SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs10593 | snp | A/G | 0.340333 | 0.233109 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405901 | TGCTGGTCTGGAACA[A/G]TGACATTGCCAACTT | 8853 |
rs870732 | snp | A/G | 0.499396 | 0.0173617 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251490 | ACCCGACGGACATCA[A/G]GGATTAGCTGTTCTG | 8853 |
rs875053 | snp | A/T | 0.29789 | 0.24537 | intron-variant | ASAP2 | GRCh38.p7 | 2:9224994 | TTGAGTCAAGGTGCG[A/T]AAGTTGGAACATTGC | 8853 |
rs875054 | snp | A/C | 0.149999 | 0.229128 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226087 | GGTGAGACTAGCTCG[A/C]ATGAGGCAGCACACA | 8853 |
rs907161 | snp | G/T | 0.499989 | 0.00239614 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230920 | GGTCCTGTGTGACCT[G/T]GGAGGTGTGTGAGGG | 8853 |
rs907162 | snp | A/G | 0.35445 | 0.227135 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270500 | ATTATTATGCACTGC[A/G]TGCCTGTATCAAAAT | 8853 |
rs1136172 | snp | C/T | 0.5 | 0 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406135 | AGTGACAAACACACA[C/T]TGAAGGCCTGAGGAA | 8853 |
rs1138459 | snp | C/T | 0 | 0 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9405017 | TCTATTTTAACAATC[C/T]TCCTGCATCTGTATT | 8853 |
rs1139804 | snp | A/G | 5.01098e-05 | 0.00500524 | missense | ASAP2 | GRCh38.p7 | 2:9388532 | CCCCGCTTCCTCCAC[A/G]GAATGTTGGCAAAGG | 8853 |
rs1473022 | snp | A/G | 0.4021 | 0.198407 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244247 | GTTGCAGTGAGCCAA[A/G]ATCGCGCCACTGCAC | 8853 |
rs1510796 | snp | C/T | 0.499801 | 0.00998203 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256874 | GGTGGACAGGACAAG[C/T]GGCTAAGAGACAGTC | 8853 |
rs1858268 | snp | C/T | 0.102014 | 0.201495 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208017 | AATTTTCAACCAAGC[C/T]TCTTCGTTCCTACGT | 8853 |
rs1877098 | snp | C/G | 0.49962 | 0.0137727 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263920 | TAGAAGGCCAGGTGC[C/G]GTGTCTCACACCTGT | 8853 |
rs1962214 | snp | C/T | 0.19646 | 0.2442 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385581 | GAATGGCTAATTATG[C/T]ACTTATAGGCAGCCT | 8853 |
rs1995924 | snp | C/T | 0.499824 | 0.00938333 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256385 | GCTAATTTCTTTATG[C/T]ACAGTTGACACTGCC | 8853 |
rs1995925 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9256149 | ttGCAGGGGACCCTA[A/G]AATAGTTTTTCTCCT | 8853 |
rs2001296 | snp | A/G | 0.128632 | 0.218563 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366761 | TTTTTCCACGTGTCA[A/G]GGGCCGGGTTGAATT | 8853 |
rs2136841 | snp | C/G | 0.499928 | 0.00598999 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222789 | GTAGGAGAAATGGCC[C/G]TTCACCTTTTCCCAT | 8853 |
rs2136842 | snp | C/T | 0.499923 | 0.00618962 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222856 | CTTTTCCTTGGGGAC[C/T]GGGATGCTTATGCTG | 8853 |
rs2175335 | snp | C/G/T | 0.133777 | 0.221342 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222979 | TCCAGACCCTCCAAG[C/G/T]CCTGTGTTTTCTCTT | 8853 |
rs2271333 | snp | A/G | 0.498794 | 0.0245311 | intron-variant | ASAP2 | GRCh38.p7 | 2:9233121 | GAGATACGGCTTTGA[A/G]ACAGTTTGAGTCATC | 8853 |
rs2356779 | snp | A/G | 0.26271 | 0.249677 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251562 | GTCAGATGAGGTAAT[A/G]CGTTTTAGTAAAGTG | 8853 |
rs2666205 | snp | A/C | 0.0592355 | 0.161582 | intron-variant | ASAP2 | GRCh38.p7 | 2:9215988 | TTCAGCAGAGCTGCA[A/C]ATTGGACCTTCTGAG | 8853 |
rs2666206 | snp | A/G | 0.163892 | 0.234703 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241698 | GGAAAATTACAGTAC[A/G]TATCTTTGGTGAGGC | 8853 |
rs2666207 | snp | C/T | 0.499902 | 0.00698814 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241137 | CATCCAGATAcagta[C/T]taccctcttatccac | 8853 |
rs2666208 | snp | G/T | 0.49998 | 0.00319482 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240553 | aaaaatcattaactt[G/T]tgggaggggctgggc | 8853 |
rs2666209 | snp | C/T | 0.499897 | 0.00718776 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240042 | TGACTAGTTTTTTCA[C/T]CCTGACTTAATTTCT | 8853 |
rs2666210 | snp | A/G | 0.304188 | 0.244057 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271039 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACGAGGT | 8853 |
rs2666211 | snp | A/G | 0.153 | 0.230415 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270850 | agccgagatcgcgcc[A/G]ctgcactccagcctg | 8853 |
rs2666212 | snp | C/T | 0.438246 | 0.16451 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251499 | ACAAAACCCACCCGA[C/T]GGACATCAGGGATTA | 8853 |
rs2666213 | snp | C/T | 0.499984 | 0.00279548 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250300 | CAGGAAGTCTGTGGT[C/T]AAATACCATTTGCTG | 8853 |
rs2666214 | snp | A/C | 0.492087 | 0.0623997 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249683 | AATCTCAGCCCAGCG[A/C]CCAGTCTCACTCAGG | 8853 |
rs2666215 | snp | A/C | 0.0498117 | 0.149749 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249110 | GTGTGGCCTCAGCCA[A/C]AAGACAGCCTCTCAG | 8853 |
rs2666216 | snp | A/C | 0.174288 | 0.23826 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268479 | GGCCTGGCTTTATTC[A/C]CACAAGGGGGGAGGT | 8853 |
rs2666217 | snp | A/G | 0.163892 | 0.234703 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262711 | TTTTTAAAGGAACAC[A/G]GCACACAAATGTGAC | 8853 |
rs2666218 | snp | A/G | 0.411746 | 0.190626 | intron-variant | ASAP2 | GRCh38.p7 | 2:9262859 | GGAATCAAAGTCCTC[A/G]GTCTCTTTCACGCGG | 8853 |
rs2666219 | snp | C/T | 0.406123 | 0.195258 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263693 | GAGGCTGCAGCCTCT[C/T]GTTGTTCATGCGTCG | 8853 |
rs2709559 | snp | C/T | 0.431029 | 0.17242 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390671 | CTCCTTCCCATGGGC[C/T]GTGGGAGTCACCACC | 8853 |
rs2709560 | snp | C/T | 0.17461 | 0.238362 | intron-variant, synonymous-codon | ASAP2 | GRCh38.p7 | 2:9389915 | AGGATCTGGGAGAGG[C/T]GGGGAGAAAGCCGCA | 8853 |
rs2709561 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228274 | TGACATAAGTATATT[C/T]TTAACACTGAAGGAA | 8853 |
rs2709562 | snp | A/G | 0.446118 | 0.155041 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251851 | GCCCATCTCTGCTCC[A/G]TCCATCACTGCCAGA | 8853 |
rs2709563 | snp | A/G | 0.499968 | 0.00399348 | intron-variant | ASAP2 | GRCh38.p7 | 2:9251836 | ATCCATCACTGCCAG[A/G]AAACTCACATTCAGT | 8853 |
rs2709564 | snp | C/T | 0.155987 | 0.23165 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240178 | CTAGTTCAATATTAG[C/T]TGGCTGCAGGCATCC | 8853 |
rs2709565 | snp | A/C | 0.499996 | 0.00139776 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239912 | TTAAACATGACAAAA[A/C]CTCATCTCTACAAAA | 8853 |
rs2709566 | snp | A/C | 0.3748 | 0.216622 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239739 | CTCATCTAAAACAAA[A/C]AAAAAAAGATGCTGC | 8853 |
rs2709567 | snp | A/G | 0.5 | 0.00019968 | intron-variant | ASAP2 | GRCh38.p7 | 2:9244833 | CTCAGAAAGGATCTA[A/G]TGAAAAGGGTTTGCC | 8853 |
rs2709568 | snp | A/G | 0.499631 | 0.0135733 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243343 | AGGTGGGTGGATCAC[A/G]AGGTCAGGAGATCGA | 8853 |
rs2709569 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249012 | ATACATAGGATGCTA[A/G]AATTTTAGGTCTAGA | 8853 |
rs2709570 | snp | C/T | 0.494651 | 0.0514399 | intron-variant | ASAP2 | GRCh38.p7 | 2:9249337 | CCCATTCTGCCCTCA[C/T]GTCTCTAGAGAGGAC | 8853 |
rs2709571 | snp | A/G | 0.216048 | 0.247684 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367004 | GCAAAGGAGTTAACA[A/G]ACATGCTTTGGGAGA | 8853 |
rs2709572 | snp | C/G | 0.239326 | 0.249772 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366038 | GGGGCAGGAAGGTGG[C/G]TGTCGACCTGAGCCC | 8853 |
rs2709573 | snp | C/T | 0.243919 | 0.249926 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363687 | GCTACCCAGAAGGAT[C/T]GCATGAGCCTGGGAG | 8853 |
rs2709574 | snp | C/T | 0.195526 | 0.243993 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361606 | GACTCCAGCCTGGGT[C/T]ATGGAGTGAGACCCT | 8853 |
rs2709575 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361204 | TTTAAAACTCTGGAA[A/G]CAATTAGATTTTGAA | 8853 |
rs2709576 | snp | A/G | 0.448323 | 0.15221 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359248 | GAAATCGCTGGTGAT[A/G]AGGGAAAACAAGTAC | 8853 |
rs2709577 | snp | G/T | 0.0471551 | 0.14613 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367789 | GTGTTAATTTAATGT[G/T]TAACATGTCAGAAGA | 8853 |
rs2709578 | snp | A/T | 0.196149 | 0.244131 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368779 | AGAGCCTCACTCGCC[A/T]CTGGTGGGTGGAAGA | 8853 |
rs2709579 | snp | A/C/T | 0.0479342 | 0.147301 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369910 | gcaatgatgtgatct[A/C/T]ggctcactgcagcat | 8853 |
rs2709580 | snp | C/T | 0.427727 | 0.175821 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374444 | CCTGAATAAGAAGGG[C/T]GTGGAGGTGACGAGG | 8853 |
rs2709581 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387917 | aaggcagttttccct[C/G]ctctcgcttgctctc | 8853 |
rs2709582 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387916 | aggcagttttccctg[C/G]tctcgcttgctctct | 8853 |
rs2709583 | snp | A/C | 0.42666 | 0.176893 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382821 | tgtcaggcgactaca[A/C]ttggtgtatggggtc | 8853 |
rs2709584 | snp | G/T | 0.499563 | 0.0147699 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265521 | TTTGATAATTTTTTC[G/T]AATTAAAGAAAATGA | 8853 |
rs2709585 | snp | A/G | 0.173965 | 0.238157 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263212 | ACTAGCTCAGGAAAA[A/G]AATCACAAACAAGAG | 8853 |
rs2709586 | snp | C/T | 0.425123 | 0.178415 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377518 | GGACTCCCAGATCTG[C/T]GGTAAACTGCCTGTG | 8853 |
rs2709587 | snp | A/G | 0.488302 | 0.0755777 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260303 | CAGATTCTGGATCCC[A/G]CCTCATCCTCATGAC | 8853 |
rs2709588 | snp | C/G | 0.382085 | 0.212258 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259637 | AGGGGGCCTGAGAGC[C/G]CCAAGGAGCAAGGTG | 8853 |
rs2709589 | snp | C/T | 0.498774 | 0.02473 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258987 | GCAGGCCCAGGGTCC[C/T]GGTCTGGCCCCGCGA | 8853 |
rs2709590 | snp | C/T | 0.499984 | 0.00279548 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258715 | CTGTTCCTCAAGAGA[C/T]CTAAAGAAGTTGCAA | 8853 |
rs2709591 | snp | C/T | 0.49277 | 0.0596899 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356162 | AATTTAACACAGCGT[C/T]GCTCTTGTTTTTCTA | 8853 |
rs2709592 | snp | C/T | 0.35574 | 0.226537 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376131 | AGCTCAGAGCCTGCA[C/T]GGACATGCCTGTTAC | 8853 |
rs2709593 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9268751 | TGTCCCTTCTTCTCA[A/G]GCTGGCCTTTCGTCC | 8853 |
rs2709594 | snp | A/T | 0.17138 | 0.237316 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270431 | TCAGTATTTTTTTTT[A/T]AATTTTTGATTATTG | 8853 |
rs2709595 | snp | C/T | 0.472989 | 0.113031 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270828 | gacggagtctcgctc[C/T]gtcgcccaggctgga | 8853 |
rs2709596 | snp | A/G | 0.464309 | 0.12873 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271090 | GAGCCACCGCGCCCG[A/G]CCCTGTTTTCATTTT | 8853 |
rs2709597 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375481 | tgtaatcattccatg[A/G]tgtaaacatagatca | 8853 |
rs2715855 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376693 | CTTCTCATTTATTTC[C/T]CATGGAGTCAGGAGA | 8853 |
rs2715856 | snp | C/T | 0.177824 | 0.239355 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377427 | GATTAGAAACCAGAG[C/T]ACTGGATTATGGGTG | 8853 |
rs2715857 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381626 | ctgtagccccagtta[C/T]ccaggaggctaaggt | 8853 |
rs2715858 | snp | C/T | 0.425586 | 0.17796 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383619 | gcagaattcagaccc[C/T]tcccataatcctaat | 8853 |
rs2715859 | snp | C/T | 0.425894 | 0.177655 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384836 | tcttcccccagggta[C/T]agggtgagaccctct | 8853 |
rs2715860 | snp | C/G | 0.454722 | 0.143489 | missense | ASAP2 | GRCh38.p7 | 2:9388407 | AAACCTTGCCAAGGA[C/G]AAGCAGAGGGCTTTC | 8853 |
rs2715861 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, missense | ASAP2 | GRCh38.p7 | 2:9390139 | CCTTTTTCTTTTTGC[C/T]GTTCCTGTCCCTAGC | 8853 |
rs2715862 | snp | C/T | 0.0535932 | 0.154675 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390301 | GCCTTGCATTTGGGG[C/T]GGACCTGGCTCCCCA | 8853 |
rs2715863 | snp | C/T | 0.216649 | 0.247765 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353417 | TTAAAAATAGTGCAG[C/T]ATGGTGACATGTGCC | 8853 |
rs2715864 | snp | A/G | 0.24932 | 0.249999 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353832 | GGTGGAATTGGGGCC[A/G]GGGGCAGTGGCTCAC | 8853 |
rs2715865 | snp | C/T | 0.222035 | 0.248431 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354061 | TTCTGGGAGCTCATC[C/T]AATCCATTGCCTGCA | 8853 |
rs2715866 | snp | A/G | 0.448066 | 0.152544 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355520 | TAAAACTGTGCTGAC[A/G]CCAGCAGTATGTAAG | 8853 |
rs2715867 | snp | C/T | 0.21725 | 0.247846 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359667 | ATGTAGGGAATTTAA[C/T]GTCAAGAGCAATAGT | 8853 |
rs2715868 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | ASAP2 | GRCh38.p7 | 2:9359730 | TCCTCTCAAGGGGCC[A/G]TCAGTCTTATTGATG | 8853 |
rs2715869 | snp | A/G | 0.200801 | 0.245111 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360539 | CCGTCCCCAACAAAT[A/G]TTTAACAGTCAACTC | 8853 |
rs2715870 | snp | C/T | 0.239326 | 0.249772 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363197 | aaatccattcgtcca[C/T]tggtggcatttaggt | 8853 |
rs2715871 | snp | A/T | 0.0766824 | 0.180169 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363495 | AACAGGTGTGAGATG[A/T]TCGTGGTTTTAATTT | 8853 |
rs2715872 | snp | A/G | 0.239326 | 0.249772 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365058 | TGAGCACCAAAGCAT[A/G]TACTTACTTACATAT | 8853 |
rs2715873 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366154 | TCTATGGGCTGAAAC[A/G]TAAACTGGAACTTGG | 8853 |
rs2715874 | snp | C/T | 0.21695 | 0.247806 | intron-variant | ASAP2 | GRCh38.p7 | 2:9367284 | CCGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGG | 8853 |
rs2715875 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368020 | tTAGCTTTCCTGGCT[C/T]AGTGCCGCTTCACTC | 8853 |
rs2715876 | snp | G/T | 0.0726307 | 0.176182 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370640 | GCATTGGGGGCATGA[G/T]CGGGATGATGGGGTC | 8853 |
rs2715877 | snp | C/T | 0.193966 | 0.243639 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370654 | AGCGGGATGATGGGG[C/T]CAGACATGTGGTGCT | 8853 |
rs2715878 | snp | G/T | 0.490836 | 0.0670685 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375405 | TAGAATAAACTAGGG[G/T]TTTTTCTTTTCAGTA | 8853 |
rs2715879 | snp | A/G | 0.367913 | 0.220446 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375422 | TTTTCTTTTCAGTAG[A/G]AAAATAATTGTATCT | 8853 |
rs2952791 | snp | A/C | 0.446118 | 0.155041 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369001 | GTTATTGTTGATACA[A/C]AACTTGACGGAGAAG | 8853 |
rs2952792 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387248 | tttggccacccctgC[C/T]CCCCCCTGAAGGTTA | 8853 |
rs2953361 | snp | C/T | | | intron-variant, missense | ASAP2 | GRCh38.p7 | 2:9389928 | CCGCCTCTCCCAGAT[C/T]CTGCAGGCAGGCATC | 8853 |
rs3053782 | in-del | -/AA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266148 | aaaaaaaaaaaaaaa[-/AA]gataaaaaGGCAATC | 8853 |
rs3811594 | snp | A/G | 0.191775 | 0.243125 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388672 | CCCTTTAGGAAGCAA[A/G]CAGAAAATAACTACA | 8853 |
rs3811598 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327676 | GTATCGCCTGGATTC[C/G]GTAACCGTTTCTTTA | 8853 |
rs3811599 | snp | C/T | 0.333261 | 0.235728 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318331 | TGAATAGAGGGCTAA[C/T]GAAAAGTCTAGGTCT | 8853 |
rs3811600 | snp | A/G | 0.149514 | 0.228916 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297284 | CTGCAACAGAATGAC[A/G]GAGGTGCTGTGAGTC | 8853 |
rs3828264 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327465 | AGGTCCCTTACTTTA[C/G]GAACAATAACTGCTA | 8853 |
rs3938075 | snp | A/C | 0 | 0 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211304 | TGCTGCAACCAGAGT[A/C]TGCCCTGTGCTTTTG | 8853 |
rs4233868 | snp | A/G | 0.31357 | 0.241783 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362034 | AATTATGTCTGACAC[A/G]CCGTTAAGAACCATA | 8853 |
rs4294977 | snp | C/T | 0.203882 | 0.245709 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346940 | TGCCCCAGTTTTTGG[C/T]AGATAGTACGGTTAT | 8853 |
rs4305239 | snp | A/G | 0.431177 | 0.172264 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395701 | caagttccgcttccc[A/G]ggttcacaccattct | 8853 |
rs4312451 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343602 | CCAGCGCCTGCCACC[A/G]TACCTAGCTAATTTT | 8853 |
rs4392227 | snp | A/G | 0.318735 | 0.240365 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335208 | ATTTTGAAAGATTGC[A/G]GTTTTCACCCCATTC | 8853 |
rs4401187 | snp | C/T | 0.228842 | 0.249103 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352915 | ATCCCTCCTCCTTCC[C/T]TGCTTGTCTTCCAGT | 8853 |
rs4467242 | snp | A/G | 0.499824 | 0.00938333 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258458 | ACTAAAATGCAAGCT[A/G]TTTTAAAGGTGGTAC | 8853 |
