SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4125 | snp | A/G | 0.379354 | 0.213933 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285829 | CCTGCCACTTCTTCC[A/G]GGAAGCCTTCCCTGT | 64446 |
rs735147 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298115 | GCCATGATTAATTCA[A/G]GAGCCTTGACTCAGT | 64446 |
rs1320037 | snp | A/G | 0.491629 | 0.0641526 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304852 | GGTGGGCCACCCTGC[A/G]TCCCCTCCCTGGGTC | 64446 |
rs1531493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285420 | ACTCCTCCTGATGCC[C/T]GGTCAGCCCTTGTAC | 64446 |
rs1870990 | snp | C/T | 0.373598 | 0.21731 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290572 | TAGCTCTCTGCCTGG[C/T]ACCTACATGTTTATT | 64446 |
rs1877686 | snp | G/T | 0.490673 | 0.0676508 | intron-variant | DNAI2 | GRCh38.p7 | 17:74274443 | CCCCCCAAGAGGAAT[G/T]TTTGGCACTCTTGGT | 64446 |
rs1877687 | snp | C/T | 0.465263 | 0.127129 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274303 | TCTCTGGGGAAGCGT[C/T]CAATCCACGGTCGCG | 64446 |
rs1979370 | snp | A/G | 0.243582 | 0.249918 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312180 | TTCGACATCATCTTC[A/G]CAGAGCTGAAGAAGA | 64446 |
rs1979371 | snp | A/G | 0.0832709 | 0.186283 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312308 | CTGCTTCTGCTTGCC[A/G]ACTTCCTGGGTGACC | 64446 |
rs2021862 | snp | A/G | 0.275732 | 0.248672 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286204 | AGGAGGCCGAGGCAG[A/G]AGAATTGCTTGAACC | 64446 |
rs2054400 | snp | A/G | 0.225301 | 0.248777 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314337 | ACTGGGTGGTGGGCT[A/G]GGAGCATCGGGCCCT | 64446 |
rs2126695 | snp | A/G | 0.480931 | 0.0957637 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287879 | caacctccgcctccc[A/G]ggttcaagtgattct | 64446 |
rs2126696 | snp | C/T | 0.480853 | 0.0959518 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287848 | cctgcctcagcatcc[C/T]gagtagctgggatta | 64446 |
rs2279122 | snp | A/G | 0.00498343 | 0.0496677 | synonymous-codon, nc-transcript-variant, intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312080 | GAAGGAGAAGGGTAA[A/G]GCGGAGGGCAGGGAT | 64446 |
rs2290955 | snp | C/T | 0.498497 | 0.02737 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309395 | AGCTTGAAGGTCACG[C/T]GCATGTCCCTCCTTG | 64446 |
rs2290956 | snp | C/T | 0.498878 | 0.0236607 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309549 | TGCAGCGATTGCTTT[C/T]GAGCGTGTGCTCCTA | 64446 |
rs2290957 | snp | C/T | 0.191918 | 0.243159 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309614 | GGTAGCACAACAGAA[C/T]CACCTGGGGGAAATT | 64446 |
rs2382648 | snp | C/T | 0.493432 | 0.0569306 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298752 | ctactcgggaggctg[C/T]tactcgggaggctgc | 64446 |
rs2382839 | snp | C/T | 0.487049 | 0.0794222 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285958 | ATATACACACACACA[C/T]ATATATATATATAGA | 64446 |
rs2382840 | snp | G/T | 0.47743 | 0.103805 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285972 | ACATATATATATATA[G/T]AGAGAGAGAGAGAGA | 64446 |
rs2891037 | snp | C/T | 0.428635 | 0.174898 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275892 | TCTTTGTTGTTGTTG[C/T]TTTTGGGACAGTGTT | 64446 |
rs3056091 | in-del | -/AG | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285995 | gagagagagagagag[-/AG]attaataattttatt | 64446 |
rs3803792 | snp | C/T | 0.489761 | 0.0708128 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281740 | TATCTCCACAGGTCC[C/T]GCCAGGACAGCTCCA | 64446 |
rs4007904 | snp | A/G | 0.488302 | 0.0755777 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305914 | GAGGCCGAGGTGGGC[A/G]GATCACCTGAGGTCA | 64446 |
rs4007906 | in-del | -/TT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305691 | ttttttttttttttt[-/TT]gagacagtctcgctt | 64446 |
rs4239008 | snp | A/G | 0.245339 | 0.249957 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312264 | GTTGGGTGGGTTGGG[A/G]ACTGGGCGGGACACA | 64446 |
rs4239009 | snp | A/G | 0.154917 | 0.231213 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312271 | AGTGCCATGTGTCCC[A/G]CCCAGTCCCCAACCC | 64446 |
rs4324163 | snp | A/G | 0.386313 | 0.209568 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295131 | tggatgtggtggctc[A/G]tgcctggaaacctag | 64446 |
rs4375697 | snp | G/T | 0.482979 | 0.0906686 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295037 | ccatcctgtagcttc[G/T]ctgctatatttttat | 64446 |
rs4528607 | snp | A/T | 0.118933 | 0.212888 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295141 | ggctcgtgcctggaa[A/T]cctagcactttggga | 64446 |
rs4789051 | snp | A/G | 0.489893 | 0.0703642 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295095 | tttgttctttctttt[A/G]aaaataatttctgtc | 64446 |
rs4789053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306165 | CGGGTGCCTTGGCAC[A/G]ATTCAGCAGTGAGGC | 64446 |
rs4789054 | snp | A/G | 0.49907 | 0.0215454 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315314 | GGTGACCTTGGCAGG[A/G]ACCCAAAGTGCCCTT | 64446 |
rs4789645 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279726 | tagagatgggttttc[G/T]ccatgttggccaggc | 64446 |
rs4789646 | snp | C/T | 0.330947 | 0.236533 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279774 | CCTCAAGTGATCCAC[C/T]GGCCTCGGCCACCCA | 64446 |
rs5822035 | in-del | -/AGCCGCGACC | 0.472616 | 0.113763 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274285 | TTTGAGGAGCACCGG[-/AGCCGCGACC]GTGGATTGAACGCTT | 64446 |
rs5822036 | in-del | -/GA | 0 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285996 | AGAGAGAGAGAGAGA[-/GA]TTAATAATTTTATTT | 64446 |
rs6501705 | snp | A/G | 0.489492 | 0.0717183 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282731 | CTTATCTTGAGGGTC[A/G]TGGTCATGTGTTCAG | 64446 |
rs6501706 | snp | A/G | 0.0247719 | 0.1085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285228 | TCCTGCCCCAGCTGC[A/G]AGAGCCCCATCCATC | 64446 |
rs7210620 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304186 | ttctttttctttttt[C/T]ttttttttttttttt | 64446 |
rs7211923 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292478 | ctggagtgcagtggt[A/G]taatcactgctcatt | 64446 |
rs7215726 | snp | A/G | 0.482609 | 0.0916147 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275588 | AAATTCTGGCCGGGT[A/G]CAGTGGCTCACGCCT | 64446 |
rs7216193 | snp | C/G | 0.482831 | 0.0910472 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275883 | TGACAGAGCAACACT[C/G]TCCCAAAAGCAACAA | 64446 |
rs7217436 | snp | A/G | 0.198634 | 0.244666 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312749 | TCACCTGAGCTGGTC[A/G]CTTCACTTCTGGCTT | 64446 |
rs7221177 | snp | A/G | 0.475789 | 0.107327 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288746 | TGGAAGGAGTTGCAG[A/G]AAGTGGGTGGAAGTG | 64446 |
rs7222456 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284519 | ccaggttcaagtgat[C/T]ctcctgcctcagcct | 64446 |
rs7223470 | snp | C/T | 0.497387 | 0.0360476 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279123 | agtgagctgagatcg[C/T]gccactgcactccag | 64446 |
rs7224054 | snp | A/T | 0 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293916 | agcctcccgagtagc[A/T]gggattacaggtgca | 64446 |
rs7503505 | snp | A/C | 0.49306 | 0.0584955 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306128 | GATTGGGTGTGAACC[A/C]AGGAAGCTTGGCTGG | 64446 |
rs8067840 | snp | G/T | 0.213635 | 0.247341 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305047 | GATGGGGTCTGAGGA[G/T]CCCGGGAAGAGTGGG | 64446 |
rs8069083 | snp | A/G | 0.490287 | 0.0690083 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304718 | ACCGACTGCCAGGTA[A/G]CTTCCTGAGTGCTGG | 64446 |
rs8073148 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283127 | TTGTGAGAGCTGGCT[A/T]AAAAATggaaaggag | 64446 |
rs8073660 | snp | A/G | 0.498916 | 0.0232526 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305293 | CAAGACGTCAGCTGA[A/G]AAGATTGTGTGCACC | 64446 |
rs8075243 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279735 | gttttcgccatgttg[A/G]ccaggctggtcttga | 64446 |
rs8076337 | snp | A/G | 0.453444 | 0.145294 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301041 | GTCGCCCCTCCTCCC[A/G]CCAGGTCATGTGGTG | 64446 |
rs8081850 | snp | C/T | 0.205417 | 0.245993 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289387 | caaaaattagccagg[C/T]gtggtggtgtgcgcc | 64446 |
rs9892679 | snp | A/G | 0.499527 | 0.0153681 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273624 | GGCGTAGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 64446 |
rs9893381 | snp | A/G | 0.264358 | 0.249587 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277469 | GTTGAGTTGCTCTGG[A/G]GCTAGGAGTGGGATG | 64446 |
rs9894673 | snp | A/G | 0.483053 | 0.0904792 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294880 | tgtgacttccattat[A/G]tgtatgttggcatgc | 64446 |
rs9900615 | snp | C/T | 0.32768 | 0.237625 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276968 | TTTTTCACAAGGCCG[C/T]AGCTTTGTCCATGTG | 64446 |
rs9901263 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291832 | AATGAGTTGGGAAGT[A/G]TTCCCTTCTGGAAGT | 64446 |
rs9904370 | snp | C/T | 0.483053 | 0.0904792 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295485 | tttctttagttcttt[C/T]gatgtgacttccttt | 64446 |
rs9904599 | snp | A/G | 0.262435 | 0.249691 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275189 | GACCACAGTCTTTCC[A/G]TCAAGGAGACCACAA | 64446 |
rs9904729 | snp | C/T | 0.490063 | 0.0697833 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304081 | GAGCTGAGATCGCAC[C/T]GCTGCACTCCAGCCT | 64446 |
rs9905633 | snp | A/G | 0.368119 | 0.220336 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291291 | TCAGCCTCCCGAGTC[A/G]CTGAGATTACAGGCA | 64446 |
rs9906135 | snp | A/T | 0 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74274733 | GAAGATGGGCCCTTT[A/T]AGAGGAGAGCTTTCT | 64446 |
rs9907364 | snp | C/T | 0.476833 | 0.105105 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291921 | CAGGCCGGAGTGCAG[C/T]GGTGCAGTCTCAGCT | 64446 |
rs9908396 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302078 | gaaggaaAgaaggaa[A/G]gaaggaaggaaggaa | 64446 |
rs9908476 | snp | A/C | 0.0678174 | 0.1712 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312152 | GCTGGTCAGCAAGGC[A/C]GAGGAGGAGTTCTTC | 64446 |
rs9908915 | snp | C/T | 0.47934 | 0.0995154 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293124 | aggcgtgagccaccg[C/T]acctggcctgtccag | 64446 |
rs9909910 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293572 | agccaggtgtggtga[C/T]acgcacctgtaatcc | 64446 |
rs9910454 | snp | C/G | 0.387453 | 0.208822 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296976 | cagagttctgaaaaa[C/G]ttgattctgaccatt | 64446 |
rs9910602 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301910 | gaaggaaggaaggaa[A/G]gaaggaaggaaggaa | 64446 |
rs9912615 | snp | C/T | 0.282369 | 0.247896 | intron-variant | DNAI2 | GRCh38.p7 | 17:74274989 | TTCAGACCCTATGTG[C/T]TTTCCTCTCGAATCC | 64446 |
rs9912714 | snp | A/G | 0.240765 | 0.249829 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276274 | ATGCGGGAGACGCCT[A/G]AATCTTTGATGTCTG | 64446 |
rs9913670 | snp | A/G | 0.387453 | 0.208822 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297291 | tagagacggggtttc[A/G]ctgtgttagccagga | 64446 |
rs10451226 | snp | C/G/T | 0.0629771 | 0.165899 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302521 | gcggtgagccaagat[C/G/T]gcatcattgcactcc | 64446 |
rs10459893 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74286176 | tggcacatgcctgta[A/G]tcccagctacttagg | 64446 |
rs10637482 | in-del | -/AAT/AATAAT/AATAATAAT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74286297 | AATAATAATAATAAT[-/AAT/AATAAT/AATAATAAT]TTTGTTTGTCTAGCA | 64446 |
rs10852751 | snp | A/C | 0.481319 | 0.0948228 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300364 | TCCTCCCCTCCCTCC[A/C]TCTCTTATGTCTGCC | 64446 |
rs11077736 | snp | A/G | 0.379746 | 0.213696 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287442 | GGCCTGCACTCATGC[A/G]AGTATATCCATGAAT | 64446 |
rs11077738 | snp | C/T | 0.386504 | 0.209444 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294709 | cagctttgattatga[C/T]gtttctaggtatgga | 64446 |
rs11077740 | snp | A/G | 0.387453 | 0.208822 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298366 | CTGGAGTGCAATGGC[A/G]TGATCTCAGCTCACT | 64446 |
rs11077741 | snp | C/T | 0.451234 | 0.14834 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304704 | GGACGAGTTACATCA[C/T]CGACTGCCAGGTAAC | 64446 |
rs11650202 | snp | G/T | 0 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307036 | caggCTTGTGACTCA[G/T]CCAGTCCTTGCTTTG | 64446 |
rs11652758 | snp | C/T | 0.380333 | 0.213338 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283896 | taatcccagcacttc[C/T]agaggctgaggccag | 64446 |
rs11652975 | snp | C/T | 0.476833 | 0.105105 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292260 | agttacaattcagtc[C/T]gtttatttgttatag | 64446 |
rs11653157 | snp | A/G | 0.169435 | 0.236663 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309676 | TCCTACCCACAGGCC[A/G]ATTCCTTCAGAGCCC | 64446 |
rs11654252 | snp | A/C | 0.488424 | 0.0751925 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306680 | TGAAGTGCAATGGCG[A/C]GATCTCGGCTCACTG | 64446 |
rs11655226 | snp | A/G | 0.488241 | 0.0757703 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306704 | CTCACTGCAACCTCC[A/G]CCTCCCGAGTTCATG | 64446 |
rs11655542 | snp | C/T | 0.162581 | 0.234218 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313868 | CAGGAGGAGCTAGCC[C/T]GAGGCCTCCCAGTCT | 64446 |
rs11656329 | snp | C/T | 0.48155 | 0.0942576 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306802 | TTTGTATTTTTAGTA[C/T]AGACAGAGTTTCCCC | 64446 |
rs11656969 | snp | C/T | 0.106278 | 0.204558 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315038 | GCCCAAGTCTCAGAA[C/T]TCGTGACGGGGCACA | 64446 |
rs11657608 | snp | A/G | 0.380333 | 0.213338 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283897 | aatcccagcacttcc[A/G]gaggctgaggccagt | 64446 |
rs11867486 | snp | A/G | 0.498534 | 0.052819 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307310 | TGGTGGACCTGTGTC[A/G]TAGAACCTGGGTCTC | 64446 |
rs11869916 | snp | A/G | 0 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289348 | cctaggaaacatggt[A/G]aaaacctgtctctac | 64446 |
rs11870186 | snp | A/G | 0.475877 | 0.107142 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280908 | CCTGGGTAAAATGGC[A/G]AGACCCCATCTCTAC | 64446 |
rs12051676 | snp | C/T | 0.499824 | 0.00938333 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309654 | ACAAAAGCAGGTACC[C/T]GGCATCTCCTACCCA | 64446 |
rs12103882 | snp | A/G | 0.344592 | 0.231414 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278995 | acacggtgaaacccc[A/G]tctctactaaaaata | 64446 |
rs12449500 | snp | A/G | 0.472616 | 0.113763 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303259 | AACTCTGAGGCCCAG[A/G]GTGTCCACCTGCAGC | 64446 |
rs12449937 | snp | C/T | 0.47885 | 0.100637 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303078 | GGTGCACACTGTGTG[C/T]TGGACACTTGTGGCT | 64446 |
rs12449982 | snp | C/T | 0.472616 | 0.113763 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303222 | AGTACCTGGTAAAGC[C/T]GGGACTCAAACCCAG | 64446 |
rs12450048 | snp | C/T | 0.479663 | 0.0987666 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303533 | GCAACATCCACCTCC[C/T]GGGCTCAAGCCTCAG | 64446 |
rs12451602 | snp | A/G | 0.472616 | 0.113763 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303440 | CAACTTGAAGCCCAG[A/G]TTTTTGTTTTGTTTT | 64446 |
rs12452656 | snp | G/T | 0.121717 | 0.214577 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287175 | CAAAGGCAACTCCTT[G/T]CCATCGCTGCATGCC | 64446 |
rs12453118 | snp | A/G | 0.151001 | 0.229563 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293035 | agacggggtttcacc[A/G]tgttagccaggatgg | 64446 |
rs12936009 | snp | A/C | 0.482979 | 0.0906686 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294217 | ttcctatatgtctta[A/C]atctttttgttcttt | 64446 |
rs12936473 | snp | G/T | 0.363948 | 0.223495 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279424 | tatattgcatgccta[G/T]agcaaaacatctcct | 64446 |
rs12936905 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308696 | ccggctaattttttt[A/T]ttttttgtagaaaca | 64446 |
rs12937668 | snp | C/T | 0.481242 | 0.0950111 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288885 | ATGCGGAGGGGAAGC[C/T]TGTGGACCTGGGGCA | 64446 |
rs12938263 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304187 | tctttttcttttttc[C/T]ttttttttttttttt | 64446 |
rs12938436 | snp | G/T | 0.0832709 | 0.186283 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311480 | TAGCCAGGCATGGCG[G/T]CACATGCCTGTAATC | 64446 |
rs12938663 | snp | A/G | 0.136847 | 0.222927 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282659 | AACTACCCAGCTTGA[A/G]AAAAGGGAAGTGTCC | 64446 |
rs12939645 | snp | A/G | 0.229723 | 0.249176 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296382 | aggagggagggaggg[A/G]gagagagagagagag | 64446 |
