SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs372116298 | in-del | -/AT | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303806 | CTGCATAATAAAACA[-/AT]ATGTTTTTTAAAAAA | 64446 |
rs372129512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278154 | CAGTTTCTTCATCTC[A/G]AAAATGGGCTCATGC | 64446 |
rs372155299 | snp | A/G | 3.29549e-05 | 0.00405911 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286941 | TCTGAAAGGACCTCC[A/G]TTTACTGCGGAGAAC | 64446 |
rs372196782 | snp | A/G | 8.23961e-05 | 0.00641804 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305255 | ACCGAGCAGGGCATC[A/G]TCATCTCCTGCAACC | 64446 |
rs372237155 | snp | G/T | 1.89611e-05 | 0.00307899 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310197 | GGGAAAATCCCTCCA[G/T]CACGTCCCGACCTGG | 64446 |
rs372259857 | snp | C/T | 0.000236064 | 0.0108617 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312167 | CGAGGAGGAGTTCTT[C/T]GACATCATCTTCGCA | 64446 |
rs372357313 | snp | C/G | 6.59511e-05 | 0.00574206 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281895 | GGACCGCCAGGCCGA[C/G]CTGAACATCGACATC | 64446 |
rs372389817 | in-del | -/A | 0.489259 | 0.0724914 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284222 | GAGAGACCCTCTCTT[-/A]AAAAAAAAAAAAAGG | 64446 |
rs372422186 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302459 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 64446 |
rs372522923 | snp | C/T | 5.03031e-05 | 0.00501488 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309243 | CCATGATGTGGTCTA[C/T]CTCCCACAGGTACCA | 64446 |
rs372571023 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284093 | CAGTGAGCCGAGATT[A/C]CGCCATTGCATTCCA | 64446 |
rs372577045 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301966 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA | 64446 |
rs372646357 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301902 | GAAGGAAGGAAGGAA[A/G]GAAGGAAAGAAGGAA | 64446 |
rs372682936 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293792 | CATAGTTTTGTTTTG[G/T]TTTGTTTTTGAGACA | 64446 |
rs372738024 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284443 | TTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCAGG | 64446 |
rs372749080 | snp | A/G | 0.00038342 | 0.0138406 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282037 | CCTGGCCTGTCAGGT[A/G]TGGCCAGGCAGGGCG | 64446 |
rs372751337 | snp | A/G | 1.67181e-05 | 0.00289115 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312104 | CAGGGATGAGGAGCA[A/G]ACCGATGAGGAGCTG | 64446 |
rs372767763 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279376 | ATGCTTGAGGGGATG[A/G]ATGGATACCCCATTT | 64446 |
rs372777336 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287154 | ACCCCCATGCATGGG[C/T]GCCTCCAAAGGCAAC | 64446 |
rs372790528 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, synonymous-codon, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312933 | TGAAAGAGCCAAAGA[A/G]CAGCGTGGAAGGGAA | 64446 |
rs372940037 | snp | C/G/T | 9.91595e-05 | 0.00704066 | missense, synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309328 | TACCACCAGGATGGA[C/G/T]GGAACCCTGGATATC | 64446 |
rs372958277 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287681 | CGGGGCAGTCTGGGC[A/T]TGGTGGCTCACGCCT | 64446 |
rs372972684 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279620 | GCAACGTCTACCTTC[C/T]AGGTTTAAGCGATTC | 64446 |
rs372975955 | snp | C/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74287011 | AGCAGAACAATGCCA[C/T]TGACATCTATGAAGA | 64446 |
rs372977582 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301918 | GAAGGAAAGAAGGAA[A/G]GAAGGAAGGAAGGAA | 64446 |
rs373090022 | snp | C/T | 0.000711617 | 0.0188495 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312220 | ACGCCATAAAGCTGA[C/T]GCCAGTGCCTGTAGG | 64446 |
rs373204831 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74297972 | CTAAGGCCCCGATCT[C/T]CCTCTCAGACCTGCT | 64446 |
rs373222442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298746 | TAGCAGGCAGCCTCC[C/T]GAGTAACAGCCTCCC | 64446 |
rs373253119 | snp | A/G | 0.000263752 | 0.0114807 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301029 | CGAAGTCTCACTGTC[A/G]CCCCTCCTCCCACCA | 64446 |
rs373294214 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74288468 | GTATGTGTGTATATA[C/T]GTGTAGATGTATGTT | 64446 |
rs373358488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282939 | ACCAACTGCTCCCCC[A/G]GGGATGAGAAGGACT | 64446 |
rs373360376 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294166 | TTACATTAATTTAAT[A/T]ACTGATAAAGTTTAC | 64446 |
rs373420833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311411 | CTGAGGTCGGGAGTT[C/T]GAGACCAGCCTGACC | 64446 |
rs373525217 | snp | C/G | 3.29891e-05 | 0.00406122 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301011 | AGGGGAAATACAGGG[C/G]CTCGAAGTCTCACTG | 64446 |
rs373540176 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74298776 | CGAGTAGCATGTGCC[A/G]CCATGCCCAGCTAGG | 64446 |
rs373803565 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295647 | TGGCATGTCTTATAA[A/T]TTTTTTTTTATTAAA | 64446 |
rs373836524 | snp | C/T | 3.29533e-05 | 0.00405901 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305373 | ACCCGAAGAACTTCC[C/T]GACGGTTGGCGACTG | 64446 |
rs373950256 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74310392 | TCACGTCACTCTCCA[A/G]GATTCAGTTTTTTAC | 64446 |
rs373961361 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309504 | CCAGGTGTGTTTGGG[A/C]CTCTGTGGGGGAGCC | 64446 |
rs374057086 | snp | C/T | 9.89503e-05 | 0.00703316 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314108 | AACACTTCTGTGCTG[C/T]CTTCCCCTGCAGCAG | 64446 |
rs374059513 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295659 | TAATTTTTTTTTTAT[A/T]AAAAACTATACTTTT | 64446 |
rs374070900 | snp | A/G | 0.000412143 | 0.0143493 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281928 | GCCCAACCCTGAGCT[A/G]GCCGAGCAGTTCGTG | 64446 |
rs374152390 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304161 | GTTCTTTTTTCTTTT[C/T]TTTTCTTTTTTCTTT | 64446 |
rs374155875 | snp | A/C | 1.66507e-05 | 0.00288532 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299712 | CTTCATCTCCTTCCT[A/C]ACCAGCCTGCTGGGA | 64446 |
rs374199953 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292869 | GAGTCTTGCTCTTTC[C/G]CCCAGGCTGGAGTGC | 64446 |
rs374267839 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278495 | GGGCATGCAGGAAGC[A/G]CGCCTGGAAACTGTT | 64446 |
rs374277039 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301103 | GTTGTGATCTTGGAC[A/G]TCACCAAGAAGGAAC | 64446 |
rs374314079 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279385 | GGGATGGATGGATAC[A/C]CCATTTCCCATGATT | 64446 |
rs374316836 | snp | C/T | 6.67902e-05 | 0.00577846 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299684 | AGGAAGCCTGTGCCC[C/T]CTTCCACTCCTTCTT | 64446 |
rs374338856 | snp | C/T | 1.66095e-05 | 0.00288175 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289562 | GGGGAACCTCACATC[C/T]AGCCTTCTGCTCTCT | 64446 |
rs374347041 | snp | C/T | 3.52199e-05 | 0.00419628 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287130 | GCAGGTGTCTGGCCA[C/T]CCTCCGTCACCCCCA | 64446 |
rs374365135 | in-del | -/AATAATAATAAT | 0.283158 | 0.247791 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286298 | AAGACTGTGTCTCAA[-/AATAATAATAAT]AATAATAATAATAAT | 64446 |
rs374387132 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304179 | TTCTTTTTTCTTTTT[C/T]TTTTTTCTTTTTTTT | 64446 |
rs374447879 | snp | C/T | 3.30006e-05 | 0.00406192 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289748 | CTGGGTGAGAAGCAG[C/T]GGGGTCCTGGTGGCC | 64446 |
rs374469085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284562 | GGACTACAGGCGCCC[A/G]CCACCACGCCCGGCT | 64446 |
rs374540771 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296857 | GAACTGCAGAGTGTG[C/T]GATCTTAACTAGGGC | 64446 |
rs374559225 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290266 | GGTTGCAGTGAGCCG[A/C]GATCATGCCACTGCA | 64446 |
rs374646932 | snp | A/C | | | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313940 | TCCCCCAGCTCTGCC[A/C]ACTTTCCGCACTGTC | 64446 |
rs374687041 | snp | C/T | | | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305305 | TGAAAAGATTGTGTG[C/T]ACCTTCCCGGGCCAT | 64446 |
rs374695677 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277768 | ATTGCTAGGCCCTGC[C/T]CCAGGCATCTAGTTC | 64446 |
rs374710603 | snp | C/T | 5.11845e-05 | 0.00505862 | missense, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312012 | GCCCAGATGTTTGAG[C/T]GTGAGACCCGGCGAG | 64446 |
rs374715330 | snp | A/C/T | 8.25122e-05 | 0.00642262 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281963 | GGAACCCAGTGGACA[A/C/T]GGGCATCCAGTGCTC | 64446 |
rs374744652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303891 | AGCACTTTGGGAAGC[C/T]GATGTGTGCAGATCA | 64446 |
rs374775584 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292906 | GCGATCTTGGCCCAC[C/T]GCAAGCTCTGCCTCC | 64446 |
rs374828965 | snp | A/G | 6.65679e-05 | 0.00576884 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310003 | TACCTGGGTCTGCCC[A/G]GCCCCTTCAATAGGT | 64446 |
rs374889136 | snp | G/T | | | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312113 | GGAGCAGACCGATGA[G/T]GAGCTGGCCGTAGAC | 64446 |
rs374899939 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74298997 | TGAACTTGGAGAAAT[A/T]CTAAGTCAAAGCTTA | 64446 |
rs374914591 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301922 | GAAAGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA | 64446 |
rs374948276 | snp | A/G | | | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315096 | TCCTGACCCTGCACG[A/G]TCATCAACTGTGGGC | 64446 |
rs375036015 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276429 | CACTGCTCCCGTCCC[C/G/T]GCTCTGTCACCCCAT | 64446 |
rs375080382 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289005 | TTCATTTCACTACCA[C/T]GACTGACTTAGGGGC | 64446 |
rs375109564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290918 | CCAGGCTTCCCCCTC[C/T]GCCACCATGCCCCCG | 64446 |
rs375117336 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74286981 | GTCCCCCCTAGATCA[C/T]GGAGCACTGCATCAA | 64446 |
rs375252019 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286565 | AGCTGGGATTACAGG[C/T]GGCTGCCACCATGCC | 64446 |
rs375270004 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292930 | TGCCTCCTGGGTTCA[C/T]GCCATTCTCCTGCCT | 64446 |
rs375483840 | snp | A/G | 8.23866e-05 | 0.00641767 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286950 | ACCTCCATTTACTGC[A/G]GAGAACTTCCAATGT | 64446 |
rs375487523 | snp | A/C | 1.64974e-05 | 0.00287201 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314081 | GGGGAAGGCCTGTCC[A/C]CTACCAACACCAACA | 64446 |
rs375488917 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303168 | CCGTACTTGCCAGAC[A/G]CACACGATGAGTCTT | 64446 |
rs375552543 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301906 | GAAGGAAGGAAGGAA[A/G]GAAAGAAGGAAGGAA | 64446 |
rs375613600 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301974 | GAAGGAAAGAAGGAA[A/G]GAAGGAAGGAAGGAA | 64446 |
rs375622235 | in-del | -/AGCTG | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304322 | CAGGTTCACCAGCTG[-/AGCTG]CAGAGGACATCTGAG | 64446 |
rs375716674 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295656 | TTATAATTTTTTTTT[A/T]ATTAAAAACTATACT | 64446 |
rs375725669 | snp | A/C | 6.75379e-05 | 0.00581071 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281776 | GGGGCCGGTGGGGTC[A/C]CTCACCCCACACCCT | 64446 |
rs375806637 | snp | C/T | 1.65888e-05 | 0.00287996 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309280 | TTACCTCACTGATGC[C/T]GCCTGGAGCCCCGTG | 64446 |
rs375817444 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284633 | TAGCGAGGACGGTCT[C/T]GATCTCCTGACCTCG | 64446 |
rs375840422 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277906 | CTCAAAGTTGGCTAC[A/C]CATGGAATTGCCTGG | 64446 |
rs375844510 | in-del | -/GA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296381 | AAGGAGGGAGGGAGG[-/GA]GAGAGAGAGAGAGAG | 64446 |
rs375896715 | snp | C/G/T | 8.2485e-05 | 0.00642157 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305396 | GGCGACTGGACAGCC[C/G/T]GCATTTGGTCTGAAG | 64446 |
rs375965264 | snp | A/C | | | intron-variant, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74274385 | GTCGGAGGCTAAAGA[A/C]TAGAGTGGAGAGTGA | 64446 |
rs375973900 | snp | A/G | 1.64876e-05 | 0.00287116 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314156 | AGACCAGGTGGTGGA[A/G]GAGGGAGAGGAAGCA | 64446 |
rs376036019 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307125 | GGGCAGTGCATTGTT[C/G]CAGGCCTCATAGCAA | 64446 |
rs376092651 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278910 | CGGTGGCTCACGCCT[A/G]TAATCCCAGCATTTT | 64446 |
rs376247013 | snp | C/G | | | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285156 | TTTCCGGAAGAAAGT[C/G]GAGAAAGATGAGAAC | 64446 |
rs376252250 | snp | C/T | 1.65138e-05 | 0.00287343 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285068 | GGTTTGAGATGGAGA[C/T]CCGGGGAGTTAACCA | 64446 |
rs376265471 | snp | C/T | 1.67377e-05 | 0.00289284 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312122 | CGATGAGGAGCTGGC[C/T]GTAGACCTGGAGGCG | 64446 |
rs376307484 | snp | A/T | | | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305222 | CTCCTTCCACAGCCC[A/T]CCAAGTTCATGGTGG | 64446 |
rs376327428 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305230 | ACAGCCCACCAAGTT[C/T]ATGGTGGGGACCGAG | 64446 |
rs376354122 | in-del | -/AAAG | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275442 | ATAAGAAAGAGAAAG[-/AAAG]CTGGGTGCGGTTTTC | 64446 |
rs376385306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299072 | AACAGCTCTGAGTGA[C/T]AGGGTGAGCCCTCAT | 64446 |
rs376412921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288045 | AAACCAAAACAAAGC[C/T]GGTGCAGAACAGGGT | 64446 |
rs376454603 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279092 | GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC | 64446 |
rs376484986 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309744 | GGTGGCCAGAGCTGA[A/G]CCCCACTGGCTGGGG | 64446 |
rs376504060 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74311165 | AGGCATGAGCCACCA[C/G]GCCCAGCCTGAAGAC | 64446 |
rs376541043 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312110 | TGAGGAGCAGACCGA[C/T]GAGGAGCTGGCCGTA | 64446 |
rs376611195 | snp | A/G | 0.000175116 | 0.0093556 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310201 | AAATCCCTCCAGCAC[A/G]TCCCGACCTGGCCCC | 64446 |
rs376701847 | snp | C/G | 0.000115366 | 0.00759405 | utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314249 | CGGCGCTATCCCTGT[C/G]TGCCTTCCTTTCCCA | 64446 |
rs376719069 | snp | A/G | 0.00011653 | 0.00763225 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305183 | CAGAATTGATGGTTC[A/G]TGGAGTCTTCCCCTC | 64446 |
rs376793537 | snp | A/G/T | 0.00249391 | 0.0352241 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309554 | CGATTGCTTTTGAGC[A/G/T]TGTGCTCCTACAAAG | 64446 |
rs376843946 | snp | A/C | 3.32436e-05 | 0.00407685 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285002 | GGGTTTGGGAGTATA[A/C]CAGGGTGACGTCTTC | 64446 |
rs376885226 | snp | A/G/T | 9.88328e-05 | 0.00702906 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291067 | CCATCGTCTCCACTC[A/G/T]TGACGTTGGAGTTCA | 64446 |
rs376934195 | snp | C/T | 1.64939e-05 | 0.0028717 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301014 | GGAAATACAGGGCCT[C/T]GAAGTCTCACTGTCG | 64446 |
rs376939832 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279734 | GGTTTTCGCCATGTT[A/G]GCCAGGCTGGTCTTG | 64446 |
rs377022335 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295233 | AACCCCATCTCTACT[A/T]AAAAAAAAAAAAAAA | 64446 |
rs377052916 | snp | C/T | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305298 | CGTCAGCTGAAAAGA[C/T]TGTGTGCACCTTCCC | 64446 |
rs377083699 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292948 | CATTCTCCTGCCTCA[G/T]CCTTCCGAGTAGCTG | 64446 |
rs377159884 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299738 | TGGGACACCCGAAAG[A/G]GCAGCCTGGTGGCGG | 64446 |
rs377168200 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302342 | GGAGGCCAAGGCGGG[C/T]GGATCACCTGAGGTT | 64446 |
rs377218223 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297319 | GGATGGTCTTGATCT[C/G]TTGACCTCGTGATCT | 64446 |
rs377310209 | snp | C/T | 0.000154606 | 0.00879085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287108 | GTTCAGGTAGCGCCA[C/T]AGCCAGGCAGGTGTC | 64446 |
rs377411748 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288487 | TAGATGTATGTTTAC[A/G]TGCCTGATGTGAGGA | 64446 |
rs377451242 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294168 | ACATTAATTTAATTA[A/C/T]TGATAAAGTTTACAT | 64446 |
rs377460124 | snp | C/T | | | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315055 | CGTGACGGGGCACAG[C/T]GGGGACGGGAGCCCA | 64446 |
rs377468198 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304124 | CAGAACCTGTCTCGA[G/T]AAATAAATAAATAAA | 64446 |
rs377499410 | snp | A/G | 0.000216139 | 0.0103934 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312221 | CGCCATAAAGCTGAC[A/G]CCAGTGCCTGTAGGG | 64446 |
rs377539420 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275214 | CCACAAGGTAGTTGT[G/T]AGGGCAGGTAGTCAC | 64446 |
rs377582813 | snp | C/T | 0.000184148 | 0.00959376 | missense, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312060 | AGGCACCGGGAGATG[C/T]GGCTGAAGGAGAAGG | 64446 |
rs377584814 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302406 | AACCCCATCTCTACT[A/C]AAAATACAAAATTAG | 64446 |
rs377590277 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295211 | ACCAGCATGGGCAAC[A/G]TGGTCAAACCCCATC | 64446 |
rs377616393 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292904 | GCGCGATCTTGGCCC[A/C]CTGCAAGCTCTGCCT | 64446 |
rs377618720 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74276554 | TGACCTTGCTATTCA[C/T]CTGTGTGCCCTGCTA | 64446 |
rs377712998 | in-del | -/AA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295233 | ACCCCATCTCTACTT[-/AA]AAAAAAAAAAAAAAA | 64446 |
rs377734816 | snp | A/G | 0.000603361 | 0.0173585 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287136 | GTCTGGCCACCCTCC[A/G]TCACCCCCATGCATG | 64446 |
rs386799129 | multinucleotide-polymorphism | CA/TG | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283896 | TAATCCCAGCACTTC[CA/TG]GAGGCTGAGGCCAGT | 64446 |
rs386799130 | multinucleotide-polymorphism | AA/GC | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290577 | ACATGTAGGTGCCAG[AA/GC]AGAGAGCTAACGCCC | 64446 |
rs397515358 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74286974 | CCAATGTGTCCCCCC[G/T]AGATCATGGAGCACT | 64446 |
rs397515565 | snp | C/G/T | 1.72792e-05 | 0.00293927 | DNAI2 | 17 | allele_origin=G(germline)/C(unknown) | 17:74310164 | AACGTAGCCTCTTCC[C/G/T]TAAGCACCGGGTGCC | 64446 |
rs397765396 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273763 | TCAAAAAAAAAAAAA[-/A]TTCCCCAGCTTCTAC | 64446 |
rs397825955 | in-del | -/T | 0 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282323 | AGACATTTTTTTTTT[-/T]AAACAGGGTCTCACT | 64446 |
rs398041890 | in-del | -/A | 0.5 | 0 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278280 | ACAAAAAAAAAAAAA[-/A]TTAGTCTGATGTGGT | 64446 |
rs527259910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289180 | TGTTGCCCTCCAGCC[C/G]TGCTGGGCTCTAACC | 64446 |
rs527276675 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279553 | CTGTTTTTGAGATAG[A/C]GTCTTGCTCTGTCAT | 64446 |
rs527354147 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300896 | ACAGAACAGCAATCC[C/T]CAAAGTGTATTTGCT | 64446 |
rs527396707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283152 | AAGGAGATGGGAGTG[A/G]CTTCATGAGGATGGG | 64446 |
rs527511075 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305737 | AGTGCAGTGGCGTGA[A/T]CTCGGCTCACTGCAG | 64446 |
rs527596155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294331 | CTTTTTTTTTTAGAG[A/G]CAAGGTCTCACTCTG | 64446 |
rs527624967 | in-del | -/TT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74297261 | AGCTAATGTTTTGTA[-/TT]TTTTTTTTTTTTAGT | 64446 |
rs527739411 | snp | A/G | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274050 | CGTAGGCTTGGATAA[A/G]CGCCTTGGCAACGCC | 64446 |
rs527769503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311283 | AGCCCTGCAGGCAAC[A/C]CCCCAGAACCATGGG | 64446 |
rs527807651 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275818 | TCGCTTGAACTTGGG[A/T]GGCAGAGGTTGGAGT | 64446 |
rs527864510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293727 | AAAAATAAAATAAAA[A/T]AATAAAGTATGTCTC | 64446 |
rs528004510 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287713 | TAATCCCAGCACTTT[G/T]GGAGGCCAAGGCGGG | 64446 |
rs528063452 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307955 | GGCGCCCACCAACAC[C/T]CCTGGATAATTTTTT | 64446 |
rs528100566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313481 | CACCACTCCTGGCCT[A/G]TCCAGCCCTGCAGAA | 64446 |
rs528159839 | in-del | -/GACAGAAC | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300880 | GGTGTGGGAACTGTG[-/GACAGAAC]AGCAATCCTCAAAGT | 64446 |
rs528160905 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308562 | GGTCTCACTACGTTG[C/T]CCAGGCTGGAGTACA | 64446 |
rs528199833 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272788 | CTCTTGGGACCCCCC[A/C]CAGACTGGCCCTGGC | 64446 |
rs528254413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291214 | TTCCCAGGCTGGAGT[A/G]TAGTGGTGCAATTTT | 64446 |
rs528259728 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279181 | CAAAATAAATAAATA[A/C]ATAAAAATAACTAAC | 64446 |
rs528273100 | snp | A/C | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314846 | AATGCTTTCTGTTAT[A/C]CTAATTCTTGTAAAA | 64446 |
rs528315804 | in-del | -/CCCAGTCTCCCACGCTGACACTCCTCCTC | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276073 | CCAGCTTGCCTCCTT[lengthTooLong]CCCATCACTCCCTTG | 64446 |
rs528326806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290495 | GCTGGCAAGACACAG[A/G]CAGGGACAGGGTGGT | 64446 |
rs528337518 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296919 | CTGCTGTTTTTCTTG[A/C]ATAAACATTCTCCCG | 64446 |
rs528389057 | snp | C/T | 6.89132e-05 | 0.00586957 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285227 | CTCCTGCCCCAGCTG[C/T]AAGAGCCCCATCCAT | 64446 |
rs528429825 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74286157 | AAAAATTAGCCAGGT[A/G]TGGTGGCACATGCCT | 64446 |
rs528658086 | snp | A/G | 7.68315e-05 | 0.00619757 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312247 | TAGGGGCCTGGACAG[A/G]GGTTGGGTGGGTTGG | 64446 |
rs528766085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312642 | TAGCGGTGTGCACGT[C/T]ATGCTGGCTTACCCA | 64446 |
rs528891079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294043 | CCACCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 64446 |
rs529091622 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274170 | ATGGCCTGCGCTTCC[C/G]ACGTGGCAGGAAAGG | 64446 |
rs529092396 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315056 | GTGACGGGGCACAGC[A/G]GGGACGGGAGCCCAG | 64446 |
rs529186794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304883 | TTCTTTACTCTCTCT[C/G]TAAACAAACATTCAG | 64446 |
rs529323661 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314608 | TCAACCAGACTTGCA[A/T]GGCCATGGCAGGGCC | 64446 |
rs529350025 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290362 | ACTGAGAAGGGACTC[A/C]AGGGGCGGCGGAATG | 64446 |
rs529362677 | snp | C/G | 0.0103295 | 0.0711199 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273637 | GCACCTGTAGTCCCA[C/G]CTACTCGGGAGGCTG | 64446 |
rs529362689 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280490 | CCATGTCCCGCCTGT[G/T]GGGGAAGCCCCTGGC | 64446 |
rs529401265 | snp | A/C/T | 3.41853e-05 | 0.00413421 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287103 | AATGTGTTCAGGTAG[A/C/T]GCCATAGCCAGGCAG | 64446 |
rs529411008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304137 | GAGAAATAAATAAAT[A/G]AACTAGGAGTTCTTT | 64446 |
rs529413087 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293005 | GGCTAATTTTTTGTA[-/T]TTTTTTTTTAGTAGA | 64446 |
rs529471578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303666 | GACATGATCTTGGCT[C/T]GCTGCAACCTCTGCC | 64446 |
rs529502142 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306888 | CTCCCGAAGGGCTGG[A/G]ATTACAGGCATGAGC | 64446 |
rs529546503 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298634 | TTGAGACAGGGTCTT[G/T]CTCTGTCACCCAGGC | 64446 |
rs529594507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292075 | TCACTATGTTGGCCA[A/G]ACTTGTCTCAAATTC | 64446 |
rs529709715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277478 | CTCTGGGGCTAGGAG[C/T]GGGATGGGGTGGTAC | 64446 |
rs529715720 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279775 | CTCAAGTGATCCACC[A/G]GCCTCGGCCACCCAA | 64446 |
rs529720413 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312289 | GACACATGGCACTTG[G/T]GTTCTGCTTCTGCTT | 64446 |
rs529835799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301497 | GCCCAGGACCAACAT[C/T]GGGAGGCCTGGACTC | 64446 |
rs529870396 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303100 | CTTGTGGCTGCCTGA[C/T]TTAATAAGCTTGTGC | 64446 |
rs529899054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289832 | AGGAGGTCAAGGACA[C/T]TCACGCGGTTGGTGC | 64446 |
rs529960234 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295614 | ATTCCTGTGTTTGGG[A/C]CATACATTTGTATTT | 64446 |
rs530015943 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305767 | GCCTCCACCTCCCAG[G/T]TTCAAGAGACTCTCC | 64446 |
rs530210216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281667 | GATGCAGCTTCTGGA[C/G]AAATTCCTAGGATCT | 64446 |
rs530222468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306569 | ATCTTTGGTTCCAGT[A/G]CTTCCCAAATCTGGT | 64446 |
rs530291321 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74297696 | CCAAACTGCTTTTTT[C/T]TTTTTTTAATCTCCA | 64446 |
rs530300437 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290369 | AGGGACTCAAGGGGC[A/G]GCGGAATGGAACTTG | 64446 |
rs530358190 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294207 | TTGCTTTTTTTTCCT[A/G]TATGTCTTACATCTT | 64446 |
rs530440812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282061 | CAGGGCGGCCAGCTG[A/G]GGCCGGTGAGTGGTT | 64446 |
rs530495841 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303786 | AATTTTCTGGTAGAA[G/T]AAAACTGCATAATAA | 64446 |
rs530529397 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304193 | TCTTTTTTCTTTTTT[C/T]TTTTTTTTTTTTTTT | 64446 |
rs530562600 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308716 | TTGTAGAAACAGGGT[A/C]TTTCCATGTTGTCCA | 64446 |
rs530689109 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277176 | CGGATCACTTGAGAT[A/C]AGGAGTTCAAGAACA | 64446 |
rs530746620 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279119 | TTGCAGTGAGCTGAG[A/T]TCGTGCCACTGCACT | 64446 |
rs530856600 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303120 | TAAGCTTGTGCAGTC[A/G]CCTACAACCATCTCG | 64446 |
rs530915616 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296928 | TTCTTGAATAAACAT[C/T]CTCCCGACTGCCCTA | 64446 |
rs530943193 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304884 | TCTTTACTCTCTCTG[C/T]AAACAAACATTCAGG | 64446 |
rs530975161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296344 | GAGAGGAGAGAGAGA[A/G]AGGAGAGAGAGAGGA | 64446 |
rs530987023 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291814 | GTAATACTGGCCTTA[C/T]AGAATGAGTTGGGAA | 64446 |
rs531049751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312667 | TACCCAGGTTTGGTG[C/T]CAGGAGTGTGACCTG | 64446 |
rs531121906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307806 | AAATCTCCAGATGTT[C/T]CTTTTTTTGGGGGGA | 64446 |
rs531221521 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300580 | TTTATATATGGATTC[C/T]AATATTTTGTTGCTA | 64446 |
rs531246343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302515 | GGGGTTGCGGTGAGC[C/T]AAGATCGCATCATTG | 64446 |
rs531350973 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74274895 | GAGTTCCTCCGGAGC[A/G]TGTGCAGTTCCTCCT | 64446 |
rs531392212 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289098 | ACTCATGGTGTGCAA[A/G]CAGGGCCAGTGGCTG | 64446 |
rs531444568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310362 | CTGCTGGGTAGCTAA[A/G]TGGCCTTCAGTAAGT | 64446 |
rs531511243 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305615 | CCACTCCACAAAGTG[A/G]TAAGCTTCAAACACT | 64446 |
rs531514142 | snp | C/T | 5.00555e-05 | 0.00500252 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299842 | CGAGTGCTTCTCAGC[C/T]TCCACGGATGGGCAG | 64446 |
rs531602401 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280636 | ACAATTGGGTGGGGA[G/T]TTGGGTCATTGGGTT | 64446 |
rs531674819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309806 | AGGGTGACTGTGAGG[C/T]GGAACTGAAGGGGTG | 64446 |
rs531678672 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306926 | CTGGTGGAGGAGTGA[-/T]TTTTTTTAAAATCCA | 64446 |
rs531681570 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284627 | CCGTGTTAGCGAGGA[C/T]GGTCTCGATCTCCTG | 64446 |
rs531846824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287223 | TGTGCTCTGAGCTTG[A/T]TAAGTGACGTGGTGA | 64446 |
rs531865537 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281420 | TGCACCACCATGCCC[A/G]GCTAATTTTTGTATT | 64446 |
rs531918860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299112 | ATGGGAAAATGGAAA[C/T]GAAATCTAACAGGAC | 64446 |
rs531927017 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308247 | GAAGGGAGAGGAGGT[A/C]TGGGTGAAAATCTGA | 64446 |
rs532019899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290590 | AGGCAGAGAGCTAAC[A/G]CCCGACATTCCAACA | 64446 |
rs532046902 | snp | A/G | 8.23974e-05 | 0.00641809 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314202 | GATGAAGAAGTGGAA[A/G]AAGACTTAGCCTAGA | 64446 |
rs532090167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313387 | GGTAATACAGGTGGG[A/G]CAGAGAGCTCCCTCC | 64446 |
rs532132547 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277586 | GCTCCAGGGCCCAAG[A/T]TCCCCCTGGCACATG | 64446 |
rs532158476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289839 | CAAGGACACTCACGC[A/G]GTTGGTGCCTCAAGG | 64446 |
rs532192521 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296278 | TCAGGAGTTTGAAAC[G/T]AGCCTGTGCAGCATA | 64446 |
rs532235064 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284669 | TGCTCGCCTCGGCCT[A/C]CCAAAGTGCTGGGAT | 64446 |
rs532293992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290442 | GCCTGCAGGGGCAGC[A/G]TGTCCATTTATTAGC | 64446 |
rs532296027 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284246 | AAAAAGGAAAGAAGG[A/G/T]AAAGTGGCGACACCC | 64446 |
rs532365765 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74282706 | CAGAGGGGCCTCCAC[A/G]ATAAGAGAACTTATC | 64446 |
rs532646514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301683 | ATGACAAAGAAATAT[A/C]AAAGTTCAGGTCGGG | 64446 |
rs532647326 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74276319 | TGATTCTGCGTGTTC[C/T]TGTGTTTGAGACTCA | 64446 |
rs532752439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283022 | GGGGGCCCTCCTGTC[A/G]TTTCCAGCAGCTCTG | 64446 |
rs532876553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276351 | AGTGGTGTTCTTCAC[A/G]CCTCTGGGACTCTAG | 64446 |
rs532954622 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314500 | GCCCACCCCAAGGCC[G/T]AGGCCACCTTAGTCC | 64446 |
rs532964010 | snp | C/T | | | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314885 | ATCGTAACAATGCCA[C/T]GAGTTAGTACGTGTG | 64446 |
rs532986830 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304329 | CACCAGCTGCAGAGG[A/C]CATCTGAGCCCGTTG | 64446 |
rs533152825 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291912 | TCTGTCGCCCAGGCC[A/G]GAGTGCAGTGGTGCA | 64446 |
rs533158427 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279800 | ACCCAAAGTGCTGGG[A/T]TTATAGGCATGAGCC | 64446 |
rs533226862 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274045 | ACAAACGTAGGCTTG[C/G]ATAAGCGCCTTGGCA | 64446 |
rs533278735 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74288571 | CTGTTGTTTGAAGCC[A/T]CGCAGTTTGTGGGAC | 64446 |
rs533307113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308524 | CTGTGCCCAGAGCCC[C/T]TTCTTTATTTTATTT | 64446 |
rs533425618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279161 | GACAGAGGGAGACTC[C/T]GTCTCAAAATAAATA | 64446 |
rs533451291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303502 | CTGGAGTGCAGTTGT[A/G]TAATCTCAGCTTACT | 64446 |
rs533488318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292604 | GTAGTTTTTTTAGTC[A/G]CAAGGTTTCATCATG | 64446 |