rs4507066 | snp | G/T | 0.499968 | 0.00399348 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268003 | ACGCCCTCAGAAGCT[G/T]CCCCTGCCCTGACTG | 8853 |
rs4508567 | snp | C/G | 0.217851 | 0.247924 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353168 | TGATTCTGGCTGATT[C/G]AGGAGCATCTGTCTT | 8853 |
rs4560084 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388097 | TGTGTGTTTCCTTCA[C/T]GAGACACAAGGAGGA | 8853 |
rs4599081 | snp | G/T | 0.315758 | 0.241197 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373721 | GGGGAGCAGCCGCAT[G/T]TGTCCTCAGATTGTA | 8853 |
rs4610024 | snp | A/G | 0.490007 | 0.0699769 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294682 | CCCTTCCCTTTGGGT[A/G]TTCACTTAGAGCAAC | 8853 |
rs4627537 | snp | C/T | 0.333261 | 0.235728 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319277 | TTGTGGCTGCCTTCT[C/T]GGGAGACTCAAATTC | 8853 |
rs4632318 | snp | C/G | 0.109108 | 0.206518 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293516 | AGATCTTTCCAGAAA[C/G]TTTATTCCCAAGCTA | 8853 |
rs4640358 | snp | A/G | 0.333722 | 0.235565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267217 | ATATTGCATGATGCT[A/G]AGTTTTGGGGCATGA | 8853 |
rs4668615 | snp | A/G | 0.29789 | 0.24537 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283913 | attattatgcttccc[A/G]atggccccatctcca | 8853 |
rs4668616 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304549 | TAGGTGGGAGGGCTG[C/T]AGTTGTGGGGGTGTA | 8853 |
rs4668617 | snp | A/G | 0.181978 | 0.240568 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348527 | GCTAATACTTAATCT[A/G]TGTACTTAATATTTA | 8853 |
rs4668618 | snp | G/T | 0.496483 | 0.0417852 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387078 | GGGCTTGGTGGTGGG[G/T]GGGGGGGCGCCTGTA | 8853 |
rs4669380 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209599 | TTTGTTACGGAGTTT[C/T]GCTCTTGTTGCCCAG | 8853 |
rs4669381 | snp | A/G | 0.41441 | 0.188333 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282659 | ATCACGAGAATAAAG[A/G]CCAAAGGCAATTCCT | 8853 |
rs4669382 | snp | C/G/T | 0.0158469 | 0.0875917 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331150 | CTGTGCCCTGCTGGG[C/G/T]ACACGCGGGCCTCTG | 8853 |
rs4669383 | snp | A/G | 0.110872 | 0.20771 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345281 | AAAAGACATCTCAGT[A/G]ATTTTATTATTGAAA | 8853 |
rs4669384 | snp | A/G | 0.18134 | 0.240387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348893 | TAAGTCCAGGCAAGC[A/G]ACCGCCTTCCATGGA | 8853 |
rs4669385 | snp | C/T | 0.0820865 | 0.185216 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9350888 | GAAGTGCTTTGACCT[C/T]ATTTCACGTAAGGCT | 8853 |
rs4669386 | snp | A/G | 0.311859 | 0.242226 | intron-variant | ASAP2 | GRCh38.p7 | 2:9363036 | attttgcatataaat[A/G]agatcttgcaggatt | 8853 |
rs5829203 | in-del | -/A | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245500 | TCTCAAAGTGATGAC[-/A]GTTACCTTCTGTAAC | 8853 |
rs5829204 | in-del | -/A | 0.499824 | 0.00938333 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256418 | TTAACATGCTGTGCC[-/A]ATGATGATGCTGTCC | 8853 |
rs5829205 | in-del | -/A | 0.38286 | 0.211774 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260418 | TGGATTGTAGAAAAA[-/A]TGAAAGGTTCATGCC | 8853 |
rs5829207 | in-del | -/T | 0.0256215 | 0.110247 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295713 | ATCTGGTCTCAGAAA[-/T]TTCATTTAATTTATC | 8853 |
rs5829208 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307219 | TTTCTGATTCCGCAG[-/G]TCTGGGATAGGGCCC | 8853 |
rs6431991 | snp | A/G | 0.499937 | 0.0055907 | intron-variant | ASAP2 | GRCh38.p7 | 2:9226197 | ACACCAGAAATCAAC[A/G]TTATAATAAAACTCT | 8853 |
rs6431992 | snp | C/T | 0.499087 | 0.0213463 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235627 | GGGCACGTGAGCTGC[C/T]GTGGTAGCGTGCGGG | 8853 |
rs6431993 | snp | A/G | 0.499759 | 0.0109798 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9235882 | TGGGCTTAGGCAGAT[A/G]GAGCTGCTCCACCTG | 8853 |
rs6431995 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276263 | CTATCGTGGAGGTGG[C/G]AAGGCATCAGAGGCC | 8853 |
rs6431996 | snp | C/G | 0.369958 | 0.21934 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278145 | GCTTCATTTAGTTTT[C/G]ATAGGATAGCCTGTG | 8853 |
rs6431997 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349310 | CCCTAAAATTTGCAC[A/G]TGTACAGTTGTGTCA | 8853 |
rs6431998 | snp | A/C | 0.286564 | 0.247312 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378264 | AATGTGACAGTGGCC[A/C]TGTTTGCTAGGATTG | 8853 |
rs6431999 | snp | A/G | 0.335788 | 0.23482 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388043 | AGATTACAATTCGAG[A/G]TGAGATTTGGGTGGG | 8853 |
rs6706329 | snp | C/T | 0.0429648 | 0.14013 | intron-variant, missense | ASAP2 | GRCh38.p7 | 2:9389847 | ATGAAGCCACACAGT[C/T]GCATCTCCTCCCTGT | 8853 |
rs6710137 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295400 | GCTTTGAATAAGTGA[C/T]GCCTGTTGCTGCTGT | 8853 |
rs6710839 | snp | A/T | 0.245346 | 0.249957 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280986 | GCTGTGTCAGGGTTG[A/T]GTGCAGTGAGTGGCC | 8853 |
rs6712780 | snp | C/T | 0.430583 | 0.172886 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396372 | ctcgacctcctgggc[C/T]caggtgatcctccca | 8853 |
rs6715958 | snp | G/T | 0.131723 | 0.220251 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309395 | aaaaggcgtacatgc[G/T]ggatgattccagata | 8853 |
rs6715973 | snp | A/G | 0.132066 | 0.220435 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309427 | cgtatataaaattcc[A/G]gaaagtgcagtgttc | 8853 |
rs6716232 | snp | A/G | 0.131723 | 0.220251 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309621 | tcatactttaaatgt[A/G]tgtggtttattgtct | 8853 |
rs6717443 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9385212 | TGGCCGAGTGTATGA[G/T]CAACAGCACTGACCA | 8853 |
rs6719453 | snp | C/T | 0.499933 | 0.00579035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227317 | CCCTGCAGTGCCTGA[C/T]GCATGAGTGTTGTGC | 8853 |
rs6721798 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9386543 | CTAAGACTCATCCAC[C/G]CTGCTCACCTGATTC | 8853 |
rs6721935 | snp | C/T | 0.298905 | 0.24517 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399167 | AGACAGGGTTCATTC[C/T]GAGCAGCGAAGGGAG | 8853 |
rs6724010 | snp | C/G | 0.115438 | 0.210697 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281365 | CTGGCCCAGTGGCTG[C/G]CAGTACAGCTTATAA | 8853 |
rs6724103 | snp | C/T | 0.231482 | 0.249313 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344413 | GAGAAAGGGAAATTT[C/T]TCCAATTTTTGTTGT | 8853 |
rs6724124 | snp | C/T | 0.164546 | 0.234942 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404643 | AAATTTGCATATAGG[C/T]TTGGAAAGTGAGGCA | 8853 |
rs6724714 | snp | C/T | 0.427879 | 0.175668 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375028 | TCCAGTACTTTACTT[C/T]AGGAGGCCAAGGCGG | 8853 |
rs6725109 | snp | C/T | 0.46703 | 0.124089 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259286 | TGAGAATAAATGGCC[C/T]TTGCTGACCCTAGCA | 8853 |
rs6725215 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399555 | GATGGGGCTTGAGCC[C/T]GTGGTCAGCCACATT | 8853 |
rs6727610 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287837 | TGTGGAATCCTGTCC[A/G]CAGTGACCACTGCAT | 8853 |
rs6727761 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229492 | GACAGGAGAAATAGC[C/T]GTCCCCCTTGGGCAC | 8853 |
rs6728908 | snp | A/G | 0.0738231 | 0.177374 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9393645 | GAAGAAGCCTGCGCC[A/G]GGGTAAGCCACCCCC | 8853 |
rs6729267 | snp | C/G | 0.0748431 | 0.178382 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275319 | aaacattcttcccac[C/G]ttggcctcccaaagc | 8853 |
rs6730743 | snp | A/G | 0.33693 | 0.2344 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389165 | AAACCAAAGCTCTCA[A/G]AAGTTAAGTAATTTG | 8853 |
rs6731034 | snp | C/T | 0.430434 | 0.173042 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396566 | acaggcatgaggcac[C/T]gcgcctcacctcttt | 8853 |
rs6731175 | snp | C/G | 0.256897 | 0.249905 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270823 | tttgagacggagtct[C/G]gctccgtcgcccagg | 8853 |
rs6733940 | snp | A/G | 0.029116 | 0.117091 | intron-variant | ASAP2 | GRCh38.p7 | 2:9389498 | AGGGTGGCTGAGGCC[A/G]GGAGACCTGGCCCAG | 8853 |
rs6736216 | snp | A/G | 0.417521 | 0.185571 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303714 | TTGTTTGATCGAGAC[A/G]ATGAACAAATAAGGC | 8853 |
rs6736437 | snp | A/G | 0.343701 | 0.231776 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303885 | TTGGGCAAAGATAGC[A/G]TGGTGAGGCCTTGGG | 8853 |
rs6736998 | snp | A/T | 0.5 | 0.000399361 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227273 | ATGTGCTCTGTGAAG[A/T]GGGGGACTTGGGGTT | 8853 |
rs6737102 | snp | C/T | 0.271162 | 0.249103 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227327 | CCTGACGCATGAGTG[C/T]TGTGCTGACCCTCCC | 8853 |
rs6739246 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303742 | GGCTGGTGTCAGATA[C/T]CTACATTTTGGTTGT | 8853 |
rs6739854 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9313196 | GCCGACCAAGTGGGT[A/C]TGCATGTCCGTGGAG | 8853 |
rs6740258 | snp | C/T | 0.279991 | 0.248195 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378514 | CAGCCTCCGTCCTCC[C/T]GTGGGACAGGATGGA | 8853 |
rs6740880 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9314059 | tgtcatcttggctca[A/C]tgcaacctccgcctc | 8853 |
rs6741052 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329493 | TTATGAAAAGGCAAA[A/G/T]CAGTGATGGGGAGAG | 8853 |
rs6742922 | snp | C/T | 0.221737 | 0.248397 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399534 | GTGCTGGCCCAGAGG[C/T]TCATGGATGGGGCTT | 8853 |
rs6743955 | snp | C/T | 0.412416 | 0.190055 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299303 | tcagaatcagaatgg[C/T]ggtgaacttctcagc | 8853 |
rs6744570 | snp | C/T | 0.408017 | 0.193729 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284718 | TGCCATGGGTGTGGG[C/T]GGGTAATAGGTGCCC | 8853 |
rs6744693 | snp | C/T | 0.499154 | 0.0205497 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254731 | aaaacccagtatata[C/T]aggatttggtactgt | 8853 |
rs6746487 | snp | A/G | 0.195083 | 0.243894 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237748 | GGCTAGATTCTGAGC[A/G]ACCAGGAGACTGAGT | 8853 |
rs6747915 | snp | A/G | 0.308661 | 0.24302 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228091 | TTGAAATGGAATGGG[A/G]GTGAATCTTTTAATA | 8853 |
rs6747946 | snp | C/T | 0.0970103 | 0.197722 | upstream-variant-2KB, nc-transcript-variant | ASAP2, LOC100506317 | GRCh38.p7 | 2:9205259 | CAGCATATTCCCTCA[C/T]GTCAAAAACTGTAGC | 8853 |
rs6748624 | snp | A/G | 0.304937 | 0.243889 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402090 | TGGCACAGCTCCGCA[A/G]CTGAGCTCAGAGCAG | 8853 |
rs6751628 | snp | C/T | 0.130694 | 0.219696 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402030 | GGCTTGAATGGGGCG[C/T]GGACAGAAAGCCCCA | 8853 |
rs6753873 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299186 | TCTCCAAGTTGAGAG[A/G]CTCACAAGTACCCAG | 8853 |
rs6755161 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313587 | CGGACAGCGACTCTA[A/G]TCCTCCCTGTAGGCT | 8853 |
rs6755900 | snp | G/T | 0.358728 | 0.225118 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229883 | GCCAGGCTGTTGGGG[G/T]CATTTGTGGGCCTGG | 8853 |
rs6758064 | snp | C/T | 0.276267 | 0.248616 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217739 | TCTGTCTCCGCCTCC[C/T]GAGTAGCTGGGACTA | 8853 |
rs6758158 | snp | C/T | 0.452597 | 0.146474 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313569 | GCTGCCCCCGCCAGC[C/T]GCCGGACAGCGACTC | 8853 |
rs6758205 | snp | A/G | 0.248471 | 0.249995 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240209 | tttgccttcaatcac[A/G]acatgtctctgttca | 8853 |
rs6758558 | snp | C/T | 0.16911 | 0.236552 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393777 | ACATAACTAATTCAT[C/T]GGGGCTGAAGGGTCT | 8853 |
rs6759684 | snp | C/T | 0.168135 | 0.236216 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263579 | CTCTAAGATAGGGAT[C/T]CTGGCGAAGCCCATG | 8853 |
rs6760513 | snp | A/G | 0.110167 | 0.207236 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309771 | agcaagtctctagcc[A/G]catgtgactattgca | 8853 |
rs7424162 | snp | G/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322169 | CAAAGGGTCTCCTGT[G/T]TGTTTATTTTTCACT | 8853 |
rs7558333 | snp | C/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279891 | ATATATTTACACATA[C/T]ATATTTTTTAAACCC | 8853 |
rs7559179 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348085 | AGATGAAACCGTTCT[A/G]TATCTCAATTAACTG | 8853 |
rs7559731 | snp | C/T | 0.499801 | 0.00998203 | intron-variant | ASAP2 | GRCh38.p7 | 2:9219206 | TTTTCTTATATCCAG[C/T]GAGCTTCCTAGATTT | 8853 |
rs7561296 | snp | A/G | 0.330714 | 0.236612 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383776 | cccaaatgtctgtca[A/G]tgatagactggatta | 8853 |
rs7562705 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290467 | tgcccatctcggcct[C/T]ccaaagtgctgggat | 8853 |
rs7562917 | snp | C/T | 0.412583 | 0.189912 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290602 | AAGTTTTATTTATTC[C/T]TTACGTTGTTATTAT | 8853 |
rs7564293 | snp | C/T | 0.19334 | 0.243495 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351540 | GGCAGGGTTAGAGTC[C/T]AGGGGAAGAAAGGGC | 8853 |
rs7564980 | snp | A/G | 0.499824 | 0.00938333 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257255 | GGTTCAGCTAATGAA[A/G]AGTCTCAATTGCCTT | 8853 |
rs7565731 | snp | A/G | 0.330714 | 0.236612 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383066 | tgaaatcataagagt[A/G]tgagaaacagccctt | 8853 |
rs7567672 | snp | A/G | 0.331874 | 0.236213 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280003 | TATTTTTTAAAAGTC[A/G]TTAAGTGACTATATA | 8853 |
rs7568731 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257981 | GGTTGGAGAGTCATG[C/T]GCCATAATCTGTGTG | 8853 |
rs7569295 | snp | C/T | 0.323671 | 0.238899 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327686 | GTTACGGAATCCAGG[C/T]GATACTAAGTGTCGA | 8853 |
rs7570823 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364800 | AACAGGAAATTGACT[A/C]TCAGTGGTCATTTAC | 8853 |
rs7571556 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294513 | TGCACCGATcctcct[A/G]ccaactctatggtct | 8853 |
rs7573908 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365182 | TTTTCCCTGCACACC[A/G]GAGTGTCCTTTTGTG | 8853 |
rs7577674 | snp | A/G | 0.499831 | 0.00918375 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257723 | ATGGGGTTTCACCAC[A/G]TTGGCTAGGCTGGTC | 8853 |
rs7578783 | snp | A/C | 0.493703 | 0.0557558 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406060 | ACCTCTGTGACATCT[A/C]GTCTTCCTCAGGCCT | 8853 |
rs7580743 | snp | C/T | 0.450734 | 0.149016 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330863 | TTTATGGACATGATC[C/T]CAGTAACCTTTAAAA | 8853 |
rs7581593 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258894 | GGACTCAGCATTTTA[A/G]AGTCTGTAGGTCCAT | 8853 |
rs7582857 | snp | A/G | 0.35207 | 0.228214 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327598 | GACTGTCTTATTATT[A/G]GGAGTTTTTGGCACT | 8853 |
rs7583426 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9363002 | ctgctctctacttct[A/G]tgagttcagcttttt | 8853 |
rs7583670 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341910 | GTTCATTTCTCCCCT[C/T]CTGGGCTCTGCTTGT | 8853 |
rs7583915 | snp | A/G | 0.406986 | 0.194565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294727 | CTCCTCTTGGTTTGA[A/G]GGACACCACGAGGCT | 8853 |
rs7584756 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397752 | tatatatatatatat[A/T]ttttttttttttttt | 8853 |
rs7586595 | snp | C/T | 0.118547 | 0.21265 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348116 | ATGACACTTTTTTGT[C/T]TGTTTGTTTGTTTGT | 8853 |
rs7587474 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343579 | agcctcccgcatacc[C/T]gggactaccagcgcc | 8853 |
rs7588636 | snp | A/G | 0.412583 | 0.189912 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290649 | TAGTTTAGAAAATTT[A/G]GAAAGTTCAGAAAAG | 8853 |
rs7588846 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383929 | cagaaaaccaaacac[C/T]gcacgttctcactca | 8853 |
rs7588849 | snp | C/T | 0.320096 | 0.239972 | intron-variant | ASAP2 | GRCh38.p7 | 2:9383933 | aaaccaaacaccgca[C/T]gttctcactcatagg | 8853 |
rs7589827 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336215 | TTTGCATAAATATTA[A/G]GGAAGTGGACATTTT | 8853 |
rs7589919 | snp | A/C | 0.489492 | 0.0717183 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370085 | CCTCGTGATCTGCCC[A/C]CCTTGGCCTCCCAAA | 8853 |
rs7590312 | snp | G/T | 0.0655868 | 0.168795 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336657 | ATTTAGTGCTAGAAA[G/T]GACCTACAACATGGT | 8853 |
rs7594724 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279860 | CTAGATTTACACATA[C/T]ATATTTTTTACACAT | 8853 |
rs7596570 | snp | A/G | 0.450859 | 0.148847 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341297 | AGTCACCTAGAGGAT[A/G]CTGAAGTAATTCGCA | 8853 |
rs7596770 | snp | A/G | 0.147991 | 0.228242 | intron-variant | ASAP2 | GRCh38.p7 | 2:9276528 | AAGCCTTCCTGTGTC[A/G]TCTTTTTTTTCTCTT | 8853 |
rs7598144 | snp | A/G | 0.450483 | 0.149354 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331955 | GGGCGGGTGTCACAG[A/G]CAGACCCCATCAGCA | 8853 |
rs7598230 | snp | C/T | 0.296619 | 0.245615 | intron-variant | ASAP2 | GRCh38.p7 | 2:9215614 | caagtttatggaccc[C/T]ctggattcagacaga | 8853 |
