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
rs80356814 0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs57920071 0.763 0.320 1 156136984 missense variant C/T snv 4.0E-06 7.0E-06 11
rs60682848 0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 11
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
rs60890628 0.776 0.200 1 156138507 missense variant C/T snv 1.5E-04 1.0E-04 9
rs142000963 0.807 0.240 1 156138719 missense variant C/A;T snv 1.2E-03 8
rs57520892 0.776 0.200 1 156137204 missense variant G/A;C snv 4.1E-05 8
rs58932704 0.776 0.200 1 156136413 missense variant C/T snv 8
rs150840924 0.807 0.240 1 156136359 missense variant C/T snv 8.0E-06 7.0E-06 7
rs58596362 0.827 0.280 1 156138613 splice region variant C/A;T snv 8.1E-06 7
rs59026483 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 7
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
rs4641 0.851 0.120 1 156137743 splice region variant C/T snv 0.26 0.21 6
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
rs57983345 0.851 0.160 1 156115034 missense variant A/G snv 6
rs59270054 0.925 0.120 1 156115162 missense variant G/A;C snv 6
rs61195471 0.827 0.160 1 156134496 missense variant G/A snv 6
rs878853220 0.827 0.200 1 156130818 intron variant T/G snv 6
rs150924946 0.882 0.120 1 156135271 missense variant A/G snv 4.8E-04 1.6E-04 5