8853 |
rs748975183 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267762 | AATTAGCTGGGCGTA[A/G]TAGTGCACACCTGTA | 8853 |
rs748978610 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284817 | GGAGGGGTGAACTTA[A/C]AATTTTAGATGTAAG | 8853 |
rs749036056 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9297222 | ATGTGTTCAGTGTTA[C/T]TCACAACCGAGAAGA | 8853 |
rs749040749 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337051 | GTTATTTACAGCTTC[A/G]CAGGAAAGTAATAAC | 8853 |
rs749054003 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338085 | ACGTCGTCCATCCGA[C/T]GGTGTTCTGCCAGGA | 8853 |
rs749063387 | snp | A/T | 1.65225e-05 | 0.00287419 | missense | ASAP2 | GRCh38.p7 | 2:9356243 | TTTAAGGGGGATGAC[A/T]ATACTGGAGAAAATA | 8853 |
rs749064988 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281407 | TTTGAAGGGAGAAGG[C/T]GCTAGTGCTTCGGTG | 8853 |
rs749068388 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9367430 | TCAAAGCACTGAGCT[C/T]GGTGCTCCCTTTTGG | 8853 |
rs749068561 | snp | A/G | 1.65924e-05 | 0.00288027 | missense | ASAP2 | GRCh38.p7 | 2:9403316 | TCATTTGTGCACTTT[A/G]TCGCTGACTGAATTG | 8853 |
rs749069883 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9372068 | CCAAGCCCTGGGCAG[A/T]TGAGTAAATACATTA | 8853 |
rs749070817 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243702 | TGAGGCAGAATGCAT[G/T]TATAACCAGGGCATT | 8853 |
rs749082822 | snp | C/T | 4.9458e-05 | 0.00497258 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9368427 | TTCATTTTTGCAGCT[C/T]GCCAAGAATATTGGG | 8853 |
rs749098421 | in-del | -/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317161 | ACACCCACTCACATC[-/CA]CACTCTCACCACACT | 8853 |
rs749117227 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397269 | AGCTCCCAGCAGTTA[C/T]TGGGACTCTGAGAAC | 8853 |
rs749120423 | snp | C/T | 0.000115564 | 0.00760055 | missense | ASAP2 | GRCh38.p7 | 2:9393515 | CGCCCCCACCCGTTG[C/T]CAAGACGCCCAGCGT | 8853 |
rs749134823 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9396690 | TTAAATGCTACTTTG[A/C]AAGATAACTTTCTAA | 8853 |
rs749138022 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378556 | GGCATCCAGAGGCCC[G/T]GCATCCAGCACAGCT | 8853 |
rs749154370 | snp | A/T | | | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214988 | GGAAACTAATCACAG[A/T]CATGCATTGCTTAAT | 8853 |
rs749174484 | snp | G/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405909 | AATGTCACTGTTCCA[G/T]ACCAGCATGAATCCT | 8853 |
rs749192275 | snp | A/G | 4.99838e-05 | 0.00499894 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380839 | CAAGGACGGGGTGGG[A/G]CACCTGTCACGGGAC | 8853 |
rs749196567 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383129 | GACTGTTTGAGTCAT[G/T]AGTCAGGTTCAGTGG | 8853 |
rs749198073 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244660 | CTGAAGGACAGAATC[A/G]CTAACCTGGGCTTTT | 8853 |
rs749200144 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230540 | TTTCCCTGGGCAGAC[A/T]CAGCCTCCTGCAGGA | 8853 |
rs749215680 | snp | C/T | 1.68354e-05 | 0.00290128 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385242 | ATCCCTCTGTTCTCT[C/T]AGCTGACCCAAGCCT | 8853 |
rs749219421 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274858 | CTGAGTTCAGGAAGC[A/C]CTACTTCCTCTTTGG | 8853 |
rs749220250 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243478 | TAGGAACTCAGACGG[-/A]AAATGTGACTGAGTC | 8853 |
rs749227171 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275519 | CTTTTCCAGAACGGC[C/T]ACTGCCCAGCTTTAG | 8853 |
rs749256636 | snp | G/T | 1.65403e-05 | 0.00287574 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368551 | CTATTCTCATTTGCT[G/T]AGTAAAGGTTTGCCT | 8853 |
rs749260978 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327081 | CTTTCCACCTCCTCC[A/T]TGGGCTGCAGAGAGA | 8853 |
rs749282876 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332341 | CGCCAGGGCTGACTG[C/T]ACTTTGAAGGGGCGT | 8853 |
rs749286096 | snp | A/C | 1.67536e-05 | 0.00289423 | utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207085 | CTGCGGCTGTGCGCC[A/C]GCGCCCTCGCGCCGA | 8853 |
rs749302239 | snp | A/G | 5.12229e-05 | 0.00506052 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9356311 | AGTGCAGAGGATGAC[A/G]GGCAATGACGTCTGC | 8853 |
rs749316058 | snp | A/T | 1.77735e-05 | 0.00298101 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350780 | CACCCAACCCCAACC[A/T]TTTTTGTTGTTTTTT | 8853 |
rs749323389 | in-del | -/ACAT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317883 | TACCCACATTCACTC[-/ACAT]ACACCCTCATGTGCA | 8853 |
rs749335173 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345562 | ACATGGGCTGGTAGA[C/G]AGCTTTGGTAACATC | 8853 |
rs749357463 | in-del | -/TCAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317040 | TGCAATCATTCCCAA[-/TCAC]TCACATCCACACTCC | 8853 |
rs749363693 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383893 | CTGGAAACCATCATT[C/T]TGAGCAAATTATTGC | 8853 |
rs749395095 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346084 | GTCATGTGATCACCA[C/G]CGTACTCCCCCTGCC | 8853 |
rs749438448 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263354 | AAAGCAGGGCACCAG[A/G]CTGGCTGGGGGGGTC | 8853 |
rs749444603 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9363501 | TGTGAGATGATCGTG[A/G]TTTTAATTTGCATTT | 8853 |
rs749449031 | snp | A/G | 1.65883e-05 | 0.00287991 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9401291 | CAAGTTGAAGCCTAA[A/G]CGGGTGAAAGCGCTC | 8853 |
rs749461543 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9259595 | GAACAGCACCATCTG[C/T]ATCTCTTTGGCCCTC | 8853 |
rs749471675 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391082 | ACAGCCTCCTCTGCT[A/G]ACACCCTGTGGAAGA | 8853 |
rs749481167 | snp | C/T | 1.66181e-05 | 0.00288249 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320267 | ATTAGTCTTGCCTAA[C/T]TTATTATTCTTTGTT | 8853 |
rs749482378 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402832 | GCCTTCCACAAGTAC[G/T]TAACTCATTGAAATG | 8853 |
rs749491038 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281665 | GAAGGAAGGCCTCTG[G/T]GGGCTTCAGAATTTT | 8853 |
rs749513034 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321109 | TCTGTGTCTTGGAGT[G/T]CTCTGAATGGAAATA | 8853 |
rs749514452 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321936 | TATCCCAAGAGGTTT[C/T]GTGATATGTAACAAC | 8853 |
rs749554920 | snp | C/T | 1.90685e-05 | 0.0030877 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374994 | AAAAAAGGCCGGCCA[C/T]GGTGGCTCATGCCTG | 8853 |
rs749556478 | snp | C/G/T | 4.56749e-05 | 0.00477868 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379078 | AGTGGGCCCGGGCCC[C/G/T]GGGGGTGGGCTCAGC | 8853 |
rs749559753 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332611 | ACGCGCTCTCACTCT[C/T]GCTCTCTGTCTGACC | 8853 |
rs749564735 | in-del | -/GTG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362565 | TCTCTTGAGCCTGGT[-/GTG]GTGGCCGGCGCCTGT | 8853 |
rs749567492 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333430 | AGAAAGTATAAGAAG[G/T]CCTCTTATAGGGGAA | 8853 |
rs749568960 | snp | A/G | 1.68655e-05 | 0.00290387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320386 | TAATTTGGGATTTCA[A/G]ATTTAAACCAACCTC | 8853 |
rs749582579 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351451 | TGAATGTTTACTCAG[A/C]ACCCCCTAAATTAAA | 8853 |
rs749587714 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9310901 | GCTCATCAGCTGTGA[C/T]ATTAGCATAATGATT | 8853 |
rs749608639 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365577 | GTAGGTGCTAAGGAC[A/G]TACAGGTGTGTGATT | 8853 |
rs749614385 | in-del | -/CCT | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278312 | AGGTCAGGAGTTTGA[-/CCT]GACCATCCTGTCTAA | 8853 |
rs749631364 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225919 | TTCCCCCTTCCCTTC[C/T]TCCTTTCATAGAGCA | 8853 |
rs749649823 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361870 | GCGCTTGGCCTCAAG[C/T]CTTTTAAAAGTATCC | 8853 |
rs749671945 | in-del | -/T/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217620 | TGTTTTTGTTTTTTG[-/T/TT]TTTTTTTTTTTGAGA | 8853 |
rs749684889 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350367 | GTGAAATTACCTTCA[C/T]TGGAAGTGAGGTTTA | 8853 |
rs749697109 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205004 | ACAGCTTTGCAATTT[C/T]ATTTTTTTGAGGCTA | 8853 |
rs749702782 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369870 | TTTTTTTTTCCCCTT[C/G]AAGACCTCTTGCCCA | 8853 |
rs749723079 | snp | A/G | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390817 | ACTCAGGAATTTTAA[A/G]TTTCATGGATTGAGA | 8853 |
rs749728984 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9282340 | TATTTCGGAACAAGC[A/G]TTGTCTACTGCAAAG | 8853 |
rs749746620 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279545 | ATGTTTCTTTTTCAG[-/A]AAGTATGTTTTGTTT | 8853 |
rs749756259 | snp | G/T | 1.66999e-05 | 0.00288958 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335057 | CCTCAGTCTTAATTT[G/T]CTGATTGGTTCTGTT | 8853 |
rs749759861 | snp | C/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212708 | CTAAGACAAATCCAG[C/G]TCTCAGCCGCCACAT | 8853 |
rs749810682 | snp | C/G | 0.000217925 | 0.0104362 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368381 | GTGTAGCAGTAGAAT[C/G]TATTAATAATTGAGT | 8853 |
rs749814599 | snp | C/T | 6.62471e-05 | 0.00575492 | missense | ASAP2 | GRCh38.p7 | 2:9400061 | CCAACAAAGGCCAAC[C/T]GAGAGGACCTGGTAA | 8853 |
rs749815952 | snp | C/T | 1.72865e-05 | 0.00293989 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335223 | AGTTTTCACCCCATT[C/T]TTGGAGGCTTTGGGT | 8853 |
rs749817234 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9298899 | TAGCAGAAAAATGAA[C/T]GTACGGGAAGACTGG | 8853 |
rs749821071 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272367 | TCTTCTTTGGAGATA[C/T]GTCTATTTATATCTT | 8853 |
rs749826242 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233671 | TGTGGCCATGGGCAA[A/G]TATGCTCATTTACTC | 8853 |
rs749859978 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9389415 | TGGAGTGGAGCCCAC[A/G]TCCCCAAATACATCC | 8853 |
rs749882512 | snp | G/T | 5.4444e-05 | 0.00521719 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318515 | TCTCCTTTTGTTTTT[G/T]TTTTTTAGATTCAGA | 8853 |
rs749887964 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9261553 | AGAGTACACACCTAC[C/T]GCTGCCTTGGTAACT | 8853 |
rs749956622 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9228177 | TGATAGGGACATACT[C/T]TTTGGCCATATAACC | 8853 |
rs749972110 | snp | A/C | 7.08491e-05 | 0.00595143 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318640 | GGGCAGCTTTTACAC[A/C]ATGTAGAGTCACAGT | 8853 |
rs749982357 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381411 | AATTATTATCAAATG[C/G]TGTAAAGCAGTTGAC | 8853 |
rs749994730 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274413 | CTGCAACCTTTGTCC[C/T]CCAGGTTCAAGCGAT | 8853 |
rs750002512 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249186 | AGCTCCAGTTTCTTT[C/G]CTCTGTCAGACAGCA | 8853 |
rs750003034 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254670 | TGAGCCACCGTCCCC[G/T]GCCTATAAACTAAAC | 8853 |
rs750023972 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9262897 | AAAGAAAACTCGGCT[A/G]TCTTACATCTCCTCT | 8853 |
rs750026226 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9401582 | CCCTTCTGAGCAGGC[C/T]TGATTATTCCCCAGG | 8853 |
rs750067767 | snp | C/T | 4.11531e-05 | 0.00453595 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378916 | CTGTGACACACTATG[C/T]TCTCTCTCTGTTCCT | 8853 |
rs750073169 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331873 | CAGCTGTTGCTCAGT[A/G]AACTTGGAATGCATG | 8853 |
rs750086570 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9356357 | CCAGGTGACCCAGGG[A/C]CCCCACCCGACCCTG | 8853 |
rs750088370 | snp | C/T | 1.76368e-05 | 0.00296953 | missense | ASAP2 | GRCh38.p7 | 2:9379035 | CTCAAGTTGCTCCTG[C/T]GGGGGAAGGCCTCCA | 8853 |
rs750097185 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9319248 | GACAGACGTGCACCA[C/T]GGAAGGGACGTGATT | 8853 |
rs750104790 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301568 | TTCAGGGCAGGTTTC[G/T]GAAAGGTTTGTTACA | 8853 |
rs750105534 | snp | A/G/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277981 | GGTGATTTCAGGAAG[A/G/T]CTGGAAGTCCAGAAT | 8853 |
rs750112193 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368176 | TACTGGTTCTCCCTG[C/T]CTCTGTCTGTACTCT | 8853 |
rs750140942 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362845 | TGAGACTGTCTCAAA[A/G]CAAAATTTTTAAGTA | 8853 |
rs750141873 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9215351 | AAAATTTTTACCATG[C/T]TCATAATGCTTCTTT | 8853 |
rs750156779 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9372632 | GCATACATTTAAGAA[A/G]GATTCTGGCTACTAA | 8853 |
rs750167487 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9389547 | AGCTTTGTGCTGCAC[A/G]TACACTCGGCTGTGC | 8853 |
rs750174209 | snp | C/T | 1.65504e-05 | 0.00287662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358745 | CAAATCTGCCCTGTT[C/T]TCTTTGGCAGATCCT | 8853 |
rs750174660 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9320420 | TTGCTTAAAGGGATT[A/G]TCCAAATAAACCTTA | 8853 |
rs750216969 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9237991 | TCCAGTGTGTGGATC[C/T]GTGGGCTGGCGTGTC | 8853 |
rs750242604 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361733 | CTACCACGCCTGGCT[A/G]AGTTTTGCATTTTTG | 8853 |
rs750246566 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249975 | ATGTGGAAGGAAGGC[A/G]GGGCTTGGGGTCAAA | 8853 |
rs750259758 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9293589 | AAAACAAAGGCACTG[A/T]ATGATTTTCTGTTCT | 8853 |
rs750288352 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291525 | GTGCAGAGTTGTGCA[C/T]AACATCACAACATTC | 8853 |
rs750289996 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9269684 | GGGGTTGGGGACATT[C/T]AGAGGCCACTGTGCT | 8853 |
rs750302531 | snp | C/T | 6.59044e-05 | 0.00574002 | missense | ASAP2 | GRCh38.p7 | 2:9334800 | TTGAAACGCTGTCTA[C/T]GGATCTTCACACGGT | 8853 |
rs750303805 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279471 | AATATTGATGACCAT[C/T]AACAAATGAGCCAGC | 8853 |
rs750335523 | snp | C/G | 1.66413e-05 | 0.0028845 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358907 | AATTTTTAAATCCTT[C/G]ATTTCAGATTGGAAA | 8853 |
rs750349706 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9292267 | GAAAGTAGGCTGGGC[A/G]TGGTGGCTTTGGGAG | 8853 |
rs750351762 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9339339 | AATCCTGGGTCTCCC[A/G]CTTCCTACCCTGCCC | 8853 |
rs750369941 | snp | C/G | 1.64906e-05 | 0.00287142 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279273 | CGCTGCTAGCGTGGT[C/G]TCAGCACAGACACGG | 8853 |
rs750376025 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254527 | CAGCTAATTTTTGGA[-/T]TTTTTTTTTTTTTTT | 8853 |
rs750384779 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275646 | CTCCCTGTGGCCTGA[-/G]TAACCTTCAAGCACA | 8853 |
rs750387025 | snp | A/G | 3.3024e-05 | 0.00406336 | missense | ASAP2 | GRCh38.p7 | 2:9388298 | TTCTCCTGCAGCCCA[A/G]TCCCAACCGGCGGGA | 8853 |
rs750389510 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9268767 | GCTGGCCTTTCGTCC[A/G]TGGAACGAGGGGAGA | 8853 |
rs750413096 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9223334 | CTGATAGGAAATCTC[C/T]TAAGGGCCCTGTTTT | 8853 |
rs750429225 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307722 | GAGCAGAAACCAGGT[C/T]AGCGATTTTCCTCCT | 8853 |
rs750453213 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9326657 | CATTCAAAAAAAATC[A/G]TATAAGTAGATCTTT | 8853 |
rs750465760 | in-del | -/A | 1.68074e-05 | 0.00289887 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403349 | CTGAACAAAAGCATT[-/A]AACAGTTATGTTCCT | 8853 |
rs750474378 | snp | A/G | 0.000131778 | 0.00811614 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9356084 | AGCTGAAGATGAACA[A/G]GAATGTCAAATGTAA | 8853 |
rs750499532 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369225 | AGTTTCACCATGTTG[A/G]CCAGGCTGGACTCGA | 8853 |
rs750504226 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211523 | ATCCATTCTGCCTTA[C/T]GTATTTGGCATTGAT | 8853 |
rs750509139 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9396441 | ACCATGCCCGGTTAA[C/T]TTATTTTTATATTTT | 8853 |
rs750523602 | in-del | -/GGCCTAAAGCGTCACA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387302 | ATTTTAAGCTCTACG[-/GGCCTAAAGCGTCACA]GGCCTAAAGCGTCAC | 8853 |
rs750526332 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258470 | GCTGTTTTAAAGGTG[A/G]TACTTTCATAGAATT | 8853 |
rs750537263 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225167 | AGATGCAACAGAGAC[C/T]GTGTATATGCAACCT | 8853 |
rs750545699 | snp | C/G | 1.65756e-05 | 0.00287881 | missense | ASAP2 | GRCh38.p7 | 2:9403278 | TTGATGGAGATCCTG[C/G]TCGCAAAGGCGCATT | 8853 |
rs750552593 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368123 | GCACAGGTCATTGGG[A/C]GGAGTGGGTAAGGAT | 8853 |
rs750557322 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397458 | CAGACGGGGATGGAC[A/G]GAGCCATGTCGTCAG | 8853 |
rs750581289 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257541 | GTTTTGTTTTTGAGA[C/G]AAGGTTTCTCTCTGT | 8853 |
rs750587382 | in-del | -/AAAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9314923 | GTGAGACTCCATCTC[-/AAAA]AAAAAAAAAAAAAAA | 8853 |
rs750598973 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276109 | GTGAATTCCAAGAAG[A/G]CACAGGCATTGCCTT | 8853 |
rs750607659 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9231576 | AGATGCCCGGGTGCC[A/G]CCACACCCCTAGCCT | 8853 |
rs750612400 | snp | C/T | 1.65217e-05 | 0.00287412 | missense | ASAP2 | GRCh38.p7 | 2:9380807 | AGCACTGTGAGGAGC[C/T]GGTGAGTCTCCCACC | 8853 |
rs750624150 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245300 | CAGTGTGTTGCTGCC[A/G]TGGCTGTTGCATTTG | 8853 |
rs750632165 | snp | C/T | 1.64868e-05 | 0.00287109 | missense | ASAP2 | GRCh38.p7 | 2:9323161 | GAACACGCCAAGCTC[C/T]ATGGGATGATTCGGA | 8853 |
rs750633413 | snp | C/T | 3.33283e-05 | 0.00408204 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393468 | CTCTGCACGTCTCTC[C/T]CTGTCCTCCGCAGAT | 8853 |
rs750637069 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243084 | GAATGTTTTGCCCTA[A/G]TGAGCCTTGAAGATT | 8853 |
rs750649568 | snp | A/G | 0.000145478 | 0.00852747 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9393501 | CCTGACCCCCACGCC[A/G]CCCCCACCCGTTGCC | 8853 |
rs750663985 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286983 | CTAAATAAAAACTTT[A/T]TGTGAATTCCATCCT | 8853 |
rs750669838 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271631 | GGATAGTGGACATAC[A/G]ATCCAATTTCTTTTT | 8853 |
rs750672904 | snp | G/T | 5.014e-05 | 0.00500674 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323285 | AGGTCCTACAGCCCA[G/T]GCTGTGCCGGCTCTG | 8853 |
rs750682594 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315813 | ATGCTTAAGGCTGAT[C/G]TTAGCAAGACATAGC | 8853 |
rs750715566 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333168 | TGACATATGTGAAAC[C/G]CAGATCACTTTTTAA | 8853 |
rs750728278 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9251334 | TTCCCATCTTCTGGG[C/T]TCCATCTGCTTGGTA | 8853 |
rs750730633 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9357367 | ACATGTAGTCCCAGC[G/T]ACATAGGAGGCTGAG | 8853 |
rs750734558 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9360002 | TTGTTCATGTAATAA[G/T]GCACGTAACCTACAG | 8853 |
rs750737580 | snp | A/G | 1.6566e-05 | 0.00287797 | missense | ASAP2 | GRCh38.p7 | 2:9327886 | TTACTTCAGAATCTG[A/G]TCAAATACTTTCATG | 8853 |
rs750744169 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219485 | AATTCCATAGTTCTT[C/T]GTATTCATATATACT | 8853 |
rs750749762 | snp | A/C | 1.74998e-05 | 0.00295797 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385220 | TGTATGAGCAACAGC[A/C]CTGACCATCCCTCTG | 8853 |
rs750760474 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318976 | GATCCTAGCAAGGGT[-/G]TATTTTCCTGCTGGG | 8853 |
rs750760523 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232870 | ATCCTTAAAAAAGTA[A/G]AAATATGTTTGTGCC | 8853 |
rs750761742 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9374596 | AAGACCAGTGCAGCC[A/G]TAGAACCACATGGCG | 8853 |
rs750768890 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345361 | ATCAGAGTCTATGCA[A/G]GAAAAAACGGAGCCC | 8853 |
rs750805562 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294106 | TAGGTTCAAGTGATT[-/C]TCCTGCCTCAGCCTC | 8853 |
rs750814659 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384612 | GCTCATAGAACTCAG[A/G]GAGACACTTGTGTTT | 8853 |
rs750827230 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276967 | GACATGGGTGTCTTC[C/G]ACTGTCTGTGGGGAG | 8853 |
rs750829344 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263856 | CCTGGTTCTTCTATA[A/G]TAGGTTAAGTATTTT | 8853 |
rs750909690 | snp | G/T | 1.7856e-05 | 0.00298792 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374725 | GTAGAAGCCCTTCAT[G/T]ATTTGCAAGGCAATT | 8853 |
rs750909764 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284493 | GATTAAAAGCTAGCA[A/G]TGCCACTCAAAAAGC | 8853 |
rs750921796 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9282154 | TTGGGCTCATGTCCT[C/T]TTTGAGGCCCCGCAC | 8853 |
rs750949098 | snp | A/T | 1.65261e-05 | 0.0028745 | missense | ASAP2 | GRCh38.p7 | 2:9374802 | ACATCGAGAGGAGAT[A/T]CGCAAGGAAGAAGCA | 8853 |
rs750969907 | snp | C/T | 1.66771e-05 | 0.00288761 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320363 | TCGTTTTTAAATTTA[C/T]GTATAGGTAATTTGG | 8853 |
rs750970759 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9306642 | GTGCCCCTTTGTCCT[C/T]GGGTTGATGAGCCCA | 8853 |
rs750972416 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9204779 | GTTATTTATTGGAAG[C/T]TACTCATTCTTATAT | 8853 |
rs750982396 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9220639 | GCAAGTAATAATTTC[C/T]ATTTTGTAGATTGTT | 8853 |
rs750983493 | snp | C/T | 0.000147053 | 0.00857351 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9379052 | GGGGAAGGCCTCCAT[C/T]GAGATAGGTGAGTGG | 8853 |
rs750991732 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352350 | TGATGTCTGCCAGTG[G/T]CTGGGGCTAACTCAG | 8853 |
rs750992065 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9375680 | ACCTAGTGGTTTATT[C/T]TTACACCAAAAATGT | 8853 |
rs750992615 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9334958 | CCTGTCCTCTGTCTT[A/G]GTGGGAGGGAAGGTT | 8853 |
rs751004914 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364719 | ACTTAACGACTTACA[A/G]CTGTCTTCTAAGTTC | 8853 |
rs751016492 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9323676 | CAGTGTCTGTGAGTG[A/G]ATGGGAAGTCCAGTC | 8853 |
rs751021676 | snp | C/T | 1.64825e-05 | 0.00287071 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344654 | CGTGAGGGGGTGTGG[C/T]TAGAGTTTAAATGTA | 8853 |
rs751043506 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365411 | CTGTTCTCTCCTGGG[A/G]TGAGTCAGAGAAGAA | 8853 |
rs751057631 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364895 | AATGGAGAGCTCCAT[G/T]TTTAAAAAAAGACCA | 8853 |
rs751095309 | snp | G/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207761 | CAGGGCGGCCTGGCT[G/T]CGCTCCACCCGTGCC | 8853 |
rs751096998 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9393759 | TACTCCAGCGTGGGC[A/G]CCACATAACTAATTC | 8853 |
rs751104033 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9394223 | AGGCTGGAGTGCAGT[A/G]GCGTGATCTCGGCTC | 8853 |
rs751130597 | snp | A/G | 6.59652e-05 | 0.00574267 | intron-variant, synonymous-codon, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391150 | ATCTTCGTCAGATCC[A/G]CCAGCTGTCCATCCA | 8853 |
rs751152114 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9392487 | TGCCGGCAGCAGAGC[C/T]GGGAGCAGTGGGTCT | 8853 |
rs751154001 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277702 | CCCTCAGTGAACCGA[C/T]AGGGACACATCACTC | 8853 |
rs751161261 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381297 | CAGCCCTGGCCTTGC[C/T]GGGGGCTCCCCAGCT | 8853 |
rs751176999 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260275 | GTAGCAGTGACTCCC[A/G]CAGTAAGCCTGGGTC | 8853 |
rs751179279 | snp | A/G | 1.64996e-05 | 0.0028722 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9358763 | TTTGGCAGATCCTAC[A/G]TGGCTTTCCACCAAC | 8853 |
rs751187963 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274169 | TAGGTTTTTCCAAAT[A/G]TAAGATCACATCATC | 8853 |
rs751188540 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9273045 | GGTCTTTTGTGGTTC[C/T]ATATAAATCTTAGGG | 8853 |
rs751200821 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9299686 | GACGACGTAGGAGAC[A/G]GGTGGAGGCCCGGGT | 8853 |
rs751211039 | snp | A/G/T | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390971 | TTCATAAGGGGGAGG[A/G/T]TCAATAACGCAGTGT | 8853 |
rs751228516 | snp | C/T | 3.3451e-05 | 0.00408954 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358927 | CAGATTGGAAACAAA[C/T]GAGCTGTAAGCTAAA | 8853 |
rs751242283 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275694 | GGGAAGCACTGTTGC[C/T]TGGCACTTGAGCCCC | 8853 |
rs751242307 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9298818 | CACACAGAGCTGCCT[A/G]TTAGCTTCCTGGTGC | 8853 |
rs751244068 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9329624 | TGTGGGCAATTGCTT[A/G]TGTACACAGCTCCTG | 8853 |
rs751246685 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9235914 | CAGTTTAGCCTCCCA[A/G]GGGACTTCTGGCAAG | 8853 |
rs751260336 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9296330 | CACCTGTGTCCCCTC[C/G]CCCATTCCTACCCAC | 8853 |
rs751278363 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9372541 | CTACCATGTATTTCT[A/G]ATCATGAGAACATCA | 8853 |
rs751303436 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227847 | TTTCAAGGTTCATAT[A/G]TGCATTGTTTGTTGC | 8853 |
rs751362123 | snp | A/G | 1.65644e-05 | 0.00287783 | missense | ASAP2 | GRCh38.p7 | 2:9400031 | TTTGTAGGGCTGACA[A/G]GTCCACCCCACTGAC | 8853 |
rs751388894 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254306 | TATAATTATTCTATT[A/C]GTCATTGTTGTTAAT | 8853 |
rs751397044 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387746 | TTTGGTATGTGTGTG[G/T]TTACTAGTCAGTTCT | 8853 |
rs751403237 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236324 | CCACTTGAATATATT[A/G]AGTTCGTCGACATCT | 8853 |
rs751412052 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247261 | AGCTGGAAATCCTAA[C/T]GAGGATGAACTCTTC | 8853 |
rs751421059 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9261393 | TTAAACTCTTTGAGT[C/G]AGTTTCTTCTCCTTT | 8853 |
rs751423265 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307999 | GTGTATGATAGACCT[C/T]AAGGCAATTCTGTGG | 8853 |
rs751435590 | snp | A/G | 1.64743e-05 | 0.00287 | missense, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9279371 | AAATCCGTGAAAGCA[A/G]TCAACAGCTCTGGGC | 8853 |
rs751462341 | in-del | -/GT | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208338 | TGGGCTAGCAGGAGT[-/GT]GTGTGTGTGGGTGGG | 8853 |
rs751473795 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313043 | CCGCCTGGGCAACAG[A/C]GTGAAACTGTGTCTT | 8853 |
rs751474620 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9319191 | ACAGGGCTAGAGGCG[C/T]GTTTGCCAGGCAGCG | 8853 |
rs751479586 | snp | C/T | 3.33211e-05 | 0.0040816 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344515 | AGATTAAAAACACAC[C/T]CTTCACCATTTTTTA | 8853 |
rs751484471 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9320159 | TGGTTCTTTATTTTT[C/T]GTGGGATTACATACG | 8853 |
rs751495410 | snp | G/T | | | splice-donor-variant | ASAP2 | GRCh38.p7 | 2:9279390 | ACAGCTCTGGGCTGG[G/T]TGAGTATACATCCTT | 8853 |
rs751499536 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267495 | CTTTTTTATGGCTGC[A/G]TCATATTCCATGGTG | 8853 |
rs751538314 | snp | G/T | 3.29511e-05 | 0.00405887 | missense | ASAP2 | GRCh38.p7 | 2:9388390 | TTGGCCAGAGATGCT[G/T]CAAACCTTGCCAAGG | 8853 |
rs751553633 | snp | C/G | 1.65034e-05 | 0.00287253 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297281 | TGAGACTCACAGCAC[C/G]TCCGTCATTCTGTTG | 8853 |
rs751554827 | snp | A/T | 1.84681e-05 | 0.0030387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374968 | GTGGGTTGTTGCTAC[A/T]TTAAAAAAAAAAAAA | 8853 |
rs751556644 | snp | C/G | 0.00177142 | 0.0297081 | missense | ASAP2 | GRCh38.p7 | 2:9388473 | CCTCCTGAGTGGCAG[C/G]CCACCTCCCGCCCAG | 8853 |
rs751557361 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338480 | TCTGCCTCTGGGTTC[A/G]CGTATCTTACATGCC | 8853 |
rs751617859 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337777 | GTGACCTCACACCTC[C/G]CAATCACTGGCCATT | 8853 |
rs751642279 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9223040 | CAAGAGTCCCACTTT[A/C]ATTTGGGATTTTAGG | 8853 |
rs751648530 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9255593 | CGTGGATTCGGCAGA[C/T]GGTGTCGTCAGAGAT | 8853 |
rs751649452 | snp | A/G | 1.7521e-05 | 0.00295976 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9356338 | CTGCTGTGACTGTGG[A/G]GCGCCAGGTGACCCA | 8853 |
rs751653298 | snp | C/T | 1.68159e-05 | 0.0028996 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323301 | GCTGTGCCGGCTCTG[C/T]CCTCACCTGTGGGAG | 8853 |
rs751673941 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209593 | TATTTATTTGTTACG[C/G]AGTTTTGCTCTTGTT | 8853 |
rs751678453 | snp | C/T | 2.84831e-05 | 0.00377369 | missense | ASAP2 | GRCh38.p7 | 2:9393509 | CCACGCCGCCCCCAC[C/T]CGTTGCCAAGACGCC | 8853 |
rs751716538 | snp | A/G | 0.000319483 | 0.0126349 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9393567 | GAGCAAGCCTGCCCC[A/G]CCTGGGATCTCACAG | 8853 |
rs751729604 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9285316 | AAGCTCCCAGGTGAC[A/G]GCACTGGACTTTGAG | 8853 |
rs751733301 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9242632 | CGCGGGATCACCTTT[C/T]AAAGGAACGCAGTCC | 8853 |
rs751760804 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243459 | GATTACAATCACTGT[C/T]GTTTAGGAACTCAGA | 8853 |
rs751767646 | snp | C/G | 1.97541e-05 | 0.00314271 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207170 | CTACAAGGCGCCCAC[C/G]GCCTCCAGCTTCACC | 8853 |
rs751768453 | snp | C/T | 1.69258e-05 | 0.00290905 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385238 | GACCATCCCTCTGTT[C/T]TCTCAGCTGACCCAA | 8853 |
rs751779611 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9339015 | AGATTCCATCTCTAC[C/G]AAAAGTCAAAAAAAT | 8853 |
rs751787446 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9323998 | GGTTAATTCCTCCTG[A/G]CAGTGCCAGCGAAGC | 8853 |
rs751810829 | snp | A/G | 3.32325e-05 | 0.00407617 | missense | ASAP2 | GRCh38.p7 | 2:9327899 | TGATCAAATACTTTC[A/G]TGCCCAATGCAAGTA | 8853 |
rs751829306 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9314703 | CTTTGGGAGGCCGAG[A/G]CAGGTGGATCACTTG | 8853 |
rs751852366 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208426 | GTTTTTTTTTTTTTT[C/T]CCCATTTGAACAAAG | 8853 |
rs751853047 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263145 | TTTCCACTGTCTCGG[C/T]GTCCCTGCTGCCTGT | 8853 |
rs751858771 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325346 | CACAAAGTATTGGTT[A/T]TTGTTTTTGTTTTTC | 8853 |
rs751880396 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244471 | AGTTTTTGAGTTTCA[C/T]GGTGTGAACAGAACA | 8853 |
rs751897098 | in-del | -/GTGG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305471 | GTAGAGGCTGTAGTA[-/GTGG]GTGGGGTATAGATAT | 8853 |
rs751898366 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9367997 | GAGCTGTGATTTGAA[A/C]CTGAGTCTTAGCTTT | 8853 |
rs751900094 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9354223 | AGAGGGAGTCAATGA[C/T]CTTCCAGGTCCACAT | 8853 |
rs751901858 | snp | C/G | 0.00010836 | 0.00735991 | intron-variant, missense, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207258 | GCGCGGCGGCTCCGG[C/G]CGCAGGTATCCCGCG | 8853 |
rs751913371 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9231372 | GGCTTAAGTCAGGTC[A/T]CATCTAACTTTAAGA | 8853 |
rs751921173 | in-del | -/GAGTTCTGTGCCAACAGGCATC | 1.65979e-05 | 0.00288074 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323071 | CAAGGCTGTCCCGTT[-/GAGTTCTGTGCCAACAGGCATC]GAGTTCTGTGCCAAC | 8853 |
rs751933898 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230221 | TGTCAGGATACAGAG[A/G]CAGTTGCTATTGGCA | 8853 |
rs751940759 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383648 | ATCTTGAGGCCTTTC[A/G]TTAGTCTTCCAAAGG | 8853 |
rs751958625 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9396284 | TCCTGAGATCAACTA[C/G]GTTGACTGTGATTTA | 8853 |
rs751984047 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369081 | TGGAGTGCAGTGGCA[C/T]GATCTCGGCTCACTG | 8853 |
rs751989174 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286582 | ACTGAAAACATGCAC[A/G]CAGAGTTTCTGGAAA | 8853 |
rs751997267 | in-del | -/TAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9290392 | TTTTTGTATTTTTAT[-/TAA]AGATTGGGTTTCGCC | 8853 |
rs752010716 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9303282 | AATATCCGCCCTTGG[A/G]TTAGTCCTGGACTAT | 8853 |
rs752012368 | snp | C/G | 1.64743e-05 | 0.00287 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391066 | TGTGGGTTCAGTTCA[C/G]ACAGCCTCCTCTGCT | 8853 |
rs752049216 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333087 | CCTTCTGTGTGTGAC[A/G]CATTTGGTCTGAGAA | 8853 |
rs752065140 | in-del | -/ACACACACAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352217 | AACACACACAAACAC[-/ACACACACAC]ACACACACACACACA | 8853 |
rs752083888 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267268 | CTGAGCATAGTACCC[-/A]ACAGTTAGTTTTTCA | 8853 |
rs752102091 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9398758 | AGGTTGCAGTGAGCC[A/G]AGATTGTGCCACTGC | 8853 |
rs752139532 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245387 | GCCTGGCCACTTCTT[C/T]GGCTCTGTGCTTACT | 8853 |
rs752144214 | snp | A/G | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390637 | GTGCCAGCTGGGCAC[A/G]CGGTGTTCCTCTTCA | 8853 |
rs752148516 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345147 | AGAAAGCACAGAACA[A/G]CAAACTGCTCCCCCA | 8853 |
rs752173910 | snp | A/G | 1.67234e-05 | 0.00289161 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320237 | AAGTAAGTTTATCTT[A/G]CACAGAAGTGAATGA | 8853 |
rs752209473 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207984 | GCAGTACGCTCTCCA[A/G]GTCCTGGGGAGAGGA | 8853 |
rs752213554 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9293022 | GGGCGCAAAGGAGCC[A/G]TTCTTGTCCTTTTTG | 8853 |
rs752221687 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232220 | CTCCCACCCCATCTC[A/C]TCCATGCCTGTCCTC | 8853 |
rs752226584 | snp | A/C | | | missense | ASAP2 | GRCh38.p7 | 2:9388486 | AGCCCACCTCCCGCC[A/C]AGCCTGCAGCCCCCA | 8853 |
rs752246868 | snp | A/T | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404823 | ATGATGTTGTATAGC[A/T]ATCGCTTTTTACCTT | 8853 |
rs752262463 | snp | G/T | 1.6504e-05 | 0.00287258 | missense | ASAP2 | GRCh38.p7 | 2:9335164 | GAAATCCGCATTGCA[G/T]GTTGAACAGAAAGAG | 8853 |
rs752288273 | snp | A/G | 1.65625e-05 | 0.00287766 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9400053 | CCCACTGACCAACAA[A/G]GGCCAACCGAGAGGA | 8853 |
rs752302470 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271736 | AGGCTGCTGAGTCCT[C/T]GGCAGTGGCTCAGTG | 8853 |
rs752305457 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281985 | TCCCCAGAGAGCCAC[A/G]TTTTATGCCTTCTTC | 8853 |
rs752309028 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9251211 | CACATCAGGAGTTTA[G/T]TCCGCAAGTAGAGGT | 8853 |
rs752318330 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281275 | GAAATAAAAATGAAA[G/T]AATCTGTGTCTTATG | 8853 |
rs752319636 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9310534 | AAGAATCCTGTCTAG[C/T]TTCAGGCTTCTAGAT | 8853 |
rs752321344 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271478 | TGGTGTAATCATCAG[C/T]GATCCCTTGGACAGT | 8853 |
rs752334720 | snp | A/T | | | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391458 | AGCATTTCAGCAACA[A/T]TTCCTCCTTTACACA | 8853 |
rs752365528 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311812 | GGCCCCCACGCACTT[C/G]TTCTCTGGCCCAGAC | 8853 |
rs752367293 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9368475 | GATCATGGAATGTTG[C/T]CTACCAGCTGAGGAC | 8853 |
rs752370076 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301259 | GCGTGAAAGAATGTT[-/T]ATAAAGCAGTTGGAA | 8853 |
rs752372095 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322718 | AGCTGGCCTGGCTTC[A/C]CTGAGTGAGGAGGTG | 8853 |
rs752375931 | snp | C/G | 1.66183e-05 | 0.00288251 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400719 | GATGGGATGTCTTAA[C/G]CTGCTTCATTTTTGC | 8853 |
rs752395174 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341616 | TTTTTTTCTCCCCCA[A/G]ATCAATAGACGTATT | 8853 |
rs752397693 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311354 | GGGTGAGAGGCACTC[C/T]CTCAAAAAAAAAAAG | 8853 |
rs752407990 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245756 | ACGCTGTGTGCCATG[-/C]ATTAGTCGGTTCGTC | 8853 |
rs752414473 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229923 | GATTTCTGCAGCCCT[-/G]GCGGTTGTCAGTGTG | 8853 |
rs752426686 | snp | A/G | 1.64792e-05 | 0.00287042 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9388413 | TGCCAAGGAGAAGCA[A/G]AGGGCTTTCATGCCC | 8853 |
rs752448992 | in-del | -/GCT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227522 | TGGCTATTTTCAAAC[-/GCT]GCTATTCGGGTGGGA | 8853 |
rs752470049 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381146 | GTAAGCTGTTTACTT[A/G]CTACTTTGCAGGACA | 8853 |
rs752480388 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260203 | GAACACTGAGGCCCA[C/G]GTGATCAAGTAATTT | 8853 |
rs752480830 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405491 | AGGATGCTATTTTGA[A/G]ATGTATGATATTCAG | 8853 |
rs752485307 | snp | A/C | 0.000322583 | 0.012696 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9388476 | CCTGAGTGGCAGCCC[A/C]CCTCCCGCCCAGCCT | 8853 |
rs752511116 | snp | A/G | 1.65018e-05 | 0.00287239 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297472 | TGTGTATGAAATGCT[A/G]CGGTTACTTCAGTTG | 8853 |
rs752535236 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258935 | ACAGACTGGGGTCTG[A/C]AGCCCTCCAGTGATA | 8853 |
rs752542512 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9334718 | GAAATGTCATCTCTG[C/T]TTCTTCTTTTTCCTG | 8853 |
rs752548990 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9340590 | ACCTGTCATATCTTC[A/G]GAAGATGGGGGAATG | 8853 |
rs752573155 | snp | A/G | 3.29554e-05 | 0.00405914 | missense | ASAP2 | GRCh38.p7 | 2:9376915 | TTTTTCAGGAGCCGG[A/G]TGAAACGGCCCTCCA | 8853 |
rs752608159 | in-del | -/CT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317527 | CAATCACACCCCACA[-/CT]CAAATCCACACAATC | 8853 |
rs752624042 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9399758 | GCCCAGCATCACTCC[A/G]GACCCTGGCCATCGG | 8853 |
rs752624282 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9329436 | ACCCTGGGGTCTCAT[C/G]GGGGAGGCAAGTAGG | 8853 |
rs752632049 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9289172 | CTTTTGGCTGCTCTC[C/T]GTTACCTGGGATGAA | 8853 |
rs752632172 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9277250 | TGTTTCTGGCACAGC[C/T]CTGAGCACAACCTCA | 8853 |
rs752682870 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9288021 | GCCGCATGCATCTGT[A/G]AGACATGGGGCTGCA | 8853 |
rs752686777 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9363882 | AGCCTAGCATTACTT[A/C]TTTTCCAATGGAATG | 8853 |
rs752696654 | snp | C/T | 1.65181e-05 | 0.00287381 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377032 | GGCACTCGTTTTCTC[C/T]TTGGTATTTCTGGGG | 8853 |
rs752699509 | snp | C/T | 1.64857e-05 | 0.00287099 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9356188 | TTCTAGATGGATGTC[C/T]GTGCTGCAAAATAGC | 8853 |
rs752785185 | snp | C/T | 2.08028e-05 | 0.00322505 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207185 | GGCCTCCAGCTTCAC[C/T]ACCCGCACGGCGCAG | 8853 |
rs752797890 | snp | C/T | 0.000181227 | 0.00951738 | missense | ASAP2 | GRCh38.p7 | 2:9376936 | CGGCCCTCCACCTTG[C/T]AGTCAGATCCGTGGA | 8853 |
rs752808199 | in-del | -/TCACACAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317800 | CATACACAATCGCAT[-/TCACACAC]TCACACAATCACACC | 8853 |
rs752810773 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9375970 | TGCAGTAACATACCA[A/G]CACCCAAGTGGGGTG | 8853 |
rs752811922 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387586 | GCTGGCCACCCTGTG[A/G]GGTAGCATAAGAAGG | 8853 |
rs752814864 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236262 | GGATGTTTCATAAGC[A/G]GAGGCTTGTAGGTAA | 8853 |
rs752818199 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221147 | ATTGAGGCTCCCTTG[A/C]ATTTCCATATGAATT | 8853 |
rs752861646 | snp | C/T | 1.65201e-05 | 0.00287398 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388291 | CCCAATGTTCTCCTG[C/T]AGCCCAGTCCCAACC | 8853 |
rs752862972 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266336 | ACTTTTTGTAGAGAT[A/G]GGGTCTCACTGTGTT | 8853 |
rs752865024 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9385841 | GAAAAGTTGACTTGG[C/T]CAAAGTGAAGCAGCT | 8853 |
rs752874193 | snp | A/G | 1.68134e-05 | 0.00289938 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385368 | TTGCAGGTCTGTGCC[A/G]GGTTGCTAACCATTA | 8853 |
rs752912544 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348748 | CGAAGTGAGAAATCT[A/G]TCTTTGATAGTAGTT | 8853 |
rs752915609 | snp | C/G/T | 6.59994e-05 | 0.00574421 | missense, synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374818 | CGCAAGGAAGAAGCA[C/G/T]GCGGATAACGCGGCG | 8853 |
rs752927351 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253940 | TGGCCGGGCACGGTG[C/G]CTCATGTCTGTAATC | 8853 |
rs752933805 | snp | C/T | 6.5937e-05 | 0.00574144 | missense | ASAP2 | GRCh38.p7 | 2:9374865 | GCGAGGCCGTCAAAA[C/T]GAGAGATATTTTTGG | 8853 |
rs752937743 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351263 | GTTTTCAAGAACTTA[C/T]ATAATTTGGGTGATG | 8853 |
rs752954717 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337537 | TTATAAAAATTCTAA[A/C]CCTCCCTGTGTAATA | 8853 |
rs752990844 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294686 | TCCCTTTGGGTGTTC[A/G]CTTAGAGCAACACTG | 8853 |
rs753014483 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9222035 | TCTCGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 8853 |
rs753021956 | snp | C/G/T | 8.65937e-05 | 0.00657957 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350917 | CTCCCTCTGAGATGC[C/G/T]GCGCCATAGAGACGT | 8853 |
rs753067748 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284218 | GGAGGAGACGTTATT[C/T]TGTCTACCACACCTC | 8853 |
rs753069588 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249204 | CTGTCAGACAGCAAT[-/G]GCCTCATGTCTTGTT | 8853 |
rs753076041 | in-del | -/AAT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286447 | AAAAGGAAAAAAAAA[-/AAT]ATATATATATATACT | 8853 |
rs753078643 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9367842 | ACATCTGGAGCTAAT[A/G]TATTACATTTTTAGT | 8853 |
rs753080062 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212473 | GTCTTCTGTACCTGC[C/T]TCCCTGCCTTAGGTA | 8853 |
rs753088087 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9396017 | CCCCATCCAGACACC[A/G]TCCGTTTTGCCCTCT | 8853 |
rs753116948 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315616 | CCTGGAGGCGGGAAC[G/T]GTGACGGGAGTTTCA | 8853 |