rs7600712 | snp | C/T | 0.201418 | 0.245234 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351457 | TTTACTCAGCACCCC[C/T]TAAATTAAAGGGCCC | 8853 |
rs7600853 | snp | G/T | 0.261056 | 0.249755 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271603 | GCAAAGGAGTTTAAA[G/T]AGTGGAGGTTCTGGA | 8853 |
rs7602301 | snp | A/G | 0.322245 | 0.239334 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269414 | gtgtgcccacccTGA[A/G]CCAGGTCATCTCCTC | 8853 |
rs7605562 | snp | A/G | 0.132066 | 0.220435 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275915 | TATTGTTTTAACgtg[A/G]cacttagccacattt | 8853 |
rs7605582 | snp | A/G | 0.452227 | 0.146984 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275961 | CACGTGCTGGTAGCT[A/G]CTGTAGTGGATGGCT | 8853 |
rs7605589 | snp | A/G | 0.45235 | 0.146814 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275973 | GCTGCTGTAGTGGAT[A/G]GCTGTGGCCTAGAGG | 8853 |
rs7609466 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331263 | ACTACGTAGATATGC[A/G]TTATTTTGCTTTTTC | 8853 |
rs9287705 | snp | G/T | 0.289165 | 0.246913 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213126 | AGTCATGCATAACAT[G/T]GGGATAGAAAGTGGT | 8853 |
rs9677219 | snp | C/T | 0.313082 | 0.241911 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369030 | AGCTTTTTTTTTTTT[C/T]TCTGGGAGACGGAGT | 8853 |
rs9679129 | snp | A/G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387077 | cgggcttggtggtgg[A/G/T]tgggggggcgcctgt | 8853 |
rs9710920 | snp | A/T | 0.17332 | 0.23795 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395489 | tcaaaaataaaaaaa[A/T]aaagaaTTTGGAGAC | 8853 |
rs10153575 | snp | C/G | 0.406986 | 0.194565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296975 | GGCTGAGTCTGGTGA[C/G]TTGTGCCATCATTTG | 8853 |
rs10153576 | snp | G/T | 0.154661 | 0.231107 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297022 | CGGAGAGGTGGAAAT[G/T]TTGTGTGTCCTTGGC | 8853 |
rs10164433 | snp | C/G/T | 0.0158557 | 0.0876905 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302503 | tgtttgaaacagagt[C/G/T]tcactgtgtcgccca | 8853 |
rs10164744 | snp | C/G | 0.414905 | 0.187899 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290242 | AGATGGAGTCTCGCT[C/G]TGTCACCCAGGCTGG | 8853 |
rs10164869 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290407 | taaagattgggtttc[A/G]ccctgttggccaggc | 8853 |
rs10165366 | snp | C/T | 0.128632 | 0.218563 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377997 | CTCCATGCACATTTT[C/T]AGGGGGCAGGAGAGG | 8853 |
rs10166341 | snp | A/G | 0.133093 | 0.220981 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394269 | TCCAGGGTTCTTGCC[A/G]TTCTCCTGCCTGAGC | 8853 |
rs10166616 | snp | A/G | 0.4941 | 0.0539917 | intron-variant, downstream-variant-500B | ASAP2, LOC107985851 | GRCh38.p7 | 2:9215189 | ttacagtatttatgt[A/G]tggtatttgtgtatc | 8853 |
rs10169339 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | ASAP2 | GRCh38.p7 | 2:9336948 | CTGCTGGGGCCAAAT[A/G]GCCCTCTGGGCACAG | 8853 |
rs10169465 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337046 | AACTGGTTATTTACA[A/G]CTTCGCAGGAAAGTA | 8853 |
rs10169849 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395430 | cagggagctgagatc[A/G]cgtcattgtactcca | 8853 |
rs10170027 | snp | A/G | 0.146314 | 0.227484 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300460 | TGTTACAGCTGGTAC[A/G]TTGCTCACCACCCTG | 8853 |
rs10170149 | snp | C/T | 0.480107 | 0.0977272 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279286 | GTCTCAGCACAGACA[C/T]GGTTTAATGACTGTA | 8853 |
rs10172687 | snp | A/T | 0.412249 | 0.190198 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300773 | AACACTCCAAACCCA[A/T]GTTGTTGTCATTGTG | 8853 |
rs10173551 | snp | G/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406143 | GCCTTCAGTGTGTGT[G/T]TGTCACTGAGTGGAC | 8853 |
rs10174135 | snp | C/G | 0.456095 | 0.141508 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274943 | GTAAATGATCAGGGA[C/G]GGGTGTGTCCCATGA | 8853 |
rs10174704 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293126 | CCAGTAAACTAAAAA[A/G]CACACAACAAAACCT | 8853 |
rs10177742 | snp | A/G | 0.406986 | 0.194565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293800 | AAAATCCCCAACTAG[A/G]CCAGTGCACAAAGAT | 8853 |
rs10177932 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326872 | ATCTTCTTTTCTGTT[C/T]ATCTTTGTAAACTTT | 8853 |
rs10178636 | snp | C/T | 0.418491 | 0.184691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301856 | TGAGACGGAGTCTCG[C/T]TCTGTTGTCCAGGCT | 8853 |
rs10179415 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302639 | gccaccacacccagc[C/T]aagttttgtattttt | 8853 |
rs10179475 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9287633 | AACTGGGTGAGCAGA[C/G]TGAGCGGCGAGCTGG | 8853 |
rs10179619 | snp | C/T | 0.265727 | 0.249505 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281792 | CCTTTCCCAATTCAT[C/T]TGTCGATGAAACTGT | 8853 |
rs10179702 | snp | A/G | 0.21875 | 0.248039 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273084 | tctatttctgtgaag[A/G]aaagcattggtattt | 8853 |
rs10180856 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300597 | TGATGAGCACCCACC[A/G]GTGTAGCAATCACTG | 8853 |
rs10180881 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335535 | CCTACCCTGACATAC[A/G]TGGACTCTGCCCCTT | 8853 |
rs10181337 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325196 | CATATCATGTGTAGT[A/G]TAAGAGGTTGCATTC | 8853 |
rs10181704 | snp | G/T | 0.451732 | 0.147663 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325558 | GACTACTTAAAATGC[G/T]TACTGAATTTTGACA | 8853 |
rs10181884 | snp | G/T | 0.115788 | 0.21092 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278715 | GCTGAATATTATATA[G/T]GAGAGTACCTCTATC | 8853 |
rs10181930 | snp | A/G | 0.133777 | 0.221342 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376263 | CAGGGCAGGCGGCCT[A/G]GGAAGCACCTTCCTT | 8853 |
rs10182138 | snp | A/G | 0.136506 | 0.222754 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376464 | AGCATTCGTAGCCTT[A/G]TCTGTAAGTGTAGAA | 8853 |
rs10183519 | snp | A/G | 0.456095 | 0.141508 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274619 | TGAGCCACCGCGTCC[A/G]GCCTAACACTCAATC | 8853 |
rs10183546 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301005 | CCAGAGGAAGGCCCA[G/T]TGGCGGCTCCTGCAA | 8853 |
rs10184450 | snp | C/T | 0.159292 | 0.232964 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388964 | AGCTCATGGCCCCTG[C/T]GATTACTTCTTACCC | 8853 |
rs10185363 | snp | C/G | 0.46754 | 0.123192 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329672 | GATGACGATGGCCCA[C/G]CTGGCTTCGTGACAG | 8853 |
rs10186044 | snp | A/G | 0.232651 | 0.249397 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345703 | GTGTGAGTGGATGAT[A/G]GTAACCGTCTTTCCT | 8853 |
rs10186062 | snp | A/G | 0.393065 | 0.205018 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402157 | TTCTTTGTCGAGTGC[A/G]AGGAGTTTGGACACT | 8853 |
rs10187824 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329755 | TGCCTGTCTGCTTAC[C/T]TTCCCAGAGCAGGCT | 8853 |
rs10188737 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250930 | TTAAAACAGTGAACT[A/G]TGAAACGAGGCGTGG | 8853 |
rs10189014 | snp | G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275089 | ATTTGTCTGTTTTTT[G/T]TTTTTTTTTAAGAGA | 8853 |
rs10189139 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355802 | ATTGAATAGCTTCAG[A/T]TTTTAGAAGCGGCGT | 8853 |
rs10190411 | snp | A/G | 0.181978 | 0.240568 | intron-variant | ASAP2 | GRCh38.p7 | 2:9272982 | aagtaaggtaatgtg[A/G]ttcctccagttttgt | 8853 |
rs10191238 | snp | A/G | 0.407845 | 0.193868 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287205 | GTGGAGAAAACAAGC[A/G]GCAACGTGGGGAACA | 8853 |
rs10191814 | snp | A/G | 0.0634278 | 0.166406 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379072 | TAGGTGAGTGGGCCC[A/G]GGCCCCGGGGGTGGG | 8853 |
rs10192441 | snp | A/C | 0.412416 | 0.190055 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282397 | TCTCCTGTCATGTTG[A/C]TGACATCATTCACAG | 8853 |
rs10192751 | snp | G/T | 0.183568 | 0.241012 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278977 | GTAACCAAGGAGAAC[G/T]GAGGGTTCGGCTGGA | 8853 |
rs10192759 | snp | A/G | 0.180702 | 0.240204 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279005 | GGAGTAATTCACTTC[A/G]CTGCAGAGGGCTCAC | 8853 |
rs10193043 | snp | A/G | 0.311224 | 0.242395 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9279282 | CGTGGTCTCAGCACA[A/G]ACACGGTTTAATGAC | 8853 |
rs10193254 | snp | A/G | 0.178144 | 0.239451 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279454 | TGAAGTCCTGGTACC[A/G]TAATATTGATGACCA | 8853 |
rs10193503 | snp | C/T | 0.301177 | 0.244706 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396963 | GCCAAGATCACACCA[C/T]TGCACTCCAGCCTGG | 8853 |
rs10194649 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331960 | GGTGTCACAGACAGA[A/C]CCCATCAGCAGACAC | 8853 |
rs10195639 | snp | A/G | 0.499995 | 0.00159744 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218273 | GCAGTCCCCATTGTC[A/G]CTGAATGTGATTGCC | 8853 |
rs10196137 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9375127 | aaaaaaaaaaaaaaa[A/G]taaaattggccaggc | 8853 |
rs10196837 | snp | G/T | 0.232651 | 0.249397 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345672 | TAGTAGTGCATGCAA[G/T]CCAGCAGCCTTGGGC | 8853 |
rs10197626 | snp | C/T | 0.415563 | 0.18732 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312779 | TTTTTGTTTCCTAAC[C/T]CATCCGTACACCCCC | 8853 |
rs10200085 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329937 | TCCTCCTGTGTTGCC[A/G]CCACACCGTCTGCTT | 8853 |
rs10200904 | snp | A/G | 0.128976 | 0.218754 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387244 | CATATAACCTTCAGG[A/G]GGGAGCAGGGGTGGC | 8853 |
rs10200984 | snp | C/T | 0.040671 | 0.13668 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339662 | GGATACTGCTGCTGT[C/T]GTTGTGTGTGACATA | 8853 |
rs10202068 | snp | A/T | 0.161924 | 0.233971 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395783 | tggccaattttttat[A/T]tttttagtagagatg | 8853 |
rs10202390 | snp | A/G | 0.312104 | 0.242163 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311737 | TGCTGGACACACAGA[A/G]GAAGCCCAGAGCCTG | 8853 |
rs10203328 | snp | G/T | 0.33303 | 0.235809 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319857 | GCCTTTCTATTTCTG[G/T]CGTTGGGCTTAAAGC | 8853 |
rs10204214 | snp | C/T | 0.215314 | 0.247582 | intron-variant | ASAP2 | GRCh38.p7 | 2:9400720 | ATGGGATGTCTTAAG[C/T]TGCTTCATTTTTGCC | 8853 |
rs10204847 | snp | A/G | 0.41408 | 0.188621 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291507 | GAGGAAATGGTCTCC[A/G]CTGTGCAGAGTTGTG | 8853 |
rs10205660 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258503 | GTATCTAGAAGCTCA[A/G]AGGAGAAGTGGCTCA | 8853 |
rs10206005 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337168 | AAATGAACCTCCTTT[A/G]CTATTCTTCTTTGGC | 8853 |
rs10206011 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217972 | ATTTCATTTCTCTGA[A/G]CTTTAATTCTGTATT | 8853 |
rs10206331 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218301 | GCCTGGAGGTCATCA[A/G]ACACTAACTCCTGGG | 8853 |
rs10206519 | snp | A/C | 0.181978 | 0.240568 | intron-variant | ASAP2 | GRCh38.p7 | 2:9346453 | AAAAAAAAAAAAAAG[A/C]CATTCTTTCCATGCG | 8853 |
rs10207470 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291799 | GGGCTGGGTAGCCAT[A/G]AGGCTGGTGCACCCT | 8853 |
rs10208073 | snp | A/G | 0.32627 | 0.238082 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292375 | ATACAAAAATTAGCC[A/G]GAAGTGGTGGTGTGC | 8853 |
rs10208656 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337310 | GCAAGTTGGACAATC[C/T]TTGAACACAGTTGCA | 8853 |
rs10208740 | snp | C/T | 0.36606 | 0.221428 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337422 | ATTTGCAATAAGAAT[C/T]GATCATTTGGTCATT | 8853 |
rs10208888 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9391758 | ttttttttttttttg[G/T]atttttagtagagat | 8853 |
rs10208984 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354621 | actccactccaacct[A/G]ggcagcagagtgaga | 8853 |
rs10210194 | snp | C/T | 0.172997 | 0.237846 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402086 | CAAGTGGCACAGCTC[C/T]GCAACTGAGCTCAGA | 8853 |
rs10210443 | snp | C/T | 0.32627 | 0.238082 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292294 | GGAGGCTGAGGAGGG[C/T]GGATCATGAGATCAG | 8853 |
rs10210616 | snp | A/G | 0.132409 | 0.220618 | intron-variant, synonymous-codon | ASAP2 | GRCh38.p7 | 2:9390032 | TGTCACGGGAGGAAA[A/G]ATTTTATTTTGTTCC | 8853 |
rs10210653 | snp | A/C | 0.467642 | 0.123012 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322820 | TTACTAGAGGGCAGG[A/C]AGGCTCTGAATGCTG | 8853 |
rs10210949 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301820 | GTGTGTATCCATCAt[C/T]ttttttttttttttt | 8853 |
rs10210957 | snp | C/T | 0.195526 | 0.243993 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9277662 | CCTTTGTTAACATCC[C/T]GCACTACAAGTGGTA | 8853 |
rs10211017 | snp | A/G | | | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390423 | ATGGGGTCACACCTA[A/G]CACCTGGGCCCTGTG | 8853 |
rs10211042 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301846 | tttttttttttgaga[C/T]ggagtctcgttctgt | 8853 |
rs10439230 | snp | C/T | 0.195837 | 0.244062 | intron-variant | ASAP2 | GRCh38.p7 | 2:9277205 | TGAGAGCTGTGCTGT[C/T]TGACATGTGGTCTAA | 8853 |
rs10519965 | snp | C/G | 0.100944 | 0.200705 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212253 | AAGAGGAACAGAATC[C/G]TGTAAACAAATCAGT | 8853 |
rs10803699 | snp | A/G | 0.345704 | 0.230956 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304912 | TAGTGGGGTGTAGAT[A/G]TTAGTGGAGAGGCTG | 8853 |
rs10929571 | snp | C/T | 0.405603 | 0.195673 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270947 | acaggtgcccgccac[C/T]acgcccggctaattt | 8853 |
rs10929573 | snp | C/T | 0.186105 | 0.241697 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347120 | ATCCTGCAGGGGTGG[C/T]AGGTGGGGCTGTCTT | 8853 |
rs10929574 | snp | C/T | 0.231189 | 0.249291 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347507 | CACATAGCTGCGAAG[C/T]AGGTCTTTAAGAAAT | 8853 |
rs10929575 | snp | C/G | 0.231482 | 0.249313 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347875 | AGAAAGAAGAAAACA[C/G]CTTCCTTCTAAAAGC | 8853 |
rs10929576 | snp | G/T | 0.130351 | 0.219509 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349886 | TAATCCCAAATTCAG[G/T]TTTTTTTCATCTTGA | 8853 |
rs10929577 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368990 | TTTGTGTTTGTGTTA[C/T]TGTTGATACACAACT | 8853 |
rs10929578 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370405 | TTGAGAATTGGATAA[C/T]GTGTGGTTTTACATA | 8853 |
rs11537588 | snp | C/G/T | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404910 | TAAAGCACTACATCT[C/G/T]TTTTCACTAATTGTT | 8853 |
rs11537589 | snp | A/G | 0.168785 | 0.236441 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403723 | ATTATTATTTTAGGC[A/G]GCCAGTGAACTGCTG | 8853 |
rs11674007 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385625 | AAAGGTGTGTGTGGC[C/G]GGGGGGTTGATTCCA | 8853 |
rs11674019 | snp | A/G | 0.183568 | 0.241012 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338761 | ATTGGGGTGCAGTGT[A/G]ATGAGAGCACTCGTG | 8853 |
rs11674625 | snp | A/C | 0.414576 | 0.188188 | intron-variant | ASAP2 | GRCh38.p7 | 2:9403092 | TGTGGTGAGGAAAAA[A/C]GGACAAAAATCATTT | 8853 |
rs11674903 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278437 | agaattgcttgaacc[C/T]aggaggcagaggctg | 8853 |
rs11674905 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278444 | cttgaacccaggagg[C/T]agaggctgcagtgag | 8853 |
rs11674936 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293838 | GACCTCAACTGGTAC[A/G]GTGTGAGCATCAGAA | 8853 |
rs11674949 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278552 | acaaaGGACTTTTTA[C/G]CTTTGTATCTGTTGT | 8853 |
rs11676012 | snp | A/G | 0.333491 | 0.235646 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299886 | ccataaggtcagtca[A/G]tgtcatccccacttt | 8853 |
rs11676283 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344232 | GGGAGCCTCATGTCA[C/T]TGTCAGGGGGTTAAG | 8853 |
rs11676340 | snp | G/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324554 | caggacatcacatgg[G/T]gggggcctcacaaga | 8853 |
rs11676717 | snp | A/C | 0.168785 | 0.236441 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406172 | GCCTCTGTGACATCT[A/C]GTCTTCCTCAGGCCT | 8853 |
rs11676816 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231784 | TCTCTGTGCCGTCTC[A/G]CATGCCATCCTTGAG | 8853 |
rs11676820 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291972 | AGCAAATGAAGAAAC[A/G]GTTTTTGCTGTGGGa | 8853 |
rs11677305 | snp | G/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232726 | GGCAACTACAGCTTA[G/T]ATTGCAGGGAGTGAG | 8853 |
rs11677445 | snp | A/G | 0.426507 | 0.177046 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397908 | ggactacaggcgccc[A/G]ccaccacgcccggct | 8853 |
rs11677488 | snp | C/T | 0.131038 | 0.219882 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380417 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 8853 |
rs11677929 | snp | C/G | 0.311369 | 0.242351 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310383 | AAAGCTGATTATCCT[C/G]GAAGAGAGTTGGATT | 8853 |
rs11678359 | snp | C/T | 0.0807149 | 0.183963 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210151 | ggactttgaacttgg[C/T]tcctgctgttttcag | 8853 |
rs11678445 | snp | C/T | 0.273856 | 0.248859 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245839 | TTCTTCGCCACCAGA[C/T]CCCCAGTGCCCAGAG | 8853 |
