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
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs6198 0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs375382379 0.882 0.160 5 143399792 missense variant T/C snv 4.0E-06 5
rs550659379 0.882 0.160 5 143399780 missense variant T/C snv 4.0E-06 7.0E-06 5
rs752834812 0.882 0.160 5 143399885 missense variant T/C snv 8.0E-06 5
rs772651364 0.882 0.160 5 143400050 missense variant C/T snv 4.0E-06 5