Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397508267 1.000 0.120 7 117590353 missense variant A/C snv 4.0E-06 1
rs121909037 1.000 0.120 7 117611653 missense variant A/C;G snv 4.0E-06 1
rs397508288 0.882 0.200 7 117590409 missense variant A/C;G snv 4.0E-06 1
rs397508464 0.851 0.160 7 117530918 missense variant A/C;G snv 8.0E-06 1
rs79635528 1.000 0.120 7 117611695 missense variant A/C;G snv 4.0E-06 1
rs397508314 1.000 0.120 7 117592026 missense variant A/C;G;T snv 8.6E-06; 4.3E-06 1
rs76371115 0.807 0.160 7 117531041 missense variant A/C;G;T snv 8.0E-06 1
rs121909042 1.000 0.120 7 117652875 missense variant A/C;T snv 4.0E-06 1
rs121909008 0.925 0.160 7 117603612 missense variant A/G snv 4.0E-06 7.0E-06 1
rs121909031 1.000 0.120 7 117530951 missense variant A/G snv 1
rs150691494 1.000 0.120 7 117540132 missense variant A/G snv 2.9E-04 1.8E-04 1
rs1800103 0.925 0.160 7 117592588 missense variant A/G snv 7.7E-04 4.4E-04 1
rs191456345 0.925 0.160 7 117536576 missense variant A/G snv 1.8E-04 1.1E-04 1
rs201124247 0.882 0.160 7 117592008 missense variant A/G snv 3.1E-05 1
rs397508225 0.925 0.160 7 117559609 missense variant A/G snv 4.0E-06 1
rs397508277 1.000 0.120 7 117590379 missense variant A/G snv 1
rs397508428 1.000 0.120 7 117603624 missense variant A/G snv 1
rs397508553 1.000 0.120 7 117614654 missense variant A/G snv 3.6E-05 4.9E-05 1
rs397508621 1.000 0.120 7 117642592 missense variant A/G snv 4.0E-06 1
rs75389940 0.882 0.120 7 117627753 missense variant A/G snv 4.0E-06 1
rs1800074 1.000 0.120 7 117504330 missense variant A/G;T snv 4.0E-06 1
rs397508306 1.000 0.120 7 117591968 missense variant A/G;T snv 4.3E-06; 4.3E-06 1
rs1177201180 1.000 0.120 7 117592160 missense variant A/T snv 1
rs121909033 1.000 0.120 7 117592110 missense variant A/T snv 1
rs397508804 1.000 0.120 7 117536663 missense variant A/T snv 1.2E-05 1