rs12940226 | snp | C/T | 0.497613 | 0.0344622 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275287 | CGTCCTGCCCTCAAC[C/T]TTCACTTTCCTTGGG | 64446 |
rs12940754 | snp | A/G | 0.149999 | 0.229128 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300290 | ATAATACATGCCCAC[A/G]GAACAGAATCTAAAG | 64446 |
rs12941546 | snp | A/T | 0.0345262 | 0.126772 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307703 | gttaaatctgaattt[A/T]aaaaaaaaaaactat | 64446 |
rs12943749 | snp | A/G | 0.1652 | 0.235179 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295268 | tcagccaggtgaggt[A/G]gagtgcacctgcaat | 64446 |
rs12943843 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277335 | gtttgcaatgagcct[A/G]gatcttgccactgca | 64446 |
rs12943990 | snp | A/C | 0.145978 | 0.227331 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300601 | tttgttgctaccccc[A/C]aaaaaatacagcaaa | 64446 |
rs12944044 | snp | A/T | 0.498206 | 0.0298983 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308722 | AAACAGGGTCTTTCC[A/T]TGTTGTCCAGGCTGG | 64446 |
rs12944104 | snp | A/G | 0.498392 | 0.028309 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308782 | CTGCCTTGGCCTCCC[A/G]AAGTGCTGGGATTAC | 64446 |
rs12944390 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308697 | cggctaattttttta[A/T]tttttgtagaaacag | 64446 |
rs12946840 | snp | C/T | 0.451732 | 0.147663 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304008 | TGTGTGCTTGTGGTC[C/T]CTACGTGGGAGGCTG | 64446 |
rs12946901 | snp | A/G | 0.465368 | 0.126951 | intron-variant | DNAI2 | GRCh38.p7 | 17:74274690 | ATGGAAAAAAAAGAA[A/G]AAAAACAGCCTCCGG | 64446 |
rs12947030 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311312 | GGGAACACTGTGGAA[C/T]TGAAAACCCCTAGTG | 64446 |
rs12948999 | snp | A/C | 0.387453 | 0.208822 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298761 | CGAGTAACAGCCTCC[A/C]GAGTAGCATGTGCCA | 64446 |
rs12951862 | snp | A/G | 0.198014 | 0.244535 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272727 | ACAGATCCCAAACCC[A/G]CTGAGGGCTTCCCAT | 64446 |
rs16967130 | snp | A/T | 0.0818113 | 0.184966 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286361 | TGTCTAGCATGGTGT[A/T]CTTCAACCTTTTCTT | 64446 |
rs17192691 | snp | A/G | 0.474363 | 0.110278 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275108 | ATCACAGTCACTAAC[A/G]CAGCAGGTGACAGGA | 64446 |
rs17882048 | snp | A/G | 0.481319 | 0.0948228 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289192 | GCCCTGCTGGGCTCT[A/G]ACCTCGTATATGGAC | 64446 |
rs28463022 | snp | A/G/T | 0.0170251 | 0.090679 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279794 | TCGGCCACCCAAAGT[A/G/T]CTGGGATTATAGGCA | 64446 |
rs28574791 | snp | A/G | 0.127944 | 0.218179 | intron-variant, missense, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312848 | TCTTTTGTACCAGCG[A/G]AGAGAGGAAGAAAAG | 64446 |
rs28612762 | snp | C/T | 0.21303 | 0.247251 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287845 | CTGTAATCCCAGCTA[C/T]TCGGGATGCTGAGGC | 64446 |
rs28615526 | snp | A/G | 0.493013 | 0.058691 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306277 | AGACCAGAGAAGCTT[A/G]GACTATCACATCCCC | 64446 |
rs28647353 | snp | A/G | 0.117537 | 0.212022 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291464 | CCACCACACCTGGCC[A/G]GGACCCAGATTCATA | 64446 |
rs28692188 | snp | C/T | 0.230603 | 0.249246 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287666 | ACCTGGTAAAGCGAG[C/T]GGGGCAGTCTGGGCA | 64446 |
rs28725418 | snp | A/G | 0.18118 | 0.240341 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310152 | AGGAATGAGAAGAAC[A/G]TAGCCTCTTCCGTAA | 64446 |
rs28882071 | snp | C/T | 0.179105 | 0.239737 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295950 | GTGAGCATGCCTTTA[C/T]ACTCAGCCAGGCAGT | 64446 |
rs33997393 | in-del | -/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304845 | GATCTGGGTGGGCCA[-/C]CCCTGCGTCCCCTCC | 64446 |
rs34064840 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279260 | TATTAATATCTAGTA[-/T]TTTGATAGCACAACA | 64446 |
rs34075831 | snp | A/G | 0.236144 | 0.249616 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293489 | TTGGTTACCATTTGC[A/G]TGGTATATCTTTCCC | 64446 |
rs34138799 | in-del | -/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74276996 | TGGTAAAAACACACT[-/G]GGGGCACCCCGCTAC | 64446 |
rs34159194 | snp | C/T | 0.241814 | 0.249866 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299827 | GTCGAAGACGGGCAC[C/T]GAGTGCTTCTCAGCT | 64446 |
rs34192490 | in-del | -/TG | 0.491834 | 0.0633738 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303629 | GACAGAGTCTCACTC[-/TG]TTGCCCAGGCTGGAG | 64446 |
rs34248832 | in-del | -/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74310388 | AAGTCACGTCACTCT[-/C]CCAGGATTCAGTTTT | 64446 |
rs34306690 | in-del | -/T | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274205 | CGTGCTCCGGGGTCC[-/T]TTCCGCGTCGCCCCG | 64446 |
rs34333197 | in-del | -/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295814 | TGTATTCCCTGTCAC[-/G]GTGTGACCACTTATA | 64446 |
rs34392071 | snp | A/G | 0.0302059 | 0.119124 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305284 | CCGCAAGGCCAAGAC[A/G]TCAGCTGAGAAGATT | 64446 |
rs34458816 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299961 | CTTTAACACATTTTA[-/T]TTTTGAGATGGAGTT | 64446 |
rs34558513 | snp | G/T | 0.119281 | 0.213102 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308733 | TTCCTTGTTGTCCAG[G/T]CTGGTCTCAAAATCC | 64446 |
rs34598117 | snp | A/G | 0.149665 | 0.228982 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294021 | CTCCTGGCCTCAAGC[A/G]ATATGCCCACCTCGG | 64446 |
rs34608668 | snp | A/G | 0.124144 | 0.21601 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277153 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 64446 |
rs34628493 | in-del | -/A | 0 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285593 | CATACTTGCCAGTGC[-/A]AAAAAAAAAAATTGT | 64446 |
rs34811061 | in-del | -/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304657 | TCAGACAAGCTCGTG[-/C]CCCTCAAAGAGCTCA | 64446 |
rs34812711 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300601 | TTGTTGCTACCCCCC[-/A]AAAAAATACAGCAAA | 64446 |
rs34824670 | snp | A/C | 0.375 | 0.216506 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284576 | CACCACCACGCCCGG[A/C]TAATGTTTTGTATTT | 64446 |
rs34852424 | in-del | -/T | 0.36955 | 0.219562 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292834 | CCGGTGTAGTTTTCC[-/T]TTTTTTTTTTTTTGG | 64446 |
rs34880269 | snp | C/T | 0.377187 | 0.215229 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300965 | TGGCTGACCCCAGGA[C/T]GGTGGGGTGAGGGCG | 64446 |
rs34893675 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305671 | CTTAATTTTATTTCC[C/T]TTTTTTTTTTTTTTT | 64446 |
rs34911667 | in-del | -/A | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277401 | AAAAAAAAAAAAAAA[-/A]GAAAAAAGAAAAAAA | 64446 |
rs34919463 | in-del | -/C | | | upstream-variant-2KB, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74274215 | GGTCCTTCCGCGTCG[-/C]CCCCGCGCGTCCGGA | 64446 |
rs35013359 | snp | A/G | 0.260504 | 0.249779 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287978 | AAAAAAAGCAGTGCA[A/G]CTTCTTATGTGCTGA | 64446 |
rs35082870 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283675 | AAAGAAGGCAGAGGC[A/G]AGAGGATCACTTCCG | 64446 |
rs35091234 | in-del | -/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277563 | TCTCCCCACCTGCTG[-/C]CCCAGCTGCTCCAGG | 64446 |
rs35097253 | in-del | -/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279275 | TTTGATAGCACAACA[-/G]GGGTGACTATAGTCA | 64446 |
rs35159044 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74289520 | AAGACTCCATCTGAC[-/A]AAAAAAAAAAAAAAG | 64446 |
rs35302128 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287955 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 64446 |
rs35388033 | in-del | -/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299965 | AACACATTTTATTTT[-/G]GAGATGGAGTTTCAC | 64446 |
rs35429929 | snp | A/G | 0.250168 | 0.25 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295988 | TCTGCCTTAGTGTCT[A/G]TGCAGAGATGAGGTC | 64446 |
rs35579788 | in-del | -/C | | | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312453 | GGCAGGAACCATACT[-/C]CCATGCCTCCTGGTA | 64446 |
rs35604335 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74289521 | AAGACTCCATCTGAC[-/A]AAAAAAAAAAAAAGG | 64446 |
rs35636875 | snp | A/T | 0.00586717 | 0.0538439 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289716 | TGGGCATGAGCAGCG[A/T]TTCATACATCTGGGA | 64446 |
rs35652186 | snp | A/G | 0.000231256 | 0.0107506 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309332 | ACCAGGATGGACGGA[A/G]CCCTGGATATCTGGG | 64446 |
rs35732837 | in-del | -/TC | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309983 | ACATAACTTTGCTCC[-/TC]TCTCCTCTACCTGGG | 64446 |
rs35785992 | in-del | -/T | 0.498589 | 0.02652 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282313 | AGACATTTTTTTTTT[-/T]AAACAGGGTCTCACT | 64446 |
rs35812512 | in-del | -/A | 0.497121 | 0.0378299 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273750 | TCAAAAAAAAAAAAA[-/A]TTCCCCAGCTTCTAC | 64446 |
rs35967811 | snp | A/C | 0.125874 | 0.217008 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287594 | GAACAAGCTAAGTCC[A/C]TCCATAGGGGACTGG | 64446 |
rs35985071 | snp | A/G | 0.00588801 | 0.0539383 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285090 | AGTTAACCATGTCGA[A/G]GGGGGCTGGCCCAAG | 64446 |
rs36055191 | in-del | -/T/TT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74291867 | AAGAATTGATATTAA[-/T/TT]TTTTTTTTTTTTTTG | 64446 |
rs36098842 | in-del | -/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74276374 | ACTCTAGGTTCCCAC[-/G]GGGGGGAGGATCTCC | 64446 |
rs55909647 | snp | A/G | 0.247053 | 0.249983 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297117 | TTGAGACAGAGTCTC[A/G]CTGTGTCACCTAGGC | 64446 |
rs56013644 | in-del | -/TTT | 0 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292432 | TTTTTTTTTTTTTTT[-/TTT]GAGACAGAGTTTTAC | 64446 |
rs56066632 | snp | G/T | 0.294064 | 0.246086 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278695 | AGCAGGAGAACCACT[G/T]GAACGCAGGAGGCGG | 64446 |
rs56181128 | snp | A/G | 0.26078 | 0.249767 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288407 | GATGTAGCCAACATC[A/G]TTAGATAAGGAGCAT | 64446 |
rs56331794 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292960 | TCAGCCTTCCGAGTA[A/G]CTGGGACTACAGGTG | 64446 |
rs56696514 | in-del | -/T | 0 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304212 | TTTTTTTTTTTTTTT[-/T]GAGGTAGGGCCTTGC | 64446 |
rs56716237 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275985 | GTAGGGGCTGTACCA[A/G]GGACCAAGAAGAAGA | 64446 |
rs56790193 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301323 | ACGTGTGTGGCCTTT[A/T]CAACAACTTTCCAGC | 64446 |
rs56951763 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296334 | GAGAGAGAGAGAGAG[A/G]AGAGAGAGAGAGGAG | 64446 |
rs57113634 | in-del | -/AATAATAAT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74286331 | AATAATAATAATAAT[-/AATAATAAT]TTTGTTTGTCTAGCA | 64446 |
rs57143936 | in-del | -/A/AA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295252 | AAAAAAAAAAAAAAA[-/A/AA]TCAGCCAGGTGAGGT | 64446 |
rs57241428 | in-del | -/A/AA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287969 | AAAAAAAAAAAAAAA[-/A/AA]GCAGTGCAACTTCTT | 64446 |
rs57341715 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276016 | GGAAAATGTTCTCAT[C/T]TCCTTATTCCACTAG | 64446 |
rs57387665 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307727 | AAACTATTTTTTTTT[-/T]AGTATAAGTATGTCC | 64446 |
rs57623495 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285604 | TGCAAAAAAAAAAAA[-/A]TTGTTTTAAGGAAAA | 64446 |
rs57688909 | snp | C/T | 0.0490535 | 0.14873 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273643 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 64446 |
rs57843748 | snp | A/T | 0.105569 | 0.204058 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306718 | CACCTCCCGAGTTCA[A/T]GCGATTCTCCTGCCT | 64446 |
rs57863144 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284235 | TTAAAAAAAAAAAAA[-/A]GGAAAGAAGGGAAAG | 64446 |
rs58014408 | in-del | -/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304186 | TTCTTTTTCTTTTTT[-/C]TTTTTTTTTTTTTTT | 64446 |
rs58022186 | in-del | -/GT | 0 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303630 | ACAGAGTCTCACTCT[-/GT]TGCCCAGGCTGGAGT | 64446 |
rs58224225 | in-del | -/A | 0 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289534 | ACAAAAAAAAAAAAA[-/A]GGGGGAGAAATTGGG | 64446 |
rs58369361 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304337 | GCAGAGGACATCTGA[A/G]CCCGTTGACAAAGGC | 64446 |
rs58528569 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297785 | CCTGAACCTGGAGTC[A/G]CCAGACACCCAACCC | 64446 |
rs58530220 | snp | A/G | 0.105569 | 0.204058 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306881 | CCTCAGCCTCCCGAA[A/G]GGCTGGGATTACAGG | 64446 |
rs58634425 | snp | G/T | 0.499598 | 0.0141716 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272279 | GTCTTCAGAGAGCCC[G/T]CGGCTTCCCAGGGCT | 64446 |
rs58831344 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305534 | AGTCCCGAGCCTCCA[C/T]ATGTAAAATGGAGAA | 64446 |
rs58988578 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74297918 | AGCCAGGATGGCTGA[A/G]AAACTCCTCCTCTGA | 64446 |
rs59034534 | snp | A/G | 0.105569 | 0.204058 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306878 | CTGCCTCAGCCTCCC[A/G]AAGGGCTGGGATTAC | 64446 |
rs59197211 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303612 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC | 64446 |
rs59499600 | snp | A/G | 0.00763166 | 0.0612992 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305362 | AAACCCCTTCTACCC[A/G]AAGAACTTCCTGACG | 64446 |
rs59546087 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307714 | ATTTTAAAAAAAAAA[-/A]CTATTTTTTTTTTAG | 64446 |
rs59552528 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309983 | AACTTTGCTCCTCTC[-/T]CCTCTACCTGGGTCT | 64446 |
rs59728283 | snp | A/G | 0.0861826 | 0.188849 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311950 | CCCAGCACTGGAGTC[A/G]CTTGCCATCCTGCCC | 64446 |
rs59746831 | in-del | -/GAGA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285994 | AGAGAGAGAGAGAGA[-/GAGA]TTAATAATTTTATTT | 64446 |
rs60023825 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288641 | GAGCACCTTTGTAGG[G/T]TGTACAAAAGAAGCT | 64446 |
rs60042096 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295846 | TCTCTGCTTAGCTTA[A/G]TGATTAGTTAATGAT | 64446 |
rs60399157 | in-del | -/AA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74281106 | AAAAAAAAAAAAAAA[-/AA]GCCCTAAAAACAAAA | 64446 |
rs60523779 | snp | C/G/T | 0.0185938 | 0.0946107 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303150 | GTGGGGTAATGTTAT[C/G/T]ATCCGTACTTGCCAG | 64446 |
rs60607279 | snp | C/T | 0.137867 | 0.223442 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307007 | CCAGGAATGGGTTTG[C/T]TAAGGAGCAACCCCA | 64446 |
rs60685363 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310819 | TGCTGGGATTATAGG[C/T]GTGAGCCACCGTGCC | 64446 |
rs61016714 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314499 | AGCCCACCCCAAGGC[C/T]GAGGCCACCTTAGTC | 64446 |
rs61034209 | snp | A/T | 0.105569 | 0.204058 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306933 | GAGGAGTGATTTTTT[A/T]AAAATCCAGATTCTC | 64446 |
rs61123316 | snp | C/T | 0.133093 | 0.220981 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306916 | AGCCACCGTGCCTGG[C/T]GGAGGAGTGATTTTT | 64446 |
rs61153755 | in-del | -/GA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296399 | AGAGAGAGAGAGAGA[-/GA]AAGAAAGAAAATAGG | 64446 |
rs61180859 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74297408 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTTGC | 64446 |
rs61351092 | snp | A/C | 0.177503 | 0.239258 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311851 | ATTCAGCCCTCCTTC[A/C]TTGACACCAGCCCTG | 64446 |
rs61689842 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298889 | TCGGCCTCCTAATGC[G/T]CTAGGATTACAAGCA | 64446 |
rs61736879 | snp | C/T | 0.00506906 | 0.0500883 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310131 | CCTGGGCTCTCTACC[C/T]TCCAGAGGAATGAGA | 64446 |
rs62063568 | snp | A/T | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307700 | TTAGTTAAATCTGAA[A/T]TTTAAAAAAAAAAAC | 64446 |
rs62063569 | snp | C/T | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311379 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 64446 |
rs62063570 | snp | A/G | 0.171704 | 0.237423 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313651 | GGTTCACAGAACTTG[A/G]CCCCTTCCTCCTCCT | 64446 |
rs62065702 | snp | A/G | 0.137527 | 0.223271 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281550 | GTTGTCAGCTACCGC[A/G]CCTGGCCAAAATTTT | 64446 |
