Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2227307 0.851 0.240 4 73740952 intron variant T/G snv 0.45 6
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs193922500 0.851 0.160 7 117548798 missense variant T/C snv 2.0E-04 4.9E-05 5
rs11575934 0.882 0.040 19 18075808 missense variant T/C snv 0.28 0.25 4
rs7512462 0.882 0.200 1 205930467 intron variant T/C snv 0.38 4
rs778055276 3 122555701 missense variant T/C snv 4.4E-05 3.5E-05 1
rs121909005 0.851 0.160 7 117587801 missense variant T/A;C;G snv 4.0E-06; 8.0E-06 5
rs121917834 0.790 0.080 8 22163096 missense variant T/A;C snv 3.6E-05 10
rs17580 0.776 0.160 14 94380925 missense variant T/A snv 2.3E-02 2.9E-02 14
rs1965708 0.851 0.200 10 79557289 missense variant G/T snv 0.22 0.25 6
rs113857788 0.882 0.160 7 117664780 missense variant G/C;T snv 1.0E-03; 6.0E-05 5
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs75541969 0.827 0.200 7 117614699 missense variant G/C snv 4.0E-04 3.2E-04 9
rs1800076 0.763 0.200 7 117509093 missense variant G/A;T snv 1.5E-02; 8.0E-06 10
rs78655421 0.716 0.240 7 117530975 missense variant G/A;C;T snv 1.5E-03; 1.2E-05 18
rs77932196 0.790 0.280 7 117540270 missense variant G/A;C;T snv 2.4E-05; 2.4E-05 8
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs1130866 0.827 0.160 2 85666618 missense variant G/A;C snv 0.50 9
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs213950 0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs75527207 0.732 0.440 7 117587806 missense variant G/A snv 1.8E-04 3.0E-04 15