rs533594899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288692 | AACAGGGATGGGGAG[A/G]AGCCTGGGGAAGAAG | 64446 |
rs533682602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297024 | TGCTATTATGGAGGA[C/G]AGAATTTTTGGAGGT | 64446 |
rs533770272 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277964 | ATGAGAGATTCTGAT[A/G]TAGTTGTTCTGGGGT | 64446 |
rs533772611 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293565 | GTCTTGTAGCCAGGT[G/T]TGGTGACACGCACCT | 64446 |
rs533814143 | snp | A/G | 0.000181445 | 0.0095231 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281856 | CAAGAAGCGCAGCGA[A/G]TTCGGGAAGCAGTGC | 64446 |
rs533875474 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296514 | TGAGCCACTGTACTC[A/G]GCCCAGCTTTTCCTT | 64446 |
rs533885803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311478 | ATTAGCCAGGCATGG[A/C]GTCACATGCCTGTAA | 64446 |
rs534019253 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299434 | TGTTCCCCTGCCACT[A/C]TGCCTGTCCTATCCC | 64446 |
rs534103236 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280076 | CATGGTGTGATATGG[C/G]AGGTACACAGGTCAA | 64446 |
rs534160949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279581 | CATCCAGGCTGGAGT[A/G]CAGTGGCACAATCTC | 64446 |
rs534223470 | snp | G/T | 0.00117892 | 0.0242502 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309401 | AAGGTCACGCGCATG[G/T]CCCTCCTTGTGCATC | 64446 |
rs534259620 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303064 | CTGGCCCTTGCAGGG[-/T]TGCACACTGTGTGTT | 64446 |
rs534294269 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302736 | TGAGTCTTGGTTTAC[A/G]TCTTAGTGCAGCCCA | 64446 |
rs534401707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303323 | GCCACTCAGATCTGG[A/G]TGGCCTTTCTCTCTG | 64446 |
rs534503619 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315181 | GGGTGCCCTGAAACC[C/G]CAGCTCAACAGAGCA | 64446 |
rs534557760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284326 | AACTTGGAGTTTTAA[C/T]GTTCAATTTTTGTGA | 64446 |
rs534779579 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312492 | TCCCCCCAGAGAGGG[A/C]ACATGGTGAAAATGC | 64446 |
rs534807555 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301617 | TGAGGTCAAAGCAGG[C/T]TCCTTGGAAAACCAG | 64446 |
rs534979181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295889 | TCCTTAAGCATTTGT[C/T]ACCAAAAAATCTCCC | 64446 |
rs535037734 | snp | A/C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280452 | TGACCAGTAGCACGC[A/C/G]TCAGAGGCTTTCCCA | 64446 |
rs535045634 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295368 | GATTGTGCCACTGCA[C/G]TCCAGGCTGGGCAAC | 64446 |
rs535089669 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286804 | TTGTACCTAAAAAGC[A/T]ATATTATTTTACCCC | 64446 |
rs535182801 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299215 | CTGTGAGTTTCTTTC[C/T]AACAGAGGCAGCAGA | 64446 |
rs535218983 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280281 | GCCTCTGATGCTGCT[A/G]GAGCACTTTCATTTC | 64446 |
rs535232391 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293759 | TGTAGATTACATGTA[C/G]CTGGCATACAAGTGA | 64446 |
rs535244837 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306070 | CTGGGCTACAGAAAG[C/G]CCAAGCCACTTGCTC | 64446 |
rs535323698 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301244 | CAGGCCATTGCTAGG[A/T]TATCAGGTGCTCGTG | 64446 |
rs535427514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293476 | ACTCCAGCCCTCTTT[A/G]GTTACCATTTGCATG | 64446 |
rs535459572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313704 | CTCTCTTAGTCTGCA[A/G]TTGGCCCAAAACGCT | 64446 |
rs535490932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292964 | CCTTCCGAGTAGCTG[A/G]GACTACAGGTGCCTG | 64446 |
rs535559561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287277 | CCCTGCTCTGGGGGC[A/G]GGTCTGGTTGATGGA | 64446 |
rs535612262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304493 | AAGACAGAACAGTAA[A/G]CAAGGAAGGGCATTG | 64446 |
rs535639058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291388 | AGGCTGGTCTCGCAC[C/T]CCTGACCTCAGGTGA | 64446 |
rs535778175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285469 | GACTCCCAAAGTGCC[C/G]CACCCAGCAGCCAAT | 64446 |
rs535830006 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272509 | TGTCCCGAGAAACTG[A/G]TGCGAGCCAGAACGG | 64446 |
rs535849333 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311525 | GGCTGAGGCAGGAGA[A/T]TTGCTTGAACGTGGG | 64446 |
rs535882161 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285980 | ATATATAGAGAGAGA[G/T]AGAGAGAGAGAGAGA | 64446 |
rs536074555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290873 | AAGGTGGACCAGGGG[A/G]TGCAGGCTGGGGAAA | 64446 |
rs536091657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294362 | TCACCCAAGCTGGAG[C/T]GCAGTGCTGTGATCA | 64446 |
rs536106412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288151 | AAATCCAGGAGAAAC[C/T]GTACTTCAAGTACCC | 64446 |
rs536218727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299968 | CACATTTTATTTTGA[A/G]ATGGAGTTTCACTCT | 64446 |
rs536266246 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285546 | CTGCCAGGCACAGTA[A/G]AGGTTGCAAAATGAA | 64446 |
rs536384953 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278417 | CCTGGATGACAGAGC[A/G]AGACACTGTCTCATA | 64446 |
rs536410188 | snp | C/T | 3.32662e-05 | 0.00407824 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310014 | GCCCGGCCCCTTCAA[C/T]AGGTGTGTGACGAGG | 64446 |
rs536509276 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276105 | ACACTCCTCCTCCCC[A/G]TCACTCCCTTGGCCT | 64446 |
rs536542287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305076 | GGGACTGCTCTCCAG[G/T]AGGGGCCACAGCCCT | 64446 |
rs536569194 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282686 | GTCCCACAGAAAGTT[A/C]CAGCCAGAGGGGCCT | 64446 |
rs536614830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297183 | CTCCGCCTCCCAGGT[C/T]CATGCCATTCTCCTG | 64446 |
rs536680930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303352 | TGGCTCACTGACGGG[C/T]GGCGTGCAGTCGGCT | 64446 |
rs536685250 | snp | A/G | 0.000148477 | 0.00861489 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305397 | GCGACTGGACAGCCC[A/G]CATTTGGTCTGAAGA | 64446 |
rs536842342 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315323 | GGCAGGGACCCAAAG[G/T]GCCCTTGAAAAATGC | 64446 |
rs537137295 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306526 | ACAGACTCCTGCAAC[A/G]TCAAAGCCACCAGCA | 64446 |
rs537137505 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280745 | TTTAGTCCAACATCA[C/T]CACCATCAATATTTC | 64446 |
rs537168391 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284898 | AGGAATTTCCTTGCC[A/T]GCATTTGAAAATACT | 64446 |
rs537248899 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303895 | CTTTGGGAAGCCGAT[A/G]TGTGCAGATCACTTG | 64446 |
rs537281546 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307097 | CTACAGGGGTGGGAA[C/T]GCTGGCTGACAAGGG | 64446 |
rs537322175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308094 | TGAGCCACCGCGCCC[A/G]GCCCAGATCCTTTCT | 64446 |
rs537346890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302779 | CCTTGGGGGTGTCAC[C/T]TGTTTGCTTCGGGGT | 64446 |
rs537429474 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290577 | ACATGTAGGTGCCAG[A/G]CAGAGAGCTAACGCC | 64446 |
rs537493017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290107 | GATCACCTGAAGTCA[A/G]GAGTTCAAGACCAGC | 64446 |
rs537565522 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74274813 | GCAGGTGTTTTAAGT[G/T]CTTTCTTTCATTTCT | 64446 |
rs537571452 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277244 | ATACAAAAATTAGCC[A/G]CGAATGGTGGCATGT | 64446 |
rs537573075 | snp | A/G | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272366 | ATCATGGAGTGGATC[A/G]TTTCCTATTCTTGGA | 64446 |
rs537579505 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283752 | CTACAGAAGAAAAAC[A/C]AAAACAAAAATTAGC | 64446 |
rs537677280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298888 | CTCGGCCTCCTAATG[C/T]GCTAGGATTACAAGC | 64446 |
rs537684103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301344 | ACTTTCCAGCAGGGG[A/G]CAGCAGAGCTTCTCG | 64446 |
rs537728615 | snp | C/G | | | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313345 | ATTTGGGGGTACTTG[C/G]TTATGAGATGTTTTC | 64446 |
rs537766870 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296297 | CTGTGCAGCATAGTG[A/T]GATCTTGCCTTTAAA | 64446 |
rs537816710 | snp | C/T | 4.95372e-05 | 0.00497656 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309367 | CATGTTCGAGCAGTG[C/T]GATCCCACCCTCAGC | 64446 |
rs537854520 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314674 | CTCCATGATCGACCC[C/T]CCTCGTCCACCTACA | 64446 |
rs537856445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308918 | AAAATAAAATATTAG[C/T]TGGGTGTGGTGACGG | 64446 |
rs537886329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287427 | ACAGGCCCCCGCCGC[A/G]GCCTGCACTCATGCG | 64446 |
rs537909153 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275402 | GTCCCTCAGGACCCC[A/G]GAATTCCAGAAGGTG | 64446 |
rs537948326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304537 | GTCATGCTCAGAGAC[A/G]CGAGGGGAGCACTGG | 64446 |
rs538031304 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286141 | TCTCTACTAAAAATA[C/G]AAAAATTAGCCAGGT | 64446 |
rs538077256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304956 | CAGAGGGGGCTAGTG[A/G]CCTGACAACCCTCCA | 64446 |
rs538099077 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285593 | CATACTTGCCAGTGC[A/T]AAAAAAAAAAATTGT | 64446 |
rs538147313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293494 | TACCATTTGCATGGT[A/G]TATCTTTCCCCATCC | 64446 |
rs538233263 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273736 | AGCCTGGGCGACAGA[A/G]CGAGACTCCGTCTCA | 64446 |
rs538263899 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312333 | GTGACCTTGAGCAAG[G/T]AGTCTTACCTGCTAG | 64446 |
rs538430982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283385 | GACCAAGGTGGGAGG[A/G]TGCTTGAGGCCACGA | 64446 |
rs538439339 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308955 | GTAATCCCAGTTACT[C/T]GGGAGGCTGAGACAG | 64446 |
rs538447244 | in-del | -/C/CC | 0.020998 | 0.100702 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301773 | GGGTACATAATGAGA[-/C/CC]CCCCCCCCACCGCCC | 64446 |
rs538488206 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279962 | GTGCAACCCCAGGAG[C/T]CTTGCACAGATCCTC | 64446 |
rs538517608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277030 | CTGGGCTTCTCATCC[C/G]ACCCTGTGCCCTCTA | 64446 |
rs538543314 | snp | A/C/G/T | 0.000117013 | 0.00764828 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312108 | GATGAGGAGCAGACC[A/C/G/T]ATGAGGAGCTGGCCG | 64446 |
rs538718556 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302277 | CCCTACATAAGAAAA[A/G]AAAAAAAGGGCCAGG | 64446 |
rs538764319 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295228 | GGTCAAACCCCATCT[C/G]TACTTAAAAAAAAAA | 64446 |
rs538925735 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277978 | TGTAGTTGTTCTGGG[A/G]TTCAAACAGCATTGT | 64446 |
rs538989656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294650 | ATGATCCTGTGTATG[C/T]GATGAGTCATTTTTC | 64446 |
rs539039472 | snp | A/G | | | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301127 | AAGGAACAGTTGGAA[A/G]ATGCCTTGGGGGCCA | 64446 |
rs539052962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300731 | TAACATTGCCGGATA[C/T]TGCCTTATTGTGGGG | 64446 |
rs539152539 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286250 | GCAGTGAGTCCAGAT[C/T]GCACCCCTGCACTCT | 64446 |
rs539190887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305511 | GGGAGCCCAGCTGGG[C/T]CCCGGAGAGTCCCGA | 64446 |
rs539191515 | snp | A/G | | | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312442 | AGGCTCCTTACAGGC[A/G]GGAACCATACTCCAT | 64446 |
rs539205013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311404 | AGATCACCTGAGGTC[A/G]GGAGTTCGAGACCAG | 64446 |
rs539385816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298728 | CCACCTCAGCCTCCC[A/G]AGTAGCAGGCAGCCT | 64446 |
rs539461253 | snp | C/G/T | 0.000164717 | 0.00907384 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291066 | GCCATCGTCTCCACT[C/G/T]GTGACGTTGGAGTTC | 64446 |
rs539500799 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272323 | AAAGGGTTGCATTAT[G/T]ATTGCAACCCCAGCC | 64446 |
rs539526455 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292866 | ACGGAGTCTTGCTCT[G/T]TCGCCCAGGCTGGAG | 64446 |
rs539537506 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74286700 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG | 64446 |
rs539574144 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74289343 | ACCAGCCTAGGAAAC[A/G]TGGTAAAAACCTGTC | 64446 |
rs539618937 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272941 | CTCACGCCATGCCCT[C/T]CCCCAATCTGGAACG | 64446 |
rs539675330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302522 | CGGTGAGCCAAGATC[A/G]CATCATTGCACTCCA | 64446 |
rs539708680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297234 | GGGACTACAGGTGCC[C/T]GCCACCACGCCCAGC | 64446 |
rs539747979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290632 | TCTGGCAGCAGCCCT[A/G]TGGGGTGGACTCCGT | 64446 |
rs539881209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284950 | CAGCATCCAGCCCTG[A/G]GAGCCCCCGTGGGAC | 64446 |
rs539953434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278823 | TAAGACCTACTATTT[A/G]ATAGGACAACAAGGT | 64446 |
rs539958286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313047 | AAATGTGAGGGCCCT[C/T]GTTTAAAAAGTATTA | 64446 |
rs540161849 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274061 | ATAAGCGCCTTGGCA[A/G]CGCCCCTACAAATAT | 64446 |
rs540186199 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298909 | GATTACAAGCATGAG[A/C]CACTGTGCTTGGCTG | 64446 |
rs540243142 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292564 | TGAGCCTACAGGCAT[A/G]TGCCACCACACTCGG | 64446 |
rs540274408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74274988 | TTTCAGACCCTATGT[A/G]TTTTCCTCTCGAATC | 64446 |
rs540282262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298462 | GGTGCCTGCCACCAC[A/G]CCCAGCTAATTTTTT | 64446 |
rs540305543 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305524 | GGCCCCGGAGAGTCC[C/T]GAGCCTCCATATGTA | 64446 |
rs540397562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280473 | GGCTTTCCCAAAGGC[C/T]TCCATGTCCCGCCTG | 64446 |
rs540440889 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304446 | AGGCTCAGGCCCTGC[A/T]GGTGGAGGTTGTTCA | 64446 |
rs540447499 | snp | A/G | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74287016 | AACAATGCCATTGAC[A/G]TCTATGAAGAGTATT | 64446 |
rs540450475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308531 | CAGAGCCCTTTCTTT[A/G]TTTTATTTGAGACAG | 64446 |
rs540508872 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272726 | CACAGATCCCAAACC[C/T]GCTGAGGGCTTCCCA | 64446 |
rs540659952 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295578 | GGCTTCTTGGGGACA[A/C]TCTCTATTTATTGCT | 64446 |
rs540661863 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302343 | GAGGCCAAGGCGGGC[A/G]GATCACCTGAGGTTG | 64446 |
rs540747650 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302920 | TGACCCCCTCCCCAG[A/G]GGACAAGGCACTGGG | 64446 |
rs540796541 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273202 | TTATCTAATAAGCAC[C/T]GCCACTGTCCTGCCA | 64446 |
rs540926157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301441 | GGGCAATCTTTTGAC[A/G]GAACAATTCCAGAAA | 64446 |
rs540993717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282825 | AGATAAAATGATAAC[A/G]AAATCACTTGATTTG | 64446 |
rs540993824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275877 | CCTGGGTGACAGAGC[A/G]ACACTGTCCCAAAAG | 64446 |
rs540994651 | snp | A/C/G | 0.00239393 | 0.0345281 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289804 | CACAAGTGGAGGAGC[A/C/G]GGAGGGAGGGGCAGG | 64446 |
rs541130570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276254 | ATCTGACTGCCTCCC[C/T]GGGGATGCGGGAGAC | 64446 |
rs541159994 | in-del | -/A | 0.487621 | 0.0776941 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287954 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 64446 |
rs541238522 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74297327 | TTGATCTCTTGACCT[C/T]GTGATCTGCCTGCCT | 64446 |
rs541482375 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273853 | AAGGATGGTAGCAGA[C/G]GGGAGGGCAGAGTTA | 64446 |
rs541504909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311727 | TTGTTGGGCCAAAGC[C/T]GCCATATTTCATAGC | 64446 |
rs541546179 | snp | A/G | 0.00874735 | 0.0655527 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273436 | AGTACATTTCGTGCC[A/G]ATCACCCAGCTAAGC | 64446 |
rs541626125 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74311156 | TGGGATTATAGGCAT[A/G]AGCCACCACGCCCAG | 64446 |
rs541658747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300289 | GATAATACATGCCCA[C/T]GGAACAGAATCTAAA | 64446 |
rs541670194 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290030 | GCTCCTAAGGAGCAT[A/G]TCAGGCCGGGCTCGG | 64446 |
rs541702121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288284 | CAACTATAGGCTAAT[A/G]TAAGTGTTCTGAGCA | 64446 |
rs541769050 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285954 | TGCCATATACACACA[C/T]ACACATATATATATA | 64446 |
rs541792432 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279728 | GAGATGGGTTTTCGC[A/C]ATGTTGGCCAGGCTG | 64446 |
rs541820111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276269 | CGGGGATGCGGGAGA[C/T]GCCTGAATCTTTGAT | 64446 |
rs541937957 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314890 | AACAATGCCACGAGT[C/T]AGTACGTGTGATGCA | 64446 |
rs542080905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297309 | GTGTTAGCCAGGATG[A/G]TCTTGATCTCTTGAC | 64446 |
rs542104210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284614 | AGACGGGGTTTCACC[A/G]TGTTAGCGAGGACGG | 64446 |
rs542149351 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313156 | AGCACCCACCCATGA[C/T]GCCTGCTTGAAGAAG | 64446 |
rs542154815 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292347 | TAGGAACTTTTCCAT[G/T]TCATCAAGTTGTCTA | 64446 |
rs542157417 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284613 | GAGACGGGGTTTCAC[C/T]GTGTTAGCGAGGACG | 64446 |
rs542172362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308261 | TCTGGGTGAAAATCT[A/G]AAGGCTGCACTGTGT | 64446 |
rs542230705 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302546 | CACTCCAGCCTGGAC[A/G]ACAAGAGCGAAACTC | 64446 |
rs542308179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303422 | CCACTTGCCCTTGAC[A/G]CCCAACTTGAAGCCC | 64446 |
rs542425763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277454 | AACAGTCTGGTTAAG[G/T]TTGAGTTGCTCTGGG | 64446 |
rs542439989 | snp | C/T | 0.00100546 | 0.0223991 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281940 | GCTGGCCGAGCAGTT[C/T]GTGGAGCGGAACCCA | 64446 |
rs542455902 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303597 | CCAAGCCAGGCTGAT[-/T]TTTTTTTTTTTTTTT | 64446 |
rs542494591 | snp | A/G/T | 8.84989e-05 | 0.00665154 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309436 | TCCTCAGGGAGCCAG[A/G/T]TCCCGGCGTGGGTGT | 64446 |
rs542506057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310991 | TCGGTCCTCCCACCT[C/T]AGCCTCCTGAGTTGC | 64446 |
rs542539193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312650 | TGCACGTCATGCTGG[C/T]TTACCCAGGTTTGGT | 64446 |
rs542544011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277938 | GAATTAAAGAAAAAA[A/G]GCATATACTGATGAG | 64446 |
rs542566143 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300324 | GCAAAAAAGAAAATG[A/C]CTTCCTCTCACCTCT | 64446 |
rs542571832 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284364 | ATTGTCAGTGATAGG[A/G]TGGCATTGTTAATGA | 64446 |
rs542586318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293618 | CTAAGGCACGAGAAT[C/T]GCTTGAACCTGGGAA | 64446 |
rs542647831 | snp | A/G | 1.67245e-05 | 0.00289171 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299671 | CCTGCCCTAAGGAAG[A/G]AAGCCTGTGCCCCCT | 64446 |
rs542825287 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275087 | AGAAGCCTGGTAGGC[A/G]CTGGTATCACAGTCA | 64446 |
rs542850730 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281328 | CAATGGTGTGATCTC[A/G]GCTCACTGCAACGTT | 64446 |
rs542873456 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304141 | AATAAATAAATAAAC[G/T]AGGAGTTCTTTTTTC | 64446 |
rs542897628 | snp | G/T | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273512 | ATCCCAGCACTTTGG[G/T]AGGCCGAGGCAGGCG | 64446 |
rs542985041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290950 | TACCCACCCGCAGAA[A/G]GGGTGAAACTGGTTG | 64446 |
rs543309250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296150 | ACATCATGCTTCAGC[C/T]TTTCCTTTTACTTAT | 64446 |
rs543378147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284647 | TCGATCTCCTGACCT[C/T]GTGATCTGCTCGCCT | 64446 |
rs543524124 | in-del | -/GG | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284194 | ACTGCACTCCAGCCT[-/GG]GGGCAACAGAGTGAG | 64446 |
rs543524201 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307090 | CCTCATTCTACAGGG[G/T]TGGGAACGCTGGCTG | 64446 |
rs543573022 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301851 | GGAAAGAAAAGGAAA[G/T]AAGGAAGGAAAGAAG | 64446 |
rs543965164 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312175 | AGTTCTTCGACATCA[C/T]CTTCGCAGAGCTGAA | 64446 |
rs544062512 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294787 | GTAGATTATTTTTTT[A/T]AAAATCAAATATGGA | 64446 |
rs544154012 | snp | C/T | 2.35946e-05 | 0.00343464 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309473 | GGGGTGCTGTGAGCA[C/T]GTGTGCAGTGTGTGG | 64446 |
rs544181157 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273980 | GGGCTTCCCAAGCAC[C/T]GACTATTCTTCCTTG | 64446 |
rs544181693 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279780 | GTGATCCACCGGCCT[C/T]GGCCACCCAAAGTGC | 64446 |
rs544215970 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314927 | ACCCAGAGCCTGTCA[C/T]GTTATCTCGTGTAAC | 64446 |
rs544235819 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297371 | TGCTGGGATTACAGG[A/C]ATGAGCCACCGTGCC | 64446 |
rs544242961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280396 | AGAACTTGAAATCAG[A/G]GCCGAGCCCAGCCCA | 64446 |
rs544448422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292542 | CCACCCCAGCCTCCC[A/G]AGTAGCTGAGCCTAC | 64446 |
rs544526327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286877 | GGTGGATGGGAAAAG[C/T]CCCTGGCTATGTCCT | 64446 |
rs544526991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278032 | TTTCTAAATGTGCAG[C/T]CAGGACTAACAATCA | 64446 |
rs544535079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313739 | GTCACAAAGTACCGC[A/G]TGGTACTGAAGCTGT | 64446 |
rs544546976 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307814 | AGATGTTTCTTTTTT[G/T]GGGGGGATGAAGTCT | 64446 |
rs544550370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303988 | AAATTAGCTGACCCT[A/G]GTGGTGTGTGCTTGT | 64446 |
rs544612689 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302646 | AGGAGGGAAGCTTCC[G/T]AGAAGCAGTAAAGGA | 64446 |
rs544685208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298376 | ATGGCATGATCTCAG[C/T]TCACTGCAACATCTG | 64446 |
rs544869608 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279098 | CGTGAACCCGGGAGG[A/C]GGAGCTTGCAGTGAG | 64446 |
rs544942894 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305703 | TTTTTGAGACAGTCT[C/G]GCTTAGTTCCCCAGA | 64446 |
rs544944619 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294952 | TTCTCTTTTCTTTCT[A/C]TTCCTCAGACTACAT | 64446 |
rs545003499 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307512 | ATCTCTAATAAAAAT[A/G]CAAAAAATCAGCTGG | 64446 |
rs545101362 | snp | C/G | 3.30087e-05 | 0.00406242 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281966 | ACCCAGTGGACACGG[C/G]CATCCAGTGCTCGAT | 64446 |
rs545118328 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289105 | GTGTGCAAGCAGGGC[A/C]AGTGGCTGTCAGCAA | 64446 |
rs545196802 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287379 | GAGTAAGTACAAGTA[C/T]CAAGCATGAGCAGCT | 64446 |
rs545227972 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275804 | CTGAGGCACAAGAAT[C/G]GCTTGAACTTGGGAG | 64446 |
rs545275994 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275726 | CTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAT | 64446 |
rs545316247 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74276858 | AAAGTCAGAGACAGG[A/C]AGCCCTAATTGCCTG | 64446 |
rs545361882 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285817 | CTGCTGAAGGGAACA[A/G]GGAAGGCTTCCTGGA | 64446 |
rs545425948 | snp | C/T | 8.36547e-05 | 0.00646687 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285193 | AACGCCATCATGCAG[C/T]TCGGCTCTGTAAGGC | 64446 |
rs545494551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279084 | AGGCAGAAGAATGGC[A/G]TGAACCCGGGAGGCG | 64446 |
rs545497139 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74297148 | TGGAGTGCAATGTCA[C/T]GATCTTGGCTCACTG | 64446 |
rs545536618 | snp | C/T | 4.98641e-05 | 0.00499295 | stop-gained, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299732 | GCCTGCTGGGACACC[C/T]GAAAGGGCAGCCTGG | 64446 |
rs545630923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296802 | CCAGGCTGCTGTTTT[C/T]CATCAGGAGTGCAGA | 64446 |
rs545669181 | in-del | -/GCCATGGTGTA | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282958 | ATGAGAAGGACTGTG[-/GCCATGGTGTA]GCCAATAAGCAGAAT | 64446 |
rs545672271 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277459 | TCTGGTTAAGGTTGA[A/G]TTGCTCTGGGGCTAG | 64446 |
rs545732470 | in-del | -/A | 0.394171 | 0.204242 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284139 | GCGAAACTCCTTTTC[-/A]AAAAAAAAAAAAAAA | 64446 |
rs545733700 | snp | A/G | | | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313199 | AGTTCTTGGTCCCTG[A/G]TAGAGTGGACAGAGC | 64446 |
rs545810193 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291542 | GGGCTCGGCCACAGA[A/G]GACTAAGTGGGGTGA | 64446 |
rs545902601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312630 | GGGCTGGGACATTAG[C/T]GGTGTGCACGTCATG | 64446 |
rs545915201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277364 | CACTCCAGCCTGGAC[A/G]ACAGAGCGAGAATCC | 64446 |
rs545950207 | snp | C/G | 0.000742115 | 0.0192486 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307280 | CCTTTCGCAGGGCTG[C/G]TTCCTAGAGGGACTT | 64446 |
rs546028074 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285483 | CCCACCCAGCAGCCA[A/G]TAGGGATCATTCATT | 64446 |
rs546036204 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303006 | TTTCTAGGCCAAGTG[A/C]TAGACATGCAGCCAC | 64446 |
rs546084374 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304167 | TTTTCTTTTCTTTTC[A/T]TTTTTCTTTTTCTTT | 64446 |
rs546238083 | snp | C/T | | | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315020 | GGAGCGGTACAGGGA[C/T]GTGCCCAAGTCTCAG | 64446 |
rs546240174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292934 | TCCTGGGTTCACGCC[A/G]TTCTCCTGCCTCAGC | 64446 |
rs546296756 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307641 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 64446 |
rs546296781 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302490 | GAGAATTGCTTGAAC[C/G]TGGGAGGCGGGGGTT | 64446 |
rs546334955 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280609 | GAGTCTGGCAACCAA[C/T]GAGCCTTTTGGACAA | 64446 |
rs546505988 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272971 | GCCCTCCCCACTCCT[A/C]TTCCCTGCAACTCAT | 64446 |
rs546671853 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293368 | CTTATAATTGTTAAG[G/T]TTTCCTAGTGAATTA | 64446 |
rs546837384 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286705 | GCTGGGATTACAGGC[A/G/T]TGAGCCACCGCACCC | 64446 |
rs546846102 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279841 | GCCTAATCTCTTGGG[A/C]GTTGAAAGGCCTTTG | 64446 |
rs546901509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304359 | GACAAAGGCCCTCCC[C/T]TCAGTGTGCCCCTCC | 64446 |
rs546926769 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309637 | GGGAAATTTAAAAAG[A/C]AACAAAAGCAGGTAC | 64446 |
rs546962126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279572 | TTGCTCTGTCATCCA[C/G]GCTGGAGTGCAGTGG | 64446 |
rs546975805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291383 | TGGCCAGGCTGGTCT[C/T]GCACTCCTGACCTCA | 64446 |
rs547050991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285442 | AGGAGGAGTCTGACC[G/T]TGGGCAAAGGTGACT | 64446 |
rs547131811 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308142 | TCCCACTGTGGTCTG[A/G]CTGTCAACACACTAG | 64446 |
rs547212542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300489 | TTTCCATTGTGTGTA[C/T]CTTGGAGATAGTTTC | 64446 |
rs547227810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298507 | AGATGGGGTTTCATC[A/T]TGTTGGCCAGGCTGG | 64446 |
rs547247936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297543 | CATGCCACCACGCCT[A/G]GCTAATTTTTGTATT | 64446 |
rs547432256 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275256 | GGTCTCCAATTCTGG[A/G]GACCTCTTCCCAACT | 64446 |
rs547477346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283947 | GTTCAAAACCAGCCT[A/G]GCCAACATGGTGAAA | 64446 |
rs547555929 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280728 | CCCAGCATGGCAGGG[A/C]ATTTAGTCCAACATC | 64446 |
rs547558422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305740 | GCAGTGGCGTGATCT[C/T]GGCTCACTGCAGCCT | 64446 |
rs547609783 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300957 | TGGCCCAGTGGCTGA[C/T]CCCAGGACGGTGGGG | 64446 |
rs547693786 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | DNAI2 | GRCh38.p7 | 17:74274469 | GGGGGCTTCCTTCTG[C/G]GATAGCTCTGCCAGA | 64446 |
rs547767152 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272789 | TCTTGGGACCCCCCA[A/C]AGACTGGCCCTGGCT | 64446 |
rs547785439 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310499 | CAATGAAGGCTTAGT[A/G]TTGTATTATATTATA | 64446 |
rs547816957 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315229 | GAGACATTGGGAGGT[C/T]GAGAGGGCACTTCAG | 64446 |
rs547926379 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294786 | TGTAGATTATTTTTT[A/T]AAAAATCAAATATGG | 64446 |
rs548024993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303345 | TTCTCTCTGGCTCAC[C/T]GACGGGCGGCGTGCA | 64446 |
rs548055686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295388 | GGCTGGGCAACAAAG[C/T]GAAACTCTGTCTTCA | 64446 |
rs548087247 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278426 | CAGAGCAAGACACTG[A/T]CTCATAAAAAGAAAT | 64446 |
rs548250604 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303689 | CCTCTGCCTCCCAGG[A/T]TCAAGTGATTCTCGT | 64446 |
rs548296172 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308620 | TCGACCTCCTGGGCT[C/G]AAGCGATCCTCCCAT | 64446 |
rs548388114 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290535 | ACGCTCTCCAGCTTC[A/C]CTTCGTTGTCAGCAT | 64446 |
rs548458981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313511 | AGGCAAAGATGACAC[C/T]GGCCACCTTTTACAA | 64446 |
rs548521485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290038 | GGAGCATATCAGGCC[A/G]GGCTCGGTGGCCCAT | 64446 |
rs548526331 | in-del | -/T | 0.178785 | 0.239642 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307718 | TAAAAAAAAAAACTA[-/T]TTTTTTTTTAGTATA | 64446 |
rs548561056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296313 | GATCTTGCCTTTAAA[A/G]AGAGAGAGAGAGAGA | 64446 |
rs548601121 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283448 | TTCATTTCTACACTT[C/T]TTTTTTTTAATTACC | 64446 |
rs548884789 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302156 | CAATGTGAGGCAAGG[C/T]GCCGTGGCTCACACC | 64446 |
rs548957933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293824 | AGTCTTACTCTGTCA[C/T]CCAGGCTGGAGTGCA | 64446 |
rs548988225 | snp | C/T | 0.000131791 | 0.00811655 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305283 | ACCGCAAGGCCAAGA[C/T]GTCAGCTGAAAAGAT | 64446 |
rs548990416 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301256 | AGGATATCAGGTGCT[C/T]GTGGAACCCAGCACC | 64446 |
rs549006196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298028 | ATTATGGAATAGACC[C/T]GGGCTCCCATAAACG | 64446 |
rs549019570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293482 | GCCCTCTTTGGTTAC[C/T]ATTTGCATGGTATAT | 64446 |
rs549023938 | snp | C/T | 0.0023933 | 0.0345097 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315061 | GGGGCACAGCGGGGA[C/T]GGGAGCCCAGGCAGC | 64446 |
rs549111687 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314669 | TTCTCCTCCATGATC[A/G]ACCCTCCTCGTCCAC | 64446 |