rs62065703 | snp | A/C | 0.139564 | 0.224285 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283369 | TCCCAGTACTTTGGG[A/C]GACCAAGGTGGGAGG | 64446 |
rs62065706 | snp | C/T | 0.221404 | 0.248359 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289566 | AACCTCACATCCAGC[C/T]TTCTGCTCTCTTCCC | 64446 |
rs62065707 | snp | A/G | 0.221526 | 0.248373 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289767 | GTCCTGGTGGCCTGG[A/G]AGGGCTGAGGGCTGG | 64446 |
rs62065709 | snp | A/G | 0.386504 | 0.209444 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296284 | GTTTGAAACTAGCCT[A/G]TGCAGCATAGTGAGA | 64446 |
rs62065711 | snp | A/C | 0.162909 | 0.23434 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298176 | CATGCCAGCTCATAC[A/C]AGCCCAGACTCTGGT | 64446 |
rs62065712 | snp | G/T | 0.5 | 0 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299809 | TGGCACCATCTGGCT[G/T]CAGTCGAAGACGGGC | 64446 |
rs62065714 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303299 | AGTCTGAGGCTAGAG[C/G]CACGATGGGCCACTC | 64446 |
rs66769719 | in-del | -/CT | 0.219386 | 0.248119 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309978 | CACATAACTTTGCTC[-/CT]CTCTCCTCTACCTGG | 64446 |
rs67206880 | snp | G/T | 0.499539 | 0.0151687 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273141 | CCAGTAGCTCTGGAC[G/T]GGGGCTGGACACGCC | 64446 |
rs67791260 | in-del | -/A | 0.140581 | 0.224783 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298139 | ACTCAGTCATTATTC[-/A]ATAACCTCTTTCAGT | 64446 |
rs67934770 | snp | C/T | 0.482309 | 0.0923707 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277494 | GGGATGGGGTGGTAC[C/T]GTCTTCAAGACACAA | 64446 |
rs71157051 | in-del | -/T | 0 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281057 | TACTGTCACCCAGGC[-/T]TGGAGTGCAGTGGTG | 64446 |
rs71157052 | in-del | -/TTA | 0 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286317 | TTATTATTATTATTA[-/TTA]TTATTATTATTATTA | 64446 |
rs71354840 | multinucleotide-polymorphism | ATA/CTC | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285976 | TCTCTCTCTCTCTCT[ATA/CTC]TATATATATATATGT | 64446 |
rs71361608 | in-del | -/CC | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276387 | ACGGGGGGAGGATCT[-/CC]CCCCCCAAAACTCCA | 64446 |
rs71361609 | in-del | -/AA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277385 | GCGAGAATCCATCTC[-/AA]AAAAAAAAAAAAAAA | 64446 |
rs71361610 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278274 | AACTCTACAAAAAAA[-/A]AAAAAATTAGTCTGA | 64446 |
rs71361612 | in-del | AG/CCA | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286721 | TGAGCCACCGCACCC[AG/CCA]CCCATCAAATGTTAA | 64446 |
rs71361613 | in-del | -/T | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291875 | ATTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC | 64446 |
rs71361615 | in-del | -/C | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311591 | CATTCCAGCCTGGGC[-/C]AACAAGAGTGAAACT | 64446 |
rs72328271 | in-del | -/AG | 0.208169 | 0.246476 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290688 | TTGGAAGAAACCGGC[-/AG]AGAGTTGACTTTGTG | 64446 |
rs72656915 | snp | C/G | 0.0227456 | 0.10419 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282051 | TGTGGCCAGGCAGGG[C/G]GGCCAGCTGGGGCCG | 64446 |
rs72656916 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299926 | TCCCTGGTTCCCCAT[C/G]AGAACCCCTGGGGAC | 64446 |
rs72848273 | snp | C/G | 0.379354 | 0.213933 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286722 | GAGCCACCGCACCCA[C/G]CCCATCAAATGTTAA | 64446 |
rs72848283 | snp | G/T | 0.476574 | 0.105661 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295590 | ACAATCTCTATTTAT[G/T]GCTTTTTTATTCCTG | 64446 |
rs72848284 | snp | C/T | 0.051973 | 0.152595 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299691 | CTGTGCCCCCTTCCA[C/T]TCCTTCTTCATCTCC | 64446 |
rs72848287 | snp | A/C | 1.74729e-05 | 0.0029557 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305442 | CCATCATGTGGACCA[A/C]GTAAGAGGCGATGCT | 64446 |
rs72848291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312631 | GGCTGGGACATTAGC[A/G]GTGTGCACGTCATGC | 64446 |
rs73358676 | snp | A/C | 0.0494327 | 0.149241 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272565 | CATTTAGGTGCTTGT[A/C]TTTGGTTAGTGCGGC | 64446 |
rs73358678 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276478 | GCCTTGCTTGGGGAA[A/G]CCCACCCTCTAGCAC | 64446 |
rs73358689 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295563 | TTAGTCCAATATCTG[A/G]GCTTCTTGGGGACAA | 64446 |
rs73360668 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305569 | CTTTCCACAAACACC[C/T]GAGCTCGTGTTAGCA | 64446 |
rs73360669 | snp | A/C | 0.105569 | 0.204058 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305996 | TTCATAATCCTCAAA[A/C]TATCCCCAGGAGGAG | 64446 |
rs73360670 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306113 | CTAGTGAGGAGCCGA[A/G]ATTGGGTGTGAACCA | 64446 |
rs73360678 | snp | A/C | 0.105569 | 0.204058 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306577 | TTCCAGTGCTTCCCA[A/C]ATCTGGTTGCATCAG | 64446 |
rs73360700 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310486 | TGTGGAAACTTTCCA[A/G]TGAAGGCTTAGTATT | 64446 |
rs73995218 | snp | A/G | 0.132066 | 0.220435 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300980 | CGGTGGGGTGAGGGC[A/G]GAGAAGGCAAAAGCC | 64446 |
rs73996949 | snp | C/G | 0.0287295 | 0.116359 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281606 | CAATAACTAAACAGG[C/G]TAATGCTTAGCATAT | 64446 |
rs74473987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296493 | CAGCCTCCCAAAGTA[C/T]AGGCGTGAGCCACTG | 64446 |
rs74567646 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283106 | TGCTGATCCAGATTT[C/T]ACCTTTTGTGAGAGC | 64446 |
rs74695549 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307704 | TTAAATCTGAATTTT[A/T]AAAAAAAAAACTATT | 64446 |
rs74699154 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289020 | CGACTGACTTAGGGG[C/T]CTGGGAAGTACCTAG | 64446 |
rs74755315 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292847 | TCCTTTTTTTTTTTT[G/T]GGGACGGAGTCTTGC | 64446 |
rs74794062 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74274809 | GGTGGCAGGTGTTTT[A/G]AGTGCTTTCTTTCAT | 64446 |
rs74815973 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278237 | GAGTTTGAGACAAGC[C/T]TGGGCAACATAGTGA | 64446 |
rs74817645 | snp | A/T | 0.666667 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297261 | CAGCTAATGTTTTGT[A/T]TTTTTTTTTTTTAGT | 64446 |
rs74852894 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302280 | TACATAAGAAAAGAA[A/G]AAAAGGGCCAGGCAC | 64446 |
rs75037789 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305006 | GGGCTTCATTCAGCA[C/T]AGGCTCCTTGAGCAG | 64446 |
rs75186766 | snp | C/G | 0.0807149 | 0.183963 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299355 | CTCCCTCCATCCTGA[C/G]GCTCATCTTCCATCT | 64446 |
rs75405011 | snp | A/T | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303597 | ACCAAGCCAGGCTGA[A/T]TTTTTTTTTTTTTTT | 64446 |
rs75433269 | snp | G/T | 0.140242 | 0.224618 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281023 | AGCCCGGGGGTTGAG[G/T]CTGCAGTGAGCTGTG | 64446 |
rs75465040 | snp | A/C/G/T | 0.00835141 | 0.0640778 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306334 | CTTGTCTAAAAGTGC[A/C/G/T]CTTTCTCCTCCTCCC | 64446 |
rs75583793 | snp | C/T | 0.000219954 | 0.0104847 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311975 | CTGCCCTCTCCCCAC[C/T]GGGCTCTCTCTGTCC | 64446 |
rs75597688 | snp | A/G | 0.22263 | 0.248497 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303738 | GGCCATGTTCTGGGT[A/G]TTTTCTAGAGATTTT | 64446 |
rs75835340 | snp | A/C | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309063 | GCAAGAGTGTCTCAA[A/C]AAAAAAAAAAAAAAA | 64446 |
rs76069905 | snp | A/G | 0 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284154 | AAAAAAAAAAAAAAA[A/G]AGCTGTAGTGAGTCA | 64446 |
rs76329846 | snp | A/C | 0.0360663 | 0.129354 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307042 | TGTGACTCAGCCAGT[A/C]CTTGCTTTGGGAGCA | 64446 |
rs76457864 | snp | G/T | 0.0428495 | 0.13996 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307275 | ATAGGCCTTTCGCAG[G/T]GCTGGTTCCTAGAGG | 64446 |
rs76578892 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277848 | CCCAGGTTTCAGAAA[C/T]GCTGGTTGAGAGATT | 64446 |
rs76581699 | snp | G/T | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292850 | TTTTTTTTTTTTTGG[G/T]ACGGAGTCTTGCTCT | 64446 |
rs76621464 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288818 | AAAAAGCAAGGCCGT[C/T]CAATCAGATGAGTGG | 64446 |
rs76743596 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283501 | TGGTCCCAGTTACTT[A/G]GGAGGTGGAGGCGGG | 64446 |
rs76777799 | in-del | -/AAA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74289532 | TGACAAAAAAAAAAA[-/AAA]GGGGGAGAAATTGGG | 64446 |
rs76791458 | snp | G/T | 0.49962 | 0.0137727 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285974 | ATATATATATATAGA[G/T]AGAGAGAGAGAGAGA | 64446 |
rs76845324 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292821 | ATTCTGCTTATTGTC[C/T]GGTGTAGTTTTCCTT | 64446 |
rs76871435 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299210 | CTCCTCTGTGAGTTT[C/G]TTTCCAACAGAGGCA | 64446 |
rs77002632 | snp | C/T | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292835 | CCGGTGTAGTTTTCC[C/T]TTTTTTTTTTTTGGG | 64446 |
rs77043505 | snp | C/T | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297690 | CCCAGCCCAAACTGC[C/T]TTTTTTTTTTTTTAA | 64446 |
rs77145463 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279409 | CATGATTGTATATTG[C/T]ATATTGCATGCCTAT | 64446 |
rs77421074 | snp | C/T | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285592 | ACATACTTGCCAGTG[C/T]AAAAAAAAAAAATTG | 64446 |
rs77564993 | snp | A/G | 0.040671 | 0.13668 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276986 | CTTTGTCCATGTGGT[A/G]AAAACACACTGGGGC | 64446 |
rs77937702 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275142 | TTGGGCCCCTTCTAT[A/G]TGCCAGTCCCTGGGG | 64446 |
rs77940705 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294312 | TCTTTTTTTTTTTTC[C/T]TTTCTTTTTTTTTTA | 64446 |
rs78135922 | snp | G/T | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310471 | ACACTTTTTTTTTTT[G/T]GTGGAAACTTTCCAA | 64446 |
rs78226187 | snp | A/T | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295655 | CTTATAATTTTTTTT[A/T]TATTAAAAACTATAC | 64446 |
rs78288350 | snp | C/T | 0.0209421 | 0.100162 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272499 | AAGAGTTCTTTGTCC[C/T]GAGAAACTGGTGCGA | 64446 |
rs78419794 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280783 | CCTGTCAATAAACAC[C/T]GATTCAGTAAAAACC | 64446 |
rs78440886 | snp | A/T | 0.0364509 | 0.129988 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307077 | CCTGGTTCGATGTCC[A/T]CATTCTACAGGGGTG | 64446 |
rs78461565 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276687 | GCCTCTGTTCTCACT[C/T]GGGGCTTGGCCTTGG | 64446 |
rs78598790 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280669 | AGAGGAGGGGTTCAA[C/G]AAGAGGCCCAGGGGT | 64446 |
rs78937721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305133 | CTAGCGCCTGCAGAC[A/C]CCCCAAGCAAGCTCC | 64446 |
rs79044798 | snp | C/T | 4.94425e-05 | 0.0049718 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314246 | CTGCGGCGCTATCCC[C/T]GTGTGCCTTCCTTTC | 64446 |
rs79049406 | snp | G/T | 0 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292431 | TTTTTTTTTTTTTTT[G/T]TTTGAGACAGAGTTT | 64446 |
rs79119096 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276207 | CTCACTGCACAAGAC[A/G]AGTTTTGTTTTTATA | 64446 |
rs79668554 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293436 | AGTAGCATTTTTCAT[C/G]TCAAAGTCTGTCTTT | 64446 |
rs79693163 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273169 | GCCCCTGTGTTGTCT[C/T]TCACTTAATCCTCCC | 64446 |
rs79952779 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309137 | AGTCAGACACAAGGA[A/G]GAACTTCCTACCTAG | 64446 |
rs80040606 | snp | G/T | | | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305389 | GACGGTTGGCGACTG[G/T]ACAGCCCGCATTTGG | 64446 |
rs80060855 | snp | A/T | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303596 | CACCAAGCCAGGCTG[A/T]TTTTTTTTTTTTTTT | 64446 |
rs80197728 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280400 | CTTGAAATCAGGGCC[A/G]AGCCCAGCCCACTTC | 64446 |
rs80231453 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284165 | AAAAAAGCTGTAGTG[A/G]GTCAAGATCATGCCA | 64446 |
rs80326419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288796 | GCCTCGGTTTTGACC[A/G]TGAAGAAAAAAGCAA | 64446 |
rs111405402 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272639 | CACTAAAGGCAGGTG[G/T]GTAGTGGTGACAACA | 64446 |
rs111425457 | snp | A/C | 0.137867 | 0.223442 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307403 | CAGGTGCAGTGGGCT[A/C]ATGCCTGTAATCCCA | 64446 |
rs111434543 | snp | A/G | 0.105214 | 0.203807 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296617 | GTTGCCTGCAATTAC[A/G]CCCTGATGAAAAGAC | 64446 |
rs111447064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276085 | CTTCCCAGTCTCCCA[C/T]GCTGACACTCCTCCT | 64446 |
rs111455773 | snp | C/T | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289848 | TCACGCGGTTGGTGC[C/T]TCAAGGGAAGGGCCC | 64446 |
rs111529591 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298393 | CACTGCAACATCTGC[C/T]TCCCAGGTGCGAGTG | 64446 |
rs111673823 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305021 | CAGGCTCCTTGAGCA[C/G]CTTCCAAAAAGATGG | 64446 |
rs111692501 | snp | A/G | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284643 | GGTCTCGATCTCCTG[A/G]CCTCGTGATCTGCTC | 64446 |
rs111701344 | in-del | -/TAA | 0 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286299 | GACTGTGTCTCAAAA[-/TAA]TAATAATAATAATAA | 64446 |
rs111977308 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279177 | GTCTCAAAATAAATA[A/G]ATAAATAAAAATAAC | 64446 |
rs111992603 | snp | C/T | 0.236144 | 0.249616 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307470 | GTCAGGAGTTCAAGA[C/T]GAGCCTGGCCAATAT | 64446 |
rs112035800 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293905 | TCTCCTGCCTCAGCC[A/T]CCCGAGTAGCTGGGA | 64446 |
rs112052702 | snp | C/G | 0.137187 | 0.223099 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309054 | GGCAACAGAGCAAGA[C/G]TGTCTCAAAAAAAAA | 64446 |
rs112109136 | snp | C/T | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74274567 | CCAAGTCGCAGGACC[C/T]TGCAGCCTCTGTACA | 64446 |
rs112286523 | snp | C/T | 0.168785 | 0.236441 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308557 | GACAGGGTCTCACTA[C/T]GTTGCCCAGGCTGGA | 64446 |
rs112296200 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284952 | GCATCCAGCCCTGGG[A/G]GCCCCCGTGGGACCT | 64446 |
rs112626441 | snp | A/T | 0.137867 | 0.223442 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307615 | TCAAGACCAGCCGAG[A/T]TTGCGCCACTGCACT | 64446 |
rs112636741 | snp | A/G | 0.205417 | 0.245993 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290271 | CAGTGAGCCGAGATC[A/G]TGCCACTGCACTCCA | 64446 |
rs112650114 | snp | A/G | 1.65113e-05 | 0.00287322 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74287040 | GAGTATTTCAATGAC[A/G]AGGAGGCCATGGAAG | 64446 |
rs112697053 | snp | C/G | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296065 | CTCTGGGCGTGCACA[C/G]AGCTCTATCCATGCT | 64446 |
rs112732262 | snp | G/T | 0.162581 | 0.234218 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308719 | TAGAAACAGGGTCTT[G/T]CCATGTTGTCCAGGC | 64446 |
rs112751477 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295382 | ACTCCAGGCTGGGCA[A/G]CAAAGCGAAACTCTG | 64446 |
rs112830002 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297171 | GCTCACTGCAAGCTC[C/T]GCCTCCCAGGTTCAT | 64446 |
rs112866422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287599 | AGCTAAGTCCATCCA[C/T]AGGGGACTGGTTCTA | 64446 |
rs112938258 | snp | C/T | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275125 | AGCAGGTGACAGGAG[C/T]CTTGGGCCCCTTCTA | 64446 |
rs112955150 | snp | A/G | 0.138207 | 0.223612 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307658 | ACAGAGTGAGACTCC[A/G]TCTCAAAAAAAAATA | 64446 |
rs112963616 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301374 | GAAGAAGGACACCAT[A/C]GTCATCATGGCACCA | 64446 |
rs113049803 | in-del | -/T | 0.48955 | 0.071525 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294298 | TTCTTTTTTTTTTTT[-/T]CTTTTCTTTTTTTTT | 64446 |
rs113161351 | snp | A/G | 0.108402 | 0.206034 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281125 | CTAAAAACAAAAGAC[A/G]AAAACTGTATCATTT | 64446 |
rs113164069 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277243 | AATACAAAAATTAGC[C/T]GCGAATGGTGGCATG | 64446 |
rs113190193 | snp | C/T | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310001 | TCTACCTGGGTCTGC[C/T]CGGCCCCTTCAATAG | 64446 |
rs113275322 | snp | C/G | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292903 | GGCGCGATCTTGGCC[C/G]ACTGCAAGCTCTGCC | 64446 |