rs11678891 | snp | C/T | 0.375 | 0.216506 | intron-variant | ASAP2 | GRCh38.p7 | 2:9225754 | AGCATTGGCCACTGC[C/T]GTGGGAAGTGGTTGT | 8853 |
rs11679067 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | ASAP2 | GRCh38.p7 | 2:9301478 | TTTCCTCTTCCCCAA[A/T]GGATGTGAGAATCCT | 8853 |
rs11679398 | snp | G/T | 0.133093 | 0.220981 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376787 | ACTCTATGTAAGAGA[G/T]AAGTTTCTCGAAGGG | 8853 |
rs11680394 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9247731 | GGAGTAGGTGTTCAG[G/T]GAATGCAGAAGCTAT | 8853 |
rs11680400 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9223781 | GTGCCCTACAGCTAA[A/G]GCCAATGGGAGGGAG | 8853 |
rs11680620 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278438 | gaattgcttgaaccc[A/G]ggaggcagaggctgc | 8853 |
rs11680838 | snp | A/T | 0.140581 | 0.224783 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303038 | TCACTCAATATAGAC[A/T]TCTTGCTACCAGAGG | 8853 |
rs11681751 | snp | C/T | 0.441977 | 0.16014 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343458 | TTTGTTTGGTTTTTG[C/T]TTTTTTGAGACAAGG | 8853 |
rs11682006 | snp | C/G | 0.406986 | 0.194565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288003 | CTGTGGGCCAACCTG[C/G]TGGCCGCATGCATCT | 8853 |
rs11682319 | snp | A/G/T | 0.0976535 | 0.198429 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401252 | GCAGCCACACTAACC[A/G/T]TTGTTCCCTCTCCTG | 8853 |
rs11682638 | snp | C/T | 0.499154 | 0.0205497 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253174 | tttttgtttttgttt[C/T]tgtttttttaaacag | 8853 |
rs11682729 | snp | A/T | 0.0810805 | 0.184299 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209735 | ccaccatgcacagct[A/T]attttttgtatttag | 8853 |
rs11682874 | snp | A/G | 0.188 | 0.24219 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271312 | AATCTTCAGCTGATC[A/G]TCCTTAGCCAGTCCA | 8853 |
rs11683040 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308895 | TTATTCAGGCCATTT[C/T]AGTCAGTACCTTGTG | 8853 |
rs11683712 | snp | C/T | 0.17654 | 0.238964 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384376 | atgttcttgtaaagg[C/T]ggtttcacaagcagc | 8853 |
rs11684556 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214134 | ACTAAAGAGAGGTGA[C/T]GTTCCGTGATATGAA | 8853 |
rs11685369 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245425 | ATTCACTGTGCTAGG[A/T]GTGGAGGGTTCTATA | 8853 |
rs11685799 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255254 | TCAGATCATACAATG[C/T]ATCATGAGAGTAGAG | 8853 |
rs11686324 | snp | C/T | 0.204189 | 0.245767 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9235933 | ACTTCTGGCAAGGTC[C/T]GGAGTCATGTTTGAT | 8853 |
rs11686872 | snp | C/T | 0.310878 | 0.242475 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321431 | TGCAGGTCCATTCAG[C/T]CCAGGGAGGCCCCCA | 8853 |
rs11687078 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344212 | AGGGCTACTGTGGCC[A/G]TAGTGGGAGCCTCAT | 8853 |
rs11687353 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303906 | AGGCCTTGGGCGTGG[A/G]AGGGAGAACTCACAG | 8853 |
rs11687534 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227203 | ATTATCCCCACTTCC[C/T]ACATTTTCAGGGCAC | 8853 |
rs11688469 | snp | A/G | 0.490453 | 0.0684267 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253432 | gcttcccaaagtgct[A/G]ggattacaggcatga | 8853 |
rs11688558 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232265 | TCACTGCCCTGCGCC[C/T]GATCCTTTTACACAG | 8853 |
rs11688760 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232713 | aataaaACTGACAGG[C/T]AACTACAGCTTAGAT | 8853 |
rs11688860 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250457 | GATGCCAGACATGTG[A/G]CCCTTGGGTGGGAAT | 8853 |
rs11689214 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245283 | TATCGAATTGTCAGT[A/G]CCAGTGTGTTGCTGC | 8853 |
rs11689650 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229416 | CCCTGTCGATGAACC[A/G]ACCTGAGTACTGTGC | 8853 |
rs11689743 | snp | A/G | 0.23031 | 0.249223 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283802 | tccctgtaccctcac[A/G]tggcagcgagagaaa | 8853 |
rs11691689 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255521 | GGAATGGTTGATTTG[A/G]TGTAAATGCACACTG | 8853 |
rs11692186 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259999 | TGGGAAACTCTGTGG[G/T]TGAGGAACCCCACTT | 8853 |
rs11692260 | snp | A/G | 0.162253 | 0.234095 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391529 | TTCAATATTTTGGGG[A/G]CAGTCACTTGGATTA | 8853 |
rs11692473 | snp | A/C | 0.26518 | 0.249539 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236706 | GTGTGTATGTATGAG[A/C]GACACAGACAGTGCA | 8853 |
rs11692729 | snp | A/T | 0.408017 | 0.193729 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285268 | TTCAGCAGGTCAGGG[A/T]TGGAGCCTGAGTATT | 8853 |
rs11693008 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9335676 | CAGAAATCCTTAGTT[C/T]TCTTACTTCCCCTCT | 8853 |
rs11693820 | snp | G/T | 0.257096 | 0.249899 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212899 | TGCGAAGCACTGTTC[G/T]AGACGGaaccccggc | 8853 |
rs11694787 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229333 | GTGGTGCCCGCCACA[G/T]TGAGCCTCAGCCCCA | 8853 |
rs11694891 | snp | A/G | 0.00943375 | 0.0680285 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354691 | TGCCATGGTGTTGTA[A/G]AAAGTGGTCGGGCCA | 8853 |
rs11695501 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342089 | gataacagtactccc[C/T]taattgatctacaca | 8853 |
rs11695558 | snp | A/C | 0.125182 | 0.216612 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372319 | CCCTAAGAGGAGAAC[A/C]TGCAGGAATAAAATG | 8853 |
rs11695677 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232341 | GCCTGTTCTGTGAAG[G/T]TCAGCCCAGTGCCCC | 8853 |
rs11695817 | snp | A/G | 0.337923 | 0.235947 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390392 | TTTGCCCTACAGGCC[A/G]TGCACAGCCTCCAAC | 8853 |
rs11695975 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272088 | acagcagtggaattg[A/C]tggatcatatcatag | 8853 |
rs11888409 | snp | C/T | 0.0500184 | 0.150025 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9380745 | TTGAATTTTAGCAAA[C/T]GAGTCAGGAGAGACT | 8853 |
rs11892019 | snp | C/T | 0.305685 | 0.24372 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252901 | agcctcgcgacaaag[C/T]gagactccgtctcaa | 8853 |
rs11892025 | snp | C/T | 0.404384 | 0.196635 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313117 | TTGCCCACTAGGCTG[C/T]GGGCCCTGTTCCCAG | 8853 |
rs11893104 | snp | A/G | 0.314301 | 0.241589 | intron-variant | ASAP2 | GRCh38.p7 | 2:9250263 | AGGAATGTTACACAC[A/G]TGGTAATTATTACTA | 8853 |
rs11894514 | snp | A/C | 0.330714 | 0.236612 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384893 | CAGAAAAGTGGGGGA[A/C]GATAAGAGTCCTGCC | 8853 |
rs11897394 | snp | C/T | 0.293807 | 0.246132 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217404 | CCCTGGCAGGAGGCC[C/T]TCCCTGCTAACAGTG | 8853 |
rs11900151 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9333889 | TCACAGCATTGAGTT[C/T]TCAGCCTTAAAATAA | 8853 |
rs11902094 | snp | C/T | 0.309894 | 0.242719 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235035 | CCAGCCTTCTGCTTG[C/T]TCTGCCTCTCACCTG | 8853 |
rs11904728 | snp | A/G | 0.312837 | 0.241974 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384810 | TATGGAAGCTTCTTG[A/G]TGTCAGCATCTCTTC | 8853 |
rs12185533 | snp | G/T | 0.0941369 | 0.195465 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290492 | TGGGATTACAGGCGT[G/T]AGCCACTGCACCTGG | 8853 |
rs12463392 | snp | A/C | 0.277778 | 0.248452 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293698 | GTTGTCGTGGTGGGC[A/C]CCGTGCTAGGTGTTA | 8853 |
rs12463488 | snp | A/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338288 | AGATCTCAAGTATGG[A/T]TGctctctctctctc | 8853 |
rs12464209 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ASAP2 | GRCh38.p7 | 2:9330775 | GGATTTCCTTCCCCC[A/G]CCCCTTTATTTTGCC | 8853 |
rs12464411 | snp | C/G | 0.154661 | 0.231107 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296530 | GAGATGTAAGCACCT[C/G]GTATGTTTTTTCTGC | 8853 |
rs12464997 | snp | G/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397116 | TGCCTCTATACCAAA[G/T]TGGCCACAGGCCATG | 8853 |
rs12467000 | snp | C/T | 0.155274 | 0.231359 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380830 | CTCCCACCACAAGGA[C/T]GGGGTGGGGCACCTG | 8853 |
rs12467228 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338874 | CTGGGATGGAGCTTA[A/G]AAGGATGATTAGGAG | 8853 |
rs12468457 | snp | C/T | 0.252702 | 0.249985 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287725 | GTGAGGACGTGGGCT[C/T]GAAGGCCCTGGAGAT | 8853 |
rs12469510 | snp | C/T | 0.161924 | 0.233971 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288419 | GAGGCTCCAGGATCT[C/T]GTGAAACCACAGGAG | 8853 |
rs12471083 | snp | C/T | 0.166382 | 0.237126 | intron-variant | ASAP2 | GRCh38.p7 | 2:9284523 | CCTGTGACATTAGGA[C/T]GATTATTTTACCTTT | 8853 |
rs12472609 | snp | A/G | 0.252702 | 0.249985 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287462 | CTCCTTGTAGGACGG[A/G]TATCTGAAGGACGCG | 8853 |
rs12472679 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348983 | cttgttggaatccta[A/G]cttccccgctcccta | 8853 |
rs12472937 | snp | A/G | 0.187369 | 0.242028 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373931 | GTCTTTCCAAGGCCC[A/G]GGACCCACTGTGTGT | 8853 |
rs12473825 | snp | A/C | 0.254385 | 0.249962 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282837 | TCACAGATTGGCCCC[A/C]TTTGACCCATCTCTG | 8853 |
rs12475160 | snp | C/T | 0.471578 | 0.115772 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323325 | GTGGGAGCATCTCAC[C/T]GGTACCAGCGGCTTC | 8853 |
rs12476023 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254238 | aaaaaaaaaaaaaaa[A/T]atatatatatatata | 8853 |
rs12476627 | snp | A/C | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360914 | taggagcccgacccc[A/C]ccaTCTGTTATAATT | 8853 |
rs12476665 | snp | A/G | 0.144969 | 0.226867 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282688 | CTGTATAGGAAGAGC[A/G]CTCATTTTATGTACG | 8853 |
rs12477546 | snp | A/G | 0.254385 | 0.249962 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283102 | TCTTTTTTTGAGATG[A/G]TGCTTCACTCTGTTG | 8853 |
rs12478179 | snp | C/T | 0.200182 | 0.244986 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270956 | CGCCACTACGCCCGG[C/T]TAATTTTTTTGTATT | 8853 |
rs12478944 | snp | C/T | 0.311859 | 0.242226 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306946 | AGAATTCCAGCCTCT[C/T]GGAGGCCTGCAAAGC | 8853 |
rs12478982 | snp | C/T | 0.33533 | 0.234987 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307106 | ATGCGCAGCCCCAGC[C/T]TCCACACCTCACCTG | 8853 |
rs12479189 | snp | A/G | 0.125182 | 0.216612 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214540 | CCGCTGCGCCCGGCT[A/G]CCTTTCCAGGTGCTT | 8853 |
rs12615983 | snp | A/C | 0.496649 | 0.0407971 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212455 | CTAAGCTGGTTCATT[A/C]TGGTCTTCTGTACCT | 8853 |
rs12622238 | snp | A/G | 0.453939 | 0.144598 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212519 | CTGAGGTGGTGGCCA[A/G]CTCGGCGTCTGCGGT | 8853 |
rs12623538 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397750 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTT | 8853 |
rs12623912 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9213853 | TCAGAATCCAGGCCA[G/T]CTCTGTGCTGCTTGA | 8853 |
rs12624061 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402583 | CAACCTGACCACAGG[A/C]TTAGCCATGTGGAAA | 8853 |
rs12692380 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334096 | tctgtcgccaggcca[A/G]aatgcagtggcatga | 8853 |
rs12692381 | snp | A/C | 0.119351 | 0.215659 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334345 | ataggcatgagccac[A/C]gcacccggccTCTGC | 8853 |
rs12692382 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334385 | CTTTTCCATGTCGCG[A/G]TCGCCTGTTGCGGCA | 8853 |
rs12692383 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334397 | GCGGTCGCCTGTTGC[A/G]GCACATTCTTCAGTG | 8853 |
rs12986548 | snp | A/T | 0.495368 | 0.0478996 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286447 | AAAAGGAAAAAAAAA[A/T]ATATATATATATATA | 8853 |
rs12991865 | snp | A/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357654 | TTTTAAAATGCCAAG[A/T]CAGTGTGGGTAATAT | 8853 |
rs12993934 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9216486 | ttttttttgagacgg[G/T]gtctcactctgtcac | 8853 |
rs12995750 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9334040 | TCTCTGTCTTTCTCC[C/T]ttttttttttttttt | 8853 |
rs12998014 | snp | A/T | 0.412917 | 0.189626 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264198 | CCTGTCTCAAAAAAA[A/T]AATAATAATAATAAT | 8853 |
rs12998022 | snp | A/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264207 | AAAAAATAATAATAA[A/T]AATAATAATAATAAT | 8853 |
rs13002296 | snp | C/G | 0.489665 | 0.0711382 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349914 | TGAAGTGACCGGTGG[C/G]CAAGGGAAGTGGGGC | 8853 |
rs13003365 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9395595 | CTTGTGTTTTTTTTC[C/T]ttttttttttttttt | 8853 |
rs13005379 | snp | C/T | 0.48978 | 0.0707512 | intron-variant | ASAP2 | GRCh38.p7 | 2:9280299 | AGTGCCTTAGATGGT[C/T]GTGGTGTCAGGAGGG | 8853 |
rs13008339 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323422 | AGCGTTAGCCTCCTG[A/G]AGGGTAGAATTAGGT | 8853 |
rs13009593 | snp | A/G | 0.499154 | 0.0205497 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254298 | tatattgttataatt[A/G]ttctattagtcattg | 8853 |
rs13010031 | snp | A/T | 0.499154 | 0.0205497 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254502 | ggattacaggcatgc[A/T]ccactacccccagct | 8853 |
rs13015504 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254520 | actacccccagctaa[A/T]ttttggatttttttt | 8853 |
rs13015507 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254528 | cagctaatttttgga[A/T]ttttttttttttttt | 8853 |
rs13015804 | snp | C/G | 0.499653 | 0.0131743 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239516 | AGCCTGAACTCATTA[C/G]TTCTTATAACCCATA | 8853 |
rs13017331 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352232 | acacacacacacaca[A/C]acacacacacacaca | 8853 |
rs13018974 | snp | A/T | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9235981 | tggggtgctggtggc[A/T]tctggtgggtggagg | 8853 |
rs13024143 | snp | A/T | | | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391204 | ATCTACCAGTACGTT[A/T]TTTTCCTTTTTCCTT | 8853 |
rs13024159 | snp | A/T | | | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391229 | TTCCTTTCTTGCCCG[A/T]GGGCTTTGTAGATCT | 8853 |
rs13030252 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345023 | ttaattttaattttt[A/T]ttttttattttAGCC | 8853 |
rs13033403 | snp | A/T | 0.121022 | 0.21416 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380004 | TCAAAAAAAAAAAAA[A/T]AAATAAAGTATATAC | 8853 |
rs13033439 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254167 | gcagagattgcacca[C/G]tgcactgcactccag | 8853 |
rs13034079 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254460 | cgggttcaagcaatt[C/T]tcctgcctcagcctc | 8853 |
rs13035741 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9345003 | atgtttttttttttt[A/T]aattttaattttaat | 8853 |
rs13384605 | snp | C/T | 0.46703 | 0.124089 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323506 | AATGTTCTTTCTGGC[C/T]TCACGTACGTACTCT | 8853 |
rs13384638 | snp | A/C | 0.191147 | 0.242974 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278293 | TGAGGCAGGTGGATC[A/C]CCTGAGGTCAGGAGT | 8853 |
rs13384955 | snp | A/G | 0.155325 | 0.23138 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296151 | TGGCTGCCCTGTTGT[A/G]CCTGTAAATAGTTGT | 8853 |
rs13384967 | snp | A/G | 0.349233 | 0.229462 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296179 | TGTGTTATATTTCCA[A/G]TTGAACTGATGAAAA | 8853 |
rs13386896 | snp | A/G | 0.140581 | 0.224783 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340210 | GTAGTTTTAGTAGAG[A/G]CGGGGTTTCACCATG | 8853 |
rs13387963 | snp | C/T | 0.33533 | 0.234987 | intron-variant | ASAP2 | GRCh38.p7 | 2:9309066 | CACTTCCCCCAGGTC[C/T]TCATGTGGCTCTCTG | 8853 |
rs13388441 | snp | A/C | 0.270892 | 0.249126 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270652 | CCCTGTTTCTATCAA[A/C]TACTAGATCTTATTC | 8853 |
rs13388656 | snp | A/C | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234798 | CCCAGCCTGGAGCCC[A/C]CTTCCGGCCTTGCGA | 8853 |
rs13389148 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321798 | AGACACACATGGGTA[C/G]GATGGGGACAGAATT | 8853 |
rs13390738 | snp | C/T | 0.44755 | 0.153212 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395439 | gagatcacgtcattg[C/T]actccagcctgggca | 8853 |
rs13391979 | snp | A/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332909 | AGAGTATAAAATAAA[A/G]AATGATGTGTCTGTC | 8853 |
rs13394050 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316066 | gctcatgcctgtaat[C/G]ccagcactttgagag | 8853 |
rs13397012 | snp | A/G | 0.146314 | 0.227484 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294378 | GAGGGATGATAAGGA[A/G]TGCTTTTGTATTTCT | 8853 |
rs13397193 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9372689 | cagtaagataatgat[G/T]cacccacttattcca | 8853 |
rs13398867 | snp | C/G | 0.040671 | 0.13668 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340570 | GTGCCCATGTGGGTG[C/G]ACATACCTGTCATAT | 8853 |
