Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2273697
ABCC2
0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 11
rs10211
CYP3A7 ; CYP3A7-CYP3A51P ; ZSCAN25
1.000 0.080 7 99705371 3 prime UTR variant T/C snv 0.25 1
rs11190164 0.776 0.080 10 99591947 intergenic variant A/G snv 0.19 10
rs2193352 0.790 0.080 10 99586852 intergenic variant A/G snv 0.15 9
rs1035209 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 9
rs6702619
LINC01708
0.851 0.200 1 99580690 intron variant T/G snv 0.35 4
rs6584283
LINC01475
0.776 0.080 10 99530544 intron variant T/C snv 0.56 12
rs12412391
LINC01475
0.790 0.080 10 99529178 intron variant A/G;T snv 9
rs1573496
ADH7
0.827 0.160 4 99428512 missense variant C/G snv 8.5E-02; 4.9E-04 7.8E-02 7
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1590
TGFBR1
0.882 0.120 9 99153883 3 prime UTR variant T/C;G snv 5
rs868
TGFBR1
0.851 0.160 9 99149374 3 prime UTR variant A/G snv 0.17 4
rs67687202
TGFBR1
1.000 0.080 9 99147870 intron variant TCTTT/- delins 1
rs10988706
TGFBR1
1.000 0.080 9 99108020 intron variant T/C snv 0.22 1
rs6478972
TGFBR1
1.000 0.080 9 99106996 intron variant G/A snv 0.24 1
rs11466445
TGFBR1
0.851 0.160 9 99105256 inframe insertion GCGGCGGCGGCGGCG/-;GCG;GCGGCG;GCGGCGGCG;GCGGCGGCGGCG;GCGGCGGCGGCGGCGGCG;GCGGCGGCGGCGGCGGCGGCG;GCGGCGGCGGCGGCGGCGGCGGCG;GCGGCGGCGGCGGCGGCGGCGGCGGCG delins 5
rs531564
LINC00599 ; MIR124-1
0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs2229765
IGF1R
0.807 0.280 15 98934996 synonymous variant G/A snv 0.40 0.39 7
rs34405347 0.776 0.080 9 98917470 regulatory region variant T/C;G snv 10
rs1407508 0.790 0.080 9 98882256 regulatory region variant T/C snv 4.1E-02 9
rs3808348
C7orf50 ; CYP2W1
0.925 0.080 7 988812 missense variant C/T snv 0.21 0.17 2
rs145364999
CHD1
0.776 0.080 5 98870378 intron variant T/A snv 1.9E-03 10
rs145236923
GALNT12
0.851 0.120 9 98831947 missense variant G/A snv 1.2E-03 1.3E-03 4
rs149726976
GALNT12
0.882 0.120 9 98831929 missense variant C/T snv 2.7E-04 4.5E-04 3
rs1298178636
OLFM2
1.000 0.080 19 9857818 missense variant G/A snv 1