Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs405509 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24