rs113380189 | snp | C/G | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297938 | TCCTCCTCTGAAGCT[C/G]TCTGTAGTCAGCTGC | 64446 |
rs113788129 | snp | C/T | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304629 | AGCTCAGTTCGTGGG[C/T]GATGGACCCATGTCA | 64446 |
rs113981159 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296058 | GACACAGCTCTGGGC[A/G]TGCACACAGCTCTAT | 64446 |
rs113988709 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287233 | GCTTGATAAGTGACG[C/T]GGTGATAAGTCACCC | 64446 |
rs114212809 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304886 | TTTACTCTCTCTGTA[A/G]ACAAACATTCAGGAT | 64446 |
rs114363241 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283257 | GCTGCTGCAGTGTAC[A/G]CTTTAAAGTGGTTAT | 64446 |
rs114400019 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276860 | AGTCAGAGACAGGCA[A/G]CCCTAATTGCCTGAG | 64446 |
rs114544856 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275936 | GTCCTCTCCTGCCAG[A/G]TGCCATGCAGGGCCC | 64446 |
rs114912242 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284264 | AGTGGCGACACCCAC[G/T]TGTAAAACTGTCCTC | 64446 |
rs115106226 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297833 | AGTCTTGACCCTGGG[C/T]GTAAAAAGCATTCCC | 64446 |
rs115266636 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288715 | GGAAGAAGGACTCCT[C/T]GGCCTTGAAGTCTGG | 64446 |
rs115299472 | snp | A/G | 0.00145855 | 0.0269656 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310077 | TGTCTCATCGCCTGC[A/G]GCTCCCAGCTGGGGA | 64446 |
rs115446442 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276616 | AATGGGTTGTCTTCC[C/T]GTCACCAGGCCAGTC | 64446 |
rs115613688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287241 | AGTGACGTGGTGATA[A/G]GTCACCCAGCAGAGA | 64446 |
rs115685762 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279875 | GTAAATCTACCAAGG[A/C]AAGCTCTCCTTCAGT | 64446 |
rs115814164 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275398 | GTGAGTCCCTCAGGA[C/T]CCCGGAATTCCAGAA | 64446 |
rs115850728 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301786 | AGACCCCCCCCACCG[C/T]CCGCCCAGTCTTTAC | 64446 |
rs116307129 | snp | C/T | 0.021333 | 0.101051 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285290 | GCTGTGCCTGGCCAT[C/T]GCTGTGAGGCTCGTG | 64446 |
rs116309227 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292619 | ACAAGGTTTCATCAT[A/G]CTGCCCAGGCTGGTC | 64446 |
rs116458549 | snp | C/G | 0.00111338 | 0.023568 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307305 | GGACTTGGTGGACCT[C/G]TGTCGTAGAACCTGG | 64446 |
rs116819123 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311676 | GAGAGCCTCCTGGCT[C/T]TGCCTGAGACTGGGA | 64446 |
rs116863240 | snp | C/T | 0.00778631 | 0.0619074 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307246 | AAAGGAGCAGGGTGT[C/T]GAGCACAGCACCCAT | 64446 |
rs116915295 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303815 | AAAACAATATGTTTT[C/T]TAAAAAAATAAAAAT | 64446 |
rs117075898 | snp | C/G/T | 0.00544243 | 0.0518812 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301028 | TCGAAGTCTCACTGT[C/G/T]GCCCCTCCTCCCACC | 64446 |
rs117096441 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277917 | CTACACATGGAATTG[C/G]CTGGAGAATTAAAGA | 64446 |
rs117101427 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299110 | TCATGGGAAAATGGA[A/G]ACGAAATCTAACAGG | 64446 |
rs117123801 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307070 | GCAGAAACCTGGTTC[A/G]ATGTCCTCATTCTAC | 64446 |
rs117302064 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308187 | CTGGGAAGTGTAGTC[G/T]GCCTTGCTCACCAGG | 64446 |
rs117400621 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286487 | GTGCAGTGGCGTGAT[C/G]TTGGGTCTCTGCAAT | 64446 |
rs117482863 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276377 | TCTAGGTTCCCACGG[C/G]GGGAGGATCTCCCCC | 64446 |
rs117547977 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308353 | AACCAAGTAGGAAGT[A/G]ACACTCTCCTTATCT | 64446 |
rs117580787 | snp | A/G | 0.00782402 | 0.0620548 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307220 | GTCCTGCAGGCTGCC[A/G]GGGCTGTGTGAAAGG | 64446 |
rs117643450 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305052 | GGTCTGAGGAGCCCG[A/G]GAAGAGTGGGGACTG | 64446 |
rs117932646 | snp | A/G | 0.00707846 | 0.0590688 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312168 | GAGGAGGAGTTCTTC[A/G]ACATCATCTTCGCAG | 64446 |
rs118024434 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275301 | CCTTCACTTTCCTTG[G/T]GGGGCTCAGCCATGC | 64446 |
rs118104009 | snp | A/G | 0.0310518 | 0.120672 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314277 | CCACCTCTTGGTATT[A/G]CCCCGCTCTCACAAG | 64446 |
rs137852998 | snp | C/G/T | 3.31418e-05 | 0.00407063 | DNAI2 | 17 | allele_origin=T(germline)/C(germline) | 17:74299780 | ATTGAGTCCAGCCAC[C/G/T]GAGACCCTGTGTATG | 64446 |
rs137867075 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299133 | CTAACAGGACAAAGG[A/T]CAGATAACCTTTCCA | 64446 |
rs137875814 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275202 | CCGTCAAGGAGACCA[C/G]AAGGTAGTTGTGAGG | 64446 |
rs137970711 | in-del | -/GAA | 0.00953873 | 0.0683987 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288701 | GGGGAGAAGCCTGGG[-/GAA]GAAGGACTCCTCGGC | 64446 |
rs138029872 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282877 | AGGTGGGTGTGGGTG[A/G]TTTCAGTGACTCACA | 64446 |
rs138113130 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312539 | CGAGGGAACATGTGT[G/T]TTGAGTGACTGAACG | 64446 |
rs138196027 | snp | A/G | 6.59022e-05 | 0.00573993 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301082 | AAGATGAGCGAGCCC[A/G]CTGAAGTTGTGATCT | 64446 |
rs138264021 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291466 | ACCACACCTGGCCGG[G/T]ACCCAGATTCATAGT | 64446 |
rs138377190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288186 | AACCATTCTGTTTTC[C/T]ACCCTCAGTACAGTA | 64446 |
rs138386864 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295486 | TTCTTTAGTTCTTTT[G/T]ATGTGACTTCCTTTA | 64446 |
rs138489039 | snp | A/G | 4.94295e-05 | 0.00497115 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305271 | TCATCTCCTGCAACC[A/G]CAAGGCCAAGACGTC | 64446 |
rs138550758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296099 | GACCTTCTAGACTCC[C/T]AGGAATATGTCAGAT | 64446 |
rs138631553 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306777 | CGCACGCCAGCACAC[C/G]CAGCTAATTTTTGTA | 64446 |
rs138636168 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284349 | TTTTGTGACACTGAC[A/T]TTGTCAGTGATAGGG | 64446 |
rs138643456 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307973 | TGGATAATTTTTTTA[G/T]TTTTAGTAGAGGCAG | 64446 |
rs138711618 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302246 | GACCAGCCTGGACAA[C/T]ATAGCAAGACACTGT | 64446 |
rs138837180 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308761 | TCCTGGCTTCAAGCG[A/G]TCTTCCTGCCTTGGC | 64446 |
rs138885031 | snp | C/T | 0.000131817 | 0.00811735 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289691 | TGCTTGGATTTTCAG[C/T]GGGCACCTGTGGGCA | 64446 |
rs138901894 | in-del | -/TG/TGTG | 0.100076 | 0.200775 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287503 | ATTCATCCCACAGGT[-/TG/TGTG]TGTGTGTGTGTGTGT | 64446 |
rs138917551 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292186 | AATTCTTGAAATGTT[C/T]GGTAGAACTCATCAG | 64446 |
rs139006875 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298890 | CGGCCTCCTAATGCG[A/C]TAGGATTACAAGCAT | 64446 |
rs139051164 | snp | A/G | 0.000317925 | 0.012604 | missense, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312061 | GGCACCGGGAGATGC[A/G]GCTGAAGGAGAAGGG | 64446 |
rs139125983 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302436 | GCTGGGCGTGGAGGC[A/G]CACGCCTGTAATCCC | 64446 |
rs139168160 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293575 | CAGGTGTGGTGACAC[A/G]CACCTGTAATCCCAG | 64446 |
rs139228886 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300011 | TGGAGTGCAATGGCA[C/T]GATCTTGGTTCACTG | 64446 |
rs139319121 | snp | C/T | 0.000281692 | 0.0118645 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309292 | TGCTGCCTGGAGCCC[C/T]GTGAGGCCGACCGTT | 64446 |
rs139392038 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276529 | GGAGACCTCCTGAGA[C/T]GCCCTTTGCTGACCT | 64446 |
rs139420980 | snp | A/G | 0.00177845 | 0.0297668 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314238 | GCCTTCGACTGCGGC[A/G]CTATCCCTGTGTGCC | 64446 |
rs139466545 | in-del | -/T | 0.2462 | 0.249971 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276144 | GCTTGGAAAACACAC[-/T]TTCCCTTAAGCCACC | 64446 |
rs139474667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277069 | CTCCCACCCAGGAAA[G/T]AGAATTTCCAAACTA | 64446 |
rs139551482 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272524 | GTGCGAGCCAGAACG[A/G]ATCAGGAGAGATTGG | 64446 |
rs139595301 | snp | C/T | 0.00755907 | 0.0610114 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273567 | CCATCCTGGCTAACA[C/T]GGAGAAACCCCGTCT | 64446 |
rs139791957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293361 | GCACATGCTTATAAT[C/T]GTTAAGTTTTCCTAG | 64446 |
rs139877506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290264 | GAGGTTGCAGTGAGC[C/T]GAGATCATGCCACTG | 64446 |
rs139915367 | snp | C/T | 0.000183991 | 0.00958967 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312107 | GGATGAGGAGCAGAC[C/T]GATGAGGAGCTGGCC | 64446 |
rs139935771 | snp | A/G | 0.00029988 | 0.0122413 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305419 | GTCTGAAGACAGCCG[A/G]GAATCGTCCATCATG | 64446 |
rs140040744 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281163 | AAGAGCTTTGGAATG[A/G]GGGCAGACCAGCTGC | 64446 |
rs140047250 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273018 | CCAGTTCCAACCCCA[A/G]TCCCACTTCTTGGAT | 64446 |
rs140088698 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302587 | AAAAAACAAAGAAAA[C/G]AAAAACAGGAAATAT | 64446 |
rs140132848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285668 | TCTCTTATACATCCT[C/G]TCCCAAAGAGATTGC | 64446 |
rs140145001 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291025 | TGCTTTATAGAAAAC[C/T]CCAACAAGCCTGAAC | 64446 |
rs140217124 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282213 | CGCCTTCCTCGAGCC[A/G]GGGAAGTGCAAATCA | 64446 |
rs140295057 | snp | A/G | 4.98087e-05 | 0.00499017 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299815 | CATCTGGCTGCAGTC[A/G]AAGACGGGCACCGAG | 64446 |
rs140326154 | snp | A/G | 0.000614072 | 0.0175117 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299747 | CGAAAGGGCAGCCTG[A/G]TGGCGGAGCTATCCA | 64446 |
rs140339199 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311561 | GAGGTTGTGGTGAGC[C/T]GAGATCGTGCCATTG | 64446 |
rs140358589 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314671 | CTCCTCCATGATCGA[A/C]CCTCCTCGTCCACCT | 64446 |
rs140525194 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304601 | AGTCCGCAGTGAAGT[A/G]AATAACTACTAAAGC | 64446 |
rs140550346 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299296 | AATGGAGTCTTTCCA[C/T]GTGCTTTTCCCTACG | 64446 |
rs140566944 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294732 | GGTATGGATATCTTT[C/G]AGTTTATCCCACTTG | 64446 |
rs140598637 | in-del | -/AC | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285947 | AGATGAGTGCCATAT[-/AC]ACACACACACATATA | 64446 |
rs140655558 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278050 | GGACTAACAATCACT[G/T]CTTTAGAGCCAGACA | 64446 |
rs140784879 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311336 | CCTAGTGCTAGGGCC[A/G]GGTGTGGTGGCTCAC | 64446 |
rs140871777 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309959 | GGGGCCAGTTAATCA[G/T]ACACACATAACTTTG | 64446 |
rs140964616 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313707 | TCTTAGTCTGCAATT[A/G]GCCCAAAACGCTGGT | 64446 |
rs141008082 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282987 | AATAAGCAGAATGGC[C/T]GCTATGTGGGCCACA | 64446 |
rs141019803 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273777 | AATTCCCCAGCTTCT[A/G]CTCCCAAGGAGTTTC | 64446 |
rs141049070 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287667 | CCTGGTAAAGCGAGC[A/G]GGGCAGTCTGGGCAT | 64446 |
rs141079076 | snp | C/T | 0.000568134 | 0.0168447 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299847 | GCTTCTCAGCTTCCA[C/T]GGATGGGCAGGTACC | 64446 |
rs141092589 | in-del | -/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74288085 | CCACTTTTTGTGGCA[-/G]GTCCCCAACTTAAAC | 64446 |
rs141118738 | snp | C/G/T | 4.95342e-05 | 0.00497645 | missense, synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281976 | CACGGGCATCCAGTG[C/G/T]TCGATCAGCATGTCG | 64446 |
rs141122120 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307556 | CGCCTGTAATCCCAG[C/G]ACTTTGGGAGGCCGA | 64446 |
rs141162397 | snp | A/G | 0.00716266 | 0.059414 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274135 | TCTCCTAACTCAGGA[A/G]ACCTCCAAAAAGAAG | 64446 |
rs141165687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299062 | CTTTCCTAGAAACAG[C/T]TCTGAGTGACAGGGT | 64446 |
rs141256139 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276386 | CCACGGGGGGAGGAT[C/T]TCCCCCCAAAACTCC | 64446 |
rs141367010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300966 | GGCTGACCCCAGGAC[A/G]GTGGGGTGAGGGCGG | 64446 |
rs141472171 | snp | A/T | 1.64991e-05 | 0.00287215 | stop-gained, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305225 | CTTCCACAGCCCACC[A/T]AGTTCATGGTGGGGA | 64446 |
rs141578771 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288816 | GAAAAAAGCAAGGCC[A/G]TCCAATCAGATGAGT | 64446 |
rs141580345 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291228 | TGTAGTGGTGCAATT[C/T]TGGCTCACTGCAACC | 64446 |
rs141581673 | snp | A/C/T | 0.000962309 | 0.0219146 | synonymous-codon, stop-gained, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312024 | GAGCGTGAGACCCGG[A/C/T]GAGAGAAGATCCTGG | 64446 |
rs141730618 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306710 | GCAACCTCCACCTCC[C/T]GAGTTCATGCGATTC | 64446 |
rs141836809 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279609 | CTCGACTCACTGCAA[C/T]GTCTACCTTCCAGGT | 64446 |
rs141858231 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308119 | CTTTCTTTAGTCTTG[A/C]TCATTTCTCCCACTG | 64446 |
rs141893867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313045 | GAAAATGTGAGGGCC[C/T]TCGTTTAAAAAGTAT | 64446 |
rs141991485 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305732 | GACTGAGTGCAGTGG[C/T]GTGATCTCGGCTCAC | 64446 |
rs142051197 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281566 | CCTGGCCAAAATTTT[G/T]ATTGCCCTCCTCAGA | 64446 |
rs142115365 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293554 | ATCTAAAGTATGTCT[C/T]GTAGCCAGGTGTGGT | 64446 |
rs142292902 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294020 | ACTCCTGGCCTCAAG[C/T]GATATGCCCACCTCG | 64446 |
rs142396454 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277495 | GGATGGGGTGGTACT[A/G]TCTTCAAGACACAAT | 64446 |
rs142449741 | in-del | -/TTTTGT | 0.379942 | 0.213577 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293781 | ACAAGTGAATCATAG[-/TTTTGT]TTTTGTTTTGTTTTG | 64446 |
rs142497825 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310829 | ATAGGCGTGAGCCAC[C/T]GTGCCCAGCCTAATT | 64446 |
rs142547549 | snp | C/T | 0.039522 | 0.134904 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296540 | TCCTTTTAAGCTTTT[C/T]GGTAGGTCTATTCCT | 64446 |
rs142571722 | snp | A/G | 0.000164764 | 0.00907495 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305377 | GAAGAACTTCCTGAC[A/G]GTTGGCGACTGGACA | 64446 |
rs142653126 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307404 | AGGTGCAGTGGGCTA[A/T]TGCCTGTAATCCCAG | 64446 |
rs142656395 | snp | A/G | 0.00235337 | 0.034222 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299752 | GGGCAGCCTGGTGGC[A/G]GAGCTATCCACCATT | 64446 |
rs142710343 | snp | C/T | 0.000371918 | 0.0136316 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312206 | GAAGAAGGAGGCAGA[C/T]GCCATAAAGCTGACG | 64446 |
rs142757084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306413 | GAGTCATTCACCACC[A/G]AGCACTGCCATGTGT | 64446 |
rs142778194 | in-del | -/TT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292416 | ATCATTTTCTTTTTC[-/TT]TTTTTTTTTTTTTTT | 64446 |
rs142798398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299322 | CTACGTTAGGGACTC[A/G]GCTCTCCTCTCGCCT | 64446 |
rs142912779 | snp | C/T | 0.000185684 | 0.00963366 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307309 | TTGGTGGACCTGTGT[C/T]GTAGAACCTGGGTCT | 64446 |
rs142913282 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296345 | AGAGGAGAGAGAGAG[A/G]GGAGAGAGAGAGGAA | 64446 |
rs143033449 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293069 | CGATCTCCTGACCTC[A/G]TGATCCGCCCGCCTC | 64446 |
rs143056843 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275619 | GTAGTCCCAGCTACT[C/T]GGCAGGTGGAGGCAG | 64446 |
