Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1046175 0.851 0.080 10 133391446 stop gained C/A;G;T snv 1.2E-05; 0.88 4
rs11540478 0.851 0.080 15 90085305 synonymous variant G/A;C snv 3.5E-02; 6.4E-06 4
rs1171287261 0.851 0.080 7 55191839 missense variant G/A snv 4
rs11778573 0.851 0.080 8 133216687 intron variant T/G snv 0.59 4
rs1226168728 0.851 0.080 19 45398021 missense variant G/C snv 7.0E-06 4
rs1362623672 0.851 0.080 19 45421317 missense variant G/C snv 1.4E-05 4
rs1878022 0.851 0.080 12 108305255 intron variant C/T snv 0.70 4
rs2293347 0.851 0.080 7 55201223 synonymous variant C/T snv 0.14 9.5E-02 4
rs2977536 0.851 0.080 8 133207034 intron variant G/C snv 0.36 4
rs3805213 0.851 0.080 4 139044570 intron variant C/T snv 0.23 4
rs4065 0.851 0.080 10 73916706 3 prime UTR variant C/T snv 0.51 4
rs4978754 0.851 0.080 9 108884801 intron variant T/C snv 0.92 4
rs662959 0.851 0.080 3 159983443 intron variant G/A snv 0.16 4
rs677844 0.851 0.080 1 12184261 intron variant T/C snv 0.22 4
rs7170924 0.851 0.080 15 81290798 intron variant G/T snv 0.30 4
rs750758481 0.851 0.080 5 132603476 missense variant T/C snv 8.0E-06 7.0E-06 4
rs753254929 0.851 0.080 14 20455915 missense variant G/A;C snv 1.6E-05 4
rs7631358 0.851 0.080 3 189630622 upstream gene variant G/A snv 0.13 4
rs778561687 0.851 0.080 19 40235953 missense variant C/A;T snv 4.0E-06; 4.0E-06 4
rs928508 0.851 0.080 1 40757742 intron variant G/A;T snv 0.50 4
rs9535826 0.851 0.080 13 51991990 intron variant T/C;G snv 4
rs967591 0.851 0.080 19 45406676 5 prime UTR variant G/A;C;T snv 0.22; 6.7E-06 4
rs1026411 0.827 0.080 8 127014165 intron variant G/A;C snv 0.25 5
rs107822 0.827 0.120 6 33207798 upstream gene variant C/T snv 0.27 0.28 5
rs1423493595 0.851 0.080 20 50082836 missense variant G/A snv 4.0E-06 7.0E-06 5