rs549123898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292112 | TCAAGTGATCCTCCC[A/T]CCTTGGCCTTCCAAA | 64446 |
rs549248126 | snp | A/C | 0.00358779 | 0.0422022 | upstream-variant-2KB, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74274219 | CCTTCCGCGTCGCCC[A/C]GCGCGTCCGGAGCCA | 64446 |
rs549259220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292681 | CTTGGCTGGCCTCCC[A/G]AAGTGCTGGGATGAA | 64446 |
rs549281114 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299307 | TCCACGTGCTTTTCC[A/C]TACGTTAGGGACTCG | 64446 |
rs549333712 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279911 | TTCCTCCCACCAGCA[C/G/T]CAGCCACTCATCCAC | 64446 |
rs549349657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290390 | ATGGAACTTGTGCCT[C/T]TGTCCCATCTGTCCT | 64446 |
rs549390800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286672 | TCAAGTGATCCACCC[A/G]CTTCGGCCTCCCAAA | 64446 |
rs549406809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286021 | TTTATTTGGGCTGGG[C/T]TTGGTGGCTCACACC | 64446 |
rs549432065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307114 | CTGGCTGACAAGGGC[A/G]GTGCATTGTTCCAGG | 64446 |
rs549467476 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285682 | TGTCCCAAAGAGATT[A/G]CAGTCCATTGGAGGT | 64446 |
rs549518218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289394 | TAGCCAGGCGTGGTG[C/G]TGTGCGCCTGTAATC | 64446 |
rs549547023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284027 | CCTGTAATCCCAGCT[A/G]CTGGGGAGGCTGAAG | 64446 |
rs549717288 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309723 | GGACCTTCCCCTTCA[C/T]GTCAGGGTGGCCAGA | 64446 |
rs549880425 | in-del | -/AA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309060 | GAGCAAGAGTGTCTC[-/AA]AAAAAAAAAAAAAAA | 64446 |
rs549935442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275311 | CCTTGGGGGGCTCAG[C/T]CATGCTTAGTGCTAT | 64446 |
rs549990106 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279836 | GCCCGGCCTAATCTC[C/T]TGGGCGTTGAAAGGC | 64446 |
rs550039734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283352 | CTGGCTCAAGCCTGT[A/G]ATCCCAGTACTTTGG | 64446 |
rs550115875 | snp | A/G | 6.59718e-05 | 0.00574296 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301015 | GAAATACAGGGCCTC[A/G]AAGTCTCACTGTCGC | 64446 |
rs550218331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311843 | ACCCCAATATTCAGC[C/T]CTCCTTCCTTGACAC | 64446 |
rs550218846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275910 | ACAACAACAAAGAAA[A/G]AGGGAAGGAAGTCCT | 64446 |
rs550269973 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294088 | ACGCCCAGCTTGGAT[C/T]GTGGTTTTTTCCTTT | 64446 |
rs550292414 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300651 | TTGTTGCACACATGC[A/G]GGGATATATCTACAG | 64446 |
rs550308267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303795 | GTAGAAGAAAACTGC[A/G]TAATAAAACAATATG | 64446 |
rs550386077 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281677 | CTGGACAAATTCCTA[C/G]GATCTCCCCACCACC | 64446 |
rs550442937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297910 | GGAGTGGGAGCCAGG[A/G]TGGCTGAGAAACTCC | 64446 |
rs550454748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311352 | GGTGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 64446 |
rs550692353 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304196 | TTTTTCTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 64446 |
rs550716863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279122 | CAGTGAGCTGAGATC[A/G]TGCCACTGCACTCCA | 64446 |
rs550765646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307400 | GGCCAGGTGCAGTGG[A/G]CTAATGCCTGTAATC | 64446 |
rs550780620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313564 | CATGCTTTGTGACAT[A/G]TGTCCCAAAACGTGC | 64446 |
rs550808252 | in-del | -/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306650 | TGAGATGGAGTCTTA[-/C]TCTGTCACCCAGGCT | 64446 |
rs550852548 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272883 | CCACCCACCATCCTC[A/G]CAAAATGCCTTTCTT | 64446 |
rs550931190 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74274948 | CCACATTCTCTTGAA[A/C]CACAGAAGTGCGTCT | 64446 |
rs550941938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314052 | TCCTCGTGGGGTTCA[C/T]ATCCCAGGGGAGTGG | 64446 |
rs550973311 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296357 | GAGAGGAGAGAGAGA[A/G]GAAGGGGGAAGGAGG | 64446 |
rs551013077 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290578 | CATGTAGGTGCCAGG[A/C]AGAGAGCTAACGCCC | 64446 |
rs551084703 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285314 | GCTCGTGTGAATGCT[G/T]GGGGGAAGGGGACCA | 64446 |
rs551104139 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294306 | ATCATTTCTTTTTTT[C/T]TTTTCTTTTCTTTTT | 64446 |
rs551163932 | snp | A/G | 0.00024707 | 0.0111119 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305296 | GACGTCAGCTGAAAA[A/G]ATTGTGTGCACCTTC | 64446 |
rs551235814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303135 | GCCTACAACCATCTC[A/G]TGGGGTAATGTTATT | 64446 |
rs551346993 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288598 | GGACCTCGTTGCAGC[A/T]GCCCCAGGAACAGAA | 64446 |
rs551363710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300397 | CAGAGCTAGTCTCTG[A/C]GTATGCAAGGAAACA | 64446 |
rs551422275 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310366 | TGGGTAGCTAAGTGG[A/C]CTTCAGTAAGTCACG | 64446 |
rs551425992 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304965 | CTAGTGACCTGACAA[A/C]CCTCCAGGACTGGAG | 64446 |
rs551495552 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282235 | TGCAAATCACAATGT[G/T]CCCTCTCCCAAGAGC | 64446 |
rs551514798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293217 | TTGTTGATCTTTCAC[A/G]TAGTAATTATGTCTA | 64446 |
rs551651340 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287231 | GAGCTTGATAAGTGA[C/T]GTGGTGATAAGTCAC | 64446 |
rs551686536 | in-del | -/C | 0.0154538 | 0.0865337 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285592 | ACATACTTGCCAGTG[-/C]AAAAAAAAAAAATTG | 64446 |
rs551714016 | in-del | -/CTTTTTTTTTTTTTTTTTTT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304186 | TTCTTTTTCTTTTTT[-/CTTTTTTTTTTTTTTTTTTT]TTTTTTTGAGGTAGG | 64446 |
rs551715321 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274335 | CCAGAAGCAGAAGGA[A/G]CGGACCCAGGGTAAG | 64446 |
rs551739910 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315112 | TCATCAACTGTGGGC[C/G]AGGTGCTGTGCAGGC | 64446 |
rs551775136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279990 | CTCAATCTGAGCCCC[C/T]GGAAACTTGCTATCA | 64446 |
rs551778827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280645 | TGGGGAGTTGGGTCA[C/T]TGGGTTGGAGAGGAG | 64446 |
rs551786490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277646 | CTCTCAGGGGCCAGC[A/G]GCCAGGACCCACTGG | 64446 |
rs551843709 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307880 | TTGGCTCACTACAAC[C/T]TTCACCTCCTGGGTT | 64446 |
rs551899473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312805 | GAGATGTTGCTATAA[A/G]GATGGTGTCTGGTCA | 64446 |
rs551963437 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284922 | AAATACTGTGGCTCC[A/G]GCCAGGGCGCCTCAG | 64446 |
rs552045557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284707 | GTGAGCCACTGCACC[C/T]GGCCAATTATTCACC | 64446 |
rs552276266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313429 | AGGCAAAACTAGAAT[C/T]CTGGATTCTGACGCC | 64446 |
rs552367549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295815 | TGTATTCCCTGTCAC[A/G]TGTGACCACTTATAG | 64446 |
rs552458073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276352 | GTGGTGTTCTTCACG[C/T]CTCTGGGACTCTAGG | 64446 |
rs552486137 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280042 | CAGGTGGCTGGCAGA[C/T]GGAAATCTCTGCTAA | 64446 |
rs552605658 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307015 | GGGTTTGCTAAGGAG[C/G]AACCCCAGGCTTGTG | 64446 |
rs552605741 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301135 | GTTGGAAAATGCCTT[A/G]GGGGCCATCTCCCTG | 64446 |
rs552610697 | snp | A/G | 4.9436e-05 | 0.00497148 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289692 | GCTTGGATTTTCAGC[A/G]GGCACCTGTGGGCAT | 64446 |
rs552654000 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303333 | TCTGGGTGGCCTTTC[A/T]CTCTGGCTCACTGAC | 64446 |
rs552742121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301696 | ATCAAAGTTCAGGTC[A/G]GGCAGGGTGGCTCAC | 64446 |
rs552790763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286789 | ATGTATTTCCATGCT[G/T]TGTACCTAAAAAGCA | 64446 |
rs552829812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283033 | TGTCGTTTCCAGCAG[C/T]TCTGCCTTTTCCAGA | 64446 |
rs552866790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306681 | GAAGTGCAATGGCGA[A/G]ATCTCGGCTCACTGC | 64446 |
rs552956633 | in-del | -/T | 0.000331345 | 0.0128671 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291170 | TTATTTTTATTTTTA[-/T]TTTTTTTTAGATGGA | 64446 |
rs552978636 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291551 | CACAGAAGACTAAGT[A/G]GGGTGAGGGCCTCCC | 64446 |
rs553047194 | in-del | -/GACTGAAC | | | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312546 | ACATGTGTGTTGAGT[-/GACTGAAC]GAGGGTCCTAGAGGT | 64446 |
rs553111047 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284250 | AGGAAAGAAGGGAAA[A/G]TGGCGACACCCACGT | 64446 |
rs553120879 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308993 | GCTTGAACCCAGGAG[A/G]CAGAGATTGCAGTGA | 64446 |
rs553149600 | in-del | -/G | 0.000104604 | 0.00723127 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281761 | TGTGGAGATAGGGAA[-/G]GGGCCGGTGGGGTCC | 64446 |
rs553214151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303401 | GACCTCTCAAGCTTG[A/G]TCTTTCCACTTGCCC | 64446 |
rs553266191 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74281285 | TTATTTTGAGACAGA[A/G]TCTTGCTCTGTCACC | 64446 |
rs553289286 | in-del | -/TTG | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286428 | GCCTCCATAAAATGT[-/TTG]TTGTTGTTGAGACAG | 64446 |
rs553289670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298119 | TGATTAATTCAAGAG[C/T]CTTGACTCAGTCATT | 64446 |
rs553351066 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303877 | AGGTCTGTAATCCCA[G/T]CACTTTGGGAAGCCG | 64446 |
rs553425057 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272330 | TGCATTATGATTGCA[A/G]CCCCAGCCAGCCACT | 64446 |
rs553472139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313613 | CATTCTACATGAAGA[A/G]GTTGAGCCTTGGAAG | 64446 |
rs553492690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290685 | TGGTTGGAAGAAACC[A/G]GCAGAGAGTTGACTT | 64446 |
rs553501329 | snp | C/T | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273201 | ATTATCTAATAAGCA[C/T]CGCCACTGTCCTGCC | 64446 |
rs553503731 | snp | C/T | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272786 | CTCTCTTGGGACCCC[C/T]CACAGACTGGCCCTG | 64446 |
rs553516193 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300619 | AAAATACAGCAAAGA[A/G]CATCTTTATACACAG | 64446 |
rs553555702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306093 | ACTTGCTCCTGCTCT[C/T]CCAGCTAGTGAGGAG | 64446 |
rs553563090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284580 | ACCACGCCCGGCTAA[C/T]GTTTTGTATTTTTAG | 64446 |
rs553591160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275111 | ACAGTCACTAACGCA[A/G]CAGGTGACAGGAGTC | 64446 |
rs553648502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288049 | CAAAACAAAGCCGGT[A/G]CAGAACAGGGTGTGC | 64446 |
rs553707931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294034 | GCGATATGCCCACCT[C/T]GGCCTCCCAAAGTGC | 64446 |
rs553708947 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310959 | GGCCCACTGCAGCCT[A/C]TACCTCCCAGGCTGA | 64446 |
rs553772490 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277989 | TGGGGTTCAAACAGC[A/C]TTGTGATTTCACAAA | 64446 |
rs553772596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276101 | GCTGACACTCCTCCT[C/T]CCCATCACTCCCTTG | 64446 |
rs553864148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305525 | GCCCCGGAGAGTCCC[C/G]AGCCTCCATATGTAA | 64446 |
rs553893886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299439 | CCCTGCCACTATGCC[C/T]GTCCTATCCCCAGAG | 64446 |
rs553901601 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306226 | GAGGAGAGCAACAGA[C/G]AGGGAGCTTGAGACA | 64446 |
rs553905028 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294815 | GGAATATTTACAACC[A/G]TTATTTATTCAAATA | 64446 |
rs553952872 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287562 | CACTGCAGAGGGTGT[A/T]TGCCAGCCAAAGACT | 64446 |
rs553978334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280143 | ACCCAGTGGAGTCTA[A/G]TGATGTCATGGGGGA | 64446 |
rs554016202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304623 | TACTAAAGCTCAGTT[C/T]GTGGGCGATGGACCC | 64446 |
rs554045040 | in-del | -/CTCT | 9.6652e-05 | 0.00695102 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311979 | CCTCTCCCCACCGGG[-/CTCT]CTCTGTCCCTGGGTG | 64446 |
rs554047836 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296550 | CTTTTCGGTAGGTCT[A/G]TTCCTTTCCCCACCT | 64446 |
rs554103158 | snp | C/T | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281869 | GAGTTCGGGAAGCAG[C/T]GCAATTTCTCGGACC | 64446 |
rs554124252 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309899 | TCCTGTGGGCAGAGG[A/C]GTCCTGAGGATGTTT | 64446 |
rs554227167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297149 | GGAGTGCAATGTCAC[A/G]ATCTTGGCTCACTGC | 64446 |
rs554290241 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296613 | GTCAGTTGCCTGCAA[C/T]TACACCCTGATGAAA | 64446 |
rs554321573 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314873 | AAAATTAAATGAATC[A/G]TAACAATGCCACGAG | 64446 |
rs554411027 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302399 | ATGGAGAAACCCCAT[C/G]TCTACTAAAAATACA | 64446 |
rs554449239 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312525 | GTTGAGTGACTGAAC[A/G]AGGGAACATGTGTGT | 64446 |
rs554491261 | snp | A/G | 0.000391087 | 0.0139782 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309444 | GAGCCAGGTCCCGGC[A/G]TGGGTGTGAGTGTGG | 64446 |
rs554598446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307255 | GGGTGTCGAGCACAG[C/T]ACCCATAGGCCTTTC | 64446 |
rs554618757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280520 | CTTTCTCTCTGTCTG[A/G]GATTGACTCTCAGCT | 64446 |
rs554643876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276670 | TCCAGACACAAGACA[A/G]TGCCTCTGTTCTCAC | 64446 |
rs554818131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307483 | GACGAGCCTGGCCAA[C/T]ATGGTGAATCCCCAT | 64446 |
rs554940399 | snp | C/T | | | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309375 | AGCAGTGCGATCCCA[C/T]CCTCAGCTTGAAGGT | 64446 |
rs555168095 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280814 | GTATTGTACCACGTG[A/C]GATGGCTCATACCTG | 64446 |
rs555175092 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301790 | CCCCCCCACCGCCCG[C/T]CCAGTCTTTACCAAG | 64446 |
rs555207968 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300877 | CCAGGTGTGGGAACT[G/T]TGGACAGAACAGCAA | 64446 |
rs555245494 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74311173 | GCCACCACGCCCAGC[C/G]TGAAGACTTAGTAGA | 64446 |
rs555278579 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304518 | GCATTGCGTGATGGA[A/G]GGGGTCATGCTCAGA | 64446 |
rs555295699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280306 | CATTTCACTTCTCAG[A/C]ATCCTGTGGGTGTGT | 64446 |
rs555349032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301257 | GGATATCAGGTGCTC[A/G]TGGAACCCAGCACCA | 64446 |
rs555357054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286805 | TGTACCTAAAAAGCA[A/G]TATTATTTTACCCCC | 64446 |
rs555456256 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293844 | GCTGGAGTGCAGTGG[C/T]GTGATCTCGGCTCAC | 64446 |
rs555512518 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314913 | GTGATGCATCCTGCA[A/C]CCAGAGCCTGTCACG | 64446 |
rs555561670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291428 | CTGGGCCTCCCAAAG[C/T]GCTGGGATTACAGGT | 64446 |
rs555606259 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298187 | ATACCAGCCCAGACT[A/C]TGGTGCTCCGCTGCT | 64446 |
rs555679845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292987 | GGTGCCTGCCACCAC[A/G]CTGGGCTAATTTTTT | 64446 |
rs555773326 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273067 | CCCAGTCCAAATTTC[C/T]GATGTCAGCATCTGA | 64446 |
rs555794460 | in-del | -/A | 0.281049 | 0.248064 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281087 | ACAAGCCTTTGTCTC[-/A]AAAAAAAAAAAAAAA | 64446 |
rs555798331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303918 | ATCACTTGAGCTTAG[G/T]AGTTTGAGACCAGTC | 64446 |
rs555834730 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272512 | CCCGAGAAACTGGTG[C/T]GAGCCAGAACGGATC | 64446 |
rs555874511 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308844 | AACAGCCTGTCAGAC[A/C]CCTGAGGTCAAGAGT | 64446 |
rs555888989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285506 | CATTCATTCATTTGA[C/T]AAATTTGGACTGAAC | 64446 |
rs555938890 | snp | C/T | | | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312000 | CTGTCCCTGGGTGCC[C/T]AGATGTTTGAGCGTG | 64446 |
rs555951443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301359 | GCAGCAGAGCTTCTC[A/G]AAGAAGGACACCATA | 64446 |
rs556013723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311526 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACGTGGGA | 64446 |
rs556023419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278963 | ATGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 64446 |
rs556037447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282688 | CCCACAGAAAGTTCC[A/G]GCCAGAGGGGCCTCC | 64446 |
rs556174491 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276145 | CTTGGAAAACACACT[A/T]TCCCTTAAGCCACCG | 64446 |
rs556219736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288152 | AATCCAGGAGAAACC[A/G]TACTTCAAGTACCCA | 64446 |
rs556281450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294064 | CTGGGATTACAGGCA[C/T]GAGCCACCACGCCCA | 64446 |
rs556286696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300000 | GTTGCCCAGGCTGGA[A/G]TGCAATGGCACGATC | 64446 |
rs556547267 | snp | A/G | 0.000369462 | 0.0135866 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305425 | AGACAGCCGGGAATC[A/G]TCCATCATGTGGACC | 64446 |
rs556556977 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296987 | AAAAGTTGATTCTGA[A/C]CATTTTTGCCAGTTT | 64446 |
rs556678002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291490 | TCATAGTCAGAGCCA[A/G]TCCTGCTGCTATAGG | 64446 |
rs556844360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305087 | CCAGGAGGGGCCACA[A/G]CCCTTGCCAAGGCTT | 64446 |
rs556919699 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297191 | CCCAGGTTCATGCCA[C/T]TCTCCTGCCTCAGCC | 64446 |
rs557000601 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302882 | GAGAGATGAATGTTG[A/C]TGGAAGGAGGAGACA | 64446 |
rs557025142 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277273 | GTGCCTGTAATCCCA[A/G]CTACGGGAGGCTGAG | 64446 |
rs557040349 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74288887 | GCGGAGGGGAAGCCT[G/T]TGGACCTGGGGCAGA | 64446 |
rs557104574 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304741 | AGTGCTGGTTGGTCA[C/T]CTGCTCTGAGTTCTC | 64446 |
rs557181711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307618 | AGACCAGCCGAGATT[A/G]CGCCACTGCACTCCA | 64446 |
rs557196953 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74289476 | AGGTTGCAGTGAGCC[A/G]AGATTATGCCACTGC | 64446 |
rs557252473 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302098 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA | 64446 |
rs557343311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284930 | TGGCTCCGGCCAGGG[C/T]GCCTCAGCATCCAGC | 64446 |
rs557415582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277849 | CCAGGTTTCAGAAAC[A/G]CTGGTTGAGAGATTA | 64446 |
rs557465135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313026 | ATTGCAGGCACTGCA[A/G]AATGAAAATGTGAGG | 64446 |
rs557495330 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295994 | TTAGTGTCTGTGCAG[A/G]GATGAGGTCAGCCAG | 64446 |
rs557536022 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302262 | ATAGCAAGACACTGT[A/C]CCTACATAAGAAAAG | 64446 |
rs557561638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275437 | AGGACATAAGAAAGA[A/G]AAAGAAAGCTGGGTG | 64446 |
rs557589526 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295461 | TTTGGTGAGAGATCA[G/T]CTCATGCTTTTCTTT | 64446 |
rs557668070 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299413 | CCTTCCCTGACCACC[C/T]TCATGTGTTCCCCTG | 64446 |
rs557668886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290181 | ATTAGTTGTGCTTGA[C/T]GGTGGGTGCCTGTAA | 64446 |
rs557692864 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74274847 | TCAACCTGGGAGCTG[G/T]CGTTCTCGTGTGATC | 64446 |
rs557716808 | snp | C/T | 4.95364e-05 | 0.00497652 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309393 | TCAGCTTGAAGGTCA[C/T]GCGCATGTCCCTCCT | 64446 |
rs557718682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304002 | TGGTGGTGTGTGCTT[A/G]TGGTCCCTACGTGGG | 64446 |
rs557724360 | snp | C/T | 0.000362444 | 0.013457 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289648 | CTGGCACCCCGATGG[C/T]AACAGGAAGTTGGCA | 64446 |
rs557740709 | snp | C/T | 3.34711e-05 | 0.00409078 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281788 | GTCCCTCACCCCACA[C/T]CCTCCCTCTGCCCCC | 64446 |
rs557807525 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293546 | CTCTTTGAATCTAAA[A/G]TATGTCTTGTAGCCA | 64446 |
rs557855595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304541 | TGCTCAGAGACGCGA[A/G]GGGAGCACTGGACCA | 64446 |
rs557893323 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273765 | CAAAAAAAAAAAAAT[G/T]CCCCAGCTTCTACTC | 64446 |
rs557934521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293055 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 64446 |
rs557978996 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308931 | AGCTGGGTGTGGTGA[C/T]GGGCGCCAGTAATCC | 64446 |
rs558085635 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279033 | TTAGCCGGGTGTGGT[G/T]GTGGGCACCTGTAGT | 64446 |
rs558123448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286895 | CTGGCTATGTCCTGT[C/T]CCTCCCAGACTCCAT | 64446 |
rs558140844 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314806 | GGGGACGGGCGGGAC[A/G]AGCTTGGCTGTTCTG | 64446 |
rs558144754 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275649 | GAAGAATTGCTTAAA[C/T]CTGGGAGGTGGAGGT | 64446 |
rs558346585 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283427 | GCCTGGGCAACATAG[G/T]GAGACTTCATTTCTA | 64446 |
rs558551038 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304168 | TTTCTTTTCTTTTCT[C/T]TTTTCTTTTTCTTTT | 64446 |
rs558604322 | snp | A/G | 0.219049 | 0.248077 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289534 | ACAAAAAAAAAAAAA[A/G]GGGGGAGAAATTGGG | 64446 |
rs558604453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282730 | ACTTATCTTGAGGGT[C/T]ATGGTCATGTGTTCA | 64446 |
rs558665753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288858 | GGAGGCTGGAATAGA[A/G]CAGCTGGGGAAATGC | 64446 |
rs558769570 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312401 | TCCCTTCCTTCCAAA[A/G]CATCCCAAGTCTCCA | 64446 |
rs558952142 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275600 | GGTGCAGTGGCTCAC[A/G]CCTGTAGTCCCAGCT | 64446 |
rs558954150 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301502 | GGACCAACATCGGGA[A/G]GCCTGGACTCCAACC | 64446 |
rs558973562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300803 | TTTGATTCAGTAGGT[C/T]GAGGGCGAGGCCTCA | 64446 |
rs559034224 | in-del | -/AGCACAGCT | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309110 | TGGATGAGTGAGGTC[-/AGCACAGCT]AGAAGTCAGACACAA | 64446 |
rs559042652 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278153 | TCAGTTTCTTCATCT[C/T]GAAAATGGGCTCATG | 64446 |
rs559081402 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313479 | CTCACCACTCCTGGC[C/T]TATCCAGCCCTGCAG | 64446 |
rs559209668 | snp | C/T | 1.70145e-05 | 0.00291667 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285219 | AAGGCTTCCTCCTGC[C/T]CCAGCTGCAAGAGCC | 64446 |
rs559250300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300167 | TGGCCAGGCTGGTCT[C/T]GAACTCTGACCTCAG | 64446 |
rs559276153 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74298666 | GGGGTGTAGTGGCAC[A/G]ATCATGGCTCACTGC | 64446 |
rs559291415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290492 | AGGGCTGGCAAGACA[C/T]AGGCAGGGACAGGGT | 64446 |
rs559342379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305964 | GGTGTGAGCCACCGC[G/T]TCTGGCTGGCTTAAT | 64446 |
rs559403981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313947 | GCTCTGCCCACTTTC[C/T]GCACTGTCTGGGCCC | 64446 |
rs559558540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296293 | TAGCCTGTGCAGCAT[A/G]GTGAGATCTTGCCTT | 64446 |
rs559562674 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306032 | ATTGCTCTTCTCTTC[A/G]TCTCATTTTTCATGT | 64446 |
rs559643233 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291205 | TGCTCTTGTTTCCCA[G/T]GCTGGAGTGTAGTGG | 64446 |
rs559856153 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303046 | AGGGCCATCTCCTCC[A/G]TGCCTGGCCCTTGCA | 64446 |
rs559910643 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315045 | TCTCAGAACTCGTGA[C/T]GGGGCACAGCGGGGA | 64446 |
rs560084585 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277372 | CCTGGACGACAGAGC[A/G]AGAATCCATCTCAAA | 64446 |
rs560196216 | in-del | -/AA/AAA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295237 | CATCTCTACTTAAAA[-/AA/AAA]AAAAAAAAAAAAAAA | 64446 |
rs560286294 | snp | A/C | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273826 | AGATGTCTTTATTAC[A/C]GAAAGTGGAGGAAGG | 64446 |
rs560307857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303534 | CAACATCCACCTCCT[A/G]GGCTCAAGCCTCAGC | 64446 |
rs560319154 | snp | C/T | 6.63108e-05 | 0.00575769 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299766 | CGGAGCTATCCACCA[C/T]TGAGTCCAGCCACCG | 64446 |
rs560366460 | snp | A/G | 1.66225e-05 | 0.00288287 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74287065 | TGGAAGTGATGGAGG[A/G]GGACCCTTCAGCTAA | 64446 |
rs560403862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309655 | CAAAAGCAGGTACCC[A/G]GCATCTCCTACCCAC | 64446 |
rs560413121 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280483 | AAGGCCTCCATGTCC[C/T]GCCTGTTGGGGAAGC | 64446 |
rs560421207 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304593 | GTGCATTCAGTCCGC[A/C]GTGAAGTGAATAACT | 64446 |
rs560444006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304880 | GTCTTCTTTACTCTC[C/T]CTGTAAACAAACATT | 64446 |
rs560445314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297582 | AAACAGAGTTTTGTC[A/C]TGTTGGCCAGGCTGT | 64446 |
rs560553351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279842 | CCTAATCTCTTGGGC[A/G]TTGAAAGGCCTTTGG | 64446 |
rs560601238 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305692 | TTTTTTTTTTTTTTT[-/T]GAGACAGTCTCGCTT | 64446 |
rs560713533 | snp | C/T | 0.000166127 | 0.0091124 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282021 | TCCCTGCCCCAAGGG[C/T]CCTGGCCTGTCAGGT | 64446 |
rs560860099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283956 | CAGCCTGGCCAACAT[G/T]GTGAAACCCCGTCTC | 64446 |
rs560906751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276255 | TCTGACTGCCTCCCC[A/G]GGGATGCGGGAGACG | 64446 |
rs561234655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311753 | ATAGCTCCAAAGGGC[A/G]CTCTTCTGCCTGTGG | 64446 |
rs561299153 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273450 | CAATCACCCAGCTAA[A/G]CTGTAAAAATCCCCA | 64446 |
rs561317996 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300060 | TTCAAGCAATTCTCC[C/T]GCCTCAGCCTCCCAA | 64446 |
rs561357116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282848 | TTGATTTGGCCAAAA[C/T]ACGTCCAACAGTCAG | 64446 |
rs561359505 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272832 | TTCCTCTCTCATTTT[G/T]CCCCTGCAGGGACTC | 64446 |
rs561525192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308683 | CTCACCACCACACCC[A/G]GCTAATTTTTTTATT | 64446 |
rs561540806 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287800 | TCTCTACTAAAAATA[C/T]AAAAATTAACTGGGT | 64446 |
rs561631430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297476 | GCTCACTGCCACCTC[C/T]GCCTCCTGGGTTCAA | 64446 |
rs561701451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314035 | CCATTTGGCTGCTTT[G/T]GTCCTCGTGGGGTTC | 64446 |
rs561775600 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304149 | AATAAACTAGGAGTT[C/T]TTTTTTCTTTTCTTT | 64446 |
rs561780132 | snp | A/T | | | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309296 | GCCTGGAGCCCCGTG[A/T]GGCCGACCGTTTTCT | 64446 |
rs561813814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286392 | CATTATTGGCCTTCA[C/T]GTTTTTTCTAATGGC | 64446 |
rs561830846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309171 | GACTCTGAGATCCTG[A/G]AGCCCAGAAGGGACC | 64446 |
rs561911124 | snp | C/T | 3.29582e-05 | 0.00405931 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289642 | CCTCTCCTGGCACCC[C/T]GATGGCAACAGGAAG | 64446 |
rs561993367 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279117 | GCTTGCAGTGAGCTG[A/C]GATCGTGCCACTGCA | 64446 |
rs562043936 | snp | C/T | | | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312121 | CCGATGAGGAGCTGG[C/T]CGTAGACCTGGAGGC | 64446 |
rs562056700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285957 | CATATACACACACAC[A/G]CATATATATATATAG | 64446 |
rs562198173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302514 | GGGGGTTGCGGTGAG[C/T]CAAGATCGCATCATT | 64446 |
rs562259938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307343 | TTGTCCTCCTCCTGC[A/G]TAAGGTTAAACAAAT | 64446 |
rs562454129 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311050 | TGGCTCATTTTTTAA[A/T]TTTTGTAGAGACAGG | 64446 |
rs562532881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294868 | CTCCTCTCCTTCTGT[G/T]ACTTCCATTATGTGT | 64446 |
rs562548558 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293619 | TAAGGCACGAGAATC[A/G]CTTGAACCTGGGAAG | 64446 |
rs562653455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275747 | AAAAAAAAATTAGCC[A/G]AGTGTGGTGGCATGC | 64446 |
rs562666333 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315062 | GGGCACAGCGGGGAC[A/G]GGAGCCCAGGCAGCT | 64446 |
rs562810554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293138 | GCACCTGGCCTGTCC[A/G]GTGGAGTTTTCTATA | 64446 |
rs562818296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281419 | GTGCACCACCATGCC[C/T]GGCTAATTTTTGTAT | 64446 |
rs562907695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287191 | CCATCGCTGCATGCC[C/T]TGGGTGCAGCACTGT | 64446 |
rs562945643 | snp | A/T | 4.94417e-05 | 0.00497176 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291004 | CTGGTGGGGATAATT[A/T]TTTTGTGCTTTATAG | 64446 |
rs562947150 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274302 | CCGCGACCGTGGATT[A/G]AACGCTTCCCCAGAG | 64446 |
rs562949578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284658 | ACCTCGTGATCTGCT[C/T]GCCTCGGCCTCCCAA | 64446 |
rs563007197 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313344 | CATTTGGGGGTACTT[G/T]GTTATGAGATGTTTT | 64446 |
rs563067854 | snp | C/T | | | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314318 | AGCTCCGCCTTAAAG[C/T]AGCACTGGGTGGTGG | 64446 |
rs563085701 | snp | A/T | 1.65274e-05 | 0.00287462 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285155 | GTTTCCGGAAGAAAG[A/T]GGAGAAAGATGAGAA | 64446 |
rs563511988 | snp | A/G | 0.000189304 | 0.00972709 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307205 | TCCCAATGTCTTCAG[A/G]TCCTGCAGGCTGCCA | 64446 |
rs563582592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301615 | AATGAGGTCAAAGCA[A/G]GCTCCTTGGAAAACC | 64446 |
rs563616405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277025 | ACAATCTGGGCTTCT[C/T]ATCCCACCCTGTGCC | 64446 |
rs563627487 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296177 | TTATTTACTTTTGTT[C/G]TTTAAATGTAATAGA | 64446 |
rs563688126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279088 | AGAAGAATGGCGTGA[A/G]CCCGGGAGGCGGAGC | 64446 |
rs563714401 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276713 | CTTGGGAAACACCAA[C/G]AAGGAAAGCAAAGCT | 64446 |
rs563785321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306985 | AACATAGAATCTTGG[G/T]CTTAGCCCAGGAATG | 64446 |
rs563808276 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276335 | TGTGTTTGAGACTCA[C/T]AGTGGTGTTCTTCAC | 64446 |
