Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs587777623 0.882 0.120 11 686986 missense variant G/A snv 4.0E-06 8
rs730882242 0.807 0.280 5 141573518 stop gained G/A snv 7
rs202080674 0.851 0.160 10 49482848 missense variant G/A snv 8.0E-06 4
rs1057519087 0.925 0.120 1 39967632 missense variant C/T snv 7.0E-06 4
rs775277800 0.851 0.120 18 70166989 missense variant C/G;T snv 4.0E-06 4
rs1131692040 0.882 0.160 X 154399844 missense variant A/G snv 4
rs727505397 0.882 0.240 X 41553782 missense variant C/T snv 3
rs587777034 0.882 0.120 5 62361319 missense variant G/A snv 3
rs587777333 0.925 0.120 3 49104420 missense variant A/G snv 4.0E-06 3
rs34832477 0.925 0.120 10 133293066 missense variant G/A snv 4.0E-04 1.6E-03 3
rs587783390 0.925 0.120 9 120409290 stop gained G/A snv 2.6E-05 7.0E-06 2
rs1372862248 1.000 0.120 16 46926991 missense variant G/A snv 2
rs199422124 0.925 0.120 8 6409336 missense variant C/G;T snv 4.0E-06 2
rs1018001612 0.925 0.120 6 161548873 missense variant C/T snv 2.8E-05 2
rs773550500 0.925 0.120 6 162054128 missense variant C/T snv 4.0E-06 2
rs1554263624 0.925 0.120 7 6391932 missense variant A/G snv 2
rs1554264268 0.925 0.120 7 6402337 missense variant G/A snv 2
rs774912957 0.925 0.200 19 36054999 missense variant G/C;T snv 7.3E-05 2
rs201053854 0.925 0.200 19 36058791 missense variant G/T snv 6.6E-04 1.6E-04 2
rs387907082 0.925 0.120 19 36081512 missense variant G/A snv 1.4E-05 2
rs387907084 0.925 0.120 19 36058795 missense variant G/A snv 2
rs1455698435 1.000 0.120 7 15385551 frameshift variant T/- delins 8.0E-06 1.4E-05 1
rs766476013 1.000 0.120 8 6409342 missense variant C/G snv 1.6E-05 7.0E-06 1