Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1060500137 1.000 0.080 1 237772077 missense variant G/A snv 1
rs1060500142 1.000 0.080 1 237330939 missense variant C/T snv 4.0E-06 1
rs1185619003 1.000 0.080 1 237830557 missense variant A/G snv 1
rs1188352725 1.000 0.080 1 237798091 missense variant G/C snv 1
rs1202962809 1.000 0.080 1 237784184 missense variant A/C snv 1
rs1218096653 1.000 0.080 1 237828391 missense variant T/G snv 1
rs1234963411 1.000 0.080 1 237784188 missense variant A/C snv 1
rs1235005255 1.000 0.080 1 237648548 missense variant T/A snv 1
rs1239093704 1.000 0.080 1 237759849 missense variant G/T snv 4.0E-06 1
rs1242723821 1.000 0.080 1 237828429 missense variant T/C snv 1
rs1323621379 1.000 0.080 1 237791464 missense variant G/A snv 1
rs1349176732 1.000 0.080 1 237445485 missense variant A/T snv 1
rs1349585791 1.000 0.080 1 237784148 missense variant G/A snv 1
rs1359163728 1.000 0.080 1 237793903 missense variant G/C snv 1
rs1363298408 1.000 0.080 1 237819144 missense variant A/G snv 1
rs1373714510 1.000 0.080 1 237784038 missense variant T/C;G snv 1
rs1385881911 1.000 0.080 1 237784083 missense variant G/C snv 1
rs1456929288 1.000 0.080 1 237640988 missense variant G/A snv 1
rs1457271141 1.000 0.080 1 237791448 missense variant T/G snv 1
rs1472508624 1.000 0.080 1 237759782 missense variant C/T snv 1
rs1475453069 1.000 0.080 1 237830579 missense variant C/T snv 1
rs1553263875 1.000 0.080 1 237639095 missense variant G/C snv 1
rs1553339084 1.000 0.080 1 237819187 missense variant T/C snv 1
rs1553339086 1.000 0.080 1 237819192 missense variant G/T snv 1
rs1553426678 1.000 0.080 1 237377374 missense variant G/A snv 1