rs753123810 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395886 | TGCTGGGATTACAGG[C/T]TTGAGCCACTGTGCC | 8853 |
rs753145518 | in-del | -/AGC | 1.65034e-05 | 0.00287253 | cds-indel | ASAP2 | GRCh38.p7 | 2:9374814 | GATACGCAAGGAAGA[-/AGC]ACGCGGATAACGCGG | 8853 |
rs753148312 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279938 | AAAGATGACAAGTAG[A/G]TCACCTGTAGCATAC | 8853 |
rs753153351 | snp | G/T | 3.29478e-05 | 0.00405867 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391073 | TCAGTTCAGACAGCC[G/T]CCTCTGCTAACACCC | 8853 |
rs753166332 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213499 | CCATTTTAAAGACTT[C/T]ACTGTGGTTCTAGGG | 8853 |
rs753179223 | snp | C/T | 1.64746e-05 | 0.00287002 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356009 | TTGTGTATGGATTGC[C/T]GTCTGGGCTCACAGT | 8853 |
rs753180773 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9382537 | GAAAATAGCCACACA[C/G]ATCATTTTCTACAGC | 8853 |
rs753203185 | in-del | -/G | 1.6516e-05 | 0.00287362 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335084 | GTTGTGTGTGTGTGT[-/G]TTTTAAAGATCAAAC | 8853 |
rs753207524 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275217 | TGGGATTACAGGTGC[A/G]TGTTCCCATGCCCGG | 8853 |
rs753211023 | snp | A/G/T | 0.000148776 | 0.00862372 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323117 | TCCTTGCTTTCACAC[A/G/T]TAGAACCAAGATAGA | 8853 |
rs753213397 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301701 | GGAGCCAATGGGTGC[C/T]GAGGAGAGGACAGAG | 8853 |
rs753226014 | snp | A/G | 1.67153e-05 | 0.00289091 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320372 | AATTTACGTATAGGT[A/G]ATTTGGGATTTCAAA | 8853 |
rs753245120 | snp | C/T | 1.6516e-05 | 0.00287362 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391167 | CAGCTGTCCATCCAC[C/T]GCTGCCCCCTCTTCG | 8853 |
rs753245751 | snp | A/G | 4.94499e-05 | 0.00497217 | missense | ASAP2 | GRCh38.p7 | 2:9344545 | AGGACTCCCAAATTC[A/G]TCAGAGCACAGCTTA | 8853 |
rs753253126 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229999 | TAGCCTTGCTCAAGA[A/G]GTAAAGAAGCTGCTG | 8853 |
rs753256331 | in-del | -/AT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9241964 | TTATCAGGCGGACAC[-/AT]ATGTGAATTTCACAC | 8853 |
rs753258248 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250110 | TACCTCAATTGCTTT[G/T]TAGGGTTTCATAAAG | 8853 |
rs753261711 | snp | A/G | 6.59152e-05 | 0.00574049 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380713 | GGGTTTTGCCTTAAC[A/G]CCTCCTTTGCTCGCC | 8853 |
rs753267161 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343302 | CTACGAGCAGCCCTC[A/G]GCCCTTTCCTGGTTG | 8853 |
rs753269668 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274570 | TCAAGTAATCCGGCC[A/T]TCTCGGCCTCCCAAA | 8853 |
rs753272511 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217433 | TGTTAATAACGATGT[C/T]ATTTTTCCACTCCAT | 8853 |
rs753347642 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9231074 | GTCACTTTCCCCAGG[C/T]CACTTCCTTCCTTTT | 8853 |
rs753347718 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350990 | CTGCATTCGGAAGAA[C/T]TGGTTTTTGAAGAGA | 8853 |
rs753355128 | snp | C/T | 1.80286e-05 | 0.00300233 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374711 | AGGCCGGACGGCGGG[C/T]AGAAGCCCTTCATGA | 8853 |
rs753391883 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263665 | CTGTGGGCGCTGCTT[A/C]CTTAAACTGCAGGAG | 8853 |
rs753418588 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9372796 | GTCCCACTGTGGGAC[A/G]CAGTCACACCCACGT | 8853 |
rs753420068 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9215446 | ATGAATATAAACAAT[A/G]CGAGATATTTCTAAT | 8853 |
rs753437369 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9280963 | GCTCAGACCCTGATG[C/G]TCTTACTGCTGTGTC | 8853 |
rs753443904 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281984 | TTCCCCAGAGAGCCA[C/T]GTTTTATGCCTTCTT | 8853 |
rs753445297 | in-del | -/GTGT/GTGTGTGTGT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361974 | TATCTCTTTCTCTGC[-/GTGT/GTGTGTGTGT]GTGTGTGTGTGTGTG | 8853 |
rs753446888 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263033 | GGAAGGCTGACCTCA[C/T]GCCCAGCTGAAGGTC | 8853 |
rs753472117 | snp | A/C | 6.65314e-05 | 0.00576726 | missense | ASAP2 | GRCh38.p7 | 2:9400826 | TGCCTAGGAAGTCGC[A/C]GGCAGTAAGTGACGA | 8853 |
rs753475002 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9403166 | ACCAATCTTGCTTTT[C/G]TTCACCAAACGCTCT | 8853 |
rs753478709 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9320504 | ATGTGTTTGGTGATG[C/G]TGTCTTCTTCTTCTA | 8853 |
rs753506040 | snp | A/G | 1.64814e-05 | 0.00287061 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344647 | ACGGGTACGTGAGGG[A/G]GTGTGGCTAGAGTTT | 8853 |
rs753508196 | snp | G/T | | | stop-gained | ASAP2 | GRCh38.p7 | 2:9344589 | CCTCAGGGAAACAAG[G/T]AACATGGGACCGAGC | 8853 |
rs753517373 | snp | C/T | 5.24627e-05 | 0.00512139 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318631 | TGACACCAGGGGCAG[C/T]TTTTACACCATGTAG | 8853 |
rs753520322 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321519 | TGGGAAGGGACCAGC[A/G]GATTCCTGCTTTGCA | 8853 |
rs753527243 | in-del | -/TTTT/TTTTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275082 | TTTTTCATTTGTCTG[-/TTTT/TTTTT]TTTTTTTTTTTTTTT | 8853 |
rs753540024 | snp | A/C/G | 1.69123e-05 | 0.0029079 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350901 | CTCATTTCACGTAAG[A/C/G]CTCCCTCTGAGATGC | 8853 |
rs753552708 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9255065 | CGTATGAGAGTTCCA[A/G]TTCCTTCACTTCCTC | 8853 |
rs753559575 | in-del | -/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9293998 | TATAAGGACAAGAAT[-/TT]TTTTTTTTTTTTTTT | 8853 |
rs753605647 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9379241 | TTCCACGAGGCCGCA[C/T]TCACCATCTGTTACT | 8853 |
rs753626940 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9310387 | CTGATTATCCTCGAA[A/G]AGAGTTGGATTCTGT | 8853 |
rs753653114 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257626 | CAGGTTCAAGCTATT[C/G]TCCTGCCTCAGCCTC | 8853 |
rs753654958 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225565 | GCTGGATTATGGAGG[A/G]CTGAGCATGTCAGTT | 8853 |
rs753663629 | snp | A/G | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390450 | TGTGCACCTGAGCTT[A/G]GAGGTTTGTGAGGCA | 8853 |
rs753669891 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281880 | CCAGATGAGTTCCGA[A/G]CTCTTGTGCATTGCC | 8853 |
rs753682161 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9246091 | GCCCTGGTTTGGGAG[C/T]GTTGGCTTTATCCCT | 8853 |
rs753683799 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349894 | AATTCAGGTTTTTTT[A/C]ATCTTGAAGTGACCG | 8853 |
rs753688934 | snp | A/G | 1.75801e-05 | 0.00296475 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9356341 | CTGTGACTGTGGGGC[A/G]CCAGGTGACCCAGGG | 8853 |
rs753696703 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9360298 | AACCTGATGACCTTG[G/T]TATATTATCCCCATT | 8853 |
rs753703563 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364343 | CAAAACCCCATCTCT[A/G]CAAAAAAAAAAAAGT | 8853 |
rs753719219 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295769 | ATGTTAAAAAAGAAA[A/C]AGGACTCAAACAGTG | 8853 |
rs753754793 | in-del | -/GT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338306 | TCTCTCTCTCTCTCT[-/GT]CTGTCTGTCTGTGTC | 8853 |
rs753757128 | in-del | -/TCTG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338306 | CTCTCTCTCTCTCTC[-/TCTG]TCTGTCTGTGTCTGT | 8853 |
rs753762142 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9226316 | TCTGTAAAGCACACT[A/G]TATGGCTGTGTACCC | 8853 |
rs753782471 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369386 | TTGCCCATCTTATCA[A/G]AGTGTCAGTGGCCAT | 8853 |
rs753808547 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9299169 | AAAATGGAACGGAAG[A/G]GTCTCCAAGTTGAGA | 8853 |
rs753847557 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9347652 | CGGGAGATTCGTTCA[A/G]AGCCCGAGTTGAATT | 8853 |
rs753870495 | snp | A/G | 1.65932e-05 | 0.00288034 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358733 | TTACTGGAAGCTCAA[A/G]TCTGCCCTGTTCTCT | 8853 |
rs753903290 | snp | G/T | 3.29723e-05 | 0.00406018 | missense | ASAP2 | GRCh38.p7 | 2:9374872 | CGTCAAAACGAGAGA[G/T]ATTTTTGGATTGCTC | 8853 |
rs753907080 | in-del | -/GAGGTTGGTGG | 3.3437e-05 | 0.00408869 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344842 | TCTGCTGTATTAGGT[-/GAGGTTGGTGG]GAGGTTGGTGTTGGA | 8853 |
rs753909448 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9279362 | AAAATGAAGAAATCC[A/G]TGAAAGCAATCAACA | 8853 |
rs753938173 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384731 | CCCTCCCTGGGTGCC[A/C]CCCTCCAGGACCCTC | 8853 |
rs753938837 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9385706 | GATTTCCCCCAGTCT[A/G]GGTGATCACATTCTC | 8853 |
rs753955887 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9399503 | CTCATGTGTTTCTAC[C/T]TTGTGGCTTTGGGGT | 8853 |
rs753963221 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370116 | GTGCTGGGATTACAG[A/G]CATGAGCCACTGTAC | 8853 |
rs753963984 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233009 | TCCTTTATTATTTCC[A/G]AATTGCTGCCTCTTA | 8853 |
rs753966179 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247028 | AATGTTTTTGTAGAG[A/T]TGGGGTCTGTGTTGT | 8853 |
rs753971424 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9377277 | CTTGGGGACCCCATG[A/G]CCACCCTCTGTGCAC | 8853 |
rs753982367 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245734 | TTCCTCCCGTCTCTG[C/T]AGTCTGACGCTGTGT | 8853 |
rs753994149 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9398335 | GAAAACATAGTGAGA[C/T]CATGTCTTTACAAAA | 8853 |
rs754018442 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265310 | CATTACGAATTGAGC[A/G]TCCTTGGATTTTGGA | 8853 |
rs754037735 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217060 | TGGAGCTTGGAGGTG[A/G]TGAAGCCAGGATTCA | 8853 |
rs754041988 | snp | C/T | 1.66142e-05 | 0.00288216 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391181 | CCGCTGCCCCCTCTT[C/T]GCGTGACATCTACCA | 8853 |
rs754069772 | in-del | -/CAA | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211155 | AGTGAAACTGCGTCT[-/CAA]AAAAAAAAAAAAAAG | 8853 |
rs754100774 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333944 | CAAGTTCTCTACCCA[C/T]GGTTTCCTACCCCGC | 8853 |
rs754102493 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9277196 | CTCTATGTGTGAGAG[C/T]TGTGCTGTCTGACAT | 8853 |
rs754109461 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9323011 | CTGCCTGTGCTGAAA[C/T]GTGTGGTGAGCGTTG | 8853 |
rs754110796 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9304063 | CCACTGGCAGCCTGC[A/G]GAGCCCTGAGGGTAC | 8853 |
rs754111877 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260976 | GTGTCCCTGGTGAAC[-/T]TTTAGATTCTTGTGC | 8853 |
rs754123407 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240437 | TTTTTGTAGAGATGG[A/G]GTTTCTCCATGTTTC | 8853 |
rs754125034 | snp | A/G | 3.33056e-05 | 0.00408065 | missense | ASAP2 | GRCh38.p7 | 2:9403253 | TTTTCTCCATTTCAG[A/G]TTGGCCACATTGATG | 8853 |
rs754132936 | snp | C/T | 1.64923e-05 | 0.00287156 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9323151 | GGAGAAAAAGGAACA[C/T]GCCAAGCTCCATGGG | 8853 |
rs754133386 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402328 | CCTCGTTTGCCCTTA[A/G]TGGATTGAAAGTGTC | 8853 |
rs754143324 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219612 | ATCTTCAAGTTGAAT[G/T]ATTTATTTTTGAAAA | 8853 |
rs754166942 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9235143 | CTGTCCTGTTGTAGG[C/T]GGGGATCTGTGTGTG | 8853 |
rs754175338 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346358 | GGAGAATTGCTTAAA[C/T]GCAGGAGGCAGAGTT | 8853 |
rs754177986 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9363577 | ACCTGTTGGTCATTT[-/A]GTAGGTCTTCTCTTT | 8853 |
rs754186931 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9220854 | TGAGGTAGGGGTCCA[A/G]CTTCATTCTTTTGCA | 8853 |
rs754196886 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9376733 | AATCTCCAAATTGCA[C/T]GTTCCCAAGGGCAAA | 8853 |
rs754207395 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405317 | ACATTGTAGATATCT[A/G]TTTATATTTAAAGTT | 8853 |
rs754210189 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336583 | TGCCACAGCGCTCAT[G/T]TAGTAGGATTTTGGT | 8853 |
rs754222977 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9375871 | CCCACTGTGCTCCCC[C/G]TCAGAGGGAATAGAG | 8853 |
rs754257584 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210958 | GTCAGGAGTTCGAAA[C/G]CAGCCTGACCAACAT | 8853 |
rs754265152 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9335271 | CATGTCTTCTAGGAG[C/T]TCACAGTTCACTCGG | 8853 |
rs754273258 | in-del | -/ACACACACACAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352215 | AAAACACACACAAAC[-/ACACACACACAC]ACACACACACACACA | 8853 |
rs754282527 | snp | C/T | 1.6531e-05 | 0.00287493 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393453 | GCCTGGCGGCTGACC[C/T]TCTGCACGTCTCTCC | 8853 |
rs754289910 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9391805 | GGCCAGCCTGGTCTC[A/G]AACTCCTGACCTCAG | 8853 |
rs754291396 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325072 | ACAAGCAAATATTTT[A/T]AAATATTCACTTGAT | 8853 |
rs754310834 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321525 | GGGACCAGCGGATTC[C/T]TGCTTTGCAGAGGGA | 8853 |
rs754311803 | snp | A/G | 1.80589e-05 | 0.00300485 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385202 | TCCAGATGCATGGCC[A/G]AGTGTATGAGCAACA | 8853 |
rs754348841 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9273247 | TTTTATAGTTTTCGC[G/T]GTAGAGATCCTGTAC | 8853 |
rs754350840 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9283982 | ATCTGGGGGAAGGGA[C/T]GCAATTCAGTCCCAT | 8853 |
rs754364545 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313007 | GAGGTTGCAGTGAGC[C/T]AAGATCGTGCCACTG | 8853 |
rs754381389 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9293825 | AAAGATTCCCACTGA[C/T]CTCAACTGGTACAGT | 8853 |
rs754398309 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366395 | CTCATAGAGGGGGCC[A/T]CAGTGATTTTTGTCA | 8853 |
rs754408037 | snp | C/G | 1.64792e-05 | 0.00287042 | missense | ASAP2 | GRCh38.p7 | 2:9368500 | GAGGACTCAGTCAAA[C/G]CCAACCCAGGCAGCG | 8853 |
rs754408281 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305010 | TGGAGTAGTGGGGTA[A/T]AGATATTGGTGGAGG | 8853 |
rs754412793 | snp | G/T | 2.92847e-05 | 0.00382642 | utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207060 | TGCGGCAGTTGAGGC[G/T]GCGGCGCCCCTGCGG | 8853 |
rs754414100 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358420 | CTGCTAGTGTGACCA[A/C]GTTGGTGATGGGCAT | 8853 |
rs754415184 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9323729 | ACCTCACCTGCTCAG[A/G]CGGGGGCACTCATCT | 8853 |
rs754446110 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402496 | GTGTGGTGGCAGGCA[C/T]CTGTAATCCCAGCTA | 8853 |
rs754449725 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9388225 | AGGTTTTCACCCCTG[A/T]GTTGAATGTTATCAC | 8853 |
rs754466573 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291817 | GCTGGTGCACCCTGC[C/T]TTCGTTCTGTTATGC | 8853 |
rs754476594 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9320568 | CATAGTGGTTATAGG[A/G]TGTTATTTTCAGGAA | 8853 |
rs754506079 | snp | C/T | 1.648e-05 | 0.0028705 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380707 | TTTGCTGGGTTTTGC[C/T]TTAACGCCTCCTTTG | 8853 |
rs754524176 | snp | A/G | 1.67349e-05 | 0.0028926 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358928 | AGATTGGAAACAAAT[A/G]AGCTGTAAGCTAAAT | 8853 |
rs754533550 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302808 | AGGTGTGAGCCACCA[C/T]GCCTGGTCAGAAGAC | 8853 |
rs754538805 | snp | C/T | 0.000123877 | 0.00786914 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393682 | CTCGGCCATCCGTGC[C/T]CCTGCCCTCTGACCT | 8853 |
rs754543480 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9292408 | CTGTAGTCTCAGCTA[C/T]TCGGGAGGCTGAGGC | 8853 |
rs754562524 | snp | C/G | 1.64781e-05 | 0.00287033 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334816 | GGATCTTCACACGGT[C/G]AGTAGCTTCCCTCCC | 8853 |
rs754576608 | snp | C/T | 1.64887e-05 | 0.00287125 | missense | ASAP2 | GRCh38.p7 | 2:9358774 | CTACATGGCTTTCCA[C/T]CAACCTGGGCATCCT | 8853 |
rs754580686 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217555 | GCAGTCAGGATTGTC[A/G]GGACCTCTTTCCCCA | 8853 |
rs754587996 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250165 | TGGGGGCAGAAACTG[C/T]CAGGATCATTTTTAG | 8853 |
rs754593307 | snp | C/T | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390493 | GTGACCTGGAAAATG[C/T]CATCTCTTGTGGGTC | 8853 |
rs754593399 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378576 | CCAGCACAGCTGGCC[A/G]GCCTAGCACAGCAGC | 8853 |
rs754594447 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373234 | AAGTGCCAGAGCACA[A/G]GTTCACCAGGTGCCC | 8853 |
rs754602788 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9223619 | AGGGCGTACATTAGA[C/T]CTGGAAGTAAACAAA | 8853 |
rs754609995 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9403176 | CTTTTCTTCACCAAA[C/T]GCTCTATGTAATGCT | 8853 |
rs754627420 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229830 | GTGCCTGGCCCTGGA[A/G]GTGTGTGCCCCTCCT | 8853 |
rs754642611 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321564 | AGTCAGTGGTTTCTG[C/T]TTGTCAGCCAGTAAG | 8853 |
rs754650356 | snp | C/T | 1.64925e-05 | 0.00287158 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9335155 | AGATATTTTGAAATC[C/T]GCATTGCAGGTTGAA | 8853 |
rs754702997 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9316390 | TGCCATTTTATCTTC[C/G]TATTTAAGATAATTA | 8853 |
rs754730540 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9310431 | GGTGAGCCCTGGGAA[A/G]ACCTGTTATTTTCTA | 8853 |
rs754734925 | in-del | -/T | 0.000140853 | 0.00839085 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374979 | TACTTTAAAAAAAAA[-/T]AAAAAGGCCGGCCAC | 8853 |
rs754746521 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212478 | CTGTACCTGCCTCCC[C/T]GCCTTAGGTAAATAT | 8853 |
rs754760684 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327238 | CGGAGGGGATGGGGA[C/T]TCATGAAGTCCTTCT | 8853 |
rs754772345 | snp | C/T | 1.65633e-05 | 0.00287774 | missense | ASAP2 | GRCh38.p7 | 2:9400039 | GCTGACAAGTCCACC[C/T]CACTGACCAACAAAG | 8853 |
rs754775942 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9298428 | TTCTCCCCGTCTTCA[C/T]TTATGAACATTTCTG | 8853 |
rs754786610 | snp | A/G | 1.65053e-05 | 0.0028727 | missense | ASAP2 | GRCh38.p7 | 2:9388307 | AGCCCAGTCCCAACC[A/G]GCGGGAAGACCGGCC | 8853 |
rs754824167 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9379271 | TTAGACTTTGGGCGC[A/G]TTTACAGGCATTTTA | 8853 |
rs754830559 | snp | G/T | 1.64743e-05 | 0.00287 | missense, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9279372 | AATCCGTGAAAGCAA[G/T]CAACAGCTCTGGGCT | 8853 |
rs754832964 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370130 | GACATGAGCCACTGT[A/G]CCTGGCCTAGATTTT | 8853 |
rs754844322 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350906 | TTCACGTAAGGCTCC[C/G]TCTGAGATGCCGCGC | 8853 |
rs754850973 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328170 | AGAGACAGAAAGCAG[G/T]TGAGTGATTGCCGCA | 8853 |
rs754872733 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9399932 | TCACACACTCTGAGC[C/T]TGAACTCAGAAGGTT | 8853 |
rs754877873 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244724 | GGGACTCTTCCCTGA[A/G]CACCTTCCCAGGTAC | 8853 |
rs754879377 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9246170 | GAATGGGGATTCTCT[C/G]TATGGTTTCTCCAAA | 8853 |
rs754891312 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9357499 | AACAAACAAAAAACC[C/T]GAAAATACGTTTTTG | 8853 |
rs754894633 | snp | A/T | 1.80879e-05 | 0.00300726 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374969 | TGGGTTGTTGCTACT[A/T]TAAAAAAAAAAAAAA | 8853 |
rs754949147 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9287781 | TCCAGCCTTCTCCCC[G/T]CTGCTGGCTAACAAC | 8853 |
rs754968280 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272177 | TTACATTCCCACCAA[G/T]AGTGTACAGGGGTTC | 8853 |
rs754971541 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9206366 | ATCCTCCGGCAGGGG[A/G]CGAGCTCCGCACCCC | 8853 |
rs754972054 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258811 | TTTACTTATTTATTT[C/T]TCTCGCTCTCTCTCC | 8853 |
rs754984724 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263962 | TTTAGGAGGCCAAGG[C/T]GGGCGGATCAGTTGA | 8853 |
rs754985599 | snp | A/T | 1.6473e-05 | 0.00286988 | missense | ASAP2 | GRCh38.p7 | 2:9356092 | ATGAACAGGAATGTC[A/T]AATGTAAGTTACATG | 8853 |
rs754987458 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9304105 | CAGGGAGCAGTGACT[C/T]CCCGCCCTGAGCCCT | 8853 |
rs755007638 | snp | C/T | 8.57596e-05 | 0.00654771 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9393510 | CACGCCGCCCCCACC[C/T]GTTGCCAAGACGCCC | 8853 |
rs755064390 | snp | C/G/T | 3.376e-05 | 0.00410841 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385240 | CCATCCCTCTGTTCT[C/G/T]TCAGCTGACCCAAGC | 8853 |
rs755077354 | snp | C/T | 2.47804e-05 | 0.00351988 | utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207081 | GCCCCTGCGGCTGTG[C/T]GCCAGCGCCCTCGCG | 8853 |
rs755091235 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205013 | CAATTTTATTTTTTT[C/G]AGGCTACTAAAGCTT | 8853 |
rs755114893 | in-del | -/AA | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205234 | ACAAATCAAGACTTG[-/AA]AAGTTATTCAGCATA | 8853 |
rs755153322 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233055 | GCCAGTCTGTGCTCT[A/G]TGTTTTTTTTGCTCA | 8853 |
rs755154467 | snp | C/G | 1.66382e-05 | 0.00288424 | missense | ASAP2 | GRCh38.p7 | 2:9385355 | CATGGATGAGAAATT[C/G]CAGGTCTGTGCCAGG | 8853 |
rs755161636 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345567 | GGCTGGTAGACAGCT[C/T]TGGTAACATCTCAAG | 8853 |
rs755177357 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265333 | ATTTTGGAATTCAAC[A/G]GAATCCCGGAATTAA | 8853 |
rs755186131 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221034 | CCTTTATGCTAGTAC[C/T]ATAAAGCCTTAATTA | 8853 |
rs755186348 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9375917 | TCCTTTCCTGGGGGA[A/G]CTGTCTTGAGAGGGT | 8853 |
rs755189153 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253011 | CTATTTAGTTGTTCA[C/T]TGCAGCCCTCAAAAG | 8853 |
rs755204883 | snp | C/T | 1.98837e-05 | 0.00315301 | missense, utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207172 | ACAAGGCGCCCACGG[C/T]CTCCAGCTTCACCAC | 8853 |
rs755239774 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9385712 | CCCCAGTCTAGGTGA[G/T]CACATTCTCCTGGTT | 8853 |
rs755240239 | in-del | -/AT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301414 | CTCCAGAAATGTGAC[-/AT]GTGTGAAATTAAAGT | 8853 |
rs755258804 | in-del | -/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219775 | GGTTTTTAGTGTACT[-/CA]CAAAGTTGTGTAGCC | 8853 |
rs755277752 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9235144 | TGTCCTGTTGTAGGC[A/G]GGGATCTGTGTGTGG | 8853 |
rs755313773 | snp | A/G | 3.30246e-05 | 0.0040634 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374806 | CGAGAGGAGATACGC[A/G]AGGAAGAAGCACGCG | 8853 |
rs755322380 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9299654 | GGGGCCTAGAAAGCA[G/T]CCAGCCCAGGACGGC | 8853 |
rs755338012 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9312324 | CCGTGAATGAAACCA[A/G]AATCCCCCTCATTGA | 8853 |
rs755368137 | in-del | -/TTTTTTTTTTTTTTTCTTTTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9391580 | TTTTCTTTTTCTTTT[-/TTTTTTTTTTTTTTTCTTTTT]TTTTTTTTTTTTTGA | 8853 |
rs755369265 | snp | A/G | 1.67231e-05 | 0.00289159 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344841 | TGTCTGCTGTATTAG[A/G]TGAGGTTGGTGTTGG | 8853 |
rs755385620 | snp | C/T | 1.67086e-05 | 0.00289033 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320240 | TAAGTTTATCTTGCA[C/T]AGAAGTGAATGATTA | 8853 |
rs755386945 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294565 | TGAACTGCACTTGAT[C/T]CAGAAGAAAATAGGG | 8853 |
rs755390319 | snp | C/T | 0.000582536 | 0.0170566 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400850 | GTGACGAGCCCCCTT[C/T]CCTGCCTCTCTGCTC | 8853 |
rs755390881 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9323045 | TCGCCAGGCTGGGTA[C/G]TGGGGTGGCTTCAAG | 8853 |
rs755408663 | snp | C/T | 1.66604e-05 | 0.00288616 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401257 | CACACTAACCGTTGT[C/T]CCCTCTCCTGACCCA | 8853 |
rs755410048 | in-del | -/ACAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352212 | TTAAAACACACACAA[-/ACAC]ACACACACACACACA | 8853 |
rs755418501 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239629 | TCCCCTAATATTAAC[C/T]GAGCACCATTTATGT | 8853 |
rs755429634 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208104 | TTTGAGGCACATCCT[A/C]ACCTGCAGTCCTCCT | 8853 |
rs755432456 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9354181 | TTGTGAGGTGACCCA[A/G]GTGAGTCCCCTGAGT | 8853 |
rs755536351 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274425 | TCCCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 8853 |
rs755549327 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9296688 | ACATGCTGAGTGCAA[A/G]GATAGGAGAGGTGCC | 8853 |
rs755560250 | in-del | -/TTAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9382906 | CAGCAGAGAAAGAGT[-/TTAA]TTATGGCAAGCTGGC | 8853 |
rs755568943 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301652 | ACGGTCTGCAGAACC[C/T]GCTCCACATGAAGAT | 8853 |
rs755575975 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236383 | TCTTATATTCCTGAC[A/G]TATTCTTATCCTTGC | 8853 |
rs755594137 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9273454 | TGGGTTCACCTTGCC[A/C]GCTGCTGCCTAGACC | 8853 |
rs755607658 | snp | C/T | 3.3253e-05 | 0.00407742 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399983 | AAAGGGGCAGGTGCC[C/T]TCCGGTAGCAGTAAA | 8853 |
rs755623988 | snp | C/G | 3.31235e-05 | 0.00406948 | missense | ASAP2 | GRCh38.p7 | 2:9400054 | CCACTGACCAACAAA[C/G]GCCAACCGAGAGGAC | 8853 |
rs755628550 | snp | A/G | 1.67998e-05 | 0.00289821 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368374 | GGGTAATGTGTAGCA[A/G]TAGAATGTATTAATA | 8853 |
rs755630368 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9215359 | TACCATGCTCATAAT[A/G]CTTCTTTACTAAAGC | 8853 |
rs755649539 | snp | C/T | 3.29533e-05 | 0.00405901 | missense | ASAP2 | GRCh38.p7 | 2:9368495 | CAGCTGAGGACTCAG[C/T]CAAACCCAACCCAGG | 8853 |
rs755661841 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331885 | AGTGAACTTGGAATG[C/T]ATGGTCAAGATAAGG | 8853 |
rs755663277 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313522 | CTTCCCCACAACCCA[C/T]CTTATCACTGGATGG | 8853 |
rs755665966 | snp | A/G | 1.64879e-05 | 0.00287118 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9344540 | TTTTTAGGACTCCCA[A/G]ATTCGTCAGAGCACA | 8853 |
rs755669856 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361765 | TAGAGATGGTCTTTC[A/G]CCATGTCCAGGCTGG | 8853 |
rs755695741 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343249 | GTCCCTGTTTCTCCC[A/G]TTATGGAATGAACTG | 8853 |
rs755696385 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9388040 | TGAAGATTACAATTC[A/G]AGGTGAGATTTGGGT | 8853 |
rs755708939 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250003 | AAATCTGGGTATACA[A/G]CTCTTCCCTTCTTTC | 8853 |
rs755713728 | snp | C/T | 1.64822e-05 | 0.00287068 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279402 | TGGGTGAGTATACAT[C/T]CTTCCCTAGAGGTTT | 8853 |
rs755718499 | snp | C/T | 1.66913e-05 | 0.00288883 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335197 | GAGGGGATTTAATTT[C/T]GAAAGATTGCAGTTT | 8853 |
rs755765732 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9290470 | CCATCTCGGCCTCCC[-/A]AAGTGCTGGGATTAC | 8853 |
rs755767129 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9297327 | ATGAAGAGCAGTACA[C/T]CCAGGCTCTGGAGAA | 8853 |
rs755768445 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9319257 | GCACCACGGAAGGGA[C/T]GTGATTGTGGCTGCC | 8853 |
rs755794299 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9360360 | TTCAGTATGCCTAGG[A/G]TTATGAAGCTTTTAA | 8853 |
rs755796221 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249305 | TGGCTCAGCCTGCCC[A/G]TGGCCTGTCTGTCTG | 8853 |
rs755799494 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9401702 | GGTCATCACCCCCCA[A/T]TGCTGGATTAGTGGA | 8853 |
rs755809463 | in-del | -/AA | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211157 | TGAAACTGCGTCTCA[-/AA]AAAAAAAAAAAAAGT | 8853 |
rs755858325 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279609 | CCCCTGTCATCCCCT[A/G]TCATCCTCCGTGCTG | 8853 |
rs755883091 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243213 | TCCCGGGTTCACGCC[A/G]TTCTCCTGCCTCAGC | 8853 |
rs755891795 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9252477 | TACTCAGGAGGCTAC[A/G]GCAGGAGAATCGCTT | 8853 |
rs755908859 | snp | C/T | 3.36412e-05 | 0.00410115 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9388479 | GAGTGGCAGCCCACC[C/T]CCCGCCCAGCCTGCA | 8853 |
rs755917956 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237170 | AGCTTTTTTAAAAAA[-/AG]AGAGTTAAAAAAAAA | 8853 |
rs755919519 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349847 | TCTGTCCAGGTGTAG[A/C]TGCATATGTGTATGT | 8853 |
rs755942484 | in-del | -/G | | | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405541 | GGTTGCAGCACAACT[-/G]GTATATATTGTATAA | 8853 |
rs755943396 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9238125 | AGCACTTACTAACAC[C/T]GTTAGCTGACCCGCT | 8853 |
rs755947220 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9222502 | TTGCTTTCTATCAAC[A/G]TTGCCTTGATTTGGT | 8853 |
rs755951955 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358121 | CTCCCTGGCGACCTC[A/G]AGCCTGAGCATCGCA | 8853 |
rs755967574 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9389612 | TCACAGACCCTCACA[C/T]GGCTCTGCCCCTGTC | 8853 |
rs755969329 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327605 | TTATTATTAGGAGTT[C/T]TTGGCACTTCAATAT | 8853 |
rs755992125 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325524 | GTAAAGTAGACATCT[A/G]TTTACCTAAACACTT | 8853 |
rs755995156 | snp | C/T | 1.64776e-05 | 0.00287028 | missense | ASAP2 | GRCh38.p7 | 2:9376921 | AGGAGCCGGATGAAA[C/T]GGCCCTCCACCTTGC | 8853 |
rs756041908 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384972 | CTCCATGTTATAACC[A/G]AAGACTGTAACAAGG | 8853 |
rs756049199 | snp | A/C | 1.64939e-05 | 0.0028717 | missense | ASAP2 | GRCh38.p7 | 2:9356205 | TGCTGCAAAATAGCA[A/C]AGAAGAAGCTTTAAA | 8853 |
rs756078741 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9259355 | TTCCCCTCCCTTCTG[C/T]GCCATCCTGCAGTGG | 8853 |
rs756085041 | in-del | -/AG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331750 | CCCAGCCTGGGCGAC[-/AG]AGCGATTTTTTTTTT | 8853 |
rs756087665 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378515 | AGCCTCCGTCCTCCC[A/G]TGGGACAGGATGGAT | 8853 |
rs756088767 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257543 | TTTGTTTTTGAGACA[A/G]GGTTTCTCTCTGTCA | 8853 |
rs756101499 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9269875 | GACTTCCCTTACCCA[A/C]AGTGTGCACCGTCCC | 8853 |
rs756110613 | snp | C/T | | | intron-variant, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9287027 | GTTGGGTCCTGTCCA[C/T]TGACAGATGAGCTCA | 8853 |
rs756113644 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243516 | TAACTGTTAAAATAC[A/G]ACTTTGCTTACAATA | 8853 |
rs756118709 | snp | C/G | 1.68335e-05 | 0.00290111 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385369 | TGCAGGTCTGTGCCA[C/G]GTTGCTAACCATTAA | 8853 |
rs756126919 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315824 | TGATCTTAGCAAGAC[A/G]TAGCTGATGACATTG | 8853 |
rs756143980 | snp | A/G | 3.50539e-05 | 0.00418637 | missense | ASAP2 | GRCh38.p7 | 2:9356339 | TGCTGTGACTGTGGG[A/G]CGCCAGGTGACCCAG | 8853 |
rs756144211 | snp | C/G | 1.75075e-05 | 0.00295862 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327778 | GAAGCTCCTTTTAAA[C/G]TCGTATTCTGCTTAC | 8853 |
rs756159862 | snp | C/G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362812 | TCTTGCCACTGCACT[C/G/T]CAGCCTGGGCAACAG | 8853 |
rs756170798 | in-del | -/TG | 1.99938e-05 | 0.00316172 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378925 | ACTATGCTCTCTCTC[-/TG]TTCCTGTTCTCGGGC | 8853 |
rs756194937 | in-del | -/TG | 3.48099e-05 | 0.00417178 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335224 | TTTTCACCCCATTCT[-/TG]TGGAGGCTTTGGGTC | 8853 |
rs756232293 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9285476 | GTCTTCAAAATGATG[A/G]CAACCCAGCCAGCTG | 8853 |
rs756264148 | snp | C/T | 7.2998e-05 | 0.006041 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350765 | ATTTTCCATTCCTTC[C/T]ACCCAACCCCAACCT | 8853 |
rs756265850 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9216968 | TTAAATTCTTTACAT[A/G]TATCAATTATTAACT | 8853 |
rs756279360 | snp | C/T | 1.65157e-05 | 0.0028736 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9388296 | TGTTCTCCTGCAGCC[C/T]AGTCCCAACCGGCGG | 8853 |
rs756293047 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384617 | TAGAACTCAGGGAGA[C/T]ACTTGTGTTTACTGG | 8853 |
rs756295888 | snp | A/G | 3.29696e-05 | 0.00406001 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374866 | CGAGGCCGTCAAAAC[A/G]AGAGATATTTTTGGA | 8853 |
rs756311488 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244605 | TTCAGAAGCACTTCG[C/T]ATTAAGCTCCTGTGC | 8853 |
rs756321905 | snp | C/T | 3.30022e-05 | 0.00406202 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279267 | GGTGCTCGCTGCTAG[C/T]GTGGTCTCAGCACAG | 8853 |
rs756351976 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397152 | CTTGGCTTCTGGGCT[A/C]TCTTCTGCCTTCCCT | 8853 |
rs756381909 | snp | C/T | 1.66835e-05 | 0.00288816 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320250 | TTGCACAGAAGTGAA[C/T]GATTAGTCTTGCCTA | 8853 |
rs756406340 | snp | A/C | 1.66158e-05 | 0.0028823 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401270 | GTTCCCTCTCCTGAC[A/C]CAGACCAAGTTGAAG | 8853 |
rs756414521 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317356 | ACACACCCTCACACA[A/G]TCATTCACATTCACC | 8853 |
rs756414977 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361711 | TAGCTGAGACTACAG[A/G]CAAGTGCTACCACGC | 8853 |
rs756422662 | in-del | -/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214776 | GATGGCCTGGACGTC[-/T]TAAAAAAAAAAAAAA | 8853 |
rs756429460 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9296517 | AGTAAAATGCCATGA[A/G]ATGTAAGCACCTGGT | 8853 |
rs756439979 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321772 | GGATAACATCAAATT[C/T]TGTAAAATCGAGACA | 8853 |
rs756441295 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9319082 | TAGCCACCATAAGCA[C/T]GCAGGCCAGGAGCTG | 8853 |
rs756449430 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9251342 | TTCTGGGCTCCATCT[A/G]CTTGGTACTCACGTG | 8853 |
rs756452157 | snp | G/T | | | upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9204829 | GCTATGTTTTGCTCT[G/T]GTCTTGCTTTAATTC | 8853 |
rs756474416 | snp | G/T | 8.36421e-05 | 0.00646638 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320374 | TTTACGTATAGGTAA[G/T]TTGGGATTTCAAATT | 8853 |
rs756479913 | snp | A/G | 0.000115322 | 0.00759261 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9391050 | CGTCTGTGTGCATGC[A/G]TGTGGGTTCAGTTCA | 8853 |
rs756485714 | snp | A/G | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403615 | CAAGATCCTGCCTCT[A/G]CGGAATTAGCTAAAC | 8853 |
rs756497944 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9293362 | AAAGTCCCTCCCAGG[C/T]CAGTGATTATTGGAT | 8853 |
rs756525801 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9374609 | CCGTAGAACCACATG[A/G]CGGCCACTCCCGCTT | 8853 |
rs756527015 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333293 | TACACCAAACTTTGC[A/G]GGTACTTTGTGTCTC | 8853 |
rs756544771 | snp | C/T | 3.29468e-05 | 0.00405861 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391076 | GTTCAGACAGCCTCC[C/T]CTGCTAACACCCTGT | 8853 |
rs756551722 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263638 | TCCGAGGCACAGACC[G/T]CCCGGGAGTGCCTGT | 8853 |
rs756561213 | snp | C/T | 8.6259e-05 | 0.00656674 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379071 | ATAGGTGAGTGGGCC[C/T]GGGCCCCGGGGGTGG | 8853 |
rs756571675 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219546 | GGAACAAAAATCAGC[C/T]AGGAATGGCTAGTTG | 8853 |
rs756594531 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365473 | GACATGAAAACAGGA[C/T]AGGAGGTTTCCCTGC | 8853 |
rs756639591 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322952 | AAGACCCGGTTTGAC[A/G]TCTTCGTGAGGACAC | 8853 |
rs756648054 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239519 | CTGAACTCATTACTT[C/T]TTATAACCCATAGGT | 8853 |
rs756653046 | snp | C/T | 3.29538e-05 | 0.00405904 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380723 | TTAACGCCTCCTTTG[C/T]TCGCCCTTGAATTTT | 8853 |
rs756718320 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405266 | TCTTAGTTATTTGCT[C/T]CTTGCAAATTAAAAA | 8853 |
rs756727248 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9282239 | GCCATCTATTATGTC[A/T]TGCCAAGTTTGAGTT | 8853 |
rs756728313 | in-del | -/TTTTG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395555 | ACTGTGTTTTTGTTT[-/TTTTG]TTTTGTTTTGTTTTG | 8853 |
rs756737670 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9312955 | TCCCAGCTACCTGGG[A/T]GGCTGAGGCAGAGGA | 8853 |
rs756745659 | in-del | -/GT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361975 | TATCTCTTTCTCTGC[-/GT]GTGTGTGTGTGTGTG | 8853 |
rs756776792 | snp | A/C | 1.66319e-05 | 0.00288369 | missense | ASAP2 | GRCh38.p7 | 2:9388489 | CCACCTCCCGCCCAG[A/C]CTGCAGCCCCCAGCA | 8853 |
rs756817110 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371613 | CTGTGAATCCCAAGA[C/T]GGATCTTGGGGGTGT | 8853 |
rs756824864 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341744 | CATTGTTCTCAGCAA[C/T]GTTGAAAGCTGGATT | 8853 |
rs756829536 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9261424 | AAGCTGGGGAAAGAG[A/G]TGGTGATTTCACAAG | 8853 |
rs756830442 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352462 | TAATAGTGAACCTAT[C/T]ACCTGGAGGTGGGTG | 8853 |
rs756843927 | snp | C/T | 1.65655e-05 | 0.00287793 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297497 | CAGTTGGGAAAGTGG[C/T]TCAGTAGAGGATAGT | 8853 |
rs756852578 | in-del | -/CTGTGAGCTCTCAGGGCCAGGCAGCA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402243 | CAGCCTCCAGAGGCG[-/CTGTGAGCTCTCAGGGCCAGGCAGCA]CTGCCTTCATTTGGC | 8853 |
rs756858723 | snp | C/G | 3.34622e-05 | 0.00409023 | missense | ASAP2 | GRCh38.p7 | 2:9388541 | CTCCACGGAATGTTG[C/G]CAAAGGTATGAAGCT | 8853 |
rs756865431 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227087 | TCCTCCTCTCCTGTG[C/G]CTCTGGAATCCTGCT | 8853 |
rs756870223 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381298 | AGCCCTGGCCTTGCC[A/G]GGGGCTCCCCAGCTT | 8853 |
rs756878009 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341064 | GAAAGTGGAGAGTAC[A/C]TTGGAGTCTCCAGGA | 8853 |
rs756895389 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247324 | ACCAGAGGCTGCTGT[C/G]TTGGAACTGCTCCCA | 8853 |
rs756900862 | in-del | -/CT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317218 | CCACTCACATCCACA[-/CT]CACACAATCACACAA | 8853 |
rs756910678 | in-del | -/A | 0.0598232 | 0.162274 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374971 | GGTTGTTGCTACTTT[-/A]AAAAAAAAAAAAAGG | 8853 |
rs756937823 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9386251 | TTTCTGAAACCTGTT[A/G]GACTGTCTGCTCATG | 8853 |
rs756950837 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370454 | ATGTGATCATCCTCT[C/T]TTGATGAGGATCTAA | 8853 |
rs756964481 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278342 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATG | 8853 |
rs756970901 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300392 | ATAAAAGGAATCCCT[C/T]CTTCTCCTTTATAAA | 8853 |
rs756982587 | snp | C/G | 3.30518e-05 | 0.00406507 | missense | ASAP2 | GRCh38.p7 | 2:9356247 | AGGGGGATGACAATA[C/G]TGGAGAAAATAACAT | 8853 |
rs757008186 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9401558 | GGAGCTGCTTCCTCC[A/G]TGGACACCCCCTTCT | 8853 |
rs757020134 | snp | A/G | 2.08635e-05 | 0.00322976 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378910 | TCCAGCCTGTGACAC[A/G]CTATGCTCTCTCTCT | 8853 |
rs757035130 | in-del | -/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336181 | TTCATTGTTGTAGAC[-/TT]TATTAAAGGCTGAAG | 8853 |
rs757037797 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318697 | GCCAGTACGTTCTCA[C/T]TGGGACGATAGGATG | 8853 |
rs757078009 | snp | A/G | 8.84551e-05 | 0.00664979 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9393522 | ACCCGTTGCCAAGAC[A/G]CCCAGCGTAATGGAA | 8853 |
rs757091335 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248712 | AACTTTCACTCCTAT[A/C]TACCAGCCATTTGGT | 8853 |
rs757091526 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359906 | CCTTAGTTACTTACA[A/G]TTTAAAACTAAGCTA | 8853 |
rs757096811 | in-del | -/GGG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9289992 | CAGGAAGAAGCCGGT[-/GGG]GAGAGGCATCCTTCC | 8853 |
rs757128102 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348913 | CCTTCCATGGATACC[C/G]ACGTCGAGGACAGGG | 8853 |
rs757156048 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9222385 | TGGCCACGGTGCTTG[A/G]TAGTCACTCAGGAGG | 8853 |
rs757170913 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9334792 | ACCTTCCATTGAAAC[A/G]CTGTCTACGGATCTT | 8853 |
rs757172494 | snp | C/G | 1.66896e-05 | 0.00288869 | missense | ASAP2 | GRCh38.p7 | 2:9385249 | TGTTCTCTCAGCTGA[C/G]CCAAGCCTTATCTGG | 8853 |
rs757196275 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380387 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 8853 |
rs757199050 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9226780 | GCAATCTAGCAAACG[C/G]TGTGCTCTTCCCTGG | 8853 |
rs757211831 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9223182 | TGGGTTTATTGTTCT[A/G]TATTTTAAAATTGAT | 8853 |
rs757216233 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236353 | CTTCAAAGAGTTAGA[C/T]TGAAATGCTGATCCT | 8853 |
rs757243857 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387833 | ATTCACTCACACCTC[C/G]ACATGGCTGGGAAAC | 8853 |
rs757258595 | snp | A/G | 4.94588e-05 | 0.00497262 | missense | ASAP2 | GRCh38.p7 | 2:9374873 | GTCAAAACGAGAGAT[A/G]TTTTTGGATTGCTCC | 8853 |
rs757259814 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9268716 | TTTTGTTTTTTGTTT[C/T]GTCTACTGTCTTTCA | 8853 |
rs757268479 | snp | C/T | 8.25198e-05 | 0.00642286 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279432 | TCTGTGTGGAAAATG[C/T]CGCATTTGAAGTCCT | 8853 |
rs757288572 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9308245 | GCCTCAGGAAACTTA[A/C]AATCATGGCAGAAGG | 8853 |
rs757294042 | in-del | -/AA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9374971 | GGTTGTTGCTACTTT[-/AA]AAAAAAAAAAAAGGC | 8853 |
rs757295323 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302120 | GAGCCACCGCGCCCG[A/G]CCTTTTTTTTTTTTT | 8853 |