rs143072316 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295667 | TTTTTATTAAAAACT[A/G]TACTTTTTGTATGAT | 64446 |
rs143111885 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285960 | ATACACACACACACA[C/T]ATATATATATAGAGA | 64446 |
rs143142665 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307838 | GAAGTCTCTTTGTTG[C/T]CCAGGCTGGAGTGCA | 64446 |
rs143184350 | in-del | -/AG | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296311 | AGATCTTGCCTTTAA[-/AG]AGAGAGAGAGAGAGA | 64446 |
rs143196175 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313926 | CAAGTCTGCCAGATT[C/T]CCCCAGCTCTGCCCA | 64446 |
rs143311974 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294459 | GGACAACAGGTGCAC[A/G]TCACCACACTCAGCT | 64446 |
rs143413645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301612 | GAAAATGAGGTCAAA[C/G]CAGGCTCCTTGGAAA | 64446 |
rs143470009 | snp | C/T | 5.02626e-05 | 0.00501286 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305424 | AAGACAGCCGGGAAT[C/T]GTCCATCATGTGGAC | 64446 |
rs143521233 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293786 | TGAATCATAGTTTTG[-/T]TTTTGTTTTGTTTTT | 64446 |
rs143574908 | snp | G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273123 | CTGCCACTCATTCAG[G/T]CACCAGTAGCTCTGG | 64446 |
rs143656953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303348 | TCTCTGGCTCACTGA[C/T]GGGCGGCGTGCAGTC | 64446 |
rs143664787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312655 | GTCATGCTGGCTTAC[C/T]CAGGTTTGGTGTCAG | 64446 |
rs143723454 | snp | C/T | 4.97632e-05 | 0.0049879 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310076 | GTGTCTCATCGCCTG[C/T]GGCTCCCAGCTGGGG | 64446 |
rs143794758 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301372 | TCGAAGAAGGACACC[A/G]TAGTCATCATGGCAC | 64446 |
rs143982327 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289420 | TAATCGTAGCTACTC[A/G]GGAGGCTGAGGCAGG | 64446 |
rs144018987 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288305 | GTTCTGAGCACATAG[G/T]CTGGACTAAGATGTG | 64446 |
rs144035254 | snp | C/G | 0.00338162 | 0.0409802 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310100 | GCTGGGGACAACCAC[C/G]CTGCTGGAGGTCTCG | 64446 |
rs144140666 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302508 | GGAGGCGGGGGTTGC[A/G]GTGAGCCAAGATCGC | 64446 |
rs144246213 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284877 | ACCTGTGCCCACCTG[A/C]TCACCAGGAATTTCC | 64446 |
rs144328249 | snp | A/T | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281912 | TGAACATCGACATCA[A/T]GCCCAACCCTGAGCT | 64446 |
rs144344097 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309705 | CCCTGGGGTTTGGCT[G/T]CTGGACCTTCCCCTT | 64446 |
rs144347176 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300650 | ATTGTTGCACACATG[C/T]GGGGATATATCTACA | 64446 |
rs144349276 | in-del | -/TTAAT | 0.381308 | 0.21274 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294156 | TTTAATCTATTTACA[-/TTAAT]TTAATTACTGATAAA | 64446 |
rs144444784 | snp | A/G | 6.58957e-05 | 0.00573964 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305314 | TGTGTGCACCTTCCC[A/G]GGCCATCATGGCCCC | 64446 |
rs144513269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296132 | TTTCAAAGCCCTGTG[A/G]ACACATCATGCTTCA | 64446 |
rs144519019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296926 | TTTTCTTGAATAAAC[A/G]TTCTCCCGACTGCCC | 64446 |
rs144576170 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272938 | TTGCTCACGCCATGC[C/T]CTCCCCCAATCTGGA | 64446 |
rs144730142 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306946 | TTTAAAATCCAGATT[A/C]TCAGCCCCAACCCTG | 64446 |
rs144755154 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287677 | CGAGCGGGGCAGTCT[G/T]GGCATGGTGGCTCAC | 64446 |
rs144786630 | snp | A/C/T | 0.00204211 | 0.031889 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289724 | AGCAGCGATTCATAC[A/C/T]TCTGGGACCTGGGTG | 64446 |
rs144859959 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292852 | TTTTTTTTTTTGGGA[C/T]GGAGTCTTGCTCTTT | 64446 |
rs144881094 | in-del | -/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296333 | AGAGAGAGAGAGAGA[-/G]GGAGAGAGAGAGAGG | 64446 |
rs144888139 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307439 | TTGGGAGGCTGAGGC[A/G]GGAGGATCACTTGAG | 64446 |
rs144896661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314383 | ACAAATCACTAGCCC[C/T]CACTGACTCACTGGG | 64446 |
rs144909415 | snp | A/G | 6.68941e-05 | 0.00578296 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299848 | CTTCTCAGCTTCCAC[A/G]GATGGGCAGGTACCC | 64446 |
rs144972572 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310542 | TTAATTATTTTTATT[C/T]ATTTATTTATTTTTG | 64446 |
rs145184706 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298665 | TGGGGTGTAGTGGCA[C/T]GATCATGGCTCACTG | 64446 |
rs145307826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282676 | AAAGGGAAGTGTCCC[A/C]CAGAAAGTTCCAGCC | 64446 |
rs145425741 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278895 | CTAACAGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 64446 |
rs145468414 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286710 | GATTACAGGCGTGAG[C/G]CACCGCACCCAGCCC | 64446 |
rs145480179 | snp | A/G | 0.00318978 | 0.0398085 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315021 | GAGCGGTACAGGGAC[A/G]TGCCCAAGTCTCAGA | 64446 |
rs145544459 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285853 | TGGCAGGGCTTGGTT[G/T]TCCTTTGGTGGACAT | 64446 |
rs145553576 | snp | C/T | 1.64887e-05 | 0.00287125 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281921 | ACATCATGCCCAACC[C/T]TGAGCTGGCCGAGCA | 64446 |
rs145570422 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290355 | CCAGCAGACTGAGAA[A/G]GGACTCAAGGGGCGG | 64446 |
rs145602856 | snp | C/T | 0.0016363 | 0.0285565 | missense, nc-transcript-variant, intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312082 | AGGAGAAGGGTAAGG[C/T]GGAGGGCAGGGATGA | 64446 |
rs145624900 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277853 | GTTTCAGAAACGCTG[A/G]TTGAGAGATTAAGTT | 64446 |
rs145670077 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298179 | GCCAGCTCATACCAG[C/G]CCAGACTCTGGTGCT | 64446 |
rs145675543 | snp | C/T | 9.88321e-05 | 0.00702896 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291056 | TTGCTCTGAAGCCAT[C/T]GTCTCCACTCGTGAC | 64446 |
rs145683700 | in-del | -/AGGAGA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296333 | GAGAGAGAGAGAGAG[-/AGGAGA]GAGAGAGAGAGAGGA | 64446 |
rs145716654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310026 | CAATAGGTGTGTGAC[A/G]AGGCCCTCTTCTGCC | 64446 |
rs145793904 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305803 | CAGCCTCCTGAGTAG[C/T]TGGGACTACAAGCAC | 64446 |
rs145798624 | snp | A/G | 0.0025834 | 0.0358473 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301130 | GAACAGTTGGAAAAT[A/G]CCTTGGGGGCCATCT | 64446 |
rs145944531 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293175 | TGGGAGGTCTTGTCT[A/G]TAGTGTTGGTCAAGA | 64446 |
rs145980503 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312096 | GCGGAGGGCAGGGAT[A/G]AGGAGCAGACCGATG | 64446 |
rs146064729 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306847 | GGTCTCAAACTCCTG[A/G]CCTCAGGTGATTCGC | 64446 |
rs146139153 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296024 | GAGAGTTTAGGGCTT[A/T]ATCGGTTTTCCTGAG | 64446 |
rs146257718 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308153 | TCTGGCTGTCAACAC[A/T]CTAGGTTTGCAAAGG | 64446 |
rs146307891 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276857 | AAAAGTCAGAGACAG[G/T]CAGCCCTAATTGCCT | 64446 |
rs146452121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287266 | CAGAGAAGTGGCCCT[G/T]CTCTGGGGGCGGGTC | 64446 |
rs146462823 | snp | G/T | 0.00188022 | 0.0306035 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289590 | TCTTCCCTCTCCCCT[G/T]CAGGGACCCCCAGGA | 64446 |
rs146477088 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315365 | GTGTTGGTCAGGTTT[C/T]GTGGCTCACGCCTGT | 64446 |
rs146478497 | snp | A/G | 0.000115908 | 0.00761188 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305410 | CCGCATTTGGTCTGA[A/G]GACAGCCGGGAATCG | 64446 |
rs146573973 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300815 | GGTCGAGGGCGAGGC[A/C]TCAGCATCTGGGTTG | 64446 |
rs146585944 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302563 | CAAGAGCGAAACTCC[A/G]TCTCAAAAAAAAAAC | 64446 |
rs146692089 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314573 | CCAGCAATCATTTTC[A/G]TTTGTAACCTTGCAG | 64446 |
rs146727740 | snp | A/G | 0.000337325 | 0.0129826 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312171 | GAGGAGTTCTTCGAC[A/G]TCATCTTCGCAGAGC | 64446 |
rs146769635 | snp | C/T | 0.000135793 | 0.00823883 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305433 | GGGAATCGTCCATCA[C/T]GTGGACCAAGTAAGA | 64446 |
rs146825885 | snp | A/T | 0.0158469 | 0.0875917 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273470 | AAAAATCCCCAGCTT[A/T]GCCGGGCGCGGTGGC | 64446 |
rs146925440 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | DNAI2 | GRCh38.p7 | 17:74274475 | TTCCTTCTGGGATAG[C/G]TCTGCCAGATGGTGG | 64446 |
rs147072746 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288029 | TCAGTATGTGAAAAC[A/C]AAACCAAAACAAAGC | 64446 |
rs147153695 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299287 | ATTCACCTAAATGGA[A/G]TCTTTCCACGTGCTT | 64446 |
rs147196022 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296713 | GGGAACCACCAGACC[A/G]GTCAGATAATGACAG | 64446 |
rs147272474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313606 | GCTTGAACATTCTAC[A/G]TGAAGAAGTTGAGCC | 64446 |
rs147334896 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305288 | AAGGCCAAGACGTCA[A/G]CTGAAAAGATTGTGT | 64446 |
rs147347465 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292434 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTTTTAC | 64446 |
rs147409770 | snp | G/T | 0.0490535 | 0.14873 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302291 | AGAAAAAAAGGGCCA[G/T]GCACGGTGGCTCACA | 64446 |
rs147470752 | snp | G/T | 0.000760318 | 0.0194828 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285053 | AGGCCAACTCAGAGC[G/T]GTTTGAGATGGAGAC | 64446 |
rs147514164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280173 | AGTCAGAAAGGTCAA[C/G]GGCAATATGTGGGAA | 64446 |
rs147543928 | snp | A/G | 0.00447756 | 0.0471034 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314073 | AGGGGAGTGGGGAAG[A/G]CCTGTCCCCTACCAA | 64446 |
rs147564750 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278028 | GGTGTTTCTAAATGT[A/G]CAGTCAGGACTAACA | 64446 |
rs147648047 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293985 | ATGAGGTTTTACCAT[A/G]TTGGCCAGGCTGATC | 64446 |
rs147669330 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294286 | TGTACCATTTTAATT[C/T]CCTTATCATTTCTTT | 64446 |
rs147744433 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281506 | CAGGTGATCCACCTG[G/T]CTTGGCCTCCCAATG | 64446 |
rs147848262 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297016 | TTTCTCACTGCTATT[A/G]TGGAGGAGAGAATTT | 64446 |
rs147954623 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310757 | CTGGCCAGGCTGGTC[C/T]TGAACTCTTGACCTT | 64446 |
rs147954709 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273863 | GCAGAGGGGAGGGCA[A/G]AGTTATAATTCCCAC | 64446 |
rs147964485 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277675 | GGTCTGGTGCCTTGT[A/G]GCCCTGGAGGCGGGA | 64446 |
rs148073122 | snp | A/G | 0.000798403 | 0.0199641 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281951 | AGTTCGTGGAGCGGA[A/G]CCCAGTGGACACGGG | 64446 |
rs148076276 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313022 | GGGGATTGCAGGCAC[C/T]GCAAAATGAAAATGT | 64446 |
rs148100166 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279274 | TATTTGATAGCACAA[C/T]AGGGTGACTATAGTC | 64446 |
rs148187994 | in-del | -/T | 0.128976 | 0.218754 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307700 | TTAGTTAAATCTGAA[-/T]TTTAAAAAAAAAAAC | 64446 |
rs148247110 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275989 | GGGCTGTACCAGGGA[C/T]CAAGAAGAAGAGGAA | 64446 |
rs148290308 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284883 | GCCCACCTGATCACC[A/G]GGAATTTCCTTGCCT | 64446 |
rs148321634 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294725 | GTTTCTAGGTATGGA[A/T]ATCTTTGAGTTTATC | 64446 |
rs148391075 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286715 | CAGGCGTGAGCCACC[A/G]CACCCAGCCCATCAA | 64446 |
rs148488355 | snp | A/C/T | 0.00311704 | 0.0393553 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299740 | GGACACCCGAAAGGG[A/C/T]AGCCTGGTGGCGGAG | 64446 |
rs148518996 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302517 | GGTTGCGGTGAGCCA[A/T]GATCGCATCATTGCA | 64446 |
rs148544735 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296347 | AGGAGAGAGAGAGAG[A/G]AGAGAGAGAGGAAGG | 64446 |
rs148570101 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307136 | TGTTCCAGGCCTCAT[A/G]GCAAGTAGGGGGTTC | 64446 |
rs148599490 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314485 | TCTCAGCCACCCTGA[A/G]CCCACCCCAAGGCCG | 64446 |
rs148760558 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288799 | TCGGTTTTGACCATG[A/G]AGAAAAAAGCAAGGC | 64446 |
rs148774868 | snp | G/T | 0.383632 | 0.211288 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285976 | ATATATATATAGAGA[G/T]AGAGAGAGAGAGAGA | 64446 |
rs148781636 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277309 | AGAATCGCTTGCACC[C/T]GGGAGACGGAGTTTG | 64446 |
rs148864057 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290459 | GTCCATTTATTAGCA[C/T]AAACCATTGTCTACA | 64446 |
rs148885398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278557 | ACATATTCTGGATGC[A/C]AGTTCTTTATCAAAT | 64446 |
rs148885547 | snp | A/G | 0.000131915 | 0.00812036 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281932 | AACCCTGAGCTGGCC[A/G]AGCAGTTCGTGGAGC | 64446 |
rs148947094 | snp | G/T | 0.00036483 | 0.0135012 | intron-variant, synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310049 | CTTCTGCCTCCGGGT[G/T]CAGGACAATGGGTGT | 64446 |
rs148959161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297898 | GCTGCTTCTTCGGGA[A/G]TGGGAGCCAGGATGG | 64446 |
rs149092782 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307763 | AATATTTGGTATATA[C/G]TTATACTAAAAATTA | 64446 |
rs149242223 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296102 | CTTCTAGACTCCCAG[A/G]AATATGTCAGATCTT | 64446 |
rs149326208 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272851 | CTGCAGGGACTCTCA[A/G]CCCCAGCCAGACTGA | 64446 |
rs149485866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299231 | AACAGAGGCAGCAGA[A/G]GTACAAAGGATAAGA | 64446 |
rs149487924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275599 | GGGTGCAGTGGCTCA[C/T]GCCTGTAGTCCCAGC | 64446 |
rs149528472 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295234 | CCCCATCTCTACTTA[-/A]AAAAAAAAAAAAAAA | 64446 |
rs149529436 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312626 | GGAAGGGCTGGGACA[A/T]TAGCGGTGTGCACGT | 64446 |
rs149537497 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302499 | TTGAACCTGGGAGGC[A/G]GGGGTTGCGGTGAGC | 64446 |
rs149569965 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284821 | ACCACAGCTACCAGT[G/T]GCAAAGCTGCTTAGC | 64446 |
rs149843730 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286645 | GGCCGGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 64446 |
rs149918986 | snp | A/G/T | 0.000431965 | 0.0146903 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299821 | GCTGCAGTCGAAGAC[A/G/T]GGCACCGAGTGCTTC | 64446 |
rs149926751 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293766 | TACATGTAGCTGGCA[C/T]ACAAGTGAATCATAG | 64446 |
rs150001265 | snp | C/T | 0.00768497 | 0.0615096 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309619 | CACAACAGAACCACC[C/T]GGGGGAAATTTAAAA | 64446 |
rs150010890 | snp | A/C | 0.040671 | 0.13668 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277140 | GCCTGTAATCCCAGC[A/C]CTTTGGGAGGCCGAG | 64446 |
rs150103941 | in-del | -/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74289996 | TGAAGACCTGACCCC[-/C]ATGGGATCTCAATTC | 64446 |
rs150126294 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278062 | ACTGCTTTAGAGCCA[C/G]ACATGCCTGGTGGTT | 64446 |
rs150182125 | snp | C/T | 0.000198128 | 0.00995111 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309350 | CTGGATATCTGGGAC[C/T]TCATGTTCGAGCAGT | 64446 |
rs150208047 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292165 | CCACCATGCCTGGCC[A/G]CTATTAATTCTTGAA | 64446 |
rs150283442 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273798 | AAGGAGTTTCCATTC[C/T]GGTGGTGCGGGAAGA | 64446 |
rs150334665 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307620 | ACCAGCCGAGATTGC[A/G]CCACTGCACTCCAGC | 64446 |
rs150462177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294770 | TTGAGTTTCTTGGAT[A/G]TGTAGATTATTTTTT | 64446 |