rs13398941 | snp | C/T | 0.122064 | 0.214785 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312310 | TCCAAAGAGAAAAAC[C/T]GTGAATGAAACCAGA | 8853 |
rs13399030 | snp | C/G/T | 0.0111196 | 0.0737302 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312386 | TGCCTTCTGCTGACT[C/G/T]CTCGACTGCCACGGC | 8853 |
rs13399047 | snp | C/T | 0.0811548 | 0.184367 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312425 | CCCACACCAGCACTT[C/T]GACCACCCTCTATGC | 8853 |
rs13402270 | snp | A/T | 0.18325 | 0.240924 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274141 | gttctgatagttttt[A/T]tgatggcatctttag | 8853 |
rs13404915 | snp | A/T | 0.181978 | 0.240568 | intron-variant | ASAP2 | GRCh38.p7 | 2:9274122 | tgcaaaggtagtttt[A/T]tcagttctgatagtt | 8853 |
rs13405277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354339 | CTCTGTCTCCTCCTG[C/T]TCTTCTCCCTCACGG | 8853 |
rs13405805 | snp | A/C | 0.295343 | 0.245854 | intron-variant | ASAP2 | GRCh38.p7 | 2:9229651 | AGGGAGCCAGGATTG[A/C]CTGCGTTAGGCACGG | 8853 |
rs13411008 | snp | A/G | 0.407674 | 0.194008 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287218 | GCAGCAACGTGGGGA[A/G]CACCCTACGTGCCAC | 8853 |
rs13411023 | snp | A/C/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352212 | tttaaaacacacaca[A/C/G]acacacacacacaca | 8853 |
rs13411384 | snp | C/G | 0.0535823 | 0.154661 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378926 | CTATGCTCTCTCTCT[C/G]TTCCTGTTCTCGGGC | 8853 |
rs13414373 | snp | A/G | 0.333261 | 0.235728 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318052 | GTGTGCCTTTGCAGC[A/G]GACAGAAGACTCTGC | 8853 |
rs13414635 | snp | A/T | 0.131381 | 0.220067 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312143 | tttaggacattttct[A/T]ctccccttaaggacc | 8853 |
rs13415167 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217614 | AGAGGTATGtttttg[G/T]tttttgttttttttt | 8853 |
rs13415169 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217621 | TGtttttgttttttg[G/T]ttttttttttgagac | 8853 |
rs13416389 | snp | C/T | 0.154993 | 0.231244 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292680 | CCCAGTTCAATGTCT[C/T]CTTGCCATCTGAGTC | 8853 |
rs13418227 | snp | A/G | 0.144296 | 0.226554 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326392 | TTTTAAAGCTATGGA[A/G]CCCTTTCTTCAAAAT | 8853 |
rs13418453 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356731 | TTATCCTACTTTGCA[G/T]AACTTCTGAAGTagc | 8853 |
rs13418854 | snp | A/G | 0.310878 | 0.242475 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316189 | TAGCCAAGCATGTTG[A/G]CCCGTGCCTATAGTC | 8853 |
rs13421131 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289404 | GTGCTTGCTGGAGAA[C/T]AGACTTTCAGTGTGA | 8853 |
rs13423996 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217620 | ATGtttttgtttttt[G/T]tttttttttttgaga | 8853 |
rs13424046 | snp | A/T | 0.406986 | 0.194565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295967 | TTCCCTCGTTTTCCC[A/T]CATTGTCAGGCCCAG | 8853 |
rs13424953 | snp | C/T | 0.341685 | 0.232581 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340438 | GTCAAACTGGTTCTC[C/T]GGAGTCTTTTAAAAA | 8853 |
rs13425491 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300108 | cgtggtggctcacgg[C/T]tgtagtccctgctac | 8853 |
rs13425800 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240218 | aatcacgacatgtct[C/T]tgttcatgtcatgtc | 8853 |
rs13426594 | snp | A/G | 0.144296 | 0.226554 | intron-variant | ASAP2 | GRCh38.p7 | 2:9318669 | GTAGCTTGGCCTGCC[A/G]GGCAGCAGCCACGCC | 8853 |
rs13426880 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406116 | ACCTCTGTGACATCT[A/C]GTCTTCCTCAGGCCT | 8853 |
rs13429635 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301567 | TTTCAGGGCAGGTTT[C/T]TGAAAGGTTTGTTAC | 8853 |
rs13429713 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301642 | AGATGTCCTCACGGT[C/T]TGCAGAACCCGCTCC | 8853 |
rs13430809 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314281 | gagccaccacactca[G/T]ccTCCTTTGTAAATT | 8853 |
rs13431740 | snp | A/G | 0.263809 | 0.249618 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214135 | CTAAAGAGAGGTGAC[A/G]TTCCGTGATATGAAC | 8853 |
rs13432133 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292767 | TATCTTTCCCCAGGC[A/G]TTCATCCCAGCCATG | 8853 |
rs13432470 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9301908 | agctctctgcaagct[C/T]tgcctcccaggttca | 8853 |
rs16866958 | snp | A/G | 0.224412 | 0.248687 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9212388 | ATATGATGTCGTACC[A/G]TTGAGTCTTGAAGTC | 8853 |
rs16866964 | snp | A/G | 0.138886 | 0.22395 | intron-variant | ASAP2 | GRCh38.p7 | 2:9218483 | TTGAGGCTGCCACTG[A/G]AGGGTGAATCATGGA | 8853 |
rs16866972 | snp | C/T | 0.310878 | 0.242475 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261133 | GTGTGGAAGTAGCAG[C/T]CCCCTTGCCTGTAGC | 8853 |
rs16866981 | snp | A/G | 0.395453 | 0.203331 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289489 | CAATGAATGAATAAA[A/G]GTAAATGCGGATACA | 8853 |
rs16866985 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291865 | GTTCAGGTTAATGGT[A/C]CATGCACTTGACTGG | 8853 |
rs16866995 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345108 | GATAAGCCAGGTTGT[A/C]TTTATTTAGAAGCCT | 8853 |
rs16866998 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | ASAP2 | GRCh38.p7 | 2:9345890 | TCACAGCAGCAAGGA[G/T]TGTGTTCCTCTGGGG | 8853 |
rs16866999 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9348757 | AAATCTATCTTTGAT[A/G]GTAGTTAAGAACGAA | 8853 |
rs16867001 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349236 | TGTATTTATCAAAGC[A/G]CACAAACCTTAGATA | 8853 |
rs16867002 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350042 | CAAGATTTCTAAGAG[G/T]TATTCTGCTGTTCGA | 8853 |
rs16867003 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350450 | TTACCTGGCAAATCA[A/T]CTGTGTTGTCGGTAG | 8853 |
rs16867005 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350496 | GTTTTGGGCTTAGCC[A/G]TGCAATATCTTGATC | 8853 |
rs16867009 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351013 | TGAAGAGACATACCC[A/T]TTTTCTAGTGATATG | 8853 |
rs16867010 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352599 | CTCCACCTTTTTACA[A/G]CACAGCAGGCAGCAG | 8853 |
rs16867021 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380134 | GAATCGCTTTATTCA[A/G]TGAGTTACAGTTTGG | 8853 |
rs16867022 | snp | A/G | 0.00567755 | 0.0529768 | intron-variant | ASAP2 | GRCh38.p7 | 2:9388248 | GTTATCACCAGGAGC[A/G]GTTCATATTTGTCTC | 8853 |
rs16867023 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399361 | TAGCTCTGGAGTTGA[C/T]GGATCTTGTGTCACA | 8853 |
rs17522163 | snp | A/G | 0.192401 | 0.243274 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320105 | TTTAAGAGAAAGAAA[A/G]GAAATGCCACCACTG | 8853 |
rs17522184 | snp | C/T | 0.180064 | 0.240019 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320861 | ATTCTTGGATGTGAA[C/T]TACGGTTTCTACAAG | 8853 |
rs17627122 | snp | C/T | 0.273318 | 0.24891 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261642 | TTCCCTGGGAGCACT[C/T]TGGGAGCTTTGGAGG | 8853 |
rs17627209 | snp | C/G | 0.212425 | 0.24716 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289571 | ATGCAGTAGCCCAGT[C/G]TCCACTCTTCACCCT | 8853 |
rs17627283 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ASAP2 | GRCh38.p7 | 2:9291945 | AGAGCTGAAGATAGC[A/G]ACAATGTCATTAGCA | 8853 |
rs17627531 | snp | A/C | 0.33303 | 0.235809 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315212 | AGGAATAAGTAGTTT[A/C]GTCTTTATTAGGGAC | 8853 |
rs17634152 | snp | C/G | 0.264358 | 0.249587 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242653 | AACGCAGTCCAGAGG[C/G]CTTTGCTTCCTCAGG | 8853 |
rs17673165 | snp | A/G | 0.230603 | 0.249246 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295012 | CATGTCTTGACCGCT[A/G]ATTTTGAGATAGTTT | 8853 |
rs17685287 | snp | A/G | 0.21695 | 0.247806 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242214 | CGTGATCTTAGGGGC[A/G]CATGCTTTGGCGGTT | 8853 |
rs17855821 | snp | C/T | 0 | 0 | missense, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9297356 | AAGTTTGGCGGCAAC[C/T]GTGTATGCAGAGATG | 8853 |
rs28464564 | snp | C/T | 0.499992 | 0.00199679 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230334 | GGGACCCAGAGGGGC[C/T]GCGTGGGCCTGCTGC | 8853 |
rs28485612 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332532 | CACCATTCATCGTCA[C/T]GCTGGAAACAGCATC | 8853 |
rs28575639 | snp | C/T | 0.418491 | 0.184691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306623 | TGTGAGCTGTGGAGA[C/T]CCTGTGCCCCTTTGT | 8853 |
rs28578512 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352238 | ACACACACACACACA[A/C]ACACACACAAACACA | 8853 |
rs28590379 | snp | C/T | 0.152667 | 0.230274 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307532 | TGGGTTCTCCAGTGC[C/T]GCCCTCCGGCTCCCA | 8853 |
rs28601889 | snp | C/T | 0.311859 | 0.242226 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303042 | TCAATATAGACATCT[C/T]GCTACCAGAGGTCCT | 8853 |
rs28616843 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315519 | GAGGGTGGGAGAGAG[A/G]GCTTTGTAGGAAGGA | 8853 |
rs28661553 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349379 | GGTGGGTGTACACCC[G/T]TGTTAAAGTACTTGG | 8853 |
rs33912331 | in-del | -/A | 0.494651 | 0.0514399 | intron-variant | ASAP2 | GRCh38.p7 | 2:9353554 | ACAGCAAGACTGTCT[-/A]AAAAAAAAAAAAGAC | 8853 |
rs33914823 | in-del | -/TTTACACATACATATTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9279881 | TTTACACATATATAT[-/TTTACACATACATATTT]TTACACATATATATT | 8853 |
rs33928425 | in-del | -/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9391756 | TTTTTTTTTTTTTTT[-/TT]GTATTTTTAGTAGAG | 8853 |
rs33930824 | snp | C/T | 0.333277 | 0.235722 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9374788 | CATCACAGCCAAGTA[C/T]ATCGAGAGGAGATAC | 8853 |
rs33952815 | in-del | -/CT/TC | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9343406 | GGCACTGGTGGCCTC[-/CT/TC]CTACTCTCAACTCAG | 8853 |
rs33958512 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9245501 | CTCAAAGTGATGACG[-/A]TTACCTTCTGTAACC | 8853 |
rs33969163 | snp | C/G | 0.306679 | 0.24349 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252065 | TGTACAAAACCTTCC[C/G]TCTGGGAAATGCTGG | 8853 |
rs34011431 | snp | A/G | 0.179744 | 0.239925 | intron-variant | ASAP2 | GRCh38.p7 | 2:9332169 | TAGACAACAAAATTT[A/G]ATTGGGTAATGTTGA | 8853 |
rs34022109 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9284140 | ACAATTTCAATTCCT[-/A]CTTTGCCAAGTAGCA | 8853 |
rs34036536 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9332599 | GGCTCATGCTCACGC[-/A]GCTCTCACTCTCGCT | 8853 |
rs34043237 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266944 | TCCTAAGTCCCTTTT[-/T]GCTTCCTGTGGTCAA | 8853 |
rs34052263 | snp | A/G | 0.0123654 | 0.0776517 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9356320 | ACAGTCACAGCAGAC[A/G]TCATTGCCCGTCATC | 8853 |
rs34057310 | snp | C/T | 0.194278 | 0.243711 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283549 | GCATTCCTTAGCTCA[C/T]GGCTCCCTTCCATCT | 8853 |
rs34061651 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9306881 | ATTGGTGCCCCAGGG[-/G]CCCTGGCCGGACATC | 8853 |
rs34070129 | in-del | -/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240267 | TTTTTTTTTTTTTTT[-/T]ATTTGAGACAGGGTC | 8853 |
rs34087697 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9379267 | TACTTAGACTTTGGG[-/G]CGCGTTTACAGGCAT | 8853 |
rs34127308 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209564 | GAACTAGCAAACTAA[-/A]TTTTATATTTATTTA | 8853 |
rs34130016 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9380990 | AGTCTACAGGGAAAC[-/C]TAGGGGGACCCACCC | 8853 |
rs34194837 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401855 | TAAGAATTCAGACTT[A/G]GCCACTCAGGGGCTG | 8853 |
rs34206428 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240671 | TCTTCTTTACCATTT[-/T]CATGAATAGAAGACC | 8853 |
rs34230772 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9222190 | ATTGATGAACTTCGG[-/G]TATTAAAAATCAGTT | 8853 |
rs34254156 | snp | A/G | 0.2776 | 0.248472 | intron-variant | ASAP2 | GRCh38.p7 | 2:9208538 | AGTCAATAAAAGGGA[A/G]TCAAAAGTAACATTC | 8853 |
rs34257349 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225145 | TGTAAACAAAATCCC[-/C]AGAAGAAGATGCAAC | 8853 |
rs34262151 | in-del | -/A | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404458 | GGTAGTAGAGGATTA[-/A]GGTTGTCTATTATAA | 8853 |
rs34360769 | in-del | -/AA | 0.295599 | 0.245806 | intron-variant | ASAP2 | GRCh38.p7 | 2:9314942 | AAAAAAAAAAAAAAA[-/AA]TAGAAAAGAAAATAT | 8853 |
rs34387039 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9228740 | TGAACTGGCATACCC[-/C]AAATGCAAATTATTT | 8853 |
rs34389294 | in-del | -/A | | | intron-variant, frameshift-variant | ASAP2 | GRCh38.p7 | 2:9390094 | CTGGTTTCCCGAAGT[-/A]CTTGGAATTCAAGGG | 8853 |
rs34408894 | in-del | -/T | 0.375 | 0.216506 | intron-variant | ASAP2 | GRCh38.p7 | 2:9217913 | GCCACCACGCCTGGC[-/T]TTTTTTTTTTTTTAC | 8853 |
rs34458205 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9358024 | TAAATGTATGGTAGG[-/G]TCATGTTAGTGAGTA | 8853 |
rs34459563 | in-del | -/TAAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9379647 | TGAAGGACTGTTAAA[-/TAAA]GAGGAAAGAATAGAA | 8853 |
rs34463422 | snp | C/T | 0.2776 | 0.248472 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208132 | CCTTTTCCTTACCCA[C/T]CAAACGGGATTAGTA | 8853 |
rs34464740 | snp | C/T | 0.0160816 | 0.0882166 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9376937 | ATCCACGGATCTGAC[C/T]GCAAGGTGGAGGGCC | 8853 |
rs34469167 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9266558 | CTCACTGCTGGGGGG[-/G]CCTGCAGGTCTGGGT | 8853 |
rs34469603 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9402940 | TTCATTGAAAAATGG[-/G]CAAGTGGGAAGTAGT | 8853 |
rs34474684 | in-del | -/A | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9214797 | AAAAAAAAAAAAAAA[-/A]AGTGAACAGGACTAG | 8853 |
rs34494884 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9388763 | GCAGAGTTGTGGCAT[-/A]CTGCCTGGCTTGGGT | 8853 |
rs34500955 | in-del | -/A | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256181 | AAAAAAAAAAAAAAA[-/A]GAAAGCAAGTAATTC | 8853 |
rs34518071 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9215681 | TTTTTTTTTTTTTTT[-/T]GGAGTGATGGATTCT | 8853 |
rs34520841 | in-del | -/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9281151 | ATTTTTTTTTTTTTT[-/TT]ACTGCGTTCACTTGG | 8853 |
rs34527258 | snp | A/G | 0.000962144 | 0.0219122 | synonymous-codon | ASAP2 | GRCh38.p7 | 2:9403318 | AGCAATTCAGTCAGC[A/G]ATAAAGTGCACAAAT | 8853 |
rs34528995 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258353 | TTTTTTTTTTTTTTT[-/T]GAGACTTTTGGTCAG | 8853 |
rs34539855 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9379405 | CTCACCCCCACCTGA[-/A]GGCCACACTTGGCCC | 8853 |
rs34570938 | in-del | -/TA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9254254 | ATATATATATATATA[-/TA]CACGTGTGTGTGTAT | 8853 |
rs34622125 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9272822 | TTGTCCTTTCCCCAG[-/C]TGTATGTTCTTGGCA | 8853 |
rs34624339 | snp | A/G | 0.264358 | 0.249587 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210632 | CGATCCCCACTCACT[A/G]CAAGCCCCGCCTCCC | 8853 |
rs34643055 | snp | C/T | 0.327914 | 0.237549 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268888 | AGGAAGCCAGCCTCT[C/T]CCCACCCCTGCTGGT | 8853 |
rs34666140 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9304135 | GGGTCCCTGCTTCCC[-/C]TGGATCCCTGAGGGT | 8853 |
rs34685283 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9376843 | GTACACGATTTCACC[-/C]GGTGTTGGACACAGA | 8853 |
rs34691545 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9372277 | AGGAATGGAGCATCT[-/A]CCCTGGGTGTCACAC | 8853 |
rs34716094 | snp | A/G | 0.206336 | 0.246157 | intron-variant | ASAP2 | GRCh38.p7 | 2:9215941 | CATCTGATCCCACAG[A/G]TCAGTTCATATACTT | 8853 |
rs34716225 | in-del | -/A | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267907 | GCAAGACTCTATCTC[-/A]AAAAAAAAAAAAAAA | 8853 |
rs34722605 | in-del | -/A | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258245 | AAAAAAAAAAAAAAA[-/A]TTTCTATGATTACCA | 8853 |
rs34753836 | in-del | -/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387075 | GCCGGGCTTGGTGGT[-/G]GGTGGGGGGGCGCCT | 8853 |
rs34779336 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9389067 | TACCAGTGTCTTAGG[-/G]CAAAAAGCATGCTTT | 8853 |
rs34822448 | in-del | -/CA | 0.375 | 0.216506 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260044 | GGCTGGCCTCTCCCC[-/CA]GAGTCAGGCACCAGT | 8853 |
rs34854302 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9299236 | ACCCTGAGGCATCCC[-/C]TGTGTGAACTTGCAA | 8853 |
rs34860767 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361587 | TTCCTTTTCTTTTTT[-/T]GACAGGGTCTCACTC | 8853 |
rs34862955 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9225695 | GGGATCCTGGGGGAG[-/C]ATGGAGCAGGCTGGA | 8853 |
rs34867294 | in-del | -/T | 0.271702 | 0.249056 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344991 | TGCAGCCTGTTTATG[-/T]TTTTTTTTTTTTAAT | 8853 |
rs34870515 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9227034 | TCGGGTCCTGCTCCC[-/C]TGGCGAGAAGGAAGT | 8853 |
rs34880051 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9232581 | TCTCCCCTTCTCCCC[-/C]ATTAGATCATAAGCT | 8853 |
rs34971423 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239182 | ACCATATGGTTTCCC[-/C]TTTTTTAGCTTGTTA | 8853 |
