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
rs121918597 0.925 0.080 1 237634937 missense variant C/T snv 2
rs121918598 0.851 0.080 1 237648523 missense variant G/A;C snv 4
rs121918599 0.925 0.080 1 237784024 missense variant C/G snv 2
rs121918600 0.882 0.080 1 237791441 missense variant C/T snv 5
rs121918601 0.925 0.120 1 237640938 missense variant A/T snv 2
rs121918602 0.925 0.120 1 237454396 missense variant T/C snv 3
rs121918603 0.882 0.080 1 237639068 missense variant C/T snv 3
rs121918604 0.882 0.080 1 237798037 missense variant G/A;T snv 1.7E-05 3
rs121918605 0.925 0.080 1 237784314 missense variant A/G snv 2
rs121918606 0.925 0.080 1 237819181 missense variant C/G snv 3
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
rs1273246817 0.882 0.080 1 237784169 missense variant A/C snv 3
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