Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11575937 0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs386134243 0.708 0.360 1 156135967 missense variant C/A;T snv 4.0E-06 16
rs57920071 0.763 0.320 1 156136984 missense variant C/T snv 4.0E-06 7.0E-06 11
rs57077886 0.776 0.240 1 156114947 missense variant C/T snv 9
rs60890628 0.776 0.200 1 156138507 missense variant C/T snv 1.5E-04 1.0E-04 9
rs57520892 0.776 0.200 1 156137204 missense variant G/A;C snv 4.1E-05 8
rs60864230 0.790 0.280 1 156130658 missense variant G/A;C;T snv 4.0E-06 7
rs267607555 0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 6
rs150924946 0.882 0.120 1 156135271 missense variant A/G snv 4.8E-04 1.6E-04 5
rs56793579 0.851 0.240 1 156115102 missense variant C/G;T snv 5
rs57629361 0.827 0.280 1 156137207 missense variant C/A;G;T snv 9.3E-06 5
rs58672172 0.882 0.160 1 156136251 missense variant C/T snv 1.2E-05 1.4E-05 3
rs59914820 0.925 0.160 1 156115000 missense variant C/G;T snv 3
rs770850320 0.882 0.120 17 17816960 missense variant G/A snv 2.0E-05 2.8E-05 3
rs28928900 0.925 0.120 1 156115096 missense variant C/G;T snv 2
rs57830985 0.925 0.080 1 156138534 missense variant G/A;T snv 8.2E-06 7.0E-06 2
rs61282106 0.925 0.080 1 156136934 missense variant G/A snv 2
rs267607543 1.000 0.080 1 156137033 splice region variant G/A;C snv 1
rs59981161 1.000 0.080 1 156136998 missense variant G/C;T snv 1
rs61214927 1.000 0.080 1 156134853 missense variant G/A snv 1
rs62636506 1.000 0.080 1 156136371 missense variant C/T snv 2.4E-05 1.4E-05 1
rs863225024 1.000 0.080 1 156138749 frameshift variant -/G delins 1
rs918645468 1.000 0.080 1 156138533 missense variant C/T snv 1