Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267607613 0.925 0.120 1 156137678 missense variant C/T snv 7.0E-06 2
rs61046466 1.000 0.120 1 156114934 stop gained C/T snv 2
rs56699480 1.000 0.120 1 156137017 stop gained C/T snv 1
rs61195471 0.827 0.160 1 156134496 missense variant G/A snv 6
rs59332535 0.827 0.160 1 156134911 missense variant G/A snv 5
rs60662302 0.882 0.200 1 156138593 missense variant G/A snv 2.1E-04 7.7E-04 5
rs267607637 0.925 0.120 1 156136402 missense variant G/A snv 2
rs57207746 0.925 0.120 1 156134860 missense variant G/A snv 2
rs58105277 1.000 0.120 1 156135971 missense variant G/A snv 2.8E-05 1
rs60446065 1.000 0.120 1 156115045 missense variant G/A snv 1
rs61177390 1.000 0.120 1 156135992 missense variant G/A snv 3.6E-05 2.8E-05 1
rs57520892 0.776 0.200 1 156137204 missense variant G/A;C snv 4.1E-05 8
rs61444459 0.851 0.160 1 156137667 missense variant G/A;C snv 5
rs267607632 0.851 0.120 1 156134976 splice donor variant G/A;C snv 4
rs267607634 0.925 0.120 1 156136045 missense variant G/A;C snv 2
rs58362413 0.925 0.160 1 156137183 stop gained G/A;C snv 2
rs267607539 1.000 0.120 1 156137237 splice region variant G/A;C snv 1
rs60864230 0.790 0.280 1 156130658 missense variant G/A;C;T snv 4.0E-06 7
rs267607545 0.882 0.200 1 156136121 missense variant G/A;C;T snv 3
rs60695352 0.925 0.120 1 156115067 splice donor variant G/A;C;T snv 9.5E-06 2
rs11575937 0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs61672878 0.776 0.200 1 156136094 missense variant G/A;T snv 11
rs60458016 0.827 0.120 1 156136036 stop gained G/A;T snv 5
rs267607571 0.882 0.160 1 156134458 missense variant G/A;T snv 4
rs13768 1.000 0.120 1 156138660 missense variant G/A;T snv 2.4E-05 1