Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs61742245 16 31094624 missense variant C/A;T snv 2.4E-03 2
rs72558191 10 94947919 missense variant T/G snv 1
rs104894542 16 31091243 missense variant A/C snv 1
rs104894539 16 31094645 missense variant C/A snv 4.3E-06 1.4E-05 1
rs104894540 16 31094596 missense variant A/G snv 1
rs104894541 16 31094558 missense variant T/C snv 4.1E-06 1
rs72547529 16 31093399 missense variant C/T snv 2.0E-04 8.4E-04 1
rs755767348 16 31093366 missense variant T/A snv 8.0E-06 1
rs770703948 16 31094654 missense variant C/A;G;T snv 8.6E-06; 4.3E-06 1