rs563885920 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287152 | TCACCCCCATGCATG[A/G]GCGCCTCCAAAGGCA | 64446 |
rs563935266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311844 | CCCCAATATTCAGCC[C/T]TCCTTCCTTGACACC | 64446 |
rs563942048 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274013 | TTTTCTGGGTGCCTT[C/G]CTCGATGCAAATGCA | 64446 |
rs563975630 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278730 | TGCAGTGAGCAGATA[C/T]GCCACTCCACTCCAG | 64446 |
rs563989579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283707 | TCAGGAGTTTGACAC[C/T]AGCCTGGGCAACATG | 64446 |
rs564023859 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300697 | GTGGGACTTCTAGGT[C/T]GGAGCACACATGCAT | 64446 |
rs564035231 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314679 | TGATCGACCCTCCTC[A/G]TCCACCTACAAATCA | 64446 |
rs564137462 | snp | A/G | | | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311714 | ATTGAGCTGGTCCTT[A/G]TTGGGCCAAAGCCGC | 64446 |
rs564144030 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305139 | CCTGCAGACCCCCCA[A/C]GCAAGCTCCTGTCCA | 64446 |
rs564191348 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315010 | GGAGGTTCCAGGAGC[A/G]GTACAGGGACGTGCC | 64446 |
rs564204947 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304819 | AGGGAAGGCTCTGCC[A/C]ATCCCATGAGTGATC | 64446 |
rs564317490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313838 | CTCTCTATGGGTGAG[A/G]GGGCCAAGGAGACTC | 64446 |
rs564337753 | snp | A/G | 9.94085e-05 | 0.00704942 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309293 | GCTGCCTGGAGCCCC[A/G]TGAGGCCGACCGTTT | 64446 |
rs564385542 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273504 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA | 64446 |
rs564479035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308451 | CAGGTCCAGCAACAC[A/G]TGCCTGCTGCCTGGA | 64446 |
rs564516165 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297382 | CAGGCATGAGCCACC[A/G]TGCCCAGACTTTTTT | 64446 |
rs564585302 | in-del | -/G | 0.00795532 | 0.062565 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313837 | CCTCTCTATGGGTGA[-/G]GGGGCCAAGGAGACT | 64446 |
rs564618273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291895 | TTGAGATGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 64446 |
rs564640976 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300623 | TACAGCAAAGAGCAT[C/G]TTTATACACAGATTG | 64446 |
rs564663710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303145 | ATCTCGTGGGGTAAT[C/G]TTATTATCCGTACTT | 64446 |
rs564716215 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302707 | TTCCCTTGTTGTTGG[C/G]TTTTGGTTTGGGCTG | 64446 |
rs564739720 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294966 | TATTCCTCAGACTAC[A/G]TAATCTCAATTGACC | 64446 |
rs564870163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306371 | CTCCTAAATTAGGTA[A/G]TAAGCCCGAATTCTA | 64446 |
rs564879976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289106 | TGTGCAAGCAGGGCC[A/C]GTGGCTGTCAGCAAG | 64446 |
rs564894784 | snp | A/T | 1.65042e-05 | 0.0028726 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281969 | CAGTGGACACGGGCA[A/T]CCAGTGCTCGATCAG | 64446 |
rs564960636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288220 | AGAAAATTACATGAG[A/C]TGTTCACCTCTTTAT | 64446 |
rs565040402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295553 | CTTTGTCTAGTTAGT[C/T]CAATATCTGGGCTTC | 64446 |
rs565068766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311568 | TGGTGAGCCGAGATC[A/G]TGCCATTGCATTCCA | 64446 |
rs565200793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311139 | TCAGCCTCCCAAACT[A/G]CTGGGATTATAGGCA | 64446 |
rs565223671 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287687 | AGTCTGGGCATGGTG[A/G]CTCACGCCTGTAATC | 64446 |
rs565230804 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275811 | ACAAGAATCGCTTGA[A/C]CTTGGGAGGCAGAGG | 64446 |
rs565394964 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74288546 | TCCGGAACTGTGATA[A/G]AATCAATTTCTGTTG | 64446 |
rs565404563 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314768 | GACACATTGCCACGA[C/T]AGGAGCCTCCAAGTA | 64446 |
rs565486497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293220 | TTGATCTTTCACGTA[A/G]TAATTATGTCTATTA | 64446 |
rs565486981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293693 | TGGGTGACAGAGCGA[A/G]ACTCCATCTCAAAAA | 64446 |
rs565514094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313048 | AATGTGAGGGCCCTC[A/G]TTTAAAAAGTATTAA | 64446 |
rs565643978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307948 | GATTACAGGCGCCCA[C/G]CAACACCCCTGGATA | 64446 |
rs565686619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284708 | TGAGCCACTGCACCC[A/G]GCCAATTATTCACCT | 64446 |
rs565686672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277115 | AACAAGGCTGGGTGC[A/G]GTGGCTCATGCCTGT | 64446 |
rs565701361 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, missense, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312830 | TGGTCATCTTCCAGG[A/C]CCTCTTTTGTACCAG | 64446 |
rs565855039 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312482 | TATCCTCCCCTCCCC[C/G]CAGAGAGGGCACATG | 64446 |
rs565936174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295353 | GTTGCAGTAAGTTGA[A/G]ATTGTGCCACTGCAC | 64446 |
rs565981893 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283035 | TCGTTTCCAGCAGCT[C/T]TGCCTTTTCCAGACT | 64446 |
rs566074810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301713 | GCAGGGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 64446 |
rs566172324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311412 | TGAGGTCGGGAGTTC[A/G]AGACCAGCCTGACCA | 64446 |
rs566199137 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295859 | TAGTGATTAGTTAAT[G/T]ATTGAACAAAGATTT | 64446 |
rs566207357 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301567 | GCTGGTCACCTGCCT[A/T]CCTCTGGGGAAGGAA | 64446 |
rs566257321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311935 | GAAGCCCCACCTGGC[C/T]CCAGCACTGGAGTCG | 64446 |
rs566297194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276375 | ACTCTAGGTTCCCAC[A/G]GGGGGAGGATCTCCC | 64446 |
rs566333978 | snp | C/T | 1.64817e-05 | 0.00287064 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301190 | GTCCCTTGCTGTCCC[C/T]TCCCCGACTTGCATT | 64446 |
rs566376239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314282 | TCTTGGTATTGCCCC[A/G]CTCTCACAAGTGGGA | 64446 |
rs566395602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306686 | GCAATGGCGAGATCT[C/T]GGCTCACTGCAACCT | 64446 |
rs566411349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287276 | GCCCTGCTCTGGGGG[C/T]GGGTCTGGTTGATGG | 64446 |
rs566442902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293755 | CTCTTGTAGATTACA[C/T]GTAGCTGGCATACAA | 64446 |
rs566453388 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292955 | CTGCCTCAGCCTTCC[A/G]AGTAGCTGGGACTAC | 64446 |
rs566628367 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277277 | CTGTAATCCCAGCTA[C/T]GGGAGGCTGAGGCAG | 64446 |
rs566692331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308774 | CGATCTTCCTGCCTT[A/G]GCCTCCCAAAGTGCT | 64446 |
rs566718899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297070 | TTTGCTGATGGCACA[C/T]CTGGAAAACTGATTT | 64446 |
rs566761169 | snp | G/T | 0.168135 | 0.236216 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285978 | ATATATATAGAGAGA[G/T]AGAGAGAGAGAGAGA | 64446 |
rs566791253 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304396 | TCACTCAGCTGTTCT[G/T]TCCATTTGGAATGCT | 64446 |
rs566925052 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74288786 | ATGCTCTGTGGCCTC[A/G]GTTTTGACCATGAAG | 64446 |
rs566956363 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272990 | CCTGCAACTCATAAC[C/G]ATTTTTCAAGGCCCA | 64446 |
rs567025080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291965 | ACCTCTCGGATTCAA[A/G]TGATTCTCCTGCCTC | 64446 |
rs567116640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294350 | GGTCTCACTCTGTCA[C/T]CCAAGCTGGAGCGCA | 64446 |
rs567125298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285445 | AGGAGTCTGACCTTG[C/G]GCAAAGGTGACTCCC | 64446 |
rs567178970 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74311282 | CAGCCCTGCAGGCAA[C/T]CCCCCAGAACCATGG | 64446 |
rs567271550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276103 | TGACACTCCTCCTCC[C/G]CATCACTCCCTTGGC | 64446 |
rs567377861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294035 | CGATATGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 64446 |
rs567437449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299949 | CTGGGGACATTTCCT[G/T]TAACACATTTTATTT | 64446 |
rs567522765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280762 | ACCATCAATATTTCC[G/T]CCTGCCCTGTCAATA | 64446 |
rs567531807 | snp | A/G | 4.94434e-05 | 0.00497184 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305384 | TTCCTGACGGTTGGC[A/G]ACTGGACAGCCCGCA | 64446 |
rs567666283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281627 | CTTAGCATATAGTCG[A/G]CACTCAGGATTTTTT | 64446 |
rs567768651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297897 | TGCTGCTTCTTCGGG[A/G]GTGGGAGCCAGGATG | 64446 |
rs567952885 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285522 | AAATTTGGACTGAAC[C/T]TCAAGCCTCTGCCAG | 64446 |
rs568016820 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284227 | ACCCTCTCTTAAAAA[A/C]AAAAAAAAGGAAAGA | 64446 |
rs568222938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312958 | AGGGAAAAGAAACAG[C/T]GGGTATATGCCAGGA | 64446 |
rs568246514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277835 | TTTTAAGGAAGATCC[C/T]AGGTTTCAGAAACGC | 64446 |
rs568458202 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296314 | ATCTTGCCTTTAAAG[A/T]GAGAGAGAGAGAGAG | 64446 |
rs568466186 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301784 | TGAGACCCCCCCCAC[C/T]GCCCGCCCAGTCTTT | 64446 |
rs568491715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284380 | TGGCATTGTTAATGA[C/T]AGAGTGAAGAAAGGC | 64446 |
rs568616823 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307085 | GATGTCCTCATTCTA[C/T]AGGGGTGGGAACGCT | 64446 |
rs568624318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295931 | AGGGGCTCTGTGTGC[A/G]TGTGTGAGCATGCCT | 64446 |
rs568721974 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295920 | CTTCTCTGCTAAGGG[G/T]CTCTGTGTGCGTGTG | 64446 |
rs568749461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309764 | ACTGGCTGGGGCCAC[A/G]GAAGGGTGGGGGCAT | 64446 |
rs568750530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302160 | GTGAGGCAAGGCGCC[A/G]TGGCTCACACCTGTA | 64446 |
rs568860105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293909 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 64446 |
rs568860167 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287355 | GGTGGGGCATGTTCC[A/T]GCAGGGCAGAGTAAG | 64446 |
rs568934435 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304918 | TTTATGGCCAAATGC[A/T]TCGAGGACACAGTGG | 64446 |
rs568962159 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280865 | GCTGAGGCAGGTGGA[A/T]CACTTGAGCCCAGAA | 64446 |
rs568996957 | snp | C/T | | | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301075 | CATCCGAAAGATGAG[C/T]GAGCCCACTGAAGTT | 64446 |
rs569062596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314042 | GCTGCTTTGGTCCTC[A/G]TGGGGTTCACATCCC | 64446 |
rs569096282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292158 | GCGTGAGCCACCATG[C/T]CTGGCCGCTATTAAT | 64446 |
rs569280352 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273105 | ATAACCTCATTCCCC[A/G]AGCTGCCACTCATTC | 64446 |
rs569296312 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304536 | GGTCATGCTCAGAGA[C/T]GCGAGGGGAGCACTG | 64446 |
rs569413507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312718 | GGCCCCAGCTCTAAA[A/G]CACTTTCTAGCTGTA | 64446 |
rs569413768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286704 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCACC | 64446 |
rs569428863 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290514 | GGACAGGGTGGTGGT[A/G]GCTTCACGCTCTCCA | 64446 |
rs569524781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289400 | GGCGTGGTGGTGTGC[A/G]CCTGTAATCGTAGCT | 64446 |
rs569560079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286113 | CCAGCCTGGCCAACA[C/T]AGCAAAACCCCATCT | 64446 |
rs569611576 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302272 | ACTGTCCCTACATAA[A/G]AAAAGAAAAAAAGGG | 64446 |
rs569637444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277027 | AATCTGGGCTTCTCA[C/T]CCCACCCTGTGCCCT | 64446 |
rs569749751 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280013 | TGCTATCAAAGGCAC[A/C]ATTTCTGAAAGTGCA | 64446 |
rs569797297 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308863 | GAGGTCAAGAGTTTG[A/C]GAGCAGCCTGGCCAA | 64446 |
rs569850626 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294502 | TTTAATTTTTGTAGA[G/T]ATAGGGTCTTGCTAT | 64446 |
rs570011038 | in-del | -/A | 0.314057 | 0.241654 | intron-variant | DNAI2 | GRCh38.p7 | 17:74278268 | GACCCTCAACTCTAC[-/A]AAAAAAAAAAAATTA | 64446 |
rs570065680 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306629 | GTTTGTTTGTTAAAA[A/T]GCTTTTGAGATGGAG | 64446 |
rs570108010 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295192 | CTGAACTCAGGAGTT[C/G]AAGACCAGCATGGGC | 64446 |
rs570168701 | snp | A/G | 0.0036673 | 0.0426638 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301114 | GGACATCACCAAGAA[A/G]GAACAGTTGGAAAAT | 64446 |
rs570215992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305874 | ATGGGATTTTGCCAC[A/G]TTGGCCAGGCTGGTC | 64446 |
rs570252099 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310808 | GCCTCCGAAAGTGCT[A/G]GGATTATAGGCGTGA | 64446 |
rs570346486 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294194 | TACATCTGCCATTTT[G/T]CTTTTTTTTCCTATA | 64446 |
rs570364596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311380 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 64446 |
rs570459052 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304198 | TTTCTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTG | 64446 |
rs570488188 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298716 | CAAGCAATTCTCCCA[C/T]CTCAGCCTCCCGAGT | 64446 |
rs570623182 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286536 | AGCAATTCTCCTGCC[A/T]CAGCCTCCCAAGTAG | 64446 |
rs570645028 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272304 | AGGGCTGGAGGTGGA[A/G]TGGAAAGGGTTGCAT | 64446 |
rs570652041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308114 | AGATCCTTTCTTTAG[C/T]CTTGATCATTTCTCC | 64446 |
rs570653301 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313576 | CATATGTCCCAAAAC[A/G]TGCTCCTCACCATGG | 64446 |
rs570860628 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74274922 | TCCTTCCTGCTCAAG[G/T]TCAAGGTTTACCACA | 64446 |
rs570867024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284931 | GGCTCCGGCCAGGGC[A/G]CCTCAGCATCCAGCC | 64446 |
rs570869299 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291292 | CAGCCTCCCGAGTCG[A/C]TGAGATTACAGGCAC | 64446 |
rs570973974 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74298329 | GTTTTGTTTTTGAGA[A/C]AGCCTTGCTTTGTTG | 64446 |
rs571069635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298674 | GTGGCACGATCATGG[C/T]TCACTGCAGCCTCAA | 64446 |
rs571106788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298704 | ACCTCCCAGGCTCAA[A/G]CAATTCTCCCACCTC | 64446 |
rs571145583 | in-del | -/AAAA | 0.481473 | 0.0944461 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295234 | ACCCCATCTCTACTT[-/AAAA]AAAAAAAAAAAAAAA | 64446 |
rs571160863 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296364 | GAGAGAGAGGAAGGG[A/G]GAAGGAGGGAGGGAG | 64446 |
rs571300276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309812 | ACTGTGAGGCGGAAC[C/T]GAAGGGGTGGGGCGG | 64446 |
rs571350616 | snp | C/T | 1.67736e-05 | 0.00289595 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299862 | CGGATGGGCAGGTAC[C/T]CACCAGCCAGACACT | 64446 |
rs571412312 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310382 | CTTCAGTAAGTCACG[C/T]CACTCTCCAGGATTC | 64446 |
rs571583404 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315180 | GGGGTGCCCTGAAAC[C/T]GCAGCTCAACAGAGC | 64446 |
rs571674819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299431 | ATGTGTTCCCCTGCC[A/G]CTATGCCTGTCCTAT | 64446 |
rs571749627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301429 | GCTGAACACAGAGGG[C/T]AATCTTTTGACAGAA | 64446 |
rs571751512 | snp | A/G | 0.000746826 | 0.0193095 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307223 | CTGCAGGCTGCCAGG[A/G]CTGTGTGAAAGGAGC | 64446 |
rs571890931 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273773 | AAAAAATTCCCCAGC[C/T]TCTACTCCCAAGGAG | 64446 |
rs571920613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276601 | TGCTCTGGGTCCTTG[A/G]ATGGGTTGTCTTCCC | 64446 |
rs571934757 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290723 | AAACTTTAGTATCAA[A/C]ACCTCGTTTCACACC | 64446 |
rs572062175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290300 | CATCCTGGGCAACAG[A/G]GTGAGACTCTATCTC | 64446 |
rs572121401 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296079 | ACAGCTCTATCCATG[C/G]TTGTGACCTTCTAGA | 64446 |
rs572181287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276232 | TTTATAGTGAGTGAA[A/G]GTTCCCATCTGACTG | 64446 |
rs572451895 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278633 | GTTAACATTGTTGGC[C/T]GGGCATGGTGGCGCA | 64446 |
rs572566254 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273291 | AGATTAGTAGGTAGC[A/C]AATCTGGGATTCAAA | 64446 |
rs572604159 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288221 | GAAAATTACATGAGC[G/T]GTTCACCTCTTTATT | 64446 |
rs572657110 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300193 | CTCAGGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 64446 |
rs572658020 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294722 | GATGTTTCTAGGTAT[A/G]GATATCTTTGAGTTT | 64446 |
rs572666103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294093 | CAGCTTGGATCGTGG[G/T]TTTTTCCTTTTAATC | 64446 |
rs572720210 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305515 | GCCCAGCTGGGCCCC[A/G]GAGAGTCCCGAGCCT | 64446 |
rs572797018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300809 | TCAGTAGGTCGAGGG[C/T]GAGGCCTCAGCATCT | 64446 |
rs572865717 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74289409 | GTGTGCGCCTGTAAT[C/T]GTAGCTACTCGGGAG | 64446 |
rs572936195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287761 | GGAGTTCAAGACTAG[C/T]CTGGCCAACATGGCA | 64446 |
rs572962137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314329 | AAAGCAGCACTGGGT[A/G]GTGGGCTGGGAGCAT | 64446 |
rs573010190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74292321 | ATTGCTTTTGGTAGT[C/T]TCTGTCTTTCTAGGA | 64446 |
rs573053821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297292 | AGAGACGGGGTTTCA[C/T]TGTGTTAGCCAGGAT | 64446 |
rs573109907 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291589 | ACCAACTGCAGACAC[A/G]GGTGAGGCAGGTTTG | 64446 |
rs573116041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303409 | AAGCTTGGTCTTTCC[A/G]CTTGCCCTTGACGCC | 64446 |
rs573243102 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284421 | TCTTTTTTCTTTTTC[-/T]TTTTTTTTTGAGACG | 64446 |
rs573347299 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290860 | CCAGATTCTGGCCAA[A/C/G]GTGGACCAGGGGGTG | 64446 |
rs573370158 | in-del | -/AGAGAG | 0.0154538 | 0.0865337 | intron-variant | DNAI2 | GRCh38.p7 | 17:74296312 | AGATCTTGCCTTTAA[-/AGAGAG]AGAGAGAGAGAGAGA | 64446 |
rs573376357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303075 | CAGGGTGCACACTGT[A/G]TGTTGGACACTTGTG | 64446 |
rs573402329 | in-del | -/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272285 | GAGAGCCCTCGGCTT[-/C]CCCAGGGCTGGAGGT | 64446 |
rs573464702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284602 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 64446 |
rs573542268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277923 | ATGGAATTGCCTGGA[A/G]AATTAAAGAAAAAAA | 64446 |
rs573604290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310961 | CCCACTGCAGCCTCT[A/G]CCTCCCAGGCTGAAT | 64446 |
rs573607189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74277410 | AAAAAAAGAAAAAAG[A/G]AAAAAAGAAAGAAAA | 64446 |
rs573607195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284985 | CTTGCAGAAGTGGCC[A/G]AGGGTTTGGGAGTAT | 64446 |
rs573675457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293123 | CAGGCGTGAGCCACC[A/G]CACCTGGCCTGTCCA | 64446 |
rs573675508 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299622 | ACCACATACCTGCCA[A/C]ACCAGAAGCAGCAGC | 64446 |
rs573709365 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291712 | GAGAATATTTGACTA[-/G]GGGGCCGCCATAAAG | 64446 |
rs573742711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281290 | TTGAGACAGAGTCTT[A/G]CTCTGTCACCCATGC | 64446 |
rs573772345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74288074 | GTGTGCAGAGTGCCA[A/C]TTTTTGTGGCAGTCC | 64446 |
rs573780036 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300309 | CAGAATCTAAAGGGT[G/T]CAAAAAAGAAAATGC | 64446 |
rs573794143 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278008 | TGATTTCACAAAGCC[C/T]TGCAGGTGTTTCTAA | 64446 |
rs573804092 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281182 | CAGACCAGCTGCAGC[-/A]TGCATTAGCTATAGG | 64446 |
rs573862151 | snp | A/G | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273437 | GTACATTTCGTGCCA[A/G]TCACCCAGCTAAGCT | 64446 |
rs573898139 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273801 | GAGTTTCCATTCTGG[G/T]GGTGCGGGAAGATGT | 64446 |
rs573945175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275656 | TGCTTAAACCTGGGA[A/G]GTGGAGGTTGCAGTG | 64446 |
rs574010309 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275086 | GAGAAGCCTGGTAGG[C/T]GCTGGTATCACAGTC | 64446 |
rs574071851 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290371 | GGACTCAAGGGGCGG[C/T]GGAATGGAACTTGTG | 64446 |
rs574112157 | snp | A/G/T | 0.00182605 | 0.0301628 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309511 | TGTTTGGGCCTCTGT[A/G/T]GGGGAGCCGTGTGCA | 64446 |
rs574208921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290944 | CCCCGCTACCCACCC[A/G]CAGAAGGGGTGAAAC | 64446 |
rs574253849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304693 | CAGTGGTAGGGGGAC[A/G]AGTTACATCACCGAC | 64446 |
rs574388553 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302765 | CAGGCCTGGTTCCCC[C/G]TTGGGGGTGTCACTT | 64446 |
rs574472604 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308713 | TTTTTGTAGAAACAG[G/T]GTCTTTCCATGTTGT | 64446 |
rs574563091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307271 | ACCCATAGGCCTTTC[A/G]CAGGGCTGGTTCCTA | 64446 |
rs574594577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306945 | TTTTAAAATCCAGAT[C/T]CTCAGCCCCAACCCT | 64446 |
rs574769552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283550 | GAGTTCACAGCAGCA[A/G]TGAGCTGTGATTGCA | 64446 |
rs574781775 | snp | C/T | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273219 | CCACTGTCCTGCCAC[C/T]TTGCAGATGAGGATA | 64446 |
rs574807351 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302178 | GCTCACACCTGTAAT[C/T]CCAGCACTTTGGGAG | 64446 |
rs574808872 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278984 | CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTC | 64446 |
rs574883139 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280544 | CTCAGCTCTGTCCTG[A/G]TTGGAGAGAAGAGAT | 64446 |
rs574916916 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301818 | AAGAAAGAAAGAAAG[A/C]AAGAGAGGGAGAGAG | 64446 |
rs575045111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289006 | TCATTTCACTACCAC[A/G]ACTGACTTAGGGGCC | 64446 |
rs575122014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280341 | TCTCAGAAAGACTAA[A/G]TGGCCCTGCCTAGGT | 64446 |
rs575123454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300917 | TGTATTTGCTCCCAC[A/G]AATTGCCGGGAGCTC | 64446 |
rs575222865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308845 | ACAGCCTGTCAGACA[C/T]CTGAGGTCAAGAGTT | 64446 |
rs575223567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74295383 | CTCCAGGCTGGGCAA[A/C]AAAGCGAAACTCTGT | 64446 |
rs575242910 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303687 | AACCTCTGCCTCCCA[C/G]GTTCAAGTGATTCTC | 64446 |
rs575273870 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273900 | GATGCGGAAACTGAA[A/G]GAAGGCAGGACAACA | 64446 |
rs575349955 | in-del | -/AG | 0.00119737 | 0.0244387 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272270 | AAATAATGTGTCTTC[-/AG]AGAGCCCTCGGCTTC | 64446 |
rs575386212 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313258 | GATAACTGGTTCCAT[A/C]TTGTGATTTCTTCCC | 64446 |
rs575581048 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311479 | TTAGCCAGGCATGGC[A/G]TCACATGCCTGTAAT | 64446 |
rs575581215 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303446 | GAAGCCCAGGTTTTT[C/G]TTTTGTTTTGTTGAG | 64446 |
rs575617381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74306815 | TATAGACAGAGTTTC[C/T]CCATGTTGGCCAGGC | 64446 |
rs575644983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286438 | AATGTTTGTTGTTGT[C/T]GAGACAGAGTCTCAT | 64446 |
rs575674131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303953 | CAACATAGGGAGACT[C/T]CATCTCTACAAAAAT | 64446 |
rs575786714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311092 | TTGCCCAGGCTGGTC[C/T]GAAACTCCAGGGCTC | 64446 |
rs575822709 | in-del | -/AAAA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277398 | TCAAAAAAAAAAAAA[-/AAAA]GAAAAAAGAAAAAAA | 64446 |
rs575832298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297344 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 64446 |
rs575947958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74311536 | GAGAATTGCTTGAAC[G/T]TGGGAAGCAGAGGTT | 64446 |
rs576026025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74294080 | GAGCCACCACGCCCA[A/G]CTTGGATCGTGGTTT | 64446 |
rs576110883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301363 | CAGAGCTTCTCGAAG[A/C]AGGACACCATAGTCA | 64446 |
rs576167211 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74275785 | GTCTCAGCTACTCAG[G/T]AGACTGAGGCACAAG | 64446 |
rs576194449 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282720 | CGATAAGAGAACTTA[C/T]CTTGAGGGTCATGGT | 64446 |
rs576230151 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275496 | TTGAGAGGCCCAGGA[G/T]GATGGATCACTTGAG | 64446 |
rs576332621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276154 | CACACTTTCCCTTAA[A/G]CCACCGGAGGTTCTC | 64446 |
rs576361576 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273720 | CGCGCCACTGCACTC[C/T]AGCCTGGGCGACAGA | 64446 |
rs576490204 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299115 | GGAAAATGGAAACGA[A/C]ATCTAACAGGACAAA | 64446 |
rs576504243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286221 | GAATTGCTTGAACCC[A/G]AGAGACGGAAGCTGC | 64446 |
rs576542479 | in-del | -/AAA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277399 | CAAAAAAAAAAAAAA[-/AAA]GAAAAAAGAAAAAAA | 64446 |
rs576545577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305099 | ACAGCCCTTGCCAAG[G/T]CTTGATCTGAGGGCC | 64446 |
rs576567291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285690 | AGAGATTGCAGTCCA[C/T]TGGAGGTCAAAGACA | 64446 |
rs576683556 | snp | G/T | 0.000675169 | 0.0183611 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291094 | TTCAACCCCAAAGAT[G/T]CCCACGTACTCCTGG | 64446 |
rs576756991 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291533 | TGGCAGCCTGGGCTC[A/C/G]GCCACAGAAGACTAA | 64446 |
rs576845799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74279083 | GAGGCAGAAGAATGG[C/T]GTGAACCCGGGAGGC | 64446 |
rs576952990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302951 | CAGGGAGGTTGGGGT[C/G]GCGAGGGCTCAGGAA | 64446 |
rs577007971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74302473 | TCGGGAGGCTGAGGC[A/G]GGAGAATTGCTTGAA | 64446 |
rs577022294 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297220 | CCTCCCGAGTAGCTG[A/G]GACTACAGGTGCCCG | 64446 |
rs577158939 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279091 | AGAATGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 64446 |
rs577232589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74303357 | CACTGACGGGCGGCG[G/T]GCAGTCGGCTTGAAT | 64446 |
rs577437466 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74276789 | GAGTTTCCTCATTCT[C/G]TTCAATCTCCTTGTG | 64446 |
rs577536668 | in-del | -/T | 0.29175 | 0.246489 | intron-variant | DNAI2 | GRCh38.p7 | 17:74297392 | CCACCGTGCCCAGAC[-/T]TTTTTTTTTTTTTTT | 64446 |
rs577558748 | in-del | -/C/TC | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294310 | TTCTTTTTTTTTTTT[-/C/TC]CTTTTCTTTTTTTTT | 64446 |
rs577576856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DNAI2 | GRCh38.p7 | 17:74274905 | GGAGCGTGTGCAGTT[C/T]CTCCTTCCTGCTCAA | 64446 |
rs577583581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284538 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 64446 |
rs577597669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74304578 | AGGAGACCAGCCTTT[A/G]TGCATTCAGTCCGCA | 64446 |
rs577643981 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74283762 | AAAACAAAAACAAAA[A/T]TTAGCCACGTGTGGT | 64446 |
rs577659287 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307657 | GACAGAGTGAGACTC[C/T]GTCTCAAAAAAAAAT | 64446 |
rs577694930 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306164 | GCGGGTGCCTTGGCA[C/T]AATTCAGCAGTGAGG | 64446 |
rs577934976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74308935 | GGGTGTGGTGACGGG[C/T]GCCAGTAATCCCAGT | 64446 |
rs577952653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74298404 | CTGCCTCCCAGGTGC[A/G]AGTGATTCTCATGCC | 64446 |
rs578003730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74293056 | GCCAGGATGGTCTCG[A/G]TCTCCTGACCTCGTG | 64446 |
rs578025788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74280450 | CATGACCAGTAGCAC[A/G]CGTCAGAGGCTTTCC | 64446 |
rs578131933 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272689 | AAGTGGGAGAGAAAC[A/G]TTTGCTTCCTTCCTG | 64446 |
rs745320942 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283031 | CCTGTCGTTTCCAGC[A/C]GCTCTGCCTTTTCCA | 64446 |
rs745353428 | in-del | -/G | 1.64958e-05 | 0.00287187 | frameshift-variant, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285090 | AGTTAACCATGTCGA[-/G]GGGGGCTGGCCCAAG | 64446 |
rs745364046 | snp | A/G | 1.65759e-05 | 0.00287883 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299765 | GCGGAGCTATCCACC[A/G]TTGAGTCCAGCCACC | 64446 |
rs745366458 | snp | A/G | | | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312623 | GAGGGAAGGGCTGGG[A/G]CATTAGCGGTGTGCA | 64446 |
rs745419846 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302835 | GGGAGGCCCTGGCCT[C/T]GAACATACCTGGGCA | 64446 |
rs745460132 | snp | C/T | 0.000500042 | 0.0158041 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281683 | AAATTCCTAGGATCT[C/T]CCCACCACCCCTTGC | 64446 |
rs745468920 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289633 | TGCCACACACCTCTC[C/T]TGGCACCCCGATGGC | 64446 |
rs745627986 | snp | C/T | 3.5412e-05 | 0.0042077 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287135 | TGTCTGGCCACCCTC[C/T]GTCACCCCCATGCAT | 64446 |
rs745715756 | snp | A/C/T | 0.000362572 | 0.0134595 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301202 | CCCTTCCCCGACTTG[A/C/T]ATTGACAGGGCAGCC | 64446 |
rs745727788 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74291716 | AATATTTGACTAGGG[G/T]CCGCCATAAAGGGAT | 64446 |
rs745743753 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278109 | ACTGTGACCTTTGGC[C/T]CTGTATTAATACTTC | 64446 |
rs745755917 | snp | A/G | 1.6631e-05 | 0.00288362 | intron-variant, splice-acceptor-variant | DNAI2 | GRCh38.p7 | 17:74310016 | CCGGCCCCTTCAATA[A/G]GTGTGTGACGAGGCC | 64446 |
rs745774035 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279530 | CAGGCAAACCTGCTC[A/C]CGTAATCCTGTTTTT | 64446 |
rs745814926 | snp | A/G | 2.2924e-05 | 0.00338548 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309574 | CTCCTACAAAGGTTA[A/G]GGGGCCTGGGGGATT | 64446 |
rs745914412 | snp | A/C | 1.65332e-05 | 0.00287512 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281824 | GCCGGCACCATGGAG[A/C]TTGTGTACGTGTACG | 64446 |
rs745920426 | snp | C/G | | | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291026 | GCTTTATAGAAAACC[C/G]CAACAAGCCTGAACT | 64446 |
rs745986211 | in-del | -/CT | 1.6631e-05 | 0.00288362 | frameshift-variant, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310117 | TGCTGGAGGTCTCGC[-/CT]GGGCTCTCTACCCTC | 64446 |
