Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
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
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249