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
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs763351020 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs3809021 0.882 0.080 11 104164894 upstream gene variant T/G snv 0.61 4