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 0.15 264
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs7209436 0.851 0.200 17 45792776 intron variant C/T snv 0.43 5
rs121434622 1.000 0.080 X 147936534 missense variant T/A snv 2
rs182830086 1.000 0.080 X 147944892 missense variant G/T snv 5.5E-06 1