rs746037775 | snp | C/T | 4.94205e-05 | 0.0049707 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305326 | CCCGGGCCATCATGG[C/T]CCCATCTACGCCCTC | 64446 |
rs746084496 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275558 | GGTGAAACCCCATCT[C/T]TACTAAAAATACAAA | 64446 |
rs746125918 | snp | A/G | 2.00419e-05 | 0.00316552 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310206 | CCTCCAGCACGTCCC[A/G]ACCTGGCCCCACAGC | 64446 |
rs746293418 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275557 | TGGTGAAACCCCATC[-/T]TTACTAAAAATACAA | 64446 |
rs746323026 | snp | A/G | 6.66056e-05 | 0.00577047 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299828 | TCGAAGACGGGCACC[A/G]AGTGCTTCTCAGCTT | 64446 |
rs746342853 | snp | A/G | 1.65897e-05 | 0.00288003 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285026 | CGTCTTCCCTCCTGC[A/G]GCTCTCTGTTTAGGC | 64446 |
rs746398135 | snp | C/T | 3.3243e-05 | 0.00407681 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282022 | CCCTGCCCCAAGGGC[C/T]CTGGCCTGTCAGGTG | 64446 |
rs746441846 | in-del | -/TT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292418 | CATTTTCTTTTTCTT[-/TT]TTTTTTTTTTTTTTT | 64446 |
rs746460303 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280913 | GTAAAATGGCGAGAC[A/C]CCATCTCTACAAAAC | 64446 |
rs746463932 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295339 | CCCAGGAGGCAGAGG[G/T]TGCAGTAAGTTGAGA | 64446 |
rs746567136 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74311567 | GTGGTGAGCCGAGAT[C/T]GTGCCATTGCATTCC | 64446 |
rs746568626 | snp | C/T | | | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281874 | CGGGAAGCAGTGCAA[C/T]TTCTCGGACCGCCAG | 64446 |
rs746594269 | snp | C/T | 1.82693e-05 | 0.00302231 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309443 | GGAGCCAGGTCCCGG[C/T]GTGGGTGTGAGTGTG | 64446 |
rs746614043 | snp | C/T | 1.66788e-05 | 0.00288775 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281799 | CACACCCTCCCTCTG[C/T]CCCCCAGCAGCCGGC | 64446 |
rs746625773 | in-del | -/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74274565 | CCCCAAGTCGCAGGA[-/C]CCTGCAGCCTCTGTA | 64446 |
rs746651381 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74282850 | GATTTGGCCAAAACA[C/T]GTCCAACAGTCAGGT | 64446 |
rs746666477 | snp | A/C | 1.8696e-05 | 0.00305739 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312276 | GGGGACTGGGCGGGA[A/C]ACATGGCACTTGGGT | 64446 |
rs746761761 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302632 | TGCAAATGTGTTAGA[A/G]GAGGGAAGCTTCCTA | 64446 |
rs746771364 | snp | C/G/T | 5.25098e-05 | 0.00512373 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281757 | GACCTGTGGAGATAG[C/G/T]GAAGGGGCCGGTGGG | 64446 |
rs746790023 | in-del | -/GAAA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302066 | AAGGAAGGAAGGAAG[-/GAAA]GAAAGAAGGAAGGAA | 64446 |
rs746846546 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303421 | TCCACTTGCCCTTGA[C/T]GCCCAACTTGAAGCC | 64446 |
rs746846793 | in-del | -/G | 0.000195238 | 0.00987831 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305493 | GAGACAGGAGGGGAT[-/G]GAGGGAGCCCAGCTG | 64446 |
rs746854630 | snp | C/T | 1.64762e-05 | 0.00287016 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287150 | CGTCACCCCCATGCA[C/T]GGGCGCCTCCAAAGG | 64446 |
rs746865882 | snp | A/C | 1.66585e-05 | 0.00288599 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312229 | AGCTGACGCCAGTGC[A/C]TGTAGGGGCCTGGAC | 64446 |
rs746896738 | snp | A/G | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305234 | CCCACCAAGTTCATG[A/G]TGGGGACCGAGCAGG | 64446 |
rs746897622 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290372 | GACTCAAGGGGCGGC[A/G]GAATGGAACTTGTGC | 64446 |
rs746940559 | snp | A/G | 0.00014835 | 0.0086112 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301206 | TCCCCGACTTGCATT[A/G]ACAGGGCAGCCAGGG | 64446 |
rs746968131 | snp | C/T | 1.66059e-05 | 0.00288144 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310101 | CTGGGGACAACCACC[C/T]TGCTGGAGGTCTCGC | 64446 |
rs747104814 | snp | A/G | 0.000230798 | 0.0107399 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281902 | CAGGCCGAGCTGAAC[A/G]TCGACATCATGCCCA | 64446 |
rs747116126 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291128 | GCTGCTACAATGGAC[A/G]GATAGGTAAGGAGGG | 64446 |
rs747137529 | in-del | -/GTAG | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293016 | TTGTATTTTTTTTTA[-/GTAG]AGACGGGGTTTCACC | 64446 |
rs747152551 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299928 | CCTGGTTCCCCATCA[A/G]AACCCCTGGGGACAT | 64446 |
rs747260853 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314801 | TGGGAGGGGACGGGC[A/G]GGACGAGCTTGGCTG | 64446 |
rs747311219 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74274559 | GATCCGCCCCAAGTC[G/T]CAGGACCCTGCAGCC | 64446 |
rs747312852 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287693 | GGCATGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 64446 |
rs747447796 | snp | A/G | 0.000201481 | 0.0100349 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312038 | GCGAGAGAAGATCCT[A/G]GAGGCCAGGCACCGG | 64446 |
rs747464491 | snp | A/G | 1.9728e-05 | 0.00314063 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311976 | TGCCCTCTCCCCACC[A/G]GGCTCTCTCTGTCCC | 64446 |
rs747475424 | snp | C/T | 1.71062e-05 | 0.00292451 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285221 | GGCTTCCTCCTGCCC[C/T]AGCTGCAAGAGCCCC | 64446 |
rs747602265 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306050 | TCATTTTTCATGTTA[C/G]GGAACTGGGCTACAG | 64446 |
rs747634246 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292080 | ATGTTGGCCAGACTT[C/G]TCTCAAATTCCTGAC | 64446 |
rs747733080 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280810 | AACCGTATTGTACCA[C/T]GTGCGATGGCTCATA | 64446 |
rs747748164 | snp | A/C | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301105 | TGTGATCTTGGACAT[A/C]ACCAAGAAGGAACAG | 64446 |
rs747773936 | snp | A/G | 1.86827e-05 | 0.0030563 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309447 | CCAGGTCCCGGCGTG[A/G]GTGTGAGTGTGGGGT | 64446 |
rs747804291 | in-del | -/TGCCCTTGAAAAA | | | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315323 | GGCAGGGACCCAAAG[-/TGCCCTTGAAAAA]TGCCCTTGAAAAATG | 64446 |
rs747888220 | snp | A/G | 1.64901e-05 | 0.00287137 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281880 | GCAGTGCAATTTCTC[A/G]GACCGCCAGGCCGAG | 64446 |
rs747934977 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281813 | GCCCCCCAGCAGCCG[G/T]CACCATGGAGATTGT | 64446 |
rs747980486 | snp | G/T | 0.000313095 | 0.012508 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301185 | TGAGTGTCCCTTGCT[G/T]TCCCTTCCCCGACTT | 64446 |
rs747996068 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280799 | GATTCAGTAAAAACC[A/G]TATTGTACCACGTGC | 64446 |
rs747999106 | snp | A/T | 1.74281e-05 | 0.00295191 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281759 | CCTGTGGAGATAGGG[A/T]AGGGGCCGGTGGGGT | 64446 |
rs748060837 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302558 | GACGACAAGAGCGAA[A/G]CTCCATCTCAAAAAA | 64446 |
rs748081418 | snp | C/T | 3.72828e-05 | 0.00431741 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312280 | ACTGGGCGGGACACA[C/T]GGCACTTGGGTTCTG | 64446 |
rs748184664 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277947 | AAAAAAAGCATATAC[A/T]GATGAGAGATTCTGA | 64446 |
rs748220116 | in-del | -/ACAT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285957 | CATATACACACACAC[-/ACAT]ATATATATATAGAGA | 64446 |
rs748244848 | snp | A/C | | | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301140 | AAAATGCCTTGGGGG[A/C]CATCTCCCTGGAGTT | 64446 |
rs748264709 | snp | C/T | 9.96876e-05 | 0.00705931 | intron-variant, synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310025 | TCAATAGGTGTGTGA[C/T]GAGGCCCTCTTCTGC | 64446 |
rs748406327 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299045 | TTATTTTACAAAACG[A/G]CCTTTCCTAGAAACA | 64446 |
rs748484158 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309550 | GCAGCGATTGCTTTT[C/G]AGCGTGTGCTCCTAC | 64446 |
rs748489679 | snp | C/T | | | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311700 | ACTGGGATCTCACCA[C/T]TGAGCTGGTCCTTGT | 64446 |
rs748500534 | snp | A/T | 3.43731e-05 | 0.00414552 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291159 | ACCTAGGCTTTTTTA[A/T]TTTTATTTTTATTTT | 64446 |
rs748541099 | snp | A/T | 1.67304e-05 | 0.00289222 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312118 | AGACCGATGAGGAGC[A/T]GGCCGTAGACCTGGA | 64446 |
rs748542322 | in-del | -/GGGCTGAGGGCT | 1.65266e-05 | 0.00287455 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289769 | CCTGGTGGCCTGGGA[-/GGGCTGAGGGCT]GGGACCAGCACAAGT | 64446 |
rs748564730 | snp | C/G | | | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314515 | GAGGCCACCTTAGTC[C/G]TAGTCCTGGATGTCT | 64446 |
rs748634048 | in-del | -/TTTT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292416 | ATCATTTTCTTTTTC[-/TTTT]TTTTTTTTTTTTTTT | 64446 |
rs748717910 | snp | C/T | 3.35182e-05 | 0.00409365 | missense, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312051 | CTGGAGGCCAGGCAC[C/T]GGGAGATGCGGCTGA | 64446 |
rs748786040 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305123 | GAGGGCCTTTCTAGC[A/G]CCTGCAGACCCCCCA | 64446 |
rs748824135 | snp | C/T | 1.71835e-05 | 0.00293111 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281673 | GCTTCTGGACAAATT[C/T]CTAGGATCTCCCCAC | 64446 |
rs748836734 | snp | A/C | 1.67489e-05 | 0.00289381 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312128 | GGAGCTGGCCGTAGA[A/C]CTGGAGGCGCTGGTC | 64446 |
rs748846654 | snp | A/G | 1.75056e-05 | 0.00295846 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287126 | CCAGGCAGGTGTCTG[A/G]CCACCCTCCGTCACC | 64446 |
rs748855872 | snp | A/G | 3.30038e-05 | 0.00406212 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74287035 | ATGAAGAGTATTTCA[A/G]TGACGAGGAGGCCAT | 64446 |
rs749016231 | in-del | -/TC | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309979 | ACATAACTTTGCTCC[-/TC]TCTCCTCTACCTGGG | 64446 |
rs749027901 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279657 | CTCAGCCTCCTGAGT[A/C]GCTGTGATTACAGGC | 64446 |
rs749072778 | snp | A/C/T | 8.23763e-05 | 0.00641733 | missense, synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301121 | ACCAAGAAGGAACAG[A/C/T]TGGAAAATGCCTTGG | 64446 |
rs749163971 | snp | G/T | 1.93455e-05 | 0.00311005 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309555 | GATTGCTTTTGAGCG[G/T]GTGCTCCTACAAAGG | 64446 |
rs749172812 | snp | C/G | 1.64885e-05 | 0.00287123 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281892 | CTCGGACCGCCAGGC[C/G]GAGCTGAACATCGAC | 64446 |
rs749177713 | snp | A/G | 0.00022182 | 0.010529 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309474 | GGGTGCTGTGAGCAC[A/G]TGTGCAGTGTGTGGC | 64446 |
rs749213632 | snp | A/G | 6.59435e-05 | 0.00574172 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314160 | CAGGTGGTGGAGGAG[A/G]GAGAGGAAGCAGCGG | 64446 |
rs749297556 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74289198 | CTGGGCTCTAACCTC[A/G]TATATGGACCACCAG | 64446 |
rs749303157 | snp | G/T | 6.59087e-05 | 0.00574021 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289661 | GGCAACAGGAAGTTG[G/T]CAGTGGCATACTCCT | 64446 |
rs749318882 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74281180 | GGCAGACCAGCTGCA[G/T]CATGCATTAGCTATA | 64446 |
rs749432259 | snp | C/T | 3.29609e-05 | 0.00405948 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305254 | GACCGAGCAGGGCAT[C/T]GTCATCTCCTGCAAC | 64446 |
rs749468635 | snp | A/G | 8.24423e-05 | 0.00641984 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285109 | GGCTGGCCCAAGGAC[A/G]TGAACCCCCTGGAGC | 64446 |
rs749481140 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277512 | CTTCAAGACACAATG[A/T]ATATGGATGCAAAGG | 64446 |
rs749540243 | snp | C/T | 1.65987e-05 | 0.00288082 | intron-variant, synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310040 | CGAGGCCCTCTTCTG[C/T]CTCCGGGTGCAGGAC | 64446 |
rs749632284 | in-del | -/CCAGGTCCTCAGGGAG | 0.000150669 | 0.00867824 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309416 | TCCCTCCTTGTGCAT[-/CCAGGTCCTCAGGGAG]CCAGGTCCCGGCGTG | 64446 |
rs749633905 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292549 | AGCCTCCCGAGTAGC[C/T]GAGCCTACAGGCATG | 64446 |
rs749635049 | snp | A/C | 1.66012e-05 | 0.00288103 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285018 | CAGGGTGACGTCTTC[A/C]CTCCTGCGGCTCTCT | 64446 |
rs749688750 | snp | A/C | 1.65743e-05 | 0.00287869 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309290 | GATGCTGCCTGGAGC[A/C]CCGTGAGGCCGACCG | 64446 |
rs749741473 | snp | C/T | 5.29544e-05 | 0.00514533 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291175 | TTTTATTTTTATTTT[C/T]TTTAGATGGAATTTT | 64446 |
rs749771781 | in-del | -/AC | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285946 | AGATGAGTGCCATAT[-/AC]ACACACACACACATA | 64446 |
rs749778901 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284699 | TTACAGGTGTGAGCC[A/T]CTGCACCCGGCCAAT | 64446 |
rs749840684 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74298682 | ATCATGGCTCACTGC[A/G]GCCTCAACCTCCCAG | 64446 |
rs749872998 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279725 | GTAGAGATGGGTTTT[C/T]GCCATGTTGGCCAGG | 64446 |
rs749917864 | snp | A/G | 1.64942e-05 | 0.00287173 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314104 | CACCAACACTTCTGT[A/G]CTGTCTTCCCCTGCA | 64446 |
rs749949776 | snp | C/T | 1.68658e-05 | 0.0029039 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281778 | GGCCGGTGGGGTCCC[C/T]CACCCCACACCCTCC | 64446 |
rs749966359 | snp | A/G | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289730 | GATTCATACATCTGG[A/G]ACCTGGGTGAGAAGC | 64446 |
rs749987292 | in-del | -/TG | 1.64776e-05 | 0.00287028 | frameshift-variant, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301050 | CCTCCCACCAGGTCA[-/TG]TGGTGGGACATCCGA | 64446 |
rs749994035 | in-del | -/GGGGTTGGGTGGGTT | 5.35662e-05 | 0.00517496 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312246 | GTAGGGGCCTGGACA[-/GGGGTTGGGTGGGTT]GGGGACTGGGCGGGA | 64446 |
rs750005900 | snp | A/G | 5.63079e-05 | 0.00530573 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312272 | GGTTGGGGACTGGGC[A/G]GGACACATGGCACTT | 64446 |
rs750011687 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299334 | CTCGGCTCTCCTCTC[A/G]CCTGGCTCCCTCCAT | 64446 |
rs750042859 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285843 | CTGGAAGAAGTGGCA[A/G]GGCTTGGTTGTCCTT | 64446 |
rs750124541 | snp | A/G | | | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315243 | TCGAGAGGGCACTTC[A/G]GTGCCAACCTTGCAC | 64446 |
rs750191854 | snp | C/G | 1.65081e-05 | 0.00287293 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285073 | GAGATGGAGACCCGG[C/G]GAGTTAACCATGTCG | 64446 |
rs750207891 | snp | A/C/G | 8.84125e-05 | 0.00664826 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310173 | TCTTCCGTAAGCACC[A/C/G]GGTGCCTGGGGAAAA | 64446 |
rs750213486 | snp | C/T | 6.5999e-05 | 0.00574414 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305223 | TCCTTCCACAGCCCA[C/T]CAAGTTCATGGTGGG | 64446 |
rs750220881 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275006 | TTCCTCTCGAATCCT[C/T]GGTTTCAAATCCTTT | 64446 |
rs750246993 | snp | A/G | 4.97888e-05 | 0.00498918 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310088 | CTGCGGCTCCCAGCT[A/G]GGGACAACCACCCTG | 64446 |
rs750277765 | snp | A/G | 1.65723e-05 | 0.00287852 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299793 | ACCGAGACCCTGTGT[A/G]TGGCACCATCTGGCT | 64446 |
rs750307672 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305950 | GCGTTGGGATTACAG[A/G]TGTGAGCCACCGCGT | 64446 |
rs750326519 | snp | A/G/T | 4.98752e-05 | 0.00499355 | intron-variant | DNAI2 | GRCh38.p7 | 17:74284997 | GCCGAGGGTTTGGGA[A/G/T]TATACCAGGGTGACG | 64446 |
rs750360417 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306759 | AGTAGCTGGGATTAC[A/G]GGCGCACGCCAGCAC | 64446 |
rs750477345 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74282530 | GGTCTCAAGCTCCTG[A/G]GCCCAAGTAGTCCTC | 64446 |
rs750519729 | snp | C/T | 1.66477e-05 | 0.00288506 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74287070 | GTGATGGAGGAGGAC[C/T]CTTCAGCTAAAACCA | 64446 |
rs750564140 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302507 | GGGAGGCGGGGGTTG[C/T]GGTGAGCCAAGATCG | 64446 |
rs750572110 | snp | C/T | | | intron-variant, synonymous-codon, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312894 | GTCACCTCCTTCAGG[C/T]CCCACAGATAAGATG | 64446 |
rs750592127 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74289024 | TGACTTAGGGGCCTG[A/G]GAAGTACCTAGCCCA | 64446 |
rs750625351 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303154 | GGTAATGTTATTATC[C/T]GTACTTGCCAGACAC | 64446 |
rs750660614 | snp | A/G | 1.64762e-05 | 0.00287016 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286964 | CGGAGAACTTCCAAT[A/G]TGTCCCCCCTAGATC | 64446 |
rs750750518 | snp | A/G | 8.23784e-05 | 0.00641735 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301072 | GGACATCCGAAAGAT[A/G]AGCGAGCCCACTGAA | 64446 |
rs750756036 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290057 | TCGGTGGCCCATGCC[G/T]GTAATCCCAGCACTT | 64446 |
rs750794863 | snp | G/T | 1.6851e-05 | 0.00290263 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285207 | GCTCGGCTCTGTAAG[G/T]CTTCCTCCTGCCCCA | 64446 |
rs750813377 | snp | A/G | 3.29924e-05 | 0.00406142 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300997 | AGAAGGCAAAAGCCA[A/G]GGGAAATACAGGGCC | 64446 |
rs750885565 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278819 | TGAATAAGACCTACT[A/G]TTTGATAGGACAACA | 64446 |
rs750890543 | snp | A/T | 1.77008e-05 | 0.00297491 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309437 | CCTCAGGGAGCCAGG[A/T]CCCGGCGTGGGTGTG | 64446 |
rs750914015 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308558 | ACAGGGTCTCACTAC[A/G]TTGCCCAGGCTGGAG | 64446 |
rs750964634 | in-del | -/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302761 | AGCCCAGGCCTGGTT[-/C]CCCCTTGGGGGTGTC | 64446 |
rs751007987 | snp | A/G | 4.81684e-05 | 0.00490733 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309522 | CTGTGGGGGAGCCGT[A/G]TGCAGGCTGACTGCA | 64446 |
rs751017955 | snp | G/T | 3.29891e-05 | 0.00406122 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281858 | AGAAGCGCAGCGAGT[G/T]CGGGAAGCAGTGCAA | 64446 |
rs751029617 | in-del | -/CCGCGACCGT | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274287 | TGAGGAGCACCGGAG[-/CCGCGACCGT]GGATTGAACGCTTCC | 64446 |
rs751056551 | in-del | -/A | 1.64827e-05 | 0.00287073 | frameshift-variant, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314188 | CGGGGGAAGAAGGGG[-/A]TGAAGAAGTGGAAGA | 64446 |
rs751121542 | snp | A/G | 3.29859e-05 | 0.00406102 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281862 | GCGCAGCGAGTTCGG[A/G]AAGCAGTGCAATTTC | 64446 |
rs751171647 | snp | A/T | 1.64811e-05 | 0.00287059 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291002 | GCCTGGTGGGGATAA[A/T]TTTTTTGTGCTTTAT | 64446 |
rs751272500 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283789 | TGGTGGTACATGCCT[A/G]TAGTCCCAGCTACTT | 64446 |
rs751280204 | snp | C/G | 1.6498e-05 | 0.00287206 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289745 | GACCTGGGTGAGAAG[C/G]AGCGGGGTCCTGGTG | 64446 |
rs751342415 | snp | A/G | | | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313335 | TGCATTTTGCATTTG[A/G]GGGTACTTGGTTATG | 64446 |
rs751368254 | snp | C/T | 3.29468e-05 | 0.00405861 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305307 | AAAAGATTGTGTGCA[C/T]CTTCCCGGGCCATCA | 64446 |
rs751423227 | in-del | -/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74289520 | CAAGACTCCATCTGA[-/C]AAAAAAAAAAAAAAG | 64446 |
rs751426797 | snp | A/G | 1.80637e-05 | 0.00300525 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310183 | GCACCGGGTGCCTGG[A/G]GAAAATCCCTCCAGC | 64446 |
rs751438337 | snp | A/G/T | 0.000214231 | 0.0103476 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314229 | TAGAAGTCAGCCTTC[A/G/T]ACTGCGGCGCTATCC | 64446 |
rs751474359 | in-del | -/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285769 | AGAAGCATGACTTGT[-/C]CTTTGACTCCATGAG | 64446 |
rs751496866 | snp | G/T | 1.67315e-05 | 0.00289231 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285192 | TAACGCCATCATGCA[G/T]CTCGGCTCTGTAAGG | 64446 |
rs751653596 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295001 | TTCACGTTCAGTGAT[G/T]CTTCTGCCTGCTCAA | 64446 |
rs751662181 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74289019 | ACGACTGACTTAGGG[C/G]CCTGGGAAGTACCTA | 64446 |
rs751678408 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74311042 | ACCATGCCTGGCTCA[C/T]TTTTTAATTTTTGTA | 64446 |
rs751695519 | snp | A/G | 3.62404e-05 | 0.00425663 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281720 | CCCCAACCAGATTGA[A/G]AACCTGGAGCTGTCC | 64446 |
rs751745489 | snp | C/T | 3.34745e-05 | 0.00409098 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309247 | GATGTGGTCTACCTC[C/T]CACAGGTACCACATG | 64446 |
rs751751038 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300865 | TCTGATGATCAGCCA[A/G]GTGTGGGAACTGTGG | 64446 |
rs751781536 | snp | C/T | 2.27892e-05 | 0.00337551 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281625 | TGCTTAGCATATAGT[C/T]GGCACTCAGGATTTT | 64446 |
rs751794241 | snp | A/C | 0.000185822 | 0.00963724 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307257 | GTGTCGAGCACAGCA[A/C]CCATAGGCCTTTCGC | 64446 |
rs751915388 | snp | A/G | 1.7063e-05 | 0.00292082 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287101 | TCAATGTGTTCAGGT[A/G]GCGCCATAGCCAGGC | 64446 |
rs751931749 | snp | C/T | 1.64808e-05 | 0.00287057 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301179 | CTTTGGTGAGTGTCC[C/T]TTGCTGTCCCTTCCC | 64446 |
rs751933779 | snp | C/T | 3.29506e-05 | 0.00405884 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286972 | TTCCAATGTGTCCCC[C/T]CTAGATCATGGAGCA | 64446 |
rs751965421 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305671 | CTTAATTTTATTTCC[-/T]TTTTTTTTTTTTTTT | 64446 |
rs751982696 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74289866 | AAGGGAAGGGCCCGC[A/C]GTCGAGGAGGAACAC | 64446 |
rs751987024 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301374 | GAAGAAGGACACCAT[-/A]GTCATCATGGCACCA | 64446 |
rs752020598 | snp | C/T | 3.29516e-05 | 0.00405891 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301081 | AAAGATGAGCGAGCC[C/T]ACTGAAGTTGTGATC | 64446 |
rs752266938 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74276165 | TTAAGCCACCGGAGG[G/T]TCTCTCCAGGAATTA | 64446 |
rs752311201 | snp | A/C | 0.000465441 | 0.0152481 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309980 | CATAACTTTGCTCCT[A/C]TCTCCTCTACCTGGG | 64446 |
rs752358412 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299661 | TCCCCTGCTCCCTGC[C/T]CTAAGGAAGGAAGCC | 64446 |
rs752367523 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301898 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAAGAA | 64446 |
rs752393507 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296236 | TCCTAACACTTTGAG[A/G]AGCTGAGGCGGGAGG | 64446 |
rs752419194 | snp | C/T | 1.64806e-05 | 0.00287054 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314231 | GAAGTCAGCCTTCGA[C/T]TGCGGCGCTATCCCT | 64446 |
rs752440806 | snp | A/G | 3.29875e-05 | 0.00406112 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281948 | AGCAGTTCGTGGAGC[A/G]GAACCCAGTGGACAC | 64446 |
rs752504916 | snp | C/G | 0.000196115 | 0.00990045 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305494 | AGACAGGAGGGGATG[C/G]AGGGAGCCCAGCTGG | 64446 |
rs752506783 | snp | A/G | 1.64757e-05 | 0.00287012 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291016 | ATTTTTTTGTGCTTT[A/G]TAGAAAACCCCAACA | 64446 |
rs752532123 | in-del | -/A | 0.000399319 | 0.0141245 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291170 | TTTATTTTTATTTTT[-/A]TTTTTTTTAGATGGA | 64446 |
rs752538640 | snp | C/G | 1.67153e-05 | 0.00289091 | missense, nc-transcript-variant, intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312098 | GGAGGGCAGGGATGA[C/G]GAGCAGACCGATGAG | 64446 |
rs752650994 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305873 | GATGGGATTTTGCCA[C/T]GTTGGCCAGGCTGGT | 64446 |
rs752651250 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283686 | AGGCGAGAGGATCAC[G/T]TCCGCTCAGGAGTTT | 64446 |
rs752702719 | snp | A/G | | | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313057 | GCCCTCGTTTAAAAA[A/G]TATTAATAATTTTAA | 64446 |
rs752757483 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74291554 | AGAAGACTAAGTGGG[C/G]TGAGGGCCTCCCATA | 64446 |
rs752816207 | snp | C/G/T | 3.35995e-05 | 0.00409864 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299876 | CCCACCAGCCAGACA[C/G/T]TGGAGAGAGGAGGGA | 64446 |
rs752834029 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279182 | AAAATAAATAAATAA[A/G]TAAAAATAACTAACA | 64446 |
rs752834126 | snp | C/T | 3.32281e-05 | 0.0040759 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299820 | GGCTGCAGTCGAAGA[C/T]GGGCACCGAGTGCTT | 64446 |
rs752885121 | snp | A/C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280265 | GTGGCCTGTGAACCC[A/C/T]GCCTCTGATGCTGCT | 64446 |
rs752924362 | snp | A/C/G | 0.0002477 | 0.0111262 | stop-gained, missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309345 | GAACCCTGGATATCT[A/C/G]GGACTTCATGTTCGA | 64446 |
rs752981998 | snp | A/C/G | 8.34065e-05 | 0.00645734 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312266 | TGGGTGGGTTGGGGA[A/C/G]TGGGCGGGACACATG | 64446 |
rs753042488 | snp | A/G | 2.39754e-05 | 0.00346224 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281737 | ACCTGGAGCTGTCCT[A/G]GCAGGACCTGTGGAG | 64446 |
rs753068722 | snp | A/C | 0.000306607 | 0.0123778 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281669 | TGCAGCTTCTGGACA[A/C]ATTCCTAGGATCTCC | 64446 |
rs753085588 | snp | C/T | 1.66183e-05 | 0.00288251 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309268 | GTACCACATGGCTTA[C/T]CTCACTGATGCTGCC | 64446 |
rs753113481 | snp | C/T | 3.30464e-05 | 0.00406474 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289582 | TTCTGCTCTCTTCCC[C/T]CTCCCCTGCAGGGAC | 64446 |
rs753169829 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300833 | AGCATCTGGGTTGTA[C/T]GAAGCTTGCCGGCGA | 64446 |
rs753170867 | snp | C/G | 2.36482e-05 | 0.00343854 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312202 | TGAAGAAGAAGGAGG[C/G]AGACGCCATAAAGCT | 64446 |
rs753203086 | snp | G/T | 6.65159e-05 | 0.00576659 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305186 | AATTGATGGTTCGTG[G/T]AGTCTTCCCCTCCTG | 64446 |
rs753232860 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301540 | TGGCCCTGCCTGGCA[C/T]GGGGTCCCTAGGCTG | 64446 |
rs753234877 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287590 | ACTAGAACAAGCTAA[A/G]TCCATCCATAGGGGA | 64446 |
rs753284790 | snp | A/G | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289613 | CCCCAGGAAATCAAG[A/G]GGGCTGCCACACACC | 64446 |
rs753309767 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74291581 | CATAGCTGACCAACT[G/T]CAGACACGGGTGAGG | 64446 |
rs753355539 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274336 | CAGAAGCAGAAGGAG[C/T]GGACCCAGGGTAAGG | 64446 |
rs753361006 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300770 | CATATACCGATTCTT[A/G]GCCTTGCACCTGGAG | 64446 |
rs753401353 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287498 | CCAGGGATTCATCCC[A/G]CAGGTTGTGTGTGTG | 64446 |
rs753506134 | snp | A/G | 6.59294e-05 | 0.00574111 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301196 | TGCTGTCCCTTCCCC[A/G]ACTTGCATTGACAGG | 64446 |
rs753524089 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275177 | GAGTGAATAAAAGAC[A/C]ACAGTCTTTCCGTCA | 64446 |
rs753615842 | snp | C/G | 1.67843e-05 | 0.00289687 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282049 | GGTGTGGCCAGGCAG[C/G]GCGGCCAGCTGGGGC | 64446 |
rs753622026 | snp | G/T | 0.000322174 | 0.0126879 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311980 | CTCTCCCCACCGGGC[G/T]CTCTCTGTCCCTGGG | 64446 |
rs753634290 | snp | A/C | 1.66715e-05 | 0.00288712 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299700 | CTTCCACTCCTTCTT[A/C]ATCTCCTTCCTCACC | 64446 |
rs753670586 | snp | A/C | 0.000190386 | 0.00975482 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307336 | GTCTCCCTTGTCCTC[A/C]TCCTGCATAAGGTTA | 64446 |
rs753678803 | in-del | -/CTT | 1.66735e-05 | 0.00288729 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299694 | TGCCCCCTTCCACTC[-/CTT]CTTCATCTCCTTCCT | 64446 |
rs753728960 | snp | A/G/T | 4.94184e-05 | 0.00497063 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291122 | TGGGTGGCTGCTACA[A/G/T]TGGACAGATAGGTAA | 64446 |
rs753792011 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74281682 | CAAATTCCTAGGATC[G/T]CCCCACCACCCCTTG | 64446 |
rs753793879 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296088 | TCCATGCTTGTGACC[A/T]TCTAGACTCCCAGGA | 64446 |
rs753795381 | snp | C/T | | | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313911 | AGCCAGGCGTGAACC[C/T]AAGTCTGCCAGATTC | 64446 |
rs753885946 | in-del | -/AATAATAAT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74286301 | ACTGTGTCTCAAAAT[-/AATAATAAT]AATAATAATAATAAT | 64446 |
rs753890976 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303247 | ACCCAGGGCTCCAAC[A/T]CTGAGGCCCAGAGTG | 64446 |
rs753933951 | snp | C/T | 1.69275e-05 | 0.0029092 | missense, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312021 | TTTGAGCGTGAGACC[C/T]GGCGAGAGAAGATCC | 64446 |
rs753955995 | snp | A/C | 1.64768e-05 | 0.00287021 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286956 | ATTTACTGCGGAGAA[A/C]TTCCAATGTGTCCCC | 64446 |
rs753961397 | snp | C/G | 1.68883e-05 | 0.00290584 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299897 | AGAGGAGGGAAGGGA[C/G]GGGCAGTAACTGTTC | 64446 |
rs753974997 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290293 | TGCACTCCATCCTGG[C/G]CAACAGAGTGAGACT | 64446 |
rs754125549 | snp | A/G | 1.69847e-05 | 0.00291411 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309426 | TGCATCCAGGTCCTC[A/G]GGGAGCCAGGTCCCG | 64446 |
rs754176149 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294745 | TTGAGTTTATCCCAC[G/T]TGGAATTCATTGAGT | 64446 |
rs754177370 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284159 | AAAAAAAAAAAAGCT[A/G]TAGTGAGTCAAGATC | 64446 |
rs754203047 | snp | A/G | 3.32298e-05 | 0.004076 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299822 | CTGCAGTCGAAGACG[A/G]GCACCGAGTGCTTCT | 64446 |
rs754259575 | snp | A/G | 0.000131952 | 0.0081215 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314087 | GGCCTGTCCCCTACC[A/G]ACACCAACACTTCTG | 64446 |
rs754278109 | snp | C/G | 3.70083e-05 | 0.00430148 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312269 | GTGGGTTGGGGACTG[C/G]GCGGGACACATGGCA | 64446 |
rs754350448 | snp | A/G | 1.83913e-05 | 0.00303238 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281742 | GAGCTGTCCTGGCAG[A/G]ACCTGTGGAGATAGG | 64446 |
rs754377571 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299653 | CCCCTCTCTCCCCTG[C/T]TCCCTGCCCTAAGGA | 64446 |
rs754419439 | snp | C/T | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289721 | ATGAGCAGCGATTCA[C/T]ACATCTGGGACCTGG | 64446 |
rs754430392 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287532 | GTGTGTGAAATCACC[A/G]CAGGCGTGGATATTC | 64446 |
rs754458156 | snp | A/C | 1.70557e-05 | 0.0029202 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309529 | GGAGCCGTGTGCAGG[A/C]TGACTGCAGCGATTG | 64446 |
rs754485412 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275188 | AGACCACAGTCTTTC[C/G]GTCAAGGAGACCACA | 64446 |
rs754497256 | snp | A/C | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274340 | AGCAGAAGGAGCGGA[A/C]CCAGGGTAAGGGGCG | 64446 |
rs754639147 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74297051 | AGGTCCTTACTTCAC[A/G]GATTTTGCTGATGGC | 64446 |
rs754642773 | snp | A/C | 1.64939e-05 | 0.0028717 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314128 | CCCTGCAGCAGCAAC[A/C]AAGTCCAGAAGAAGA | 64446 |
rs754676358 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306913 | ATGAGCCACCGTGCC[C/T]GGTGGAGGAGTGATT | 64446 |
rs754710939 | snp | C/G/T | 0.000149725 | 0.00865112 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281803 | CCCTCCCTCTGCCCC[C/G/T]CAGCAGCCGGCACCA | 64446 |
rs754840643 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74311443 | ACATGAAGAAACCTC[A/G]TCTCTACTAAAAATA | 64446 |