rs757297702 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9309258 | CTGGCTAGACGGCAG[G/T]GTAGCCATATGATGG | 8853 |
rs757307815 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337807 | TCATGTTTTGTTCTT[C/G]ATATTTTCTGCTCTC | 8853 |
rs757312137 | snp | A/G/T | 0.000331645 | 0.0128731 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9401303 | TAAGCGGGTGAAAGC[A/G/T]CTCTATAACTGTGTG | 8853 |
rs757316469 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267600 | TACAAATGACATTTA[A/C]AGAATGATTATGAAG | 8853 |
rs757320048 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9280751 | AGAAGGTGGCCATCC[A/G]TCTCTAGCTTTTTTA | 8853 |
rs757330109 | snp | A/G | 3.45197e-05 | 0.00415435 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401405 | GTGGTGGGTGAGTCA[A/G]GGGTGGGCCTGGGAG | 8853 |
rs757340531 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295761 | TTACTGGAATGTTAA[A/C]AAAGAAAAAGGACTC | 8853 |
rs757345604 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9223119 | GGTGATGACATTTAA[A/C]GTTGGCCTCCTTTCC | 8853 |
rs757357284 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9255715 | GTGGTGCTCCAGAGG[G/T]TCTTCAGGGGTCTGC | 8853 |
rs757364445 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327432 | GACATGATGCCAAGC[A/T]TCTCAGCTACAATAC | 8853 |
rs757401759 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395168 | AGGAAGTCATCAGTT[C/T]CACCTCTCAATAAAG | 8853 |
rs757406935 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230270 | CCTTCAGGAGTGAAC[A/G]GGGCTTGTTTGCTCA | 8853 |
rs757425299 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9354859 | AGAGAGGTGGCGTGT[C/T]CACTCACTTTTAGGA | 8853 |
rs757439788 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9356054 | CTATGCAGATGACAG[A/G]ACTTACCACTTTCAA | 8853 |
rs757442409 | in-del | -/TAAAT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384170 | AGTATAATAAAAAAA[-/TAAAT]TAATTAAAAAGAAAA | 8853 |
rs757456352 | snp | C/G | 1.66145e-05 | 0.00288218 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391182 | CGCTGCCCCCTCTTC[C/G]CGTGACATCTACCAG | 8853 |
rs757466266 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274639 | AACACTCAATCTTAA[A/G]CAATCATTCTAGCTT | 8853 |
rs757473545 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378413 | TTCCCAGGGCAAACA[A/G]GCCGAGGAGCCTGGG | 8853 |
rs757476237 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9269003 | GGGTGCAGGGGCCGC[G/T]GGTGCTGTGGGAGGG | 8853 |
rs757499704 | snp | A/G | 1.64909e-05 | 0.00287144 | missense | ASAP2 | GRCh38.p7 | 2:9323152 | GAGAAAAAGGAACAC[A/G]CCAAGCTCCATGGGA | 8853 |
rs757499987 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395457 | TCCAGCCTGGGCAAC[A/G]AGAATGAAACTCCAT | 8853 |
rs757503105 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229925 | TTTCTGCAGCCCTGG[A/C]GGTTGTCAGTGTGGG | 8853 |
rs757525385 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212660 | GTGGAGCATATACAT[A/G]CATTCCAGGCCCGCA | 8853 |
rs757531224 | in-del | -/C | 5.4802e-05 | 0.00523431 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350764 | GATTTTCCATTCCTT[-/C]CACCCAACCCCAACC | 8853 |
rs757557489 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9261196 | AAGCAGGGGTAATGC[C/T]GGGTGGTTATTTTCC | 8853 |
rs757560050 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368009 | GAACCTGAGTCTTAG[C/G]TTTCCTGGCTCAGTG | 8853 |
rs757561220 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9326617 | TTGACATTTAAGTAA[A/T]CATCTTTATATGTCC | 8853 |
rs757607997 | snp | A/G | 1.64757e-05 | 0.00287012 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380732 | CCTTTGCTCGCCCTT[A/G]AATTTTAGCAAACGA | 8853 |
rs757614930 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332239 | CTCAACTTAAGAAAA[G/T]TTTCTGGGGCTATGT | 8853 |
rs757615953 | snp | A/G | 1.65012e-05 | 0.00287234 | missense | ASAP2 | GRCh38.p7 | 2:9380791 | AAGCGCCTCAAGCAC[A/G]AGCACTGTGAGGAGC | 8853 |
rs757621065 | in-del | -/AA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265708 | TTTCTTTGCTTTTAC[-/AA]TTTGTGTGTGTGTGT | 8853 |
rs757648211 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302923 | GCAGAGGGGCATCCT[A/G]GCTTGGCTGCATTGG | 8853 |
rs757664991 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9363222 | TTAGGTTGATTCCCT[A/G]TCTCGACTATTGTGA | 8853 |
rs757675714 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9355590 | CTTGATTTAGCTACA[-/T]TTCTAGTATTTGATT | 8853 |
rs757688419 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383723 | ACACGTATGTTTATT[G/T]CGGCACTATTCACAA | 8853 |
rs757697381 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9251215 | TCAGGAGTTTAGTCC[A/G]CAAGTAGAGGTGGGC | 8853 |
rs757703193 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301990 | CGCCATGCCCGGCTA[A/G]TTTTTGGTATTTTTA | 8853 |
rs757706650 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9320665 | CACTTTGTCCATTCC[A/G]TTACTGTTTTTGATA | 8853 |
rs757722244 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373408 | TTGAGGCCTGGCAGA[C/T]GCTGGCAAGAGACCT | 8853 |
rs757730465 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263767 | TCTCACTTATCTGTT[C/T]ATACCGCATGACACC | 8853 |
rs757730723 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341948 | TTGGTTGTCAGTTCA[A/G]TAATGGAGAGTGCCT | 8853 |
rs757731597 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317669 | TTACACAATCACTCA[-/C]ATCCATAATCACATC | 8853 |
rs757733550 | snp | C/T | 2.9093e-05 | 0.00381388 | utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207065 | CAGTTGAGGCGGCGG[C/T]GCCCCTGCGGCTGTG | 8853 |
rs757750826 | snp | A/G | 1.65622e-05 | 0.00287764 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9400062 | CAACAAAGGCCAACC[A/G]AGAGGACCTGGTAAT | 8853 |
rs757752239 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368383 | GTAGCAGTAGAATGT[A/G]TTAATAATTGAGTAT | 8853 |
rs757768649 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | ASAP2 | GRCh38.p7 | 2:9368507 | CAGTCAAACCCAACC[C/T]AGGCAGCGACATGTA | 8853 |
rs757840133 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9216184 | GAGACTTTGCAGTGT[A/G]TGTTATTTTCAGTGA | 8853 |
rs757857408 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9282100 | TGTTCAAAGTCACAA[A/C]GCTCTACAGTGACAG | 8853 |
rs757858736 | snp | C/T | 1.64792e-05 | 0.00287042 | missense | ASAP2 | GRCh38.p7 | 2:9344559 | CGTCAGAGCACAGCT[C/T]ATAGCTTACATCAGC | 8853 |
rs757877632 | in-del | -/TCTC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9372109 | AAAGGAAGTCCACTT[-/TCTC]TCTATCCCTTTCCTG | 8853 |
rs757886451 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322739 | TGAGGAGGTGATGAC[A/G]GAGACTAGGGAGGAA | 8853 |
rs757889105 | in-del | -/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317920 | ACTCTTATACTCAAG[-/CA]CAGTCACACCTTTAC | 8853 |
rs757892056 | snp | C/T | 1.68823e-05 | 0.00290532 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388558 | AAAGGTATGAAGCTG[C/T]CCGTCATCCCTGTGA | 8853 |
rs757913370 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361418 | TGGTCATGGTGTCGT[A/G]GCTCTAAACCTTATT | 8853 |
rs757937798 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321638 | GCCTCCCTTGCTGCC[C/T]GTCTCTGTGGCTGAT | 8853 |
rs757947401 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272585 | CCATTTATCTGTTTT[C/T]GCTTTGGTTGCCTGT | 8853 |
rs757957318 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380585 | ACAATTACAAGATAC[A/G]TTCAGCCTCGACTAG | 8853 |
rs757967045 | in-del | -/CTCGTGAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271018 | CAGGATAGTCTCGAT[-/CTCGTGAC]CTCGTGATCCACCTG | 8853 |
rs757977976 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364698 | AAAGCTCCTCAAAGA[C/T]GAAGAACTTAACGAC | 8853 |
rs757978691 | snp | A/G | 3.52609e-05 | 0.00419872 | missense | ASAP2 | GRCh38.p7 | 2:9379036 | TCAAGTTGCTCCTGC[A/G]GGGGAAGGCCTCCAT | 8853 |
rs758006147 | snp | C/T | 0.000170885 | 0.00924192 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327942 | TTATGTTATCTTAAA[C/T]GTTTGTTCATGTGTG | 8853 |
rs758006387 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9392209 | CTGAAAACCTTGGGT[A/G]AAGAAGCGGGAGGAG | 8853 |
rs758028294 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239094 | GGGTTGCCTTCTGTT[C/G]CTAGTTTGCTGGTTT | 8853 |
rs758032293 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350269 | ACTTAAGTGACAGTG[A/G]TGGTTGGCATTTAGG | 8853 |
rs758051573 | snp | G/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207985 | CAGTACGCTCTCCAG[G/T]TCCTGGGGAGAGGAA | 8853 |
rs758057004 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9340633 | CAGCCCTCCTGGGCA[C/G]AGAAATTTTAAGCTT | 8853 |
rs758064633 | snp | C/T | 4.96257e-05 | 0.004981 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358747 | AATCTGCCCTGTTCT[C/T]TTTGGCAGATCCTAC | 8853 |
rs758065201 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9226936 | CTGGAGGGGTGCACC[A/G]TGGGCCTGGGATAGG | 8853 |
rs758066563 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271909 | CTTTTTTATGGCTGA[A/G]TAGTACTCCATTGTG | 8853 |
rs758133468 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9298605 | CCCTGCCTCAGCCCC[A/G]TGCCCTGGACACTGG | 8853 |
rs758139127 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9299583 | GAAAGCAAGCAGTGG[A/G]AGGGAATTCCAAGAG | 8853 |
rs758147451 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328397 | AACATAAAAAATCTG[C/T]AGTAATTGCCAGATA | 8853 |
rs758180020 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245889 | TGTTCTCAATAAATA[A/G]TTTGTTATTGTTGTT | 8853 |
rs758205018 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9287700 | GTCTCTGAGGAAGTT[A/G]TAGAGGGAGGTGAGG | 8853 |
rs758236486 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380005 | CAAAAAAAAAAAAAT[A/T]AATAAAGTATATACT | 8853 |
rs758248178 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370360 | TTTATGTTTGAATCC[G/T]GTAACAAGTGTTTGT | 8853 |
rs758277494 | snp | A/G | 1.73297e-05 | 0.00294356 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385402 | GTTTTGATCAGCTTC[A/G]TCCAGAACAGTGTGG | 8853 |
rs758287104 | snp | A/C/G | 1.64817e-05 | 0.00287064 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334825 | CACGGTGAGTAGCTT[A/C/G]CCTCCCACTGTGGTT | 8853 |
rs758302402 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233282 | AGGAATTGCGAAGCC[A/G]TACTATGTTGAGGTC | 8853 |
rs758302722 | snp | A/G | 1.64743e-05 | 0.00287 | missense, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9279368 | AAGAAATCCGTGAAA[A/G]CAATCAACAGCTCTG | 8853 |
rs758321390 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9251504 | CCTGATGTCCGTCGG[A/G]TGGGTTTTGTATGCT | 8853 |
rs758324503 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405600 | ATGCAGTGATTTATA[A/G]TTAGAGCATGTTTAA | 8853 |
rs758337691 | snp | A/C | 1.6492e-05 | 0.00287154 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279278 | CTAGCGTGGTCTCAG[A/C]ACAGACACGGTTTAA | 8853 |
rs758340969 | in-del | -/TTCA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402909 | ACTTGTGACACTCAG[-/TTCA]TTCATTCATTCATTC | 8853 |
rs758348187 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265517 | CTTTTCATTTTCTTT[A/T]ATTCGAAAAAATTAT | 8853 |
rs758349713 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267259 | ACCCAGGTACTGAGC[A/G]TAGTACCCAACAGTT | 8853 |
rs758369349 | snp | A/G | 1.65083e-05 | 0.00287296 | missense | ASAP2 | GRCh38.p7 | 2:9388304 | TGCAGCCCAGTCCCA[A/G]CCGGCGGGAAGACCG | 8853 |
rs758388536 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9385888 | GGGACTGCACGAAGG[C/G]TCTTGCCTCCTCCTC | 8853 |
rs758422200 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318448 | TTATCAAATGTTCTC[G/T]CTAATGTCCTTGCTG | 8853 |
rs758439760 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9399831 | TTTAGGATCAGAAAC[A/G]TTGAATTTAGCACTT | 8853 |
rs758444077 | snp | A/G | 1.64868e-05 | 0.00287109 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9323166 | CGCCAAGCTCCATGG[A/G]ATGATTCGGACTGAA | 8853 |
rs758454095 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9277256 | TGGCACAGCCCTGAG[C/G]ACAACCTCAGTCTGC | 8853 |
rs758458173 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9289233 | CCAGCCCTTCCCCAT[C/G]CTCTGGACACACCAA | 8853 |
rs758469629 | snp | C/T | 3.31483e-05 | 0.004071 | missense | ASAP2 | GRCh38.p7 | 2:9403280 | GATGGAGATCCTGGT[C/T]GCAAAGGCGCATTCC | 8853 |
rs758476768 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9376130 | GGTAACAGGCATGTC[C/T]GTGCAGGCTCTGAGC | 8853 |
rs758487578 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9323858 | GGACACTCTCAGAGC[A/G]TTTCTCTGAGATCAG | 8853 |
rs758488197 | snp | A/G | 6.56944e-05 | 0.00573087 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393471 | TGCACGTCTCTCCCT[A/G]TCCTCCGCAGATCCC | 8853 |
rs758506059 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353956 | CTGTAGCCTGGGTAA[C/T]AGAGGGAGACCTTGT | 8853 |
rs758581479 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266418 | TTCCAAAGTGTTGGG[G/T]TTACAAGCATGAGCC | 8853 |
rs758588055 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337712 | TGCTGCTGTTTCCTT[G/T]TGACCCTGCAGCTTT | 8853 |
rs758589620 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221166 | TCCATATGAATTTTA[A/G]GATCAACTTTTCAAT | 8853 |
rs758604797 | snp | C/T | 3.30961e-05 | 0.0040678 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380817 | GGAGCTGGTGAGTCT[C/T]CCACCACAAGGACGG | 8853 |
rs758607815 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9242122 | ATCTTGGAAGAGAGG[A/G]GGGAGGTCTGTGCTC | 8853 |
rs758618572 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387657 | GGTTGAGATAACTTC[A/G]ACTCATAAGATAAAT | 8853 |
rs758620794 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9255511 | TTGTTACTATGGAAT[A/G]GTTGATTTGATGTAA | 8853 |
rs758621617 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9255864 | GAAGTCTTGGTAAAC[A/G]TTGGGCTGGGGGGCA | 8853 |
rs758625131 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9394354 | TATTTCTAGTAGAGA[C/T]GAGGTTTCGCCGTGT | 8853 |
rs758626379 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209408 | TTTAATAACAATTGA[C/T]GTGTACAGTATTTTG | 8853 |
rs758629076 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284274 | TGAATCAGTTTCCAC[C/T]GTTTTGTTCAGCTAC | 8853 |
rs758634683 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9323829 | TTCCCTTAGTGAGGC[A/G]GAGACAGCAGGATGG | 8853 |
rs758647512 | snp | A/C/T | 8.12095e-05 | 0.00637167 | utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207073 | GCGGCGGCGCCCCTG[A/C/T]GGCTGTGCGCCAGCG | 8853 |
rs758668316 | snp | A/C | 1.71787e-05 | 0.00293071 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385229 | AACAGCACTGACCAT[A/C]CCTCTGTTCTCTCAG | 8853 |
rs758690539 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307255 | TTTGCATTTCCTGTT[-/C]CTAGTCACGCTGGCC | 8853 |
rs758691696 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9282106 | AAGTCACAAAGCTCT[A/G]CAGTGACAGGGCTGG | 8853 |
rs758741203 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264161 | CACACCACTGCACTC[C/T]ACCCTGGGCAGTGAG | 8853 |
rs758746674 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343318 | GCCCTTTCCTGGTTG[A/C]CCTGTGAACACTTGG | 8853 |
rs758754539 | snp | C/T | 1.78248e-05 | 0.00298531 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374728 | GAAGCCCTTCATGAT[C/T]TGCAAGGCAATTACG | 8853 |
rs758760649 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331084 | TTCCCCCACCACACA[C/G]GCCCAGTTTCCGCTT | 8853 |
rs758767912 | snp | A/G | 1.64972e-05 | 0.00287199 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368526 | CAGCGACATGTAAGT[A/G]TGGGACTGGCTATTC | 8853 |
rs758799254 | in-del | -/AAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9314924 | TGAGACTCCATCTCA[-/AAA]AAAAAAAAAAAAAAA | 8853 |
rs758811686 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213868 | GCTCTGTGCTGCTTG[A/G]TGTGACTGGTTATAG | 8853 |
rs758828370 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341524 | GTGAGACCTGAAAAT[C/T]GCTCTGATTAATATG | 8853 |
rs758834442 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343837 | GCTAGTCCTCGCTTA[C/T]CCTAAGAAGCTGATA | 8853 |
rs758843172 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370201 | TTGCAGGACCTGTAT[A/T]CTTTCTGCGTTTTGC | 8853 |
rs758845346 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9339474 | AATTTCTGTAGAGCA[C/T]TTACCATATTATCTT | 8853 |
rs758846517 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275231 | CATGTTCCCATGCCC[A/G]GCTAACTTATTTTTA | 8853 |
rs758863436 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313297 | TCTATTATTAACAGC[A/C]CCTAAGTTCTTATTG | 8853 |
rs758863511 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325263 | TCCTGGCCTACCTCA[C/T]AGAGTGGCAGAGAAA | 8853 |
rs758882679 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9293996 | GTATAAGGACAAGAA[-/T]TTTTTTTTTTTTTTT | 8853 |
rs758915186 | snp | A/G | 1.64836e-05 | 0.0028708 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344656 | TGAGGGGGTGTGGCT[A/G]GAGTTTAAATGTACG | 8853 |
rs758919014 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232027 | AGCTGCAGTGGGTGC[C/G]CCTGTCATTTGTCAG | 8853 |
rs758929071 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230075 | TGCTTCTTTTACATA[C/G]TGCATTAAAGGTCCC | 8853 |
rs758940119 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263074 | ACTCTGAGCTCGGCT[C/G]CCTTCTGCATCGCCA | 8853 |
rs758944455 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9372844 | GGGGCCTTTGAGACA[C/T]AGCAGTTAGCCGAAC | 8853 |
rs758969973 | snp | A/G | 1.65715e-05 | 0.00287845 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344807 | CATGGTACCGTAAGT[A/G]TTCTCTTTTAATCCA | 8853 |
rs758993694 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9261793 | GGAGAGGGGCAGACC[C/T]GGGGTTACCTCAGTC | 8853 |
rs759001565 | snp | A/T | 8.72715e-05 | 0.00660516 | splice-acceptor-variant, intron-variant | ASAP2 | GRCh38.p7 | 2:9318522 | TTGTTTTTGTTTTTT[A/T]GATTCAGAATATGAA | 8853 |
rs759014514 | in-del | -/TTGTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258333 | GATAGTAATCAGTAG[-/TTGTT]TTTTTTTTTTTTTTT | 8853 |
rs759016238 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345994 | TTCTCGGTGACCTCT[A/G]GTCTAGGGGTTTGAA | 8853 |
rs759023682 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276596 | AGGCTGGAGTGTAGC[A/G]GCACAATCTTGGCTC | 8853 |
rs759027708 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384243 | TGATTCAAACTTACA[C/T]CACAAACTAAATTCT | 8853 |
rs759085449 | snp | C/T | 1.87261e-05 | 0.00305985 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401446 | GCTGAGCCACGTCCC[C/T]GCCCACCTGGCTGGA | 8853 |
rs759108686 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232508 | TGCAGAGAACTTGTC[G/T]GATTTGTTTAACCAC | 8853 |
rs759134599 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9316865 | GGGGGCACCAAGGCT[C/T]TTGCCCTTCCTGTTC | 8853 |
rs759142444 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9220037 | AACATGGATTTGTAC[-/T]TTTATTTCTTTTTAT | 8853 |
rs759156684 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9292924 | ATCCTCTGGCAGTGC[C/T]GTGTTGGTGGCTTGC | 8853 |
rs759162329 | snp | C/T | 1.64887e-05 | 0.00287125 | missense | ASAP2 | GRCh38.p7 | 2:9380779 | CTGGACATTGCCAAG[C/T]GCCTCAAGCACGAGC | 8853 |
rs759219354 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364466 | ACTGAGATTGTGCCA[C/T]TGCTCTCCAGCCTGG | 8853 |
rs759221711 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294324 | TTAAAAAGAAAAAAA[C/T]TTAACCTACACCAGG | 8853 |
rs759227503 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300048 | CCAGCCTGGGCAACA[-/T]TGGGGAACCCCTGTT | 8853 |
rs759234061 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9385103 | AAGTAGGCAGAGGGG[C/T]GGGGGCTTCACCTGA | 8853 |
rs759245436 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9334615 | TAAGGTTCTGTTCAT[A/G]CAGTCTTTTCCCCCA | 8853 |
rs759254805 | snp | A/G | 1.64751e-05 | 0.00287007 | missense | ASAP2 | GRCh38.p7 | 2:9368464 | GGCTTTAATGAGATC[A/G]TGGAATGTTGCCTAC | 8853 |
rs759262472 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264728 | TTTTTTTCTCCCTGT[G/T]TACCATTGGCCCTCT | 8853 |
rs759297012 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9251171 | GAAGGAGATTTTGAA[A/T]GGAGGAACGTGGCCA | 8853 |
rs759310710 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366816 | AGGCTACCCCACATA[A/G]TTCTTCTGTTTTTAA | 8853 |
rs759324431 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227693 | AACCCAGAACCAGCT[A/G]AGTATTTGGGAGGTC | 8853 |
rs759332567 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341540 | GCTCTGATTAATATG[C/T]GCGGCACGAACAGTG | 8853 |
rs759351359 | snp | C/T | 1.6636e-05 | 0.00288405 | missense | ASAP2 | GRCh38.p7 | 2:9388474 | CTCCTGAGTGGCAGC[C/T]CACCTCCCGCCCAGC | 8853 |
rs759358038 | in-del | -/GGGTG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387075 | GCCGGGCTTGGTGGT[-/GGGTG]GGGGGGCGCCTGTAG | 8853 |
rs759365673 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260023 | CCCACTTACAAGGCC[C/T]CAGGCAGGCTGGCCT | 8853 |
rs759370018 | snp | C/T | 1.66449e-05 | 0.00288482 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344516 | GATTAAAAACACACT[C/T]TTCACCATTTTTTAG | 8853 |
rs759383109 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322511 | CAAGCCCACCTTAGC[A/C]GCCACGATTACCCTG | 8853 |
rs759385623 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205811 | TTTGACTGGTATCTT[C/T]AGAGCTTCTGGATTT | 8853 |
rs759393286 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351968 | ATCCTGTGTCAAACA[A/C]CCATCCTGACTCAGT | 8853 |
rs759412190 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239966 | CTGGTAAGAAGGAGG[A/T]CTTCTGTTTCTAAGT | 8853 |
rs759419342 | snp | C/T | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390543 | CATCTGTGTCTGCTT[C/T]CAGCCAGAAATATGT | 8853 |
rs759434743 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9312795 | CATCCGTACACCCCC[C/T]TCTCCTGCCACCACT | 8853 |
rs759445524 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9273970 | CATCTTTGTTTCAAA[A/G]CTAAACTGTAAGTTC | 8853 |
rs759466388 | in-del | -/AAGTGGATGTTAATCTAAGCA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244408 | TGTCTTTGGAAGATT[-/AAGTGGATGTTAATCTAAGCA]AAGTGGATTCTGTAA | 8853 |
rs759475473 | snp | C/G | 1.66067e-05 | 0.00288151 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9400809 | GCAGCCCCCTGCACC[C/G]ATGCCTAGGAAGTCG | 8853 |
rs759476220 | snp | G/T | 0.000115425 | 0.00759599 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297457 | CCTGGTAAGCAGCTC[G/T]GTGTATGAAATGCTG | 8853 |
rs759499289 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381980 | CGAGCTCATTTAATC[-/T]TTTTTTTTTTTTTTT | 8853 |
rs759563363 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295966 | GTTCCCTCGTTTTCC[C/T]ACATTGTCAGGCCCA | 8853 |
rs759618078 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9288995 | TTTTCTGTTACCAGC[A/C]CCCAGAAAATGTACT | 8853 |
rs759635089 | snp | A/C | 6.83364e-05 | 0.00584496 | missense | ASAP2 | GRCh38.p7 | 2:9393643 | CAGAAGAAGCCTGCG[A/C]CGGGGTAAGCCACCC | 8853 |
rs759637332 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387435 | GACAAAAAACAGGTG[A/G]TAGTCCATAGGCCAC | 8853 |
rs759662012 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | ASAP2 | GRCh38.p7 | 2:9358834 | GAGAGCTGGGGGTTC[A/G]TTATTCCAGGATGCA | 8853 |
rs759663172 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9288473 | GCCCTCCATGGAGTT[-/G]GGTGGGGGCAGCGTG | 8853 |
rs759668456 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214001 | AGACTGAGGGATCTG[C/T]TCATGCGACCCTCTG | 8853 |
rs759671437 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9379228 | CTCTCCCTGCCTGTT[C/G]CACGAGGCCGCATTC | 8853 |
rs759696295 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9312646 | TTGAAGTTCCATGGT[G/T]TCTCATTCCTGGCTC | 8853 |
rs759708662 | snp | A/G | 2.09028e-05 | 0.00323279 | intron-variant, synonymous-codon, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207263 | GCGGCTCCGGCCGCA[A/G]GTATCCCGCGCCCCA | 8853 |
rs759712217 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371184 | ACATCCCCCAACCCC[A/G]GGCTTTTTTCAAAAT | 8853 |
rs759722483 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9391576 | TTTCTTTTCTTTTTC[-/T]TTTTTTTTTTTTTTT | 8853 |
rs759724320 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260952 | CAGGGTGGTTAGGGG[C/G]GTTGTGCCTGTGTCC | 8853 |
rs759731472 | snp | A/G | 1.66333e-05 | 0.00288381 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358720 | CTGACCCTCTTTTTT[A/G]CTGGAAGCTCAAATC | 8853 |
rs759748294 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9298548 | TCCCCCTTCATCCTT[A/G]TCCTAGAGTGGCGGC | 8853 |
rs759771225 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267178 | TAGATCGGGGGGTAC[A/G]TGTGTAGGTTTGCTA | 8853 |
rs759778110 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9347638 | TTGAGGATAACATCC[A/G]GGAGATTCGTTCAAA | 8853 |
rs759780449 | in-del | -/AA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265486 | AGAGAAAAGGGTAAC[-/AA]AGTATAGGATAGTAC | 8853 |
rs759783901 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295394 | GTTTGTGCTTTGAAT[A/G]AGTGACGCCTGTTGC | 8853 |
rs759789878 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209240 | AGCAAATCTACATAC[A/G]TGCTATGATGATGGT | 8853 |
rs759819362 | snp | A/T | 1.64754e-05 | 0.00287009 | missense | ASAP2 | GRCh38.p7 | 2:9334784 | AGCCTCAAACCTTCC[A/T]TTGAAACGCTGTCTA | 8853 |
rs759819508 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9319083 | AGCCACCATAAGCAC[A/G]CAGGCCAGGAGCTGT | 8853 |
rs759821640 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9251084 | GAAAACACACTGAGG[C/T]GTGGAAACCCACAGG | 8853 |
rs759826290 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278044 | ATGATAGGTTGTTGC[A/G]GGTTTTTATGATCTA | 8853 |
rs759841377 | snp | G/T | 1.65138e-05 | 0.00287343 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335085 | GTTGTGTGTGTGTGT[G/T]TTTAAAGATCAAACA | 8853 |
rs759843844 | in-del | -/T | 1.67465e-05 | 0.00289361 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368384 | TAGCAGTAGAATGTA[-/T]TAATAATTGAGTATC | 8853 |
rs759857364 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9289961 | GCCCGGGGTGTTGGA[A/G]AAGGCGGAGGAAGTG | 8853 |
rs759872394 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9268347 | GTAATTTTAATTTTT[A/T]AAGATAATACCAAAA | 8853 |
rs759874920 | snp | C/T | 3.30513e-05 | 0.00406504 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388286 | TCTGCCCCAATGTTC[C/T]CCTGCAGCCCAGTCC | 8853 |
rs759895832 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9241911 | ATGTTAGGGTCCCAA[A/T]AAGTTTAGGGGAGCA | 8853 |
rs759903612 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307822 | ACACTTAGGATCAGC[A/G]TGGGCTCCCCCTTCT | 8853 |
rs759913024 | in-del | -/TTTG | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404877 | TTATATCTGTAGTTT[-/TTTG]TTTTTGTTTTTTTTT | 8853 |
rs759922093 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9323777 | GGCCTGGGGAGCGCC[C/T]CTCTGCTCCACTCCA | 8853 |
rs759945563 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395806 | TAGAGATGGGGTTTC[A/G]CCGGGTTAGCCAGGA | 8853 |
rs759955478 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272817 | AAAAAATTGTCCTTT[-/C]CCCAGTGTATGTTCT | 8853 |
rs759962971 | snp | C/G | 1.648e-05 | 0.0028705 | missense | ASAP2 | GRCh38.p7 | 2:9388350 | CCAGCTGGGCTCCAA[C/G]CAGCTTCAGTCTAAC | 8853 |
rs759964900 | snp | C/T | 1.64833e-05 | 0.00287078 | missense | ASAP2 | GRCh38.p7 | 2:9374856 | ACAGTCTTTGCGAGG[C/T]CGTCAAAACGAGAGA | 8853 |
rs759981241 | snp | A/G | 1.65479e-05 | 0.0028764 | missense | ASAP2 | GRCh38.p7 | 2:9374921 | GTGGATCTTACGGAA[A/G]AAATCCCACTGGCCA | 8853 |
rs759981470 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9242796 | CCGTCTGGGGAAGCA[C/T]GATGCTGGGGAAGTA | 8853 |
rs759994811 | snp | A/G | 1.64754e-05 | 0.00287009 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356000 | CTTTTGGAATTGTGT[A/G]TGGATTGCTGTCTGG | 8853 |
rs760069256 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9255239 | CATGTAAGTTGGTTC[A/T]CAGATCATACAATGC | 8853 |
rs760076948 | snp | C/T | 5.89067e-05 | 0.00542677 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9393492 | CGCAGATCCCCTGAC[C/T]CCCACGCCGCCCCCA | 8853 |
rs760081749 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9285107 | AGAGTGGGGCCCTCA[C/T]GATGGGGTTAGTGCC | 8853 |
rs760095224 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343729 | TGGGATTACAGGCAT[A/G]AGCCACTGCGCCCAG | 8853 |
rs760105645 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9326019 | TCTTTCCATGGGTGA[A/G]AAAGATCATTTGAAA | 8853 |
rs760126330 | snp | G/T | 1.67416e-05 | 0.00289318 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327817 | CATTTCCTTTTCATT[G/T]TTCAACAGTATCTGC | 8853 |
rs760147152 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325120 | TAAAGCCTTTAATTA[A/C]ACTTAAAGGGTTCTT | 8853 |
rs760167397 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9356470 | GCAGCTCAGCCTGAG[C/T]TCATCCCATTACACA | 8853 |
rs760203147 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275194 | TAAGTGATCCTCCCT[C/T]CTCAGCCTGGGATTA | 8853 |
rs760217566 | in-del | -/AGC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281860 | GAGTAAATACTGCAG[-/AGC]AGCACCAGATGAGTT | 8853 |
rs760233129 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9314069 | GCTCACTGCAACCTC[C/T]GCCTCCTGGATTCAA | 8853 |
rs760243987 | snp | A/G | 1.64963e-05 | 0.00287192 | missense | ASAP2 | GRCh38.p7 | 2:9380786 | TTGCCAAGCGCCTCA[A/G]GCACGAGCACTGTGA | 8853 |
rs760249084 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244101 | CTAGCACTTTGGGAG[A/G]CCAGTCTGGGCAACA | 8853 |
rs760273463 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9270431 | TCAGTATTTTTTTTT[-/A]AATTTTTGATTATTG | 8853 |
rs760312098 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291615 | CCAGGCTGCTGCCAT[A/G]GAGAACATATGTCTC | 8853 |
rs760314853 | snp | A/G | 3.33406e-05 | 0.00408279 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344836 | CATGGTGTCTGCTGT[A/G]TTAGGTGAGGTTGGT | 8853 |
rs760344020 | snp | A/G | 7.22061e-05 | 0.00600815 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374705 | AAAGGGAGGCCGGAC[A/G]GCGGGTAGAAGCCCT | 8853 |
rs760348501 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205719 | AAAGGTTTTTGTAAA[A/G]TTTCTCTTGGTTTTA | 8853 |
rs760354118 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373192 | GGGCAGAACTGGAGC[C/T]GGAGCAGGAGGGAGG | 8853 |
rs760357147 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302699 | AGGCTGGTCTCGAAC[A/T]CCTGACCTCAAGTGA | 8853 |
rs760366112 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9303709 | GCACATTGTTTGATC[A/G]AGACAATGAACAAAT | 8853 |
rs760381236 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9360078 | GATGATGGCATAGAT[C/T]GGAGGTTGTCATGGT | 8853 |
rs760405024 | snp | C/G | 4.94425e-05 | 0.0049718 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344644 | GTGACGGGTACGTGA[C/G]GGGGTGTGGCTAGAG | 8853 |
rs760431902 | snp | C/T | 0.000100771 | 0.00709756 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374782 | GGACTACATCACAGC[C/T]AAGTACATCGAGAGG | 8853 |
rs760434203 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275793 | AGGCACTGGGGATAC[A/G]ATGAACAAATATCAG | 8853 |
rs760434449 | snp | C/T | 6.59272e-05 | 0.00574101 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344723 | TGTTTCTCCCACTTA[C/T]CCACAAGGATCCGAA | 8853 |
rs760454104 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9280759 | GCCATCCGTCTCTAG[C/G]TTTTTTACCTGGATT | 8853 |
rs760475522 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350640 | GATGAAGTTCAAAGG[A/C]CTCTGTAACTTGTCC | 8853 |
rs760491344 | in-del | -/CT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338292 | TCAAGTATGGTTGCT[-/CT]CTCTCTCTCTCTCTC | 8853 |
rs760505637 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9235137 | CTTTTCCTGTCCTGT[G/T]GTAGGCGGGGATCTG | 8853 |
rs760524374 | snp | C/T | 1.73261e-05 | 0.00294325 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318622 | TTGACACTGTGACAC[C/T]AGGGGCAGCTTTTAC | 8853 |
rs760533259 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9403106 | ACGGACAAAAATCAT[C/T]TGGATGTTTTACCTA | 8853 |
rs760556107 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362868 | TTTAAGTATACAGTA[C/T]GTTATTATTAAGTAG | 8853 |
rs760565468 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346620 | TCTGTGGTTTGCTTT[C/T]GAATTGGTGTCCACT | 8853 |
rs760571911 | snp | C/G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9282648 | ATAGTGTTTTGATCA[C/G/T]GAGAATAAAGACCAA | 8853 |
rs760592953 | in-del | -/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240246 | GTCTTCCTCCCATAA[-/TT]TTTTTTTTTTTTTTT | 8853 |
rs760597223 | snp | C/T | 3.29554e-05 | 0.00405914 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9391035 | ATGTGTGCGTGCATG[C/T]GTCTGTGTGCATGCG | 8853 |
rs760597537 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373971 | GTGTTGACGCACATA[C/T]GTCTCATGGTGCTAC | 8853 |
rs760619146 | snp | A/G | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404467 | AGGATTAGGTTGTCT[A/G]TTATAAAACCAAAAC | 8853 |
rs760632837 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250913 | GCTTGCTCCCGGGGA[A/C]CTTAAAACAGTGAAC | 8853 |
rs760684874 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9238894 | ATGATTTTGTCTTCT[A/G]TGAACGCTGTTTGCC | 8853 |
rs760716539 | in-del | -/ATT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245591 | GACTTCTGAATCTAA[-/ATT]AAGAGCACCACTCTT | 8853 |
rs760717599 | in-del | -/CAAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317399 | CCACACACACACCCT[-/CAAA]CACACACATGCTCCC | 8853 |
rs760748396 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371026 | CCAAGCACCAGGGGT[A/T]CCTAACGAAAGCAGG | 8853 |
rs760757117 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322279 | ACTCTAGTCCTCCTT[G/T]CCCTAATGACAGGGA | 8853 |
rs760763822 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9340313 | GGCATGAGCCACCGC[A/G]CCCGGCCAGCCATGT | 8853 |
rs760771309 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9310274 | TCTCATAAATTGGGC[A/G]TATTCAAATAAGTGA | 8853 |
rs760771690 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9299108 | GCAGGTGTTTTAGAA[A/C]GAGAGAAGGTTGTCA | 8853 |
rs760805639 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9288702 | CATACAACAAATGTT[G/T]AATTCACCTCTTGGC | 8853 |
rs760826058 | snp | A/G | 1.65811e-05 | 0.00287929 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374932 | GGAAAAAATCCCACT[A/G]GCCAACGGACATGTA | 8853 |
rs760839486 | snp | C/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213563 | GAGACCAGTTGTGGG[C/G]TGAGGGGCTATTGCA | 8853 |
rs760843202 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351728 | CCTGTATTATTGAGG[A/G]CTAGGAAGTCACTTG | 8853 |
rs760855378 | snp | A/G | 1.64928e-05 | 0.00287161 | missense | ASAP2 | GRCh38.p7 | 2:9335102 | TTAAAGATCAAACAG[A/G]CCCAGGATGAAGAAA | 8853 |
rs760855667 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380266 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAACCT | 8853 |
rs760865958 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272867 | GAGTTCACTGTAAAT[A/G]TATGGATTTATTTCT | 8853 |
rs760895714 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258511 | AAGCTCAGAGGAGAA[G/T]TGGCTCACCTAAGGC | 8853 |
rs760899973 | snp | C/T | 3.31565e-05 | 0.0040715 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400008 | AGTAAATCTACTTTT[C/T]CCCTGTCTTTGTAGG | 8853 |
rs760929165 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248922 | TGGAAGCTCTCCATG[C/T]CCCCAAATCCAGAAG | 8853 |
rs760930057 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9220753 | CATAATACAGTCACA[A/G]AGATTTACACCTATA | 8853 |
rs760941869 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328930 | ATAATACAGGGACCT[C/G]ATTTAGATAAAGATT | 8853 |
rs760951088 | snp | G/T | 1.64738e-05 | 0.00286995 | missense, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9279352 | GGTTCTTTACAAAAT[G/T]AAGAAATCCGTGAAA | 8853 |
rs760953884 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9259877 | GCACCCTGATGAGCC[C/T]CTGCAGTGTCCTGCA | 8853 |
rs760958143 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274306 | TGGCATAAGACTGTT[G/T]CTAGCATTCAATCTT | 8853 |
rs760971797 | snp | A/G | 8.2513e-05 | 0.00642259 | missense | ASAP2 | GRCh38.p7 | 2:9388453 | CAGAATGAGACTTAC[A/G]GAGCCCTCCTGAGTG | 8853 |
rs761000085 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9385522 | GTTTTACCCTTCCCA[C/T]TACCATCTCCTGTCT | 8853 |
rs761003398 | in-del | -/GCCCCCACA | 1.6659e-05 | 0.00288604 | cds-indel | ASAP2 | GRCh38.p7 | 2:9393600 | CAGGCCCCCACCTCT[-/GCCCCCACA]GCCGCCCAGCCGCCT | 8853 |
rs761004524 | snp | A/G | 1.65206e-05 | 0.00287403 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297261 | GGGAGTGAGGGTGGC[A/G]TGCCTGAGACTCACA | 8853 |
rs761009021 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245328 | TTGAATGGGCTCTGG[A/C]GACACCTGGGGTGGG | 8853 |
rs761043247 | snp | A/G | 6.73265e-05 | 0.00580161 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403353 | AACAAAAGCATTAAC[A/G]GTTATGTTCCTGTTT | 8853 |
rs761052618 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265626 | GATTATTTTCTTTCT[-/G]TATCTTTATATACAG | 8853 |
rs761066423 | snp | C/T | 1.64735e-05 | 0.00286993 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356019 | ATTGCTGTCTGGGCT[C/T]ACAGTTGAAATTCCT | 8853 |
rs761134858 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9323659 | CAGACCATGGCCTGT[-/G]TCAGTGTCTGTGAGT | 8853 |
rs761136797 | snp | C/T | 1.64942e-05 | 0.00287173 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376868 | CACAGAATTGAATGC[C/T]CCCATTAGAATTCTG | 8853 |
rs761146931 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315791 | CTTTTCAGCATTTAA[A/C]AATTTAATGCTTAAG | 8853 |
rs761161090 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9400874 | TCTGCTCTAGCCAGG[A/G]GGGTGCAGGTGGTTT | 8853 |
rs761174674 | snp | A/G | 1.66112e-05 | 0.00288189 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323265 | GGTAAGGCGGTGGTG[A/G]AGGCAGGTCCTACAG | 8853 |
rs761200954 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348395 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC | 8853 |
rs761203330 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266636 | GCCACCACCCCGTTC[C/T]AGTCAAGATGGGAAT | 8853 |
rs761205865 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221855 | GCTGGAGTGCATGGC[A/G]CCATCTCGGCTCACT | 8853 |
rs761212653 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353972 | AGAGGGAGACCTTGT[C/G]TCTTTAAAAAAAGAA | 8853 |
rs761216549 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9288940 | CATACTACATTTTCA[A/C]TGAGGAAATTCCTCT | 8853 |
rs761230731 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253730 | GATTACAATGTTACA[C/T]GTATCTTTAGACCAC | 8853 |
rs761236027 | in-del | -/T | 9.24274e-05 | 0.00679744 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374967 | GTGGGTTGTTGCTAC[-/T]TTTAAAAAAAAAAAA | 8853 |
rs761252436 | snp | C/T | 9.85173e-05 | 0.00701776 | intron-variant, missense, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207244 | AGGTGAGGCGGCCTG[C/T]GCGGCGGCTCCGGCC | 8853 |
rs761257460 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337237 | CAGTCTCCTAGTTGT[A/G]GGCGTGTTGTGTTTT | 8853 |
rs761259674 | in-del | -/TA | 4.94246e-05 | 0.0049709 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279311 | CTGTATTCTCTACAT[-/TA]TTTAGGCTTTGGACG | 8853 |
rs761270110 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254838 | AAGTGATGGGCATTT[G/T]GGTTCTTTCCAGTTT | 8853 |
rs761281715 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307566 | CCGGCCTTCAGCTGG[C/T]GTCAGTGTGGTTGTT | 8853 |
rs761297328 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9367671 | GAACCTGAGGTAGGA[A/G]GGTCACCTGAGCCTG | 8853 |
rs761306169 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336443 | GCCCCATTTGAATCA[C/T]AGCCTATTCCTCTTT | 8853 |
rs761317081 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343006 | GCTTCCATCACACTG[A/G]TTTTCCTGCGTTAGT | 8853 |
rs761348711 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366333 | CCATCTCCCCACCCC[C/T]ATCTGCTTAACACAA | 8853 |
rs761383824 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369854 | GGGAGAGAATTTAGA[-/T]TTTTTTTTTCCCCTT | 8853 |
rs761396457 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274215 | TTCAACTTCATCCTT[C/T]CAATTTGGAGGCCCT | 8853 |
rs761396661 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9242729 | TTTTTTCTGTTTCCT[C/T]TACTGTTCCAACTTT | 8853 |
rs761402184 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209117 | AAGAGACTGGATTTG[A/G]TCATTTCATTAAATT | 8853 |
rs761414693 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9323703 | AGTCACCTGTTTTGA[C/G]TTCCTGCTAGACCTC | 8853 |
rs761427084 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9241833 | ATCTGGACCTGAAAG[G/T]TTGAATCTAATAAGT | 8853 |
rs761439424 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302169 | TGTGAGTTAGAAGCC[-/T]TTTTTTTTTTTTTTT | 8853 |
rs761442141 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9241498 | AATCCCAGCACACTG[A/G]GAGGCCAAAGAAGCA | 8853 |
rs761445602 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351008 | TTTTTGAAGAGACAT[-/A]ACCCTTTTTCTAGTG | 8853 |
rs761457631 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9355386 | CTCTAGTGTTTTCTC[A/G]TGAGTGGATTGAGGT | 8853 |
rs761460562 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239264 | TTATGTGTGGGGTAA[A/G]CACAGATTTGGTGTC | 8853 |
rs761463891 | snp | C/T | 1.65214e-05 | 0.0028741 | missense | ASAP2 | GRCh38.p7 | 2:9320300 | CAGGATCTGAAAAAG[C/T]CTTTTGATAAAGCTT | 8853 |
rs761477328 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9228485 | ATTTGGTCTTTGGTC[A/T]CTTTCTTTGGGGAAG | 8853 |
rs761482159 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9382290 | CACCTGACCTGTCTC[A/G]TTTAATCTTCATAGC | 8853 |
rs761496519 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274993 | TGTCAGAGTTCAATT[A/G]TGTTATTAAGGTATG | 8853 |
rs761504964 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373154 | ACGTTGAGGCACCCG[C/T]CTTAACCTAGGCCCT | 8853 |
rs761518412 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313899 | CTACTATGTGGTATT[C/T]TTAGAATTTTACATT | 8853 |
rs761526914 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9355843 | TTGAATGAGGGAAAG[A/G]GCAGGTTTATTTTGC | 8853 |
rs761528938 | snp | C/T | 1.75121e-05 | 0.00295901 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318632 | GACACCAGGGGCAGC[C/T]TTTACACCATGTAGA | 8853 |
rs761540224 | snp | G/T | 1.6513e-05 | 0.00287336 | missense | ASAP2 | GRCh38.p7 | 2:9344787 | ATGGTTTTCTGACCA[G/T]ATCCCATGGTACCGT | 8853 |
rs761542366 | snp | A/G | 1.64874e-05 | 0.00287113 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374833 | CGCGGATAACGCGGC[A/G]AAGCTTCACAGTCTT | 8853 |
rs761554879 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302628 | TATAGGCGCGAGCCA[A/C]CACACCCAGCTAAGT | 8853 |
rs761560481 | snp | A/G | 1.65203e-05 | 0.002874 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9350837 | TGCAAAGCTCAACCT[A/G]CTAACCTGCCAGGTG | 8853 |
rs761569639 | snp | G/T | 1.64754e-05 | 0.00287009 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9391048 | TGCGTCTGTGTGCAT[G/T]CGTGTGGGTTCAGTT | 8853 |
rs761583047 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9285003 | ATCGTTACCTGCACA[A/G]TAACCTCAGTATTGC | 8853 |
