Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4641 0.851 0.120 1 156137743 splice region variant C/T snv 0.26 0.21 6
rs60890628 0.776 0.200 1 156138507 missense variant C/T snv 1.5E-04 1.0E-04 9
rs141490569 1.000 0.040 1 156136258 missense variant G/A snv 8.0E-05 9.8E-05 1
rs760318158 1.000 0.040 1 156126897 missense variant C/T snv 2.3E-04 6.3E-05 1
rs138592977 1.000 0.040 1 156135968 missense variant G/A snv 5.6E-05 6.3E-05 3
rs267607578 0.925 0.120 1 156136952 missense variant G/A;C snv 1.4E-05 3
rs397517907 0.925 0.080 1 156134914 missense variant C/T snv 4.0E-06 1.4E-05 2
rs267607574 1.000 0.040 1 156135916 missense variant G/A snv 1.6E-05 1.4E-05 1
rs58672172 0.882 0.160 1 156136251 missense variant C/T snv 1.2E-05 1.4E-05 3
rs397517889 0.925 0.120 1 156136093 missense variant C/T snv 7.0E-06 3
rs59026483 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 7
rs60682848 0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 11
rs56657623 0.827 0.120 1 156138540 missense variant G/A snv 1.6E-05 7.0E-06 5
rs150840924 0.807 0.240 1 156136359 missense variant C/T snv 8.0E-06 7.0E-06 7
rs267607560 0.925 0.040 1 156115192 missense variant C/T snv 7.0E-06 2
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
rs61672878 0.776 0.200 1 156136094 missense variant G/A;T snv 11
rs58034145 0.827 0.160 1 156134830 missense variant A/C snv 10
rs57077886 0.776 0.240 1 156114947 missense variant C/T snv 9
rs142000963 0.807 0.240 1 156138719 missense variant C/A;T snv 1.2E-03 8
rs56984562 0.827 0.200 1 156137666 missense variant C/A;G;T snv 6
rs57045855 0.882 0.040 1 156134464 missense variant A/G;T snv 6
rs61195471 0.827 0.160 1 156134496 missense variant G/A snv 6
rs28933093 0.882 0.160 1 156130741 missense variant G/A snv 5