Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs238406 0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs1799950 0.752 0.240 17 43094464 missense variant T/C snv 4.7E-02 4.6E-02 13