rs761608446 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301534 | TGCTGAGAAGTGGCT[C/T]TCTAATGAAAGGCTG | 8853 |
rs761618330 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315621 | AGGCGGGAACTGTGA[C/T]GGGAGTTTCATTCCT | 8853 |
rs761638124 | in-del | -/AA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286438 | TTTTTTAAAAAAGGA[-/AA]AAAAAAAAAATATAT | 8853 |
rs761652157 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9280450 | AAGCCACAATCGGGA[A/C]GAATCTAGCAGGAAA | 8853 |
rs761659270 | snp | A/G | 1.73201e-05 | 0.00294274 | missense | ASAP2 | GRCh38.p7 | 2:9379014 | CTGACCGACAATGCC[A/G]AGTGCCTCAAGTTGC | 8853 |
rs761661220 | snp | A/G | 1.64798e-05 | 0.00287047 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391134 | GTGGAAGCCGGCAGC[A/G]ATCTTCGTCAGATCC | 8853 |
rs761673164 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217044 | CACGGTACCAAGTTC[A/G]TGGAGCTTGGAGGTG | 8853 |
rs761674758 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402151 | GGGAACTTCTTTGTC[A/G]AGTGCGAGGAGTTTG | 8853 |
rs761677655 | snp | C/T | 2.46606e-05 | 0.00351137 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379090 | CCCCGGGGGTGGGCT[C/T]AGCTGCACCCTGGCC | 8853 |
rs761679855 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362656 | CCAGCCTGACCAACA[C/T]AGGGAGACCTCCATC | 8853 |
rs761681681 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250838 | AGGCCACCATGGGCC[A/G]TCTGTGAGCAAAGTG | 8853 |
rs761707204 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291465 | CAAGTGAGGTCGGAA[A/G]CAGGTGGCATGTACA | 8853 |
rs761713136 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9372549 | TATTTCTGATCATGA[A/G]AACATCACCAAACTT | 8853 |
rs761750528 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9273973 | CTTTGTTTCAAAGCT[-/A]AACTGTAAGTTCCTC | 8853 |
rs761762913 | snp | A/G | | | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9215255 | ATCTTATGAGAGGTC[A/G]TCTGTGTGGTTCATT | 8853 |
rs761778049 | in-del | -/CACT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317749 | TCACATCCACACTCA[-/CACT]CACATCCGTACACAA | 8853 |
rs761824196 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258064 | CCACAACCAGTGCTG[G/T]TATCATCACATTTGT | 8853 |
rs761883078 | snp | C/T | 1.6489e-05 | 0.00287128 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376882 | CTCCCATTAGAATTC[C/T]GGAATGCCTTTGTTT | 8853 |
rs761896077 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332629 | TCTCTGTCTGACCGT[A/G]GGGAGAATTGCCAGG | 8853 |
rs761903078 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9310210 | GAGCAGCATTTGCTC[A/G]AATTAAAATCTCCCC | 8853 |
rs761905470 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9226118 | CTGGGGCACGTAAGA[A/G]GGGCTCAGAAGGTCA | 8853 |
rs761908349 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281786 | CTTAACCCTTTCCCA[A/G]TTCATCTGTCGATGA | 8853 |
rs761912069 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254487 | CCTCCCAAGTAGCTG[C/G]GATTACAGGCATGCA | 8853 |
rs761926794 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9269631 | GGCACCGCCCTCAGG[C/T]GGTACAGTGGGGCCC | 8853 |
rs761933601 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225105 | AAAAGTGTAAGCTAA[A/C]AATGGTGTTTATGGT | 8853 |
rs761935035 | snp | A/G | 1.64762e-05 | 0.00287016 | missense | ASAP2 | GRCh38.p7 | 2:9344610 | GGGACCGAGCGGAAC[A/G]GCAGCCTCTACAAGA | 8853 |
rs761940253 | snp | C/T | 3.29506e-05 | 0.00405884 | synonymous-codon, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9297403 | TGCGTTCCTGAAGTT[C/T]TCAGTGTTTACAAAG | 8853 |
rs761949475 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9238733 | AAATTTACCCTAAGA[A/G]TACACTTTGATGAAT | 8853 |
rs761961153 | snp | A/G | 1.64762e-05 | 0.00287016 | missense | ASAP2 | GRCh38.p7 | 2:9388369 | CTTCAGTCTAACGCT[A/G]TATCTTTGGCCAGAG | 8853 |
rs761968954 | snp | A/G | 1.64795e-05 | 0.00287045 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356163 | ATTTAACACAGCGTT[A/G]CTCTTGTTTTTCTAG | 8853 |
rs761976416 | snp | A/G | 1.66059e-05 | 0.00288144 | missense | ASAP2 | GRCh38.p7 | 2:9403262 | TTTCAGATTGGCCAC[A/G]TTGATGGAGATCCTG | 8853 |
rs761987745 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321254 | TTTCCAGTGGTGAAG[A/G]ATCACAAAGCTCAAA | 8853 |
rs762001250 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219170 | GTAATGTGGACTGTT[-/G]GAACTTCAAGAAAAT | 8853 |
rs762007182 | snp | C/T | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390378 | TTCTAGGCCTAGCCT[C/T]TGCCCTACAGGCCGT | 8853 |
rs762007216 | snp | C/T | 1.65081e-05 | 0.00287293 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297278 | GCCTGAGACTCACAG[C/T]ACCTCCGTCATTCTG | 8853 |
rs762076013 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369101 | TCGGCTCACTGCAAC[C/G]TCTGCCTCCCAGGTT | 8853 |
rs762079645 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9357490 | TTTAAAACAAACAAA[A/C]AAAAAACCCGAAAAT | 8853 |
rs762082658 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9340268 | CCTCGTGATCTGCCC[A/G]CCTCCGCCTCCCAAA | 8853 |
rs762088552 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205124 | TTTGTCCTTGTAGAA[C/G]TATTGATTAGTCTGG | 8853 |
rs762093442 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327976 | ACTTCTGGTAGATCT[A/G]TAGATAGCTCATAGG | 8853 |
rs762099333 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9287500 | TGGTTTCGGAAGGGG[C/T]AGGAGAGGGCGTACA | 8853 |
rs762099957 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212782 | GGCTCAGCAACCACC[A/G]GGAGAGCCATCACCT | 8853 |
rs762105675 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286505 | AGAAAATAACAAAAT[C/T]AGAATAATCTTTACT | 8853 |
rs762117502 | in-del | -/G | | | upstream-variant-2KB, intron-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9206108 | CTGGGACTTTTAGTA[-/G]GGGCCCCTCACCGCT | 8853 |
rs762122398 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245112 | TTTGATACCCACTTT[A/G]TAGGACTGCGGTAAG | 8853 |
rs762125391 | snp | A/G | 1.65061e-05 | 0.00287277 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377020 | GAAATTAAGGGAGGC[A/G]CTCGTTTTCTCCTTG | 8853 |
rs762135629 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9297958 | TTTCAGCCGTGGGAA[C/T]GCGGTGCTGGTGCCT | 8853 |
rs762138158 | snp | C/G | 1.69275e-05 | 0.0029092 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403362 | ATTAACAGTTATGTT[C/G]CTGTTTCGTTATTGG | 8853 |
rs762157634 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271319 | AGCTGATCGTCCTTA[C/G]CCAGTCCAAGCTCTA | 8853 |
rs762181323 | snp | A/G | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403859 | CTTGGAAATTTACAC[A/G]TTAGCATTGTACTTT | 8853 |
rs762223313 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358207 | ACTCTTAGATTTGAT[A/G]CAAAAGTGCTCTGTG | 8853 |
rs762247244 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232662 | CCAGAATTGCACTGG[A/G]CACATCATATATGTT | 8853 |
rs762271258 | snp | A/G | | | missense | ASAP2 | GRCh38.p7 | 2:9385348 | ATGACGACATGGATG[A/G]GAAATTGCAGGTCTG | 8853 |
rs762273765 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307396 | GGAGGTCAGAGCTAC[-/T]TCCTAAACCTGGATT | 8853 |
rs762277144 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277620 | AACTTTCCAAATACC[C/T]GTTCCCCTTGACATG | 8853 |
rs762284748 | snp | A/G | 1.70886e-05 | 0.00292301 | missense | ASAP2 | GRCh38.p7 | 2:9356313 | TGCAGAGGATGACGG[A/G]CAATGACGTCTGCTG | 8853 |
rs762299157 | snp | C/T | 0.000116242 | 0.00762282 | missense | ASAP2 | GRCh38.p7 | 2:9393499 | CCCCTGACCCCCACG[C/T]CGCCCCCACCCGTTG | 8853 |
rs762299640 | snp | G/T | 1.65888e-05 | 0.00287996 | missense | ASAP2 | GRCh38.p7 | 2:9327838 | CAGTATCTGCTGAAG[G/T]TCAACGAAATCAAGA | 8853 |
rs762311379 | snp | C/T | 3.58931e-05 | 0.00423619 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385205 | AGATGCATGGCCGAG[C/T]GTATGAGCAACAGCA | 8853 |
rs762313222 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234648 | TGGGCTGTTTCTAAT[C/T]AGTTAAAATGAGTAG | 8853 |
rs762317924 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9398984 | GATGTCTGCAGAGAC[A/G]TTTACACCCAGAGAC | 8853 |
rs762326006 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384567 | GGTTCCCACAGCCCC[C/T]TCTTTGGGTTTGAAT | 8853 |
rs762326535 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210679 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 8853 |
rs762334256 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276879 | TTTTCTCCCTTTACA[C/T]TTGCTGGCCCATGGA | 8853 |
rs762334308 | snp | A/G | 5.63502e-05 | 0.00530772 | synonymous-codon, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207125 | GGACCAGATCTCCGT[A/G]TCGGAATTCGTGGCC | 8853 |
rs762354138 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264930 | AATCACTTGAGCCCA[C/G]GAGTTTGAGACCAGC | 8853 |
rs762426873 | snp | A/G | 1.64754e-05 | 0.00287009 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391055 | GTGTGCATGCGTGTG[A/G]GTTCAGTTCAGACAG | 8853 |
rs762429240 | snp | C/G | 1.79554e-05 | 0.00299623 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374717 | GACGGCGGGTAGAAG[C/G]CCTTCATGATTTGCA | 8853 |
rs762430569 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336260 | TACACTTTTGCTGCT[C/G]TTCCTTTATGAAGAT | 8853 |
rs762430699 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266284 | CACCAGTAACTGGGA[C/T]CACAGGCACCTACCA | 8853 |
rs762430706 | snp | C/G | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390740 | TCCAAGTGCAGTGTT[C/G]GCAAGAGAACATTGT | 8853 |
rs762450051 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9303900 | ATGGTGAGGCCTTGG[A/G]CGTGGGAGGGAGAAC | 8853 |
rs762450113 | in-del | -/GT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332875 | TATTCAGAAAAAAAC[-/GT]ATTAAAATACAGGAA | 8853 |
rs762481679 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9334922 | TGCCGTGCCGCCCAC[A/G]TGGAGTGTGGCGTTC | 8853 |
rs762484751 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294425 | AGTCTACTATCAGTG[A/T]GAAGGCCGGCTCCTC | 8853 |
rs762504235 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9220539 | ACTATCTATTCAAAT[C/T]CTTTGCCATGTTTAT | 8853 |
rs762533601 | in-del | -/TG | 1.74257e-05 | 0.0029517 | frameshift-variant | ASAP2 | GRCh38.p7 | 2:9356333 | GACGTCTGCTGTGAC[-/TG]TGGGGCGCCAGGTGA | 8853 |
rs762543207 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253532 | ACCCTACAGATGTAA[C/T]GTAGCAGAGTGCCGT | 8853 |
rs762547166 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9208760 | TTCCTAAGTGCCAGT[G/T]AAAAAGCACGGTGTT | 8853 |
rs762570905 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9252439 | TACAGAAAATTAGCT[G/T]GGCATGGTGGCACAC | 8853 |
rs762574771 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265435 | ATTTTTGTGCTCAGA[C/G]TTAAAGACCTCAATA | 8853 |
rs762584465 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9320991 | TAGAGTAGAGAGAGT[C/T]GAGCTACAGGGAATT | 8853 |
rs762592822 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272992 | ATGTGGTTCCTCCAG[C/T]TTTGTTCTTTTTGCT | 8853 |
rs762599531 | snp | A/T | 4.94515e-05 | 0.00497225 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391142 | CGGCAGCGATCTTCG[A/T]CAGATCCGCCAGCTG | 8853 |
rs762607605 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366142 | CTGGAGGGGTTCTCT[A/G]TGGGCTGAAACGTAA | 8853 |
rs762610686 | snp | C/T | 3.3243e-05 | 0.00407681 | missense | ASAP2 | GRCh38.p7 | 2:9401347 | ATGAGCTCACCTTCT[C/T]CGAGGGGGATGTGAT | 8853 |
rs762615199 | snp | C/T | 1.65638e-05 | 0.00287778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379110 | GCACCCTGGCCTCTG[C/T]CTCCTGTCTGCCATC | 8853 |
rs762632326 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9393728 | CTGCAGGAATGTTTG[C/T]AATCCCCAGGGCTCC | 8853 |
rs762634917 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305509 | GAGGCTGTAGTAGTG[A/G]GGTATAGATATTGGT | 8853 |
rs762664525 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9323520 | CTTCACGTACGTACT[A/C]TTGCTAAAATATTTA | 8853 |
rs762702580 | snp | A/T | 3.31532e-05 | 0.0040713 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323091 | TCTGTGCCAACAGGC[A/T]TCTTGATGTATCCTT | 8853 |
rs762710524 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9394974 | TCAGCTGGGCTGTGA[C/G]CAGAACACCTACATG | 8853 |
rs762724658 | snp | C/G | 1.648e-05 | 0.0028705 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9380763 | GTCAGGAGAGACTCC[C/G]CTGGACATTGCCAAG | 8853 |
rs762744101 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338431 | CAGTTTGTGCCACCC[A/C]GGCAGCCAAGGTCCA | 8853 |
rs762755480 | snp | C/T | | | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9215154 | CCACTGTGTTGAATA[C/T]CGTGGTAACTGCGAC | 8853 |
rs762767303 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300316 | CTTGGAGCACTCCAC[A/G]CCATGGAATCCGGAC | 8853 |
rs762774632 | snp | G/T | 1.66599e-05 | 0.00288611 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358914 | AAATCCTTGATTTCA[G/T]ATTGGAAACAAATGA | 8853 |
rs762775912 | snp | A/C | | | missense | ASAP2 | GRCh38.p7 | 2:9401341 | ACCCCGATGAGCTCA[A/C]CTTCTCCGAGGGGGA | 8853 |
rs762783711 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214223 | GCCCTTCCAGGTACT[C/T]TTTTTCTTTTCTTTT | 8853 |
rs762807030 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9382167 | TTTTATATTTTTAAT[A/G]GAGACGGGGTTTCAC | 8853 |
rs762812194 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9342905 | TACCCTGATTCTGTG[C/G]CAGTTCTTGCCTTCA | 8853 |
rs762812508 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284764 | TTATACATTATCAGG[-/T]TTCCTGCTGTATGTA | 8853 |
rs762816336 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229134 | AGATGTACTAAACAT[C/T]TGTACAGATGTGGAG | 8853 |
rs762821900 | snp | C/T | 1.64787e-05 | 0.00287038 | missense | ASAP2 | GRCh38.p7 | 2:9368438 | AGCTCGCCAAGAATA[C/T]TGGGAATGCAGGCTT | 8853 |
rs762822683 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9312922 | AGCTGGGCATGGCAT[A/G]GTGGCGTGTGCCTGT | 8853 |
rs762847965 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301407 | CAGACGGCTCCAGAA[A/G]TGTGACATGTGTGAA | 8853 |
rs762856329 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9330839 | GTGGAAAAGTGAAGT[A/G]GTTGGCCTTTTATGG | 8853 |
rs762858554 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9262483 | ATTCCCAATTTATAG[A/T]TGAAGAAACAGAAGT | 8853 |
rs762859607 | snp | A/G | 1.65012e-05 | 0.00287234 | missense | ASAP2 | GRCh38.p7 | 2:9388310 | CCAGTCCCAACCGGC[A/G]GGAAGACCGGCCCAT | 8853 |
rs762861411 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248693 | TACTGTTTACTCTGC[G/T]TGTAACTTTCACTCC | 8853 |
rs762867612 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381185 | AACCTCCTTTCTTTG[C/T]TCCTCAGCCCCAGAT | 8853 |
rs762903870 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227741 | TGAGTTAAAAAAATA[C/T]GTGGGTAAGGTATTT | 8853 |
rs762905828 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9242618 | GGCTGATAGCTGGTC[A/G]CGGGATCACCTTTCA | 8853 |
rs762912311 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9261179 | GGAACAGGGTTTAGA[C/G]AAAGCAGGGGTAATG | 8853 |
rs762971727 | snp | C/T | 3.40913e-05 | 0.0041285 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318607 | GAAAGGGGTATGACA[C/T]TGACACTGTGACACC | 8853 |
rs762979328 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236282 | CTTGTAGGTAATCAA[A/G]TGCCACGAAGTAAAG | 8853 |
rs762982469 | snp | A/G | 5.04028e-05 | 0.00501985 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344507 | CCTGGACAAGATTAA[A/G]AACACACTCTTCACC | 8853 |
rs763006251 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362513 | TATCTGTCACCTCAC[A/C]TGCTTATGTTTTGTG | 8853 |
rs763023347 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291330 | TAGTTGGGATGATTC[C/T]AGAAATAAAGTTCTG | 8853 |
rs763043761 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9320070 | TTGCTTTTGTGTACA[C/T]TTAGTATATTCTATA | 8853 |
rs763044072 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343515 | GCAGTGGTGCTATCA[G/T]GACTCACTGCAACCT | 8853 |
rs763059262 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373136 | GGGAGCATGTGCCGG[A/G]GGACGTTGAGGCACC | 8853 |
rs763076150 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348769 | GATAGTAGTTAAGAA[C/T]GAACACCTTTCCCCG | 8853 |
rs763103616 | snp | C/T | 3.2962e-05 | 0.00405954 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376905 | CTTTGTTTGGTTTTT[C/T]AGGAGCCGGATGAAA | 8853 |
rs763108350 | snp | A/G | 1.71062e-05 | 0.00292451 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403370 | TTATGTTCCTGTTTC[A/G]TTATTGGTACCAAAA | 8853 |
rs763145364 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9304887 | ATAGATATTGGTGGA[C/G]AGGCTGGAGTAGTGG | 8853 |
rs763145821 | in-del | -/TG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217632 | TTGTTTTTTTTTTTG[-/TG]AGACGGAGTCTTCGC | 8853 |
rs763148263 | in-del | -/TGTG/TGTGTGTGTG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361971 | TCTTATCTCTTTCTC[-/TGTG/TGTGTGTGTG]TGCGTGTGTGTGTGT | 8853 |
rs763159298 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9285267 | GTTCAGCAGGTCAGG[A/G]TTGGAGCCTGAGTAT | 8853 |
rs763162276 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9226222 | AACTCTTAAAAATCC[A/G]ATCTTATCTCTACTT | 8853 |
rs763193204 | snp | C/T | 1.65124e-05 | 0.00287331 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377029 | GGAGGCACTCGTTTT[C/T]TCCTTGGTATTTCTG | 8853 |
rs763203282 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9308958 | TTCTTTCAGATAAGC[A/G]GCCTTTAGAAAGAAC | 8853 |
rs763213826 | snp | A/G | 3.44501e-05 | 0.00415016 | missense | ASAP2 | GRCh38.p7 | 2:9356321 | ATGACGGGCAATGAC[A/G]TCTGCTGTGACTGTG | 8853 |
rs763231081 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378270 | ACAGTGGCCATGTTT[C/G]CTAGGATTGAGGGCC | 8853 |
rs763254373 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237709 | ACAGGCATGAGCCAC[C/T]GTGCCTGGCCTGCTC | 8853 |
rs763264412 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9268484 | GGCTTTATTCCCACA[A/T]GGGGGGAGGTTCGTT | 8853 |
rs763281332 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9224674 | TTTCTTCTGTAGAAC[C/G]TTCCCTAACACTCCT | 8853 |
rs763281481 | snp | A/G | 1.89827e-05 | 0.00308075 | missense, utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207154 | CCGAGACCCATGAGG[A/G]CTACAAGGCGCCCAC | 8853 |
rs763281925 | snp | C/G | 0.000145672 | 0.00853315 | missense | ASAP2 | GRCh38.p7 | 2:9393558 | GAGCCAGCCGAGCAA[C/G]CCTGCCCCGCCTGGG | 8853 |
rs763289356 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257158 | TTACACGTGTCGGGC[A/G]TTCCACTGGTGCTGG | 8853 |
rs763350701 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276053 | GGCTCCTGTTTTCAT[C/T]GTTAATTTGTGTTTC | 8853 |
rs763365115 | snp | A/C | 5.32099e-05 | 0.00515772 | missense | ASAP2 | GRCh38.p7 | 2:9393631 | AGCCGCCTCCCGCAG[A/C]AGAAGCCTGCGCCGG | 8853 |
rs763375048 | snp | A/G | 1.64912e-05 | 0.00287147 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9385322 | ACTCCACGAAGACCT[A/G]GATGAAAGTGATGAC | 8853 |
rs763376658 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212255 | GAGGAACAGAATCCT[A/G]TAAACAAATCAGTGC | 8853 |
rs763389137 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9326436 | AAATTCAGTATGTCA[A/T]ATAGGTAGTACAGAC | 8853 |
rs763389715 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9231174 | TGGCTGGGTGTTTCT[C/T]TCTGCTGGAAGGGTT | 8853 |
rs763411745 | in-del | -/CACACCCT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317276 | ACACACACTCATATC[-/CACACCCT]CACACCCTCACAATC | 8853 |
rs763443583 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212372 | GGTGAGGGAGGGCCT[C/T]ATATGATGTCGTACC | 8853 |
rs763457425 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245011 | AGTCCTCCCGTCATA[A/T]AAAAGGTAAAAGTCT | 8853 |
rs763457551 | snp | C/T | 1.65228e-05 | 0.00287422 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374803 | CATCGAGAGGAGATA[C/T]GCAAGGAAGAAGCAC | 8853 |
rs763459636 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9356698 | GCTTCCTTGCTTGGA[A/G]TCTGCTCTCTTCTCC | 8853 |
rs763465038 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378809 | TCCCACCACCTTGGC[A/G]ATGATTTACAGAAAC | 8853 |
rs763482262 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275920 | TTTTAACGTGGCACT[A/T]AGCCACATTTCAGGT | 8853 |
rs763484002 | snp | C/G | 0.000324834 | 0.0127401 | intron-variant, synonymous-codon, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207254 | GCCTGCGCGGCGGCT[C/G]CGGCCGCAGGTATCC | 8853 |
rs763508621 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9287780 | TCCAGCCTTCTCCCC[-/G]GCTGCTGGCTAACAA | 8853 |
rs763537113 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286353 | CAGTGAGCTGAAACT[A/G]CACCACTGCACTTCA | 8853 |
rs763555998 | snp | C/G | 5.72863e-05 | 0.00535162 | missense, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207114 | GAGGCGATGCCGGAC[C/G]AGATCTCCGTGTCGG | 8853 |
rs763602369 | snp | G/T | 1.64803e-05 | 0.00287052 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344645 | TGACGGGTACGTGAG[G/T]GGGTGTGGCTAGAGT | 8853 |
rs763610857 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302469 | AGCCACCATGCCTGG[-/C]CAACTTTTTTTGTTT | 8853 |
rs763629463 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9282902 | CACTGCTTCCTGAGT[A/G]TGTGCCAGCTGTACT | 8853 |
rs763630146 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240160 | TGTTCCAAGACCCTC[A/G]GTGGATGCCTGCAGC | 8853 |
rs763646194 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364722 | TAACGACTTACAACT[A/G]TCTTCTAAGTTCACC | 8853 |
rs763646297 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207447 | AGACCTCCCCTCTCT[A/C]GGCCTCGTGGCCCTC | 8853 |
rs763675466 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350989 | ACTGCATTCGGAAGA[A/G]TTGGTTTTTGAAGAG | 8853 |
rs763675652 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366183 | GGCAGAACTGCAAGG[C/T]AGCACGTTTCTCTAG | 8853 |
rs763687265 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9368496 | AGCTGAGGACTCAGT[C/T]AAACCCAACCCAGGC | 8853 |
rs763699620 | snp | C/T | 3.61553e-05 | 0.00425163 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374707 | AGGGAGGCCGGACGG[C/T]GGGTAGAAGCCCTTC | 8853 |
rs763700121 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9393753 | GGCTCCTACTCCAGC[A/G]TGGGCGCCACATAAC | 8853 |
rs763702748 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336363 | GAAGCCCCACCTCTG[G/T]AGCGCTGCCTCTGAT | 8853 |
rs763711331 | snp | A/C | 8.29456e-05 | 0.0064394 | missense | ASAP2 | GRCh38.p7 | 2:9400745 | TTTGCCCTACAGTGG[A/C]TCTCTCTGCAACGGA | 8853 |
rs763712528 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275511 | CTGGCTGGCTTTTCC[-/A]GAACGGCTACTGCCC | 8853 |
rs763720059 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294430 | ACTATCAGTGAGAAG[C/G]CCGGCTCCTCTCTCC | 8853 |
rs763721707 | in-del | -/T | | | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405430 | TACACAGACTAAGAG[-/T]TAACTGTGTGATCTG | 8853 |
rs763743157 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214235 | ACTTTTTTTCTTTTC[C/T]TTTTCTTTTTTATTT | 8853 |
rs763763721 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9289250 | TCTGGACACACCAAG[C/T]GCCTTGAATTCCCCA | 8853 |
rs763805993 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227757 | GTGGGTAAGGTATTT[G/T]TGAGTACACGTGCAT | 8853 |
rs763816852 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341637 | TAGACGTATTTCTTG[G/T]TTGTGCAGTTGAGTC | 8853 |
rs763827322 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260623 | TGGCTTTGTGCAGGG[-/C]CCCCAGCAATCCTGG | 8853 |
rs763861667 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352222 | ACACAAACACACACA[A/C]ACACACACACACACA | 8853 |
rs763867380 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9273031 | CTTTGGCTATTCTGG[G/T]TCTTTTGTGGTTCTA | 8853 |
rs763892551 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9226991 | CGCCCAGCCAGAAGG[C/G]TAAGGGAGCTCAGAT | 8853 |
rs763896680 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9241695 | CATGCCTCACCAAAG[A/G]TATGTACTGTAATTT | 8853 |
rs763918419 | snp | G/T | 1.64827e-05 | 0.00287073 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9344731 | CCACTTATCCACAAG[G/T]ATCCGAAAAGTGTGG | 8853 |
rs763949268 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9226418 | GCATGGGTCTACTTT[A/C]CGCCCCTCTTGAGCT | 8853 |
rs763959566 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254022 | ACCAGCCTGGCCAAT[A/G]TAGTGAAACCCCGTC | 8853 |
rs763964963 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338440 | CCACCCAGGCAGCCA[A/G]GGTCCACCACAGCCA | 8853 |
rs763972822 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9367511 | CACGCCTGTAATCCC[A/T]GCACTTTGGGAGGCT | 8853 |
rs763984768 | snp | C/T | 8.65673e-05 | 0.00657846 | missense | ASAP2 | GRCh38.p7 | 2:9379012 | GCCTGACCGACAATG[C/T]CGAGTGCCTCAAGTT | 8853 |
rs763995447 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249889 | GTTTTGGGCTGGTCC[C/T]GCTCAGGATCTGTGA | 8853 |
rs764004562 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9312954 | ATCCCAGCTACCTGG[A/G]AGGCTGAGGCAGAGG | 8853 |
rs764005366 | in-del | -/AC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300539 | GCTGTCCAGCTTTCT[-/AC]AGAGAGTAAAGGTAT | 8853 |
rs764006206 | snp | A/G | 1.73972e-05 | 0.00294929 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318627 | ACTGTGACACCAGGG[A/G]CAGCTTTTACACCAT | 8853 |
rs764019472 | snp | A/C | 3.30262e-05 | 0.0040635 | missense | ASAP2 | GRCh38.p7 | 2:9388297 | GTTCTCCTGCAGCCC[A/C]GTCCCAACCGGCGGG | 8853 |
rs764046978 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9372535 | CAGTTCCTACCATGT[A/G]TTTCTGATCATGAGA | 8853 |
rs764052635 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359682 | CGTCAAGAGCAATAG[A/T]CTTGACAGAAAATCA | 8853 |
rs764057290 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9319190 | GACAGGGCTAGAGGC[A/G]CGTTTGCCAGGCAGC | 8853 |
rs764078878 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9309065 | GCACTTCCCCCAGGT[C/T]CTCATGTGGCTCTCT | 8853 |
rs764080613 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279139 | AGTCTTCCACACCAC[A/G]CTGAGGGCTTGTCTC | 8853 |
rs764081688 | snp | A/C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248710 | GTAACTTTCACTCCT[A/C/G]TCTACCAGCCATTTG | 8853 |
rs764082436 | in-del | -/C | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212467 | TTCTGGTCTTCTGTA[-/C]CCTGCCTCCCTGCCT | 8853 |
rs764141696 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9330844 | AAAGTGAAGTAGTTG[A/G]CCTTTTATGGACATG | 8853 |
rs764142432 | snp | C/T | 5.27227e-05 | 0.00513406 | missense | ASAP2 | GRCh38.p7 | 2:9356340 | GCTGTGACTGTGGGG[C/T]GCCAGGTGACCCAGG | 8853 |
rs764182536 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278318 | AGGAGTTTGAGACCA[C/T]CCTGTCTAACATGGT | 8853 |
rs764193335 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9222067 | TGCTGGGATTAGAGG[C/T]GTGAGCCACCGCGCT | 8853 |
rs764210733 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307993 | GCATGTGTGTATGAT[A/G]GACCTCAAGGCAATT | 8853 |
rs764217932 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271152 | AGGAGTTACACTAGT[C/T]CAAGTTAAAAGCGGA | 8853 |
rs764223574 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9388838 | TCCCGGGGCTGGGCC[A/G]AAAGACACACTCCTT | 8853 |
rs764230901 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9223027 | TCCAGAGGAGACTCA[A/G]GAGTCCCACTTTAAT | 8853 |
rs764250136 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9268580 | GGAAATATTTGACAC[C/T]GTCATTAATGCTCTC | 8853 |
rs764277223 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9356970 | GGTGGGGAGTGGGGG[-/T]TCGGGGACTACACAG | 8853 |
rs764294039 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9255579 | CTGTGTGTCCTTGCC[A/G]TGGATTCGGCAGATG | 8853 |
rs764313334 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286933 | TGGTAATAAATACTC[-/A]ATGAGGTATTTGTTA | 8853 |
rs764330315 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338905 | TTGGCAGGCCAGGCA[C/T]GGTGGCTCACAGCTA | 8853 |
rs764340667 | snp | A/G | 1.65113e-05 | 0.00287322 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297269 | GGGTGGCATGCCTGA[A/G]ACTCACAGCACCTCC | 8853 |
rs764364639 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325290 | GAAATCAGCGAGACA[A/G]CATGAGACAGGGACT | 8853 |
rs764365099 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9367913 | AAGTATAGGTATCAT[A/C]CCATTTTACTGATGA | 8853 |
rs764384134 | snp | A/G | 1.65389e-05 | 0.00287562 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393445 | AGTGGGAAGCCTGGC[A/G]GCTGACCCTCTGCAC | 8853 |
rs764385953 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243426 | AGATTTTTTTTATAA[A/T]GTGCATTTTTGTCCA | 8853 |
rs764400825 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9396150 | GATTTTTGGCTAATT[C/G]TTCTGCATACTACCT | 8853 |
rs764404463 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373524 | CAGGATCTCTACTCC[C/T]TGCCTCCAGTGGCAT | 8853 |
rs764419115 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286520 | CAGAATAATCTTTAC[C/T]GTTTGGCAAGCTTAC | 8853 |
rs764419337 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9283914 | TTATTATGCTTCCCG[A/G]TGGCCCCATCTCCAG | 8853 |
rs764437665 | snp | A/C/T | 3.29464e-05 | 0.00405861 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356024 | TGTCTGGGCTCACAG[A/C/T]TGAAATTCCTCTTGC | 8853 |
rs764446601 | in-del | -/CTAT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9310874 | TCTGTGCCTTCTGGC[-/CTAT]CTTTGTTTGCTCATC | 8853 |
rs764448254 | in-del | -/TTTATCTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9241197 | TTATTAGCTCACATA[-/TTTATCTT]TTAGGATACAATCTT | 8853 |
rs764454175 | snp | C/T | 0.000214853 | 0.0103624 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323118 | CCTTGCTTTCACACG[C/T]AGAACCAAGATAGAA | 8853 |
rs764454985 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9355907 | TGGAGGATATGAGGG[A/C]GTGCCTGATTTTATA | 8853 |
rs764480854 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9269603 | AGGGCCTCCGGGTGA[C/T]CCCAGAGGTGGTGGC | 8853 |
rs764487256 | in-del | -/AG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253353 | ATTTTTAGTAGAGAC[-/AG]AGATTCACCATGTTG | 8853 |
rs764493800 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275264 | TTTTGTAGAGACAGG[G/T]TGTCACTGTTGGCCA | 8853 |
rs764494497 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9398547 | GCACAGTGGCTCACA[-/C]CCGTAATCCTAGCAC | 8853 |
rs764536580 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257203 | GAAGGTGCGGGCCCC[C/T]ATCCTGAAGGAGTGA | 8853 |
rs764541960 | snp | A/G | 3.32353e-05 | 0.00407634 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323267 | TAAGGCGGTGGTGAA[A/G]GCAGGTCCTACAGCC | 8853 |
rs764546518 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370081 | TGACCTCGTGATCTG[-/C]CCCACCTTGGCCTCC | 8853 |
rs764568527 | in-del | -/A/AA | 0.0879479 | 0.190842 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374970 | GGTTGTTGCTACTTT[-/A/AA]AAAAAAAAAAAAAAG | 8853 |
rs764593757 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9326535 | AGAAAATTGGTTAAT[A/G]TAAGAAAATATATAT | 8853 |
rs764623654 | in-del | -/TTTGGGACTGAG | 4.96923e-05 | 0.00498434 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400085 | CTGGTAATTATTTAA[-/TTTGGGACTGAG]TTTGTTTCTGCTTGG | 8853 |
rs764639905 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9231224 | CCTTCACTCCCTCCT[A/G]TAGCCAGGACCTTGT | 8853 |
rs764651817 | in-del | -/AGG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9394875 | GGGGTGGTTGGACAC[-/AGG]AGGTGACTCGTTGGC | 8853 |
rs764663984 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263707 | TCGTTGTTCATGCGT[C/T]GTTTTTTCATAGTGT | 8853 |
rs764667469 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9396075 | TAGGTTGGGCAGGGC[A/G]GCGGCTAAGGCTACT | 8853 |
rs764673554 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291896 | AAGGTTGTACATTGT[C/T]GCTGTCTTCAGCTCT | 8853 |
rs764687014 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327138 | CCCCTACCCCACCCC[C/T]GCCCATCCTTTACAG | 8853 |
rs764705379 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214058 | GATACTTATGGGCAT[C/T]GTCAGATGCCTGGGA | 8853 |
rs764705597 | snp | C/T | 0.0015388 | 0.0276953 | missense | ASAP2 | GRCh38.p7 | 2:9393497 | ATCCCCTGACCCCCA[C/T]GCCGCCCCCACCCGT | 8853 |
rs764709912 | in-del | -/TGCCTTCCTCCCCCGCCACC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9400358 | CCCTCCCCCATCTCA[-/TGCCTTCCTCCCCCGCCACC]TGCCTTCCTCCCCCG | 8853 |
rs764742198 | snp | A/G | 1.66765e-05 | 0.00288756 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400837 | TCGCAGGCAGTAAGT[A/G]ACGAGCCCCCTTTCC | 8853 |
rs764745850 | snp | A/G | 1.67402e-05 | 0.00289306 | missense | ASAP2 | GRCh38.p7 | 2:9388543 | CCACGGAATGTTGGC[A/G]AAGGTATGAAGCTGT | 8853 |
rs764764869 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9403178 | TTTCTTCACCAAACG[C/G]TCTATGTAATGCTCT | 8853 |
rs764777519 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9251190 | GGAACGTGGCCAGAG[C/T]GTTGTCACATCAGGA | 8853 |
rs764780219 | snp | C/G | | | upstream-variant-2KB, intron-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9206029 | CTTCCCAGGGTGGGT[C/G]CTGGCCTAGTACCCT | 8853 |
rs764795326 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346068 | AACCCAGCTTTCACT[A/G]GTCATGTGATCACCA | 8853 |
rs764798795 | snp | A/G | 0.000181994 | 0.0095375 | missense | ASAP2 | GRCh38.p7 | 2:9374796 | CCAAGTACATCGAGA[A/G]GAGATACGCAAGGAA | 8853 |
rs764838749 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207453 | CCCCTCTCTCGGCCT[C/T]GTGGCCCTCGCGGGG | 8853 |
rs764850926 | snp | C/T | 1.65381e-05 | 0.00287555 | missense | ASAP2 | GRCh38.p7 | 2:9344799 | CCATATCCCATGGTA[C/T]CGTAAGTATTCTCTT | 8853 |
rs764854625 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336596 | ATTTAGTAGGATTTT[C/G]GTAAACATGGGTCAA | 8853 |
rs764884389 | in-del | -/AAAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313066 | TGTGTCTTAAAAAAT[-/AAAA]AAAAAAGCTGCAATT | 8853 |
rs764885135 | snp | C/G/T | 4.94306e-05 | 0.00497124 | missense | ASAP2 | GRCh38.p7 | 2:9334812 | CTACGGATCTTCACA[C/G/T]GGTGAGTAGCTTCCC | 8853 |
rs764898770 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9226401 | AGGCCATGCAGAACT[C/T]GGCATGGGTCTACTT | 8853 |
rs764907557 | snp | C/T | 6.59e-05 | 0.00573983 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9391049 | GCGTCTGTGTGCATG[C/T]GTGTGGGTTCAGTTC | 8853 |
rs764939141 | snp | C/T | 3.521e-05 | 0.00419569 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318637 | CAGGGGCAGCTTTTA[C/T]ACCATGTAGAGTCAC | 8853 |
rs764943786 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9282703 | GCTCATTTTATGTAC[A/G]ATTGAAAGAACAGTG | 8853 |
rs764945512 | snp | A/G/T | 0.000177008 | 0.00940611 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391228 | TTTCCTTTCTTGCCC[A/G/T]TGGGCTTTGTAGATC | 8853 |
rs764963417 | snp | A/T | 1.71029e-05 | 0.00292424 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350909 | ACGTAAGGCTCCCTC[A/T]GAGATGCCGCGCCAT | 8853 |
rs764999053 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9340504 | ATTTGAAAGCATTGT[C/T]CTTAGACCATGGCTC | 8853 |
rs765000563 | snp | C/G | 1.73887e-05 | 0.00294857 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9379022 | CAATGCCGAGTGCCT[C/G]AAGTTGCTCCTGCGG | 8853 |
rs765014470 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364497 | GTGACAGAGTAAGAC[C/G]CTGTCTCAAAACAAA | 8853 |
rs765031920 | snp | G/T | 1.65869e-05 | 0.00287979 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358896 | GAGCTGCTGGTAATT[G/T]TTAAATCCTTGATTT | 8853 |
rs765032137 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275131 | TGTCACCCAGGCTAT[A/C]GGGCAGTGGCGCAAT | 8853 |
rs765043252 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239039 | AGCCCCTCTCTGTCC[C/T]GTGGCGTTAGCAGCA | 8853 |
rs765045348 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9252307 | CCTTTGGGGCTGTGC[G/T]CAGTGGCTCTTGCCT | 8853 |
rs765053118 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311033 | TGTCAGACATATCCA[A/G]GTGAACTCGGGGGGA | 8853 |
rs765079453 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9312840 | CTCCTTTACAGTGGT[C/T]ATCAGAGCTGTCCTT | 8853 |
rs765085408 | snp | G/T | 1.65589e-05 | 0.00287736 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358742 | GCTCAAATCTGCCCT[G/T]TTCTCTTTGGCAGAT | 8853 |
rs765099447 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212916 | GACGGAACCCCGGCT[A/G]CACACTGGAGTTGCT | 8853 |
rs765166961 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359666 | CATGTAGGGAATTTA[A/G]CGTCAAGAGCAATAG | 8853 |
rs765171526 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9334795 | TTCCATTGAAACGCT[A/G]TCTACGGATCTTCAC | 8853 |
rs765172774 | in-del | -/CAAT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317036 | ACATGCAATCATTCC[-/CAAT]CAATCACTCACATCC | 8853 |
rs765181103 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9385802 | CCCCTTCCTTTATCA[C/G]TTTGGGATATTGAAG | 8853 |
rs765203936 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247071 | TGAACTCCTGGGCTC[A/G]TGCAGTCTGCCTGCC | 8853 |
rs765255466 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260173 | TAGCTATTACTGCCC[A/G]CATTTTAAGGATAGG | 8853 |
rs765262954 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9304990 | ATAGATATTGGTGGA[C/G]AAGCTGGAGTAGTGG | 8853 |
rs765271326 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351259 | TTCTGTTTTCAAGAA[C/G]TTACATAATTTGGGT | 8853 |
rs765290857 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9319086 | CACCATAAGCACGCA[A/G]GCCAGGAGCTGTTTA | 8853 |
rs765294334 | in-del | -/C | 5.14275e-05 | 0.00507061 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400850 | TGACGAGCCCCCTTT[-/C]CCTGCCTCTCTGCTC | 8853 |
rs765337326 | snp | C/T | 0.000318387 | 0.0126132 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393669 | CACCCCCAGCCAGCT[C/T]GGCCATCCGTGCTCC | 8853 |
rs765338184 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318405 | GCACAGTACATGCAC[C/T]GGCCAGGTTTTAGGT | 8853 |
rs765367992 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9401198 | CTGAGACCGGGGAAG[G/T]CAGGGTGCTTGAGCT | 8853 |
rs765382688 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9290868 | ATAACATCTAGAAAG[C/T]ACTTGGCCTGGGACC | 8853 |
rs765384289 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266005 | TCTTGAACTCCTGAC[C/G]TCAAGTGATCCACCC | 8853 |
rs765388137 | in-del | -/AGCCCAAAACCTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9259553 | GAGGGCACAGTTTTC[-/AGCCCAAAACCTT]AGCCCAAAACCTTAA | 8853 |
rs765394519 | snp | A/G | 1.66344e-05 | 0.0028839 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374947 | GGCCAACGGACATGT[A/G]AGAGTGTGGGTTGTT | 8853 |
rs765394549 | snp | A/G | 1.66236e-05 | 0.00288297 | missense | ASAP2 | GRCh38.p7 | 2:9388472 | CCCTCCTGAGTGGCA[A/G]CCCACCTCCCGCCCA | 8853 |
rs765398186 | in-del | -/TCTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381943 | ATAAGTAACAGGTCC[-/TCTT]TCTAAGCACTGTACA | 8853 |
rs765402115 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9347706 | CTGGCCCTAGGAAGA[A/C]GTGATCCTTGAGACA | 8853 |
rs765427909 | snp | A/C | 1.65866e-05 | 0.00287976 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9403270 | TGGCCACATTGATGG[A/C]GATCCTGGTCGCAAA | 8853 |
rs765433478 | snp | G/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236242 | TTGCAGTATGAAGTT[G/T]ACCTGGATGTTTCAT | 8853 |
rs765443714 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267213 | GGATATATTGCATGA[C/T]GCTGAGTTTTGGGGC | 8853 |
rs765448815 | snp | C/G | 1.64798e-05 | 0.00287047 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356166 | TAACACAGCGTTGCT[C/G]TTGTTTTTCTAGATG | 8853 |
rs765468476 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348622 | TGTGTGTTTTGTGGA[A/C]CCATTCTTATGGTTG | 8853 |
rs765494183 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9376832 | TTTGGAAGAGTTGTA[C/T]ACGATTTCACCGGTG | 8853 |
rs765514202 | snp | C/T | 5.09654e-05 | 0.00504778 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403366 | ACAGTTATGTTCCTG[C/T]TTCGTTATTGGTACC | 8853 |
rs765517181 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213356 | AGAAGGATGAGAGAC[A/G]GGCAGAGGGGTGGGC | 8853 |
rs765517506 | snp | A/G | 1.71358e-05 | 0.00292704 | missense | ASAP2 | GRCh38.p7 | 2:9356316 | AGAGGATGACGGGCA[A/G]TGACGTCTGCTGTGA | 8853 |
rs765518971 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361562 | TTCCTTCCTTTCTTT[C/T]CTTTTCCTTTTCCTT | 8853 |
rs765522412 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9255251 | TTCTCAGATCATACA[A/G]TGCATCATGAGAGTA | 8853 |
rs765530366 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336696 | CCTAGTCTAGAGAAT[G/T]TAGGCCCTGACGCTT | 8853 |
rs765530634 | snp | C/T | 5.7919e-05 | 0.00538109 | missense | ASAP2 | GRCh38.p7 | 2:9393500 | CCCTGACCCCCACGC[C/T]GCCCCCACCCGTTGC | 8853 |
rs765537606 | snp | A/C | 3.31208e-05 | 0.00406931 | missense | ASAP2 | GRCh38.p7 | 2:9327881 | TAGATTTACTTCAGA[A/C]TCTGATCAAATACTT | 8853 |
rs765550196 | snp | A/G | 1.78551e-05 | 0.00298784 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385210 | CATGGCCGAGTGTAT[A/G]AGCAACAGCACTGAC | 8853 |
rs765556965 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405379 | GGCATTTTGCATGCC[A/G]TTCTCCATCAGATCT | 8853 |
rs765561824 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279169 | CCCAGAAACAGGTGC[C/G]GAGGGACCTGGCAGA | 8853 |
rs765567451 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302994 | GGTTAAGTGTGAGCT[G/T]ATTGTCCATATTAGT | 8853 |
rs765588335 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209286 | TTTATAACTAAATTT[C/G]AAAGTTGTTCACTTT | 8853 |
rs765602663 | snp | C/T | 1.66999e-05 | 0.00288958 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323283 | GCAGGTCCTACAGCC[C/T]AGGCTGTGCCGGCTC | 8853 |
rs765602689 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284211 | TGGTGGTGGAGGAGA[C/T]GTTATTCTGTCTACC | 8853 |
rs765610462 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9255050 | CATTTCCACTAACCA[C/T]GTATGAGAGTTCCAG | 8853 |
rs765614504 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253896 | GAGAAAGAGACCACA[C/T]TCACATAACTTTTAT | 8853 |
rs765617936 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9314425 | TTATCTGAAGCCCCT[A/G]TAGATTCTGTCTTTC | 8853 |
rs765632270 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229933 | GCCCTGGCGGTTGTC[A/G]GTGTGGGCTGGGGTA | 8853 |
rs765643168 | snp | C/G/T | 5.55081e-05 | 0.00526798 | utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207069 | TGAGGCGGCGGCGCC[C/G/T]CTGCGGCTGTGCGCC | 8853 |
rs765647703 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9222936 | TTTCCTCTTTGTTTT[C/T]TCTTGACTTTCATTG | 8853 |
rs765661549 | snp | C/G/T | 3.73694e-05 | 0.00432245 | synonymous-codon, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207140 | GTCGGAATTCGTGGC[C/G/T]GAGACCCATGAGGAC | 8853 |
rs765697793 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9367815 | GAAGATTGATTGGCA[A/G]GTAAAGACCTTACAT | 8853 |
rs765734125 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239703 | TTTGTTGTTGTCGTT[A/G]TTGTTGAAACCACTG | 8853 |
rs765757256 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9215373 | TGCTTCTTTACTAAA[A/G]CATTTAATAACAAGA | 8853 |
rs765762128 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337466 | TCATTCCCTTTGGTT[A/G]GATTTTCTTCTGTGA | 8853 |
rs765770631 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9396016 | CCCCCATCCAGACAC[C/T]GTCCGTTTTGCCCTC | 8853 |
