Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs41423247 0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs6189 0.827 0.240 5 143400774 missense variant C/A;T snv 4.0E-06; 1.8E-02 6
rs495225 0.882 0.040 3 172448243 synonymous variant G/A;C;T snv 0.66 4