Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33