rs765777604 | in-del | -/CACA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317419 | ACACACATGCTCCCT[-/CACA]CACCTACACATACTC | 8853 |
rs765819952 | snp | A/G | 0.000148435 | 0.00861369 | missense | ASAP2 | GRCh38.p7 | 2:9385287 | AATTCTCACGTTCAC[A/G]TTGAATATGAATGGC | 8853 |
rs765837008 | snp | C/T | 1.64868e-05 | 0.00287109 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391143 | GGCAGCGATCTTCGT[C/T]AGATCCGCCAGCTGT | 8853 |
rs765856595 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391057 | GTGCATGCGTGTGGG[C/T]TCAGTTCAGACAGCC | 8853 |
rs765866868 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9231028 | GCGGGGAGATGCTGC[C/T]CAGGCTCGGCTGCTT | 8853 |
rs765894412 | snp | C/T | 1.79191e-05 | 0.00299319 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374719 | CGGCGGGTAGAAGCC[C/T]TTCATGATTTGCAAG | 8853 |
rs765922239 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9363017 | ATGAGTTCAGCTTTT[C/T]TAGATTTTGCATATA | 8853 |
rs765927891 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343762 | TGATATCATTTGTTA[A/G]ACACCAGTTGAGCCA | 8853 |
rs765929213 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383366 | CTCAAGCGATCCTCT[C/T]ACCTCAGCCTCCCGA | 8853 |
rs765931180 | snp | A/G | 4.98782e-05 | 0.00499366 | missense | ASAP2 | GRCh38.p7 | 2:9401349 | GAGCTCACCTTCTCC[A/G]AGGGGGATGTGATCA | 8853 |
rs765941978 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9356580 | GAGTAAAGAGGGTTT[G/T]ACAGAGCTGCAAAGT | 8853 |
rs765942970 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348372 | TCAGGTGATCTACCT[A/G]CCTCAGCCTCCCAAA | 8853 |
rs765943041 | snp | A/G | 3.54428e-05 | 0.00420953 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9379040 | GTTGCTCCTGCGGGG[A/G]AAGGCCTCCATCGAG | 8853 |
rs765973932 | in-del | -/GT | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208337 | CCTGGGCTAGCAGGA[-/GT]GTGTGTGTGGGTGGG | 8853 |
rs765982642 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229610 | AGCCTGAATCTCAGT[C/T]GAGCCTGGAAGGACA | 8853 |
rs765995666 | snp | C/T | 1.64827e-05 | 0.00287073 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380694 | TGGATGTCAGGCCTT[C/T]GCTGGGTTTTGCCTT | 8853 |
rs766004735 | snp | A/G | 1.66693e-05 | 0.00288693 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320362 | CTCGTTTTTAAATTT[A/G]CGTATAGGTAATTTG | 8853 |
rs766091685 | snp | C/T | 3.31417e-05 | 0.00407059 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323095 | TGCCAACAGGCATCT[C/T]GATGTATCCTTGCTT | 8853 |
rs766107020 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9215615 | AAGTTTATGGACCCC[C/T]TGGATTCAGACAGAG | 8853 |
rs766111790 | snp | C/G | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390403 | GGCCGTGCACAGCCT[C/G]CAACATGGGGTCACA | 8853 |
rs766115798 | snp | C/T | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404471 | TTAGGTTGTCTATTA[C/T]AAAACCAAAACTCAT | 8853 |
rs766118185 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373974 | TTGACGCACATACGT[C/T]TCATGGTGCTACTGT | 8853 |
rs766118194 | in-del | -/T | 1.65739e-05 | 0.00287865 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320344 | ACAAAAATGTGAGTG[-/T]TTCTCGTTTTTAAAT | 8853 |
rs766123083 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321485 | ATCCTTTATTTGTGT[A/G]CCAGTTGGGTGAAAT | 8853 |
rs766125300 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250051 | TATTTACTTACTCAC[C/T]TGAGTTTCAGTTTTA | 8853 |
rs766136388 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281796 | TCCCAATTCATCTGT[C/T]GATGAAACTGTCACT | 8853 |
rs766156444 | snp | A/G | 1.66649e-05 | 0.00288655 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358915 | AATCCTTGATTTCAG[A/G]TTGGAAACAAATGAG | 8853 |
rs766167069 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271743 | TGAGTCCTCGGCAGT[A/G]GCTCAGTGACTGGGG | 8853 |
rs766169846 | snp | A/G | 1.64841e-05 | 0.00287085 | missense | ASAP2 | GRCh38.p7 | 2:9335141 | TTGATACAGCTTCGA[A/G]ATATTTTGAAATCCG | 8853 |
rs766172386 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263662 | TGCCTGTGGGCGCTG[C/T]TTCCTTAAACTGCAG | 8853 |
rs766179335 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322345 | GGATGCCTTTGAAAG[A/T]ACATGCTACTTGGGT | 8853 |
rs766182124 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9293761 | GAAGCTTCAAGTTCA[G/T]TTGCAGGATGAAAAA | 8853 |
rs766186078 | in-del | -/AT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9251449 | GTCTGGGCGCAAAGC[-/AT]GTGGAGAAATTGAGA | 8853 |
rs766195870 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9280849 | CTTGTGCTTTCTGTA[A/C]ATTGTGCTAATCTTG | 8853 |
rs766213005 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380267 | CAGTGGCACAATCTC[A/G]GCTCACTGCAACCTC | 8853 |
rs766220109 | snp | A/G | 1.65685e-05 | 0.00287819 | missense | ASAP2 | GRCh38.p7 | 2:9400024 | CCCTGTCTTTGTAGG[A/G]CTGACAAGTCCACCC | 8853 |
rs766268011 | snp | C/G/T | 1.67061e-05 | 0.00289011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400699 | TACATCTCATGGCTG[C/G/T]GATTGATGGGATGTC | 8853 |
rs766277322 | snp | A/G | 6.58957e-05 | 0.00573964 | synonymous-codon, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9279370 | GAAATCCGTGAAAGC[A/G]ATCAACAGCTCTGGG | 8853 |
rs766297469 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318435 | TGGAGGTGAATCATT[A/G]TCAAATGTTCTCTCT | 8853 |
rs766299378 | snp | C/G | | | upstream-variant-2KB, intron-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9206132 | CACCGCTCTGAAGCA[C/G]TCACACTTGAGTCAG | 8853 |
rs766304814 | snp | C/T | 1.71625e-05 | 0.00292933 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403374 | GTTCCTGTTTCGTTA[C/T]TGGTACCAAAACTCT | 8853 |
rs766316815 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225501 | TTCCTCTGTGGTCCC[A/G]ATTTTACCTCTGAGG | 8853 |
rs766331558 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9398119 | CAGCACTCAGAAAAT[A/G]TTATTGGAACATTAG | 8853 |
rs766345147 | snp | A/G | | | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391128 | TGGACGGTGGAAGCC[A/G]GCAGCGATCTTCGTC | 8853 |
rs766433407 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341489 | TGATTCTGTTGAGAA[G/T]AATGTCCCTTATCCT | 8853 |
rs766456811 | snp | A/T | 1.64757e-05 | 0.00287012 | missense | ASAP2 | GRCh38.p7 | 2:9388385 | TATCTTTGGCCAGAG[A/T]TGCTGCAAACCTTGC | 8853 |
rs766458691 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9231829 | ACCTGGCAGCCTGGC[C/T]CTTCCCTGCAGCAGG | 8853 |
rs766459598 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250937 | AGTGAACTATGAAAC[A/G]AGGCGTGGTGAAAGT | 8853 |
rs766493666 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258564 | CTCCATGGTGCCCCC[A/G]CCGCCACACTCATCT | 8853 |
rs766502476 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245453 | ATAAAAACAAACCCT[A/G]AAAGATTAGTCATAC | 8853 |
rs766503845 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9386797 | AGACAAGAATGTGGT[C/T]AGCAAGGTTGAGTCA | 8853 |
rs766555546 | snp | C/T | 1.65138e-05 | 0.00287343 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377030 | GAGGCACTCGTTTTC[C/T]CCTTGGTATTTCTGG | 8853 |
rs766557739 | snp | C/T | 1.64868e-05 | 0.00287109 | missense | ASAP2 | GRCh38.p7 | 2:9356187 | TTTCTAGATGGATGT[C/T]TGTGCTGCAAAATAG | 8853 |
rs766575943 | snp | C/T | 1.74205e-05 | 0.00295127 | missense | ASAP2 | GRCh38.p7 | 2:9356333 | GACGTCTGCTGTGAC[C/T]GTGGGGCGCCAGGTG | 8853 |
rs766577729 | snp | C/T | 1.66037e-05 | 0.00288125 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9327897 | TCTGATCAAATACTT[C/T]CATGCCCAATGCAAG | 8853 |
rs766592566 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9299127 | AGAAGGTTGTCATCA[A/G]TGCAACAAATCTAAA | 8853 |
rs766597216 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328948 | TTAGATAAAGATTTA[A/G]GGTAGAGTTTTTTGT | 8853 |
rs766629920 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249168 | CCCTCTTGGGGCCTC[C/G]TTAGCTCCAGTTTCT | 8853 |
rs766638386 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315964 | ATTTAGCAGAATTGG[C/G]TGTGGATGCAGACGT | 8853 |
rs766641406 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333223 | AACTGGCTAAAGTTG[C/G]TGACAGTCCATCCTT | 8853 |
rs766646563 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307615 | CCAAGCTTATCCTTT[A/T]TTCTAGTGGAGAAGG | 8853 |
rs766667264 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265628 | TTATTTTCTTTCTGT[-/A]TCTTTATATACAGAG | 8853 |
rs766672524 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9375849 | GGCGGTTCCCTGGAA[C/T]CCACACCCCACTGTG | 8853 |
rs766672954 | snp | C/T | 8.2543e-05 | 0.00642376 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9385337 | GGATGAAAGTGATGA[C/T]GACATGGATGAGAAA | 8853 |
rs766678067 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9288764 | CTCCAGGCTAAAGGA[C/G]AGCCCTGCAAGTTTT | 8853 |
rs766680757 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266694 | AGAAAAATGAAAGAA[C/G]TGTTTCTCTTATGTT | 8853 |
rs766690433 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359446 | ACAGAAGCATTTTCT[A/G]TGAAGTGGCTTTCAA | 8853 |
rs766690641 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346224 | GCTGAGGTCAGGTTC[A/G]AGGCCAGCCTGGCCA | 8853 |
rs766720283 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321464 | CAGGATCCCTGGTCC[A/G]TCAGCATCCTTTATT | 8853 |
rs766727230 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358307 | GTACATAGTACGTTC[C/T]CTGTTATTATCAGCA | 8853 |
rs766729617 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9330900 | ATCTTCCATTACTTC[A/G]TTTTTGGATATGAGA | 8853 |
rs766754902 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9208591 | TAACTTGGGTAGCCT[G/T]CCTTCTCTCCATTTA | 8853 |
rs766759713 | snp | C/T | 1.91698e-05 | 0.00309589 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207158 | GACCCATGAGGACTA[C/T]AAGGCGCCCACGGCC | 8853 |
rs766762727 | snp | A/C/T | 3.30525e-05 | 0.00406514 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388285 | CTCTGCCCCAATGTT[A/C/T]TCCTGCAGCCCAGTC | 8853 |
rs766766369 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232971 | TTTGTTCTGTATCTA[C/T]TGCCAGCAGGAATCC | 8853 |
rs766768084 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247024 | TTTTAATGTTTTTGT[A/G]GAGATGGGGTCTGTG | 8853 |
rs766769690 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277845 | ATGTCTGGTGCCTTG[C/T]GATCATTTTTCCATT | 8853 |
rs766775590 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9241864 | GAGAAGAGAACTCAG[A/G]ACCTGGCAGGTGGAG | 8853 |
rs766783832 | snp | G/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209217 | CATTTCAGGTTTATT[G/T]CACTTTAAGCAAATC | 8853 |
rs766797728 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336512 | TCACCAGCTGGACCT[C/T]GAGCAGCCTGAGGAT | 8853 |
rs766800257 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221863 | GCATGGCGCCATCTC[A/G]GCTCACTGCAAGCTC | 8853 |
rs766811908 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350778 | TCCACCCAACCCCAA[C/T]CTTTTTTGTTGTTTT | 8853 |
rs766814646 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9306686 | CCTCTGCTCCTGGCT[C/T]GCTGAGGGAATTGTC | 8853 |
rs766846345 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366334 | CATCTCCCCACCCCC[A/G]TCTGCTTAACACAAA | 8853 |
rs766847798 | snp | C/T | 1.65891e-05 | 0.00287998 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344812 | TACCGTAAGTATTCT[C/T]TTTTAATCCATGGTG | 8853 |
rs766857887 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337282 | CTGCGTTGCTTTTAG[A/G]TGATGGCATTCAGCA | 8853 |
rs766873901 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263685 | AACTGCAGGAGGCTG[C/T]AGCCTCTCGTTGTTC | 8853 |
rs766899460 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365479 | AAAACAGGACAGGAG[G/T]TTTCCCTGCCCCACC | 8853 |
rs766915191 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207880 | TCACCTGCTTGAACC[C/T]GGAATGCCGCCCTTC | 8853 |
rs766920836 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9347472 | ACTTGATTAAGTGGA[A/G]GTCTAAGAGCAGAGC | 8853 |
rs766955500 | in-del | -/AG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9226115 | ACCCTGGGGCACGTA[-/AG]AGGGGCTCAGAAGGT | 8853 |
rs766970654 | snp | A/G | 9.89299e-05 | 0.00703244 | missense | ASAP2 | GRCh38.p7 | 2:9380780 | TGGACATTGCCAAGC[A/G]CCTCAAGCACGAGCA | 8853 |
rs766978710 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369917 | TGTGATCTCGGCTCA[A/C]TGCAGCATCCGCCTC | 8853 |
rs766999962 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313905 | TGTGGTATTCTTAGA[A/C]TTTTACATTCTTGGT | 8853 |
rs767023206 | snp | C/T | 8.26658e-05 | 0.00642854 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323116 | ATCCTTGCTTTCACA[C/T]GTAGAACCAAGATAG | 8853 |
rs767032136 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343690 | GGGCTCAAGCCATCC[A/G]CCCACCTTGGTCTCC | 8853 |
rs767037160 | in-del | -/AGT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9389646 | AGGGAGGCCCAGAGA[-/AGT]AGTGACAGTGAACCT | 8853 |
rs767052804 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313001 | GAGGTGGAGGTTGCA[C/G]TGAGCCAAGATCGTG | 8853 |
rs767075932 | snp | C/G | 1.65477e-05 | 0.00287638 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393431 | AGTGAGGAGGCCTGA[C/G]TGGGAAGCCTGGCGG | 8853 |
rs767085344 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9355446 | TGATGCTGCCACATC[C/T]CACACAGCCGCCTCC | 8853 |
rs767087863 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301560 | GGCTGCATTTCAGGG[C/T]AGGTTTCTGAAAGGT | 8853 |
rs767090558 | snp | C/T | 1.6782e-05 | 0.00289668 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358931 | TTGGAAACAAATGAG[C/T]TGTAAGCTAAATTTT | 8853 |
rs767090843 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325030 | TTTTCATTGAGAGAA[A/T]GTTTAGAGATATTCA | 8853 |
rs767094864 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338492 | TTCGCGTATCTTACA[C/T]GCCCAAATCTGGCCT | 8853 |
rs767114971 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274389 | GTACAGTGGTGTGAT[C/G]TCCGCTCACTGCAAC | 8853 |
rs767119353 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9354002 | AAAAGATGTAAATGA[C/G]CATGGGCTTTTCTAG | 8853 |
rs767128169 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | ASAP2 | GRCh38.p7 | 2:9368465 | GCTTTAATGAGATCA[C/T]GGAATGTTGCCTACC | 8853 |
rs767132282 | snp | A/G | 1.6563e-05 | 0.00287771 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9400041 | TGACAAGTCCACCCC[A/G]CTGACCAACAAAGGC | 8853 |
rs767143551 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9393921 | TTTGCTGCTCACCCC[A/C]CAGGTGGTCTCTGTT | 8853 |
rs767151890 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301245 | CTACCTGCTTGGAGG[C/T]GTGAAAGAATGTTTA | 8853 |
rs767170194 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9283922 | CTTCCCGATGGCCCC[A/C]TCTCCAGACACCATT | 8853 |
rs767207372 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343087 | CAGTGGCAATGATGA[A/G]AGTGGCCCTAGACTC | 8853 |
rs767207893 | in-del | -/CA | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211155 | AGTGAAACTGCGTCT[-/CA]AAAAAAAAAAAAAAA | 8853 |
rs767211500 | in-del | -/TC | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9405121 | CCAGTCCCAAACTAA[-/TC]TGTCAGGTTCACTGG | 8853 |
rs767217242 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229848 | GTGTGCCCCTCCTGT[C/G]CCCTGTAAATTGTGG | 8853 |
rs767240379 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9290443 | TTGAACTCCTGACCT[C/T]AAGAGATCTGCCCAT | 8853 |
rs767274964 | snp | A/T | 1.66632e-05 | 0.0028864 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400710 | GCTGTGATTGATGGG[A/T]TGTCTTAAGCTGCTT | 8853 |
rs767276445 | snp | A/G | | | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9215259 | TATGAGAGGTCGTCT[A/G]TGTGGTTCATTGTTG | 8853 |
rs767296380 | snp | A/G | 1.65548e-05 | 0.002877 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344523 | AACACACTCTTCACC[A/G]TTTTTTAGGACTCCC | 8853 |
rs767320581 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302637 | GAGCCACCACACCCA[C/G]CTAAGTTTTGTATTT | 8853 |
rs767322644 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248946 | CCAGAAGGAGGTAAT[C/T]TGTGTAAAATAATGC | 8853 |
rs767347703 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275001 | TTCAATTGTGTTATT[A/G]AGGTATGTTGTCTGT | 8853 |
rs767367742 | in-del | -/CTCA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317218 | CCACTCACATCCACA[-/CTCA]CACAATCACACAACC | 8853 |
rs767367843 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9292039 | TCTTGTTCCAGCTCT[A/G]CTGCAAACTCACTGT | 8853 |
rs767368573 | snp | C/T | 1.66275e-05 | 0.00288331 | missense | ASAP2 | GRCh38.p7 | 2:9388475 | TCCTGAGTGGCAGCC[C/T]ACCTCCCGCCCAGCC | 8853 |
rs767402695 | snp | C/T | 6.6012e-05 | 0.00574471 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297470 | TCTGTGTATGAAATG[C/T]TGCGGTTACTTCAGT | 8853 |
rs767408532 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349813 | TGCTGGGCCTGTAAG[C/T]GCTTGAGGGTTTCAC | 8853 |
rs767448498 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9309334 | CTACATGAATGAATC[A/G]CACAGTCATGCGCAG | 8853 |
rs767464117 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331814 | GTGATGAATGTTGAA[C/T]TGACTTGTTCTTTGA | 8853 |
rs767482973 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378458 | GGAAAGTGACTTTTC[C/T]CTTTCCTGGAGGGAA | 8853 |
rs767487986 | snp | C/G | 3.32347e-05 | 0.00407631 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358728 | CTTTTTTACTGGAAG[C/G]TCAAATCTGCCCTGT | 8853 |
rs767491777 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9298144 | TCGCTCCAGCTTTTC[A/T]TTCCTGTTTTTCTTC | 8853 |
rs767502648 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9237981 | GACCTGTGGCTCCAG[A/T]GTGTGGATCCGTGGG | 8853 |
rs767518399 | snp | C/G | 1.66955e-05 | 0.0028892 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385361 | TGAGAAATTGCAGGT[C/G]TGTGCCAGGTTGCTA | 8853 |
rs767521467 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321371 | AGTTTCATTGATGGT[A/G]TACATTCATTCAGAA | 8853 |
rs767542960 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9310226 | AATTAAAATCTCCCC[A/G]CATTTCAAAGCGTCT | 8853 |
rs767552789 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9280518 | AAGTGTATTTAGGAA[C/G]AAATTTAACAGAAGA | 8853 |
rs767589461 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211506 | CCCTCCTTTATAGCA[C/T]CATCCATTCTGCCTT | 8853 |
rs767605231 | snp | A/G | 4.94352e-05 | 0.00497143 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9376913 | GGTTTTTCAGGAGCC[A/G]GATGAAACGGCCCTC | 8853 |
rs767634277 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248864 | ACTCTGATGTGAGCT[A/C]AGTGTTAGGTGGCAA | 8853 |
rs767637785 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350556 | GCTGGCATCGCTTGT[C/T]CTCTTGTCCAGGTGG | 8853 |
rs767658310 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271412 | ATTCTGGATGCTCAA[C/T]TACAGTACCATTGCA | 8853 |
rs767668446 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286631 | TCAAGAAAAATAACA[A/G]TCTTTTTGTGGAAGG | 8853 |
rs767696499 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244512 | GATGAGAACACATGC[A/G]TAGCTCCTAGCACAG | 8853 |
rs767701321 | snp | A/C | 3.3579e-05 | 0.00409736 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327919 | CAATGCAAGTAAGTT[A/C]TTCTCTGTTATGTTA | 8853 |
rs767717757 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | ASAP2 | GRCh38.p7 | 2:9334785 | GCCTCAAACCTTCCA[C/T]TGAAACGCTGTCTAC | 8853 |
rs767742671 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328045 | AGGTGCTGACTCATG[C/T]GACAACACGGGTAAA | 8853 |
rs767772887 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9330525 | ACCAGGCCTATAACA[A/G]AACTGCACTTGTACC | 8853 |
rs767781254 | snp | C/T | 2.4403e-05 | 0.00349298 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207270 | CGGCCGCAGGTATCC[C/T]GCGCCCCAGCCCCGC | 8853 |
rs767791428 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327520 | TTAGAAATCCCATTT[A/G]TTTGAACCATCCATA | 8853 |
rs767791475 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359724 | CCATGTTCCTCTCAA[C/G]GGGCCATCAGTCTTA | 8853 |
rs767807751 | snp | C/T | 6.60458e-05 | 0.00574618 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335087 | TGTGTGTGTGTGTTT[C/T]TAAAGATCAAACAGG | 8853 |
rs767822766 | snp | A/G | 4.95626e-05 | 0.00497784 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388290 | CCCCAATGTTCTCCT[A/G]CAGCCCAGTCCCAAC | 8853 |
rs767823721 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384599 | ATTTGCTGGAGTGGC[C/T]CATAGAACTCAGGGA | 8853 |
rs767823954 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9357040 | GCTTGGCTAGAATGG[C/T]TAATCCCCTTTTCAT | 8853 |
rs767850570 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276945 | CTTCCAGAGAGCCTG[A/G]CAGGCTGACATGGGT | 8853 |
rs767861708 | in-del | -/C | 1.66094e-05 | 0.00288174 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368564 | CTGAGTAAAGGTTTG[-/C]CTTTGCCCGAGCCCC | 8853 |
rs767864391 | snp | A/G | 1.66785e-05 | 0.00288773 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320366 | TTTTTAAATTTACGT[A/G]TAGGTAATTTGGGAT | 8853 |
rs767866387 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9334929 | CCGCCCACGTGGAGT[A/G]TGGCGTTCCCACGCC | 8853 |
rs767868846 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397447 | GCTACCCGGGACAGA[C/T]GGGGATGGACGGAGC | 8853 |
rs767869162 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9261233 | GTTAGAGAAAGCCAG[C/T]GCTTCTGGCTCTGGA | 8853 |
rs767875142 | snp | A/T | 3.31033e-05 | 0.00406823 | missense | ASAP2 | GRCh38.p7 | 2:9374923 | GGATCTTACGGAAAA[A/T]ATCCCACTGGCCAAC | 8853 |
rs767901633 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9287515 | CAGGAGAGGGCGTAC[A/G]TGAAGGGCTTTCTCT | 8853 |
rs767903839 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276050 | CTGGGCTCCTGTTTT[A/C]ATCGTTAATTTGTGT | 8853 |
rs767917326 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346131 | CATGCAGTATGGATC[G/T]TAATGGGACATTATG | 8853 |
rs767925615 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234700 | ATGGATTTACTCAGG[G/T]TTCAGTTGGTTGGAC | 8853 |
rs767952216 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9374595 | GAAGACCAGTGCAGC[C/T]GTAGAACCACATGGC | 8853 |
rs767953253 | snp | C/T | 3.32956e-05 | 0.00408004 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401260 | ACTAACCGTTGTTCC[C/T]TCTCCTGACCCAGAC | 8853 |
rs767964969 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356008 | ATTGTGTATGGATTG[C/T]TGTCTGGGCTCACAG | 8853 |
rs767976112 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317088 | AATCACATCCACACA[C/T]ACACTCAACCACACT | 8853 |
rs767981965 | snp | A/G | 8.23703e-05 | 0.00641704 | missense, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9279333 | CTTTGGACGTGGACC[A/G]GATGGTTCTTTACAA | 8853 |
rs767990005 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9303925 | GAGAACTCACAGAGA[C/T]GAGGACTGGGCACCT | 8853 |
rs767999608 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9376846 | ACACGATTTCACCGG[C/T]GTTGGACACAGAATT | 8853 |
rs768010269 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9220551 | AATCCTTTGCCATGT[A/T]TATATTGGATTATTT | 8853 |
rs768019088 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217663 | TCTGCCACCCAGGCT[-/G]GAGTGCGGTGGCACA | 8853 |
rs768042053 | snp | A/G | 9.38835e-05 | 0.00685076 | missense | ASAP2 | GRCh38.p7 | 2:9393538 | CCCAGCGTAATGGAA[A/G]CCTTGAGCCAGCCGA | 8853 |
rs768042136 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337096 | AGACCAGAAGTTCTT[C/T]ATAGTTTGTTGTTTT | 8853 |
rs768048655 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9385471 | AAATGAAAATGTAGC[G/T]TACTTTATGCTTTCA | 8853 |
rs768059715 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358256 | AACACAAACTGTTAT[C/T]GCTACTACCAGCATG | 8853 |
rs768071434 | in-del | -/TG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9270102 | GTGATAAGTTCACTC[-/TG]TAAAACTTGTTTGAC | 8853 |
rs768073003 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9319434 | TCAGACACATTCCCC[A/G]TCGAGCCTTCAGGGG | 8853 |
rs768078078 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9293080 | TGCACTGGGCCTTCT[C/T]CTTGATACCAGTTTT | 8853 |
rs768083699 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9376561 | TGTAGGTGGCCTGGG[A/G]GACCTTCCTGGATCC | 8853 |
rs768085722 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9388056 | AGGTGAGATTTGGGT[A/G]GGGACACAAAGCCAA | 8853 |
rs768101290 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236841 | TTTCCTGTGTTGGAG[C/T]AAAGGTGCTGTGTGT | 8853 |
rs768114555 | snp | A/G | 1.68295e-05 | 0.00290077 | missense | ASAP2 | GRCh38.p7 | 2:9401379 | ATCGTGGACGGGGAG[A/G]AGGACCAGGAGTGGT | 8853 |
rs768128127 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352532 | ATGCTCCACAGGGAG[A/T]CCCTGCTAGATGCCA | 8853 |
rs768130435 | snp | C/T | 1.66718e-05 | 0.00288715 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327823 | CTTTTCATTGTTCAA[C/T]AGTATCTGCTGAAGG | 8853 |
rs768169618 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278763 | AAAGTGGGTATTGTT[C/T]CTGCTGGTTTCTGGA | 8853 |
rs768218602 | snp | C/T | 8.6175e-05 | 0.00656354 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327952 | TTAAATGTTTGTTCA[C/T]GTGTGGCAACTTCTG | 8853 |
rs768219520 | snp | C/T | 4.36348e-05 | 0.0046707 | missense | ASAP2 | GRCh38.p7 | 2:9393605 | CCCCACCTCTGCCCC[C/T]ACAGCCGCCCAGCCG | 8853 |
rs768234347 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9290543 | CAGGCACAGAGCACT[A/G]TAACAATCTAGCCAT | 8853 |
rs768249478 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9308508 | TGATTTTCCTGTTTA[C/G]AGTTTCCTTGTATGT | 8853 |
rs768250724 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254799 | TCCCTGAAGATAAGC[A/G]GTACTACTTGTTATC | 8853 |
rs768251871 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295106 | TAGAGTAAAACAGAA[A/G]GAATTATTGATCCAT | 8853 |
rs768300447 | in-del | -/AAAAG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256178 | AAAAAAAAAAAAAAA[-/AAAAG]AAAGCAAGTAATTCT | 8853 |
rs768302668 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307526 | GAGTCCTGGGTTCTC[C/T]AGTGCTGCCCTCCGG | 8853 |
rs768309685 | snp | C/T | 2.78959e-05 | 0.00373459 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207224 | CACTGTGGCGGCCAT[C/T]GAGGAGGTGAGGCGG | 8853 |
rs768334472 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257781 | CGCCCGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 8853 |
rs768362870 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349359 | ATAGACACAGGCTAC[A/G]TATGGGTGGGTGTAC | 8853 |
rs768378195 | snp | C/G/T | 3.34999e-05 | 0.00409256 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401229 | CTCTGCCCTGAGAGC[C/G/T]GAGGCCTGCAGCCAC | 8853 |
rs768389831 | snp | C/T | 1.66194e-05 | 0.00288261 | missense | ASAP2 | GRCh38.p7 | 2:9350814 | TTTAAACAGGCTAAC[C/T]GGCCTCCTGCAAAGC | 8853 |
rs768389916 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368572 | AGGTTTGCCTTTGCC[C/T]GAGCCCCGGGAGGCA | 8853 |
rs768408338 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9320280 | AATTTATTATTCTTT[C/G]TTTACAGGATCTGAA | 8853 |
rs768433288 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315238 | GGGACACAACCCCAG[A/G]CAAGCCTGCCATAGC | 8853 |
rs768448683 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274895 | AGGTAGAAGATTCCA[C/T]ATGGTGACCTATTTT | 8853 |
rs768448745 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243821 | GCCTTCCAGGACTCA[C/G]AGTTTAGTTGTGAGG | 8853 |
rs768456790 | in-del | -/AGA | 1.65064e-05 | 0.00287279 | cds-indel | ASAP2 | GRCh38.p7 | 2:9350869 | AGACCAACCCTGAGG[-/AGA]AGAAGTGCTTTGACC | 8853 |
rs768463808 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313729 | GATCGTGTAGATGAG[A/T]GGGCAGTGAGCATCT | 8853 |
rs768474225 | snp | A/C | 1.65976e-05 | 0.00288072 | missense | ASAP2 | GRCh38.p7 | 2:9401327 | CTGTGTGGCTGACAA[A/C]CCCGATGAGCTCACC | 8853 |
rs768486184 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325622 | TGAGGAGTAATTGGT[A/T]CCCCACTTGGCTCTG | 8853 |
rs768503107 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387077 | CGGGCTTGGTGGTGG[-/G]TGGGGGGGCGCCTGT | 8853 |
rs768504278 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383151 | GTTCAGTGGAGTCAG[C/T]TGGTCACCAGGATGC | 8853 |
rs768505400 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284909 | AAGGAAGATTTAAGA[C/T]GCCTTACAATGGAGG | 8853 |
rs768516995 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395828 | TAGCCAGGATGGTCT[C/G]AATCTCCTGACCTCG | 8853 |
rs768522652 | in-del | -/GCGCCCCTGCGGCTGTGCGCCA | 2.90213e-05 | 0.00380917 | utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207064 | GCAGTTGAGGCGGCG[-/GCGCCCCTGCGGCTGTGCGCCA]GCGCCCTCGCGCCGA | 8853 |
rs768539515 | snp | A/C/T | 3.29751e-05 | 0.00406038 | missense | ASAP2 | GRCh38.p7 | 2:9374832 | ACGCGGATAACGCGG[A/C/T]GAAGCTTCACAGTCT | 8853 |
rs768563454 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234213 | AGCCTGGGCACTCTG[A/G]CTCGAGTTCATTTTT | 8853 |
rs768569120 | snp | A/G | 1.74977e-05 | 0.00295779 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350926 | AGATGCCGCGCCATA[A/G]AGACGTTGTCTTATG | 8853 |
rs768581247 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369552 | GTTTTGTTGTGATGC[A/G]AAGTGAAACAGACGG | 8853 |
rs768606424 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294933 | TGCAGTAGACAGTGT[A/G]TAGTGACAGATGCCT | 8853 |
rs768640267 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243650 | TGAGATAGCGTTTCC[A/G]CTTACAGAAGCTTGT | 8853 |
rs768649432 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291353 | AAGTTCTGAAAATGG[G/T]TCTCTCTCACGAGAT | 8853 |
rs768662379 | in-del | -/TAATAT | | | upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9204805 | ATATTAATCTCAGAA[-/TAATAT]AGGCATTAGCTATGT | 8853 |
rs768664811 | in-del | -/TTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9293997 | GTATAAGGACAAGAA[-/TTT]TTTTTTTTTTTTTTT | 8853 |
rs768674470 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302700 | GGCTGGTCTCGAACT[C/T]CTGACCTCAAGTGAT | 8853 |
rs768678377 | snp | C/G | 3.29979e-05 | 0.00406175 | missense | ASAP2 | GRCh38.p7 | 2:9344534 | CACCATTTTTTAGGA[C/G]TCCCAAATTCGTCAG | 8853 |
rs768681146 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250725 | AGAGCCAGGGTGGAG[C/T]GGAGGTGTCTCAGCC | 8853 |
rs768702748 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9231723 | GTTCCCATGGTCCTT[A/C]TGCTAGTTGGAGCCC | 8853 |
rs768708463 | snp | C/T | 1.66665e-05 | 0.00288669 | synonymous-codon, intron-variant | ASAP2 | GRCh38.p7 | 2:9318553 | CAACATAATCTCCTT[C/T]CCTTTGGACAGTTTG | 8853 |
rs768721215 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230693 | TCACAGCTGGGAGTA[A/G]GAGCAGATATGTGCA | 8853 |
rs768723108 | snp | A/G | 1.6476e-05 | 0.00287014 | missense | ASAP2 | GRCh38.p7 | 2:9344605 | AACATGGGACCGAGC[A/G]GAACGGCAGCCTCTA | 8853 |
rs768736235 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317940 | TCACACCTTTACACA[C/G]CCACAACACCCTCAC | 8853 |
rs768757661 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239756 | TTGTTTTAGATGAGG[A/C]CTCACTGTGTCGCCC | 8853 |
rs768779263 | snp | C/G | 3.30513e-05 | 0.00406504 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368543 | GGGACTGGCTATTCT[C/G]ATTTGCTGAGTAAAG | 8853 |
rs768779368 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321186 | GAAGTCATTTCAAAT[C/G]TAAGTACAAGTATTT | 8853 |
rs768783815 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9293178 | TATGTACACATGCAT[A/G]CTGGCTTCATGATCG | 8853 |
rs768810456 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9303225 | AAACTAATGAACTAT[A/G]CTGAAATCTAGAGAC | 8853 |
rs768816073 | in-del | -/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317081 | ACACAAAATCACATC[-/CA]CACACACACACTCAA | 8853 |
rs768834729 | snp | A/G | 3.39536e-05 | 0.00412015 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344500 | ATTAGGACCTGGACA[A/G]GATTAAAAACACACT | 8853 |
rs768843023 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373877 | GTACTCTGTGACCAG[C/T]GAGCTGCTGTTTCGC | 8853 |
rs768865431 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9310093 | TGAGGTCTTTCTACA[A/G]CTGCCCACCCTTAGA | 8853 |
rs768891081 | snp | C/T | 1.65762e-05 | 0.00287886 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400109 | GAGTTTGTTTCTGCT[C/T]GGTCCATGGGGGCAA | 8853 |
rs768897360 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387170 | AGTGAGCTGGGATTG[C/T]GCCACTGCATTCCAG | 8853 |
rs768916329 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9224793 | TATCTGTCTCTGTCC[A/G]TCCATTGATCCATCT | 8853 |
rs768943718 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9340223 | AGACGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 8853 |
rs768987545 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9242830 | TTTGATTGTCCGATG[-/A]TTGTCAGGTGAGACT | 8853 |
rs769000120 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277517 | GGTAACTCTCTACTC[-/T]TTTAGTATGGCAGGA | 8853 |
rs769002716 | snp | A/G | 1.83768e-05 | 0.00303118 | missense | ASAP2 | GRCh38.p7 | 2:9378949 | TCTCGGGCAGTGGGA[A/G]CCTGGATAAACAGAC | 8853 |
rs769009726 | in-del | -/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258332 | GATAGTAATCAGTAG[-/TT]TTGTTTTTTTTTTTT | 8853 |
rs769053684 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341253 | TTTTGTACAGGCTAA[C/T]AAAGGCTATTGTTAC | 8853 |
rs769066866 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281702 | ATTGGGATAAAGATG[A/G]TTCTCTTACCACAGA | 8853 |
rs769075989 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397117 | GCCTCTATACCAAAG[C/T]GGCCACAGGCCATGC | 8853 |
rs769077247 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250415 | CAGGTGCCATGCATG[A/G]CTTTAAAGATGGGAG | 8853 |
rs769078162 | snp | G/T | 1.64844e-05 | 0.00287087 | missense | ASAP2 | GRCh38.p7 | 2:9376988 | AGACTTTTTAGTTCA[G/T]AACAGGTAGGTGTTC | 8853 |
rs769086571 | snp | A/C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9273230 | AATTTCTTACATCAT[A/C/T]GTTTTATAGTTTTCG | 8853 |
rs769088388 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275917 | TTGTTTTAACGTGGC[A/G]CTTAGCCACATTTCA | 8853 |
rs769124133 | snp | C/T | 9.91031e-05 | 0.00703859 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279433 | CTGTGTGGAAAATGT[C/T]GCATTTGAAGTCCTG | 8853 |
rs769131592 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9385134 | GACCCAGAGATTTCC[A/G]TGCATTTGCCTTGGA | 8853 |
rs769135192 | snp | A/G | 8.33743e-05 | 0.00645602 | missense, intron-variant | ASAP2 | GRCh38.p7 | 2:9318563 | TCCTTCCCTTTGGAC[A/G]GTTTGCTGAAGGGGG | 8853 |
rs769137651 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247458 | CCTTATTACCTCATG[C/T]GCTGCTTTCGGTCCA | 8853 |
rs769141664 | snp | A/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277562 | TATTTAAATAAACAT[A/T]TTTAGTTTTAGGTTC | 8853 |
rs769143553 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328738 | GGCCTCTGGCTCCTT[A/C]ACTCACCCACCCAAC | 8853 |
rs769160643 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271302 | AAACCCCATGAATCT[C/T]CAGCTGATCGTCCTT | 8853 |
rs769165124 | in-del | -/CAGC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256928 | CTGATCCTCCTGCTG[-/CAGC]CAAGGGCTGGGAGGG | 8853 |
rs769168372 | snp | G/T | 1.64933e-05 | 0.00287165 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334855 | TTAAAACCATCTTAA[G/T]GCAACAGACATTTTC | 8853 |
rs769174246 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358114 | CTCTGCACTCCCTGG[C/T]GACCTCGAGCCTGAG | 8853 |
rs769182626 | snp | A/G | 4.96225e-05 | 0.00498084 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388268 | ATATTTGTCTCACAC[A/G]CCTCTGCCCCAATGT | 8853 |
rs769192821 | snp | A/G | 4.94621e-05 | 0.00497279 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9391020 | CGTGTGTGCACGTGT[A/G]TGTGTGCGTGCATGC | 8853 |
rs769199116 | snp | C/T | 9.89087e-05 | 0.00703168 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374839 | TAACGCGGCGAAGCT[C/T]CACAGTCTTTGCGAG | 8853 |
rs769210435 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9299863 | CTTACTTAATTCTTA[C/T]GACAATCCCATAAGG | 8853 |
rs769210579 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9287474 | CGGATATCTGAAGGA[C/T]GCGGGGCTCCTGGTT | 8853 |
rs769211585 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9329745 | GGAATTGCCATGCCT[C/G]TCTGCTTACCTTCCC | 8853 |
rs769220069 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362037 | TATGTCTGACACACC[A/G]TTAAGAACCATAAAG | 8853 |
rs769245970 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358998 | GTTGTTGATATGTTG[A/C]CAGATTGGTTTGGAT | 8853 |
rs769269993 | in-del | -/CCTA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9344210 | GAGGGCTACTGTGGC[-/CCTA]CGTAGTGGGAGCCTC | 8853 |
rs769277834 | snp | G/T | 1.80218e-05 | 0.00300176 | intron-variant, missense, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207247 | TGAGGCGGCCTGCGC[G/T]GCGGCTCCGGCCGCA | 8853 |
rs769290885 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311711 | GGCTCGTTCGGCTGC[A/G]GGCCTGAGGCTGCTG | 8853 |
rs769298264 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9288410 | CCTGAGGGTGAGGCT[C/T]CAGGATCTCGTGAAA | 8853 |
rs769322209 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212712 | GACAAATCCAGCTCT[C/T]AGCCGCCACATTGCA | 8853 |
rs769331166 | snp | C/T | 1.64765e-05 | 0.00287019 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279289 | TCAGCACAGACACGG[C/T]TTAATGACTGTATTC | 8853 |
rs769353971 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276641 | CTCCCAGGTTCAAGC[C/G]ATTCTTTTGCCTCAG | 8853 |
rs769371542 | in-del | -/CT | 6.59511e-05 | 0.00574206 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297454 | AAACCTGGTAAGCAG[-/CT]CTGTGTATGAAATGC | 8853 |
rs769398489 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336052 | CTAGGAGAGTAAGTA[A/G]TTCAGTATTTTAATA | 8853 |
rs769398702 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365449 | GCAATTGTTGTCCTT[-/C]CTCATGGAGACATGA | 8853 |
rs769399916 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318747 | CTCTGATTTGCCATC[G/T]TGGGACCACCTTTCA | 8853 |
rs769413914 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212875 | GTACACCACAGGCAC[A/G]TGAGAGCTTGCGAAG | 8853 |
rs769437113 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9220385 | ACATCCTTGACAACA[C/T]TTGTTATGTTTGTCT | 8853 |
rs769439228 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9235840 | TGGATGCAGCCGGCA[A/G]TGCCTTCCCATGAAT | 8853 |
rs769439390 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346987 | ATGCTGAGAACTCAG[C/T]TTGTCACACAGCGTG | 8853 |
rs769441711 | snp | C/T | 1.65105e-05 | 0.00287315 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374902 | CCAAGCTTATGCTGA[C/T]GGTGTGGATCTTACG | 8853 |
rs769454481 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295907 | GACCATTCATAGGTC[A/G]TAGGGATTGGCTCAG | 8853 |
rs769460147 | in-del | -/TGCAGTTA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353747 | GACTGGCTGGCTGGT[-/TGCAGTTA]CTTCCTACAAGATGT | 8853 |
rs769462909 | snp | A/G | 1.8027e-05 | 0.00300219 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401431 | GGGAGGTTCCTGGGG[A/G]CTGAGCCACGTCCCT | 8853 |
rs769498164 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9296329 | TCACCTGTGTCCCCT[A/C]CCCCATTCCTACCCA | 8853 |
rs769521673 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9386555 | CACGCTGCTCACCTG[A/T]TTCTCAGCAGACAGC | 8853 |
rs769540606 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9377388 | CAAGGAGGGATCCAC[A/G]CATTAGCCATGGTCT | 8853 |
rs769577209 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9324620 | CTTCTCATAATTGTA[C/T]CACTCCCCCAGTAAT | 8853 |
rs769610429 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229061 | GTTGAAGGCTAGGGG[C/T]GGAAAGTGGACAATC | 8853 |
rs769615812 | snp | C/T | 0.000247233 | 0.0111155 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391140 | GCCGGCAGCGATCTT[C/T]GTCAGATCCGCCAGC | 8853 |
rs769627602 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307425 | TTCTTGGAGGTAATA[A/C]ATTTGAAAAAGTACT | 8853 |
rs769628628 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336895 | AAGGAAGATCCAACC[C/T]ATGAAGCAAAGCTCA | 8853 |
rs769645188 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209673 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 8853 |
rs769656215 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9326411 | TTTCTTCAAAATTCA[-/T]TTAATAAAGAAATTC | 8853 |
rs769666544 | snp | C/T | | | intron-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212054 | CTGCCCCCTGGTGAA[C/T]GCTGAATTCAGTTTC | 8853 |
rs769666641 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9208575 | CTGAATCCTGTTAAT[A/G]TAACTTGGGTAGCCT | 8853 |
rs769669019 | snp | C/G | 0.000115341 | 0.00759324 | missense | ASAP2 | GRCh38.p7 | 2:9380759 | ACGAGTCAGGAGAGA[C/G]TCCGCTGGACATTGC | 8853 |
rs769683100 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9323514 | TTCTGGCTTCACGTA[C/T]GTACTCTTGCTAAAA | 8853 |
rs769708328 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381917 | AATAATAAATGCTAT[A/G]CAAGTGTAAGATAAG | 8853 |
rs769760649 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274011 | TAGTTCAGCCTAGGC[C/G]CAGGAATGAACAAGG | 8853 |
rs769791724 | snp | C/T | 6.59478e-05 | 0.00574191 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9323187 | TCGGACTGAAATAAG[C/T]GGAGCGGAAATTGCC | 8853 |
rs769795113 | snp | C/T | 3.40379e-05 | 0.00412526 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400865 | TCCTGCCTCTCTGCT[C/T]TAGCCAGGGGGGTGC | 8853 |
rs769795490 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227753 | ATATGTGGGTAAGGT[-/A]TTTGTGAGTACACGT | 8853 |
rs769801866 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9372063 | GGCCTCCAAGCCCTG[G/T]GCAGATGAGTAAATA | 8853 |
rs769828411 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9262208 | TAGTGGAAATGAAAG[C/G]CTGGTATAAGCTGTA | 8853 |
rs769838169 | snp | A/G | 1.64757e-05 | 0.00287012 | missense | ASAP2 | GRCh38.p7 | 2:9344620 | GGAACGGCAGCCTCT[A/G]CAAGAAGAGTGACGG | 8853 |
rs769838212 | snp | G/T | 1.70664e-05 | 0.00292112 | missense | ASAP2 | GRCh38.p7 | 2:9374767 | CAGGAATGCAAGAAA[G/T]GACTACATCACAGCC | 8853 |
rs769851396 | in-del | -/AC | 1.64977e-05 | 0.00287203 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356153 | TGTTTGTGGAATTTA[-/AC]ACAGCGTTGCTCTTG | 8853 |
rs769866340 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9242557 | ACATCTTGTATTGGG[C/T]GGTGTGTGGGCTCTG | 8853 |
rs769866712 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353651 | GTGCATCTGCCAGGC[A/G]CTCCATGGTCACCCA | 8853 |
rs769872655 | in-del | -/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9401934 | GTGACAGGGAGGTCA[-/CA]CACACACACAGTCTG | 8853 |
rs769878656 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362436 | GCATGTATTTATAGT[A/G]TACAACATGATGTTT | 8853 |
rs769879273 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274794 | CTACCTCACCTTTAT[G/T]TCTAATCTGTTTAAC | 8853 |
rs769904858 | snp | C/T | 3.32027e-05 | 0.00407434 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9400803 | GGTCCTGCAGCCCCC[C/T]GCACCCATGCCTAGG | 8853 |
rs769906640 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331587 | AGCCTGGCCAACATG[A/G]TGAAACCTGGTCTCT | 8853 |
rs769920271 | snp | C/T | 3.29783e-05 | 0.00406055 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344674 | GTTTAAATGTACGTT[C/T]GTTATCTTGTGTCCA | 8853 |
rs769940237 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371317 | TTTAAAACATTTCAT[C/T]CCACTTCATAGTATA | 8853 |