rs150495039 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304706 | ACGAGTTACATCACC[A/G]ACTGCCAGGTAACTT | 64446 |
rs150597529 | in-del | -/CCCC/CCCCC | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273200 | ATTATCTAATAAGCA[-/CCCC/CCCCC]CCGCCACTGTCCTGC | 64446 |
rs150649080 | snp | A/G | 4.94328e-05 | 0.00497131 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289643 | CTCTCCTGGCACCCC[A/G]ATGGCAACAGGAAGT | 64446 |
rs150710001 | snp | G/T | 0.000939203 | 0.0216499 | missense, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312041 | AGAGAAGATCCTGGA[G/T]GCCAGGCACCGGGAG | 64446 |
rs150723882 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299074 | CAGCTCTGAGTGACA[C/G]GGTGAGCCCTCATTG | 64446 |
rs150923696 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310869 | ATTTTTATTTTATCA[A/G]TTTATTTTATTTTAC | 64446 |
rs151033547 | in-del | -/G | 0.000104604 | 0.00723127 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281760 | TGTGGAGATAGGGAA[-/G]GGGGCCGGTGGGGTC | 64446 |
rs151176313 | snp | A/G | 0.00403234 | 0.0447204 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281941 | CTGGCCGAGCAGTTC[A/G]TGGAGCGGAACCCAG | 64446 |
rs151188579 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287679 | AGCGGGGCAGTCTGG[C/G]CATGGTGGCTCACGC | 64446 |
rs151241589 | snp | C/T | 0.00461572 | 0.0478179 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312223 | CCATAAAGCTGACGC[C/T]AGTGCCTGTAGGGGC | 64446 |
rs151250789 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300007 | AGGCTGGAGTGCAAT[A/G]GCACGATCTTGGTTC | 64446 |
rs151302078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303500 | TGCTGGAGTGCAGTT[C/G]TGTAATCTCAGCTTA | 64446 |
rs180900229 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308673 | ACCACAGGTGCTCAC[C/T]ACCACACCCGGCTAA | 64446 |
rs180967967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276549 | TTTGCTGACCTTGCT[A/G]TTCATCTGTGTGCCC | 64446 |
rs180977207 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312554 | GTTGAGTGACTGAAC[A/G]AGGGTCCTAGAGGTA | 64446 |
rs181090686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280027 | CAATTTCTGAAAGTG[C/T]AGGTGGCTGGCAGAC | 64446 |
rs181107657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299089 | GGGTGAGCCCTCATT[A/G]TGCATTCATGGGAAA | 64446 |
rs181252885 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313090 | CAGTGACAATAGAGC[A/G]TTAAACCAAGCGTGG | 64446 |
rs181338913 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294336 | TTTTTTAGAGACAAG[G/T]TCTCACTCTGTCACC | 64446 |
rs181445123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276898 | GCCCCATGTGGGAGG[A/C]ACAGTTGCTTCACAC | 64446 |
rs181481701 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303364 | GGGCGGCGTGCAGTC[A/G]GCTTGAATACTTTCT | 64446 |
rs181705917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308087 | ACAGGCATGAGCCAC[C/T]GCGCCCGGCCCAGAT | 64446 |
rs181730272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289997 | TGAAGACCTGACCCC[A/G]TGGGATCTCAATTCT | 64446 |
rs181777228 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74286493 | TGGCGTGATCTTGGG[A/T]CTCTGCAATCTCCAC | 64446 |
rs181862655 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299601 | ACCAAGCCCTGATTC[C/T]AGAAAACCACATACC | 64446 |
rs181911729 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303892 | GCACTTTGGGAAGCC[A/G/T]ATGTGTGCAGATCAC | 64446 |
rs181933227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311351 | GGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 64446 |
rs181945307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298635 | TGAGACAGGGTCTTG[C/T]TCTGTCACCCAGGCT | 64446 |
rs181949954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276206 | TCTCACTGCACAAGA[C/T]GAGTTTTGTTTTTAT | 64446 |
rs181950703 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279655 | ACCTCAGCCTCCTGA[G/T]TAGCTGTGATTACAG | 64446 |
rs181952483 | snp | A/G | 0.00438332 | 0.0466095 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314886 | TCGTAACAATGCCAC[A/G]AGTTAGTACGTGTGA | 64446 |
rs182131161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281012 | AGGATCACTTGAGCC[C/T]GGGGGTTGAGGCTGC | 64446 |
rs182154378 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313948 | CTCTGCCCACTTTCC[A/C/G]CACTGTCTGGGCCCT | 64446 |
rs182184285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290279 | CGAGATCATGCCACT[G/T]CACTCCATCCTGGGC | 64446 |
rs182201411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293690 | GCCTGGGTGACAGAG[C/T]GAGACTCCATCTCAA | 64446 |
rs182402111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295905 | ACCAAAAAATCTCCC[C/T]TTCTCTGCTAAGGGG | 64446 |
rs182407881 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278199 | CTTTGGGAGGCTGAG[G/T]CAGGAGGATCACTTG | 64446 |
rs182441253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308358 | AGTAGGAAGTGACAC[C/T]CTCCTTATCTCAGCG | 64446 |
rs182509388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291238 | CAATTTTGGCTCACT[A/G]CAACCTCCGCCTCCT | 64446 |
rs182527268 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309017 | GCAGTGAGCCGACAT[C/T]GTACCACTGCACTCC | 64446 |
rs182555546 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288534 | GGACTTCTGGCATCC[A/G]GAACTGTGATAGAAT | 64446 |
rs182570014 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305514 | AGCCCAGCTGGGCCC[C/T]GGAGAGTCCCGAGCC | 64446 |
rs182674286 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304864 | TGCATCCCCTCCCTG[A/G]GTCTTCTTTACTCTC | 64446 |
rs182775168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301020 | ACAGGGCCTCGAAGT[C/G]TCACTGTCGCCCCTC | 64446 |
rs182986650 | snp | C/G | 3.3024e-05 | 0.00406336 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309359 | TGGGACTTCATGTTC[C/G]AGCAGTGCGATCCCA | 64446 |
rs182987778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283186 | TCCATCCTGGGTGAT[A/G]TAAGAGTTTTGGAAC | 64446 |
rs182990635 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286854 | CCTCCATTGAAAGCA[C/T]ATGGTTAGGTGGATG | 64446 |
rs183196535 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74289145 | AGGAGAGGGCATGGC[A/G]GGGCAGAGGCTGCCC | 64446 |
rs183212481 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306378 | ATTAGGTAATAAGCC[C/T]GAATTCTAACCACCC | 64446 |
rs183234614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300469 | CACTATTCTGTACTC[A/G]ATGTTTTCCATTGTG | 64446 |
rs183400335 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300358 | TGCACCTCCTCCCCT[C/T]CCTCCCTCTCTTATG | 64446 |
rs183451667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282179 | CGCAGTGCTCAGGGT[C/T]AGAGGAAGACCCAGC | 64446 |
rs183505620 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279928 | AGCCACTCATCCACA[C/T]CTTTTGTCCTAAGGC | 64446 |
rs183512007 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314917 | TGCATCCTGCACCCA[A/G]AGCCTGTCACGTTAT | 64446 |
rs183514797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298781 | AGCATGTGCCACCAT[A/G]CCCAGCTAGGTTTTA | 64446 |
rs183770866 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291384 | GGCCAGGCTGGTCTC[A/G]CACTCCTGACCTCAG | 64446 |
rs183820332 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313527 | GGCCACCTTTTACAA[C/T]GCAATGGTGGCTGGT | 64446 |
rs183843365 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277742 | ACCTAGGGTGATTGT[G/T]AAAAACACGAATTGC | 64446 |
rs183929301 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292219 | AAGCCATCTGGTCCC[C/T]GGCTTTTCTTTATTG | 64446 |
rs184060066 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309826 | CTGAAGGGGTGGGGC[A/G]GGAGATGAGGCAGGG | 64446 |
rs184082098 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273208 | AATAAGCACCGCCAC[C/T]GTCCTGCCACTTTGC | 64446 |
rs184103881 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310235 | GCAGAGCAGGCTAGT[C/T]AGACAAATAGATGGC | 64446 |
rs184143561 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292577 | ATGTGCCACCACACT[C/T]GGCTAATTTTTGTAG | 64446 |
rs184147791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74274456 | AACATTCCTCTTGGG[A/G]GGCTTCCTTCTGGGA | 64446 |
rs184191474 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289837 | GTCAAGGACACTCAC[A/G]CGGTTGGTGCCTCAA | 64446 |
rs184199043 | snp | A/G | 0.0109276 | 0.0731156 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307315 | GACCTGTGTCGTAGA[A/G]CCTGGGTCTCCCTTG | 64446 |
rs184237320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283831 | GCTGGAGGATCCCTT[C/T]AGCCTGAGAAGTCAA | 64446 |
rs184354915 | snp | C/G/T | 4.94322e-05 | 0.00497132 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289628 | AGGGCTGCCACACAC[C/G/T]TCTCCTGGCACCCCG | 64446 |
rs184584123 | snp | A/G | | | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314435 | TTGGAGAGAGGGAAG[A/G]GGCGGGGCTTGTCCC | 64446 |
rs184670575 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279446 | ACATCTCCTGTGCCC[C/T]ATAAATATATACACC | 64446 |
rs184673696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285255 | CATCACTGCAGCTCC[C/T]CAAGGGATGCACTGC | 64446 |
rs184724341 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74276299 | TGTCTGGACCACAGC[A/G]TCCCTGATTCTGCGT | 64446 |
rs184730745 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302498 | CTTGAACCTGGGAGG[C/T]GGGGGTTGCGGTGAG | 64446 |
rs184777847 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296707 | TTATCAGGGAACCAC[A/C]AGACCGGTCAGATAA | 64446 |
rs184828196 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303347 | CTCTCTGGCTCACTG[A/T]CGGGCGGCGTGCAGT | 64446 |
rs184887767 | snp | G/T | 3.29679e-05 | 0.00405991 | stop-gained, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314178 | GAGGAAGCAGCGGGG[G/T]AAGAAGGGGATGAAG | 64446 |
rs184926917 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278906 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 64446 |
rs185029734 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310830 | TAGGCGTGAGCCACC[C/G]TGCCCAGCCTAATTA | 64446 |
rs185066398 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275722 | ACAGACTGAGACTCC[A/G]TCTCAAAAAAAAAAA | 64446 |
rs185142578 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292772 | GCATATTGTCTATCC[C/T]GGAGAATGTTCCATG | 64446 |
rs185368282 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293926 | GTAGCTGGGATTACA[G/T]GTGCATGCCACCACG | 64446 |
rs185379060 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276563 | TATTCATCTGTGTGC[C/G]CTGCTAGCTTGTGAG | 64446 |
rs185381490 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312557 | GAGTGACTGAACGAG[A/G]GTCCTAGAGGTAAGT | 64446 |
rs185506266 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314581 | CATTTTCGTTTGTAA[C/T]CTTGCAGACCCTCAA | 64446 |
rs185618973 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297050 | GAGGTCCTTACTTCA[C/T]GGATTTTGCTGATGG | 64446 |
rs185625359 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291286 | CTGCCTCAGCCTCCC[G/T]AGTCGCTGAGATTAC | 64446 |
rs185639266 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309019 | AGTGAGCCGACATCG[C/T]ACCACTGCACTCCAG | 64446 |
rs185736785 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293691 | CCTGGGTGACAGAGC[A/G]AGACTCCATCTCAAA | 64446 |
rs185783189 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308759 | AATCCTGGCTTCAAG[C/T]GATCTTCCTGCCTTG | 64446 |
rs185881793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311840 | CCAACCCCAATATTC[A/G]GCCCTCCTTCCTTGA | 64446 |
rs185918219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290409 | CCCATCTGTCCTGAC[A/G]CTTGCCTTTAATTCA | 64446 |
rs185932993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303473 | TGAGACATCGTTTTG[C/T]TCTGTTGCCCATGCT | 64446 |
rs185967887 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286337 | AATAATAATAATAAT[A/T]ATTTTGTTTGTCTAG | 64446 |
rs186041427 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287334 | GAAATTGCCCAGCTG[C/T]GTACAGGTGGGGCAT | 64446 |
rs186361351 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308107 | CCGGCCCAGATCCTT[G/T]CTTTAGTCTTGATCA | 64446 |
rs186377537 | snp | C/T | 0.000334175 | 0.0129219 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281754 | CAGGACCTGTGGAGA[C/T]AGGGAAGGGGCCGGT | 64446 |
rs186532593 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299158 | TTTCCATCTTTCTTG[A/G]CAAAGCACTAATAAC | 64446 |
rs186560341 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304487 | GAAGTTAAGACAGAA[A/C]AGTAAACAAGGAAGG | 64446 |
rs186573068 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276939 | AAGGGGAGGATGCCA[C/T]GGGATTTGCATGCTT | 64446 |
rs186582161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313214 | ATAGAGTGGACAGAG[C/T]GAAGGATGGTGCATG | 64446 |
rs186600214 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273499 | GCTCACGCCTGTAAT[C/G]CCAGCACTTTGGGAG | 64446 |
rs186612640 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300422 | GAAACACACCTCTCT[C/T]TTCTTTACTCTTTCT | 64446 |
rs186637442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282420 | ATCCTCCCACCTCAG[C/T]CTCCCTGGTAGCTGG | 64446 |
rs186741539 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280610 | AGTCTGGCAACCAAC[A/G]AGCCTTTTGGACAAT | 64446 |
rs186820138 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295132 | GGATGTGGTGGCTCG[C/T]GCCTGGAAACCTAGC | 64446 |
rs186834818 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313981 | CCAGCCGCAGAGCTG[G/T]CACCCGGGTTCCAGG | 64446 |
rs186886333 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278645 | GGCCGGGCATGGTGG[C/T]GCATACCTGTAATCC | 64446 |
rs187132495 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290003 | CCTGACCCCATGGGA[C/T]CTCAATTCTTAGCTC | 64446 |
rs187207937 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288584 | CCACGCAGTTTGTGG[G/T]ACCTCGTTGCAGCAG | 64446 |
rs187222709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305576 | CAAACACCCGAGCTC[A/G]TGTTAGCAAGTGACT | 64446 |
rs187262894 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310253 | ACAAATAGATGGCCC[C/T]GCCCTCCCACCCCCA | 64446 |
rs187303882 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292632 | ATGCTGCCCAGGCTG[C/G]TCTTAAACTCCTGGG | 64446 |
rs187424175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301486 | GGGAAGGTCACGCCC[A/G]GGACCAACATCGGGA | 64446 |
rs187429098 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283958 | GCCTGGCCAACATGG[C/T]GAAACCCCGTCTCTA | 64446 |
rs187581577 | snp | C/T | 3.32513e-05 | 0.00407732 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310114 | CCCTGCTGGAGGTCT[C/T]GCCTGGGCTCTCTAC | 64446 |
rs187668900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286498 | TGATCTTGGGTCTCT[G/T]CAATCTCCACCTCCC | 64446 |
rs187696045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292286 | TATAGATCCTCTTCA[C/T]ATTTTCTGTTTCTTC | 64446 |
rs188041544 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277971 | ATTCTGATGTAGTTG[C/T]TCTGGGGTTCAAACA | 64446 |
rs188058840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295638 | TGTATTTCTTGGCAT[A/G]TCTTATAATTTTTTT | 64446 |
rs188107913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293760 | GTAGATTACATGTAG[C/T]TGGCATACAAGTGAA | 64446 |
rs188108363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300698 | TGGGACTTCTAGGTC[A/G]GAGCACACATGCATT | 64446 |
rs188143783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276530 | GAGACCTCCTGAGAC[A/G]CCCTTTGCTGACCTT | 64446 |
rs188149585 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302756 | AGTGCAGCCCAGGCC[C/T]GGTTCCCCCTTGGGG | 64446 |
rs188191522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279013 | TCTACTAAAAATACA[A/G]AAAATTAGCCGGGTG | 64446 |
rs188196863 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315107 | CACGGTCATCAACTG[C/T]GGGCCAGGTGCTGTG | 64446 |
rs188205001 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298882 | TTTTGCCTCGGCCTC[C/G]TAATGCGCTAGGATT | 64446 |
rs188373973 | snp | C/T | 4.94434e-05 | 0.00497184 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314237 | AGCCTTCGACTGCGG[C/T]GCTATCCCTGTGTGC | 64446 |
rs188427023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283256 | CGCTGCTGCAGTGTA[C/T]GCTTTAAAGTGGTTA | 64446 |
rs188474653 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291672 | AAAATAAACAGTTTT[A/T]AAAAACTATAGTTCA | 64446 |
rs188643631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296712 | AGGGAACCACCAGAC[C/T]GGTCAGATAATGACA | 64446 |
rs188742115 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272245 | CTTCTAACCCACTTT[C/T]CCACCCACAAAATAA | 64446 |
rs188746322 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309650 | AGAAACAAAAGCAGG[G/T]ACCCGGCATCTCCTA | 64446 |
rs188822172 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | DNAI2 | GRCh38.p7 | 17:74274587 | GCCTCTGTACACCCT[C/G]CCTCATACCCTCCTA | 64446 |
rs188917476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306518 | ACAGAACCACAGACT[C/T]CTGCAACGTCAAAGC | 64446 |
rs189030563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307822 | CTTTTTTTGGGGGGA[G/T]GAAGTCTCTTTGTTG | 64446 |