rs754901875 | snp | C/G/T | 3.2948e-05 | 0.00405871 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305313 | TTGTGTGCACCTTCC[C/G/T]GGGCCATCATGGCCC | 64446 |
rs754996132 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74282565 | CTTGGCCTCCCAAAG[A/T]GCTGGGAATACAGGC | 64446 |
rs755060592 | snp | A/G | 4.9855e-05 | 0.0049925 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299733 | CCTGCTGGGACACCC[A/G]AAAGGGCAGCCTGGT | 64446 |
rs755089551 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303363 | CGGGCGGCGTGCAGT[C/T]GGCTTGAATACTTTC | 64446 |
rs755098942 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74291505 | ATCCTGCTGCTATAG[C/G]GCAGAGCCCACATGG | 64446 |
rs755099020 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277639 | GCCCTGCCTCTCAGG[A/G]GCCAGCGGCCAGGAC | 64446 |
rs755199948 | in-del | -/ATAT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285958 | TATACACACACACAC[-/ATAT]ATATATATATATAGA | 64446 |
rs755223435 | snp | A/G | 6.58924e-05 | 0.0057395 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291129 | CTGCTACAATGGACA[A/G]ATAGGTAAGGAGGGA | 64446 |
rs755245406 | snp | A/G | 1.66701e-05 | 0.002887 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309255 | CTACCTCCCACAGGT[A/G]CCACATGGCTTACCT | 64446 |
rs755253798 | snp | A/G | 0.000590842 | 0.0171777 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281652 | TTTTTTTTTAATGCG[A/G]ATGCAGCTTCTGGAC | 64446 |
rs755261403 | snp | C/G | 2.03279e-05 | 0.00318803 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312185 | CATCATCTTCGCAGA[C/G]CTGAAGAAGAAGGAG | 64446 |
rs755263601 | snp | C/T | 0.000185649 | 0.00963277 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307269 | GCACCCATAGGCCTT[C/T]CGCAGGGCTGGTTCC | 64446 |
rs755314525 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304672 | CCCTCAAAGAGCTCA[-/T]CCCACCAGTGGTAGG | 64446 |
rs755351514 | snp | A/G | 1.67186e-05 | 0.0028912 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312109 | ATGAGGAGCAGACCG[A/G]TGAGGAGCTGGCCGT | 64446 |
rs755618314 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299680 | AGGAAGGAAGCCTGT[A/G]CCCCCTTCCACTCCT | 64446 |
rs755619913 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284476 | GGAGTGTAGTGCTGT[A/G]ATCTCGGCTCACTGC | 64446 |
rs755651450 | snp | G/T | | | splice-donor-variant, intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314272 | CTTTCCCACCTCTTG[G/T]TATTGCCCCGCTCTC | 64446 |
rs755702212 | snp | C/T | 1.64819e-05 | 0.00287066 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301192 | CCCTTGCTGTCCCTT[C/T]CCCGACTTGCATTGA | 64446 |
rs755714858 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301109 | ATCTTGGACATCACC[A/G]AGAAGGAACAGTTGG | 64446 |
rs755741675 | snp | C/T | 1.65021e-05 | 0.00287241 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281961 | GCGGAACCCAGTGGA[C/T]ACGGGCATCCAGTGC | 64446 |
rs755791569 | snp | A/G | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274150 | GACCTCCAAAAAGAA[A/G]AGGGATGGCCTGCGC | 64446 |
rs755797250 | in-del | -/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290869 | GGCCAAGGTGGACCA[-/G]GGGGTGCAGGCTGGG | 64446 |
rs755825865 | snp | C/G/T | 0.000183101 | 0.00956657 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310002 | CTACCTGGGTCTGCC[C/G/T]GGCCCCTTCAATAGG | 64446 |
rs755885584 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305058 | AGGAGCCCGGGAAGA[A/G]TGGGGACTGCTCTCC | 64446 |
rs755889871 | in-del | -/ACATAT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285957 | CATATACACACACAC[-/ACATAT]ATATATATAGAGAGA | 64446 |
rs755932648 | snp | A/G/T | 3.2961e-05 | 0.00405951 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314233 | AGTCAGCCTTCGACT[A/G/T]CGGCGCTATCCCTGT | 64446 |
rs755938555 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305962 | CAGGTGTGAGCCACC[G/T]CGTCTGGCTGGCTTA | 64446 |
rs755944944 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74291741 | AGGGATGATGAGAGC[A/G]TTGGGGAGCCCTATT | 64446 |
rs755947209 | snp | A/C | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291105 | AGATTCCCACGTACT[A/C]CTGGGTGGCTGCTAC | 64446 |
rs755972641 | snp | A/G | 4.94711e-05 | 0.00497324 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281885 | GCAATTTCTCGGACC[A/G]CCAGGCCGAGCTGAA | 64446 |
rs756035443 | snp | A/C | 4.94197e-05 | 0.00497066 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291024 | GTGCTTTATAGAAAA[A/C]CCCAACAAGCCTGAA | 64446 |
rs756053540 | snp | A/G | 9.90017e-05 | 0.00703499 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305399 | GACTGGACAGCCCGC[A/G]TTTGGTCTGAAGACA | 64446 |
rs756142741 | in-del | -/TA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74310717 | TAATTTTTGTATTTT[-/TA]TAATAGAGACAGGAT | 64446 |
rs756307459 | snp | A/G | 3.29826e-05 | 0.00406082 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285094 | AACCATGTCGAGGGG[A/G]GCTGGCCCAAGGACG | 64446 |
rs756331566 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290071 | CTGTAATCCCAGCAC[C/T]TTGGGAGGCCAAGGC | 64446 |
rs756361278 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74276338 | GTTTGAGACTCACAG[A/T]GGTGTTCTTCACGCC | 64446 |
rs756382003 | snp | A/G | 3.32171e-05 | 0.00407522 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309272 | CACATGGCTTACCTC[A/G]CTGATGCTGCCTGGA | 64446 |
rs756395499 | snp | A/G | 1.66161e-05 | 0.00288232 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285007 | TGGGAGTATACCAGG[A/G]TGACGTCTTCCCTCC | 64446 |
rs756523421 | snp | C/T | 1.65173e-05 | 0.00287374 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289587 | CTCTCTTCCCTCTCC[C/T]CTGCAGGGACCCCCA | 64446 |
rs756547324 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299648 | GCAGCCCCCTCTCTC[C/G]CCTGCTCCCTGCCCT | 64446 |
rs756552230 | snp | C/T | 3.44905e-05 | 0.0041526 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281671 | CAGCTTCTGGACAAA[C/T]TCCTAGGATCTCCCC | 64446 |
rs756600609 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308700 | CTAATTTTTTTATTT[G/T]TTGTAGAAACAGGGT | 64446 |
rs756662256 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74298719 | GCAATTCTCCCACCT[C/T]AGCCTCCCGAGTAGC | 64446 |
rs756680472 | snp | A/G | 1.73213e-05 | 0.00294284 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287118 | CGCCATAGCCAGGCA[A/G]GTGTCTGGCCACCCT | 64446 |
rs756748793 | in-del | -/GAA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285924 | TGTCTGCAAGGACAG[-/GAA]GAAGGAGATGAGTGC | 64446 |
rs756770689 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302829 | GGCTTTGGGAGGCCC[C/T]GGCCTCGAACATACC | 64446 |
rs756827065 | in-del | -/C | 5.00688e-05 | 0.00500319 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281798 | CACACCCTCCCTCTG[-/C]CCCCCCAGCAGCCGG | 64446 |
rs756837428 | in-del | -/GGCA | 2.44394e-05 | 0.00349558 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281736 | ACCTGGAGCTGTCCT[-/GGCA]GGCAGGACCTGTGGA | 64446 |
rs756854583 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74282851 | ATTTGGCCAAAACAC[A/G]TCCAACAGTCAGGTG | 64446 |
rs756868374 | snp | C/T | 0.000132732 | 0.00814544 | stop-gained, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310083 | ATCGCCTGCGGCTCC[C/T]AGCTGGGGACAACCA | 64446 |
rs756957651 | snp | C/T | 1.65261e-05 | 0.0028745 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305210 | CCTCCTGTGTCACTC[C/T]TTCCACAGCCCACCA | 64446 |
rs756978205 | snp | C/G | 1.64822e-05 | 0.00287068 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301198 | CTGTCCCTTCCCCGA[C/G]TTGCATTGACAGGGC | 64446 |
rs757025123 | in-del | -/CTC | 1.6664e-05 | 0.00288647 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299703 | CCACTCCTTCTTCAT[-/CTC]CTTCCTCACCAGCCT | 64446 |
rs757069601 | snp | C/T | 1.66399e-05 | 0.00288438 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310007 | TGGGTCTGCCCGGCC[C/T]CTTCAATAGGTGTGT | 64446 |
rs757156552 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74291626 | ACCTCAGCAGTGTCT[C/T]CTGTTACTACTGTAA | 64446 |
rs757199467 | snp | A/C/G | 0.000115365 | 0.0075941 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314235 | TCAGCCTTCGACTGC[A/C/G]GCGCTATCCCTGTGT | 64446 |
rs757220715 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305050 | GGGGTCTGAGGAGCC[C/T]GGGAAGAGTGGGGAC | 64446 |
rs757238033 | snp | A/G | 5.07327e-05 | 0.00503624 | missense, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312022 | TTGAGCGTGAGACCC[A/G]GCGAGAGAAGATCCT | 64446 |
rs757275584 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305316 | TGTGCACCTTCCCGG[A/G]CCATCATGGCCCCAT | 64446 |
rs757304123 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74311113 | TCCAGGGCTCAAGCA[A/G]TCCTTCCACCTCAGC | 64446 |
rs757344038 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74281616 | ACAGGGTAATGCTTA[G/T]CATATAGTCGGCACT | 64446 |
rs757468573 | snp | C/T | 1.94154e-05 | 0.00311566 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310202 | AATCCCTCCAGCACG[C/T]CCCGACCTGGCCCCA | 64446 |
rs757494255 | snp | C/T | 1.67756e-05 | 0.00289612 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285198 | CATCATGCAGCTCGG[C/T]TCTGTAAGGCTTCCT | 64446 |
rs757517728 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287707 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCAA | 64446 |
rs757534422 | snp | A/G | 1.68997e-05 | 0.00290682 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299899 | AGGAGGGAAGGGAGG[A/G]GCAGTAACTGTTCCC | 64446 |
rs757582356 | snp | A/C | 1.64898e-05 | 0.00287135 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285116 | CCAAGGACGTGAACC[A/C]CCTGGAGCTGGAGCA | 64446 |
rs757613765 | snp | C/T | 1.66158e-05 | 0.0028823 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299824 | GCAGTCGAAGACGGG[C/T]ACCGAGTGCTTCTCA | 64446 |
rs757638244 | snp | A/C/G | 3.37332e-05 | 0.00410678 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281777 | GGGCCGGTGGGGTCC[A/C/G]TCACCCCACACCCTC | 64446 |
rs757748358 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74276270 | GGGGATGCGGGAGAC[A/G]CCTGAATCTTTGATG | 64446 |
rs757776003 | snp | A/G | 9.73094e-05 | 0.00697461 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312270 | TGGGTTGGGGACTGG[A/G]CGGGACACATGGCAC | 64446 |
rs757802545 | snp | A/C | 1.81896e-05 | 0.0030157 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281744 | GCTGTCCTGGCAGGA[A/C]CTGTGGAGATAGGGA | 64446 |
rs757805725 | in-del | -/C | 1.64928e-05 | 0.00287161 | frameshift-variant, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305394 | TTGGCGACTGGACAG[-/C]CCGCATTTGGTCTGA | 64446 |
rs757839047 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307484 | ACGAGCCTGGCCAAT[A/G]TGGTGAATCCCCATC | 64446 |
rs757872851 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277283 | TCCCAGCTACGGGAG[G/T]CTGAGGCAGGAGAAT | 64446 |
rs757939152 | in-del | -/CAGC | 1.64928e-05 | 0.00287161 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314107 | AACACTTCTGTGCTG[-/CAGC]TCTTCCCCTGCAGCA | 64446 |
rs757942722 | in-del | -/TTT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292417 | TCATTTTCTTTTTCT[-/TTT]TTTTTTTTTTTTTTT | 64446 |
rs757961043 | snp | A/G | 3.74049e-05 | 0.00432447 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312274 | TTGGGGACTGGGCGG[A/G]ACACATGGCACTTGG | 64446 |
rs757969084 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74276174 | CGGAGGTTCTCTCCA[G/T]GAATTACTTTGCTCA | 64446 |
rs757989808 | snp | C/T | 4.97343e-05 | 0.00498645 | utr-variant-5-prime, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281814 | CCCCCCAGCAGCCGG[C/T]ACCATGGAGATTGTG | 64446 |
rs758022189 | snp | C/T | 3.36016e-05 | 0.00409874 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281782 | GGTGGGGTCCCTCAC[C/T]CCACACCCTCCCTCT | 64446 |
rs758109864 | snp | A/G | 1.64925e-05 | 0.00287158 | splice-donor-variant | DNAI2 | GRCh38.p7 | 17:74289737 | ACATCTGGGACCTGG[A/G]TGAGAAGCAGCGGGG | 64446 |
rs758128202 | snp | A/C | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289641 | ACCTCTCCTGGCACC[A/C]CGATGGCAACAGGAA | 64446 |
rs758148650 | snp | A/G | | | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313988 | CAGAGCTGGCACCCG[A/G]GTTCCAGGGTGCTCA | 64446 |
rs758174843 | in-del | AAAGTGGGTGGAAGTGAGAAAGACC/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74288746 | TGGAAGGAGTTGCAG[AAAGTGGGTGGAAGTGAGAAAGACC/G]ATGCTCTGTGGCCTC | 64446 |
rs758209243 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74282698 | GTTCCAGCCAGAGGG[A/G]CCTCCACGATAAGAG | 64446 |
rs758228934 | snp | C/T | | | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313101 | GAGCGTTAAACCAAG[C/T]GTGGGCCCTGCTGAG | 64446 |
rs758300859 | snp | A/G | 3.29957e-05 | 0.00406162 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285083 | CCCGGGGAGTTAACC[A/G]TGTCGAGGGGGGCTG | 64446 |
rs758354268 | snp | A/C | 1.6604e-05 | 0.00288127 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310097 | CCAGCTGGGGACAAC[A/C]ACCCTGCTGGAGGTC | 64446 |
rs758385841 | in-del | -/AGAA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280330 | GGTGTGTCAGGTCTC[-/AGAA]AGACTAAGTGGCCCT | 64446 |
rs758405055 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279360 | GTAACACAAAGGATA[A/G]ATGCTTGAGGGGATG | 64446 |
rs758555019 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280273 | TGAACCCCGCCTCTG[A/G]TGCTGCTGGAGCACT | 64446 |
rs758608515 | snp | A/C | 8.27096e-05 | 0.00643024 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309617 | AGCACAACAGAACCA[A/C]CTGGGGGAAATTTAA | 64446 |
rs758643189 | snp | C/T | 1.66471e-05 | 0.00288501 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305417 | TGGTCTGAAGACAGC[C/T]GGGAATCGTCCATCA | 64446 |
rs758658409 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300844 | TGTATGAAGCTTGCC[A/G]GCGACTCTGATGATC | 64446 |
rs758678063 | snp | C/T | 1.64768e-05 | 0.00287021 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286967 | AGAACTTCCAATGTG[C/T]CCCCCCTAGATCATG | 64446 |
rs758710603 | snp | A/G | 5.06333e-05 | 0.00503131 | missense, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312025 | AGCGTGAGACCCGGC[A/G]AGAGAAGATCCTGGA | 64446 |
rs758729736 | snp | C/T | 1.68852e-05 | 0.00290557 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285213 | CTCTGTAAGGCTTCC[C/T]CCTGCCCCAGCTGCA | 64446 |
rs758810046 | snp | C/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301076 | ATCCGAAAGATGAGC[C/G]AGCCCACTGAAGTTG | 64446 |
rs758893842 | snp | A/G | 3.29924e-05 | 0.00406142 | intron-variant | DNAI2 | GRCh38.p7 | 17:74300999 | AAGGCAAAAGCCAGG[A/G]GAAATACAGGGCCTC | 64446 |
rs758912244 | snp | C/T | 1.77919e-05 | 0.00298255 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309438 | CTCAGGGAGCCAGGT[C/T]CCGGCGTGGGTGTGA | 64446 |
rs758997612 | snp | A/G | 1.64942e-05 | 0.00287173 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281860 | AAGCGCAGCGAGTTC[A/G]GGAAGCAGTGCAATT | 64446 |
rs759039842 | snp | C/T | 0.000183761 | 0.00958366 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299681 | GGAAGGAAGCCTGTG[C/T]CCCCTTCCACTCCTT | 64446 |
rs759103872 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301481 | TTGTGGGGAAGGTCA[C/T]GCCCAGGACCAACAT | 64446 |
rs759140683 | in-del | -/AGAG | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285971 | CACATATATATATAT[-/AGAG]AGAGAGAGAGAGAGA | 64446 |
rs759166271 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291089 | TGGAGTTCAACCCCA[A/G]AGATTCCCACGTACT | 64446 |
rs759195732 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277113 | AAAACAAGGCTGGGT[C/G]CGGTGGCTCATGCCT | 64446 |
rs759214858 | snp | A/G | 2.13459e-05 | 0.00326687 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305488 | TGCAGGAGACAGGAG[A/G]GGATGGAGGGAGCCC | 64446 |
rs759252738 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74276093 | TCTCCCACGCTGACA[C/G]TCCTCCTCCCCATCA | 64446 |
rs759296220 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296107 | AGACTCCCAGGAATA[C/T]GTCAGATCTTTTCAA | 64446 |
rs759424350 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308113 | CAGATCCTTTCTTTA[C/G]TCTTGATCATTTCTC | 64446 |
rs759464555 | snp | C/G | 1.65274e-05 | 0.00287462 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74287047 | TCAATGACGAGGAGG[C/G]CATGGAAGTGATGGA | 64446 |
rs759495096 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308760 | ATCCTGGCTTCAAGC[C/G]ATCTTCCTGCCTTGG | 64446 |
rs759506250 | in-del | -/TTTTTA | 1.67393e-05 | 0.00289299 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291152 | GGAGGGACCTAGGCT[-/TTTTTA]TTTTTATTTTTATTT | 64446 |
rs759577580 | in-del | -/T | 0.0126045 | 0.0783798 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281636 | AGTCGGCACTCAGGA[-/T]TTTTTTTTTAATGCG | 64446 |
rs759604794 | snp | A/G | | | intron-variant, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74274849 | AACCTGGGAGCTGGC[A/G]TTCTCGTGTGATCGA | 64446 |
rs759607286 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294003 | GGCCAGGCTGATCTC[G/T]AACTCCTGGCCTCAA | 64446 |
rs759627302 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305816 | AGCTGGGACTACAAG[C/T]ACCTGCCACCATGCC | 64446 |
rs759666586 | snp | C/T | 3.45764e-05 | 0.00415776 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281766 | AGATAGGGAAGGGGC[C/T]GGTGGGGTCCCTCAC | 64446 |
rs759691143 | snp | A/G/T | 5.99957e-05 | 0.00547676 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281727 | CAGATTGAGAACCTG[A/G/T]AGCTGTCCTGGCAGG | 64446 |
rs759710323 | snp | C/T | 1.64961e-05 | 0.00287189 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314075 | GGGAGTGGGGAAGGC[C/T]TGTCCCCTACCAACA | 64446 |
rs759735240 | snp | C/G | 1.65192e-05 | 0.00287391 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309335 | AGGATGGACGGAACC[C/G]TGGATATCTGGGACT | 64446 |
rs759758608 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292956 | TGCCTCAGCCTTCCG[A/G]GTAGCTGGGACTACA | 64446 |
rs759882911 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280074 | TCCATGGTGTGATAT[A/G]GCAGGTACACAGGTC | 64446 |
rs759893306 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278268 | ACCCTCAACTCTACA[-/A]AAAAAAAAAAAATTA | 64446 |
rs759932851 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294601 | GATTTCAGGCGTGAG[A/C]CACCACACTCAACTT | 64446 |
rs759934283 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74281346 | TCACTGCAACGTTCT[C/T]CTCCCGAGTTCAAGT | 64446 |
rs759946853 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304121 | AGCCAGAACCTGTCT[C/T]GAGAAATAAATAAAT | 64446 |
rs759964418 | snp | C/T | 0.000127413 | 0.00798061 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309971 | TCAGACACACATAAC[C/T]TTGCTCCTCTCTCCT | 64446 |
rs759983526 | snp | C/T | 8.33215e-05 | 0.00645398 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305182 | CCAGAATTGATGGTT[C/T]GTGGAGTCTTCCCCT | 64446 |
rs760053842 | in-del | -/AC | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307714 | ATTTTAAAAAAAAAA[-/AC]TATTTTTTTTTTAGT | 64446 |
rs760125530 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300791 | GCACCTGGAGGTTTT[A/G]ATTCAGTAGGTCGAG | 64446 |
rs760142052 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295690 | TGTATGATTTAATGT[A/G]GCAACTTTGCAAATC | 64446 |
rs760278899 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301317 | TCCTAGACGTGTGTG[A/G]CCTTTACAACAACTT | 64446 |
rs760284240 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300702 | ACTTCTAGGTCGGAG[C/T]ACACATGCATTTTTA | 64446 |
rs760306602 | snp | G/T | 1.66779e-05 | 0.00288768 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282038 | CTGGCCTGTCAGGTG[G/T]GGCCAGGCAGGGCGG | 64446 |
rs760400323 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275038 | CTTGTTTGTCACGGT[C/T]AGCAGAGGAGGAACA | 64446 |
rs760404675 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287412 | CAGCACTGTGGGCAC[A/G]CAGGCCCCCGCCGCG | 64446 |
rs760520336 | snp | A/G | 6.72936e-05 | 0.0058002 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312158 | CAGCAAGGCCGAGGA[A/G]GAGTTCTTCGACATC | 64446 |
rs760562974 | in-del | -/T | 0.000331345 | 0.0128671 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291171 | TTATTTTTATTTTTA[-/T]TTTTTTTAGATGGAA | 64446 |
rs760605654 | snp | A/C | 0.000100822 | 0.00709934 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281693 | GATCTCCCCACCACC[A/C]CTTGCTTCCTGCCCC | 64446 |
rs760740593 | in-del | -/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74288129 | TGCAAGGCTGCAAAA[-/G]CAATGCAAATCCAGG | 64446 |
rs760779967 | snp | A/C | | | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312980 | ATGCCAGGATTTACC[A/C]TTGTAGGCAAGACTG | 64446 |
rs760797251 | snp | C/T | 1.66477e-05 | 0.00288506 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309407 | ACGCGCATGTCCCTC[C/T]TTGTGCATCCAGGTC | 64446 |
rs760813607 | snp | C/T | 1.6498e-05 | 0.00287206 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314082 | GGGAAGGCCTGTCCC[C/T]TACCAACACCAACAC | 64446 |
rs760845605 | snp | C/T | 3.30404e-05 | 0.00406437 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281832 | CATGGAGATTGTGTA[C/T]GTGTACGTCAAGAAG | 64446 |
rs760849588 | snp | C/T | 2.86447e-05 | 0.00378438 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309490 | TGTGCAGTGTGTGGC[C/T]AGGTGTGTTTGGGCC | 64446 |
rs760894839 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304539 | CATGCTCAGAGACGC[A/G]AGGGGAGCACTGGAC | 64446 |
rs761002674 | snp | A/G | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273129 | CTCATTCAGGCACCA[A/G]TAGCTCTGGACGGGG | 64446 |
rs761003028 | snp | G/T | 1.69381e-05 | 0.00291011 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281773 | GAAGGGGCCGGTGGG[G/T]TCCCTCACCCCACAC | 64446 |
rs761036084 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74282026 | GCCCCAAGGGCCCTG[G/T]CCTGTCAGGTGTGGC | 64446 |
rs761120612 | snp | G/T | 1.66158e-05 | 0.0028823 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305189 | TGATGGTTCGTGGAG[G/T]CTTCCCCTCCTGTGT | 64446 |
rs761171314 | snp | A/G | 3.29652e-05 | 0.00405974 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289715 | GTGGGCATGAGCAGC[A/G]ATTCATACATCTGGG | 64446 |
rs761194398 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308449 | ACCAGGTCCAGCAAC[A/T]CGTGCCTGCTGCCTG | 64446 |
rs761280652 | snp | A/T | 1.65121e-05 | 0.00287329 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309351 | TGGATATCTGGGACT[A/T]CATGTTCGAGCAGTG | 64446 |
rs761320355 | in-del | -/GAAG | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301863 | AAAGAAGGAAGGAAA[-/GAAG]GAAGGAAGGAAGGAA | 64446 |
rs761346320 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278717 | AGGAGGCGGAGGTTG[C/T]AGTGAGCAGATATGC | 64446 |
rs761389658 | snp | A/T | 0.000116162 | 0.00762021 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285173 | AGAAAGATGAGAACT[A/T]CGTTAACGCCATCAT | 64446 |
rs761450887 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305290 | GGCCAAGACGTCAGC[C/T]GAAAAGATTGTGTGC | 64446 |
rs761516740 | snp | C/T | 8.61675e-05 | 0.00656326 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310163 | GAACGTAGCCTCTTC[C/T]GTAAGCACCGGGTGC | 64446 |
rs761527489 | snp | A/G | | | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312501 | AGAGGGCACATGGTG[A/G]AAATGCGTGTTGAGT | 64446 |
rs761547413 | snp | A/G | 1.67178e-05 | 0.00289113 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299849 | TTCTCAGCTTCCACG[A/G]ATGGGCAGGTACCCA | 64446 |
rs761552228 | snp | C/T | 1.65677e-05 | 0.00287812 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299788 | CAGCCACCGAGACCC[C/T]GTGTATGGCACCATC | 64446 |
rs761587657 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285659 | GAAAAAGAATCTCTT[A/G]TACATCCTGTCCCAA | 64446 |
rs761640702 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287181 | CAACTCCTTGCCATC[A/G]CTGCATGCCCTGGGT | 64446 |
rs761667037 | in-del | -/GAA | 2.06652e-05 | 0.00321437 | cds-indel, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312188 | CATCTTCGCAGAGCT[-/GAA]GAAGAAGGAGGCAGA | 64446 |
rs761668503 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290345 | GACAGAGTGCCCAGC[-/A]GACTGAGAAGGGACT | 64446 |
rs761793391 | in-del | -/GA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296383 | GGAGGGAGGGAGGGA[-/GA]GAGAGAGAGAGAGAG | 64446 |
rs761805361 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74274230 | GCCCCGCGCGTCCGG[A/G]GCCAGGCCGGGGTTG | 64446 |
rs761835518 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74274926 | TCCTGCTCAAGGTCA[A/G]GGTTTACCACATTCT | 64446 |
rs761836294 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74282221 | TCGAGCCAGGGAAGT[A/G]CAAATCACAATGTTC | 64446 |
rs761844591 | snp | G/T | 3.54453e-05 | 0.00420968 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312254 | CTGGACAGGGGTTGG[G/T]TGGGTTGGGGACTGG | 64446 |
rs761883293 | snp | C/T | 3.29549e-05 | 0.00405911 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301047 | CCTCCTCCCACCAGG[C/T]CATGTGGTGGGACAT | 64446 |
rs761964297 | in-del | -/AATAATAAT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74286309 | CAAAATAATAATAAT[-/AATAATAAT]AATAATAATAATAAT | 64446 |
rs762021521 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301142 | AATGCCTTGGGGGCC[A/G]TCTCCCTGGAGTTCG | 64446 |
rs762022417 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74297849 | GTAAAAAGCATTCCC[C/T]ACTCCTCTCTGCTCT | 64446 |
rs762057771 | snp | A/G | 3.44418e-05 | 0.00414966 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309503 | GCCAGGTGTGTTTGG[A/G]CCTCTGTGGGGGAGC | 64446 |
rs762117893 | in-del | -/TA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307716 | TTTAAAAAAAAAAAC[-/TA]TTTTTTTTTTAGTAT | 64446 |
rs762136731 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304362 | AAAGGCCCTCCCCTC[A/G]GTGTGCCCCTCCCCT | 64446 |
rs762145184 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283376 | ACTTTGGGAGACCAA[A/G]GTGGGAGGATGCTTG | 64446 |
rs762164473 | snp | A/G | | | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313747 | GTACCGCGTGGTACT[A/G]AAGCTGTTTTACATA | 64446 |
rs762217686 | snp | A/G | 1.64836e-05 | 0.0028708 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314180 | GGAAGCAGCGGGGGA[A/G]GAAGGGGATGAAGAA | 64446 |
rs762241468 | in-del | -/CTC | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296244 | TTTGAGAAGCTGAGG[-/CTC]CGGGAGGATCGCCTG | 64446 |
rs762303844 | snp | A/G | 1.64925e-05 | 0.00287158 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314093 | TCCCCTACCAACACC[A/G]ACACTTCTGTGCTGT | 64446 |
rs762305426 | snp | A/G | 1.65007e-05 | 0.00287229 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281849 | TGTACGTCAAGAAGC[A/G]CAGCGAGTTCGGGAA | 64446 |
rs762351802 | snp | C/T | 1.64933e-05 | 0.00287165 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290984 | CTGTCCTTTTCTTTC[C/T]GGGCCTGGTGGGGAT | 64446 |
rs762406330 | snp | A/G | 3.53163e-05 | 0.00420201 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305445 | TCATGTGGACCAAGT[A/G]AGAGGCGATGCTGGG | 64446 |
rs762439621 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305374 | CCCGAAGAACTTCCT[A/G]ACGGTTGGCGACTGG | 64446 |
rs762446556 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74282216 | CTTCCTCGAGCCAGG[A/G]AAGTGCAAATCACAA | 64446 |
rs762541914 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74289835 | AGGTCAAGGACACTC[A/G]CGCGGTTGGTGCCTC | 64446 |
rs762596436 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277255 | AGCCGCGAATGGTGG[C/T]ATGTGCCTGTAATCC | 64446 |
rs762607200 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308188 | TGGGAAGTGTAGTCT[A/G]CCTTGCTCACCAGGG | 64446 |
rs762652711 | snp | C/T | 0.000131841 | 0.00811808 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305383 | CTTCCTGACGGTTGG[C/T]GACTGGACAGCCCGC | 64446 |
rs762659186 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293848 | GAGTGCAGTGGCGTG[A/G]TCTCGGCTCACTGCA | 64446 |
rs762668832 | snp | C/G | 1.76961e-05 | 0.00297452 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311993 | GCTCTCTCTGTCCCT[C/G]GGTGCCCAGATGTTT | 64446 |
rs762686865 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74288547 | CCGGAACTGTGATAG[-/A]ATCAATTTCTGTTGT | 64446 |
rs762708201 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283733 | ACATGGCGAAACACC[A/G]TCTCTACAGAAGAAA | 64446 |
rs762721155 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278345 | TGAGGTGGGAGGATT[A/G]CTTGAGCCTGGGAGG | 64446 |
rs762726791 | snp | C/T | 3.32878e-05 | 0.00407956 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285180 | TGAGAACTACGTTAA[C/T]GCCATCATGCAGCTC | 64446 |
rs762731907 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308956 | TAATCCCAGTTACTC[A/G]GGAGGCTGAGACAGG | 64446 |
rs762763690 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305159 | GCTCCTGTCCATGCC[C/T]GCTAATCCCAGAATT | 64446 |
rs762783286 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299273 | AATGTAGCAGAGAGA[G/T]TCACCTAAATGGAGT | 64446 |
rs762791538 | snp | C/T | 1.94782e-05 | 0.00312069 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285242 | CAAGAGCCCCATCCA[C/T]CACTGCAGCTCCCCA | 64446 |
rs762842258 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285320 | GTGAATGCTGGGGGG[-/A]AGGGGACCAGCTGCT | 64446 |
rs762976144 | snp | C/T | 4.9807e-05 | 0.00499009 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299814 | CCATCTGGCTGCAGT[C/T]GAAGACGGGCACCGA | 64446 |
rs762980383 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285317 | CGTGTGAATGCTGGG[A/G]GGAAGGGGACCAGCT | 64446 |
rs763011642 | snp | A/G | 4.97789e-05 | 0.00498868 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309396 | GCTTGAAGGTCACGC[A/G]CATGTCCCTCCTTGT | 64446 |
rs763026333 | snp | C/T | 3.33968e-05 | 0.00408623 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74287078 | GGAGGACCCTTCAGC[C/T]AAAACCATCAATGTG | 64446 |
rs763070004 | snp | G/T | 6.43811e-05 | 0.00567331 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281704 | CACCCCTTGCTTCCT[G/T]CCCCAACCAGATTGA | 64446 |
rs763157679 | snp | C/T | 1.66084e-05 | 0.00288165 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289561 | TGGGGAACCTCACAT[C/T]CAGCCTTCTGCTCTC | 64446 |
rs763193003 | snp | A/T | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301159 | CTCCCTGGAGTTCGA[A/T]TCTACTTTGGTGAGT | 64446 |
rs763194331 | snp | A/G | | | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289611 | ACCCCCAGGAAATCA[A/G]GAGGGCTGCCACACA | 64446 |
rs763228543 | in-del | -/CAA | 0.000296474 | 0.0121717 | cds-indel, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291027 | CTTTATAGAAAACCC[-/CAA]CAAGCCTGAACTTGC | 64446 |
rs763319113 | snp | A/G | | | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312727 | TCTAAAGCACTTTCT[A/G]GCTGTATCACCTGAG | 64446 |
rs763322486 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74282066 | CGGCCAGCTGGGGCC[A/G]GTGAGTGGTTCTGTG | 64446 |
rs763354596 | snp | A/C/G/T | 0.000187855 | 0.00969013 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309966 | GTTAATCAGACACAC[A/C/G/T]TAACTTTGCTCCTCT | 64446 |
rs763372278 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302934 | GAGGACAAGGCACTG[A/G]GCAGGGAGGTTGGGG | 64446 |
rs763380261 | snp | C/G | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314207 | AGAAGTGGAAGAAGA[C/G]TTAGCCTAGAAGTCA | 64446 |
rs763405700 | snp | A/G | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274376 | CAGGAGGACGTCGGA[A/G]GCTAAAGACTAGAGT | 64446 |
rs763426265 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299357 | CCCTCCATCCTGAGG[C/T]TCATCTTCCATCTCA | 64446 |
rs763444149 | snp | C/T | 4.61372e-05 | 0.00480276 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309519 | CCTCTGTGGGGGAGC[C/T]GTGTGCAGGCTGACT | 64446 |
rs763465981 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301585 | TCTGGGGAAGGAAGA[A/G]GTACTGGAGAGGAAA | 64446 |
rs763473211 | snp | C/T | 3.31818e-05 | 0.00407306 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282012 | CGAGGTGGGTCCCTG[C/T]CCCAAGGGCCCTGGC | 64446 |
rs763485792 | in-del | -/AGCCGCGACC | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274284 | TTTGAGGAGCACCGG[-/AGCCGCGACC]AGCCGCGACCGTGGA | 64446 |
rs763489979 | snp | C/T | 1.64906e-05 | 0.00287142 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281931 | CAACCCTGAGCTGGC[C/T]GAGCAGTTCGTGGAG | 64446 |
rs763598909 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307407 | TGCAGTGGGCTAATG[A/C]CTGTAATCCCAGCAC | 64446 |
rs763636160 | snp | G/T | 1.65542e-05 | 0.00287695 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305201 | GAGTCTTCCCCTCCT[G/T]TGTCACTCCTTCCAC | 64446 |
rs763679163 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277276 | CCTGTAATCCCAGCT[A/G]CGGGAGGCTGAGGCA | 64446 |
rs763721569 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308242 | TGGAGGAAGGGAGAG[C/G]AGGTCTGGGTGAAAA | 64446 |
