Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 38
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs13199524 0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 9
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 8
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 8
rs2066845 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 8
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 6
rs12191877 0.851 0.120 6 31285148 intron variant C/T snv 0.12 6
rs4921482 0.807 0.120 5 159337470 intron variant T/C;G snv 6
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs74817271 0.807 0.120 5 151090412 intron variant G/A snv 5.0E-02 6
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 5
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs2201841 0.716 0.440 1 67228519 intron variant A/G;T snv 4
rs763361 0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 4
rs744166 0.689 0.560 17 42362183 intron variant A/G snv 0.48 4
rs702873 0.882 0.120 2 60854407 intron variant C/T snv 0.35 3
rs13017599 0.882 0.160 2 60937196 non coding transcript exon variant G/A snv 0.25 3
rs2066808 0.807 0.280 12 56344189 intron variant A/G snv 0.21 3
rs33980500 0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 3
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 2
rs4683946 0.925 0.080 3 101896982 intron variant G/T snv 0.19 2
rs848 0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 2