rs769957904 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343478 | TTGAGACAAGGTCTC[A/G]CTCTGTCACTGAGGT | 8853 |
rs769971553 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9290179 | AGCTTTGGGAGAGAA[A/G]GACATATTCTAATGT | 8853 |
rs769982633 | in-del | -/TTGT | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205605 | GGGGCTTTAAAAAGA[-/TTGT]TTGACTGGTCTACTG | 8853 |
rs770011992 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9269319 | GGTCTTTCCTGTGAC[C/T]CTGTCCTTGCATTCA | 8853 |
rs770023526 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237613 | TTGTAGAGATGAGGG[C/T]CTCAGTATGTTGCCC | 8853 |
rs770025045 | snp | C/G | 1.66701e-05 | 0.002887 | missense | ASAP2 | GRCh38.p7 | 2:9388517 | GCACCACCAGCGCCC[C/G]CCCGCTTCCTCCACG | 8853 |
rs770028123 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369219 | AGACAGAGTTTCACC[A/T]TGTTGGCCAGGCTGG | 8853 |
rs770053244 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263344 | GGCTCTCCCCAAAGC[A/G]GGGCACCAGGCTGGC | 8853 |
rs770082435 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9216597 | TCCTGAGTAGCTGGG[A/G]TTACAGGTGCCAACC | 8853 |
rs770114969 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349628 | CTGACTAACCTGTAG[A/G]GGAAAAGACCAACAC | 8853 |
rs770116287 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9310047 | TGCTGCAGCCTCTGC[C/T]AAGAATGCTCTTAAT | 8853 |
rs770126504 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9329112 | AGTATGAGTAGGAGC[C/T]GGCAGATAAGGAGTG | 8853 |
rs770130985 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9356169 | CACAGCGTTGCTCTT[C/G]TTTTTCTAGATGGAT | 8853 |
rs770134400 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402721 | ATTTTGGCTGTTTTT[A/T]GCCTTTTATTTGCCT | 8853 |
rs770165709 | snp | A/G | 1.64751e-05 | 0.00287007 | missense | ASAP2 | GRCh38.p7 | 2:9358800 | ATCCTGACCTGCATC[A/G]AGTGTTCCGGAATCC | 8853 |
rs770182563 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9379658 | TAAATAAAGAGGAAA[G/T]AATAGAAAAAAGACA | 8853 |
rs770191367 | snp | A/G | 3.29603e-05 | 0.00405944 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9391016 | TGTTCGTGTGTGCAC[A/G]TGTATGTGTGCGTGC | 8853 |
rs770191566 | snp | C/T | 1.65072e-05 | 0.00287286 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377021 | AAATTAAGGGAGGCA[C/T]TCGTTTTCTCCTTGG | 8853 |
rs770205114 | in-del | -/TGGACTCAGAT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233621 | GAAGCCAGCTGGACC[-/TGGACTCAGAT]ATAGGTTTTGCTAAT | 8853 |
rs770211523 | snp | A/G | 1.84599e-05 | 0.00303803 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356374 | CCCACCCGACCCTGG[A/G]CTCTAGGACATTTCA | 8853 |
rs770236597 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281494 | CCTATATTGCTGAGC[A/G]TGTACCACAAACCTC | 8853 |
rs770262709 | snp | A/G | | | missense | ASAP2 | GRCh38.p7 | 2:9358785 | TCCACCAACCTGGGC[A/G]TCCTGACCTGCATCG | 8853 |
rs770279059 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387086 | TGGTGGGTGGGGGGG[C/T]GCCTGTAGTCCCAGC | 8853 |
rs770297487 | snp | C/G | 1.64762e-05 | 0.00287016 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9334756 | TTTTCAGGATGGACT[C/G]AAAGCCGTGGAAAGC | 8853 |
rs770298603 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9287450 | GGATGGAGAAACCTC[C/T]TTGTAGGACGGATAT | 8853 |
rs770298608 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397075 | ATTATGCTGTAATAA[A/G]TGGGCTTTCCAGTGC | 8853 |
rs770317496 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368908 | GATATGTGATTATGT[A/G]GCGTCCTTCTTGCCA | 8853 |
rs770325750 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257937 | TTCTATGTTGTTGCA[A/G]TAATATTGCCTGTGT | 8853 |
rs770330979 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257008 | TCCTGCCTGCTAACA[A/G]CCTGTCACTTTCTTC | 8853 |
rs770338165 | snp | C/G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350351 | CTGCCATTTTTGTAC[C/G/T]GTGAAATTACCTTCA | 8853 |
rs770345417 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9310835 | TGTGAAGAGATGGCT[A/G]TTTGGCTGGCTCTGT | 8853 |
rs770347473 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230509 | TGGTCAGCCCCACAG[A/C]TGGACTGCAAGCTGC | 8853 |
rs770350074 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9298789 | CGCACCTGGGTGGAT[A/G]AGCCCTTTCCATGCA | 8853 |
rs770382575 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217905 | AGGTGTGAGCCACCA[C/T]GCCTGGCTTTTTTTT | 8853 |
rs770387424 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9297568 | CTTGGGTACCCAAAA[G/T]AATTATGTTTTTATA | 8853 |
rs770410090 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212236 | GGGACCTACAGTCCA[A/G]CAAGAGGAACAGAAT | 8853 |
rs770413612 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221439 | GGATTGCAGGCATGA[A/G]CCACTGCACCTGGCC | 8853 |
rs770415360 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369745 | CTGAAGTAGAATTAA[C/T]GACACGAGTCTTCCC | 8853 |
rs770428671 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9224182 | CAGTGCGAGGGAAGG[A/G]AGGATTGCCTAGTGA | 8853 |
rs770429164 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9309359 | GCGCAGTCCCAAAAT[A/C]ATGATGCAAGAAGCC | 8853 |
rs770430193 | in-del | -/CGGGGT | 0.000199117 | 0.00997592 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380830 | CTCCCACCACAAGGA[-/CGGGGT]GGGGCACCTGTCACG | 8853 |
rs770436828 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338746 | GGGGACAGAGAAGCA[A/G]TTGGGGTGCAGTGTA | 8853 |
rs770447840 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209954 | AATCATTTTACAATT[-/A]AAATGTGCTGTTTTG | 8853 |
rs770456920 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286132 | CTGGGCACGGTGACT[A/C]ACGCCTGTAATCCTA | 8853 |
rs770457431 | snp | A/G | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390741 | CCAAGTGCAGTGTTC[A/G]CAAGAGAACATTGTG | 8853 |
rs770521039 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345826 | TGGGGTCCAGAGAAA[C/T]GGCCCTGAGGTTCAT | 8853 |
rs770536015 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247315 | TTGCCCTTCACCAGA[G/T]GCTGCTGTCTTGGAA | 8853 |
rs770538933 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346636 | GAATTGGTGTCCACT[C/T]GCTGTTTGTTTGAAC | 8853 |
rs770553054 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366634 | CTGGGAAAATTGCAA[C/T]GCAGCCTCTAGGCTT | 8853 |
rs770561532 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328531 | TTTAAAATAAGAAAA[C/T]ACTTTTATATATTAT | 8853 |
rs770562238 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233968 | ATATAAAAATTAGCT[A/G]GTCGTGGTGACAGGC | 8853 |
rs770563112 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317905 | CCCTCATGTGCATTC[A/G]CTCTTATACTCAAGC | 8853 |
rs770579188 | snp | C/T | 3.29473e-05 | 0.00405864 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356135 | TGGGCTGGACTCAGC[C/T]GTTGTTTGTGGAATT | 8853 |
rs770580525 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9246188 | TGGTTTCTCCAAACC[C/T]GTACTCCTTAGACAT | 8853 |
rs770585926 | snp | A/G | 7.39727e-05 | 0.00608119 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401441 | TGGGGGCTGAGCCAC[A/G]TCCCTGCCCACCTGG | 8853 |
rs770586352 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9357903 | TCTGAAGAGAATTGT[A/G]TTTATGGGTTGTGAT | 8853 |
rs770602598 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212658 | TTGTGGAGCATATAC[A/G]TGCATTCCAGGCCCG | 8853 |
rs770617653 | snp | C/T | 3.12086e-05 | 0.0039501 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393479 | TCTCCCTGTCCTCCG[C/T]AGATCCCCTGACCCC | 8853 |
rs770638159 | snp | G/T | 3.34275e-05 | 0.00408811 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380845 | CGGGGTGGGGCACCT[G/T]TCACGGGACAGGGAG | 8853 |
rs770650349 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264580 | TCATTTATTAATCTT[C/T]CCCATGCAAGTCATA | 8853 |
rs770688632 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294251 | TGATGCACCTGTCTC[A/G]GCCTCCCAAAGTGCT | 8853 |
rs770692138 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277502 | TTGATTATCTTGTAT[C/T]GGTAACTCTCTACTC | 8853 |
rs770692154 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264656 | TCAGTCTCCTGTCAC[C/T]GTCTTCTCTCCTCAT | 8853 |
rs770713648 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9208507 | ATGGAAAAATTTTTT[A/C]TTTGTAGCTGTAAAC | 8853 |
rs770722649 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9251855 | GCAGTGATGGATGGA[A/G]CAGAGATGGGCCTGA | 8853 |
rs770743548 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276534 | TCCTGTGTCATCTTT[C/T]TTTTCTCTTTTTTTT | 8853 |
rs770744650 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351745 | TAGGAAGTCACTTGT[A/T]ATGTGATTCAGCGCT | 8853 |
rs770749697 | in-del | -/G | 1.8573e-05 | 0.00304732 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356380 | CGACCCTGGGCTCTA[-/G]GACATTTCAATCCCA | 8853 |
rs770749931 | snp | A/G | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390329 | CCAGGGGAGGAGCTC[A/G]AAGGCTTCCTCTGGA | 8853 |
rs770762340 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346944 | CCAGTTTTTGGCAGA[C/T]AGTACGGTTATAACC | 8853 |
rs770772937 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9241062 | TGAATTGCTTATTTC[C/T]GGACTTTTCTGTGGA | 8853 |
rs770791423 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253239 | CGCGATATTGGCTCA[C/G]TGCAACCTCTGCTTC | 8853 |
rs770798027 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9334101 | CGCCAGGCCAGAATG[C/T]AGTGGCATGATCTCG | 8853 |
rs770807139 | snp | A/G | 1.65507e-05 | 0.00287664 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368555 | TCTCATTTGCTGAGT[A/G]AAGGTTTGCCTTTGC | 8853 |
rs770808256 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9220138 | GGTTGCCTCCACTTT[C/T]AGGCTATTATGAATA | 8853 |
rs770829193 | snp | A/G | 1.64923e-05 | 0.00287156 | missense | ASAP2 | GRCh38.p7 | 2:9323203 | GGAGCGGAAATTGCC[A/G]AAGAGATGGAAAAGG | 8853 |
rs770873771 | in-del | -/T | 6.62586e-05 | 0.00575543 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320281 | ATTTATTATTCTTTG[-/T]TTACAGGATCTGAAA | 8853 |
rs770881145 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9339751 | TCTTCCTTCTTCACT[A/G]TCTGACTCAAGATGC | 8853 |
rs770897020 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405974 | CATGCCAGTGATACC[A/G]TGACTGGGAAGCCAC | 8853 |
rs770907889 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249056 | TAGCATTCTCCTGGA[-/C]AAATTGCATGTTTTG | 8853 |
rs770928430 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272883 | TATGGATTTATTTCT[A/G]GGTTCTCTATTCCAT | 8853 |
rs770940974 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9262424 | GTGCTGACTGTATGG[C/G]AGACACATAAGCATT | 8853 |
rs770971152 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368992 | TGTGTTTGTGTTATT[A/G]TTGATACACAACTTG | 8853 |
rs771011740 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9283634 | TAGATGGCTCGGGCT[A/G]CTATAACAAAATACC | 8853 |
rs771018314 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343418 | GGCCTCCTACTCTCA[A/G]CTCAGAGTGTCTGCT | 8853 |
rs771032957 | snp | A/G | 3.2956e-05 | 0.00405918 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9391028 | CACGTGTATGTGTGC[A/G]TGCATGCGTCTGTGT | 8853 |
rs771038528 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371956 | CCCATCTGAGGGATC[A/C]CATTAGCAAAGCAAA | 8853 |
rs771050784 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9261941 | CAGTTGGACCAGAGC[A/G]CCTCACCCCACCATT | 8853 |
rs771056918 | snp | A/G | 0.000174969 | 0.00935168 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400877 | GCTCTAGCCAGGGGG[A/G]TGCAGGTGGTTTCAC | 8853 |
rs771064884 | snp | A/T | 1.66062e-05 | 0.00288146 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320270 | AGTCTTGCCTAATTT[A/T]TTATTCTTTGTTTAC | 8853 |
rs771095701 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387213 | GAGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAC | 8853 |
rs771099150 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300136 | TACTCGGGAGGCTGA[A/G]GCTGAAGAATTGCTT | 8853 |
rs771106986 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313519 | TTTCTTCCCCACAAC[C/G]CACCTTATCACTGGA | 8853 |
rs771124783 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350678 | GCCTTCCTCTGTCAA[A/G]TCTGAAGGCCACCTT | 8853 |
rs771128287 | snp | C/T | | | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214849 | AATAGTCTCATGTTT[C/T]ATGTGCAGTTCTGTT | 8853 |
rs771141220 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300102 | GCCAGGCGTGGTGGC[C/T]CACGGCTGTAGTCCC | 8853 |
rs771146348 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213685 | CAAACCTACTGATGG[A/G]TTGTCATTATTGTGT | 8853 |
rs771164721 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9393282 | CTTTAGGCTCCCAGC[G/T]TCCTTATTAGTTTGG | 8853 |
rs771185346 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276481 | GAGAACACCAGGAAG[C/G]CTTATAGTGCCTGGG | 8853 |
rs771200183 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9289863 | TGGGGTACCATCCAC[A/G]AAGACTGGCTGTTTC | 8853 |
rs771226301 | snp | C/G | 5.924e-05 | 0.0054421 | missense | ASAP2 | GRCh38.p7 | 2:9393638 | TCCCGCAGAAGAAGC[C/G]TGCGCCGGGGTAAGC | 8853 |
rs771229875 | snp | C/T | 5.67102e-05 | 0.00532465 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356391 | TCTAGGACATTTCAA[C/T]CCCATTCTGATTCAC | 8853 |
rs771231424 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260924 | AAGATTCTGAAACAA[A/G]GAATTGGTTACCCAG | 8853 |
rs771250155 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248268 | CCCAACAATACTGAG[C/T]ATTTAAGCCAAATTA | 8853 |
rs771263068 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9355755 | CTGTAGTGAGTTAAA[A/G]TGAAGCTATTGAGAG | 8853 |
rs771270121 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9401933 | CTGTGACAGGGAGGT[C/T]ACACACACACAGTCT | 8853 |
rs771274454 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9290981 | GTATTATCTTTTCAA[A/C]CTCCTCTCTACATTT | 8853 |
rs771297622 | in-del | -/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317386 | CCCAACTCACATCCA[-/CA]CACACACACCCTCAA | 8853 |
rs771330524 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318962 | TAGCACTGGGAAAGG[A/G]TCCTAGCAAGGGTGT | 8853 |
rs771367078 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381594 | TTTAAAAACTAGCAA[C/T]GCATGGTGGAGCATG | 8853 |
rs771389002 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383760 | AGAGACTTGGAACCA[A/G]CCCAAATGTCTGTCA | 8853 |
rs771390212 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225681 | GGCCTGGCATGGTTT[A/G]GGATCCTGGGGGAGA | 8853 |
rs771393279 | snp | C/T | 1.64751e-05 | 0.00287007 | stop-gained | ASAP2 | GRCh38.p7 | 2:9358818 | TGTTCCGGAATCCAC[C/T]GAGAGCTGGGGGTTC | 8853 |
rs771405689 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9292466 | GAGGTTGCAGTGAGC[C/T]GAGATTGCACCACTG | 8853 |
rs771407162 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9308606 | CAGCATGTGCCCAGC[C/T]TCAGCTTAGCTTAGC | 8853 |
rs771421051 | snp | C/T | 1.66687e-05 | 0.00288688 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403335 | CTGACTGAATTGCTA[C/T]TGAACAAAAGCATTA | 8853 |
rs771427856 | snp | A/G | 3.29495e-05 | 0.00405877 | missense, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9279326 | TTTTAGGCTTTGGAC[A/G]TGGACCGGATGGTTC | 8853 |
rs771465575 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9268181 | TAAGTTTGTTCTCTT[C/G]CGTTGCTGTGTAGCA | 8853 |
rs771469911 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325797 | ATCTTTCGAGCAGTC[C/T]TCAGGTAGTGCTGGG | 8853 |
rs771475737 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256495 | TATCTGAGATAAGGA[C/T]TGCAAGGAGATATTA | 8853 |
rs771481183 | snp | A/G | 1.66371e-05 | 0.00288414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335065 | TTAATTTTCTGATTG[A/G]TTCTGTTGTGTGTGT | 8853 |
rs771490426 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302722 | TCAAGTGATCCACCC[G/T]CCTGGGTCTCCCAAA | 8853 |
rs771493588 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361153 | CCCACAATGAGAAAT[C/T]AGCCAGTGCCTGCTT | 8853 |
rs771502049 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256846 | TAAAAAAGCACTGAC[C/T]GAGAGTCAGTATGAC | 8853 |
rs771504255 | in-del | -/TA | | | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9215288 | TGACTGAAATGTCAC[-/TA]TGTGGAGCACGACTG | 8853 |
rs771505165 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279953 | GTCACCTGTAGCATA[C/T]CTTCCCTTGTACAAA | 8853 |
rs771506075 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378652 | TCACCCCGGTAGTGC[A/C]CTGCCCCACCTTGGC | 8853 |
rs771517010 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9309752 | TATCTGCTTTACTGA[C/G]TCTAGCAAGTCTCTA | 8853 |
rs771526473 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349466 | CCTGGATAAGTTAGG[C/T]AATCCGATTGGTAAC | 8853 |
rs771535117 | snp | G/T | 3.29554e-05 | 0.00405914 | missense | ASAP2 | GRCh38.p7 | 2:9376970 | AACCTCTCTTCACAT[G/T]GTAGACTTTTTAGTT | 8853 |
rs771537145 | snp | C/T | 1.64751e-05 | 0.00287007 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356154 | GTTTGTGGAATTTAA[C/T]ACAGCGTTGCTCTTG | 8853 |
rs771542053 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9246565 | GCCAGGATTACAGGC[A/G]TGAGCCACCACGCCC | 8853 |
rs771557024 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9238381 | TTGACAATACTCCAG[A/G]CTTTTGTAAACAAAT | 8853 |
rs771573131 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237307 | ATTAGGACATTTCTC[A/G]TTTACATTGTGACTT | 8853 |
rs771582488 | in-del | -/AAAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9326227 | TCTACAAAAAAACAA[-/AAAC]AAACAAACAAACAAA | 8853 |
rs771617058 | in-del | -/TG | 1.64757e-05 | 0.00287012 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9391039 | GTGCGTGCATGCGTC[-/TG]TGTGCATGCGTGTGG | 8853 |
rs771627102 | snp | A/G | 1.6696e-05 | 0.00288924 | missense | ASAP2 | GRCh38.p7 | 2:9356285 | GAACTGACAAAGGAG[A/G]TCATCTCAGAAGTGC | 8853 |
rs771639702 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244040 | CACGTTGGCTCATAA[C/T]GATAATCCCAGCACT | 8853 |
rs771643070 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315356 | TGAGGCGCAGCCAAG[G/T]CAGTGGACGTGAGAA | 8853 |
rs771648327 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9296323 | CCAGAATCACCTGTG[A/T]CCCCTCCCCCATTCC | 8853 |
rs771652192 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212088 | CTTAGGCTCAAGAGT[A/G]GAAGTACTGATGCCA | 8853 |
rs771660289 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9270544 | ATGGGGCTTCCATCA[C/T]CTCAAAGCATTTAGC | 8853 |
rs771686998 | snp | C/T | 1.69246e-05 | 0.00290896 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327807 | ACTTCCATGACATTT[C/T]CTTTTCATTGTTCAA | 8853 |
rs771693642 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9340088 | AGTGCAGTGGTGCAA[C/T]CTTGGCTCACTGTAA | 8853 |
rs771698779 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9231459 | TGCGTCATGACTCGG[C/T]ACCTGCTACCCGTTC | 8853 |
rs771728266 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9356414 | TGATTCACAGAATCC[A/G]TTCATTGATTTTCAC | 8853 |
rs771754434 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244769 | AGGAAGAACAGGAGA[C/T]GGATTTAATGTGGAT | 8853 |
rs771778856 | snp | C/T | 1.68849e-05 | 0.00290554 | missense | ASAP2 | GRCh38.p7 | 2:9374778 | GAAAGGACTACATCA[C/T]AGCCAAGTACATCGA | 8853 |
rs771784721 | snp | A/G | 1.66197e-05 | 0.00288263 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9400818 | TGCACCCATGCCTAG[A/G]AAGTCGCAGGCAGTA | 8853 |
rs771809916 | in-del | -/CT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279719 | TGGATTCATTCCTGC[-/CT]CTGTCATTTGGTTTT | 8853 |
rs771819687 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346389 | TGTGGTGAGCCGATA[C/T]CACGCCACTGCACTC | 8853 |
rs771831853 | snp | A/G | 1.66724e-05 | 0.0028872 | missense, utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207205 | GCACGGCGCAGTGCC[A/G]GAACACTGTGGCGGC | 8853 |
rs771832975 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9386941 | GAGCGCGGGGGCTCA[-/G]CGCCTGTAATCCCAG | 8853 |
rs771860831 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263555 | GTTTACTGTCATCTG[C/T]TTCCGTTTCTCTAAG | 8853 |
rs771866390 | snp | C/T | 1.64849e-05 | 0.00287092 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344715 | ACTCTTATTGTTTCT[C/T]CCACTTATCCACAAG | 8853 |
rs771866846 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348486 | AGAATTTTCTCCCAT[A/G]AATTTTTCTAATAGC | 8853 |
rs771868685 | in-del | -/TG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9335073 | TGATTGGTTCTGTTG[-/TG]TGTGTGTGTGTTTTT | 8853 |
rs771870707 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9363933 | TTAATTAGTTCTGGG[G/T]AATCATGTCATCTTA | 8853 |
rs771896140 | snp | A/G/T | 9.02685e-05 | 0.0067177 | missense | ASAP2 | GRCh38.p7 | 2:9393529 | GCCAAGACGCCCAGC[A/G/T]TAATGGAAGCCTTGA | 8853 |
rs771902266 | snp | A/G | 1.68388e-05 | 0.00290158 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380855 | CACCTGTCACGGGAC[A/G]GGGAGCCAAGCCTGT | 8853 |
rs771918434 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9316312 | TGTTTCAAAAAAAAA[G/T]AAAAAAAAATTAGTA | 8853 |
rs771924783 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383983 | ACACTTGGACACAGG[A/G]CGGGGAACATCACAA | 8853 |
rs771928762 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9262310 | GACTGAGACGGTCCT[A/G]GGGTAACAGCGTCTT | 8853 |
rs771929727 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9218111 | GAGTAAGAATCCCAG[-/T]TGCTGTGGAGGAGGT | 8853 |
rs771936071 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387074 | GCCGGGCTTGGTGGT[-/G]GGGTGGGGGGGCGCC | 8853 |
rs771951647 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276343 | GGGGGAGCCACAGGT[A/G]GCTCATTATGATGGA | 8853 |
rs771965273 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9344707 | ATGTCTAAACTCTTA[C/T]TGTTTCTCCCACTTA | 8853 |
rs771977696 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9344195 | CATCACCTCCCTCCT[C/T]GAGGGCTACTGTGGC | 8853 |
rs771989083 | snp | A/C | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211361 | TGGCAGAAATTTGAA[A/C]AGTAAGGGTTTTTTG | 8853 |
rs772004684 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275665 | CCTTCAAGCACAGCT[C/G]CCGTTTCCCCTCTGG | 8853 |
rs772016757 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260207 | ACTGAGGCCCAGGTG[A/G]TCAAGTAATTTGTGT | 8853 |
rs772035480 | snp | C/G | 1.67531e-05 | 0.00289418 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401225 | AGCTCTCTGCCCTGA[C/G]AGCTGAGGCCTGCAG | 8853 |
rs772052585 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281739 | CAAAGATTTTAATGT[G/T]CTAGTAATGTGGATT | 8853 |
rs772082699 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405680 | TACTTTTAAATGGAC[A/G]TGGTTTTATTTTTAA | 8853 |
rs772090588 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333776 | AAGGGTTACACACAG[C/T]ACCCTCCAGAGGCAG | 8853 |
rs772091111 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239862 | CTCTTGAGTAGCTTG[C/G]ACTCCAGGTGCACAC | 8853 |
rs772131831 | snp | A/T | 1.67211e-05 | 0.00289142 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391190 | CCTCTTCGCGTGACA[A/T]CTACCAGTACGTTTT | 8853 |
rs772135012 | snp | G/T | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390910 | ACATGCCGGAGACAG[G/T]AGTAAAAGCATTGAG | 8853 |
rs772144578 | snp | G/T | 1.65023e-05 | 0.00287244 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368418 | AAATAGACTTTCATT[G/T]TTGCAGCTCGCCAAG | 8853 |
rs772145810 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332647 | GAGAATTGCCAGGTC[A/G]CAAAGATTCTTGGAG | 8853 |
rs772169116 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9273654 | GCTGATTGGTTGGGT[C/T]GGAGATGAACTCATA | 8853 |
rs772185936 | snp | A/G | 0.000140292 | 0.00837414 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379083 | GCCCGGGCCCCGGGG[A/G]TGGGCTCAGCTGCAC | 8853 |
rs772254159 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366410 | ACAGTGATTTTTGTC[A/T]CTCAACTTGGGAAAA | 8853 |
rs772268802 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227416 | TTGTTTCCTGTGTTT[A/G]TGTTCTTATTTCCTA | 8853 |
rs772270223 | snp | C/T | 4.96849e-05 | 0.00498397 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9323247 | CCAGCTACAGATGTG[C/T]GAGGTAAGGCGGTGG | 8853 |
rs772289359 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240603 | GCCACGCACCACGGC[C/T]GTAGCTTTTGCAGTT | 8853 |
rs772299268 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351622 | ATTTGCAGAGGACCA[C/T]GCCGGACTGTGTACT | 8853 |
rs772312335 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313557 | GGTGCCTTTGGCGCT[A/G]CCCCCGCCAGCTGCC | 8853 |
rs772314449 | snp | A/G | 1.64787e-05 | 0.00287038 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9388353 | GCTGGGCTCCAACCA[A/G]CTTCAGTCTAACGCT | 8853 |
rs772345739 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205225 | CAGCCCTCTACAAAT[A/C]AAGACTTGAAAAGTT | 8853 |
rs772357094 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300000 | CTTTGGGAGGCCAAG[A/G]TGGGCGGGTTGCTTT | 8853 |
rs772361005 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328876 | TTCTAATTAGATGTT[C/T]ACAAAATTGTTTTAA | 8853 |
rs772366046 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380193 | AACAGTTTTTGTTTT[C/T]GTTTTTGTTTTTTGT | 8853 |
rs772377079 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272730 | GGTTTGATTTTTGTG[C/T]ATGGTGAAAGATAGA | 8853 |
rs772448441 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9401764 | GCAGAGCCCCAGGCC[C/T]GAGTCTGGTCCTGAA | 8853 |
rs772457551 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300839 | TGACTGATCATAAGG[G/T]TTCAAGTTTCAACTT | 8853 |
rs772462350 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9342592 | CTTCATGACCTTGGA[G/T]TAGGCAATAGTTTCT | 8853 |
rs772466185 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9329977 | ATGACATCTTCCTTG[C/T]GTCTCTGTGCCACTG | 8853 |
rs772471580 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9288843 | ATTTGGTCTCAGAGC[A/G]CCCCTAGGAGGGAAG | 8853 |
rs772475518 | snp | A/G | 1.65685e-05 | 0.00287819 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400090 | AATTATTTAATTTGG[A/G]ACTGAGTTTGTTTCT | 8853 |
rs772481321 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234659 | TAATCAGTTAAAATG[A/T]GTAGGTAGAGCCAAG | 8853 |
rs772485854 | snp | G/T | 1.64868e-05 | 0.00287109 | missense | ASAP2 | GRCh38.p7 | 2:9388440 | GCCCAGCATCTTGCA[G/T]AATGAGACTTACGGA | 8853 |
rs772526162 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9246656 | AGAATAAAGAGAACC[A/G]TGAGAGGTCTTCAAT | 8853 |
rs772540793 | snp | C/T | 1.71202e-05 | 0.00292572 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344494 | CTAAAAATTAGGACC[C/T]GGACAAGATTAAAAA | 8853 |
rs772557752 | snp | C/T | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404600 | GGCATATGATACCCA[C/T]TTGGACTTTTAACAA | 8853 |
rs772588129 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9347244 | TCCCTGCGTGCTCTG[A/G]AAGTCAGAATCCAGA | 8853 |
rs772597778 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221950 | AGGTGCCCGCCACCA[C/T]GCCTGGCTAATTTTT | 8853 |
rs772619396 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278643 | AGCGCCTCCTATGTG[C/T]TGGACATTGTGAGTG | 8853 |
rs772619761 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210293 | TTGAGTGAGATGCCT[A/G]ACATTTTCTTATTTT | 8853 |
rs772628333 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | ASAP2 | GRCh38.p7 | 2:9344593 | AGGGAAACAAGGAAC[A/G]TGGGACCGAGCGGAA | 8853 |
rs772629070 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236039 | GCCCAGGACTGCACC[C/T]ACCACAAAGAAGTAC | 8853 |
rs772630705 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370945 | GCTTCATCTCACACT[G/T]ACGGTACCAGCACCC | 8853 |
rs772646789 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9297361 | TGGCGGCAACTGTGT[A/G]TGCAGAGATGACCCA | 8853 |
rs772657376 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214539 | GCCGCTGCGCCCGGC[C/T]GCCTTTCCAGGTGCT | 8853 |
rs772665062 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9360650 | TAAGTGAATTACTCA[A/G]TGTGAAGTTGGAAAA | 8853 |
rs772672391 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368858 | TCTTGGTCTCTCTGC[A/G]TAATCCTGAGCCACC | 8853 |
rs772690383 | in-del | -/CTCT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317563 | ACATCCACAATCACA[-/CTCT]CACACACCCACACAC | 8853 |
rs772710930 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212093 | GCTCAAGAGTAGAAG[C/T]ACTGATGCCACTCCT | 8853 |
rs772717030 | in-del | -/TG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243913 | CCAGAATAAATGTGC[-/TG]TGTGTGTGTTAGTTT | 8853 |
rs772719724 | snp | A/G | 0.000148762 | 0.00862315 | missense | ASAP2 | GRCh38.p7 | 2:9374909 | TATGCTGATGGTGTG[A/G]ATCTTACGGAAAAAA | 8853 |
rs772722253 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247721 | TGCCAGACGCGGAGT[A/C]GGTGTTCAGTGAATG | 8853 |
rs772723813 | snp | A/G | | | missense | ASAP2 | GRCh38.p7 | 2:9344793 | TTCTGACCATATCCC[A/G]TGGTACCGTAAGTAT | 8853 |
rs772737717 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256865 | AGTCAGTATGACTGT[C/T]TCTTAGCCGCTTGTC | 8853 |
rs772740584 | in-del | -/GTTG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258332 | TGATAGTAATCAGTA[-/GTTG]TTTTTTTTTTTTTTT | 8853 |
rs772752281 | in-del | -/C | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278659 | TGGACATTGTGAGTG[-/C]CATAGACAACTGCCG | 8853 |
rs772757742 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395851 | TGACCTCGTGATCTG[A/C]CCTCCTCGGCCTCCC | 8853 |
rs772764371 | snp | A/T | | | missense | ASAP2 | GRCh38.p7 | 2:9400782 | GGGTCCTCTGTCCAA[A/T]GCTATGGTCCTGCAG | 8853 |
rs772768060 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244057 | ATAATCCCAGCACTT[G/T]GGGAGGCCGAGGTGG | 8853 |
rs772769193 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327415 | AATGTCTCAGGACGA[C/G]AGACATGATGCCAAG | 8853 |
rs772794874 | snp | C/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213206 | CATTTGAGCAGGCTG[C/G]AATGCAGAGAGGAAG | 8853 |
rs772808176 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9372888 | GGATGTGGGGGAAAC[C/T]GGAGTGCCCAGAGAA | 8853 |
rs772831269 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281800 | AATTCATCTGTCGAT[A/G]AAACTGTCACTGCCT | 8853 |
rs772832823 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286190 | TCGCTTGAGCTCAGG[A/G]GTTGAAGACCAGCCT | 8853 |
rs772832949 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275036 | AGCCTTTTACATTGA[A/C]GTTTACCACCGCTTC | 8853 |
rs772886023 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9285102 | GCATGAGAGTGGGGC[C/T]CTCATGATGGGGTTA | 8853 |
rs772902840 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9356444 | CTTTCATTTCAAACA[C/T]GAAATTAAGTGCAGC | 8853 |
rs772906561 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232127 | TCTCAGCTGAAGACA[C/T]GTTGGTGGCTTCCCT | 8853 |
rs772917147 | in-del | -/T | 1.64798e-05 | 0.00287047 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356169 | ACAGCGTTGCTCTTG[-/T]TTTTTCTAGATGGAT | 8853 |
rs772932553 | snp | C/T | 1.83596e-05 | 0.00302976 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401438 | TCCTGGGGGCTGAGC[C/T]ACGTCCCTGCCCACC | 8853 |
rs772936328 | in-del | -/GGCAT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358431 | ACCAAGTTGGTGATG[-/GGCAT]GGTGTGTTTTCACCA | 8853 |
rs772944769 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315403 | TTGGAAGACGGGTCT[A/G]CGTATGTAGGGTTAA | 8853 |
rs772951408 | snp | G/T | 4.96216e-05 | 0.0049808 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379095 | GGGGTGGGCTCAGCT[G/T]CACCCTGGCCTCTGC | 8853 |
rs772980240 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9403093 | GTGGTGAGGAAAAAC[A/G]GACAAAAATCATTTG | 8853 |
rs772980550 | snp | C/T | 8.25307e-05 | 0.00642328 | missense | ASAP2 | GRCh38.p7 | 2:9350862 | CAGGTGAAGACCAAC[C/T]CTGAGGAGAAGAAGT | 8853 |
rs772995998 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387629 | GGGGAACTTCAGGGA[A/G]AATGCTGACTTAGGT | 8853 |
rs773003262 | in-del | -/AGA | 1.75412e-05 | 0.00296147 | splice-acceptor-variant, intron-variant | ASAP2 | GRCh38.p7 | 2:9318522 | TTGTTTTTGTTTTTT[-/AGA]TTCAGAATATGAACA | 8853 |
rs773011595 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317270 | TGCATCACACACACT[C/T]ATATCCACACCCTCA | 8853 |
rs773020419 | snp | C/G/T | 3.52941e-05 | 0.00420072 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391227 | TTTTCCTTTCTTGCC[C/G/T]GTGGGCTTTGTAGAT | 8853 |
rs773026756 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264422 | CATTTCCAGTGTGTC[C/T]GGGCCTCTGCTGTTC | 8853 |
rs773053678 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9303518 | GGGCTTTGAGTGAGG[A/T]GGGGAGAGAGAGTAC | 8853 |
rs773064233 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383321 | GTTGGAGTGCAATGG[C/T]GTGCTTGTGGACAGC | 8853 |
rs773068006 | snp | C/G | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404376 | ATATATAGGTCCCAG[C/G]TAATACTCCCAAACA | 8853 |
rs773070460 | snp | C/T | 1.65963e-05 | 0.0028806 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320349 | AAATGTGAGTGTTCT[C/T]GTTTTTAAATTTACG | 8853 |
rs773086867 | snp | A/G | 1.65842e-05 | 0.00287955 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323087 | GAGTTCTGTGCCAAC[A/G]GGCATCTTGATGTAT | 8853 |
rs773099229 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373965 | GCAGGTGTGTTGACG[C/T]ACATACGTCTCATGG | 8853 |
rs773110660 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | ASAP2 | GRCh38.p7 | 2:9380762 | AGTCAGGAGAGACTC[C/T]GCTGGACATTGCCAA | 8853 |
rs773134227 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380229 | TTGAGGCAGAGTCTC[A/G]CTCTGTCACCAAGGC | 8853 |
rs773151687 | in-del | -/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9310187 | TTTCCTATTTAACTC[-/TT]ATGACTGAGCAGCAT | 8853 |
rs773152454 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384026 | CATGGGGTGGGGAGA[C/T]GGGGGAGGGATAGCA | 8853 |
rs773163624 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281785 | TCTTAACCCTTTCCC[A/C]ATTCATCTGTCGATG | 8853 |
rs773173181 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365040 | AAGTCTATCAGAAAA[A/C]ATTGAGCACCAAAGC | 8853 |
rs773182592 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9238889 | CATAGATGATTTTGT[C/T]TTCTGTGAACGCTGT | 8853 |
rs773189537 | snp | A/C | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390916 | CGGAGACAGGAGTAA[A/C]AGCATTGAGGGTTCT | 8853 |
rs773192263 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350584 | TGGGTTTGTGTAGAC[C/T]ACCAAGGTGCCCTTG | 8853 |
rs773197232 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9262321 | TCCTGGGGTAACAGC[A/G]TCTTCTTAACGGCCA | 8853 |
rs773219130 | snp | A/G | 1.64876e-05 | 0.00287116 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344690 | GTTATCTTGTGTCCA[A/G]AATGTCTAAACTCTT | 8853 |
rs773219228 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9226144 | GGTCAGTTGTTTGAA[A/G]TCCCACAGCTGGCTG | 8853 |
rs773220652 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333836 | AAAAACTTGTCCAGC[C/T]TCTGTTGTATTTCCT | 8853 |
rs773221107 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9297453 | AAAACCTGGTAAGCA[A/G]CTCTGTGTATGAAAT | 8853 |
rs773224282 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248899 | GCTGGCTCTGTGTCT[A/G]CCTGTCATGGAAGCT | 8853 |
rs773247338 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9363976 | CACACCAGCTTAATA[C/T]CTTTAGATTCTAAAG | 8853 |
rs773248421 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322267 | CTCTTCTTAAACACT[C/G]TAGTCCTCCTTGCCC | 8853 |
rs773262059 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9287605 | GCCTTGACTCAGATA[C/T]GAGGGAGAGGATAAC | 8853 |
rs773273916 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9363030 | TTTTAGATTTTGCAT[A/G]TAAATGAGATCTTGC | 8853 |
rs773289880 | snp | C/T | 1.65759e-05 | 0.00287883 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400011 | AAATCTACTTTTTCC[C/T]TGTCTTTGTAGGGCT | 8853 |
rs773312916 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9299081 | TAATTCTCAAGGCCC[A/G]GCATCCAACTGGCAG | 8853 |
rs773313524 | snp | A/G | 1.70342e-05 | 0.00291836 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318606 | TGAAAGGGGTATGAC[A/G]TTGACACTGTGACAC | 8853 |
rs773315643 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239893 | CACCATGCCCCAGTA[A/G]TTTTTTTGTAGAGAT | 8853 |
rs773358663 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9296981 | GTCTGGTGAGTTGTG[C/T]CATCATTTGGTGAAG | 8853 |
rs773361629 | snp | A/G | | | intron-variant, synonymous-codon | ASAP2 | GRCh38.p7 | 2:9390056 | TTGTTCCACTGGGTC[A/G]TGGAGGGGTAAACTC | 8853 |
rs773374222 | snp | C/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212850 | AGGACAATTTTTACA[C/G]CATCTCCACGTACAC | 8853 |
rs773377377 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333052 | TGCATTAAAGGCCAC[A/G]CTGCAGTGTTTTCAC | 8853 |
rs773377658 | snp | A/C/G | 6.67061e-05 | 0.0057749 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9388518 | CACCACCAGCGCCCC[A/C/G]CCGCTTCCTCCACGG | 8853 |
rs773410799 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350187 | AAGTATGTTGTGATC[A/G]CTTGGTGTCGTGTGT | 8853 |
rs773415823 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9342636 | TACAGTACAAGTGAC[A/G]AATGAAACAGTAGGT | 8853 |
rs773415860 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328896 | AATTGTTTTAAAGTA[C/T]AGGAATCTAAGAAAG | 8853 |
rs773429399 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9400862 | CTTTCCTGCCTCTCT[C/G]CTCTAGCCAGGGGGG | 8853 |
rs773437286 | in-del | -/TTG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258333 | GATAGTAATCAGTAG[-/TTG]TTTTTTTTTTTTTTT | 8853 |
rs773462274 | snp | C/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213546 | GCATGAAAGGAAAGA[C/G]GGAGACCAGTTGTGG | 8853 |
rs773474342 | snp | A/C | 1.6476e-05 | 0.00287014 | missense | ASAP2 | GRCh38.p7 | 2:9334759 | TCAGGATGGACTCAA[A/C]GCCGTGGAAAGCCTC | 8853 |
rs773479976 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311432 | TAAGATTAATAATTT[G/T]TATTCAGGTTGCACT | 8853 |
rs773503942 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9330130 | CTTTGGAATTCTTAA[C/T]ACAGCTTTGATGATG | 8853 |
rs773518040 | snp | A/G | 3.80626e-05 | 0.00436232 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9393552 | AGCCTTGAGCCAGCC[A/G]AGCAAGCCTGCCCCG | 8853 |
rs773528387 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381051 | GTTTGCTGGTTGGCC[A/G]TGTTGGTAACATCAC | 8853 |
rs773554714 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277696 | TGGTGACCCTCAGTG[A/G]ACCGACAGGGACACA | 8853 |
rs773560263 | snp | A/G | 3.2975e-05 | 0.00406035 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9385307 | ATATGAATGGCGACT[A/G]CTCCACGAAGACCTG | 8853 |
rs773592560 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336406 | CAGTGATCTGAGTTC[A/G]CAGAGCACATCCTGT | 8853 |
rs773613880 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234810 | CCCACTTCCGGCCTT[A/G]CGAATGCTTCAGTGG | 8853 |
rs773622771 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370074 | TGAACTCCTGACCTC[A/G]TGATCTGCCCACCTT | 8853 |
rs773626979 | snp | C/G | 1.77966e-05 | 0.00298295 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9378974 | ACAGACAGGGAAAGG[C/G]AGCACAGCCCTGCAC | 8853 |
rs773629323 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9347325 | AGTTCACCCATACCA[A/G]GAAAGAGAATTGAGA | 8853 |
rs773633370 | snp | A/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236090 | GCCTGATGTTGAGAA[A/T]CGCTGGGTCAAAAGG | 8853 |
rs773642798 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266382 | AAATGCTTAGGCTCA[A/G]GTGGTCTGCCCACCT | 8853 |
rs773659826 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359186 | ACATAGACCAGCTCA[C/T]CCCATCCATTAGACA | 8853 |
rs773660820 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9399200 | TCGACAGACGGGAGC[A/G]TACAGTGGAAAGAAT | 8853 |
rs773668808 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9288648 | CATTAAAGGATGTGA[A/G]TATAATTGGGAGTAA | 8853 |
rs773714952 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371020 | TTTCTTCCAAGCACC[A/G]GGGGTACCTAACGAA | 8853 |
rs773741642 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260831 | CCCAGGAAGAGCCCC[A/G]GATTGTGTAACCTGG | 8853 |
rs773773475 | snp | A/G | 7.54916e-05 | 0.0061433 | intron-variant, synonymous-codon, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207251 | GCGGCCTGCGCGGCG[A/G]CTCCGGCCGCAGGTA | 8853 |
rs773773478 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9386880 | AGGTCTAAGTTACCT[A/G]AGTCATCATTCCATG | 8853 |
rs773783386 | snp | A/G | 3.306e-05 | 0.00406558 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388280 | CACGCCTCTGCCCCA[A/G]TGTTCTCCTGCAGCC | 8853 |
rs773786115 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9208887 | TCTTTAGAAAGCTTG[A/G]TTATGTTTAAAGTTC | 8853 |
rs773804171 | in-del | -/AGCA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9235496 | TGTAAATCATCCTGC[-/AGCA]AGCAGTTCTGTCTTG | 8853 |
rs773828587 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213028 | GGCATTTTTTAAAGC[C/T]TCCTCCCAAATAGGG | 8853 |
rs773840199 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9325705 | TCCAGGTGAATTGAT[C/T]CTGTGAACTGACTAA | 8853 |
rs773844744 | snp | C/T | 1.80556e-05 | 0.00300457 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350943 | GACGTTGTCTTATGC[C/T]CTCCTCTGGGGCGTC | 8853 |
rs773846486 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9222744 | GTGGGTGTGTTCGCT[A/C]GCAGGAATCACCCAC | 8853 |
rs773857981 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336520 | TGGACCTCGAGCAGC[C/T]TGAGGATGCCACCCT | 8853 |
rs773861353 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9376593 | TTGAACAAGATTCTT[C/G]CTTGCAGGCAGGGAT | 8853 |
rs773868662 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9355339 | AAGAGTATTGACCTG[C/T]TTTTTGGTCAGACTC | 8853 |
rs773871204 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366309 | GATTCCTGGGGAATT[A/C]TCCTCCTCCCATCTC | 8853 |
rs773871868 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267861 | CGAGAATGCACCACT[C/G]TACTCCAGCCTGAGC | 8853 |
rs773891052 | snp | G/T | 1.64844e-05 | 0.00287087 | missense | ASAP2 | GRCh38.p7 | 2:9380773 | ACTCCGCTGGACATT[G/T]CCAAGCGCCTCAAGC | 8853 |
rs773893016 | in-del | -/C | 0.000669607 | 0.0182854 | frameshift-variant | ASAP2 | GRCh38.p7 | 2:9388513 | CCAGCACCACCAGCG[-/C]CCCCCCCGCTTCCTC | 8853 |
rs773921603 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9367536 | GAGGCTGAGGTGGCC[A/G]GATTGCATGAGCCCA | 8853 |
rs773936428 | snp | G/T | 1.65704e-05 | 0.00287836 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323096 | GCCAACAGGCATCTT[G/T]ATGTATCCTTGCTTT | 8853 |
rs773959831 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313759 | TCAGGGGTTAGTAAC[G/T]GGGACAGTTACCCTT | 8853 |
rs773975393 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9308568 | ACAGGAGGGCTTTTC[A/G]ATGGAGACAGCATCT | 8853 |
rs773997110 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267831 | TGAACCCAGGAGGCA[A/G]AGGTTGTAGTGAGTC | 8853 |
rs774012197 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9324911 | GTTTAATCCATTAAC[A/G]TTGAATGTTACTATT | 8853 |
rs774013920 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9262531 | TTTTTGAGGTCACGC[A/G]GCTAGTAATTGGAGC | 8853 |
rs774019417 | in-del | -/C | 1.86085e-05 | 0.00305023 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356383 | CCCTGGGCTCTAGGA[-/C]ATTTCAATCCCATTC | 8853 |
rs774027530 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265015 | GTGGCATGTGCCTGT[A/G]CTCCCAGCTACTCAG | 8853 |
