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
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs4293393 0.827 0.200 16 20353266 intron variant A/G snv 0.20 8
rs12313273 0.882 0.160 12 121625105 upstream gene variant T/C snv 0.23 4
rs7456421 0.882 0.120 7 139715976 synonymous variant G/C snv 0.27 0.37 4
rs752977102 0.925 0.120 16 88811577 missense variant G/C snv 2.8E-05 7.0E-05 3