rs763731811 | snp | A/G | 1.65321e-05 | 0.00287502 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285054 | GGCCAACTCAGAGCG[A/G]TTTGAGATGGAGACC | 64446 |
rs763741833 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74276346 | CTCACAGTGGTGTTC[C/T]TCACGCCTCTGGGAC | 64446 |
rs763748297 | snp | A/G | 1.67295e-05 | 0.00289214 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282040 | GGCCTGTCAGGTGTG[A/G]CCAGGCAGGGCGGCC | 64446 |
rs763777128 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74298357 | TTGCCCAGGCTGGAG[G/T]GCAATGGCATGATCT | 64446 |
rs763825658 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74289055 | TCCCAGCACAGCAAG[-/A]AAAGAACTCTTTTCT | 64446 |
rs763838321 | snp | G/T | 1.66715e-05 | 0.00288712 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299698 | CCCTTCCACTCCTTC[G/T]TCATCTCCTTCCTCA | 64446 |
rs763897321 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299277 | TAGCAGAGAGATTCA[C/T]CTAAATGGAGTCTTT | 64446 |
rs763978870 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304924 | GCCAAATGCATCGAG[C/G]ACACAGTGGTGCTCT | 64446 |
rs763997928 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291109 | TCCCACGTACTCCTG[A/G]GTGGCTGCTACAATG | 64446 |
rs764044215 | snp | A/C | 1.64781e-05 | 0.00287033 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301043 | CGCCCCTCCTCCCAC[A/C]AGGTCATGTGGTGGG | 64446 |
rs764071733 | snp | C/T | 0.000189197 | 0.00972433 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307333 | TGGGTCTCCCTTGTC[C/T]TCCTCCTGCATAAGG | 64446 |
rs764106899 | in-del | -/GAG | 1.67216e-05 | 0.00289145 | cds-indel, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312111 | GAGGAGCAGACCGAT[-/GAG]GAGCTGGCCGTAGAC | 64446 |
rs764225804 | snp | A/G/T | 0.000100645 | 0.00709319 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285196 | GCCATCATGCAGCTC[A/G/T]GCTCTGTAAGGCTTC | 64446 |
rs764283914 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74282101 | CTTGTCCACCTGAAA[C/G]CCAGTTAGAGTAGAC | 64446 |
rs764299201 | in-del | -/A | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273465 | GCTGTAAAAATCCCC[-/A]GCTTTGCCGGGCGCG | 64446 |
rs764313765 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74281601 | AACTGCAATAACTAA[A/G]CAGGGTAATGCTTAG | 64446 |
rs764316301 | snp | G/T | 0.000189142 | 0.00972291 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281774 | AAGGGGCCGGTGGGG[G/T]CCCTCACCCCACACC | 64446 |
rs764371131 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74310886 | TTATTTTATTTTACT[C/T]CATTTTGAGACAGGG | 64446 |
rs764381446 | snp | C/T | 3.30224e-05 | 0.00406326 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281838 | GATTGTGTACGTGTA[C/T]GTCAAGAAGCGCAGC | 64446 |
rs764393327 | snp | C/G | 1.68437e-05 | 0.00290199 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299885 | CAGACACTGGAGAGA[C/G]GAGGGAAGGGAGGGG | 64446 |
rs764396055 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301788 | ACCCCCCCCACCGCC[C/G]GCCCAGTCTTTACCA | 64446 |
rs764398483 | snp | G/T | 1.85043e-05 | 0.00304168 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312268 | GGTGGGTTGGGGACT[G/T]GGCGGGACACATGGC | 64446 |
rs764405714 | in-del | -/CA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285958 | ATATACACACACACA[-/CA]TATATATATATAGAG | 64446 |
rs764429251 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301286 | CAGCCCAGGGAGGCC[-/A]CCCTCACTGCAGCCA | 64446 |
rs764446872 | snp | C/G | 1.6888e-05 | 0.00290581 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309422 | CTTGTGCATCCAGGT[C/G]CTCAGGGAGCCAGGT | 64446 |
rs764463332 | snp | A/G | 1.64958e-05 | 0.00287187 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314084 | GAAGGCCTGTCCCCT[A/G]CCAACACCAACACTT | 64446 |
rs764602033 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303004 | GCTTTCTAGGCCAAG[C/T]GCTAGACATGCAGCC | 64446 |
rs764732760 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74276159 | TTTCCCTTAAGCCAC[C/T]GGAGGTTCTCTCCAG | 64446 |
rs764771316 | snp | C/T | 4.94319e-05 | 0.00497127 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305376 | CGAAGAACTTCCTGA[C/T]GGTTGGCGACTGGAC | 64446 |
rs764812763 | snp | C/T | 1.66043e-05 | 0.00288129 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285174 | GAAAGATGAGAACTA[C/T]GTTAACGCCATCATG | 64446 |
rs764886751 | in-del | -/CTC | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293287 | TTGAATTGTCTATTT[-/CTC]CTTCAATTTTGTCAG | 64446 |
rs764971993 | in-del | -/A | 4.8129e-05 | 0.00490532 | frameshift-variant, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312205 | AGAAGAAGGAGGCAG[-/A]CGCCATAAAGCTGAC | 64446 |
rs764983344 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307335 | GGTCTCCCTTGTCCT[C/T]CTCCTGCATAAGGTT | 64446 |
rs765028301 | snp | A/G | 1.65946e-05 | 0.00288046 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310084 | TCGCCTGCGGCTCCC[A/G]GCTGGGGACAACCAC | 64446 |
rs765051692 | in-del | -/TAAC | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278877 | TTGTACATTTAAAAA[-/TAAC]TAACAGGCCGGGCGC | 64446 |
rs765101863 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296213 | AGCACAGTGGCTCAC[A/G]TCTGTAATCCTAACA | 64446 |
rs765144359 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283681 | GGCAGAGGCGAGAGG[A/T]TCACTTCCGCTCAGG | 64446 |
rs765154352 | snp | C/T | 1.66322e-05 | 0.00288371 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299723 | TCCTCACCAGCCTGC[C/T]GGGACACCCGAAAGG | 64446 |
rs765165851 | in-del | -/TG | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287505 | TCATCCCACAGGTTG[-/TG]TGTGTGTGTGTGTGT | 64446 |
rs765191292 | snp | A/C | 1.66382e-05 | 0.00288424 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74287069 | AGTGATGGAGGAGGA[A/C]CCTTCAGCTAAAACC | 64446 |
rs765197781 | snp | C/T | 1.65682e-05 | 0.00287817 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299790 | GCCACCGAGACCCTG[C/T]GTATGGCACCATCTG | 64446 |
rs765198335 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74282632 | AGGGAGCAGAGATTC[A/G]TATCTACAGGCAACT | 64446 |
rs765285682 | snp | A/G | 3.30524e-05 | 0.00406511 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309329 | ACCACCAGGATGGAC[A/G]GAACCCTGGATATCT | 64446 |
rs765353102 | snp | C/G | 1.6477e-05 | 0.00287024 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301147 | CTTGGGGGCCATCTC[C/G]CTGGAGTTCGAATCT | 64446 |
rs765390052 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305864 | TTTAGTAGAGATGGG[A/T]TTTTGCCACGTTGGC | 64446 |
rs765446000 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294611 | GTGAGCCACCACACT[C/T]AACTTAAGCTATTGA | 64446 |
rs765468248 | snp | C/T | 0.000247115 | 0.0111129 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286963 | GCGGAGAACTTCCAA[C/T]GTGTCCCCCCTAGAT | 64446 |
rs765512257 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280250 | GAAACCCTTCCTTGC[A/G]TGGCCTGTGAACCCC | 64446 |
rs765565303 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74281439 | AATTTTTGTATTTTT[A/G]CAGAGATGGGGTTTC | 64446 |
rs765616599 | snp | A/G | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314185 | CAGCGGGGGAAGAAG[A/G]GGATGAAGAAGTGGA | 64446 |
rs765740532 | in-del | -/GCAACACCAACA | 1.64931e-05 | 0.00287163 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314108 | ACACTTCTGTGCTGT[-/GCAACACCAACA]CTTCCCCTGCAGCAG | 64446 |
rs765760420 | snp | A/C/T | 3.48058e-05 | 0.00417156 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311999 | TCTGTCCCTGGGTGC[A/C/T]CAGATGTTTGAGCGT | 64446 |
rs765777768 | snp | C/T | 0.000494715 | 0.0157198 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314100 | CCAACACCAACACTT[C/T]TGTGCTGTCTTCCCC | 64446 |
rs765830821 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300757 | TGGGGAGTCTTGGCA[C/T]ATACCGATTCTTGGC | 64446 |
rs765870884 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291073 | TCTCCACTCGTGACG[C/T]TGGAGTTCAACCCCA | 64446 |
rs765895624 | snp | A/C/G | 4.94412e-05 | 0.00497178 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314224 | TAGCCTAGAAGTCAG[A/C/G]CTTCGACTGCGGCGC | 64446 |
rs765902505 | snp | A/C/G/T | 9.89527e-05 | 0.00703342 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290985 | TGTCCTTTTCTTTCC[A/C/G/T]GGCCTGGTGGGGATA | 64446 |
rs765922331 | snp | G/T | 6.59337e-05 | 0.0057413 | intron-variant | DNAI2 | GRCh38.p7 | 17:74290997 | TCCGGGCCTGGTGGG[G/T]ATAATTTTTTTGTGC | 64446 |
rs765949899 | snp | A/G | 1.64933e-05 | 0.00287165 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281861 | AGCGCAGCGAGTTCG[A/G]GAAGCAGTGCAATTT | 64446 |
rs766029339 | snp | A/G | 1.81622e-05 | 0.00301343 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305452 | GACCAAGTAAGAGGC[A/G]ATGCTGGGGACAGGA | 64446 |
rs766074098 | in-del | -/GTGGAGGAAGGATG | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273831 | TCTTTATTACAGAAA[-/GTGGAGGAAGGATG]GTAGCAGAGGGGAGG | 64446 |
rs766111224 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74288404 | TCAGATGTAGCCAAC[A/T]TCATTAGATAAGGAG | 64446 |
rs766139796 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305300 | TCAGCTGAAAAGATT[A/G]TGTGCACCTTCCCGG | 64446 |
rs766189697 | snp | C/G | 3.53363e-05 | 0.0042032 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310175 | TTCCGTAAGCACCGG[C/G]TGCCTGGGGAAAATC | 64446 |
rs766323256 | snp | G/T | 4.20867e-05 | 0.00458711 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281714 | TTCCTGCCCCAACCA[G/T]ATTGAGAACCTGGAG | 64446 |
rs766478158 | snp | A/G | 1.67964e-05 | 0.00289792 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299875 | ACCCACCAGCCAGAC[A/G]CTGGAGAGAGGAGGG | 64446 |
rs766478722 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303246 | AACCCAGGGCTCCAA[C/T]TCTGAGGCCCAGAGT | 64446 |
rs766488460 | snp | A/C/G | 0.000240183 | 0.010956 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281676 | TCTGGACAAATTCCT[A/C/G]GGATCTCCCCACCAC | 64446 |
rs766506690 | snp | G/T | 7.16653e-05 | 0.00598561 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312257 | GACAGGGGTTGGGTG[G/T]GTTGGGGACTGGGCG | 64446 |
rs766512138 | snp | C/T | | | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313873 | GGAGCTAGCCCGAGG[C/T]CTCCCAGTCTGCATG | 64446 |
rs766529645 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293940 | AGGTGCATGCCACCA[C/T]GCCCAGCTAATTTTT | 64446 |
rs766594026 | snp | C/T | 7.20141e-05 | 0.00600016 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281617 | CAGGGTAATGCTTAG[C/T]ATATAGTCGGCACTC | 64446 |
rs766594632 | snp | C/T | 3.3896e-05 | 0.00411666 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312179 | CTTCGACATCATCTT[C/T]GCAGAGCTGAAGAAG | 64446 |
rs766630155 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278891 | ATAACTAACAGGCCG[G/T]GCGCGGTGGCTCACG | 64446 |
rs766644122 | snp | C/T | 5.02306e-05 | 0.00501127 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74287083 | ACCCTTCAGCTAAAA[C/T]CATCAATGTGTTCAG | 64446 |
rs766652341 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74291412 | CAGGTGATTCACCCA[C/T]CTGGGCCTCCCAAAG | 64446 |
rs766662586 | snp | A/G | 1.64803e-05 | 0.00287052 | splice-donor-variant | DNAI2 | GRCh38.p7 | 17:74301169 | TTCGAATCTACTTTG[A/G]TGAGTGTCCCTTGCT | 64446 |
rs766670224 | snp | G/T | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273132 | ATTCAGGCACCAGTA[G/T]CTCTGGACGGGGGCT | 64446 |
rs766750403 | snp | C/G | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301080 | GAAAGATGAGCGAGC[C/G]CACTGAAGTTGTGAT | 64446 |
rs766833504 | snp | C/T | 4.94466e-05 | 0.00497201 | utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314263 | TGTGCCTTCCTTTCC[C/T]ACCTCTTGGTATTGC | 64446 |
rs766867824 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279869 | TTGGTTGTAAATCTA[C/T]CAAGGCAAGCTCTCC | 64446 |
rs766870839 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74311396 | AGGCGGGCAGATCAC[C/T]TGAGGTCGGGAGTTC | 64446 |
rs766992890 | snp | C/G | 0.000156348 | 0.00884022 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309975 | ACACACATAACTTTG[C/G]TCCTCTCTCCTCTAC | 64446 |
rs767000824 | snp | C/G | 1.66707e-05 | 0.00288705 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282034 | GGCCCTGGCCTGTCA[C/G]GTGTGGCCAGGCAGG | 64446 |
rs767015710 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299311 | CGTGCTTTTCCCTAC[A/G]TTAGGGACTCGGCTC | 64446 |
rs767036995 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74310570 | TTGAGACAAAGTCAC[C/G]CTCTGTTGCCCAGGC | 64446 |
rs767042349 | snp | C/T | 1.64933e-05 | 0.00287165 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281947 | GAGCAGTTCGTGGAG[C/T]GGAACCCAGTGGACA | 64446 |
rs767170365 | snp | C/T | 1.66985e-05 | 0.00288946 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299683 | AAGGAAGCCTGTGCC[C/T]CCTTCCACTCCTTCT | 64446 |
rs767182928 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299512 | GAGGGGCTCAAGGAA[C/T]TGAATGAAGCTTGCA | 64446 |
rs767299549 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285875 | GGTGGACATTTGCAA[G/T]AAAGGGGAGGGCATT | 64446 |
rs767324607 | snp | A/G | 6.68371e-05 | 0.00578049 | synonymous-codon, nc-transcript-variant, intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312083 | GGAGAAGGGTAAGGC[A/G]GAGGGCAGGGATGAG | 64446 |
rs767336743 | in-del | -/T | 0.0126045 | 0.0783798 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281637 | AGTCGGCACTCAGGA[-/T]TTTTTTTTAATGCGG | 64446 |
rs767397736 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293339 | AAGGCTATGTTATTA[C/G]GTACATGCACATGCT | 64446 |
rs767421180 | snp | A/C | | | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74315118 | ACTGTGGGCCAGGTG[A/C]TGTGCAGGCCTCTCG | 64446 |
rs767482061 | snp | A/G | 1.7009e-05 | 0.0029162 | missense, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312013 | CCCAGATGTTTGAGC[A/G]TGAGACCCGGCGAGA | 64446 |
rs767524146 | in-del | -/T | 1.71832e-05 | 0.00293109 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291165 | GCTTTTTTATTTTTA[-/T]TTTTATTTTTTTTAG | 64446 |
rs767546069 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305937 | TCGGCCTCCCAAAGC[A/G]TTGGGATTACAGGTG | 64446 |
rs767678940 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74282499 | AGAGATGAGGTTTTG[A/C]CATGTTGCCCAGGCT | 64446 |
rs767717463 | snp | A/G | 1.71605e-05 | 0.00292915 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281767 | GATAGGGAAGGGGCC[A/G]GTGGGGTCCCTCACC | 64446 |
rs767757416 | snp | A/G | 6.46405e-05 | 0.00568472 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312191 | CTTCGCAGAGCTGAA[A/G]AAGAAGGAGGCAGAC | 64446 |
rs767770535 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303125 | TTGTGCAGTCGCCTA[C/T]AACCATCTCGTGGGG | 64446 |
rs767825543 | snp | A/C | 1.65386e-05 | 0.00287559 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289574 | ATCCAGCCTTCTGCT[A/C]TCTTCCCTCTCCCCT | 64446 |
rs767842125 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277316 | CTTGCACCCGGGAGA[C/T]GGAGTTTGCAATGAG | 64446 |
rs767895543 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304482 | GCCCAGAAGTTAAGA[C/T]AGAACAGTAAACAAG | 64446 |
rs767911321 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312923 | TGCCAAGATATGAAA[A/G]AGCCAAAGAGCAGCG | 64446 |
rs767957813 | in-del | -/ACCATGATGTGGTCT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309227 | GCCTCTGTCCCTCCA[-/ACCATGATGTGGTCT]ACCTCCCACAGGTAC | 64446 |
rs767996853 | snp | A/G | 0.000131774 | 0.00811601 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291100 | CCCAAAGATTCCCAC[A/G]TACTCCTGGGTGGCT | 64446 |
rs768061384 | in-del | -/AAGA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301803 | CGCCCAGTCTTTACC[-/AAGA]AAGAAAGAAAGAAAG | 64446 |
rs768125412 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278756 | TCCAGCATGGGTAAC[A/G]AAATGAGATTCCATC | 64446 |
rs768133910 | snp | A/C | 1.64814e-05 | 0.00287061 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301188 | GTGTCCCTTGCTGTC[A/C]CTTCCCCGACTTGCA | 64446 |
rs768177641 | in-del | -/T | | | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313377 | TCTCACACTGGGTAA[-/T]ACAGGTGGGGCAGAG | 64446 |
rs768194832 | snp | C/G | | | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305246 | ATGGTGGGGACCGAG[C/G]AGGGCATCGTCATCT | 64446 |
rs768263886 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290932 | CTGCCACCATGCCCC[C/T]GCTACCCACCCGCAG | 64446 |
rs768297659 | snp | A/G | 1.65351e-05 | 0.00287528 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309314 | CCGACCGTTTTCTTT[A/G]CCACCAGGATGGACG | 64446 |
rs768312326 | snp | A/G | 3.3145e-05 | 0.0040708 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299781 | TTGAGTCCAGCCACC[A/G]AGACCCTGTGTATGG | 64446 |
rs768386683 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278518 | AAACTGTTGTTCATA[A/G]TGCTTGCAACCTGGT | 64446 |
rs768428109 | snp | A/C/G | 3.73178e-05 | 0.00431946 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312279 | GACTGGGCGGGACAC[A/C/G]TGGCACTTGGGTTCT | 64446 |
rs768440178 | in-del | -/GTTTT/GTTTTG | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293780 | TACAAGTGAATCATA[-/GTTTT/GTTTTG]GTTTTGTTTTGTTTT | 64446 |
rs768459051 | snp | A/G | 6.02065e-05 | 0.00548631 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312246 | GTAGGGGCCTGGACA[A/G]GGGTTGGGTGGGTTG | 64446 |
rs768490008 | snp | C/T | 0.000131896 | 0.00811976 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305242 | GTTCATGGTGGGGAC[C/T]GAGCAGGGCATCGTC | 64446 |
rs768511171 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300302 | CACGGAACAGAATCT[A/G]AAGGGTGCAAAAAAG | 64446 |
rs768564105 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280749 | GTCCAACATCATCAC[A/C]ATCAATATTTCCTCC | 64446 |
rs768650926 | snp | C/T | 1.66651e-05 | 0.00288657 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289545 | AAAAAGGGGGAGAAA[C/T]TGGGGAACCTCACAT | 64446 |
rs768659914 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290152 | AAAACCCTGTCTCTA[C/T]TAAAAATACAAAAAT | 64446 |
rs768661714 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74298451 | CTGGGATTACAGGTG[C/T]CTGCCACCACGCCCA | 64446 |
rs768700575 | in-del | -/GG | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296321 | TTTAAAGAGAGAGAG[-/GG]AGAGAGAGAGAGGAG | 64446 |
rs768710986 | snp | A/G | 8.61809e-05 | 0.00656377 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281697 | TCCCCACCACCCCTT[A/G]CTTCCTGCCCCAACC | 64446 |
rs768739142 | snp | A/T | 3.08038e-05 | 0.00392441 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309496 | GTGTGTGGCCAGGTG[A/T]GTTTGGGCCTCTGTG | 64446 |
rs768745055 | snp | A/T | 0.00188679 | 0.0306567 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309613 | TGGTAGCACAACAGA[A/T]CCACCTGGGGGAAAT | 64446 |
rs768747332 | snp | C/T | 1.64874e-05 | 0.00287113 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281904 | GGCCGAGCTGAACAT[C/T]GACATCATGCCCAAC | 64446 |
rs768765890 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291064 | AAGCCATCGTCTCCA[C/G]TCGTGACGTTGGAGT | 64446 |
rs768934586 | snp | A/G | 1.64844e-05 | 0.00287087 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314177 | AGAGGAAGCAGCGGG[A/G]GAAGAAGGGGATGAA | 64446 |
rs768937776 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307940 | GTAGCTGGGATTACA[A/G]GCGCCCACCAACACC | 64446 |
rs768937889 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295809 | AAAGTCTGTATTCCC[C/T]GTCACGTGTGACCAC | 64446 |
rs768984356 | snp | C/T | | | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313736 | GTGGTCACAAAGTAC[C/T]GCGTGGTACTGAAGC | 64446 |
rs768987800 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287387 | ACAAGTACCAAGCAT[G/T]AGCAGCTAGCAGCAC | 64446 |
rs769016733 | snp | C/G | 1.65622e-05 | 0.00287764 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289785 | GGCTGAGGGCTGGGA[C/G]CAGCACAAGTGGAGG | 64446 |
rs769025367 | in-del | -/AGAT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285995 | GAGAGAGAGAGAGAG[-/AGAT]TAATAATTTTATTTG | 64446 |
rs769047787 | snp | A/G | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272513 | CCGAGAAACTGGTGC[A/G]AGCCAGAACGGATCA | 64446 |
rs769092464 | snp | C/G | | | intron-variant, nc-transcript-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312729 | TAAAGCACTTTCTAG[C/G]TGTATCACCTGAGCT | 64446 |
rs769115235 | snp | A/G | 5.02567e-05 | 0.00501257 | missense, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312052 | TGGAGGCCAGGCACC[A/G]GGAGATGCGGCTGAA | 64446 |
rs769127427 | in-del | -/TGT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306818 | GACAGAGTTTCCCCA[-/TGT]TGTTGGCCAGGCTGG | 64446 |
rs769157248 | snp | A/G | 1.72036e-05 | 0.00293283 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285226 | CCTCCTGCCCCAGCT[A/G]CAAGAGCCCCATCCA | 64446 |
rs769216291 | snp | A/T | | | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314367 | TGACTCCCCAGCCCC[A/T]ACAAATCACTAGCCC | 64446 |
rs769251936 | in-del | -/G | 3.29783e-05 | 0.00406055 | frameshift-variant, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285105 | GGGGGGCTGGCCCAA[-/G]GACGTGAACCCCCTG | 64446 |
rs769348811 | snp | C/G | 3.83443e-05 | 0.00437843 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311979 | CCTCTCCCCACCGGG[C/G]TCTCTCTGTCCCTGG | 64446 |
rs769434290 | snp | A/G | 1.67304e-05 | 0.00289222 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299852 | TCAGCTTCCACGGAT[A/G]GGCAGGTACCCACCA | 64446 |
rs769450965 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302862 | GGCAACCCTAGCTCA[A/G]GGCTGAGAGATGAAT | 64446 |
rs769486647 | snp | A/C | 1.89252e-05 | 0.00307608 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285234 | CCCAGCTGCAAGAGC[A/C]CCATCCATCACTGCA | 64446 |
rs769520010 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314830 | TGTTCTGCTGCACCT[A/G]AATGCTTTCTGTTAT | 64446 |
rs769602136 | snp | A/G | 1.65891e-05 | 0.00287998 | utr-variant-5-prime, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281812 | TGCCCCCCAGCAGCC[A/G]GCACCATGGAGATTG | 64446 |
rs769629471 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290728 | TTAGTATCAAAACCT[C/T]GTTTCACACCAAACC | 64446 |
rs769668300 | snp | C/T | 2.0248e-05 | 0.00318176 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309455 | CGGCGTGGGTGTGAG[C/T]GTGGGGTGCTGTGAG | 64446 |
rs769707610 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295289 | CACCTGCAATCTCAG[C/G]TACTTGGGAGGCTGA | 64446 |
rs769723839 | snp | A/G | 1.65102e-05 | 0.00287312 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289761 | AGCGGGGTCCTGGTG[A/G]CCTGGGAGGGCTGAG | 64446 |
rs769735489 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287799 | GTCTCTACTAAAAAT[A/C]CAAAAATTAACTGGG | 64446 |
rs769780034 | snp | G/T | 8.72014e-05 | 0.00660251 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281761 | TGTGGAGATAGGGAA[G/T]GGGCCGGTGGGGTCC | 64446 |
rs769832640 | snp | A/G | 1.65121e-05 | 0.00287329 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309394 | CAGCTTGAAGGTCAC[A/G]CGCATGTCCCTCCTT | 64446 |
rs769833556 | in-del | -/CAA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275893 | ACACTGTCCCAAAAG[-/CAA]CAACAACAAAGAAAG | 64446 |
rs769837167 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299124 | AAACGAAATCTAACA[G/T]GACAAAGGACAGATA | 64446 |
rs769862483 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275586 | AAAAATTCTGGCCGG[A/G]TGCAGTGGCTCACGC | 64446 |
rs769876141 | snp | A/G | 1.64836e-05 | 0.0028708 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301207 | CCCCGACTTGCATTG[A/G]CAGGGCAGCCAGGGC | 64446 |
rs769890379 | snp | C/T | | | intron-variant, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74274862 | GCGTTCTCGTGTGAT[C/T]GAGGTCATACAGTTG | 64446 |
rs769978898 | snp | A/G | 3.32071e-05 | 0.00407461 | intron-variant, missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310027 | AATAGGTGTGTGACG[A/G]GGCCCTCTTCTGCCT | 64446 |
rs770064644 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303673 | TCTTGGCTCGCTGCA[A/T]CCTCTGCCTCCCAGG | 64446 |
rs770094044 | in-del | -/T | 1.64808e-05 | 0.00287057 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291002 | GCCTGGTGGGGATAA[-/T]TTTTTTGTGCTTTAT | 64446 |
rs770216013 | in-del | -/GGCATGAGCCACTGTGCCCAGCGTG | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74282578 | AGTGCTGGGAATACA[-/GGCATGAGCCACTGTGCCCAGCGTG]GGAGAGATATTCTGA | 64446 |
rs770232269 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74291169 | TTTTATTTTTATTTT[A/T]ATTTTTTTTAGATGG | 64446 |
rs770281851 | in-del | -/AGG | 0.00130439 | 0.0255048 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307233 | CCAGGGCTGTGTGAA[-/AGG]AGCAGGGTGTCGAGC | 64446 |
rs770299534 | snp | A/G | 0.00018558 | 0.00963098 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307279 | GCCTTTCGCAGGGCT[A/G]GTTCCTAGAGGGACT | 64446 |
rs770302178 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283125 | TTTTGTGAGAGCTGG[C/T]TTAAAAATGGAAAGG | 64446 |
rs770479962 | snp | A/G | 1.72101e-05 | 0.00293338 | stop-gained, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305437 | ATCGTCCATCATGTG[A/G]ACCAAGTAAGAGGCG | 64446 |
rs770547622 | snp | C/T | 0.000117344 | 0.00765888 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312136 | CCGTAGACCTGGAGG[C/T]GCTGGTCAGCAAGGC | 64446 |
rs770550979 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301433 | AACACAGAGGGCAAT[A/C]TTTTGACAGAACAAT | 64446 |
rs770578810 | snp | A/C | 1.64784e-05 | 0.00287035 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286936 | GGCAATCTGAAAGGA[A/C]CTCCATTTACTGCGG | 64446 |
rs770587936 | snp | C/T | | | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311794 | CCATGCTCCTTGGCA[C/T]TGAGTAACTCAGTGT | 64446 |
rs770624431 | snp | C/T | 4.95266e-05 | 0.00497603 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74287039 | AGAGTATTTCAATGA[C/T]GAGGAGGCCATGGAA | 64446 |
rs770868052 | in-del | -/TTTG | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306611 | ATCTTGGGAGGAGTT[-/TTTG]TTTGTTTGTTAAAAT | 64446 |
rs770916646 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278065 | GCTTTAGAGCCAGAC[A/G]TGCCTGGTGGTTCTG | 64446 |
rs770946088 | snp | A/C | 6.59087e-05 | 0.00574021 | stop-gained, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289672 | GTTGGCAGTGGCATA[A/C]TCCTGCTTGGATTTT | 64446 |
rs770962187 | snp | C/T | 1.96439e-05 | 0.00313393 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309557 | TTGCTTTTGAGCGTG[C/T]GCTCCTACAAAGGTT | 64446 |
rs771002059 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314819 | ACGAGCTTGGCTGTT[C/T]TGCTGCACCTGAATG | 64446 |
rs771017771 | in-del | -/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293171 | TGTCTGGGAGGTCTT[-/G]TCTATAGTGTTGGTC | 64446 |
rs771020484 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74286769 | TATATCTGTTCATGC[A/G]CTGCATGTATTTCCA | 64446 |
rs771046755 | in-del | -/T | 3.32962e-05 | 0.00408007 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291151 | AGGAGGGACCTAGGC[-/T]TTTTTTATTTTTATT | 64446 |
rs771052029 | snp | C/G | 0.000689805 | 0.0185587 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309481 | GTGAGCACGTGTGCA[C/G]TGTGTGGCCAGGTGT | 64446 |
rs771114555 | snp | G/T | 1.66341e-05 | 0.00288388 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310120 | TGGAGGTCTCGCCTG[G/T]GCTCTCTACCCTCCA | 64446 |
rs771179084 | in-del | -/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74288490 | ATGTATGTTTACATG[-/C]CTGATGTGAGGAGAA | 64446 |
rs771188981 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74281447 | TATTTTTGCAGAGAT[A/G]GGGTTTCACCATGTT | 64446 |
rs771197484 | snp | A/T | 3.33522e-05 | 0.0040835 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305173 | CCGCTAATCCCAGAA[A/T]TGATGGTTCGTGGAG | 64446 |
rs771227104 | in-del | -/AG | 1.69818e-05 | 0.00291387 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309426 | TGCATCCAGGTCCTC[-/AG]GGAGCCAGGTCCCGG | 64446 |
rs771260018 | snp | C/T | 1.65979e-05 | 0.00288074 | intron-variant, missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310041 | GAGGCCCTCTTCTGC[C/T]TCCGGGTGCAGGACA | 64446 |
rs771289946 | in-del | -/AA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277386 | CGAGAATCCATCTCA[-/AA]AAAAAAAAAAAAAAG | 64446 |
rs771351617 | snp | A/G | 1.79932e-05 | 0.00299938 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291179 | ATTTTTATTTTTTTT[A/G]GATGGAATTTTGCTC | 64446 |
rs771387611 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294411 | AACTCCTGGGCTCAA[A/G]CAATCCTCCCACCTC | 64446 |
rs771422068 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275508 | GGAGGATGGATCACT[C/T]GAGGTCAGGAGTTTG | 64446 |
rs771449338 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279787 | ACCGGCCTCGGCCAC[A/C]CAAAGTGCTGGGATT | 64446 |
rs771468802 | snp | C/T | 1.65943e-05 | 0.00288043 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285023 | TGACGTCTTCCCTCC[C/T]GCGGCTCTCTGTTTA | 64446 |
rs771487732 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280948 | CAAAACTTAGCCAGG[A/C]ATGGTACTGCACACC | 64446 |
rs771491107 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304031 | GGAGGCTGAGGTGGG[A/T]GTACTGCTTGAGCCC | 64446 |
rs771564902 | snp | G/T | 1.66156e-05 | 0.00288228 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282020 | GTCCCTGCCCCAAGG[G/T]CCCTGGCCTGTCAGG | 64446 |
rs771686170 | snp | C/G/T | 8.27378e-05 | 0.00643143 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309304 | CCCCGTGAGGCCGAC[C/G/T]GTTTTCTTTACCACC | 64446 |
rs771690910 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74311559 | CAGAGGTTGTGGTGA[A/G]CCGAGATCGTGCCAT | 64446 |
rs771705785 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280849 | CCCAGCACTTTGGGA[A/G]GCTGAGGCAGGTGGA | 64446 |
rs771773999 | snp | A/T | 0.000252302 | 0.0112289 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307312 | GTGGACCTGTGTCGT[A/T]GAACCTGGGTCTCCC | 64446 |
rs771788368 | snp | A/G | 1.67722e-05 | 0.00289583 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312144 | CTGGAGGCGCTGGTC[A/G]GCAAGGCCGAGGAGG | 64446 |
rs771816059 | snp | A/C | 3.22846e-05 | 0.00401762 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312224 | CATAAAGCTGACGCC[A/C]GTGCCTGTAGGGGCC | 64446 |
rs771835572 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275416 | CGGAATTCCAGAAGG[C/T]GCACAAGGACATAAG | 64446 |
rs771837155 | snp | A/T | 0.000123508 | 0.0078574 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281753 | GCAGGACCTGTGGAG[A/T]TAGGGAAGGGGCCGG | 64446 |
rs771881864 | snp | C/T | 3.36361e-05 | 0.00410084 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281684 | AATTCCTAGGATCTC[C/T]CCACCACCCCTTGCT | 64446 |
rs771908966 | snp | A/G | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273433 | CACAGTACATTTCGT[A/G]CCAATCACCCAGCTA | 64446 |
rs771919830 | snp | G/T | 1.6623e-05 | 0.00288292 | intron-variant, missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310020 | CCCCTTCAATAGGTG[G/T]GTGACGAGGCCCTCT | 64446 |
rs771991249 | in-del | -/T | 1.72792e-05 | 0.00293927 | splice-donor-variant | DNAI2 | GRCh38.p7 | 17:74310164 | ACGTAGCCTCTTCCG[-/T]TAAGCACCGGGTGCC | 64446 |
rs772007265 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74289290 | TTAGCACTTTGGGAG[G/T]CCCAGGTGGGCATAT | 64446 |
rs772061154 | snp | C/G | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301132 | ACAGTTGGAAAATGC[C/G]TTGGGGGCCATCTCC | 64446 |
rs772064890 | snp | C/G | 1.64985e-05 | 0.0028721 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314077 | GAGTGGGGAAGGCCT[C/G]TCCCCTACCAACACC | 64446 |
rs772122568 | snp | C/G | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314165 | GGTGGAGGAGGGAGA[C/G]GAAGCAGCGGGGGAA | 64446 |
rs772133192 | snp | G/T | 1.65463e-05 | 0.00287626 | stop-gained, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74287052 | GACGAGGAGGCCATG[G/T]AAGTGATGGAGGAGG | 64446 |
rs772185024 | snp | C/T | 3.30518e-05 | 0.00406507 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281828 | GCACCATGGAGATTG[C/T]GTACGTGTACGTCAA | 64446 |
rs772201762 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305353 | CCTCCAGAGAAACCC[C/T]TTCTACCCGAAGAAC | 64446 |
rs772245017 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291040 | CCCAACAAGCCTGAA[C/T]TTGCTCTGAAGCCAT | 64446 |
rs772285592 | snp | C/T | 2.00805e-05 | 0.00316857 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311974 | CCTGCCCTCTCCCCA[C/T]CGGGCTCTCTCTGTC | 64446 |
rs772377822 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283399 | GATGCTTGAGGCCAC[A/G]AGTTTGAGACCAGCC | 64446 |
rs772386014 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299064 | TTCCTAGAAACAGCT[C/T]TGAGTGACAGGGTGA | 64446 |
rs772452083 | snp | A/G | | | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314535 | CCTGGATGTCTCCTG[A/G]GATTCAGCTTCTCAC | 64446 |
rs772460661 | snp | C/T | 1.65416e-05 | 0.00287586 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285047 | CTGTTTAGGCCAACT[C/T]AGAGCGGTTTGAGAT | 64446 |
