Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13768 1.000 0.120 1 156138660 missense variant G/A;T snv 2.4E-05 1
rs1553265999 1.000 0.120 1 156136925 missense variant A/C snv 1
rs267607539 1.000 0.120 1 156137237 splice region variant G/A;C snv 1
rs267607540 1.000 0.120 1 156134509 inframe deletion GAA/- delins 1
rs267607614 1.000 0.120 1 156115016 missense variant A/G snv 1
rs267607629 1.000 0.120 1 156134507 missense variant C/G snv 1
rs267607630 1.000 0.120 1 156134967 missense variant T/C snv 1
rs267607633 1.000 0.120 1 156135259 missense variant T/C snv 1
rs267607638 1.000 0.120 1 156136417 missense variant T/C snv 1
rs267607641 1.000 0.120 1 156135188 missense variant T/C snv 1
rs267607642 1.000 0.120 1 156136921 missense variant G/T snv 8.0E-06 1
rs267607643 1.000 0.120 1 156134455 missense variant GG/CC mnv 1
rs56694480 1.000 0.120 1 156115021 missense variant C/G snv 1
rs56699480 1.000 0.120 1 156137017 stop gained C/T snv 1
rs57048196 1.000 0.120 1 156134965 missense variant A/G snv 1
rs57394692 1.000 0.120 1 156136946 missense variant T/C snv 1
rs57793737 1.000 0.120 1 156115106 missense variant T/A;C;G snv 1
rs58105277 1.000 0.120 1 156135971 missense variant G/A snv 2.8E-05 1
rs58541611 1.000 0.120 1 156136393 missense variant A/G;T snv 1
rs59931416 1.000 0.120 1 156115066 missense variant C/A;T snv 1
rs60446065 1.000 0.120 1 156115045 missense variant G/A snv 1
rs60992550 1.000 0.120 1 156136423 missense variant A/T snv 1
rs61177390 1.000 0.120 1 156135992 missense variant G/A snv 3.6E-05 2.8E-05 1
rs61235244 1.000 0.120 1 156136424 missense variant C/A snv 1
rs61527854 1.000 0.120 1 156135283 missense variant T/C snv 1