rs189063548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289881 | AGTCGAGGAGGAACA[C/T]ACTCTTCTCCTTCCT | 64446 |
rs189082910 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303817 | AACAATATGTTTTTT[A/T]AAAAAATAAAAATAA | 64446 |
rs189116843 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286374 | GTTCTTCAACCTTTT[A/C]TTCATTATTGGCCTT | 64446 |
rs189145513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311898 | GTACAGGGACTGTAT[A/G]GAGAGCAAGGAGAGC | 64446 |
rs189184618 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289333 | CGAGTTTGAGACCAG[C/T]CTAGGAAACATGGTA | 64446 |
rs189192906 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313528 | GCCACCTTTTACAAC[A/G]CAATGGTGGCTGGTA | 64446 |
rs189241855 | snp | G/T | 4.95307e-05 | 0.00497623 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289760 | CAGCGGGGTCCTGGT[G/T]GCCTGGGAGGGCTGA | 64446 |
rs189277462 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304191 | TTTCTTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 64446 |
rs189423876 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74297084 | ACCTGGAAAACTGAT[A/T]TTTGTTTGTTTGTTT | 64446 |
rs189433992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279578 | TGTCATCCAGGCTGG[A/G]GTGCAGTGGCACAAT | 64446 |
rs189443329 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314832 | TTCTGCTGCACCTGA[A/G]TGCTTTCTGTTATCC | 64446 |
rs189489092 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279997 | TGAGCCCCTGGAAAC[C/T]TGCTATCAAAGGCAC | 64446 |
rs189521690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307399 | GGGCCAGGTGCAGTG[C/G]GCTAATGCCTGTAAT | 64446 |
rs189705639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303356 | TCACTGACGGGCGGC[A/G]TGCAGTCGGCTTGAA | 64446 |
rs189720867 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290530 | GCTTCACGCTCTCCA[A/G]CTTCCCTTCGTTGTC | 64446 |
rs189757861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313738 | GGTCACAAAGTACCG[C/T]GTGGTACTGAAGCTG | 64446 |
rs189786341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295774 | TTGTTTCATTAATAC[A/C]TTTTCTTAGCTAGTT | 64446 |
rs189797051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278012 | TTCACAAAGCCCTGC[A/G]GGTGTTTCTAAATGT | 64446 |
rs189969398 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285325 | TGCTGGGGGGAAGGG[A/G]ACCAGCTGCTACCTC | 64446 |
rs189987289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294210 | CTTTTTTTTCCTATA[A/T]GTCTTACATCTTTTT | 64446 |
rs189993695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276683 | CAATGCCTCTGTTCT[C/T]ACTCGGGGCTTGGCC | 64446 |
rs189997691 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312684 | AGGAGTGTGACCTGT[C/G]GTCAGCTCATCTGCC | 64446 |
rs190023590 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293113 | GCTGGGATAACAGGC[A/G]TGAGCCACCGCACCT | 64446 |
rs190267488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308346 | CAGATGAAACCAAGT[A/G]GGAAGTGACACTCTC | 64446 |
rs190268373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311135 | CACCTCAGCCTCCCA[A/G]ACTGCTGGGATTATA | 64446 |
rs190306609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275959 | CAGGGCCCACCACTC[A/G]CAGGAACCCAGTAGG | 64446 |
rs190425042 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291363 | GAGACAGGGTTTCAC[C/T]ATGTTGGCCAGGCTG | 64446 |
rs190440997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309069 | GTGTCTCAAAAAAAA[A/G]AAAAAAAAAAGCAAC | 64446 |
rs190521462 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290043 | ATATCAGGCCGGGCT[C/T]GGTGGCCCATGCCTG | 64446 |
rs190747648 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286794 | TTTCCATGCTTTGTA[C/T]CTAAAAAGCAATATT | 64446 |
rs190922660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299937 | CCATCAGAACCCCTG[A/G]GGACATTTCCTTTAA | 64446 |
rs190930942 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282065 | GCGGCCAGCTGGGGC[C/T]GGTGAGTGGTTCTGT | 64446 |
rs190960691 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300468 | ACACTATTCTGTACT[C/T]GATGTTTTCCATTGT | 64446 |
rs190963158 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304811 | GTCTTGCCAGGGAAG[G/T]CTCTGCCCATCCCAT | 64446 |
rs191031963 | snp | A/G | 8.24083e-05 | 0.00641852 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305248 | GGTGGGGACCGAGCA[A/G]GGCATCGTCATCTCC | 64446 |
rs191045514 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282635 | GAGCAGAGATTCATA[C/T]CTACAGGCAACTACC | 64446 |
rs191051962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309005 | GAGGCAGAGATTGCA[A/G]TGAGCCGACATCGTA | 64446 |
rs191285865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288198 | TTCCACCCTCAGTAC[A/G]GTATTCAGAAAATTA | 64446 |
rs191531286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280726 | TGCCCAGCATGGCAG[A/G]GAATTTAGTCCAACA | 64446 |
rs191597429 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273547 | ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 64446 |
rs191601564 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295187 | ATTACCTGAACTCAG[A/G]AGTTCAAGACCAGCA | 64446 |
rs191608824 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292541 | TCCACCCCAGCCTCC[C/T]GAGTAGCTGAGCCTA | 64446 |
rs191638292 | snp | C/T | 0.000230798 | 0.0107399 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314173 | AGGGAGAGGAAGCAG[C/T]GGGGGAAGAAGGGGA | 64446 |
rs191643069 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296497 | CTCCCAAAGTACAGG[C/T]GTGAGCCACTGTACT | 64446 |
rs191647843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289836 | GGTCAAGGACACTCA[C/T]GCGGTTGGTGCCTCA | 64446 |
rs191804375 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299310 | ACGTGCTTTTCCCTA[C/T]GTTAGGGACTCGGCT | 64446 |
rs191844645 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310569 | TTTGAGACAAAGTCA[C/T]GCTCTGTTGCCCAGG | 64446 |
rs191847579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309807 | GGGTGACTGTGAGGC[A/G]GAACTGAAGGGGTGG | 64446 |
rs191863490 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277522 | CAATGTATATGGATG[C/G]AAAGGGTTAACCTTC | 64446 |
rs192070770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313338 | ATTTTGCATTTGGGG[A/G]TACTTGGTTATGAGA | 64446 |
rs192074694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292660 | GGGCTCAAGGGATCC[A/G]CCTGCCTTGGCTGGC | 64446 |
rs192223705 | snp | A/C | 0.000746423 | 0.0193043 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289565 | GAACCTCACATCCAG[A/C]CTTCTGCTCTCTTCC | 64446 |
rs192278949 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289009 | TTTCACTACCACGAC[A/T]GACTTAGGGGCCTGG | 64446 |
rs192292448 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305746 | GCGTGATCTCGGCTC[A/C]CTGCAGCCTCCACCT | 64446 |
rs192330833 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284439 | TTTTTTTGAGACGGA[G/T]TCTCGCTCTGTCGCC | 64446 |
rs192346520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302427 | ACAAAATTAGCTGGG[C/T]GTGGAGGCGCACGCC | 64446 |
rs192489362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303085 | ACTGTGTGTTGGACA[C/T]TTGTGGCTGCCTGAT | 64446 |
rs192533898 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307471 | TCAGGAGTTCAAGAC[C/G]AGCCTGGCCAATATG | 64446 |
rs192589260 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278890 | AATAACTAACAGGCC[A/G]GGCGCGGTGGCTCAC | 64446 |
rs192650313 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306799 | ATTTTTGTATTTTTA[C/G]TATAGACAGAGTTTC | 64446 |
rs192790912 | snp | A/G | 1.66468e-05 | 0.00288498 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285181 | GAGAACTACGTTAAC[A/G]CCATCATGCAGCTCG | 64446 |
rs192859355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283513 | CTTGGGAGGTGGAGG[C/T]GGGCGGATTGCTTAT | 64446 |
rs192979763 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296920 | TGCTGTTTTTCTTGA[A/G]TAAACATTCTCCCGA | 64446 |
rs193030467 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272669 | ACATATATGGAGAAG[G/T]TGGGAAGTGGGAGAG | 64446 |
rs193062360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300925 | CTCCCACGAATTGCC[A/G]GGAGCTCCATCCTTT | 64446 |
rs193070347 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275229 | GAGGGCAGGTAGTCA[C/T]TGACCCCCATCGGTC | 64446 |
rs193196672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314380 | CCTACAAATCACTAG[C/G]CCCCACTGACTCACT | 64446 |
rs193201629 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279102 | AACCCGGGAGGCGGA[A/G]CTTGCAGTGAGCTGA | 64446 |
rs193222430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291754 | GCGTTGGGGAGCCCT[A/G]TTTTGGGAGAGGTTT | 64446 |
rs199524166 | snp | A/C/G/T | 4.95391e-05 | 0.0049767 | missense, synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309358 | CTGGGACTTCATGTT[A/C/G/T]GAGCAGTGCGATCCC | 64446 |
rs199535813 | snp | A/G | 0.00199808 | 0.0315444 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285159 | CCGGAAGAAAGTGGA[A/G]AAAGATGAGAACTAC | 64446 |
rs199562768 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281979 | GGGCATCCAGTGCTC[A/G]ATCAGCATGTCGGAA | 64446 |
rs199640353 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294311 | TTCTTTTTTTTTTTT[C/T]TTTTCTTTTTTTTTT | 64446 |
rs199726930 | snp | A/C/T | 0.0001318 | 0.008117 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305361 | GAAACCCCTTCTACC[A/C/T]GAAGAACTTCCTGAC | 64446 |
rs199817659 | snp | A/G | 0.000150684 | 0.00867868 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312123 | GATGAGGAGCTGGCC[A/G]TAGACCTGGAGGCGC | 64446 |
rs199832373 | in-del | -/A | 0.0368353 | 0.130617 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279489 | CAAAAATTAAAAATT[-/A]AAAAAAAAATAGCAA | 64446 |
rs199835284 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301895 | AAGGAAGGAAGGAAG[A/G]AAGGAAGGAAGGAAA | 64446 |
rs199891805 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301951 | AAGGAAGGAAGGAAG[A/G]AAGGAAGGAAGGAAA | 64446 |
rs199932162 | in-del | -/C | 0.0103295 | 0.0711199 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294204 | ATTTTGCTTTTTTTT[-/C]CTATATGTCTTACAT | 64446 |
rs199965300 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314228 | CTAGAAGTCAGCCTT[C/T]GACTGCGGCGCTATC | 64446 |
rs199966746 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282727 | AGAACTTATCTTGAG[A/G]GTCATGGTCATGTGT | 64446 |
rs199987940 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302086 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA | 64446 |
rs200043910 | snp | A/G | 8.2763e-05 | 0.00643231 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309301 | GAGCCCCGTGAGGCC[A/G]ACCGTTTTCTTTACC | 64446 |
rs200125805 | snp | A/C | 1.65201e-05 | 0.00287398 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285152 | TCCGTTTCCGGAAGA[A/C]AGTGGAGAAAGATGA | 64446 |
rs200252022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305172 | CCCGCTAATCCCAGA[A/G]TTGATGGTTCGTGGA | 64446 |
rs200279879 | snp | C/T | 4.94466e-05 | 0.00497201 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301204 | CTTCCCCGACTTGCA[C/T]TGACAGGGCAGCCAG | 64446 |
rs200358267 | snp | A/G | 8.30489e-05 | 0.00644341 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285175 | AAAGATGAGAACTAC[A/G]TTAACGCCATCATGC | 64446 |
rs200381053 | in-del | -/G | 0.0107246 | 0.0724382 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289337 | TTTGAGACCAGCCTA[-/G]GAAACATGGTAAAAA | 64446 |
rs200490335 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301886 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA | 64446 |
rs200587166 | snp | A/G | 0.000372806 | 0.0136478 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310154 | GAATGAGAAGAACGT[A/G]GCCTCTTCCGTAAGC | 64446 |
rs200668134 | snp | A/G/T | 4.9531e-05 | 0.00497629 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285071 | TTGAGATGGAGACCC[A/G/T]GGGAGTTAACCATGT | 64446 |
rs200693763 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309278 | GCTTACCTCACTGAT[A/G]CTGCCTGGAGCCCCG | 64446 |
rs200708211 | in-del | -/AAA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277385 | GCGAGAATCCATCTC[-/AAA]AAAAAAAAAAAAAAG | 64446 |
rs200708870 | snp | C/T | 3.29527e-05 | 0.00405898 | stop-gained, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301064 | ATGTGGTGGGACATC[C/T]GAAAGATGAGCGAGC | 64446 |
rs200721742 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301925 | AGAAGGAAGGAAGGA[A/C]GGAAGGAAGGAAGGA | 64446 |
rs200799408 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74288092 | TTTGTGGCAGTCCCC[G/T]ACTTAAACCATTTTT | 64446 |
rs200825190 | snp | A/C | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74286986 | CCCTAGATCATGGAG[A/C]ACTGCATCAAGCAGA | 64446 |
rs200861036 | snp | A/G | 0.000445093 | 0.0149113 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314174 | GGGAGAGGAAGCAGC[A/G]GGGGAAGAAGGGGAT | 64446 |
rs200862518 | in-del | -/GAGAGAGAGAGAG | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296321 | CTTTAAAGAGAGAGA[-/GAGAGAGAGAGAG]GAGAGAGAGAGAGGA | 64446 |
rs200947626 | snp | C/G | 1.65075e-05 | 0.00287289 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309377 | CAGTGCGATCCCACC[C/G]TCAGCTTGAAGGTCA | 64446 |
rs200961442 | in-del | -/G | 0.00363259 | 0.0424629 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281726 | CCAGATTGAGAACCT[-/G]GAGCTGTCCTGGCAG | 64446 |
rs200978593 | snp | C/T | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273218 | GCCACTGTCCTGCCA[C/T]TTTGCAGATGAGGAT | 64446 |
rs200978738 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301981 | AGAAGGAAGGAAGGA[A/C]GGAAGGAAGGAAGGA | 64446 |
rs201064976 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309978 | CACATAACTTTGCTC[C/T]TCTCTCCTCTACCTG | 64446 |
rs201072174 | in-del | -/TGTTTT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293790 | TCATAGTTTTGTTTT[-/TGTTTT]GTTTTGTTTTTGAGA | 64446 |
rs201083051 | in-del | -/CCCACC | 0.0894459 | 0.191631 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277056 | CTCTAAGCCATTGCT[-/CCCACC]CAGGAAAGAGAATTT | 64446 |
rs201110499 | in-del | -/TTT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292416 | ATCATTTTCTTTTTC[-/TTT]TTTTTTTTTTTTTTT | 64446 |
rs201170972 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293908 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 64446 |
rs201255275 | in-del | -/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294311 | TCTTTTTTTTTTTTC[-/C]TTTTCTTTTTTTTTT | 64446 |
rs201294141 | snp | A/T | 4.95446e-05 | 0.00497693 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309342 | ACGGAACCCTGGATA[A/T]CTGGGACTTCATGTT | 64446 |
rs201298434 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74274453 | CCAAACATTCCTCTT[G/T]GGGGGCTTCCTTCTG | 64446 |
rs201327040 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301887 | AAGGAAGGAAGGAAG[C/G]AAGGAAGGAAGGAAG | 64446 |
rs201366939 | snp | A/G | 3.33e-05 | 0.00408031 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289549 | AGGGGGAGAAATTGG[A/G]GAACCTCACATCCAG | 64446 |
rs201444208 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294196 | CATCTGCCATTTTGC[-/T]TTTTTTTCCTATATG | 64446 |
rs201457010 | snp | C/T | 0.000510704 | 0.0159716 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289697 | GATTTTCAGCGGGCA[C/T]CTGTGGGCATGAGCA | 64446 |
rs201457679 | snp | C/G/T | 0.00019782 | 0.00994359 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301031 | AAGTCTCACTGTCGC[C/G/T]CCTCCTCCCACCAGG | 64446 |
rs201464593 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294310 | TTTCTTTTTTTTTTT[C/T]CTTTTCTTTTTTTTT | 64446 |
rs201477140 | in-del | -/ATTTTAATTTA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74310519 | ATTATATTATATTGT[-/ATTTTAATTTA]ATTATTTTTATTTAT | 64446 |
rs201492303 | snp | C/T | 0.00046127 | 0.0151797 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286949 | GACCTCCATTTACTG[C/T]GGAGAACTTCCAATG | 64446 |
rs201521142 | snp | A/G | 6.59881e-05 | 0.00574367 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285140 | TGGAGCAGACCATCC[A/G]TTTCCGGAAGAAAGT | 64446 |
rs201524327 | snp | A/T | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309348 | CCCTGGATATCTGGG[A/T]CTTCATGTTCGAGCA | 64446 |
rs201637697 | snp | G/T | 0.238171 | 0.24972 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285970 | ACACATATATATATA[G/T]AGAGAGAGAGAGAGA | 64446 |
rs201745965 | snp | A/C | | | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281873 | TCGGGAAGCAGTGCA[A/C]TTTCTCGGACCGCCA | 64446 |
rs201801542 | snp | A/G | 0.000165442 | 0.00909361 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309305 | CCCGTGAGGCCGACC[A/G]TTTTCTTTACCACCA | 64446 |
rs201802455 | snp | C/T | 1.65312e-05 | 0.00287495 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281990 | GCTCGATCAGCATGT[C/T]GGAACACGAGGTGGG | 64446 |
rs201832227 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302070 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA | 64446 |
rs201909971 | snp | A/G/T | 0.000527639 | 0.0162341 | splice-acceptor-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314120 | CTGTCTTCCCCTGCA[A/G/T]CAGCAACCAAGTCCA | 64446 |
