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 |