Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 15
rs3918226 0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 6
rs17367504 1.000 0.040 1 11802721 intron variant A/G snv 0.14 4
rs2282978 7 92635096 intron variant T/C snv 0.38 4