rs201925425 | snp | A/G | 0.000419094 | 0.0144697 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312137 | CGTAGACCTGGAGGC[A/G]CTGGTCAGCAAGGCC | 64446 |
rs201968524 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301943 | AAGGAAGGAAGGAAG[C/G]AAGGAAGGAAGGAAG | 64446 |
rs202170345 | in-del | -/TA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307703 | GTTAAATCTGAATTT[-/TA]AAAAAAAAAACTATT | 64446 |
rs202220110 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283052 | GCCTTTTCCAGACTT[G/T]TTTTGTTTTGTTTTG | 64446 |
rs267605036 | snp | A/C | | | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291063 | GAAGCCATCGTCTCC[A/C]CTCGTGACGTTGGAG | 64446 |
rs367596059 | snp | A/G | 1.64863e-05 | 0.00287104 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301211 | GACTTGCATTGACAG[A/G]GCAGCCAGGGCTAAA | 64446 |
rs367685084 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307605 | GATCAGGAGTTCAAG[A/C]CCAGCCGAGATTGCG | 64446 |
rs367814265 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286671 | CTCAAGTGATCCACC[C/T]GCTTCGGCCTCCCAA | 64446 |
rs367818977 | snp | A/G | 0.000140033 | 0.00836642 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309520 | CTCTGTGGGGGAGCC[A/G]TGTGCAGGCTGACTG | 64446 |
rs367835600 | snp | A/T | 1.6534e-05 | 0.00287519 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289775 | GGCCTGGGAGGGCTG[A/T]GGGCTGGGACCAGCA | 64446 |
rs367920388 | snp | A/G | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274136 | CTCCTAACTCAGGAG[A/G]CCTCCAAAAAGAAGA | 64446 |
rs367937717 | in-del | -/C | | | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311725 | CTTGTTGGGCCAAAG[-/C]CCGCCATATTTCATA | 64446 |
rs367950076 | snp | C/T | 3.29674e-05 | 0.00405988 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305387 | CTGACGGTTGGCGAC[C/T]GGACAGCCCGCATTT | 64446 |
rs367953403 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294089 | CGCCCAGCTTGGATC[A/C/G]TGGTTTTTTCCTTTT | 64446 |
rs367982356 | snp | A/G | 8.27315e-05 | 0.00643109 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305203 | GTCTTCCCCTCCTGT[A/G]TCACTCCTTCCACAG | 64446 |
rs368042584 | multinucleotide-polymorphism | CA/TG | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283897 | TAATCCCAGCACTTC[CA/TG]GAGGCTGAGGCCAGT | 64446 |
rs368063114 | snp | A/G | 5.04265e-05 | 0.00502103 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312153 | CTGGTCAGCAAGGCC[A/G]AGGAGGAGTTCTTCG | 64446 |
rs368176106 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304166 | TTTTTCTTTTCTTTT[C/T]TTTTTTCTTTTTCTT | 64446 |
rs368190304 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300002 | TGCCCAGGCTGGAGT[A/G]CAATGGCACGATCTT | 64446 |
rs368199611 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278772 | AAATGAGATTCCATC[C/T]CAAAAAAAAAGAAAG | 64446 |
rs368217836 | snp | A/G/T | 4.98818e-05 | 0.00499388 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310115 | CCTGCTGGAGGTCTC[A/G/T]CCTGGGCTCTCTACC | 64446 |
rs368225621 | snp | A/G | 3.30191e-05 | 0.00406306 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309368 | ATGTTCGAGCAGTGC[A/G]ATCCCACCCTCAGCT | 64446 |
rs368232107 | snp | A/G | 6.58892e-05 | 0.00573936 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291072 | GTCTCCACTCGTGAC[A/G]TTGGAGTTCAACCCC | 64446 |
rs368236204 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296270 | GCCTGCATTCAGGAG[C/T]TTGAAACTAGCCTGT | 64446 |
rs368286153 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305665 | CCATGGCTTAATTTT[A/T]TTTCCTTTTTTTTTT | 64446 |
rs368338657 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293791 | TCATAGTTTTGTTTT[G/T]TTTTGTTTTTGAGAC | 64446 |
rs368378867 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293555 | TCTAAAGTATGTCTT[A/G]TAGCCAGGTGTGGTG | 64446 |
rs368435643 | snp | C/T | 5.77695e-05 | 0.00537414 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285240 | TGCAAGAGCCCCATC[C/T]ATCACTGCAGCTCCC | 64446 |
rs368444912 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296230 | CTGTAATCCTAACAC[G/T]TTGAGAAGCTGAGGC | 64446 |
rs368445170 | snp | A/G | 3.29571e-05 | 0.00405924 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301157 | ATCTCCCTGGAGTTC[A/G]AATCTACTTTGGTGA | 64446 |
rs368452360 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74281552 | TGTCAGCTACCGCGC[C/T]TGGCCAAAATTTTTA | 64446 |
rs368574156 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301544 | CCTGCCTGGCACGGG[G/T]TCCCTAGGCTGGTCA | 64446 |
rs368602173 | snp | A/C | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305427 | ACAGCCGGGAATCGT[A/C]CATCATGTGGACCAA | 64446 |
rs368633797 | snp | A/G | 0.000154799 | 0.00879633 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312210 | AAGGAGGCAGACGCC[A/G]TAAAGCTGACGCCAG | 64446 |
rs368636962 | snp | A/G | 0.000132002 | 0.00812304 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289749 | TGGGTGAGAAGCAGC[A/G]GGGTCCTGGTGGCCT | 64446 |
rs368825259 | snp | A/T | | | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315169 | GGGCTGCCCTGGGGG[A/T]GCCCTGAAACCGCAG | 64446 |
rs368834672 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287897 | GAGGCGGAGGTTGCA[C/G]TGAGCCGAGATCGCA | 64446 |
rs368836198 | snp | A/G | 8.23784e-05 | 0.00641735 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286962 | TGCGGAGAACTTCCA[A/G]TGTGTCCCCCCTAGA | 64446 |
rs368886602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287538 | GAAATCACCGCAGGC[A/G]TGGATATTCACTGCA | 64446 |
rs369004270 | snp | G/T | 0.00018528 | 0.00962319 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309232 | TGTCCCTCCAACCAT[G/T]ATGTGGTCTACCTCC | 64446 |
rs369004602 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294831 | TTATTTATTCAAATA[C/T]TCTTTCCTACCCTTT | 64446 |
rs369016407 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301954 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAAGAA | 64446 |
rs369017940 | snp | A/G/T | 6.60081e-05 | 0.00574459 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281964 | GAACCCAGTGGACAC[A/G/T]GGCATCCAGTGCTCG | 64446 |
rs369021155 | snp | A/G | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273622 | CGGGCGTAGTGGCGG[A/G]CACCTGTAGTCCCAG | 64446 |
rs369033976 | snp | A/G | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272254 | CACTTTCCCACCCAC[A/G]AAATAATGTGTCTTC | 64446 |
rs369078530 | snp | A/G | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273837 | TTACAGAAAGTGGAG[A/G]AAGGATGGTAGCAGA | 64446 |
rs369083904 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294159 | AATCTATTTACATTA[A/C]TTTAATTACTGATAA | 64446 |
rs369116620 | snp | C/T | | | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299800 | CCCTGTGTATGGCAC[C/T]ATCTGGCTGCAGTCG | 64446 |
rs369243633 | in-del | -/TG | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287504 | ATTCATCCCACAGGT[-/TG]TGTGTGTGTGTGTGT | 64446 |
rs369262819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312314 | CTGCTTGCCGACTTC[C/T]TGGGTGACCTTGAGC | 64446 |
rs369270232 | snp | C/T | 0.00014832 | 0.00861035 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314234 | GTCAGCCTTCGACTG[C/T]GGCGCTATCCCTGTG | 64446 |
rs369278280 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291170 | TTTATTTTTATTTTT[A/T]TTTTTTTTAGATGGA | 64446 |
rs369283317 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283508 | AGTTACTTGGGAGGT[A/G]GAGGCGGGCGGATTG | 64446 |
rs369284382 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307984 | TTTATTTTTAGTAGA[G/T]GCAGGGTTCTGCCAT | 64446 |
rs369371635 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302577 | GCGAAACTCCATCTC[-/A]AAAAAAAAAACAAAG | 64446 |
rs369461002 | snp | C/G | 0.000199518 | 0.00998595 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284994 | GTGGCCGAGGGTTTG[C/G]GAGTATACCAGGGTG | 64446 |
rs369484279 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284070 | TTGAATCCAGGAGGC[A/G]AAGGTTGCAGTGAGC | 64446 |
rs369563704 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279460 | CCATAAATATATACA[C/G]CTACTATGTAACCAC | 64446 |
rs369630004 | snp | A/G | 1.67206e-05 | 0.00289137 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312111 | GAGGAGCAGACCGAT[A/G]AGGAGCTGGCCGTAG | 64446 |
rs369657136 | snp | A/G | 1.76643e-05 | 0.00297184 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287129 | GGCAGGTGTCTGGCC[A/G]CCCTCCGTCACCCCC | 64446 |
rs369665087 | snp | G/T | 8.24083e-05 | 0.00641852 | utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314259 | CCTGTGTGCCTTCCT[G/T]TCCCACCTCTTGGTA | 64446 |
rs369673672 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307741 | TTAGTATAAGTATGT[C/T]CCATGCAATATTTGG | 64446 |
rs369677831 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74297876 | CTCTGTATGTTCTTA[A/T]ACTTTTGCTGCTTCT | 64446 |
rs369692655 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283767 | AAAAACAAAAATTAG[A/C]CACGTGTGGTGGTAC | 64446 |
rs369708012 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278360 | GCTTGAGCCTGGGAG[G/T]TTGAGGCTGCAGCAA | 64446 |
rs369740012 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287445 | CTGCACTCATGCGAG[A/T]ATATCCATGAATAAC | 64446 |
rs369783079 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302481 | TGAGGCAGGAGAATT[-/T]GCTTGAACCTGGGAG | 64446 |
rs369894686 | snp | C/T | 1.65688e-05 | 0.00287821 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299785 | GTCCAGCCACCGAGA[C/T]CCTGTGTATGGCACC | 64446 |
rs369922267 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302014 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAAGAA | 64446 |
rs370090383 | snp | C/T | 0.000116182 | 0.00762085 | utr-variant-5-prime, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281811 | CTGCCCCCCAGCAGC[C/T]GGCACCATGGAGATT | 64446 |
rs370123370 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284756 | AGAGCAGATGGACAG[G/T]CTTCTCTGGTCCATT | 64446 |
rs370124079 | snp | C/T | 0.000108883 | 0.00737765 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287146 | CCTCCGTCACCCCCA[C/T]GCATGGGCGCCTCCA | 64446 |
rs370159896 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293023 | TTTTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 64446 |
rs370250337 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304156 | TAGGAGTTCTTTTTT[C/T]TTTTCTTTTCTTTTT | 64446 |
rs370251608 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295582 | TCTTGGGGACAATCT[C/G]TATTTATTGCTTTTT | 64446 |
rs370299295 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295657 | TATAATTTTTTTTTT[A/T]TTAAAAACTATACTT | 64446 |
rs370352545 | snp | C/T | 0.000197948 | 0.0099466 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285087 | GGGAGTTAACCATGT[C/T]GAGGGGGGCTGGCCC | 64446 |
rs370357581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277750 | TGATTGTGAAAAACA[C/T]GAATTGCTAGGCCCT | 64446 |
rs370359274 | snp | A/G | 1.67677e-05 | 0.00289544 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312140 | AGACCTGGAGGCGCT[A/G]GTCAGCAAGGCCGAG | 64446 |
rs370421003 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309319 | CGTTTTCTTTACCAC[C/T]AGGATGGACGGAACC | 64446 |
rs370424861 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304173 | TTTCTTTTCTTTTTT[C/T]TTTTTCTTTTTTCTT | 64446 |
rs370430068 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279924 | CACCAGCCACTCATC[A/C]ACATCTTTTGTCCTA | 64446 |
rs370462360 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306797 | AATTTTTGTATTTTT[-/T]AGTATAGACAGAGTT | 64446 |
rs370515891 | in-del | -/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74291716 | ATATTTGACTAGGGG[-/G]CCGCCATAAAGGGAT | 64446 |
rs370535730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288923 | GACCTTGGGTCTGGG[C/T]GATGCAGGACTAGGG | 64446 |
rs370544004 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274255 | GGGTTGCCAAGCAAC[C/T]GGTAAACGCCGCCGT | 64446 |
rs370664318 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306482 | TGCTAAAAAAAACAT[C/T]CTGGGGTTCCTTTCC | 64446 |
rs370664818 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292915 | GCCCACTGCAAGCTC[A/T]GCCTCCTGGGTTCAC | 64446 |
rs370735250 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300655 | TGCACACATGCGGGG[A/G]TATATCTACAGCAGA | 64446 |
rs370747984 | snp | C/T | | | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311811 | GAGTAACTCAGTGTC[C/T]CTGCTGCAGCCTTCC | 64446 |
rs370866845 | snp | A/G | 1.65138e-05 | 0.00287343 | stop-gained, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309346 | AACCCTGGATATCTG[A/G]GACTTCATGTTCGAG | 64446 |
rs370909237 | snp | A/C/G | 1.65784e-05 | 0.00287905 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289788 | TGAGGGCTGGGACCA[A/C/G]CACAAGTGGAGGAGC | 64446 |
rs370938447 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309167 | GCAAGACTCTGAGAT[C/T]CTGGAGCCCAGAAGG | 64446 |
rs370941339 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292518 | ACCTCCTGGGCCCGA[A/G]CAATTCTTCCACCCC | 64446 |
rs371039062 | in-del | -/A/AGAGA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296346 | AGGAGAGAGAGAGAG[-/A/AGAGA]GAGAGAGAGAGGAAG | 64446 |
rs371065329 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300493 | CATTGTGTGTACCTT[A/G]GAGATAGTTTCATAT | 64446 |
rs371091730 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284273 | ACCCACGTGTAAAAC[G/T]GTCCTCCCTGCTAGA | 64446 |
rs371217895 | snp | A/G | 3.34264e-05 | 0.00408804 | missense, nc-transcript-variant, intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312099 | GAGGGCAGGGATGAG[A/G]AGCAGACCGATGAGG | 64446 |
rs371226659 | snp | C/T | 0.000380231 | 0.013783 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285052 | TAGGCCAACTCAGAG[C/T]GGTTTGAGATGGAGA | 64446 |
rs371267856 | in-del | -/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74288034 | ATGTGAAAACCAAAC[-/C]AAAACAAAGCCGGTG | 64446 |
rs371303156 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74288297 | ATATAAGTGTTCTGA[A/G]CACATAGGCTGGACT | 64446 |
rs371326378 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294505 | AATTTTTGTAGAGAT[A/G]GGGTCTTGCTATGTT | 64446 |
rs371333933 | snp | C/G | 3.29826e-05 | 0.00406082 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314145 | AGTCCAGAAGAAGAC[C/G]AGGTGGTGGAGGAGG | 64446 |
rs371373191 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294163 | TATTTACATTAATTT[A/G]ATTACTGATAAAGTT | 64446 |
rs371384338 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309870 | TGACAACCAGTCTCC[A/G]AGTTTGAACTTCATC | 64446 |
rs371437628 | snp | A/G | 1.66932e-05 | 0.002889 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305175 | GCTAATCCCAGAATT[A/G]ATGGTTCGTGGAGTC | 64446 |
rs371451281 | snp | C/T | 9.88891e-05 | 0.00703099 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301195 | TTGCTGTCCCTTCCC[C/T]GACTTGCATTGACAG | 64446 |
rs371554981 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294160 | ATCTATTTACATTAA[A/T]TTAATTACTGATAAA | 64446 |
rs371641997 | snp | A/G | 0.000232581 | 0.0107813 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309400 | GAAGGTCACGCGCAT[A/G]TCCCTCCTTGTGCAT | 64446 |
rs371729787 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279024 | TACAAAAAATTAGCC[A/G]GGTGTGGTGGTGGGC | 64446 |
rs371736179 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74291219 | AGGCTGGAGTGTAGT[A/G]GTGCAATTTTGGCTC | 64446 |
rs371756796 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306185 | AGCAGTGAGGCATAG[C/T]CTGTCTTGCTCAGTG | 64446 |
rs371768249 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294192 | TTTACATCTGCCATT[G/T]TGCTTTTTTTTCCTA | 64446 |
rs371775540 | snp | A/C/G | 7.53627e-05 | 0.00613812 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311981 | TCTCCCCACCGGGCT[A/C/G]TCTCTGTCCCTGGGT | 64446 |
rs371817794 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286966 | GAGAACTTCCAATGT[G/T]TCCCCCCTAGATCAT | 64446 |
rs371845293 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278824 | AAGACCTACTATTTG[A/G]TAGGACAACAAGGTG | 64446 |
rs371869307 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306367 | TCATCTCCTAAATTA[C/G]GTAATAAGCCCGAAT | 64446 |
rs371869933 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275035 | TTGCTTGTTTGTCAC[A/G]GTCAGCAGAGGAGGA | 64446 |
rs371897209 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292848 | CCTTTTTTTTTTTTT[G/T]GGACGGAGTCTTGCT | 64446 |
rs371944060 | snp | G/T | 2.13815e-05 | 0.0032696 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305489 | GCAGGAGACAGGAGG[G/T]GATGGAGGGAGCCCA | 64446 |
rs371964291 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289736 | TACATCTGGGACCTG[A/G]GTGAGAAGCAGCGGG | 64446 |
rs371965225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287531 | TGTGTGTGAAATCAC[C/T]GCAGGCGTGGATATT | 64446 |
rs371989598 | snp | C/T | 0.000149245 | 0.00863714 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310070 | CAATGGGTGTCTCAT[C/T]GCCTGCGGCTCCCAG | 64446 |
rs372009842 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291057 | TGCTCTGAAGCCATC[A/G]TCTCCACTCGTGACG | 64446 |