rs34977883 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229899 | ATTTGTGGGCCTGGA[-/A]GTGATGCTGATTTCT | 8853 |
rs35003553 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9396623 | CTTGGAAAGAAATGG[-/G]AAGTAAATGTACTTA | 8853 |
rs35011056 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9314978 | GATCTGGGGGAGGGA[-/A]GGGATCACATTCTGC | 8853 |
rs35027390 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237187 | GAGTTAAAAAAAAAA[-/A]GCCCTGTTTTGTACA | 8853 |
rs35027722 | snp | C/T | 0.264358 | 0.249587 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210628 | GGCTCGATCCCCACT[C/T]ACTGCAAGCCCCGCC | 8853 |
rs35059298 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9291433 | AGAAATTGCATTCCC[-/C]ATGAGATCATGCGCC | 8853 |
rs35075609 | in-del | -/AGCCCAAAACCTT | 0.383632 | 0.211288 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259554 | GAGGGCACAGTTTTC[-/AGCCCAAAACCTT]AAGGAACAAAAATGA | 8853 |
rs35078846 | in-del | -/A | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252931 | AAAAAAAAAAAAAAA[-/A]GAATTTAGGAACACA | 8853 |
rs35131756 | in-del | -/T | 0.261056 | 0.249755 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283073 | TCTTGTAATAGATTC[-/T]TTTTTTTTTCCTCTC | 8853 |
rs35153385 | in-del | -/C | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210597 | CTCGCTCTGTCGCCC[-/C]AGGCTGGAGTGCAGT | 8853 |
rs35182001 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9397276 | GCAGTTATTGGGACT[-/A]CTGAGAACCGTGGTT | 8853 |
rs35204746 | in-del | -/AT | 0.444444 | 0.157135 | intron-variant | ASAP2 | GRCh38.p7 | 2:9239445 | GGGTAGAATGAAATC[-/AT]GTGTGTGGTGATGGA | 8853 |
rs35276607 | in-del | -/C | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278744 | CTAATTATTCAACCC[-/C]TGCAAAGTGGGTATT | 8853 |
rs35296269 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9349027 | ACCAGATTATTTGGT[-/G]CTGTCCGGGCCAGTG | 8853 |
rs35298334 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369191 | CCTGGCTAATTTTTA[-/A]TATTTTTAGTAGAGA | 8853 |
rs35315409 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9360531 | CCTATCACCGTCCCC[-/C]AACAAATGTTTAACA | 8853 |
rs35322892 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9309353 | GTCATGCGCAGTCCC[-/C]AAAATCATGATGCAA | 8853 |
rs35348989 | snp | G/T | 0.5 | 0 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406062 | CTCTGTGACATCTAG[G/T]CTTCCTCAGGCCTTC | 8853 |
rs35350089 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9303073 | ACCCTCAGTACTTCC[-/C]ATAGACTTTCTCCTA | 8853 |
rs35357758 | snp | A/G | 0.00701054 | 0.0587888 | synonymous-codon, utr-variant-5-prime | ASAP2 | GRCh38.p7 | 2:9279325 | AACCATCCGGTCCAC[A/G]TCCAAAGCCTAAAAT | 8853 |
rs35375516 | in-del | -/T/TT | | | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9237431 | TTTTTTTTTTTTTTT[-/T/TT]GACAGATTCTTGCTT | 8853 |
rs35377883 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9235329 | GAGTTGTTTTCTTTT[-/T]AAGAGGTAGCCAAGG | 8853 |
rs35389797 | snp | C/T | 0.336017 | 0.234736 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267643 | TTCTCATGCCTGTAA[C/T]CCCAGCACTTTGGGA | 8853 |
rs35390571 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9224783 | CTGTCCATTTATCTG[-/G]TCTCTGTCCATCCAT | 8853 |
rs35416254 | in-del | -/C | | | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211496 | TTAGTTAGACCCTCC[-/C]TTTATAGCACCATCC | 8853 |
rs35424556 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9344462 | TAGGCATAAGTTTCC[-/C]TTTGTGTACTGCTTT | 8853 |
rs35433389 | in-del | -/A | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267922 | AAAAAAAAAAAAAAA[-/A]GAATGATTATAAAGC | 8853 |
rs35473125 | in-del | -/G | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258335 | TAGTAATCAGTAGTT[-/G]TTTTTTTTTTTTTTT | 8853 |
rs35474923 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9342701 | CTTCAGAATCTTTTT[-/T]CAAACTCAGAAATCC | 8853 |
rs35487223 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9371193 | AACCCCGGGCTTTTT[-/T]CAAAATGAGGGCGGA | 8853 |
rs35495550 | in-del | -/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9334065 | TTTTTTTTTTTTTTT[-/T]GGGAGACAGTCTCAC | 8853 |
rs35496846 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322270 | TTCTTAAACACTCTA[-/G]TCCTCCTTGCCCTAA | 8853 |
rs35555034 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9224772 | TTATCCATCCATCTG[G/T]CCATTTATCTGTCTC | 8853 |
rs35563492 | in-del | -/TAGT | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210423 | AGTTACCAGATTATA[-/TAGT]TTAGTGAGTCCACAG | 8853 |
rs35579461 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9348468 | GAAGGATTTTAATGG[-/C]ATAGAATTTTCTCCC | 8853 |
rs35585288 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9209791 | CAGGCTGGTCTCGAA[-/A]CTCCTGACCTCAGGT | 8853 |
rs35586173 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9283337 | CAGCCTCGGCCTCCC[-/C]TGTAATAGTTTCTTA | 8853 |
rs35615681 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9290585 | TTCAGATTTCTTTTT[-/T]AAAGTTTTATTTATT | 8853 |
rs35623748 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9376904 | CCTTTGTTTGGTTTT[-/T]CAGGAGCCGGATGAA | 8853 |
rs35629199 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9226549 | CCAGCTTGCTGAAGG[-/G]CTTTGTGGTAAAGGG | 8853 |
rs35630429 | in-del | -/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364991 | TTTAGCCTTTTTTTT[-/T]AAAGCCAAGATTCTG | 8853 |
rs35643120 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267486 | GATTTAGTTCTTTTT[-/T]ATGGCTGCGTCATAT | 8853 |
rs35656522 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9356984 | GTCGGGGACTACACA[-/A]GGTGCATTTTCTGAA | 8853 |
rs35711911 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9369912 | ATGATGTGATCTCGG[-/G]CTCACTGCAGCATCC | 8853 |
rs35758474 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9314653 | ACATTTAGAAAAGGG[-/G]CTGGGTGTAGTGGCT | 8853 |
rs35768042 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234946 | ACATCCTGTTTGGGG[-/G]AAGTGATAAGAGAGG | 8853 |
rs35770426 | snp | A/G | 0.213333 | 0.247296 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264352 | AGACTGGGGGGGCCC[A/G]TGCTGGCGTCACCAC | 8853 |
rs35776705 | in-del | -/A | | | frameshift-variant | ASAP2 | GRCh38.p7 | 2:9379042 | GCTCCTGCGGGGGAA[-/A]GGCCTCCATCGAGAT | 8853 |
rs35784307 | in-del | -/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221339 | TTTTTTTTTTTTTTT[-/T]GAGACGGAATTTTCC | 8853 |
rs35796016 | in-del | -/A | 0.429538 | 0.173972 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311358 | GAGAGGCACTCTCTC[-/A]AAAAAAAAAAGAAAA | 8853 |
rs35808681 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9259146 | GAGCCCTTCCCCTCG[-/G]CTTCCTCTCTTGTTC | 8853 |
rs35823500 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9355054 | TCCCCTAGCTTTCCC[-/C]TTCTGTTAACATCTT | 8853 |
rs35890230 | snp | C/T | 0.314544 | 0.241524 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269113 | TGGCGGGCCTCAAGG[C/T]GGTATGTAGGTACTT | 8853 |
rs35894198 | snp | A/G | 0.130694 | 0.219696 | intron-variant | ASAP2 | GRCh38.p7 | 2:9221707 | TGTGTATTTGTATGT[A/G]TATTCCTTAGGATTT | 8853 |
rs35913703 | in-del | -/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270810 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 8853 |
rs35915921 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9321310 | CCTTCTATCCATGGG[-/G]AATCTTACATTTCCA | 8853 |
rs35955045 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285711 | GTGGGTGGAAAAATT[A/C]ATCTCTATCAAGAAG | 8853 |
rs35957038 | snp | C/T | 0.199254 | 0.244796 | intron-variant | ASAP2 | GRCh38.p7 | 2:9271630 | TGGATAGTGGACATA[C/T]GATCCAATTTCTTTT | 8853 |
rs35969307 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9330723 | AAGTGGGTCGCTTCC[-/C]TTGCTGATATTTTAT | 8853 |
rs36014706 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9328851 | GAAGTTAGACTGAAA[-/A]GAGACAAATTTCTAA | 8853 |
rs36039356 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9295715 | CTGGTCTCAGAAATT[-/T]CATTTAATTTATCTA | 8853 |
rs36039598 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229249 | GCGGGGCAGGTGGCC[-/C]GGTGCTGCTTCCATG | 8853 |
rs36057242 | in-del | -/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9361613 | CACTCCATGACCCAG[-/G]CTGGAGTCCAGTAGC | 8853 |
rs36078682 | in-del | -/ACTT/TC/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317453 | CATTCTCACACACAC[-/ACTT/TC/TT]ATGTGCATTCACCTT | 8853 |
rs36107587 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9355488 | ACACACAGGTCCACA[G/T]CCTGGCAAAACACTT | 8853 |
rs36112788 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9228334 | GCATATTTCTTTTTT[-/T]CACATCCTGCCTACT | 8853 |
rs36113627 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9337202 | TGCCCAGTTGGCTCC[-/C]TTGTCAAGACCTAAC | 8853 |
rs36121744 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9383669 | TTCCAAAGGCACTTT[-/T]CAAGTTCCCTAACAA | 8853 |
rs41264165 | snp | A/G | 0.165853 | 0.235413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279479 | TGACCATTAACAAAT[A/G]AGCCAGCTAGACTCC | 8853 |
rs41264167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356837 | GTGAAGGGACAGGAC[A/C]CTTTCAGCTGACACA | 8853 |
rs41264169 | snp | A/G | 0.00560757 | 0.052653 | missense | ASAP2 | GRCh38.p7 | 2:9400786 | CCTCTGTCCAATGCT[A/G]TGGTCCTGCAGCCCC | 8853 |
rs41264171 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9405631 | TAAGTTTACTCTTCT[C/T]GTTAACTAGTCATTT | 8853 |
rs41437044 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321472 | GGCACACAAATAAAG[G/T]ATGCTGACGGACCAG | 8853 |
rs55686536 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9387180 | GATTGCGCCACTGCA[C/T]TCCAGCCTGGGCAAC | 8853 |
rs55698003 | snp | A/G | 0.244205 | 0.249933 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281890 | TCCGAGCTCTTGTGC[A/G]TTGCCTGGACTCAGG | 8853 |
rs55737406 | snp | A/C | 0.224116 | 0.248656 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315539 | TGTAGGAAGGAAGAG[A/C]ATTGGAGGAAGGAGA | 8853 |
rs55746439 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ASAP2 | GRCh38.p7 | 2:9369941 | CCGCCTCCTGGGTTC[A/G]AGTGATTCTCCTGCC | 8853 |
rs55762500 | snp | C/G | 0.0425829 | 0.139564 | intron-variant | ASAP2 | GRCh38.p7 | 2:9245746 | CTGCAGTCTGACGCT[C/G]TGTGCCATGCATTAG | 8853 |
rs55850504 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323800 | CCACTCCATTCCACC[A/C/T]GCAGCCTCAGCCCTT | 8853 |
rs55892385 | snp | A/G | 0.42666 | 0.176893 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306076 | GTAGAGAGGCTGTAG[A/G]GGGTGGGGTTATGGG | 8853 |
rs55905985 | snp | A/T | 0.0681886 | 0.171594 | intron-variant | ASAP2 | GRCh38.p7 | 2:9286445 | AAAAAAGGAAAAAAA[A/T]AAATATATATATATA | 8853 |
rs55912883 | snp | C/G | 0.260227 | 0.249791 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241098 | TTTGGACTGTGGTTA[C/G]TGGAAACTGTGGAAA | 8853 |
rs55952263 | snp | C/T | 0.267364 | 0.249396 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210577 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 8853 |
rs55996345 | in-del | -/CATATTTTTTACACATA | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9279890 | ATATATTTACACATA[-/CATATTTTTTACACATA]TATATTTTTTAAACC | 8853 |
rs56017407 | snp | A/T | 0.311859 | 0.242226 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355536 | CCAGCAGTATGTAAG[A/T]GTAGGATTTTATATT | 8853 |
rs56023131 | snp | G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9334265 | ATGTTGGCCAGCTGG[G/T]CTGGAACTCCTGGTC | 8853 |
rs56035447 | snp | G/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254526 | CCCAGCTAATTTTTG[G/T]ATTTTTTTTTTTTTT | 8853 |
rs56041565 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | ASAP2 | GRCh38.p7 | 2:9324016 | GTGCCAGCGAAGCTC[C/T]CTTGCACTGGATGGT | 8853 |
rs56070465 | snp | A/G | 0.17461 | 0.238362 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390574 | TTGCGGGAGGGAGGG[A/G]GAGAGAGCCCCTCCT | 8853 |
rs56111045 | snp | G/T | 0.301681 | 0.2446 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265879 | CCCGGTTCAAGTGAT[G/T]CTCCTGCCTCAGCCT | 8853 |
rs56138030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285896 | CCTCAAATCCTTACC[A/G]TCTCCCACATACAAA | 8853 |
rs56170230 | snp | C/T | 0.267091 | 0.249415 | intron-variant | ASAP2 | GRCh38.p7 | 2:9228619 | AGTTCATGTGTGATA[C/T]ACAAATGAATGGTCT | 8853 |
rs56178313 | snp | A/G | 0.230896 | 0.249269 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294541 | TCTGGGGCAGGTGAC[A/G]TGACTCTCTGAACTG | 8853 |
rs56253420 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9379382 | ACCTGTTCACATACC[C/T]TGAGTCTACTCACCC | 8853 |
rs56323641 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | ASAP2 | GRCh38.p7 | 2:9253889 | ATATTTTGAGAAAGA[A/G]ACCACATTCACATAA | 8853 |
rs56659258 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341312 | ACTGAAGTAATTCGC[A/G]CTAAAACAGTTTCAA | 8853 |
rs56664264 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347957 | ATAATCTCTGCCTGC[A/T]TGGCAAACTCTAAAG | 8853 |
rs56706792 | in-del | -/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9229157 | TGTGGAGCCCCCCCC[-/C]GCATCATCACACTTA | 8853 |
rs56726319 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | ASAP2 | GRCh38.p7 | 2:9341727 | CCACATTCCTTCCAC[A/G]GCATTGTTCTCAGCA | 8853 |
rs56842553 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322516 | CCACCTTAGCAGCCA[C/T]GATTACCCTGGTGGC | 8853 |
rs56856344 | in-del | -/TC | 0.0325976 | 0.123435 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317542 | CTCAAATCCACACAA[-/TC]TCTCACATCCACAAT | 8853 |
rs56904067 | snp | A/T | 0.340784 | 0.232934 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264201 | GTCTCAAAAAAATAA[A/T]AATAATAATAATAAT | 8853 |
rs57008254 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294124 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGAATTAC | 8853 |
rs57039765 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347930 | CGGCACGATTAGAAT[A/G]GAGAATCACTGATAA | 8853 |
rs57184463 | snp | A/G | 0.178144 | 0.239451 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379153 | TTGGAAACAGGGCCA[A/G]CCCTGTGGGCTCTTG | 8853 |
rs57215390 | snp | A/G | 0.111928 | 0.208413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283673 | GTGGGTTAAACAACA[A/G]AAATTTATTTTCTCA | 8853 |
rs57217281 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9320590 | TTTCAGGAAAGTTCA[C/T]TGAGGGAAGTTAAGA | 8853 |
rs57269008 | in-del | -/AA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9267922 | AAAAAAAAAAAAAAA[-/AA]GAATGATTATAAAGC | 8853 |
rs57325322 | snp | A/G | 0.229136 | 0.249128 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358269 | ATTGCTACTACCAGC[A/G]TGCTGAACACAGCAT | 8853 |
rs57346156 | snp | C/G | 0.111928 | 0.208413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300007 | AGGCCAAGGTGGGCG[C/G]GTTGCTTTGAACCCA | 8853 |
rs57358804 | snp | A/G | 0.115788 | 0.21092 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278676 | ATAGACAACTGCCGT[A/G]TAGTAGCTGGTCTAT | 8853 |
rs57399297 | snp | C/T | 0.164546 | 0.234942 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377209 | GGTAATTGCAGGGTC[C/T]AACTTCTAGTGTCTG | 8853 |
rs57470511 | in-del | -/AT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9241965 | TTATCAGGCGGACAC[-/AT]GTGAATTTCACACCT | 8853 |
rs57553892 | snp | G/T | 0.174288 | 0.23826 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378663 | GTGCACTGCCCCACC[G/T]TGGCCCCACATGCTC | 8853 |
rs57600562 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398452 | GGAGTTCCGAGGCTG[C/T]GGTGAACTGATTGCC | 8853 |
rs57795045 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | ASAP2 | GRCh38.p7 | 2:9293638 | CCTTGGGGTGATCTG[C/T]AGCAGTGGGTCAGTC | 8853 |
rs57798948 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9274319 | TCTAGCATTCAATCT[-/T]TTTTTTTTTTTTTTT | 8853 |
rs57906310 | in-del | -/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9302190 | TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTCGC | 8853 |
rs57923271 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323511 | TCTTTCTGGCTTCAC[A/G]TACGTACTCTTGCTA | 8853 |
rs58023406 | snp | A/G | 0.150667 | 0.229419 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227661 | TACAGCTCTTGTTCA[A/G]TGAATGATCTTTCTG | 8853 |
rs58109723 | snp | A/G | 0.040671 | 0.13668 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322622 | ACAAGATGAATGTAG[A/G]AAGGATAATTAAGCC | 8853 |
rs58150803 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322487 | CAGAATAAAAACTCA[C/T]GGCTATTTCAAGCCC | 8853 |
rs58172848 | in-del | -/GG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9336802 | GAGGTAGTGCGAGGG[-/GG]CAGGAGCCAGAATGC | 8853 |
rs58275721 | in-del | -/CACACACACACA | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352236 | ACACACACACACACA[-/CACACACACACA]AACACACACACCACT | 8853 |
rs58279098 | snp | A/G | 0.109108 | 0.206518 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340212 | AGTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 8853 |
rs58354494 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | ASAP2 | GRCh38.p7 | 2:9361062 | TGACTTCTAATGCCT[A/G]GTTAAATTCTCCATT | 8853 |
rs58360128 | snp | A/G | 0.142609 | 0.225759 | intron-variant | ASAP2 | GRCh38.p7 | 2:9223329 | CATAGCTGATAGGAA[A/G]TCTCTTAAGGGCCCT | 8853 |
rs58394981 | snp | G/T | 0.489608 | 0.0713316 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258335 | TAGTAATCAGTAGTT[G/T]TTTTTTTTTTTTTTT | 8853 |
rs58501944 | snp | C/T | 0.345704 | 0.230956 | intron-variant | ASAP2 | GRCh38.p7 | 2:9395345 | CTGGGCATGGTGGCA[C/T]GCACCTGTAATCCCA | 8853 |