rs772477561 | snp | C/T | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272784 | GCCTCTCTTGGGACC[C/T]CCCACAGACTGGCCC | 64446 |
rs772574421 | snp | A/G/T | 4.99649e-05 | 0.00499804 | synonymous-codon, missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299830 | GAAGACGGGCACCGA[A/G/T]TGCTTCTCAGCTTCC | 64446 |
rs772610746 | snp | A/G | 3.33996e-05 | 0.0040864 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310138 | TCTCTACCCTCCAGA[A/G]GAATGAGAAGAACGT | 64446 |
rs772618588 | snp | G/T | 1.64988e-05 | 0.00287213 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285142 | GAGCAGACCATCCGT[G/T]TCCGGAAGAAAGTGG | 64446 |
rs772659542 | in-del | -/AAT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74281592 | TCAGAGAGCAACTGC[-/AAT]AACTAAACAGGGTAA | 64446 |
rs772697427 | snp | C/G | 1.78334e-05 | 0.00298603 | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311991 | GGGCTCTCTCTGTCC[C/G]TGGGTGCCCAGATGT | 64446 |
rs772788448 | snp | G/T | 1.67444e-05 | 0.00289343 | missense, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312056 | GGCCAGGCACCGGGA[G/T]ATGCGGCTGAAGGAG | 64446 |
rs772938951 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287253 | ATAAGTCACCCAGCA[A/G]AGAAGTGGCCCTGCT | 64446 |
rs773014105 | snp | A/C | 0.000444997 | 0.0149098 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301213 | CTTGCATTGACAGGG[A/C]AGCCAGGGCTAAAGA | 64446 |
rs773061334 | snp | C/T | 0.000150914 | 0.0086853 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299861 | ACGGATGGGCAGGTA[C/T]CCACCAGCCAGACAC | 64446 |
rs773246494 | in-del | -/GAGA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296381 | AAGGAGGGAGGGAGG[-/GAGA]GAGAGAGAGAGAGAG | 64446 |
rs773347706 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299113 | TGGGAAAATGGAAAC[A/G]AAATCTAACAGGACA | 64446 |
rs773370913 | snp | C/T | 3.31978e-05 | 0.00407404 | intron-variant, synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310037 | TGACGAGGCCCTCTT[C/T]TGCCTCCGGGTGCAG | 64446 |
rs773375327 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278739 | CAGATATGCCACTCC[A/T]CTCCAGCATGGGTAA | 64446 |
rs773403780 | snp | A/G | | | downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314931 | AGAGCCTGTCACGTT[A/G]TCTCGTGTAACTCAT | 64446 |
rs773403879 | snp | A/C | | | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74313862 | GAGACTCAGGAGGAG[A/C]TAGCCCGAGGCCTCC | 64446 |
rs773412901 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314668 | TTTCTCCTCCATGAT[C/T]GACCCTCCTCGTCCA | 64446 |
rs773436223 | in-del | -/C | 3.29473e-05 | 0.00405864 | frameshift-variant, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291024 | GTGCTTTATAGAAAA[-/C]CCCAACAAGCCTGAA | 64446 |
rs773502918 | snp | G/T | 1.6483e-05 | 0.00287076 | utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314255 | TATCCCTGTGTGCCT[G/T]CCTTTCCCACCTCTT | 64446 |
rs773528349 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74304503 | AGTAAACAAGGAAGG[A/G]CATTGCGTGATGGAG | 64446 |
rs773532437 | snp | G/T | 4.29581e-05 | 0.00463435 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309621 | CAACAGAACCACCTG[G/T]GGGAAATTTAAAAAG | 64446 |
rs773555176 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285006 | TTGGGAGTATACCAG[A/G]GTGACGTCTTCCCTC | 64446 |
rs773581570 | snp | C/G | | | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305394 | TTGGCGACTGGACAG[C/G]CCGCATTTGGTCTGA | 64446 |
rs773606391 | snp | C/T | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272897 | CGCAAAATGCCTTTC[C/T]TCCATGACGACTGCC | 64446 |
rs773657423 | snp | C/T | 1.6571e-05 | 0.0028784 | intron-variant | DNAI2 | GRCh38.p7 | 17:74282008 | AACACGAGGTGGGTC[C/T]CTGCCCCAAGGGCCC | 64446 |
rs773733869 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291083 | TGACGTTGGAGTTCA[A/G]CCCCAAAGATTCCCA | 64446 |
rs773735578 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74291958 | AGCCTCCACCTCTCG[A/G]ATTCAAGTGATTCTC | 64446 |
rs773817933 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279792 | CCTCGGCCACCCAAA[C/G]TGCTGGGATTATAGG | 64446 |
rs773823632 | snp | A/G | 0.00012693 | 0.00796549 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305485 | GGATGCAGGAGACAG[A/G]AGGGGATGGAGGGAG | 64446 |
rs773850046 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309192 | AGAAGGGACCAAGTG[A/G]GCCAAGCTGTGGCTC | 64446 |
rs773861763 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301978 | GAAAGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA | 64446 |
rs773866945 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290945 | CCCGCTACCCACCCG[C/T]AGAAGGGGTGAAACT | 64446 |
rs773911235 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301495 | ACGCCCAGGACCAAC[A/C]TCGGGAGGCCTGGAC | 64446 |
rs774066246 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287728 | GGGAGGCCAAGGCGG[G/T]TGCATCACCTGAGGT | 64446 |
rs774089922 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299294 | TAAATGGAGTCTTTC[A/C]ACGTGCTTTTCCCTA | 64446 |
rs774207817 | snp | A/T | | | intron-variant, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74274867 | CTCGTGTGATCGAGG[A/T]CATACAGTTGGTGAG | 64446 |
rs774323743 | snp | A/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301128 | AGGAACAGTTGGAAA[A/T]TGCCTTGGGGGCCAT | 64446 |
rs774441527 | snp | G/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289673 | TTGGCAGTGGCATAC[G/T]CCTGCTTGGATTTTC | 64446 |
rs774483437 | snp | C/T | 9.8912e-05 | 0.0070318 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301035 | CTCACTGTCGCCCCT[C/T]CTCCCACCAGGTCAT | 64446 |
rs774539792 | in-del | -/TTTTTA | 1.67393e-05 | 0.00289299 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291153 | GGAGGGACCTAGGCT[-/TTTTTA]TTTTTATTTTTATTT | 64446 |
rs774540628 | snp | C/T | 1.64958e-05 | 0.00287187 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314074 | GGGGAGTGGGGAAGG[C/T]CTGTCCCCTACCAAC | 64446 |
rs774547921 | in-del | -/CAA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277384 | AGCGAGAATCCATCT[-/CAA]AAAAAAAAAAAAAAA | 64446 |
rs774589483 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307942 | AGCTGGGATTACAGG[C/T]GCCCACCAACACCCC | 64446 |
rs774591252 | snp | A/G | 1.65938e-05 | 0.00288039 | intron-variant, missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310045 | CCCTCTTCTGCCTCC[A/G]GGTGCAGGACAATGG | 64446 |
rs774597549 | snp | C/T | 3.31851e-05 | 0.00407326 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285025 | ACGTCTTCCCTCCTG[C/T]GGCTCTCTGTTTAGG | 64446 |
rs774602317 | snp | C/G/T | 6.59048e-05 | 0.00574009 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305270 | GTCATCTCCTGCAAC[C/G/T]GCAAGGCCAAGACGT | 64446 |
rs774612838 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74293941 | GGTGCATGCCACCAC[A/G]CCCAGCTAATTTTTG | 64446 |
rs774626567 | snp | A/G/T | 6.31876e-05 | 0.00562055 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312258 | ACAGGGGTTGGGTGG[A/G/T]TTGGGGACTGGGCGG | 64446 |
rs774770773 | snp | C/T | 1.66402e-05 | 0.00288441 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310122 | GAGGTCTCGCCTGGG[C/T]TCTCTACCCTCCAGA | 64446 |
rs774858679 | snp | A/T | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272549 | GATTGGTGGCAGCAG[A/T]CATTTAGGTGCTTGT | 64446 |
rs774915500 | in-del | -/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74281546 | TACAGTTGTCAGCTA[-/C]CGCGCCTGGCCAAAA | 64446 |
rs775008914 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279374 | AAATGCTTGAGGGGA[A/T]GGATGGATACCCCAT | 64446 |
rs775110998 | snp | A/C/G | 3.31687e-05 | 0.00407228 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310071 | AATGGGTGTCTCATC[A/C/G]CCTGCGGCTCCCAGC | 64446 |
rs775147230 | snp | G/T | 0.000164163 | 0.0090584 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312226 | TAAAGCTGACGCCAG[G/T]GCCTGTAGGGGCCTG | 64446 |
rs775259526 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74299256 | ATAAGAGGAAATGGG[C/T]TAATGTAGCAGAGAG | 64446 |
rs775280929 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290781 | ATTATCACACACATA[C/T]GCACACCCCAATCCT | 64446 |
rs775320295 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308936 | GGTGTGGTGACGGGC[A/G]CCAGTAATCCCAGTT | 64446 |
rs775356868 | snp | A/C | 0.000108962 | 0.00738032 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281691 | AGGATCTCCCCACCA[A/C]CCCTTGCTTCCTGCC | 64446 |
rs775413109 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74298213 | CTGCTCCAAGAAGGG[C/T]CCCTCTAGGGCCATG | 64446 |
rs775429715 | snp | C/T | 2.5745e-05 | 0.00358773 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309482 | TGAGCACGTGTGCAG[C/T]GTGTGGCCAGGTGTG | 64446 |
rs775567813 | snp | G/T | 1.65233e-05 | 0.00287426 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281829 | CACCATGGAGATTGT[G/T]TACGTGTACGTCAAG | 64446 |
rs775577400 | in-del | -/C | | | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74311979 | CCTCTCCCCACCGGG[-/C]TCTCTCTGTCCCTGG | 64446 |
rs775610070 | snp | A/C | 1.65482e-05 | 0.00287643 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74287054 | CGAGGAGGCCATGGA[A/C]GTGATGGAGGAGGAC | 64446 |
rs775626346 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74310516 | TGTATTATATTATAT[A/T]GTATTTTAATTTAAT | 64446 |
rs775634372 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74298358 | TGCCCAGGCTGGAGT[A/G]CAATGGCATGATCTC | 64446 |
rs775644773 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309203 | AGTGAGCCAAGCTGT[C/G]GCTCAGAAGCCTCTG | 64446 |
rs775661857 | snp | A/G | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74273551 | GGTCAGGAGATCGAG[A/G]CCATCCTGGCTAACA | 64446 |
rs775665695 | in-del | -/AC | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285948 | ATGAGTGCCATATAC[-/AC]ACACACACACATATA | 64446 |
rs775671172 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295511 | CCTTTAGTTCTTTGA[A/T]CATGTTTAGCATAGC | 64446 |
rs775689647 | in-del | -/TC | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272496 | CCTAAGAGTTCTTTG[-/TC]CCGAGAAACTGGTGC | 64446 |
rs775726145 | snp | A/G | 3.29527e-05 | 0.00405898 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305275 | CTCCTGCAACCGCAA[A/G]GCCAAGACGTCAGCT | 64446 |
rs775727201 | snp | G/T | 0.00154593 | 0.0277592 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281769 | TAGGGAAGGGGCCGG[G/T]GGGGTCCCTCACCCC | 64446 |
rs775752356 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294659 | TGTATGTGATGAGTC[A/G]TTTTTCTCTTGCTGC | 64446 |
rs775769506 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306687 | CAATGGCGAGATCTC[A/G]GCTCACTGCAACCTC | 64446 |
rs775820806 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74307228 | GGCTGCCAGGGCTGT[A/G]TGAAAGGAGCAGGGT | 64446 |
rs775823680 | snp | A/C/G | 3.30771e-05 | 0.00406665 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289777 | CCTGGGAGGGCTGAG[A/C/G]GCTGGGACCAGCACA | 64446 |
rs775926673 | snp | A/G | 0.000577658 | 0.0169851 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285146 | AGACCATCCGTTTCC[A/G]GAAGAAAGTGGAGAA | 64446 |
rs776092482 | snp | C/G | 1.67354e-05 | 0.00289265 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310143 | ACCCTCCAGAGGAAT[C/G]AGAAGAACGTAGCCT | 64446 |
rs776150411 | snp | A/G | 1.65408e-05 | 0.00287578 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285157 | TTCCGGAAGAAAGTG[A/G]AGAAAGATGAGAACT | 64446 |
rs776194595 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74276071 | TTCCAGCTTGCCTCC[A/T]TCCCAGTCTCCCACG | 64446 |
rs776284600 | snp | C/G | 1.65078e-05 | 0.00287291 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309381 | GCGATCCCACCCTCA[C/G]CTTGAAGGTCACGCG | 64446 |
rs776295366 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301461 | AATTCCAGAAAAGCC[C/T]TGTTTTGTGGGGAAG | 64446 |
rs776297555 | snp | A/T | 1.70403e-05 | 0.00291888 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310158 | GAGAAGAACGTAGCC[A/T]CTTCCGTAAGCACCG | 64446 |
rs776342494 | in-del | -/CAGGCAGCCTCCCGAGTAA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74298734 | CAGCCTCCCGAGTAG[-/CAGGCAGCCTCCCGAGTAA]CAGCCTCCCGAGTAG | 64446 |
rs776404021 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308098 | CCACCGCGCCCGGCC[C/G]AGATCCTTTCTTTAG | 64446 |
rs776419137 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302772 | GGTTCCCCCTTGGGG[G/T]TGTCACTTGTTTGCT | 64446 |
rs776420686 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74278072 | AGCCAGACATGCCTG[A/G]TGGTTCTGCCTGAAC | 64446 |
rs776475567 | snp | C/T | 7.76126e-05 | 0.00622899 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281699 | CCCACCACCCCTTGC[C/T]TCCTGCCCCAACCAG | 64446 |
rs776510205 | snp | G/T | 1.74723e-05 | 0.00295564 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281758 | ACCTGTGGAGATAGG[G/T]AAGGGGCCGGTGGGG | 64446 |
rs776562930 | snp | G/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301134 | AGTTGGAAAATGCCT[G/T]GGGGGCCATCTCCCT | 64446 |
rs776613484 | in-del | -/GAG | 1.73691e-05 | 0.00294691 | cds-indel, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312153 | CTGGTCAGCAAGGCC[-/GAG]GAGGAGTTCTTCGAC | 64446 |
rs776667942 | snp | G/T | 4.94319e-05 | 0.00497127 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74289657 | CGATGGCAACAGGAA[G/T]TTGGCAGTGGCATAC | 64446 |
rs776678382 | in-del | -/AAGA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74301806 | CAGTCTTTACCAAGA[-/AAGA]AAGAAAGAAAGAAAG | 64446 |
rs776777011 | snp | C/G | 1.64784e-05 | 0.00287035 | splice-acceptor-variant | DNAI2 | GRCh38.p7 | 17:74301045 | CCCCTCCTCCCACCA[C/G]GTCATGTGGTGGGAC | 64446 |
rs776778663 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74286782 | GCGCTGCATGTATTT[C/T]CATGCTTTGTACCTA | 64446 |
rs776787499 | snp | C/T | 1.64814e-05 | 0.00287061 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314244 | GACTGCGGCGCTATC[C/T]CTGTGTGCCTTCCTT | 64446 |
rs776802277 | snp | A/G | 1.65102e-05 | 0.00287312 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281839 | ATTGTGTACGTGTAC[A/G]TCAAGAAGCGCAGCG | 64446 |
rs776826747 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275250 | CCCATCGGTCTCCAA[-/T]TCTGGGGACCTCTTC | 64446 |
rs776869031 | snp | C/T | 1.6534e-05 | 0.00287519 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309500 | GTGGCCAGGTGTGTT[C/T]GGGCCTCTGTGGGGG | 64446 |
rs776952886 | snp | A/T | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281908 | GAGCTGAACATCGAC[A/T]TCATGCCCAACCCTG | 64446 |
rs776979362 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74274795 | TTGCACACCTGCTAG[A/G]TGGCAGGTGTTTTAA | 64446 |
rs776994319 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74294569 | AATTCTCCCACCTTG[A/G]CCTCCCAAAGTGCTG | 64446 |
rs777084756 | snp | C/T | 3.47953e-05 | 0.0041709 | intron-variant | DNAI2 | GRCh38.p7 | 17:74287124 | AGCCAGGCAGGTGTC[C/T]GGCCACCCTCCGTCA | 64446 |
rs777109213 | in-del | -/CA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277384 | AGCGAGAATCCATCT[-/CA]AAAAAAAAAAAAAAA | 64446 |
rs777139936 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74281303 | TTGCTCTGTCACCCA[-/T]GCTGGAGTGCAATGG | 64446 |
rs777256906 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74310799 | CCCACCCTGGCCTCC[A/G]AAAGTGCTGGGATTA | 64446 |
rs777295125 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295324 | AGAGAATTGCTTGAA[C/T]CCAGGAGGCAGAGGT | 64446 |
rs777319707 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74274836 | TCATTTCTTCCTCAA[C/T]CTGGGAGCTGGCGTT | 64446 |
rs777369529 | snp | A/G | 0.000577029 | 0.0169759 | synonymous-codon, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74287027 | TGACATCTATGAAGA[A/G]TATTTCAATGACGAG | 64446 |
rs777389942 | snp | C/T | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272469 | CCCCTGTCAGGACCC[C/T]CAGCACCCACCCCTA | 64446 |
rs777391104 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296503 | AAGTACAGGCGTGAG[A/C]CACTGTACTCGGCCC | 64446 |
rs777425543 | snp | A/C | | | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281867 | GCGAGTTCGGGAAGC[A/C]GTGCAATTTCTCGGA | 64446 |
rs777583144 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295290 | ACCTGCAATCTCAGC[A/T]ACTTGGGAGGCTGAG | 64446 |
rs777662498 | snp | A/C | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281887 | AATTTCTCGGACCGC[A/C]AGGCCGAGCTGAACA | 64446 |
rs777672675 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74289356 | ACATGGTAAAAACCT[A/G]TCTCTACTAAAAATA | 64446 |
rs777740592 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280361 | CCTGCCTAGGTCACG[C/T]AGCTGGTGACGGGAG | 64446 |
rs777753410 | snp | A/C | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303370 | CGTGCAGTCGGCTTG[A/C]ATACTTTCTTCTCTG | 64446 |
rs777802690 | snp | A/G | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314157 | GACCAGGTGGTGGAG[A/G]AGGGAGAGGAAGCAG | 64446 |
rs777815873 | snp | C/T | 1.91503e-05 | 0.00309431 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310200 | AAAATCCCTCCAGCA[C/T]GTCCCGACCTGGCCC | 64446 |
rs777861811 | snp | A/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308830 | AGAGCCCTTTAAAGA[A/T]CAGCCTGTCAGACAC | 64446 |
rs778105683 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74300846 | TATGAAGCTTGCCGG[C/T]GACTCTGATGATCAG | 64446 |
rs778114743 | snp | C/T | 3.29777e-05 | 0.00406051 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285108 | GGGCTGGCCCAAGGA[C/T]GTGAACCCCCTGGAG | 64446 |
rs778170016 | in-del | -/CCGTTT | 1.65526e-05 | 0.00287681 | cds-indel, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309303 | GCCCCGTGAGGCCGA[-/CCGTTT]TCTTTACCACCAGGA | 64446 |
rs778190340 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74286677 | TGATCCACCCGCTTC[A/G]GCCTCCCAAAGTGCT | 64446 |
rs778200963 | in-del | -/TAAA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295233 | AACCCCATCTCTACT[-/TAAA]AAAAAAAAAAAAAAA | 64446 |
rs778212524 | snp | C/T | 1.66103e-05 | 0.00288182 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285011 | AGTATACCAGGGTGA[C/T]GTCTTCCCTCCTGCG | 64446 |
rs778221030 | snp | G/T | 1.65968e-05 | 0.00288065 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299749 | AAAGGGCAGCCTGGT[G/T]GCGGAGCTATCCACC | 64446 |
rs778246376 | snp | A/C/T | 3.6179e-05 | 0.00425305 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281745 | CTGTCCTGGCAGGAC[A/C/T]TGTGGAGATAGGGAA | 64446 |
rs778250062 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74306137 | TGAACCAAGGAAGCT[C/T]GGCTGGGAAATGCGG | 64446 |
rs778305345 | snp | G/T | 0.000282446 | 0.0118804 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281672 | AGCTTCTGGACAAAT[G/T]CCTAGGATCTCCCCA | 64446 |
rs778308456 | snp | A/G | 1.84439e-05 | 0.00303671 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281741 | GGAGCTGTCCTGGCA[A/G]GACCTGTGGAGATAG | 64446 |
rs778315009 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74274504 | GGCTGCCAGGACTAG[C/T]GCTCCTAGTGCCCTC | 64446 |
rs778368017 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275316 | GGGGGCTCAGCCATG[C/T]TTAGTGCTATCCTGG | 64446 |
rs778391861 | snp | A/G | 9.96835e-05 | 0.00705917 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312207 | AAGAAGGAGGCAGAC[A/G]CCATAAAGCTGACGC | 64446 |
rs778405695 | in-del | -/G | 1.64963e-05 | 0.00287192 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301007 | GCCAGGGGAAATACA[-/G]GGGCCTCGAAGTCTC | 64446 |
rs778468970 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295133 | GATGTGGTGGCTCGT[G/T]CCTGGAAACCTAGCA | 64446 |
rs778547622 | in-del | -/C | 1.64976e-05 | 0.00287202 | frameshift-variant, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281952 | GTTCGTGGAGCGGAA[-/C]CCAGTGGACACGGGC | 64446 |
rs778583557 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74311445 | ATGAAGAAACCTCGT[C/G]TCTACTAAAAATAGA | 64446 |
rs778604584 | snp | A/T | 0.0001924 | 0.00980628 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281680 | GACAAATTCCTAGGA[A/T]CTCCCCACCACCCCT | 64446 |
rs778718449 | snp | A/G | | | | | GRCh38.p7 | 17:74273037 | CACTTCTTGGATGAC[A/G]CACTCCTCTTCTGTC | 64446 |
rs778744125 | snp | A/G | | | | | GRCh38.p7 | 17:74280792 | AAACACTGATTCAGT[A/G]AAAACCGTATTGTAC | 64446 |
rs778774910 | snp | C/T | 0.000495066 | 0.0157254 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305220 | CACTCCTTCCACAGC[C/T]CACCAAGTTCATGGT | 64446 |
rs778793370 | snp | G/T | 8.24097e-05 | 0.00641857 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301201 | TCCCTTCCCCGACTT[G/T]CATTGACAGGGCAGC | 64446 |
rs778812649 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284184 | AAGATCATGCCACTG[C/T]ACTCCAGCCTGGGCA | 64446 |
rs778872776 | snp | A/G | 0.00013866 | 0.00832532 | intron-variant | DNAI2 | GRCh38.p7 | 17:74281764 | GGAGATAGGGAAGGG[A/G]CCGGTGGGGTCCCTC | 64446 |
rs778910329 | snp | C/T | 1.65138e-05 | 0.00287343 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289764 | GGGGTCCTGGTGGCC[C/T]GGGAGGGCTGAGGGC | 64446 |
rs778958481 | snp | C/T | 6.01269e-05 | 0.00548268 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309560 | CTTTTGAGCGTGTGC[C/T]CCTACAAAGGTTAAG | 64446 |
rs778997016 | snp | C/G | 0.000247633 | 0.0111245 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305403 | GGACAGCCCGCATTT[C/G]GTCTGAAGACAGCCG | 64446 |
rs778998306 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305320 | CACCTTCCCGGGCCA[C/T]CATGGCCCCATCTAC | 64446 |
rs779055691 | snp | C/T | 0.000119256 | 0.00772099 | intron-variant | DNAI2 | GRCh38.p7 | 17:74310205 | CCCTCCAGCACGTCC[C/T]GACCTGGCCCCACAG | 64446 |
rs779060081 | snp | A/C | 1.67806e-05 | 0.00289656 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285200 | TCATGCAGCTCGGCT[A/C]TGTAAGGCTTCCTCC | 64446 |
rs779082321 | snp | A/G | 1.69132e-05 | 0.00290797 | intron-variant | DNAI2 | GRCh38.p7 | 17:74299902 | AGGGAAGGGAGGGGC[A/G]GTAACTGTTCCCTGG | 64446 |
rs779268065 | snp | C/T | 1.64955e-05 | 0.00287184 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74285139 | CTGGAGCAGACCATC[C/T]GTTTCCGGAAGAAAG | 64446 |
rs779326889 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309584 | GGTTAAGGGGCCTGG[A/G]GGATTTGGCATCCTG | 64446 |
rs779332423 | snp | A/G | 3.31835e-05 | 0.00407316 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299753 | GGCAGCCTGGTGGCG[A/G]AGCTATCCACCATTG | 64446 |
rs779354774 | snp | A/C | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74274381 | GGACGTCGGAGGCTA[A/C]AGACTAGAGTGGAGA | 64446 |
rs779363755 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284774 | TCTCTGGTCCATTAG[A/G]ATTCAGATAAGGTCA | 64446 |
rs779364380 | snp | A/G | | | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314512 | GCCGAGGCCACCTTA[A/G]TCCTAGTCCTGGATG | 64446 |
rs779452547 | snp | C/T | 4.97905e-05 | 0.00498926 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74299751 | AGGGCAGCCTGGTGG[C/T]GGAGCTATCCACCAT | 64446 |
rs779484407 | snp | C/G | 1.80879e-05 | 0.00300726 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309441 | AGGGAGCCAGGTCCC[C/G]GCGTGGGTGTGAGTG | 64446 |
rs779560268 | snp | C/T | | | upstream-variant-2KB | DNAI2 | GRCh38.p7 | 17:74272403 | GGGTCTGATTCACCT[C/T]TGACCACACAAAGCC | 64446 |
rs779618772 | snp | A/C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305963 | AGGTGTGAGCCACCG[A/C/T]GTCTGGCTGGCTTAA | 64446 |
rs779673538 | snp | G/T | | | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314016 | TCAGCGACCCAGGCT[G/T]CAGCCATTTGGCTGC | 64446 |
rs779742315 | snp | A/G | 0.000247376 | 0.0111188 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305231 | CAGCCCACCAAGTTC[A/G]TGGTGGGGACCGAGC | 64446 |
rs779803968 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74297690 | CCCAGCCCAAACTGC[-/T]TTTTTTTTTTTTTAA | 64446 |
rs779807193 | snp | A/T | 7.49078e-05 | 0.0061195 | intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312275 | TGGGGACTGGGCGGG[A/T]CACATGGCACTTGGG | 64446 |
rs779821433 | snp | C/G | 1.64969e-05 | 0.00287196 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289741 | CTGGGACCTGGGTGA[C/G]AAGCAGCGGGGTCCT | 64446 |
rs779851526 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295036 | GCCATCCTGTAGCTT[C/T]TCTGCTATATTTTTA | 64446 |
rs779867971 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292954 | CCTGCCTCAGCCTTC[C/G]GAGTAGCTGGGACTA | 64446 |
rs779906391 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74291771 | TTTGGGAGAGGTTTC[C/T]GGGAAACCTACATGC | 64446 |
rs779934843 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74309779 | GGAAGGGTGGGGGCA[C/T]TGGGGAACCACAGGG | 64446 |
rs780040851 | snp | C/G | 1.64871e-05 | 0.00287111 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281896 | GACCGCCAGGCCGAG[C/G]TGAACATCGACATCA | 64446 |
rs780116486 | snp | C/T | 1.64732e-05 | 0.0028699 | stop-gained, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74291127 | GGCTGCTACAATGGA[C/T]AGATAGGTAAGGAGG | 64446 |
rs780180539 | snp | A/G | 1.66515e-05 | 0.00288539 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74305418 | GGTCTGAAGACAGCC[A/G]GGAATCGTCCATCAT | 64446 |
rs780206571 | snp | C/T | 0.000743356 | 0.0192646 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307252 | GCAGGGTGTCGAGCA[C/T]AGCACCCATAGGCCT | 64446 |
rs780216155 | snp | C/G | 3.29533e-05 | 0.00405901 | intron-variant | DNAI2 | GRCh38.p7 | 17:74286968 | GAACTTCCAATGTGT[C/G]CCCCCTAGATCATGG | 64446 |
rs780420957 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287274 | TGGCCCTGCTCTGGG[G/T]GCGGGTCTGGTTGAT | 64446 |
rs780463497 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284628 | CGTGTTAGCGAGGAC[A/G]GTCTCGATCTCCTGA | 64446 |
rs780506581 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74301099 | TGAAGTTGTGATCTT[A/G]GACATCACCAAGAAG | 64446 |
rs780557132 | snp | C/T | 1.68086e-05 | 0.00289896 | missense, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312034 | CCCGGCGAGAGAAGA[C/T]CCTGGAGGCCAGGCA | 64446 |
rs780577279 | snp | A/C | 1.64955e-05 | 0.00287184 | intron-variant | DNAI2 | GRCh38.p7 | 17:74301003 | CAAAAGCCAGGGGAA[A/C]TACAGGGCCTCGAAG | 64446 |
rs780598460 | snp | A/G | 0.000153116 | 0.0087484 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309540 | CAGGCTGACTGCAGC[A/G]ATTGCTTTTGAGCGT | 64446 |
rs780600994 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283170 | TCATGAGGATGGGGT[C/T]TCCATCCTGGGTGAT | 64446 |
rs780627875 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74284407 | AGGCTATTCACTTTT[G/T]CTTTTTTCTTTTTCT | 64446 |
rs780647938 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305629 | GATAAGCTTCAAACA[C/T]TCAGTTACTAAAAAT | 64446 |
rs780854075 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74290509 | GGCAGGGACAGGGTG[A/G]TGGTGGCTTCACGCT | 64446 |
rs780897001 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280451 | ATGACCAGTAGCACG[C/T]GTCAGAGGCTTTCCC | 64446 |
rs780946546 | snp | C/G | 1.86392e-05 | 0.00305274 | intron-variant | DNAI2 | GRCh38.p7 | 17:74309446 | GCCAGGTCCCGGCGT[C/G]GGTGTGAGTGTGGGG | 64446 |
rs780958998 | snp | C/T | 8.24477e-05 | 0.00642005 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74281879 | AGCAGTGCAATTTCT[C/T]GGACCGCCAGGCCGA | 64446 |
rs780969152 | snp | C/T | 1.64795e-05 | 0.00287045 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291007 | GTGGGGATAATTTTT[C/T]TGTGCTTTATAGAAA | 64446 |
rs781052507 | snp | A/G | | | intron-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314458 | CTTGTCCCGGAGCTG[A/G]CTGCCCCATTGTCTC | 64446 |
rs781125572 | snp | A/G | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74314136 | CAGCAACCAAGTCCA[A/G]AAGAAGACCAGGTGG | 64446 |
rs781137439 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74305051 | GGGTCTGAGGAGCCC[A/G]GGAAGAGTGGGGACT | 64446 |
rs781178096 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74291663 | AATTAGCTCAAAATA[A/G]ACAGTTTTAAAAAAC | 64446 |
rs781259491 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74287718 | CCAGCACTTTGGGAG[G/T]CCAAGGCGGGTGCAT | 64446 |
rs781268054 | snp | A/G | 1.66225e-05 | 0.00288287 | intron-variant | DNAI2 | GRCh38.p7 | 17:74285001 | AGGGTTTGGGAGTAT[A/G]CCAGGGTGACGTCTT | 64446 |
rs781321992 | snp | G/T | 1.66192e-05 | 0.00288259 | intron-variant, missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74310022 | CCTTCAATAGGTGTG[G/T]GACGAGGCCCTCTTC | 64446 |
rs781411031 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275488 | CCAGTGCTTTGAGAG[A/G]CCCAGGAGGATGGAT | 64446 |
rs781473279 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277963 | GATGAGAGATTCTGA[C/T]GTAGTTGTTCTGGGG | 64446 |
rs781499125 | snp | A/G | 1.67798e-05 | 0.00289648 | missense, nc-transcript-variant, downstream-variant-500B | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312042 | GAGAAGATCCTGGAG[A/G]CCAGGCACCGGGAGA | 64446 |
rs781517527 | in-del | -/G | 1.6507e-05 | 0.00287284 | intron-variant | DNAI2 | GRCh38.p7 | 17:74289760 | CAGCGGGGTCCTGGT[-/G]GCCTGGGAGGGCTGA | 64446 |
rs781533751 | in-del | -/AA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295232 | AACCCCATCTCTACT[-/AA]TAAAAAAAAAAAAAA | 64446 |
rs781567619 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74311594 | TTCCAGCCTGGGCAA[C/T]AAGAGTGAAACTCTG | 64446 |
rs781603676 | snp | G/T | 1.72389e-05 | 0.00293584 | intron-variant | DNAI2 | GRCh38.p7 | 17:74291153 | GGAGGGACCTAGGCT[G/T]TTTTATTTTTATTTT | 64446 |
rs781605510 | snp | A/C | 1.66518e-05 | 0.00288542 | missense, nc-transcript-variant | DNAI2 | GRCh38.p7 | 17:74309259 | CTCCCACAGGTACCA[A/C]ATGGCTTACCTCACT | 64446 |
rs781609665 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74275540 | GACCAGCCTGCCCAA[C/T]ATGGTGAAACCCCAT | 64446 |
rs781679398 | snp | C/T | 0.000185684 | 0.00963366 | intron-variant | DNAI2 | GRCh38.p7 | 17:74307270 | CACCCATAGGCCTTT[C/T]GCAGGGCTGGTTCCT | 64446 |
rs781712279 | snp | A/C | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant, intron-variant | DNAI2 | GRCh38.p7 | 17:74287002 | ACTGCATCAAGCAGA[A/C]CAATGCCATTGACAT | 64446 |
rs781733104 | in-del | -/GACAGGAGGGGATGCAGGA | 3.74272e-05 | 0.00432576 | intron-variant | DNAI2 | GRCh38.p7 | 17:74305461 | AGAGGCGATGCTGGG[-/GACAGGAGGGGATGCAGGA]GACAGGAGGGGATGG | 64446 |
rs794727074 | snp | A/T | | | missense, nc-transcript-variant, intron-variant | DNAI2, LOC105371891 | GRCh38.p7 | 17:74312127 | AGGAGCTGGCCGTAG[A/T]CCTGGAGGCGCTGGT | 64446 |
rs796082374 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74295656 | TTATAATTTTTTTTT[-/T]ATTAAAAACTATACT | 64446 |
rs796190813 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74292415 | AATCATTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 64446 |
rs796223330 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74291932 | GCAGTGGTGCAGTCT[C/T]AGCTCACTGCAGCCT | 64446 |
rs796248671 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279493 | AAATTAAAAATTAAA[A/G]AAAAATAGCAAAACC | 64446 |
rs796267416 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74308168 | ACTAGGTTTGCAAAG[A/G]TGACTGGGAAGTGTA | 64446 |
rs796269287 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74291838 | TTGGGAAGTATTCCC[C/T]TCTGGAAGTTTGTGA | 64446 |
rs796288214 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74285604 | GTGCAAAAAAAAAAA[-/A]TTGTTTTAAGGAAAA | 64446 |
rs796302144 | in-del | -/A | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302567 | GCGAAACTCCATCTC[-/A]AAAAAAAAAACAAAG | 64446 |
rs796350373 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296630 | ACACCCTGATGAAAA[A/G]ACTTTTCACACCAGG | 64446 |
rs796355765 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74288302 | AGTGTTCTGAGCACA[C/T]AGGCTGGACTAAGAT | 64446 |
rs796413119 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302050 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA | 64446 |
rs796427957 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74296335 | AGAGAGAGAGAGAGG[A/G]GAGAGAGAGAGGAGA | 64446 |
rs796488965 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302159 | TGTGAGGCAAGGCGC[C/T]GTGGCTCACACCTGT | 64446 |
rs796626501 | snp | C/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74279445 | AACATCTCCTGTGCC[C/G]CATAAATATATACAC | 64446 |
rs796636830 | snp | C/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302761 | AGCCCAGGCCTGGTT[C/T]CCCCTTGGGGGTGTC | 64446 |
rs796638601 | snp | A/G | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74302062 | GAAGGAAGGAAGGAA[A/G]GAAGGAAAGAAGGAA | 64446 |
rs796682632 | snp | G/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74283959 | CCTGGCCAACATGGT[G/T]AAACCCCGTCTCTAC | 64446 |
rs796729896 | in-del | -/T | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74303596 | ACCAAGCCAGGCTGA[-/T]TTTTTTTTTTTTTTT | 64446 |
rs796836513 | in-del | -/AAAA | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74277385 | GCGAGAATCCATCTC[-/AAAA]AAAAAAAAAAAAAGA | 64446 |
rs796944894 | in-del | -/ACAAT | | | intron-variant | DNAI2 | GRCh38.p7 | 17:74280926 | CCCCATCTCTACAAA[-/ACAAT]ACAATACAAAACTTA | 64446 |