rs774049164 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210136 | ATAGAGCTCTGAAGT[A/G]GACTTTGAACTTGGC | 8853 |
rs774051579 | snp | C/T | 1.65293e-05 | 0.00287479 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401445 | GGCTGAGCCACGTCC[C/T]TGCCCACCTGGCTGG | 8853 |
rs774073850 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295177 | TTGTTTGACAAGGTA[A/G]ACTTTTTAACGATGA | 8853 |
rs774083909 | in-del | -/ACTC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343410 | CACTGGTGGCCTCCT[-/ACTC]ACTCTCAACTCAGAG | 8853 |
rs774096072 | snp | A/G | 3.295e-05 | 0.00405881 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9368460 | TGCAGGCTTTAATGA[A/G]ATCATGGAATGTTGC | 8853 |
rs774103313 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9242672 | TGCTTCCTCAGGATG[A/G]ATTCAAGGAGAGAAT | 8853 |
rs774125598 | in-del | -/TGG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305353 | GTGGGGTATAGATAT[-/TGG]TGGAGGGGCTGGAGC | 8853 |
rs774146629 | in-del | -/TAAT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264204 | TCAAAAAAATAATAA[-/TAAT]AATAATAATAATAAT | 8853 |
rs774156557 | snp | A/G | 6.70736e-05 | 0.00579071 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380850 | TGGGGCACCTGTCAC[A/G]GGACAGGGAGCCAAG | 8853 |
rs774157999 | snp | A/G | 6.2079e-05 | 0.00557097 | splice-acceptor-variant | ASAP2 | GRCh38.p7 | 2:9393480 | CTCCCTGTCCTCCGC[A/G]GATCCCCTGACCCCC | 8853 |
rs774160777 | snp | A/C | 1.66023e-05 | 0.00288113 | missense | ASAP2 | GRCh38.p7 | 2:9400805 | TCCTGCAGCCCCCTG[A/C]ACCCATGCCTAGGAA | 8853 |
rs774162393 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383182 | AAAAGTCTGAAAAAA[A/T]ATCTCAAAAGATCAG | 8853 |
rs774189981 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315249 | CCAGACAAGCCTGCC[A/G]TAGCCCTGAAGCGGG | 8853 |
rs774193324 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275584 | GTTCCCTCTTCTTTG[C/T]GTAGCCTCTCCCTGA | 8853 |
rs774222510 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249892 | TTGGGCTGGTCCTGC[C/T]CAGGATCTGTGAGAA | 8853 |
rs774224487 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343532 | ACTCACTGCAACCTC[C/G]ATCTCCCAGGCTCAA | 8853 |
rs774231829 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230712 | CAGATATGTGCAAGG[C/G]AAGGACGTTGTTTCA | 8853 |
rs774243215 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9340274 | GATCTGCCCGCCTCC[A/G]CCTCCCAAAGTGCTG | 8853 |
rs774257242 | snp | A/G | 0.000121104 | 0.00778058 | missense | ASAP2 | GRCh38.p7 | 2:9379005 | TACTGCTGCCTGACC[A/G]ACAATGCCGAGTGCC | 8853 |
rs774277368 | snp | A/G | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390373 | CCCATTTCTAGGCCT[A/G]GCCTTTGCCCTACAG | 8853 |
rs774285745 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281705 | GGGATAAAGATGGTT[C/T]TCTTACCACAGATCC | 8853 |
rs774297083 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291363 | AATGGTTCTCTCTCA[C/T]GAGATGTCCACTAAG | 8853 |
rs774313622 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395832 | CAGGATGGTCTCAAT[C/T]TCCTGACCTCGTGAT | 8853 |
rs774315393 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9372472 | TTTAAGCAAAATGAT[A/G]TATAAGAAACCAGTT | 8853 |
rs774327577 | snp | A/G | 0.000148946 | 0.00862849 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368557 | TCATTTGCTGAGTAA[A/G]GGTTTGCCTTTGCCC | 8853 |
rs774331901 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9288356 | GGTAGCTACTATCTG[-/A]GGCTTTAGAGACCAT | 8853 |
rs774338564 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9292549 | CAAAAGAAAAACAGA[C/G]AAAGTATTAACAGTG | 8853 |
rs774339512 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9344621 | GAACGGCAGCCTCTA[C/T]AAGAAGAGTGACGGG | 8853 |
rs774363959 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349742 | CCAAATCCTTCACGC[C/T]GCAAGGATGGGTTCA | 8853 |
rs774389703 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230992 | TTGCTTCCTGGCAGC[A/G]CAAACCCCTGCCTGT | 8853 |
rs774400396 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9238611 | TACAGTGTTTTGTTT[G/T]CATGGGGAGGAGAGG | 8853 |
rs774417137 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205025 | TTTGAGGCTACTAAA[A/G]CTTCCTGTATCTGCA | 8853 |
rs774418980 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250748 | TCTCAGCCCCTGAGA[C/T]GTTGCAGTCTTCCTG | 8853 |
rs774418987 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362618 | CTGAGGTGAGAAGAT[C/T]GTTTGAGTCTGGGAG | 8853 |
rs774423539 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208411 | ATTTTTTTTTTCTGG[-/T]TTTTTTTTTTTTTTT | 8853 |
rs774430783 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9293204 | GATCGATTTCTCTGC[C/T]AGAGTCTCTCAGTTC | 8853 |
rs774456784 | snp | A/G/T | 8.24007e-05 | 0.00641828 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344640 | AAGAGTGACGGGTAC[A/G/T]TGAGGGGGTGTGGCT | 8853 |
rs774456809 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331701 | TGAACCCAAGAGGCG[A/G]AGGTTGCAGTGAGCT | 8853 |
rs774470544 | snp | C/T | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404056 | AAAAACTAAGGATGA[C/T]GGATTGCAAAACAGT | 8853 |
rs774474700 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9209005 | AAATTGGCATACCTT[A/T]CTCTGATTAATTTTA | 8853 |
rs774501672 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9216937 | TATGGGGCACTTATT[A/C]TGTGCCAGATATGCT | 8853 |
rs774508186 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9297940 | TGAGAGCAATGCCTC[A/G]GTTTTCAGCCGTGGG | 8853 |
rs774539594 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294994 | CAATGAAACTAAACT[A/G]CCCATGTCTTGACCG | 8853 |
rs774563271 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9269620 | CCAGAGGTGGTGGCA[C/T]CGCCCTCAGGCGGTA | 8853 |
rs774583249 | snp | A/C/T | 4.94233e-05 | 0.00497087 | synonymous-codon, missense, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9279332 | GCTTTGGACGTGGAC[A/C/T]GGATGGTTCTTTACA | 8853 |
rs774589943 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229881 | GGGCCAGGCTGTTGG[A/G]GGCATTTGTGGGCCT | 8853 |
rs774594103 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350461 | ATCAACTGTGTTGTC[A/G]GTAGGAATCAGAACT | 8853 |
rs774598324 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239799 | GGAGTGGTCACGGCT[C/T]ACTGCAGCCTTGGCC | 8853 |
rs774609318 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311003 | GATCACAGACCTTTG[A/G]CTACTTACTTACCTT | 8853 |
rs774627122 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279748 | TTTTGCTGTTAATTG[C/T]GTCACAGTGCCCTTT | 8853 |
rs774631665 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9340267 | ACCTCGTGATCTGCC[C/T]GCCTCCGCCTCCCAA | 8853 |
rs774635664 | snp | A/G | 6.89869e-05 | 0.00587271 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9393642 | GCAGAAGAAGCCTGC[A/G]CCGGGGTAAGCCACC | 8853 |
rs774649181 | in-del | -/TTTC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9320626 | TTCTCTTAGGAGGTA[-/TTTC]TTTCTGTTTTTGTTT | 8853 |
rs774664065 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322136 | ATGCATAGACTCATT[A/G]AACAACAACATCCCT | 8853 |
rs774697193 | snp | A/G | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390832 | ATTTCATGGATTGAG[A/G]AAACCTGCTGAGAAT | 8853 |
rs774715347 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212770 | GGCTACCATATTGGC[C/T]CAGCAACCACCGGGA | 8853 |
rs774716147 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332676 | AGCTGTACACCTGCT[-/C]CCTCTCCCTGGGTGG | 8853 |
rs774719140 | snp | G/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213083 | GTTACGTAACAACCT[G/T]AGGCAGTTGATACGT | 8853 |
rs774723673 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9327760 | AAATCATCTCAGTCC[C/T]CAGAAGCTCCTTTTA | 8853 |
rs774764181 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9298981 | ATAACATTAAAAATC[C/T]AACAGGAAGGGCTGG | 8853 |
rs774768252 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9398894 | CACTGCTGTCTCAGA[C/G]GATCAGGCCTTCCCT | 8853 |
rs774769078 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9246576 | AGGCATGAGCCACCA[C/T]GCCCAGCCCCACCTG | 8853 |
rs774772456 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245047 | ATGCAGGCCTAGGTT[G/T]GGTTGTGAACTTTTA | 8853 |
rs774781953 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384538 | GAACTTCTGACCAAC[C/T]GGCTTCAAGTTGGGG | 8853 |
rs774783791 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9358823 | CGGAATCCACCGAGA[A/G]CTGGGGGTTCATTAT | 8853 |
rs774800117 | snp | G/T | 1.65302e-05 | 0.00287486 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335083 | CTGTTGTGTGTGTGT[G/T]TTTTTAAAGATCAAA | 8853 |
rs774812740 | snp | C/T | 1.6486e-05 | 0.00287102 | missense | ASAP2 | GRCh38.p7 | 2:9388330 | GACCGGCCCATCAGC[C/T]TCTACCAGCTGGGCT | 8853 |
rs774814688 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369911 | CAATGATGTGATCTC[A/G]GCTCACTGCAGCATC | 8853 |
rs774891887 | snp | C/T | 0.000117636 | 0.00766839 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327813 | ATGACATTTCCTTTT[C/T]ATTGTTCAACAGTAT | 8853 |
rs774893504 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234608 | GGGGAAGTGGGCACT[A/G]TCCCCATTGTGTGGA | 8853 |
rs774914250 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264829 | ATCCAATAAAAACTA[A/G]TACAGCAATTTAAAA | 8853 |
rs774918953 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9218743 | AGCTCTTGACCTTCC[A/G]TGTCTGCTGCTGTCT | 8853 |
rs774921198 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9220498 | TTGTTTTATATGCCC[A/G]TGGCTGTGTGTATCT | 8853 |
rs774923338 | snp | C/T | 1.67486e-05 | 0.00289379 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9356290 | GACAAAGGAGATCAT[C/T]TCAGAAGTGCAGAGG | 8853 |
rs774945398 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248551 | AGTCAGCGTTTTGGG[C/T]CTCGGTTTCTTCCTC | 8853 |
rs774978292 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318032 | TTCGCACCCAGCATT[C/T]GCTCGTGTGCCTTTG | 8853 |
rs775002138 | in-del | -/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317703 | AAACCCTCACACGCC[-/CA]CACACACCCATACAC | 8853 |
rs775005602 | snp | A/G | 3.31884e-05 | 0.00407346 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323258 | TGTGCGAGGTAAGGC[A/G]GTGGTGAAGGCAGGT | 8853 |
rs775012984 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362482 | ATTGGGTGTGACTAA[A/G]TCAAGCTAGTTAACA | 8853 |
rs775059524 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9376479 | GTCTGTAAGTGTAGA[A/G]CGCAAAACTTTAAGC | 8853 |
rs775064810 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266268 | CCTCCTGCTTCAGCC[G/T]CACCAGTAACTGGGA | 8853 |
rs775065516 | snp | C/T | 5.42589e-05 | 0.00520831 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374704 | CAAAGGGAGGCCGGA[C/T]GGCGGGTAGAAGCCC | 8853 |
rs775088308 | snp | A/G | 2.98485e-05 | 0.00386308 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9393489 | CTCCGCAGATCCCCT[A/G]ACCCCCACGCCGCCC | 8853 |
rs775094325 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9320955 | GCAGTTGTAACTTCC[C/T]CAATCACAGTTTCTC | 8853 |
rs775095168 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337016 | GAGGTTTGGGAAAAC[A/G]GGCTGTTGTGAGAGA | 8853 |
rs775130699 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227726 | CAGTAACCGTTTTAT[C/T]GAGTTAAAAAAATAT | 8853 |
rs775149381 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9401087 | TTCTCTCTGCTTGGT[-/G]GGGGAGCTCTTCCCT | 8853 |
rs775160129 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236298 | TGCCACGAAGTAAAG[A/G]TCATTTCGGGCCACT | 8853 |
rs775177670 | snp | A/G | 1.7521e-05 | 0.00295976 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393670 | ACCCCCAGCCAGCTC[A/G]GCCATCCGTGCTCCT | 8853 |
rs775208327 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9312873 | AGCCTGGCCAACATG[A/T]TGAAACCCCGTCTCT | 8853 |
rs775222132 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294408 | TTGGTGCTGGAACAT[A/G]AAGTCTACTATCAGT | 8853 |
rs775271757 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378476 | TTCCTGGAGGGAATA[C/T]CAAATAATGATAGAG | 8853 |
rs775273719 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365181 | TTTTTCCCTGCACAC[C/T]AGAGTGTCCTTTTGT | 8853 |
rs775275990 | snp | C/T | | | upstream-variant-2KB, intron-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9206055 | ACCCTAAAACTATAA[C/T]CGAGAATACCTATCA | 8853 |
rs775306936 | snp | A/G | 1.64776e-05 | 0.00287028 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9391032 | TGTATGTGTGCGTGC[A/G]TGCGTCTGTGTGCAT | 8853 |
rs775310172 | snp | C/T | 6.6507e-05 | 0.0057662 | missense | ASAP2 | GRCh38.p7 | 2:9400823 | CCATGCCTAGGAAGT[C/T]GCAGGCAGTAAGTGA | 8853 |
rs775329548 | snp | A/G | 6.67947e-05 | 0.00577866 | missense | ASAP2 | GRCh38.p7 | 2:9350808 | TTTGCTTTTAAACAG[A/G]CTAACCGGCCTCCTG | 8853 |
rs775343235 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284797 | TACACTGCTTTCTTA[A/G]TGTAGGAGGGGTGAA | 8853 |
rs775364480 | snp | A/G | 1.64876e-05 | 0.00287116 | missense | ASAP2 | GRCh38.p7 | 2:9358863 | CAGTCCCTGACCTTA[A/G]ATGTACTGGGAACAT | 8853 |
rs775375165 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353797 | CTTGCTCCTAAACAG[A/G]GGCTTCCCATTCTCA | 8853 |
rs775376099 | snp | C/T | 3.29696e-05 | 0.00406001 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344717 | TCTTATTGTTTCTCC[C/T]ACTTATCCACAAGGA | 8853 |
rs775394906 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361568 | CCTTTCTTTTCTTTT[C/T]CTTTTCCTTTTCTTT | 8853 |
rs775400024 | snp | A/G | 0.000117276 | 0.00765663 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401227 | CTCTCTGCCCTGAGA[A/G]CTGAGGCCTGCAGCC | 8853 |
rs775407113 | in-del | -/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317569 | ACAATCACACTCTCA[-/CA]CACCCACACACCCGT | 8853 |
rs775426258 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9241572 | CATGGCGAAACCCCA[C/T]CTTTTACCCAGGCAT | 8853 |
rs775428325 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254749 | GATTTGGTACTGTCT[A/G]GTTTCAGGCATCCAC | 8853 |
rs775445277 | snp | G/T | 1.71455e-05 | 0.00292787 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318614 | GTATGACATTGACAC[G/T]GTGACACCAGGGGCA | 8853 |
rs775449989 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383094 | CTTGTCCACTGCATA[C/T]CATCTCGGGGGGGCC | 8853 |
rs775468556 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291208 | GTTCTGTACACACAT[C/G]TCTGATCACCTTGAT | 8853 |
rs775475637 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9382118 | CCTCCTGAGTAACTC[A/G]GATTACAGGCACCTG | 8853 |
rs775513739 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257148 | CGTGGAGTGTTTACA[C/T]GTGTCGGGCATTCCA | 8853 |
rs775533674 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229070 | TAGGGGCGGAAAGTG[G/T]ACAATCAGGATAGAG | 8853 |
rs775562948 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300475 | TTGCTCACCACCCTG[-/T]TGGCTTTGCCAGTTT | 8853 |
rs775563836 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9372171 | GTGATGATTGAAAGT[A/G]CATGAAACTGGACAA | 8853 |
rs775571827 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9262303 | TCGTAATGACTGAGA[C/T]GGTCCTGGGGTAACA | 8853 |
rs775593200 | snp | A/C/G | 1.65693e-05 | 0.00287826 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400094 | ATTTAATTTGGGACT[A/C/G]AGTTTGTTTCTGCTT | 8853 |
rs775597067 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383985 | ACTTGGACACAGGGC[-/G]GGGAACATCACAAAC | 8853 |
rs775603729 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281382 | AGTACAGCTTATAAA[C/T]AGCCCTGCATTTGAA | 8853 |
rs775609628 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9320068 | CCTTGCTTTTGTGTA[C/T]ATTTAGTATATTCTA | 8853 |
rs775610480 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227758 | TGGGTAAGGTATTTG[G/T]GAGTACACGTGCATA | 8853 |
rs775618416 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9342863 | CCCTGTGTCTTCTGT[A/G]TACTATCCACTTTGC | 8853 |
rs775620065 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237664 | GGCTCAAGAGATCCT[C/T]CTGCCTCGGCCCCTC | 8853 |
rs775657980 | snp | C/T | 0.000115402 | 0.00759524 | missense | ASAP2 | GRCh38.p7 | 2:9368426 | TTTCATTTTTGCAGC[C/T]CGCCAAGAATATTGG | 8853 |
rs775673218 | snp | C/T | 1.65023e-05 | 0.00287244 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9388452 | GCAGAATGAGACTTA[C/T]GGAGCCCTCCTGAGT | 8853 |
rs775676820 | in-del | -/AATC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317038 | CATGCAATCATTCCC[-/AATC]ACTCACATCCACACT | 8853 |
rs775689422 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9215843 | AAGGTGTTTAGAAGC[G/T]CTCTTGGCGGGGAGC | 8853 |
rs775689597 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378743 | CGTGTTATTTCCCTG[A/G]TGACCTTCTGCTAAG | 8853 |
rs775697854 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279255 | GGCACTCAACGTGGT[A/G]CTCGCTGCTAGCGTG | 8853 |
rs775704859 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9340062 | GAATCTCCCTCTGTC[A/G]TCTAGGCTGGAGTGC | 8853 |
rs775739518 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362483 | TTGGGTGTGACTAAA[G/T]CAAGCTAGTTAACAT | 8853 |
rs775750957 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9290238 | TTTGAGATGGAGTCT[C/T]GCTGTGTCACCCAGG | 8853 |
rs775772659 | snp | A/C | 0.000165826 | 0.00910416 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400003 | GTAGCAGTAAATCTA[A/C]TTTTTCCCTGTCTTT | 8853 |
rs775785729 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402802 | CCAAGAGGGAACATA[A/T]GTGGATAGAGTGAAG | 8853 |
rs775785998 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9280016 | TCGTTAAGTGACTAT[A/G]TAGTTTCATTCAGCA | 8853 |
rs775790061 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9388817 | GCCTGAGGTGGCCAA[C/T]TGGGCTCCCGGGGCT | 8853 |
rs775799113 | snp | C/G | 1.64781e-05 | 0.00287033 | missense | ASAP2 | GRCh38.p7 | 2:9388354 | CTGGGCTCCAACCAG[C/G]TTCAGTCTAACGCTG | 8853 |
rs775807620 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253524 | GTCTAAGCACCCTAC[A/G]GATGTAACGTAGCAG | 8853 |
rs775815776 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332326 | TGAAGCTTCTCCTGA[C/T]GCCAGGGCTGACTGC | 8853 |
rs775832520 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359036 | AACTCATTGATAATT[A/C]TTCATTTTTAGCTAC | 8853 |
rs775844483 | snp | C/T | 1.71528e-05 | 0.0029285 | intron-variant | ASAP2 | GRCh38.p7 | 2:9403228 | TTGGAATTTTAATAA[C/T]AACCTACACTTTTCT | 8853 |
rs775896935 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9296417 | ATGCATGCATTTGGC[A/G]TCCAGCAGGGATTGA | 8853 |
rs775923014 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9279348 | GGATGGTTCTTTACA[A/G]AATGAAGAAATCCGT | 8853 |
rs775923422 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244219 | AATAATCACTTGAAC[C/G]CGGGAGGTGGAGGTT | 8853 |
rs775923765 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257054 | TACCTGCTCCAGGGT[A/G]TCTTTCCCTAACAGC | 8853 |
rs775931084 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338750 | ACAGAGAAGCAATTG[A/G]GGTGCAGTGTAATGA | 8853 |
rs775935157 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9224632 | AATTAATATCTGATT[G/T]CTTCTTTGAAAAACA | 8853 |
rs775935548 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9298843 | TGGTGCCTCACACTT[C/G]AGTACAGATGAGCAG | 8853 |
rs775949719 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9326762 | GGCTTAGTGGCCGCA[C/T]AGTATTTTCTGTATG | 8853 |
rs775951888 | snp | C/T | 1.64969e-05 | 0.00287196 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376867 | ACACAGAATTGAATG[C/T]TCCCATTAGAATTCT | 8853 |
rs775977305 | in-del | -/C | 3.63049e-05 | 0.00426041 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393450 | AAGCCTGGCGGCTGA[-/C]CCCTCTGCACGTCTC | 8853 |
rs775978016 | snp | G/T | 1.65304e-05 | 0.00287488 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297258 | GTGGGGAGTGAGGGT[G/T]GCATGCCTGAGACTC | 8853 |
rs775981461 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9398639 | ATGGTGAAACCCCGT[C/T]TCTACTGAAAATACA | 8853 |
rs775988603 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9297574 | TACCCAAAAGAATTA[C/T]GTTTTTATACACATT | 8853 |
rs776051782 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9273128 | ATTGAATCTGTAAAT[C/T]GTTCTGGGTAGTATG | 8853 |
rs776065611 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234110 | GCGAAGCTATGTCTC[-/A]AAAAAAAAAAAAAAA | 8853 |
rs776066923 | snp | C/T | 3.35447e-05 | 0.00409527 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403346 | GCTACTGAACAAAAG[C/T]ATTAACAGTTATGTT | 8853 |
rs776070587 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358052 | GTAGCCGAGCTGTGA[A/G]GGGAAAACGTGGCTT | 8853 |
rs776075181 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9356461 | AAATTAAGTGCAGCT[C/T]AGCCTGAGTTCATCC | 8853 |
rs776101006 | snp | C/G | 3.76854e-05 | 0.00434065 | synonymous-codon, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207122 | GCCGGACCAGATCTC[C/G]GTGTCGGAATTCGTG | 8853 |
rs776119501 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244947 | TGCTTATTTGACAGG[A/G]TGACACGATGGTGTG | 8853 |
rs776119590 | snp | A/G | 2.89055e-05 | 0.00380157 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207227 | TGTGGCGGCCATCGA[A/G]GAGGTGAGGCGGCCT | 8853 |
rs776122877 | snp | G/T | 1.65504e-05 | 0.00287662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388249 | TTATCACCAGGAGCA[G/T]TTCATATTTGTCTCA | 8853 |
rs776124402 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9379765 | AATTATAGGCCGGGT[A/G]CAGTGGCTCACGAGG | 8853 |
rs776125624 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9356643 | GGTACAGTGAGAGTG[A/G]ACTCAAGGTCATGTG | 8853 |
rs776141780 | snp | C/G | 1.6546e-05 | 0.00287624 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393440 | GCCTGAGTGGGAAGC[C/G]TGGCGGCTGACCCTC | 8853 |
rs776163224 | snp | A/G | 1.65007e-05 | 0.00287229 | missense | ASAP2 | GRCh38.p7 | 2:9385281 | AGATTTAATTCTCAC[A/G]TTCACGTTGAATATG | 8853 |
rs776165223 | in-del | -/GG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284256 | TTCTTAGGATTTGGA[-/GG]TTGAATCAGTTTCCA | 8853 |
rs776184246 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384121 | TACGTATGTAACAAA[C/T]CTGCACGTTGTGCAC | 8853 |
rs776197800 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276539 | TGTCATCTTTTTTTT[C/G]TCTTTTTTTTCTTTT | 8853 |
rs776199299 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387088 | GTGGGTGGGGGGGCG[C/T]CTGTAGTCCCAGCTA | 8853 |
rs776210268 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369751 | TAGAATTAATGACAC[A/G]AGTCTTCCCAAAGGA | 8853 |
rs776215199 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9385100 | GTGAAGTAGGCAGAG[A/G]GGCGGGGGCTTCACC | 8853 |
rs776251657 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346971 | AACCGGCATTACTGG[C/G]ATGCTGAGAACTCAG | 8853 |
rs776252796 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9287455 | GAGAAACCTCCTTGT[A/T]GGACGGATATCTGAA | 8853 |
rs776253085 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9260815 | TTTTCCCTCTGAAAA[A/G]CCCAGGAAGAGCCCC | 8853 |
rs776311374 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9220173 | TGTGAATATTCTTGT[A/C]TAAATTTTTGTGTAG | 8853 |
rs776314631 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345877 | CAGCCGAAGCATGTC[A/G]CAGCAGCAAGGATTG | 8853 |
rs776323517 | snp | C/T | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404529 | TCTATTTAGTAATTG[C/T]GAGGGTAAGATTCAT | 8853 |
rs776350011 | in-del | -/CTTGAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9218347 | AGAAGTGTTTATTAA[-/CTTGAC]CTTGACCAATTGGCC | 8853 |
rs776358029 | snp | C/G | 1.6476e-05 | 0.00287014 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9391040 | TGCGTGCATGCGTCT[C/G]TGTGCATGCGTGTGG | 8853 |
rs776385532 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219093 | TAAAACTTTGTTGTG[A/C]TTTGCTTCTCTGGTG | 8853 |
rs776430734 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353418 | TAAAAATAGTGCAGT[A/G]TGGTGACATGTGCCT | 8853 |
rs776431609 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9335802 | AGATAATTTTACTAT[A/G]TTTTCACTACAATGT | 8853 |
rs776433039 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318488 | TAGATTCACAAGGAA[A/G]CTGAATAAGAATCTC | 8853 |
rs776440192 | snp | C/T | 4.98004e-05 | 0.00498976 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9401330 | TGTGGCTGACAACCC[C/T]GATGAGCTCACCTTC | 8853 |
rs776449807 | in-del | -/CACA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317567 | CCACAATCACACTCT[-/CACA]CACCCACACACCCGT | 8853 |
rs776477930 | snp | C/G | 1.65941e-05 | 0.00288041 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323079 | GTCCCGTTGAGTTCT[C/G]TGCCAACAGGCATCT | 8853 |
rs776492234 | snp | A/T | 1.64825e-05 | 0.00287071 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9344737 | ATCCACAAGGATCCG[A/T]AAAGTGTGGCAGAAA | 8853 |
rs776506630 | snp | A/G | 1.66043e-05 | 0.00288129 | missense | ASAP2 | GRCh38.p7 | 2:9350815 | TTAAACAGGCTAACC[A/G]GCCTCCTGCAAAGCT | 8853 |
rs776513072 | snp | A/G | 1.68576e-05 | 0.00290319 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344505 | GACCTGGACAAGATT[A/G]AAAACACACTCTTCA | 8853 |
rs776514810 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9228970 | AGAGGTGGAAGATCC[A/G]GTATCTCAGGAGGGA | 8853 |
rs776518516 | snp | C/G | 1.65296e-05 | 0.00287481 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9320293 | TTGTTTACAGGATCT[C/G]AAAAAGCCTTTTGAT | 8853 |
rs776527491 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365097 | TACACTTACTAAGAA[A/G]TACATACTTTGTAAA | 8853 |
rs776527794 | in-del | -/AAG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9388105 | TCCTTCACGAGACAC[-/AAG]GAGGAGTGAATTTTC | 8853 |
rs776544533 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371146 | GCCCTCCTCCAGCCT[C/T]GGCACTGTTGAAAAA | 8853 |
rs776559927 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253266 | CTTCCTGGGTTCAAG[A/C]GATTCTCGTGCGTCA | 8853 |
rs776583391 | snp | A/G | 1.65078e-05 | 0.00287291 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297277 | TGCCTGAGACTCACA[A/G]CACCTCCGTCATTCT | 8853 |
rs776594599 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9265898 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 8853 |
rs776598265 | snp | C/T | 6.92317e-05 | 0.00588312 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9379013 | CCTGACCGACAATGC[C/T]GAGTGCCTCAAGTTG | 8853 |
rs776600346 | in-del | -/ACA | 1.90456e-05 | 0.00308585 | cds-indel, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207157 | AGACCCATGAGGACT[-/ACA]AGGCGCCCACGGCCT | 8853 |
rs776603640 | snp | A/G | 1.65244e-05 | 0.00287436 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379085 | CCGGGCCCCGGGGGT[A/G]GGCTCAGCTGCACCC | 8853 |
rs776627886 | snp | A/G | 3.30518e-05 | 0.00406507 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368544 | GGACTGGCTATTCTC[A/G]TTTGCTGAGTAAAGG | 8853 |
rs776630964 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9320529 | CTTCTAATCTGTTTT[-/C]TTCTGTTCCTTTGTC | 8853 |
rs776634172 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213727 | AGAGGTAGACCCAAT[A/G]GAACTCCTGCCCCAA | 8853 |
rs776637796 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210218 | AATTCTCTAAATTAC[-/T]CCTTTGTCAGATTGA | 8853 |
rs776680910 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351908 | CCAGTACCATTTATT[C/T]TGTTCTTCAGACTCT | 8853 |
rs776709936 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9273955 | GGAAAGGGCCATTGT[A/C]ATCTTTGTTTCAAAG | 8853 |
rs776710487 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337021 | TTGGGAAAACGGGCT[G/T]TTGTGAGAGAACTGG | 8853 |
rs776713721 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9394576 | GTCACTGCTCCCACA[C/G]AGGCCCTCTGAGCTG | 8853 |
rs776727011 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349136 | TTTAGAACAGTGCCT[A/G]CCTTGTATAGGTATA | 8853 |
rs776748840 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253274 | GTTCAAGCGATTCTC[A/G]TGCGTCAGCCTCCTG | 8853 |
rs776763149 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278796 | AGAAATCTGAGGCTC[A/G]GGAAGCAATAGGACC | 8853 |
rs776771516 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9248404 | TGGGTAATTAGTGTA[C/T]GTGTAGCTCTTTATT | 8853 |
rs776778106 | snp | A/C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9367771 | TGTCTCAAAAAAAAG[A/C/T]ATGTGTTAATTTAAT | 8853 |
rs776791290 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9259963 | GCTGTCCAGTGTCTG[C/T]GCATCGCCCCCTCCC | 8853 |
rs776792184 | snp | C/G | 1.65004e-05 | 0.00287227 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377014 | TGTTCTGAAATTAAG[C/G]GAGGCACTCGTTTTC | 8853 |
rs776797223 | snp | C/G | 1.6476e-05 | 0.00287014 | missense | ASAP2 | GRCh38.p7 | 2:9344609 | TGGGACCGAGCGGAA[C/G]GGCAGCCTCTACAAG | 8853 |
rs776799840 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9319053 | CAGAGGATGTTGGCT[C/G]TTTAGGACATGCCTA | 8853 |
rs776812693 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362375 | CTGTTTCAGGGTGAC[A/C]TGCTGTGACAGCAAA | 8853 |
rs776859446 | in-del | -/AAAAAAAAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264193 | AGACCCTGTCTCAAA[-/AAAAAAAAA]AAAATAATAATAATA | 8853 |
rs776859473 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9330541 | AACTGCACTTGTACC[C/T]CATGAATTTATATTA | 8853 |
rs776904287 | snp | C/G | | | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214894 | TTGTTTGTGCCATGG[C/G]TCCCTTTGACACTCT | 8853 |
rs776907146 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9268676 | TTCTTGGCAAAGCCA[C/T]CCTGGGGGCACGGAC | 8853 |
rs776913748 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300160 | ATTGCTTAAGCCCAG[A/G]AAGCGGAGATTGCAG | 8853 |
rs776927886 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9400940 | CCCCTGGCTGGGGCA[A/G]GGCGGGGCTCTTCTT | 8853 |
rs776950097 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9296333 | CTGTGTCCCCTCCCC[A/C]ATTCCTACCCACGGT | 8853 |
rs776960593 | snp | A/C/T | 4.95481e-05 | 0.00497715 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9388461 | GACTTACGGAGCCCT[A/C/T]CTGAGTGGCAGCCCA | 8853 |
rs776969271 | snp | A/T | 1.64893e-05 | 0.0028713 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376880 | TGCTCCCATTAGAAT[A/T]CTGGAATGCCTTTGT | 8853 |
rs776974114 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9268208 | AGCATTCTGTTGTAC[A/G]AATGTCCATCATCAG | 8853 |
rs777003156 | snp | A/G | 2.90677e-05 | 0.00381221 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9393498 | TCCCCTGACCCCCAC[A/G]CCGCCCCCACCCGTT | 8853 |
rs777013117 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9308705 | TGAGCTGAGAGGAAG[A/G]GCTCTGGCTTCACTG | 8853 |
rs777033631 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254353 | ATTTATAAACTAAAC[-/T]TTTTTTTTTTTTTTT | 8853 |
rs777035431 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9319623 | GCTGTGGCACTTGGG[C/T]CTTACCTGAGGCCAT | 8853 |
rs777045567 | in-del | -/CCT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371972 | CATTAGCAAAGCAAA[-/CCT]CCTTCACAAAACCAG | 8853 |
rs777061606 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361407 | TGCTAGGAGTGTGGT[C/T]ATGGTGTCGTGGCTC | 8853 |
rs777063870 | in-del | -/TGGGATAG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9377730 | AAAATGCAAAAGCCA[-/TGGGATAG]TGGGATAGTTTGCAT | 8853 |
rs777081224 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237330 | TGTGACTTTTAGATG[A/G]AAACATAATTGATAC | 8853 |
rs777082360 | in-del | -/G | 1.67002e-05 | 0.00288961 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400839 | CAGGCAGTAAGTGAC[-/G]GAGCCCCCTTTCCTG | 8853 |
rs777088208 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9249673 | AAGTTCACAGCCTGA[A/G]TGAGACTGGGCGCTG | 8853 |
rs777098325 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278999 | TCGGCTGGAGTAATT[C/G]ACTTCGCTGCAGAGG | 8853 |
rs777106610 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307813 | TTGTGTTAAACACTT[A/T]GGATCAGCATGGGCT | 8853 |
rs777107619 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9379534 | TTGTTACTTGGCCCC[A/G]GTCCCTCCCTCTCTC | 8853 |
rs777121910 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9271997 | CAAATCTTGGCCATT[A/G]TGAACAGTGCTGCAG | 8853 |
rs777131886 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9298627 | GGACACTGGCAGGCA[G/T]GCATGGTGGGGTCTC | 8853 |
rs777158171 | snp | C/T | 1.66059e-05 | 0.00288144 | missense | ASAP2 | GRCh38.p7 | 2:9327833 | TTCAACAGTATCTGC[C/T]GAAGGTCAACGAAAT | 8853 |
rs777178807 | snp | A/G | 1.6495e-05 | 0.0028718 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279428 | GGTTTCTGTGTGGAA[A/G]ATGTCGCATTTGAAG | 8853 |
rs777210787 | snp | A/G | 3.41956e-05 | 0.00413481 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9393543 | CGTAATGGAAGCCTT[A/G]AGCCAGCCGAGCAAG | 8853 |
rs777214394 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9290757 | TCTGAGGCCCACTGC[A/G]ACTTGGAACACAGCT | 8853 |
rs777223474 | snp | C/G | 1.65616e-05 | 0.00287759 | missense | ASAP2 | GRCh38.p7 | 2:9400060 | ACCAACAAAGGCCAA[C/G]CGAGAGGACCTGGTA | 8853 |
rs777239539 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257881 | ATTTTGGTTTATCCT[A/T]ACCTATGTGGCCTTG | 8853 |
rs777271584 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338481 | CTGCCTCTGGGTTCG[C/T]GTATCTTACATGCCC | 8853 |
rs777304170 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9314091 | TGGATTCAAGTGATT[C/G]TCCTGCCTCAGCCTC | 8853 |
rs777317417 | in-del | -/TTGATTGGGTAATG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332167 | AATAGACAACAAAAT[-/TTGATTGGGTAATG]TTGATGGTAAAAGTT | 8853 |
rs777343307 | snp | A/G | 3.29745e-05 | 0.00406031 | missense | ASAP2 | GRCh38.p7 | 2:9344541 | TTTTAGGACTCCCAA[A/G]TTCGTCAGAGCACAG | 8853 |
rs777352180 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225639 | GCGTAGGGGAGTGAC[A/G]TGAGCATAGCTGGGC | 8853 |
rs777352381 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350944 | ACGTTGTCTTATGCT[C/G]TCCTCTGGGGCGTCC | 8853 |
rs777359914 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9340152 | CTCAGCCTCCCAATT[A/G]GCTGGGATTACAGGT | 8853 |
rs777377388 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9376922 | GGAGCCGGATGAAAC[A/G]GCCCTCCACCTTGCA | 8853 |
rs777401679 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9357862 | CGATATTTACCTGCC[A/G]TGAGTTTCTCAGGGC | 8853 |
rs777425864 | snp | A/G | 3.29511e-05 | 0.00405887 | missense, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9297347 | GCTCTGGAGAAGTTT[A/G]GCGGCAACTGTGTAT | 8853 |
rs777443162 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239445 | GGGTAGAATGAAATC[A/G]TGTGTGTGGTGATGG | 8853 |
rs777446962 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9224169 | AACCATTGCTGAGCA[C/G]TGCGAGGGAAGGGAG | 8853 |
rs777448531 | snp | A/C | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213030 | CATTTTTTAAAGCCT[A/C]CTCCCAAATAGGGTT | 8853 |
rs777455789 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369565 | GCAAAGTGAAACAGA[C/T]GGAAGGAAGGAGAGA | 8853 |
rs777460734 | snp | A/G | 1.65053e-05 | 0.0028727 | missense | ASAP2 | GRCh38.p7 | 2:9356223 | AAGAAGCTTTAAACA[A/G]TGCATTTAAGGGGGA | 8853 |
rs777482493 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247197 | GCAGTCTGTCTGCTC[A/G]TGAGTTTTGACGGCA | 8853 |
rs777498058 | snp | A/C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9287421 | GCATTTAAAGAAGAA[A/C/T]CTGAAAACCTTAGGG | 8853 |
rs777501354 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311482 | TTTACATAATATATT[C/T]GTTAAAAGTGAGTCA | 8853 |
rs777532791 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380613 | TAGGTCAAACTCACT[A/G]TGGATTTCATTAACC | 8853 |
rs777540234 | snp | A/G/T | 0.000472932 | 0.0153705 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393478 | CTCTCCCTGTCCTCC[A/G/T]CAGATCCCCTGACCC | 8853 |
rs777540262 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9335579 | GTAGCAGGGGACCAG[C/T]TGGGGCTCTGCCAGC | 8853 |
rs777549129 | snp | A/G | 5.6878e-05 | 0.00533252 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374989 | AAAAAAAAAAAGGCC[A/G]GCCACGGTGGCTCAT | 8853 |
rs777563429 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233566 | CCTTCAGGACCTCTC[A/G]TTATAGCTTAGCCTA | 8853 |
rs777572411 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245897 | ATAAATAGTTTGTTA[C/T]TGTTGTTGTGGGGCT | 8853 |
rs777587419 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318624 | GACACTGTGACACCA[A/G]GGGCAGCTTTTACAC | 8853 |
rs777593161 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346822 | GGAAAACAGGTCTGG[C/T]AATCCTTTGCTGACA | 8853 |
rs777595461 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370006 | ACCACACCCAGCTAA[-/T]TTTTTGTATCTTTAG | 8853 |
rs777600497 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9340712 | CACTGACTTTCTAAG[A/C]AGTGGGCAAAATGTC | 8853 |
rs777636057 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9235468 | ATGTTGTTCATTCCA[A/G]CAGAGGCCGGATGTG | 8853 |
rs777645051 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9398516 | CCCTGACTCAAAAAA[C/T]AAACACAAAGGCCAG | 8853 |
rs777645056 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9288183 | CCCCATAAACCTGTC[C/T]GCAAACCCAACCTAC | 8853 |
rs777650190 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307158 | GGAGTGCATCAGCAT[C/T]GCCTGCGTGGCTTGT | 8853 |
rs777657615 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356118 | ACATGGTGGTGGGAC[C/T]TTGGGCTGGACTCAG | 8853 |
rs777664864 | snp | A/C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395032 | GGTGGCTGGGTCCAC[A/C/G]GACAGGTCCCCAGAG | 8853 |
rs777696180 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9285846 | ATCCTAGAAAATTAT[C/T]ACATTCTTGAAAGTA | 8853 |
rs777723502 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9335039 | CACCAACGTTTCACT[G/T]TACCTCAGTCTTAAT | 8853 |
rs777733242 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276457 | AAAGCTTGCTAAAGA[C/T]GTTATTCTGAGAACA | 8853 |
rs777745428 | snp | A/G | 4.94637e-05 | 0.00497287 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9323193 | TGAAATAAGCGGAGC[A/G]GAAATTGCCGAAGAG | 8853 |
rs777748899 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253209 | ACTCTTGTCACCCAG[A/G]CTGGAGTGCAATGGC | 8853 |
rs777759699 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380047 | TAGACTGCTTGAGAG[A/G]AGGTTTAAAAGTTTG | 8853 |
rs777760631 | in-del | -/T | 3.30912e-05 | 0.00406749 | splice-donor-variant | ASAP2 | GRCh38.p7 | 2:9344801 | TATCCCATGGTACCG[-/T]TAAGTATTCTCTTTT | 8853 |
rs777824207 | snp | C/G | 1.6591e-05 | 0.00288015 | missense | ASAP2 | GRCh38.p7 | 2:9401286 | CAGACCAAGTTGAAG[C/G]CTAAGCGGGTGAAAG | 8853 |
rs777825294 | in-del | -/T | 1.64787e-05 | 0.00287038 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380716 | TTTTGCCTTAACGCC[-/T]CCTTTGCTCGCCCTT | 8853 |
rs777832751 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9220040 | CATGGATTTGTACTT[C/T]ATTTCTTTTTATGGC | 8853 |
rs777846644 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9354497 | CAGAAATTGGCCAGG[A/T]GCGGTGGCCCACGCC | 8853 |
rs777847906 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9377558 | GGGGCATATTGCTTC[A/C]GTCATGTGTTACCTG | 8853 |
rs777862794 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350777 | TTCCACCCAACCCCA[A/G]CCTTTTTTGTTGTTT | 8853 |
rs777873764 | in-del | -/TC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9303396 | TGGGTGCCTCTAAGG[-/TC]TCTGTTTCACGATGC | 8853 |
rs777909069 | snp | C/G/T | 3.50344e-05 | 0.00418524 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327780 | AGCTCCTTTTAAACT[C/G/T]GTATTCTGCTTACTT | 8853 |
rs777916995 | snp | A/G | 0.000115311 | 0.00759224 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391079 | CAGACAGCCTCCTCT[A/G]CTAACACCCTGTGGA | 8853 |
rs777917254 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9386006 | AGTCAGACTTAGGCC[C/T]TGTGACCCAAAGCCC | 8853 |
rs777931555 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9304992 | AGATATTGGTGGACA[A/G]GCTGGAGTAGTGGGG | 8853 |
rs777958303 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208207 | TCTGCTCGGCTCAGA[A/G]TAGGTTTACAAGTCA | 8853 |
rs777993492 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9273686 | GCAGTCAAAACTGTC[A/G]TTTTGTGTTGAGTCA | 8853 |
rs777997274 | snp | A/G | 1.64928e-05 | 0.00287161 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279268 | GTGCTCGCTGCTAGC[A/G]TGGTCTCAGCACAGA | 8853 |
rs778004497 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381683 | TCAAAGCTACAGTGA[A/G]CCATAATGGTGTCAC | 8853 |
rs778018921 | snp | A/C | 1.66779e-05 | 0.00288768 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320252 | GCACAGAAGTGAATG[A/C]TTAGTCTTGCCTAAT | 8853 |
rs778020275 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9392995 | TCACCCACCCACTCC[A/G]GAGACTGAGGAGCCG | 8853 |
rs778025777 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274613 | CAGGCATGAGCCACC[A/G]CGTCCAGCCTAACAC | 8853 |
rs778035672 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300870 | GCACTTTATGGAAGT[C/T]GGATTGTTGATCCTA | 8853 |
rs778043565 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230089 | ACTGCATTAAAGGTC[C/T]CAGACACTGGGGCAT | 8853 |
rs778044123 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9334040 | TCTCTGTCTTTCTCC[-/T]TTTTTTTTTTTTTTT | 8853 |
rs778085356 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351521 | TTCCTAGGTAGTTCT[C/G]TGTGGCAGGGTTAGA | 8853 |
rs778089887 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313324 | ATTGGAATTAAATAA[C/T]GAATAATCTCAAAAT | 8853 |
rs778090171 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237696 | AAGTGCTGGGATTAC[A/G]GGCATGAGCCACCGT | 8853 |
rs778092082 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266514 | TCCTGTGCGGGTGGT[-/G]GGCGTCTGCATGTAC | 8853 |
rs778099703 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353363 | TGAGGTCAGGAGTTC[A/G]AGACCAGACTGGGCA | 8853 |
rs778105105 | snp | C/T | 1.68647e-05 | 0.0029038 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320384 | GGTAATTTGGGATTT[C/T]AAATTTAAACCAACC | 8853 |
rs778112684 | in-del | -/A | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405915 | CTGTTCCAGACCAGC[-/A]ATGAATCCTGGTCTC | 8853 |
rs778119109 | in-del | -/AAA | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211156 | GTGAAACTGCGTCTC[-/AAA]AAAAAAAAAAAAAGT | 8853 |
rs778136472 | snp | C/G | 1.65734e-05 | 0.00287862 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391176 | ATCCACCGCTGCCCC[C/G]TCTTCGCGTGACATC | 8853 |
rs778152736 | in-del | -/CACT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317090 | TCACATCCACACACA[-/CACT]CAACCACACTCATAC | 8853 |
rs778153302 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209579 | ATTTTATATTTATTT[A/G]TTTATTTGTTACGGA | 8853 |
rs778159240 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9382602 | TTTACAGTGAATGAG[C/G]ACATTCATTCTCCTG | 8853 |
rs778177181 | in-del | -/GTATTTATACTTGGCTATTTTCAAACGCTATTC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227497 | AATAAGCTCTCATTT[lengthTooLong]GGGTGGGACAGGGCT | 8853 |
rs778189887 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301955 | CAGCCTCACATGTAG[C/G]TGGGACTACAGGTGC | 8853 |
rs778221964 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9238324 | CCTCAGTTTCCCCAT[C/G]TGTAACACCAGAGAG | 8853 |
rs778229431 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332010 | GTGAAGGCTGCAGGA[C/G]GGGCCCTGGCACGGT | 8853 |
rs778257789 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9261916 | AACCCTCAGTGTTCA[A/C]GAGAGAGGCCAGTTG | 8853 |