rs58519058 | snp | A/G | 0.115788 | 0.21092 | intron-variant | ASAP2 | GRCh38.p7 | 2:9308290 | GCACTTCGCATGGCC[A/G]TGGGCAGGGGCAAGA | 8853 |
rs58536406 | in-del | -/AA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9353565 | GTCTAAAAAAAAAAA[-/AA]GACATTTGGGCAGTT | 8853 |
rs58573671 | in-del | -/CCT | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347077 | TTCCAGAGGTCTCCT[-/CCT]GCCTTTAGCAGCCAT | 8853 |
rs58605449 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286447 | AAAGGAAAAAAAAAA[-/T]ATATATATATATATA | 8853 |
rs58620535 | in-del | -/TT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9217631 | TTTGTTTTTTTTTTT[-/TT]GAGACGGAGTCTTCG | 8853 |
rs58696518 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311400 | CTGCTTGTTGGTCCA[A/G]CGTTAATAGCAGTGA | 8853 |
rs58773472 | in-del | -/TC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9317566 | TCCACAATCACACTC[-/TC]ACACACCCACACACC | 8853 |
rs58786363 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286446 | AAAAGGAAAAAAAAA[-/T]AATATATATATATAT | 8853 |
rs58866959 | snp | A/G | 0.33533 | 0.234987 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302158 | AAACACAGATGATGT[A/G]AGTTAGAAGCCTTTT | 8853 |
rs58906207 | in-del | -/GTG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9289990 | AGGAAGAAGCCGGTG[-/GTG]AGAGGCATCCTTCCA | 8853 |
rs59091531 | snp | C/G | 0.103082 | 0.202275 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317534 | ACCCCACACTCAAAT[C/G]CACACAATCTCTCAC | 8853 |
rs59204833 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | ASAP2 | GRCh38.p7 | 2:9384094 | GTGCAGCACACCAAC[A/G]TGGCACATTTGTACG | 8853 |
rs59223290 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9219575 | GATAGTCCTGAAAAG[-/T]ACAACATCATTGCTG | 8853 |
rs59242662 | snp | C/G | | | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391373 | CCTCCTTCGTCACAG[C/G]TGCAAACCCCTGCCT | 8853 |
rs59319754 | snp | C/T | 0.128288 | 0.218372 | intron-variant | ASAP2 | GRCh38.p7 | 2:9342765 | ACTCTGACTCCAGCC[C/T]GTCTTGTCCACCCCT | 8853 |
rs59324084 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381638 | TTACCCAGGAGGCTA[A/G]GGTAGGAGGATCACT | 8853 |
rs59329658 | snp | A/G | 0.111224 | 0.207945 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340021 | TTTGCCCATGTCTGC[A/G]GCTTTTTGTTTGTTT | 8853 |
rs59370549 | snp | A/G | 0.029116 | 0.117091 | intron-variant | ASAP2 | GRCh38.p7 | 2:9386158 | CTTTTTTTTTTTTCT[A/G]TAATGCATTAATGTT | 8853 |
rs59395423 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | ASAP2 | GRCh38.p7 | 2:9241538 | CTTGAGCCCAGGAGT[C/T]CGAGACCAGCCTGGG | 8853 |
rs59423766 | in-del | -/T | | | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404751 | AGTTTTTTTTTTTTT[-/T]GGCATTGTACTTTTT | 8853 |
rs59603011 | snp | A/C | 0.040671 | 0.13668 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322513 | AGCCCACCTTAGCAG[A/C]CACGATTACCCTGGT | 8853 |
rs59614278 | snp | C/T | 0.140581 | 0.224783 | intron-variant | ASAP2 | GRCh38.p7 | 2:9235188 | AATGGTAGAATTAAT[C/T]GAGTTAGAGATGGGG | 8853 |
rs59634883 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258146 | TCTATTTTGAGAAAT[C/T]TAAGCCAGGGAAATG | 8853 |
rs59670261 | snp | A/C | 0.229136 | 0.249128 | intron-variant | ASAP2 | GRCh38.p7 | 2:9358637 | GTTTCCAGCTGTGTT[A/C]AGGATCAGAAAATGC | 8853 |
rs59687102 | in-del | -/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9264207 | AAAAAATAATAATAA[-/T]AATAATAATAATAAT | 8853 |
rs59824016 | in-del | -/TG | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9250595 | AAATGCAGTGTGGTG[-/TG]CTCTTTCATTTAAGC | 8853 |
rs59833056 | snp | A/T | 0.339882 | 0.233284 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264204 | TCAAAAAAATAATAA[A/T]AATAATAATAATAAT | 8853 |
rs59862328 | in-del | -/C | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9209000 | ATTAAAATTGGCATA[-/C]CCTTTCTCTGATTAA | 8853 |
rs59939019 | snp | A/C | 0.111576 | 0.20818 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283918 | TATGCTTCCCGATGG[A/C]CCCATCTCCAGACAC | 8853 |
rs59968284 | snp | A/C | 0.0277387 | 0.114455 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380820 | GCTGGTGAGTCTCCC[A/C]CCACAAGGACGGGGT | 8853 |
rs60012182 | snp | G/T | 0.118933 | 0.212888 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311390 | AAAAGTTTGCCTGCT[G/T]GTTGGTCCAACGTTA | 8853 |
rs60035102 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9258172 | AAATGCAGTGGAATT[C/T]TTCATTAAAAATTAC | 8853 |
rs60099601 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289706 | TCACTGGAAGGATGG[A/G]ATCATTAATATAAGG | 8853 |
rs60187435 | in-del | -/AAAAAAAAAAAA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387227 | CAAAAAAAAAAAAAA[-/AAAAAAAAAAAA]CCATATAACCTTCAG | 8853 |
rs60292178 | snp | A/G | 0.158302 | 0.232576 | intron-variant | ASAP2 | GRCh38.p7 | 2:9399631 | AGAGTGCTCGGACCC[A/G]TCCTGGCAAAGCCAT | 8853 |
rs60316313 | snp | A/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9235313 | CCAGCTGCCCCGGGC[A/G]GAGTTGTTTTCTTTT | 8853 |
rs60417778 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9286926 | AAGCATAGTGGTAAT[A/T]AATACTCATGAGGTA | 8853 |
rs60496602 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9296606 | CGAAGATGAATACAA[-/A]CTTAGTCTGTCAACT | 8853 |
rs60530862 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9240254 | CCCATAATTTTTTTT[C/T]TTTTTTTTTTTTTAT | 8853 |
rs60624105 | snp | G/T | 0.0498117 | 0.149749 | intron-variant | ASAP2 | GRCh38.p7 | 2:9268921 | GCATTGAGAACTCAG[G/T]GTGCTGGGGACAAAC | 8853 |
rs60655458 | in-del | -/TTGTGGCTCTTTTTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9322520 | TTAGCAGCCACGATT[-/TTGTGGCTCTTTTTT]ACCCTGGTGGCTCTT | 8853 |
rs60731896 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9222416 | CTTAGAGCCAGGCCT[C/T]GTGTGTTCTCTGCAA | 8853 |
rs60794503 | in-del | -/G | 0.362732 | 0.22314 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311041 | TATCCAAGTGAACTC[-/G]GGGGGGAAAAGCTAA | 8853 |
rs60869426 | in-del | -/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302139 | TTTTTTTTTTTTTTT[-/T]CCCAAACACAGATGA | 8853 |
rs60874735 | snp | A/G | 0.316968 | 0.240864 | intron-variant | ASAP2 | GRCh38.p7 | 2:9396831 | ACATGGCAAAACCCT[A/G]TCTCTACTAAAATTA | 8853 |
rs60911999 | in-del | -/AGCA | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9235500 | AATCATCCTGCAGCA[-/AGCA]GTTCTGTCTTGTATG | 8853 |
rs61129624 | in-del | -/A | 0.442791 | 0.15916 | intron-variant | ASAP2 | GRCh38.p7 | 2:9326477 | CGGAGAAGGCGTGAG[-/A]AGATCCTCTGTTGCT | 8853 |
rs61196009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ASAP2 | GRCh38.p7 | 2:9391518 | ATTTGGTGATTTTCA[A/G]TATTTTGGGGACAGT | 8853 |
rs61237489 | in-del | -/CTTTTT | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9235324 | GGGCAGAGTTGTTTT[-/CTTTTT]AAGAGGTAGCCAAGG | 8853 |
rs61275202 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9374984 | TAAAAAAAAAAAAAA[-/A]GGCCGGCCACGGTGG | 8853 |
rs61275565 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9403357 | AAAGCATTAACAGTT[A/G]TGTTCCTGTTTCGTT | 8853 |
rs61303081 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9387227 | TCAAAAAAAAAAAAA[-/A]CCATATAACCTTCAG | 8853 |
rs61407647 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9255548 | ACTGCAGCTTAATGA[A/G]GTAGCCTCTCTGGTT | 8853 |
rs61540303 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380475 | AGTGCTGGGATTACA[A/G]GCGTGAGCCACTGCG | 8853 |
rs61651168 | snp | C/T | 0.115088 | 0.210473 | intron-variant | ASAP2 | GRCh38.p7 | 2:9281714 | ATGGTTCTCTTACCA[C/T]AGATCCATCCAAAGA | 8853 |
rs62118644 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9230643 | TGCCTGCATCCCCTG[A/T]GCTGCTTGGCGAGGA | 8853 |
rs62118645 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9239936 | TGTTTAAGTGACTTT[A/C]CCAAGGCCTTGTAGC | 8853 |
rs62118760 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338377 | TCTTTCTCTTGCTCC[C/T]TCTTTTTCAAGCATC | 8853 |
rs62118761 | snp | C/T | 0.204803 | 0.245881 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340171 | GGGATTACAGGTACG[C/T]GCCACCACGCCTGGC | 8853 |
rs62118762 | snp | A/G | 0.203575 | 0.245652 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340318 | GAGCCACCGCGCCCG[A/G]CCAGCCATGTCTGCA | 8853 |
rs62118763 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | ASAP2 | GRCh38.p7 | 2:9340937 | TAGAATTTCATGAAA[C/G]CCTTTTGAGGTTCCA | 8853 |
rs62118791 | snp | A/C | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9352234 | ACACACACACACACA[A/C]ACACACACACACAAA | 8853 |
rs62118793 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357525 | TTTTGGCAGGAGATG[A/T]GGTAGGGGGTGATAA | 8853 |
rs62118794 | snp | A/C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362260 | AGTGAGTGTTCATTA[A/C/G]GCCCCTTGGTGCCTT | 8853 |
rs62118795 | snp | C/G | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9362262 | TGAGTGTTCATTAGG[C/G]CCCTTGGTGCCTTGT | 8853 |
rs62118796 | snp | A/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9364359 | CAAAAAAAAAAAAGT[A/T]AGCTGAGTATGGTAG | 8853 |
rs62118797 | snp | A/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9364991 | TTTAGCCTTTTTTTT[A/T]AAAGCCAAGATTCTG | 8853 |
rs62118798 | snp | A/G | 0.207559 | 0.246371 | intron-variant | ASAP2 | GRCh38.p7 | 2:9365890 | ACAGGAAGGGCGACG[A/G]ACTGGGCTGAGCTAC | 8853 |
rs62118799 | snp | A/C | 0.128632 | 0.218563 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373167 | CGCCTTAACCTAGGC[A/C]CTGTAGAGCGGGCAG | 8853 |
rs62118800 | snp | G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9374530 | AGAGGCGGGTGGGCT[G/T]AGAGAACATGGGGAG | 8853 |
rs62118801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9378859 | TGCCTTTCCTGTGCC[C/T]GTAGCCCAGGCTCCC | 8853 |
rs62118802 | snp | A/G | 0.128632 | 0.218563 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381434 | CAGTTGACACACAGC[A/G]CTCAGTAAATAGATT | 8853 |
rs62118803 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390871 | GAGCCTCTTCGGTTT[C/T]GCGAGTATCAGTGTC | 8853 |
rs62118804 | snp | C/T | 0.175576 | 0.238665 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394944 | GGTAGCTGACGCTGC[C/T]TGTCAGCCAGAGCCT | 8853 |
rs62118807 | snp | A/G | 0.316485 | 0.240998 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397852 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 8853 |
rs62118808 | snp | A/G | 0.181978 | 0.240568 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397854 | AGCTCCGCCTCCCGG[A/G]TTCACGCCATTCTCC | 8853 |
rs62118809 | snp | G/T | 0.0836354 | 0.186609 | intron-variant | ASAP2 | GRCh38.p7 | 2:9398461 | AGGCTGCGGTGAACT[G/T]ATTGCCGCACTGCAC | 8853 |
rs62118810 | snp | C/G | 0.172674 | 0.237741 | intron-variant | ASAP2 | GRCh38.p7 | 2:9401796 | CAAGCTGTGGCCGCC[C/G]AGGCGTCCAGCAGGG | 8853 |
rs62118840 | snp | G/T | 0.170733 | 0.237101 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ASAP2, ITGB1BP1 | GRCh38.p7 | 2:9406174 | CTCTGTGACATCTAG[G/T]CTTCCTCAGGCCTTC | 8853 |
rs62121268 | snp | A/T | 0.192715 | 0.243348 | intron-variant | ASAP2 | GRCh38.p7 | 2:9246581 | TGAGCCACCACGCCC[A/T]GCCCCACCTGTGTGA | 8853 |
rs62121269 | snp | A/G | 0.147321 | 0.227941 | intron-variant | ASAP2 | GRCh38.p7 | 2:9247928 | ACCTCTTTATGATGT[A/G]TCCTCCCAGCTCTCA | 8853 |
rs62121270 | snp | C/T | 0.26326 | 0.249648 | intron-variant | ASAP2 | GRCh38.p7 | 2:9254445 | GCAACCTCTGTCTCC[C/T]GGGTTCAAGCAATTC | 8853 |
rs62121272 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ASAP2 | GRCh38.p7 | 2:9263796 | CCGTCCACTTCAGGC[A/G]CAGTTGACGGCCGTC | 8853 |
rs62121273 | snp | A/T | 0.0770498 | 0.180522 | intron-variant | ASAP2 | GRCh38.p7 | 2:9269531 | AGAGGAGCCCCCACA[A/T]GGAGGAGGGTGGCCA | 8853 |
rs62121274 | snp | A/G | 0.184838 | 0.241358 | intron-variant | ASAP2 | GRCh38.p7 | 2:9273506 | GGAACTGCAGTAGAG[A/G]AAGAGTAATTCACGC | 8853 |
rs62121275 | snp | G/T | 0.187369 | 0.242028 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9278755 | AACCCTGCAAAGTGG[G/T]TATTGTTCCTGCTGG | 8853 |
rs62121298 | snp | C/T | 0.212728 | 0.247206 | intron-variant | ASAP2 | GRCh38.p7 | 2:9285977 | CAGTGTTAATTGGAA[C/T]ATGATATTAAAATAC | 8853 |
rs62121299 | snp | A/G | 0.212425 | 0.24716 | intron-variant | ASAP2 | GRCh38.p7 | 2:9287271 | TCTGAAAAATTCCAG[A/G]TGGTTTTGGTTGATT | 8853 |
rs62121300 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292397 | GTGGTGTGCGCCTGT[A/G]GTCTCAGCTACTCGG | 8853 |
rs62121301 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9292981 | GACCTGTCAAGAGCC[C/G/T]TATCTACATGTGTGG | 8853 |
rs62121303 | snp | C/G | 0.212122 | 0.247114 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295256 | AATTTGGGTTTGAAT[C/G]CCAGCTCTGCCACTT | 8853 |
rs62121304 | snp | A/G | 0.212425 | 0.24716 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295443 | TGTTATTGGTTATGC[A/G]CCAAGTGTGGTAAAC | 8853 |
rs62121305 | snp | G/T | 0.326506 | 0.238006 | intron-variant | ASAP2 | GRCh38.p7 | 2:9297728 | GGCCTCTGACTTGAA[G/T]TTTTAACAGTTTCTA | 8853 |
rs62121306 | snp | A/G | 0.146314 | 0.227484 | intron-variant | ASAP2 | GRCh38.p7 | 2:9298304 | CATTCCTGAGATGGT[A/G]ATGACAGTGGTTTTG | 8853 |
rs62121307 | snp | C/T | 0.154993 | 0.231244 | intron-variant | ASAP2 | GRCh38.p7 | 2:9299059 | GAAATAGATAAAAGA[C/T]GAGGATTAATTCTCA | 8853 |
rs62121308 | snp | C/G | 0.33303 | 0.235809 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300265 | GCAGCTAATATCTCT[C/G]TTGGGAGGCTCAGAG | 8853 |
rs62121309 | snp | A/G | 0.146314 | 0.227484 | intron-variant | ASAP2 | GRCh38.p7 | 2:9300486 | CCCTGTGGCTTTGCC[A/G]GTTTTTAATACTTCA | 8853 |
rs62121311 | snp | C/T | 0.201418 | 0.245234 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302905 | TCATATGTGCTGCAC[C/T]TGGCAGAGGGGCATC | 8853 |
rs62121312 | snp | A/G | 0.444444 | 0.157135 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305318 | TAGTGGGGTATAGAT[A/G]TTGGTGGAGGGGCTG | 8853 |
rs62121313 | snp | A/G | 0.350764 | 0.228794 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305342 | GGGGCTGTAGTAGTG[A/G]GGTATAGATATTGGA | 8853 |
rs62121314 | snp | C/T | 0.31014 | 0.242659 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305399 | TTGGTGGAGGGGCTG[C/T]AATAGTGGGGTATAG | 8853 |
rs62121315 | snp | A/G | 0.31014 | 0.242659 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305401 | GGTGGAGGGGCTGTA[A/G]TAGTGGGGTATAGAT | 8853 |
rs62121316 | snp | G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305624 | GGTATAGATATTGGT[G/T]GACAGGCTGGAGTAG | 8853 |
rs62121317 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305686 | TAGTGGGGTATAGAT[A/G]TTGGTGGAGAGGCTG | 8853 |
rs62121340 | snp | G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305693 | GTATAGATATTGGTG[G/T]AGAGGCTGTAGTAGT | 8853 |
rs62121341 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305704 | GGTGGAGAGGCTGTA[A/G]TAGTGGGGTATAGAT | 8853 |
rs62121342 | snp | G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305727 | GTATAGATATTGGTG[G/T]AGAGGCTGTAGTAGT | 8853 |
rs62121343 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305764 | TAGATATTGGTGGAG[A/G]GGCTGTAGTAGTGAG | 8853 |
rs62121344 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9305811 | GGCTGGAGTAGTGAC[A/G]TATAGATATTGGTGG | 8853 |
rs62121345 | snp | A/C | 0.334642 | 0.235236 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306038 | TATGGGATGGAGGGG[A/C]TGTGGGAGAGTATCG | 8853 |
rs62121346 | snp | A/G | 0.329783 | 0.236927 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306219 | GGGTGTATATACCAC[A/G]TGGAGAGTTGTAGTA | 8853 |
rs62121347 | snp | G/T | 0.077417 | 0.180873 | intron-variant | ASAP2 | GRCh38.p7 | 2:9306554 | TTGAGCCTGTTTCTG[G/T]GCCCCAGGGAAGGAG | 8853 |
rs62121348 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9307234 | GTCTGGGATAGGGCC[C/T]AGGGTTTTGCATTTC | 8853 |
rs62121349 | snp | C/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9311385 | AAAAAAAAAGTTTGC[C/T]TGCTTGTTGGTCCAA | 8853 |
rs62121350 | snp | C/G | 0.378568 | 0.214407 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316896 | CCTTTTATCTCCTTT[C/G]CCTAGCAACACCCCC | 8853 |
rs62121351 | snp | C/T | 0.333261 | 0.235728 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317675 | AATCACTCACATCCA[C/T]AATCACATCCTGAAA | 8853 |
rs62121352 | snp | C/T | 0.333261 | 0.235728 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319569 | GTCAGGCTGCCAGGG[C/T]GCAGGAGGAGCCAGT | 8853 |
rs62639385 | snp | A/C | 0.333491 | 0.235646 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317531 | CACACCCCACACTCA[A/C]ATCCACACAATCTCT | 8853 |
rs62639386 | snp | A/C | 0.333491 | 0.235646 | intron-variant | ASAP2 | GRCh38.p7 | 2:9317550 | CACACAATCTCTCAC[A/C]TCCACAATCACACTC | 8853 |
rs66589853 | snp | A/G | 0.128288 | 0.218372 | intron-variant | ASAP2 | GRCh38.p7 | 2:9270604 | CTCTTAGTTATTTTT[A/G]AATGTACAATAAATT | 8853 |
rs70948809 | in-del | -/AA | 0 | 0 | intron-variant, nc-transcript-variant | ASAP2, LOC107985851 | GRCh38.p7 | 2:9211170 | CAAAAAAAAAAAAAA[-/AA]GTTTGTTGTCCTGGC | 8853 |
rs70948810 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9234111 | GCGAAGCTATGTCTC[-/A]AAAAAAAAAAAAAAA | 8853 |
rs70948813 | in-del | -/TAATAA | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9264221 | TAATAATAATAATAA[-/TAATAA]TAAACACAAGTACTG | 8853 |
rs70948815 | in-del | -/GT | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9362012 | TGTGTGTGTGTGTGT[-/GT]ATTTAGAATTATGTC | 8853 |
rs71389232 | in-del | -/T/TT | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9215665 | GATTTGTTTAGCTAG[-/T/TT]TTTTTTTTTTTTTTT | 8853 |
