Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs8040868 0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 17
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs886424 0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 10
rs2279574 0.827 0.120 12 89351700 missense variant C/A;T snv 0.52 8