rs778266117 | snp | C/T | 1.66286e-05 | 0.0028834 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399986 | GGGGCAGGTGCCCTC[C/T]GGTAGCAGTAAATCT | 8853 |
rs778282609 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343995 | GTGAAGATTTTTGCA[A/G]TACTTGTTGATGTTC | 8853 |
rs778282731 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331095 | CACACGCCCAGTTTC[C/T]GCTTCTCGCCCCCAA | 8853 |
rs778283041 | in-del | -/AA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9314925 | GAGACTCCATCTCAA[-/AA]AAAAAAAAAAAAAAA | 8853 |
rs778299731 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402545 | CCCACAGTTGCCCAC[A/C]ACCCACCATCCGGAA | 8853 |
rs778316587 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9319509 | AGGCATCCCAGGCAG[A/G]GGAAAGGCGCAGGTG | 8853 |
rs778325164 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9314683 | TCATACCTGTAATCC[A/C]AGGTCTTTGGGAGGC | 8853 |
rs778326608 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9370235 | TGTAACTTGATACAG[G/T]GAAAGAGCCAGAACA | 8853 |
rs778329211 | in-del | -/TCT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9347071 | CTCCACTTCCAGAGG[-/TCT]CCTCCTGCCTTTAGC | 8853 |
rs778331813 | snp | C/G | 1.66327e-05 | 0.00288376 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9388497 | CGCCCAGCCTGCAGC[C/G]CCCAGCACCACCAGC | 8853 |
rs778354051 | snp | C/T | | | intron-variant, missense | ASAP2 | GRCh38.p7 | 2:9389815 | GGACGTCCCTGAGCA[C/T]AGAAGGCAGCTACAA | 8853 |
rs778360114 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281246 | GTCATATGTTGAAAA[C/G]GTTGCTCTTATCAGA | 8853 |
rs778375502 | in-del | -/ACAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317215 | CACCCACTCACATCC[-/ACAC]TCACACAATCACACA | 8853 |
rs778413590 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279756 | TTAATTGTGTCACAG[C/T]GCCCTTTCCGTTTCT | 8853 |
rs778423163 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362055 | AAGAACCATAAAGTA[G/T]TAGTTATCATTGTTA | 8853 |
rs778440382 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9309718 | CAATAGAACTGTTTG[C/T]GTTGATGGGAATAGT | 8853 |
rs778442229 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358536 | TGAATGGAAGGATGG[C/G]GAGATGGAGAGAGAG | 8853 |
rs778453319 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272350 | TGTTTGCCATTTGTA[G/T]GTCTTCTTTGGAGAT | 8853 |
rs778465987 | snp | C/T | 6.71242e-05 | 0.00579289 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368375 | GGTAATGTGTAGCAG[C/T]AGAATGTATTAATAA | 8853 |
rs778487438 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256662 | GAAGAGTATTGAAAT[G/T]AAAGTGCAGGCCACT | 8853 |
rs778488496 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263123 | CAGGCCGTGGCTGCA[C/T]GCTGGCTTTCCACTG | 8853 |
rs778496359 | snp | G/T | 3.80004e-05 | 0.00435876 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318509 | TAAGAATCTCCTTTT[G/T]TTTTTGTTTTTTAGA | 8853 |
rs778507271 | snp | A/C | | | intron-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212042 | GAGCCTTCCTCCCTG[A/C]CCCCTGGTGAATGCT | 8853 |
rs778512507 | snp | A/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236877 | ACTTCAGGTTTCTTT[A/T]TTGAGTGAATGGGAC | 8853 |
rs778514939 | in-del | -/TGAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9294972 | CACCAGCCCCCTTCC[-/TGAA]TGAACCCAATGAAAC | 8853 |
rs778520475 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9375372 | CAGAGGAAGACGGCA[C/T]GGAGAGGGGTACTGG | 8853 |
rs778557276 | snp | A/G | 1.82433e-05 | 0.00302016 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356356 | GCCAGGTGACCCAGG[A/G]ACCCCACCCGACCCT | 8853 |
rs778575426 | snp | G/T | 1.70269e-05 | 0.00291773 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327938 | TCTGTTATGTTATCT[G/T]AAATGTTTGTTCATG | 8853 |
rs778583364 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378596 | AGCACAGCAGCCTCG[G/T]CGCAGCCAGTGGGAC | 8853 |
rs778584289 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9310471 | GGCTAGAGCTGGAAA[A/G]ATTCTGCCCAGTGAC | 8853 |
rs778592771 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250190 | TTTTAGCATTTAACA[C/T]GCTGCCTGACACAAA | 8853 |
rs778617715 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256311 | AGGATGTTAAAAGTT[-/G]GAGTTTAGCACGAGG | 8853 |
rs778665901 | snp | C/G | 1.6582e-05 | 0.00287936 | missense | ASAP2 | GRCh38.p7 | 2:9356270 | AATAACATCGTCCAA[C/G]AACTGACAAAGGAGA | 8853 |
rs778681617 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9400599 | CAAGGTCTGCATCCA[A/C]GTCAGAAGGTTCCCT | 8853 |
rs778684307 | in-del | -/AACA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9244483 | TCACGGTGTGAACAG[-/AACA]GAGAACCCTTGATGA | 8853 |
rs778685372 | snp | C/G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9379397 | CTGAGTCTACTCACC[C/G/T]CCACCTGAGGCCACA | 8853 |
rs778703148 | snp | A/G | 1.65993e-05 | 0.00288086 | missense | ASAP2 | GRCh38.p7 | 2:9403319 | TTTGTGCACTTTATC[A/G]CTGACTGAATTGCTA | 8853 |
rs778712995 | snp | C/T | | | | | GRCh38.p7 | 2:9244747 | CCAGGTACCCAGAAG[C/T]GTTTGTAGGAAGAAC | 8853 |
rs778742052 | snp | C/T | | | | | GRCh38.p7 | 2:9350186 | AAAGTATGTTGTGAT[C/T]GCTTGGTGTCGTGTG | 8853 |
rs778742272 | snp | A/G | | | | | GRCh38.p7 | 2:9316441 | TTTGCTTGATGGTAT[A/G]AATGAATACATAAGG | 8853 |
rs778769136 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317583 | ACACACCCACACACC[C/T]GTACACAATCACATT | 8853 |
rs778771258 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9303261 | CAGTGGCTTGGGGTA[C/T]GTGGGAATATCCGCC | 8853 |
rs778773025 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9246331 | ACAGGGTCTTGCTCT[A/G]TTACCTAGACTGGAG | 8853 |
rs778785930 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245815 | CTCCTGGGGGACAGA[A/G]CCTTTGTTTTCTTCG | 8853 |
rs778797345 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402752 | ACATCATTTACACTC[C/T]TGAGATCATATTTGG | 8853 |
rs778807638 | snp | C/G/T | 0.00020953 | 0.0102335 | missense, synonymous-codon | ASAP2 | GRCh38.p7 | 2:9393528 | TGCCAAGACGCCCAG[C/G/T]GTAATGGAAGCCTTG | 8853 |
rs778848593 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278315 | GTCAGGAGTTTGAGA[A/C]CATCCTGTCTAACAT | 8853 |
rs778848854 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9360877 | ATTCCTGAAATTTTA[A/G]CAGTTGACTCATATG | 8853 |
rs778859500 | snp | A/T | 1.6473e-05 | 0.00286988 | missense | ASAP2 | GRCh38.p7 | 2:9356059 | CAGATGACAGAACTT[A/T]CCACTTTCAAGCTGA | 8853 |
rs778890108 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263992 | AGGTCAGGAGTTCAA[C/T]ACCAGCCTGGCCAAC | 8853 |
rs778897194 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9298432 | CCCCGTCTTCACTTA[C/T]GAACATTTCTGTAGG | 8853 |
rs778903472 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9285761 | ATTTTCACTTCTCTA[G/T]AATTATTCTGTCATA | 8853 |
rs778928416 | snp | A/G | 1.75041e-05 | 0.00295833 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401412 | GTGAGTCAAGGGTGG[A/G]CCTGGGAGGTTCCTG | 8853 |
rs778938210 | snp | A/G | 2.21002e-05 | 0.00332409 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207197 | CACCACCCGCACGGC[A/G]CAGTGCCGGAACACT | 8853 |
rs778946842 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307078 | TGCACCAGCAGCACC[A/G]GAATTGTTAGAAATG | 8853 |
rs778951366 | snp | C/T | 4.94605e-05 | 0.0049727 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9323160 | GGAACACGCCAAGCT[C/T]CATGGGATGATTCGG | 8853 |
rs778968834 | snp | C/G/T | 0.000118123 | 0.0076844 | missense | ASAP2 | GRCh38.p7 | 2:9393588 | GATCTCACAGATCAG[C/G/T]CCCCCACCTCTGCCC | 8853 |
rs778975189 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9218681 | GTCCTGCCTCAGTTG[C/T]GTCATTTGTAACATG | 8853 |
rs778976290 | snp | C/T | 1.66319e-05 | 0.00288369 | intron-variant, synonymous-codon, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391183 | GCTGCCCCCTCTTCG[C/T]GTGACATCTACCAGT | 8853 |
rs778980595 | snp | A/G | 1.70067e-05 | 0.002916 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385383 | AGGTTGCTAACCATT[A/G]AGAGTTTTGATCAGC | 8853 |
rs778985384 | snp | A/G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345586 | TAACATCTCAAGGCC[A/G/T]AGGTCGTTGCCTTTT | 8853 |
rs778990739 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9346501 | GTTCTGTAGACCAAG[A/G]GAAGCAAATTTATCC | 8853 |
rs779001979 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9304159 | TGAGGGTGGAGGGGC[A/G]CTGCAGTATGGCACT | 8853 |
rs779015334 | snp | G/T | 3.29484e-05 | 0.00405871 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391103 | CTGTGGAAGACAAAC[G/T]CTGTAAGTGTGGACG | 8853 |
rs779035255 | in-del | -/AAA | 0.00207022 | 0.0321064 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374971 | GGTTGTTGCTACTTT[-/AAA]AAAAAAAAAAAGGCC | 8853 |
rs779043388 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9375931 | AGCTGTCTTGAGAGG[A/G]TGGGCATCCAGCTGG | 8853 |
rs779060841 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9231781 | TCCTCTCTGTGCCGT[C/T]TCGCATGCCATCCTT | 8853 |
rs779068141 | snp | C/T | 1.64757e-05 | 0.00287012 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380735 | TTGCTCGCCCTTGAA[C/T]TTTAGCAAACGAGTC | 8853 |
rs779076093 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405456 | ATCTGTTAAGGGGTG[G/T]ATAACATAATATGCA | 8853 |
rs779080745 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9277211 | CTGTGCTGTCTGACA[C/T]GTGGTCTAAGCTTCG | 8853 |
rs779095845 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219720 | ATACCATAGAATTCA[C/T]TTACCATAAAATTCA | 8853 |
rs779099934 | snp | C/T | | | intron-variant, missense | ASAP2 | GRCh38.p7 | 2:9389884 | CCCAGGCTGGCTGGT[C/T]GGGGCCCAGGGTGGG | 8853 |
rs779140699 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263879 | AGTATTTTTTTCTCC[A/T]TTTTTTTCCCTTTTA | 8853 |
rs779141893 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364946 | CAGTGCAGGATTTAC[A/G]TTCCAACTATCAGAC | 8853 |
rs779147751 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253083 | AAAGAAACGAAAGTC[A/G]TTTTTTGTTGTTTTT | 8853 |
rs779162425 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9392698 | CTTCATGTTTCCCCA[C/T]GCCAGTTTCCTCTCT | 8853 |
rs779170647 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9283374 | TTGTAACAAATTACC[A/G]TAAAATGAGTTGGCT | 8853 |
rs779171905 | in-del | -/C | 1.78721e-05 | 0.00298927 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350778 | TCCACCCAACCCCAA[-/C]CTTTTTTGTTGTTTT | 8853 |
rs779178440 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353077 | ACCCCAGAGAGTCAT[C/T]ACAGGAAACCTGGCT | 8853 |
rs779228726 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9262130 | CTGGGAATGATAGGC[A/G]CGTGCCATCATGCCT | 8853 |
rs779230276 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275949 | GTGCTCCGTAGACAC[A/G]TGCTGGTAGCTGCTG | 8853 |
rs779254413 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343250 | TCCCTGTTTCTCCCA[C/T]TATGGAATGAACTGG | 8853 |
rs779272444 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240491 | ACTGGAGCGATTCAC[C/T]TGCCTTGGCCTCCCA | 8853 |
rs779292096 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221104 | GAGTCTTTCAACTTT[A/G]TTTTTTTTTCCCAAG | 8853 |
rs779302160 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229093 | GGATAGAGACAGGAC[-/T]CGGCAGAGAAGCGGA | 8853 |
rs779304326 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9335417 | TGGCGGTGTATAAAC[C/T]CTGTGCTCTGTCAGT | 8853 |
rs779316687 | in-del | -/TTTTTTTTTTTTTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395607 | TCTTTTTTTTTTTTT[-/TTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 8853 |
rs779326662 | in-del | -/GGA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234042 | TTGAACCCGGGAGGC[-/GGA]GGAGGTTGCAGTGAG | 8853 |
rs779328234 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211019 | AATTAGCTGGGTGTG[C/G]TGGCGCATGCCTGTA | 8853 |
rs779337947 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9299716 | TTCTGCTTCTCACTC[C/T]CAGACTGCCCTTTTA | 8853 |
rs779350459 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213245 | AGAAGATGTGGGAAT[A/G]GAACAGCTTGGGAAA | 8853 |
rs779361402 | snp | C/T | 1.66302e-05 | 0.00288355 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368399 | TTAATAATTGAGTAT[C/T]CTGAAATAGACTTTC | 8853 |
rs779373068 | snp | C/G | 1.94585e-05 | 0.00311911 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378929 | TGCTCTCTCTCTGTT[C/G]CTGTTCTCGGGCAGT | 8853 |
rs779377826 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380897 | AGGGTTTGCTGTGAA[C/T]CAGTGTCCTGAGCAG | 8853 |
rs779384449 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336124 | ATATATTCCTTTTAT[A/G]TATTAATGGTTAGTA | 8853 |
rs779386265 | in-del | -/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278318 | GGAGTTTGAGACCAT[-/G]CCTGTCTAACATGGT | 8853 |
rs779406641 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278169 | GCCTGTGATTGGCAT[C/T]GCTATCCCAGTTCAC | 8853 |
rs779419949 | in-del | -/TTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240247 | CTTCCTCCCATAATT[-/TTT]TTTTTTTTTTTTTTT | 8853 |
rs779440597 | snp | A/T | 1.65649e-05 | 0.00287788 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400078 | AGAGGACCTGGTAAT[A/T]ATTTAATTTGGGACT | 8853 |
rs779444259 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272591 | ATCTGTTTTTGCTTT[G/T]GTTGCCTGTGCTTGT | 8853 |
rs779445786 | in-del | -/GA | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209462 | ACTGAGACGAAACAT[-/GA]GAGGGTATCATGACA | 8853 |
rs779446547 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214501 | CACCTCGGCCTCACA[A/G]AGTGCTGGGATTATA | 8853 |
rs779448181 | snp | C/T | 1.64838e-05 | 0.00287083 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9368514 | ACCCAACCCAGGCAG[C/T]GACATGTAAGTATGG | 8853 |
rs779449110 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301562 | CTGCATTTCAGGGCA[A/G]GTTTCTGAAAGGTTT | 8853 |
rs779458016 | snp | C/T | 1.64841e-05 | 0.00287085 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9388428 | GAGGGCTTTCATGCC[C/T]AGCATCTTGCAGAAT | 8853 |
rs779468472 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368371 | GATGGGTAATGTGTA[G/T]CAGTAGAATGTATTA | 8853 |
rs779486035 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331060 | TTCCACGTGTGGGAG[C/T]GCCTCTCATTCCCCC | 8853 |
rs779487056 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9323813 | CCCGCAGCCTCAGCC[A/C]TTCCCTTAGTGAGGC | 8853 |
rs779506578 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313524 | TCCCCACAACCCACC[C/T]TATCACTGGATGGTT | 8853 |
rs779510055 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9342312 | TACTGGCATAAGGAG[A/G]GACATATAGACCAAT | 8853 |
rs779532459 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9228360 | CTACTCACTTGGTGT[C/T]ATCCTTGAGAAGAGA | 8853 |
rs779558504 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371799 | ATTATGTTAATTGTT[A/T]TTCTGCAAAAGCCTG | 8853 |
rs779566217 | snp | A/G | 9.97738e-05 | 0.00706236 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9400824 | CATGCCTAGGAAGTC[A/G]CAGGCAGTAAGTGAC | 8853 |
rs779571235 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383002 | GTTTTTCAAGGATGG[C/T]TGGATGGGCAAGAGG | 8853 |
rs779579303 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9392488 | GCCGGCAGCAGAGCC[A/G]GGAGCAGTGGGTCTG | 8853 |
rs779599133 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9290471 | CATCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 8853 |
rs779604417 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338925 | GCTCACAGCTATAGT[C/T]CCAGCACTTTGGGAG | 8853 |
rs779611667 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381437 | TTGACACACAGCGCT[C/T]AGTAAATAGATTAAG | 8853 |
rs779611839 | snp | A/C | 1.64773e-05 | 0.00287026 | missense | ASAP2 | GRCh38.p7 | 2:9344569 | CAGCTTATAGCTTAC[A/C]TCAGCCTCAGGGAAA | 8853 |
rs779627613 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279670 | GAGCATCGTCCTGCA[C/T]GTACCCACTTTGTCA | 8853 |
rs779641397 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236716 | ATGAGAGACACAGAC[A/G]GTGCATTTTACTTTT | 8853 |
rs779645491 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247524 | TTGCTCGCTGCGTCT[C/G]TTATTATAGAAGGGT | 8853 |
rs779662177 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378549 | TCACACAGGCATCCA[A/G]AGGCCCTGCATCCAG | 8853 |
rs779674686 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397259 | AGGAGCCGTCAGCTC[A/C]CAGCAGTTATTGGGA | 8853 |
rs779701269 | in-del | -/TG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233054 | TGCCAGTCTGTGCTC[-/TG]TGTTTTTTTTGCTCA | 8853 |
rs779703048 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9297180 | TTCCTGGTGCAGCTT[A/G]ACTTTTCTCAGATTT | 8853 |
rs779721561 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9243265 | AGGCACCCGCCACCA[C/T]GCCCAGCTAATTTTT | 8853 |
rs779728116 | snp | C/T | 1.65367e-05 | 0.00287543 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358749 | TCTGCCCTGTTCTCT[C/T]TGGCAGATCCTACAT | 8853 |
rs779767466 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9318814 | CCTGTTGGCACAACA[A/G]AGTTGGTGAGGGGAG | 8853 |
rs779778166 | in-del | -/CTCA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317951 | CACACCCACAACACC[-/CTCA]CTCAGTCGTACACAC | 8853 |
rs779784702 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361797 | CTCGAACTCCTGGAC[C/G]CAAGTGATCCTCCTG | 8853 |
rs779789242 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9285688 | ATTTTTAGCTGTTTG[A/G]CATATCAGTGGGTGG | 8853 |
rs779804240 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9308436 | CCCCAGCTCCAACAC[G/T]GGGGACTGCAATTGG | 8853 |
rs779813899 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245848 | ACCAGATCCCCAGTG[A/C]CCAGAGCAGTGCCTG | 8853 |
rs779814702 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9224508 | TATGCCTGGAAATAA[A/G]TCCATTTTGGTTTGC | 8853 |
rs779826380 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9389688 | CACTGAGTCATACCC[C/G]GAAGAACAAACCTGC | 8853 |
rs779849719 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9367370 | CAGAAATATCACAAG[C/T]GTCACTGACTCCCCA | 8853 |
rs779870543 | snp | A/G | 4.68999e-05 | 0.00484229 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207206 | CACGGCGCAGTGCCG[A/G]AACACTGTGGCGGCC | 8853 |
rs779876715 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256111 | TTGACATATTTGCAC[A/G]TTCAGACATTCATAG | 8853 |
rs779885844 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338074 | TTCCCCATCCCACGT[C/T]GTCCATCCGATGGTG | 8853 |
rs779895631 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368283 | TGGGCTTTGGGTTTT[A/G]TCCATCTTCATTAAA | 8853 |
rs779925202 | snp | C/G | 1.75096e-05 | 0.0029588 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385407 | GATCAGCTTCATCCA[C/G]AACAGTGTGGGTCCT | 8853 |
rs779944136 | in-del | -/GTTTTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380182 | GTGGCTGCTTCAACA[-/GTTTTT]GTTTTTGTTTTTGTT | 8853 |
rs779994084 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9339469 | GAGATAATTTCTGTA[C/G]AGCACTTACCATATT | 8853 |
rs780014875 | snp | C/G | 1.65075e-05 | 0.00287289 | missense | ASAP2 | GRCh38.p7 | 2:9388305 | GCAGCCCAGTCCCAA[C/G]CGGCGGGAAGACCGG | 8853 |
rs780023789 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369304 | GATTACAGGCGTGAG[C/G]CACCGTGCCTGGCCA | 8853 |
rs780033489 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9309410 | GGGATGATTCCAGAT[A/G]CCGTATATAAAATTC | 8853 |
rs780041018 | snp | A/T | 1.64762e-05 | 0.00287016 | missense | ASAP2 | GRCh38.p7 | 2:9380747 | GAATTTTAGCAAACG[A/T]GTCAGGAGAGACTCC | 8853 |
rs780043108 | snp | C/T | 3.22025e-05 | 0.00401251 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393474 | ACGTCTCTCCCTGTC[C/T]TCCGCAGATCCCCTG | 8853 |
rs780043586 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302514 | GAGTCTCACTGTGTC[A/G]CCCAAGCTAGAGTGC | 8853 |
rs780065065 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9285077 | GGGAAGTAATTAGCT[G/T]TAGATGAGGGCATGA | 8853 |
rs780076385 | snp | G/T | 1.64887e-05 | 0.00287125 | missense | ASAP2 | GRCh38.p7 | 2:9374880 | CGAGAGATATTTTTG[G/T]ATTGCTCCAAGCTTA | 8853 |
rs780079128 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9263345 | GCTCTCCCCAAAGCA[G/T]GGCACCAGGCTGGCT | 8853 |
rs780096978 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9304040 | TTAGAAGACATGTGC[C/T]GGGACAGCCACTGGC | 8853 |
rs780112968 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219580 | GTCCTGAAAAGACAA[C/T]ATCATTGCTGAATCA | 8853 |
rs780121255 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333369 | ACTAATGAATACATA[A/G]TTGCAGTTACAGCAA | 8853 |
rs780127761 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9324908 | ATTGTTTAATCCATT[A/C]ACGTTGAATGTTACT | 8853 |
rs780134444 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275452 | GTGGGAGTATCAGAG[G/T]CAGGAGGGCTGAAAT | 8853 |
rs780138997 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383807 | AGAAAATGTGGCACA[C/T]ATACACCGTGCAATA | 8853 |
rs780151619 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9276191 | TCACACCATTTTATC[C/G]AATGAAATGCTAAGC | 8853 |
rs780152482 | in-del | -/CAAT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317224 | ACATCCACACTCACA[-/CAAT]CACACAACCACACTC | 8853 |
rs780171348 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279090 | GGTTTTCAGTAATTG[A/C]CAACAAACTTCTGCT | 8853 |
rs780173789 | snp | A/G | 1.64857e-05 | 0.00287099 | missense | ASAP2 | GRCh38.p7 | 2:9323167 | GCCAAGCTCCATGGG[A/G]TGATTCGGACTGAAA | 8853 |
rs780177990 | in-del | -/CACT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317215 | ACCCACTCACATCCA[-/CACT]CACTCACACAATCAC | 8853 |
rs780178524 | snp | C/T | 9.89821e-05 | 0.00703429 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368527 | AGCGACATGTAAGTA[C/T]GGGACTGGCTATTCT | 8853 |
rs780186528 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9384724 | TTCCATGCCCTCCCT[C/G]GGTGCCACCCTCCAG | 8853 |
rs780213352 | snp | A/C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9357435 | AGTGAGCTGAGATCA[A/C/T]GCCACTGCACTCCAG | 8853 |
rs780224255 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239587 | TGAGGTCCAGCTTCT[C/T]GGAAGGTAAGAGAAA | 8853 |
rs780234834 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9204973 | TTGTTGTTTTCCACC[A/G]GCCTTGCAATGCAAC | 8853 |
rs780245534 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315978 | GCTGTGGATGCAGAC[A/G]TTATTATACACCTTA | 8853 |
rs780246180 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9374702 | GACAAAGGGAGGCCG[A/G]ACGGCGGGTAGAAGC | 8853 |
rs780248116 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9363497 | CAGGTGTGAGATGAT[C/T]GTGGTTTTAATTTGC | 8853 |
rs780267210 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9344600 | CAAGGAACATGGGAC[C/T]GAGCGGAACGGCAGC | 8853 |
rs780272607 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371641 | TGTCAGGGACGTGTA[A/C]CTGGGGGAGGTGGAG | 8853 |
rs780294792 | snp | C/T | 3.43059e-05 | 0.00414147 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385230 | ACAGCACTGACCATC[C/T]CTCTGTTCTCTCAGC | 8853 |
rs780301657 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230403 | GTGACTCTGGCAGGC[A/G]AGTTTCCCAAGCCGA | 8853 |
rs780302231 | snp | A/G | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403637 | TAGCTAAACCTAAAA[A/G]TGTTTGCATTAATGA | 8853 |
rs780337188 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9303065 | GAGGTCCTCACCCTC[A/G]GTACTTCCATAGACT | 8853 |
rs780338016 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9252680 | CAGCACTTAGGGAGG[C/T]TGAGGCGGGCAGATC | 8853 |
rs780339398 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9399607 | CAGAGGCATGGACAG[C/T]GCTGACCCAGAGTGC | 8853 |
rs780361272 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9386136 | TAAACACATTTTCAT[-/G]GTTTGGCTTTTTTTT | 8853 |
rs780362063 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217031 | AGCAAAATTAGGCCA[C/T]GGTACCAAGTTCATG | 8853 |
rs780383504 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9292390 | AGAAGTGGTGGTGTG[C/T]GCCTGTAGTCTCAGC | 8853 |
rs780421119 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361712 | AGCTGAGACTACAGG[C/T]AAGTGCTACCACGCC | 8853 |
rs780431665 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405314 | AAAACATTGTAGATA[C/T]CTATTTATATTTAAA | 8853 |
rs780440616 | snp | A/G | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9405028 | AATCCTCCTGCATCT[A/G]TATTTTATAGTCAGC | 8853 |
rs780451792 | snp | A/G | 1.77656e-05 | 0.00298035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374732 | CCCTTCATGATTTGC[A/G]AGGCAATTACGTTTG | 8853 |
rs780490300 | snp | C/T | 8.4626e-05 | 0.00650429 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388560 | AGGTATGAAGCTGTC[C/T]GTCATCCCTGTGAAT | 8853 |
rs780512938 | snp | A/G | 1.64846e-05 | 0.0028709 | missense | ASAP2 | GRCh38.p7 | 2:9358777 | CATGGCTTTCCACCA[A/G]CCTGGGCATCCTGAC | 8853 |
rs780528589 | snp | A/G | 1.6588e-05 | 0.00287988 | missense | ASAP2 | GRCh38.p7 | 2:9400783 | GGTCCTCTGTCCAAT[A/G]CTATGGTCCTGCAGC | 8853 |
rs780537753 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9335250 | GGGTCTGAAGAACAT[A/G]AAGTTCATGTCTTCT | 8853 |
rs780538688 | snp | G/T | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390774 | TGTTTATTTCCTTCT[G/T]CAAATGATACTGATA | 8853 |
rs780556292 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272319 | ATCAATGATGTTGAA[C/G]ACCTTTTTGTATGCC | 8853 |
rs780563081 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9282298 | AAAGTCCTAAGTCCT[A/G]AAACCAGAGCCTGAT | 8853 |
rs780571174 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9347568 | GGAAAACCCTTCCCA[C/G]GAAGCTGGCAGCCTC | 8853 |
rs780576194 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9221539 | CTGTTAAATTTATTC[C/G]TAAGTACTTTATTCT | 8853 |
rs780586617 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227118 | CATCTGCCATCCGGC[A/G]TCTCCAGCCCTGCTG | 8853 |
rs780598718 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9273127 | CATTGAATCTGTAAA[A/T]CGTTCTGGGTAGTAT | 8853 |
rs780616456 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9293426 | CATTTGAACAAGGGG[A/G]AGGTGAGAGTGTGAG | 8853 |
rs780627224 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9341786 | TTGGTGCCGATGTTC[C/T]GCCCTTCTGAGAAAA | 8853 |
rs780645370 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277503 | TGATTATCTTGTATC[A/G]GTAACTCTCTACTCT | 8853 |
rs780655052 | snp | A/G | 1.67038e-05 | 0.00288992 | missense, intron-variant | ASAP2 | GRCh38.p7 | 2:9318545 | AATATGAACAACATA[A/G]TCTCCTTCCCTTTGG | 8853 |
rs780664721 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9246238 | CCAACTTTTCATTTC[A/G]CCTGACTTCTCAGTA | 8853 |
rs780685891 | snp | C/G/T | 6.71123e-05 | 0.00579243 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400847 | TAAGTGACGAGCCCC[C/G/T]TTTCCTGCCTCTCTG | 8853 |
rs780730186 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9299823 | GGATAGATTATAGCC[A/C]GCCGGTGACTCTTAC | 8853 |
rs780747512 | snp | A/G | | | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9358850 | TTATTCCAGGATGCA[A/G]TCCCTGACCTTAGAT | 8853 |
rs780759691 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9392542 | GGCGAACACACCAAA[A/G]GCCAGAAGGAACCAC | 8853 |
rs780769890 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225847 | GCAACTCCTCATCTT[C/T]TAGTTTGTGCTGTCA | 8853 |
rs780796255 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9381314 | GGGGCTCCCCAGCTT[A/G]GCTTGGGAAGGAAAC | 8853 |
rs780813224 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387982 | CCAAGAACAGCAGAG[G/T]GGAACCGCTGCCATG | 8853 |
rs780861313 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247390 | GGTCCTCATTTGCAC[A/G]AGGCGAATCAGTTTA | 8853 |
rs780877420 | snp | A/G | 1.64779e-05 | 0.00287031 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279287 | TCTCAGCACAGACAC[A/G]GTTTAATGACTGTAT | 8853 |
rs780882976 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9360049 | GGTGTACATGTGGTA[A/T]CTCTTGGATAACTGA | 8853 |
rs780887930 | in-del | -/AAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264191 | GTGAGACCCTGTCTC[-/AAA]AAAATAATAATAATA | 8853 |
rs780913156 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267504 | GGCTGCGTCATATTC[A/C]ATGGTGTATATGTAC | 8853 |
rs780934399 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371622 | CCAAGACGGATCTTG[G/T]GGGTGTCAGGGACGT | 8853 |
rs780956472 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209615 | GCTCTTGTTGCCCAG[A/G]CTGGAGTGCAATGGC | 8853 |
rs780964312 | snp | C/T | 1.78312e-05 | 0.00298585 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401426 | GGCCTGGGAGGTTCC[C/T]GGGGGCTGAGCCACG | 8853 |
rs780964858 | snp | C/T | 3.30066e-05 | 0.00406229 | missense | ASAP2 | GRCh38.p7 | 2:9388309 | CCCAGTCCCAACCGG[C/T]GGGAAGACCGGCCCA | 8853 |
rs780970529 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9324139 | CCAGCTCTTAATTCC[C/G]TCTGAGCAATCAACA | 8853 |
rs780973843 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9401581 | CCCCTTCTGAGCAGG[A/C]CTGATTATTCCCCAG | 8853 |
rs780994044 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9223064 | TTTTAGGCAGAGGCC[-/T]TCCTGCATCTCTCAA | 8853 |
rs781007092 | in-del | -/GTT | 1.77847e-05 | 0.00298195 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350931 | CCGCGCCATAGAGAC[-/GTT]GTCTTATGCTCTCCT | 8853 |
rs781008975 | snp | C/T | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214400 | GACTGCCACCATGCC[C/T]GGCTGATTTTTGTAT | 8853 |
rs781066914 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278414 | GCTACTTGGGAGGCT[A/G]AGGCAGGAGAATTGC | 8853 |
rs781081631 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307341 | TGCTTCCGACTCTCA[C/T]CCTTGGCGAGATGGA | 8853 |
rs781086151 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337895 | TACTTGGAGAAAAGT[A/T]GAAAAATTGTGCAGT | 8853 |
rs781086865 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371037 | GGGTACCTAACGAAA[A/G]CAGGGCATTTGGTTG | 8853 |
rs781108154 | in-del | -/TTTG | 6.59391e-05 | 0.00574153 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376891 | GAATTCTGGAATGCC[-/TTTG]TTTGGTTTTTCAGGA | 8853 |
rs781128789 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349032 | GATTATTTGGTCTGT[C/T]CGGGCCAGTGTCTTT | 8853 |
rs781139048 | in-del | -/AAC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9287791 | TCCCCGCTGCTGGCT[-/AAC]AACAATGATTGGAAT | 8853 |
rs781158318 | snp | A/G | 1.75425e-05 | 0.00296158 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374978 | GCTACTTTAAAAAAA[A/G]AAAAAAGGCCGGCCA | 8853 |
rs781158585 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9242255 | GATCTGACCTGGTCC[A/C]TGGGAAGTGCAGATT | 8853 |
rs781162123 | snp | C/G | 1.675e-05 | 0.00289391 | intron-variant, missense, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391191 | CTCTTCGCGTGACAT[C/G]TACCAGTACGTTTTT | 8853 |
rs781174773 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9319238 | CGCCAGCCCTGACAG[A/G]CGTGCACCACGGAAG | 8853 |
rs781185358 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9354611 | CGTTTGCACCACTCC[A/T]CTCCAACCTGGGCAG | 8853 |
rs781213480 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256604 | TGGCCATCTGTTTCT[A/G]TTTACATGTGCAAAT | 8853 |
rs781215326 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395469 | AACAAGAATGAAACT[C/G]CATCTCAAAAATAAA | 8853 |
rs781215371 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274658 | TCATTCTAGCTTCTC[A/G]TCCTGACCAAGTTTA | 8853 |
rs781230860 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315779 | CCTTAAACTGCGCTT[C/T]TCAGCATTTAAAAAT | 8853 |
rs781249376 | snp | A/G | 4.97211e-05 | 0.00498579 | missense | ASAP2 | GRCh38.p7 | 2:9403281 | ATGGAGATCCTGGTC[A/G]CAAAGGCGCATTCCC | 8853 |
rs781270607 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284581 | ATGGGAATTTAATAG[G/T]TCATAGGATTGCTAG | 8853 |
rs781273180 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9351818 | TGGCTTGCTCTTATC[A/C]TCCCTGTTCCCCTTC | 8853 |
rs781325255 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9257355 | TACTTAGTAAGCATT[-/A]TGGAATGACCATAGG | 8853 |
rs781336702 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9275343 | CCAAAGCACTGGTAT[C/T]ATAGTAGGTGTGAGC | 8853 |
rs781340001 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9268726 | TGTTTTGTCTACTGT[C/T]TTTCAGAAATGTCCC | 8853 |
rs781388922 | snp | C/T | 2.39679e-05 | 0.0034617 | utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207083 | CCCTGCGGCTGTGCG[C/T]CAGCGCCCTCGCGCC | 8853 |
rs781391395 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9280931 | CTGGGTGTTCCCAAG[A/G]TGTCTGTGCAGCTGG | 8853 |
rs781394520 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250348 | GAGGGGAAAGAACAC[A/G]ACATGTGAATACACA | 8853 |
rs781400700 | snp | A/G | 1.6676e-05 | 0.00288751 | missense, intron-variant | ASAP2 | GRCh38.p7 | 2:9318564 | CCTTCCCTTTGGACA[A/G]TTTGCTGAAGGGGGA | 8853 |
rs781419075 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9373085 | GTCAGCCAGCACCGC[A/G]GTGAGCTCAGTGCAC | 8853 |
rs781428067 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9255858 | CATTTTGAAGTCTTG[A/G]TAAACATTGGGCTGG | 8853 |
rs781444144 | snp | C/G | 6.05981e-05 | 0.00550412 | missense, utr-variant-5-prime, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9207178 | CGCCCACGGCCTCCA[C/G]CTTCACCACCCGCAC | 8853 |
rs781469335 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368997 | TTGTGTTATTGTTGA[C/T]ACACAACTTGACGGA | 8853 |
rs781491646 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9315107 | CAAATTGAGCACATG[C/T]GTAGAATCAGGGAAG | 8853 |
rs781521012 | in-del | -/GTTTTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380187 | GCTTCAACAGTTTTT[-/GTTTTT]GTTTTTGTTTTTGTT | 8853 |
rs781530781 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9261947 | GACCAGAGCGCCTCA[C/T]CCCACCATTTGCCAT | 8853 |
rs781536075 | snp | A/G | 1.65941e-05 | 0.00288041 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9400794 | CAATGCTATGGTCCT[A/G]CAGCCCCCTGCACCC | 8853 |
rs781538999 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230315 | ACCCAGAGGACCAGT[G/T]TTGGGGACCCAGAGG | 8853 |
rs781539133 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230161 | CTCACAGTTTCAGAA[A/T]AAACACATATGTAAA | 8853 |
rs781539581 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364709 | AAGACGAAGAACTTA[A/C]CGACTTACAACTGTC | 8853 |
rs781569489 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9386681 | AACCTAGAAAGGGTT[C/G]GTGGTCCTGTGAGGG | 8853 |
rs781608259 | snp | G/T | 3.34622e-05 | 0.00409023 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344843 | TCTGCTGTATTAGGT[G/T]AGGTTGGTGTTGGAG | 8853 |
rs781617521 | snp | A/G | 1.85389e-05 | 0.00304452 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9379055 | GAAGGCCTCCATCGA[A/G]ATAGGTGAGTGGGCC | 8853 |
rs781624787 | snp | A/G | 1.66988e-05 | 0.00288949 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320247 | ATCTTGCACAGAAGT[A/G]AATGATTAGTCTTGC | 8853 |
rs781631191 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321654 | GTCTCTGTGGCTGAT[A/G]GGAAATGGTCCTGTG | 8853 |
rs781635011 | snp | A/G | 1.72299e-05 | 0.00293508 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388583 | CTGTGAATATATAGA[A/G]GGTCTTGTTTTGTGG | 8853 |
rs781669501 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9320686 | GTTTTTGATAGCAGG[A/G]CAGTTTTCAGACTTC | 8853 |
rs781681307 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281338 | GAGGAGAGACTTGTG[G/T]GACTCCCAAGGCTGG | 8853 |
rs781717752 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345438 | AATCTAGCTTTCAGA[A/G]GCCAGGAACTTGGAT | 8853 |
rs781722203 | in-del | -/ACACACCCAT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317628 | CACAATCACACCCAC[-/ACACACCCAT]ACACACATTTACACA | 8853 |
rs781722299 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9292573 | AACAGTGGGAACACA[C/T]AGGACTCCCTGGTAT | 8853 |
rs781723116 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291171 | GAACTTAACACATTT[C/T]AAATTTTCACTCTTT | 8853 |
rs781724892 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333148 | GAAGTAAACATCACC[C/T]CACATGACATATGTG | 8853 |
rs781741032 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9251326 | CCCACTCCTTCCCAT[C/T]TTCTGGGCTCCATCT | 8853 |
rs781743423 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9363253 | ATAGTGCTGCAGTAA[A/G]CAAGATGGTGAAGAC | 8853 |
rs781756922 | snp | G/T | | | intron-variant, missense | ASAP2 | GRCh38.p7 | 2:9390015 | CTTTTGCTGACTGTG[G/T]GTGTCACGGGAGGAA | 8853 |
rs781757836 | snp | A/T | 1.83001e-05 | 0.00302485 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356367 | CAGGGACCCCACCCG[A/T]CCCTGGGCTCTAGGA | 8853 |
rs781759220 | snp | C/T | 1.64738e-05 | 0.00286995 | intron-variant, synonymous-codon, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391072 | TTCAGTTCAGACAGC[C/T]TCCTCTGCTAACACC | 8853 |
rs781761376 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9350281 | GTGATGGTTGGCATT[G/T]AGGAATGTGAGTCTG | 8853 |
rs781762488 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317024 | CCACACTCACACAAC[A/C]TGCAATCATTCCCAA | 8853 |
rs796069566 | in-del | -/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9391740 | CACCATGCTCAGCTA[-/TT]TTTTTTTTTTTTTTT | 8853 |
rs796073287 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397834 | CTCGATCTCTGCTCA[C/T]TGCAAGCTCCGCCTC | 8853 |
rs796080837 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395942 | AGTAGAGAAATAAAG[A/T]TAAACTTTTACTTAG | 8853 |
rs796091064 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9360885 | AATTTTAACAGTTGA[C/T]TCATATGAGCTGGTA | 8853 |
rs796107480 | in-del | ACCACACAACA/TCCACATTCACACACTCACAACCACACAACACACT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317123 | CCCACGCAATCACAA[lengthTooLong]ACATCCCAATCACAC | 8853 |
rs796110243 | snp | A/G | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213283 | GAAATGCCAATGGGC[A/G]GGATCATGGAAGGAC | 8853 |
rs796113532 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250358 | AACACGACATGTGAA[A/T]ACACAGCTGTCCCTA | 8853 |
rs796136992 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9372795 | CGTCCCACTGTGGGA[C/T]GCAGTCACACCCACG | 8853 |
rs796137437 | in-del | AAC/TCTCACAAT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317122 | CCCCACGCAATCACA[AAC/TCTCACAAT]ACACAACACACATCC | 8853 |
rs796141066 | snp | A/G | | | intron-variant, missense | ASAP2 | GRCh38.p7 | 2:9390090 | ATCTCCTGGTTTCCC[A/G]AAGTCTTGGAATTCA | 8853 |
rs796153577 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264635 | TTTTCAGGTGATAGC[A/G]AAAACTCAGTCTCCT | 8853 |
rs796174123 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9233057 | AGTCTGTGCTCTGTG[-/T]TTTTTTTTGCTCAGT | 8853 |
rs796195897 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348377 | TGATCTACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 8853 |
rs796228312 | in-del | -/GT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9330920 | TGGATATGAGAGAGA[-/GT]GTGTACGCTGCCTGC | 8853 |
rs796240649 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402044 | GTGGACAGAAAGCCC[C/G]AGGCTGAGCCCACCA | 8853 |
rs796250637 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9378469 | TTTCCCTTTCCTGGA[C/G]GGAATATCAAATAAT | 8853 |
rs796253883 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9316292 | TGGGCGACACAGTGA[C/G]ACCCTGTTTCAAAAA | 8853 |
rs796300998 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9326948 | GTCAAAATGTACATA[C/T]GTTTAAAAATTTGAT | 8853 |
rs796342536 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258334 | TAGTAATCAGTAGTT[-/G]GTTTTTTTTTTTTTT | 8853 |
rs796347107 | in-del | -/CA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239444 | TGGGTAGAATGAAAT[-/CA]TGTGTGTGGTGATGG | 8853 |
rs796367657 | in-del | -/GT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258335 | TAGTAATCAGTAGTT[-/GT]TTTTTTTTTTTTTTT | 8853 |
rs796397759 | in-del | -/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302123 | CCACCGCGCCCGGCC[-/TT]TTTTTTTTTTTTTTT | 8853 |
rs796406834 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395599 | TGTTTTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 8853 |
rs796407192 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371014 | GTGTCGTTTCTTCCA[A/G]GCACCAGGGGTACCT | 8853 |
rs796412815 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9331855 | GCTGGAAACCACTGT[A/G]ACCAGCTGTTGCTCA | 8853 |
rs796425569 | in-del | -/TT | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404738 | CAAGACTGTGTAGAG[-/TT]TTTTTTTTTTTTGGC | 8853 |
rs796439963 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9359694 | TAGTCTTGACAGAAA[A/C]TCAATAGTTGTGGAC | 8853 |
rs796458018 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9300213 | CTCCACCTGGGCGAC[-/A]AGAGAGTGAGACCCT | 8853 |
rs796459824 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9356621 | TTTTGAGAAATGAAA[A/C]CTGAAGGGTACAGTG | 8853 |
rs796468685 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239630 | CCCCTAATATTAACC[A/G]AGCACCATTTATGTG | 8853 |
rs796470426 | in-del | -/TGTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348116 | TGACACTTTTTTGTC[-/TGTT]TGTTTGTTTGTTTGT | 8853 |
rs796473249 | in-del | -/TG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9335072 | TCTGATTGGTTCTGT[-/TG]TGTGTGTGTGTTTTT | 8853 |
rs796512233 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305135 | GTGGAGGGGGTTGTA[A/G]TAGTGGGGTATAGAT | 8853 |
rs796520483 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9393106 | TGGCCACAGGTCAGT[C/T]GATGTGCAAAGCAGG | 8853 |
rs796523643 | snp | A/G | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390465 | GGAGGTTTGTGAGGC[A/G]GAAGAAGGGCTTGTG | 8853 |
rs796527501 | multinucleotide-polymorphism | AGA/GGG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397852 | AAGCTCCGCCTCCCG[AGA/GGG]TCACGCCATTCTCCT | 8853 |
rs796538910 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9379691 | CATCTGCCTGAGAGC[C/T]GTGCTTATCATTAAA | 8853 |
rs796540558 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9374531 | GAGGCGGGTGGGCTG[A/G]GAGAACATGGGGAGT | 8853 |
rs796556703 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272372 | TTTGGAGATATGTCT[A/G]TTTATATCTTTTGCC | 8853 |
rs796627199 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240267 | TTTTTTTTTTTTTTT[A/T]ATTTGAGACAGGGTC | 8853 |
rs796648167 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9365220 | CTTTGGAGGCAGCAG[-/T]TTGGTCAAGCCCCTT | 8853 |
rs796676578 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9366857 | CTGCATCCTCCACTA[C/G]CCCACTAGCCCATTT | 8853 |
rs796714406 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266147 | CGATTGCCTTTTTAT[C/T]TTTTTTTTTTTTTTT | 8853 |
rs796723843 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9253745 | TGTATCTTTAGACCA[C/G]TCCTTTGCATTGCTG | 8853 |
rs796732909 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9368585 | CCCGAGCCCCGGGAG[A/G]CAGGGGAATAAGAAG | 8853 |
rs796737903 | multinucleotide-polymorphism | CAGTG/TGGCT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9360837 | ATTTTTAATAGTAGC[CAGTG/TGGCT]TTAACAGTTGGCTTG | 8853 |
rs796770791 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9386143 | TTTTCATGGTTTGGC[-/T]TTTTTTTTTTTTCTG | 8853 |
rs796782025 | in-del | AC/GCA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245499 | TTCTCAAAGTGATGA[AC/GCA]TTACCTTCTGTAACC | 8853 |
rs796790338 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229368 | TGTTGTCTTCACCCT[G/T]TGACCTCACTTGAGC | 8853 |