Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs281865545 0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93