rs71389234 | in-del | -/A/AA | 0.442655 | 0.159323 | intron-variant | ASAP2 | GRCh38.p7 | 2:9252914 | GCGAGACTCCGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 8853 |
rs71389235 | in-del | -/A | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9256162 | TCTAGGGTCCCCTGC[-/A]AAAAAAAAAAAAAAA | 8853 |
rs71389236 | in-del | -/A/AA | 0.368119 | 0.220336 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258244 | GCGATACTTCATCTC[-/A/AA]AAAAAAAAAAAAAAA | 8853 |
rs71389237 | in-del | -/C | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9260895 | TCTGCTTCTCCGCCA[-/C]CCTGGCCCTTCAGAA | 8853 |
rs71389239 | in-del | -/T/TT/TTT | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302122 | CCACCGCGCCCGGCC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 8853 |
rs71389241 | in-del | -/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9394182 | GGTCTAGTTTGTGGC[-/T]TTTTTTTTTTTTTTT | 8853 |
rs71389242 | in-del | -/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9397725 | AAAAAAAAATCAAAA[-/G]GGATATATATATATA | 8853 |
rs71437656 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315850 | CATTGTACCTTGGAG[A/G]AAGGCCAGGTACGTG | 8853 |
rs71437657 | snp | A/C | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328380 | AATAAAAGCATATAT[A/C]CAACATAAAAAATCT | 8853 |
rs71437658 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9331490 | AGCCATGGTTTGGCA[A/G]GGCATGGTGGCTCAT | 8853 |
rs71437659 | snp | G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360215 | AGATGATGTAATAAT[G/T]GTTTATTTTGTACTA | 8853 |
rs71437660 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366635 | TGGGAAAATTGCAAC[A/G]CAGCCTCTAGGCTTT | 8853 |
rs71437661 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402003 | GCAGACAGTGAGGGC[A/G]GTGGATGAACCGGCT | 8853 |
rs72534540 | in-del | -/A | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9305519 | TAGTGGGGTATAGAT[-/A]ATTGGTGGAGGGGCT | 8853 |
rs72534541 | in-del | -/TC | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9343407 | TGGCACTGGTGGYCT[-/TC]CCTACTCTCAACTCA | 8853 |
rs72773351 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231580 | GCCCGGGTGCCGCCA[C/T]ACCCCTAGCCTGCGC | 8853 |
rs72773354 | snp | A/T | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | ASAP2 | GRCh38.p7 | 2:9236591 | AATGTCTAAAGAGGA[A/T]TTTTTACCGGAGAGG | 8853 |
rs72773365 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ASAP2 | GRCh38.p7 | 2:9242140 | GAGGTCTGTGCTCTG[G/T]GCTGGAATGAAACTT | 8853 |
rs72773369 | snp | C/T | 0.272241 | 0.249009 | intron-variant | ASAP2 | GRCh38.p7 | 2:9243673 | AAGCTTGTTTTATCT[C/T]ACCTAGATTAAGTTG | 8853 |
rs72773377 | snp | A/G | 0.276267 | 0.248616 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258111 | AGGATATACGGACAT[A/G]CACATTTCATTTCTT | 8853 |
rs72773379 | snp | A/C | 0.275999 | 0.248644 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258233 | CTGGGTGACAGAGCG[A/C]TACTTCATCTCAAAA | 8853 |
rs72773380 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ASAP2 | GRCh38.p7 | 2:9258322 | TTCACAGTATTGATA[A/G]TAATCAGTAGTTGTT | 8853 |
rs72773381 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9259263 | GAGAAACATTCATCC[C/T]TCAACGCTGAGAATA | 8853 |
rs72773386 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9261677 | CCAGTGCTGCCCCCA[A/G]CCTTTAACAGTGTGG | 8853 |
rs72773389 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265458 | CCTCAATACCCTGCT[C/T]GATGGGAGGAGAAGA | 8853 |
rs72773399 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282130 | GGGCTGGGATTTTAA[C/T]GTAGCTCCTTGGGCT | 8853 |
rs72773400 | snp | C/T | 0.211516 | 0.24702 | intron-variant | ASAP2 | GRCh38.p7 | 2:9283014 | CCCACCCATTTTCAT[C/T]AAGCCTTAGCTCTCT | 8853 |
rs72775204 | snp | A/T | 0.230896 | 0.249269 | intron-variant | ASAP2 | GRCh38.p7 | 2:9290581 | GGTGCTTCAGATTTC[A/T]TTTTAAAGTTTTATT | 8853 |
rs72775207 | snp | C/G | 0.192401 | 0.243274 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296185 | ATATTTCCAGTTGAA[C/G]TGATGAAAACATAGA | 8853 |
rs72775212 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ASAP2 | GRCh38.p7 | 2:9303169 | CAATGATCATAGTAT[C/T]ATCTTTTTGGGAGGA | 8853 |
rs72775213 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | ASAP2 | GRCh38.p7 | 2:9307031 | GCACTGCCCTGGAGC[A/G]GAGGTCCTCCAAGTG | 8853 |
rs72775216 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ASAP2 | GRCh38.p7 | 2:9319224 | CTGCCCCTGCGCATC[A/G]CCAGCCCTGACAGAC | 8853 |
rs72775219 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329123 | GAGCCGGCAGATAAG[A/G]AGTGGGGGAAGAACA | 8853 |
rs72775232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9376773 | TAGAGATTAAAGAGA[C/G]TCTATGTAAGAGATA | 8853 |
rs72775242 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9393153 | AGAGCTGAGGGCCCC[A/G]GCCTCCTGCTGTTGG | 8853 |
rs73148712 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323811 | CACCCGCAGCCTCAG[A/C]CCTTCCCTTAGTGAG | 8853 |
rs73148715 | snp | A/T | 0.0130097 | 0.0795963 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327805 | TTACTTCCATGACAT[A/T]TCCTTTTCATTGTTC | 8853 |
rs73148719 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328261 | TATTGAAAATATTCC[A/G]GAAGTGAGTGCTAAT | 8853 |
rs73148721 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328366 | ATATCTTAATTAAAA[A/G]TAAAAGCATATATAC | 8853 |
rs73148722 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328757 | CACCCACCCAACACA[C/T]ATGTCAGGTGCTGGA | 8853 |
rs73148723 | snp | A/G | 0.114387 | 0.210022 | intron-variant | ASAP2 | GRCh38.p7 | 2:9328818 | GCTGGCATAGTTCCT[A/G]CTCAAAGAGTCAAGT | 8853 |
rs73148725 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329022 | CAGCACACAGTGCCC[A/G]GAACACAGTAGGTAC | 8853 |
rs73148734 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | ASAP2 | GRCh38.p7 | 2:9337743 | GTTTTAGTGTGGAGC[C/T]TGTGCCGTTCTGGTC | 8853 |
rs73148736 | snp | A/C | 0.0655868 | 0.168795 | intron-variant | ASAP2 | GRCh38.p7 | 2:9338715 | TCATCTCTTCAGGGG[A/C]TCATGCTCTGGGGGT | 8853 |
rs73148740 | snp | A/G | 0.040671 | 0.13668 | intron-variant | ASAP2 | GRCh38.p7 | 2:9339191 | CTCCAAAACAAAAAC[A/G]AAAAACTGGGGACGG | 8853 |
rs73148746 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9344167 | TTGGAAACCCCTGCC[A/T]TTCCACTCACTGCAT | 8853 |
rs73148762 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9349149 | CTGCCTTGTATAGGT[A/G]TATAATAAAAATAGC | 8853 |
rs73148774 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354865 | GTGGCGTGTCCACTC[A/G]CTTTTAGGAGCACAG | 8853 |
rs73148776 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | ASAP2 | GRCh38.p7 | 2:9355260 | TTTAGTTGTGATTTT[A/T]TCCTGGTCTCTTGCA | 8853 |
rs73148781 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9357861 | GCGATATTTACCTGC[C/T]GTGAGTTTCTCAGGG | 8853 |
rs73148796 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ASAP2 | GRCh38.p7 | 2:9366490 | GGCTATAAACCAGGC[A/G]CTCTGACATTGGGGT | 8853 |
rs73148800 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASAP2 | GRCh38.p7 | 2:9368352 | AAATAAATCATCAGA[A/T]GGGGATGGGTAATGT | 8853 |
rs73150905 | snp | C/T | 0.030278 | 0.119257 | intron-variant | ASAP2 | GRCh38.p7 | 2:9370744 | GAAGTCACATCTGTA[C/T]CCTGCATTGATTCCA | 8853 |
rs73150907 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371105 | AATGTGGAACCCTTC[A/G]GTATGAACGTTCTGT | 8853 |
rs73150909 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371692 | TTGCTCACAGGAGCC[A/G]GAACTGTTTCTCCCT | 8853 |
rs73150911 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371883 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 8853 |
rs73150914 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373120 | TAGCGCTGTGTGGAC[A/G]GGGAGCATGTGCCGG | 8853 |
rs73150916 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373217 | GGGAGGCAGTGTGAT[A/G]AAAGTGCCAGAGCAC | 8853 |
rs73150925 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377324 | TCATCCTGTGAGCCA[A/G]GTCATCGTACTGCGC | 8853 |
rs73150926 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9377920 | TCTGAGTGCCAGCCC[A/G]GCTCCTAGAACGCAG | 8853 |
rs73150927 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ASAP2 | GRCh38.p7 | 2:9379533 | GTTGTTACTTGGCCC[C/T]GGTCCCTCCCTCTCT | 8853 |
rs73150930 | snp | C/T | 0.00108726 | 0.0232905 | intron-variant | ASAP2 | GRCh38.p7 | 2:9380696 | GATGTCAGGCCTTTG[C/T]TGGGTTTTGCCTTAA | 8853 |
rs73150933 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9381082 | TGCTGTGGTGGGACA[A/G]CTGGAACAGAGGCCC | 8853 |
rs73150935 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | ASAP2 | GRCh38.p7 | 2:9382894 | ACAGTGTGATTGCAG[C/T]AGAGAAAGAGTTTAA | 8853 |
rs73150946 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9385465 | TTATAGAAATGAAAA[C/T]GTAGCTTACTTTATG | 8853 |
rs73150963 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9390827 | TTTAAATTTCATGGA[C/T]TGAGAAAACCTGCTG | 8853 |
rs73150968 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASAP2 | GRCh38.p7 | 2:9392767 | CAGAGGGAAACCCAG[C/T]GCCTTATGTGTTACC | 8853 |
rs73150988 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402323 | TGTGGCCTCGTTTGC[C/T]CTTAATGGATTGAAA | 8853 |
rs73150990 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402610 | GAAAATACCTGCTCA[A/T]TTCCAAAACTGGAAA | 8853 |
rs73150994 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | ASAP2 | GRCh38.p7 | 2:9404260 | GAGAATGTTTACTCA[A/G]TTTAGTGTCTTGTAT | 8853 |
rs73151901 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208351 | AGTGTGTGTGTGGGT[G/T]GGGGGGTGGGTGTCA | 8853 |
rs73153603 | snp | A/G | 0.10237 | 0.201756 | intron-variant, upstream-variant-2KB | ASAP2, LOC107985851 | GRCh38.p7 | 2:9210778 | CCAGGATGGTCGATG[A/G]TCTAGATCTCCTGAC | 8853 |
rs73153628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230721 | GCAAGGCAAGGACGT[C/T]GTTTCACCTTTTGAA | 8853 |
rs73153629 | snp | C/T | 0.146314 | 0.227484 | intron-variant | ASAP2 | GRCh38.p7 | 2:9231388 | CATCTAACTTTAAGA[C/T]CCAGTTTTAGCATCT | 8853 |
rs73153632 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232280 | CGATCCTTTTACACA[A/G]GTGGTCCCTCTGTTT | 8853 |
rs73153640 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | ASAP2 | GRCh38.p7 | 2:9238522 | TCCCTTGTCTTACTG[C/G]AAATGTCTTTCTCAA | 8853 |
rs73155668 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296133 | AGGTTCACACCGCAG[A/G]TCTGGCTGCCCTGTT | 8853 |
rs73155688 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310236 | TCCCCACATTTCAAA[G/T]CGTCTTTTCTACCTC | 8853 |
rs73155689 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9310328 | AAGATCCTTTGGCCA[C/T]ATTGTATATTACATG | 8853 |
rs73155694 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ASAP2 | GRCh38.p7 | 2:9311503 | AAGTGAGTCAGAACA[G/T]AAGAGAAAGCCCTAT | 8853 |
rs73155696 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9313689 | AAATTGACCTGCGCC[A/G]GTGACTCTGATTGTG | 8853 |
rs73155700 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316094 | GAGGCCGAGGAGGGC[A/G]GATTGCTTAAGTCTA | 8853 |
rs73157609 | snp | G/T | 0.114036 | 0.209795 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321566 | TCAGTGGTTTCTGCT[G/T]GTCAGCCAGTAAGAG | 8853 |
rs73157611 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | ASAP2 | GRCh38.p7 | 2:9321891 | GGATAAATAAAGGAA[A/G]TAATTCTTTATTAAT | 8853 |
rs73157614 | snp | A/G | 0.040671 | 0.13668 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322763 | GGAGGAAGTCCAGGA[A/G]GAGAAACAGTGGGTA | 8853 |
rs73157615 | snp | C/T | 0.0379754 | 0.13246 | intron-variant | ASAP2 | GRCh38.p7 | 2:9323078 | TGTCCCGTTGAGTTC[C/T]GTGCCAACAGGCATC | 8853 |
rs73912992 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ASAP2 | GRCh38.p7 | 2:9227038 | GGTCCTGCTCCCTGG[C/T]GAGAAGGAAGTATGT | 8853 |
rs73912994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9230335 | GGACCCAGAGGGGCT[C/G]CGTGGGCCTGCTGCC | 8853 |
rs73913001 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ASAP2 | GRCh38.p7 | 2:9257131 | TTCATTCATTCCATG[C/T]TCGTGGAGTGTTTAC | 8853 |
rs73915705 | snp | A/G | 0.132409 | 0.220618 | intron-variant | ASAP2 | GRCh38.p7 | 2:9275559 | GCTTTTGAACCATGG[A/G]TTCCAGCCAGTTCCC | 8853 |
rs73915709 | snp | A/G | 0.122411 | 0.214991 | intron-variant | ASAP2 | GRCh38.p7 | 2:9288876 | GCTCTCTGGTTAAGG[A/G]GAGTCTAGGGTGAGT | 8853 |
rs73915710 | snp | A/G | 0.111576 | 0.20818 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289073 | CAGTGGATTGTTTTC[A/G]CATGTTTATCTTTGT | 8853 |
rs73915711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASAP2 | GRCh38.p7 | 2:9296624 | TAGTCTGTCAACTCT[A/G]AGCACATCCGATGTA | 8853 |
rs73915712 | snp | C/G | 0.0948562 | 0.196037 | intron-variant | ASAP2 | GRCh38.p7 | 2:9304491 | GTGGAGGGGCTGTAG[C/G]GGGGGTGTAGATACA | 8853 |
rs73915714 | snp | A/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9347755 | ATCCTCTTTGCCAGA[A/T]TCGCAGGATTGCCAC | 8853 |
rs73915716 | snp | A/G | 0.00428475 | 0.046087 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350931 | CCGCGCCATAGAGAC[A/G]TTGTCTTATGCTCTC | 8853 |
rs74260089 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASAP2 | GRCh38.p7 | 2:9240599 | ACTTGCCACGCACCA[C/T]GGCCGTAGCTTTTGC | 8853 |
rs74260092 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | ASAP2 | GRCh38.p7 | 2:9312812 | CTCCTGCCACCACTG[C/T]GGCCACATGTGGCTC | 8853 |
rs74341814 | snp | G/T | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294316 | TAATTTTTTTAAAAA[G/T]AAAAAAACTTAACCT | 8853 |
rs74343764 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASAP2 | GRCh38.p7 | 2:9316475 | CAAGTCCCTCTTCTC[A/G]TCCTTCTCCTTCTCT | 8853 |
rs74359136 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASAP2 | GRCh38.p7 | 2:9402317 | CTTTCCTGTGGCCTC[A/G]TTTGCCCTTAATGGA | 8853 |
rs74416428 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | ASAP2 | GRCh38.p7 | 2:9373716 | TCGAAGGGGAGCAGC[C/T]GCATTTGTCCTCAGA | 8853 |
rs74417063 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ASAP2 | GRCh38.p7 | 2:9360551 | AATGTTTAACAGTCA[A/G]CTCTGGAGAAAAAAG | 8853 |
rs74425041 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9327388 | CAATCACATTATTTT[A/C]CTTGTAAGGGAAATG | 8853 |
rs74426864 | snp | A/G | 0.111928 | 0.208413 | intron-variant | ASAP2 | GRCh38.p7 | 2:9295556 | CGCCGCAGGCCCAGC[A/G]TCACTGTGACTTACC | 8853 |
rs74439099 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | ASAP2 | GRCh38.p7 | 2:9375528 | ATCCATTACCTCACA[G/T]GCTCATCCATTTTTA | 8853 |
rs74440525 | snp | A/C | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9354647 | TGAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAG | 8853 |
rs74448327 | snp | A/C | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9267897 | AGCAAGACTCTATCT[A/C]AAAAAAAAAAAAAAA | 8853 |
rs74450818 | snp | A/G/T | 0.0260105 | 0.111035 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329247 | AAAAGCCTTAGGGAT[A/G/T]TGGATGGCCCCAGAC | 8853 |
rs74450979 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ASAP2 | GRCh38.p7 | 2:9350598 | CCACCAAGGTGCCCT[G/T]GCAGGGAGGCAGTTG | 8853 |
rs74462475 | snp | C/G | 0.131381 | 0.220067 | intron-variant | ASAP2 | GRCh38.p7 | 2:9352092 | TGCAAGCCAGGTGTG[C/G]TGGTGTGATCCTGTA | 8853 |
rs74472937 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | ASAP2 | GRCh38.p7 | 2:9294902 | GACCATGGAGGTTGC[A/G]TTCCTGTTTCTGTCA | 8853 |
rs74478195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASAP2, LOC100506317 | GRCh38.p7 | 2:9208057 | GGGAAAGGGGCAGAG[C/T]CTGTGAGTCCAGGGG | 8853 |
rs74518557 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASAP2 | GRCh38.p7 | 2:9234244 | CTTCTTGACGCTATT[C/T]GTGCTGCCTCTCAGC | 8853 |
rs74546957 | snp | C/T | 0 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9302124 | CACCGCGCCCGGCCT[C/T]TTTTTTTTTTTTTTT | 8853 |
rs74547153 | snp | A/G | 0.5 | 0 | intron-variant | ASAP2 | GRCh38.p7 | 2:9351964 | CTTTATCCTGTGTCA[A/G]ACACCCATCCTGACT | 8853 |
rs74548936 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ASAP2 | GRCh38.p7 | 2:9282336 | TCTTTATTTCGGAAC[A/G]AGCGTTGTCTACTGC | 8853 |
rs74549764 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | ASAP2 | GRCh38.p7 | 2:9265483 | AGAAGAGAAAAGGGT[A/T]ACAAAGTATAGGATA | 8853 |
rs74550408 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | ASAP2 | GRCh38.p7 | 2:9232418 | CCCCGTACCCCTTTC[A/G]CAGCTGACTGTCCAC | 8853 |
rs74612567 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ASAP2 | GRCh38.p7 | 2:9329741 | TTGTGGAATTGCCAT[A/G]CCTGTCTGCTTACCT | 8853 |
rs74641209 | snp | A/C/G/T | | | intron-variant | ASAP2 | GRCh38.p7 | 2:9338347 | TCTCTGTCTGTCTCT[A/C/G/T]TCTCTCTCTCTCTCT | 8853 |
rs74646993 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ASAP2 | GRCh38.p7 | 2:9322957 | CCGGTTTGACATCTT[C/T]GTGAGGACACCCATT | 8853 |
rs74651263 | snp | A/C | 0.0505692 | 0.150756 | intron-variant | ASAP2 | GRCh38.p7 | 2:9371409 | CGTAATATGTTGCTT[A/C]TGGTGAACCAGTGAC | 8853 |
rs74663590 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | ASAP2 | GRCh38.p7 | 2:9315339 | GTCCTGAGAAGGAGC[A/G]GTGAGGCGCAGCCAA | 8853 |
rs74665000 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | ASAP2 | GRCh38.p7 | 2:9325423 | TAGCATTTTACAAAC[A/C]ATCAGGGTGAAATTA | 8853 |
rs74674396 | snp | A/T | 0.00465445 | 0.0480163 | intron-variant | ASAP2 | GRCh38.p7 | 2:9356386 | TGGGCTCTAGGACAT[A/T]TCAATCCCATTCTGA | 8853 |
rs74691695 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASAP2 | GRCh38.p7 | 2:9289839 | AACACAACCAGACTA[C/G]ATACATCCTGGGGTA | 8853 |
rs74704189 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASAP2 | GRCh38.p7 | 2:9224538 | CAAAATCAAGGTTGT[C/T]GTGTCATCCTTTGAA | 8853 |