Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.407 0.786 7 140753336 missense variant snp 4.0E-06 267
rs4986790 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 146
rs4986791 0.501 0.714 9 117713324 missense variant C/T snp 5.7E-02 5.1E-02 108
rs2910164 0.525 0.750 5 160485411 mature miRNA variant C/G snp 0.71; 4.1E-06 0.71 82
rs121913529 0.559 0.393 12 25245350 missense variant C/A,G,T snp 4.0E-06 70
rs121913279 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 68
rs5443 0.570 0.571 12 6845711 synonymous variant C/T snp 0.36 0.43 65
rs28934576 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 64
rs861539 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 60
rs1800470 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 46
rs1800896 0.593 0.571 1 206773552 intergenic variant T/C snp 0.40 43
rs121912651 0.618 0.464 17 7674221 missense variant G/A,C snp 4.0E-06 41
rs1799864 0.626 0.536 3 46357717 missense variant G/A snp 0.13 0.12 39
rs121913530 0.615 0.321 12 25245351 missense variant C/A,G,T snp 39
rs351855 0.642 0.357 5 177093242 missense variant G/A snp 0.33 0.27 35
rs121434568 0.642 0.321 7 55191822 missense variant T/A,G snp 33
rs121913254 0.647 0.429 1 114713909 missense variant G/A,C,T snp 33
rs121912664 0.667 0.357 17 7670699 missense variant C/A,G,T snp 1.2E-05 31
rs17576 0.647 0.571 20 46011586 missense variant A/G snp 0.39 0.38 30
rs121434569 0.667 0.321 7 55181378 missense variant C/T snp 2.8E-05 9.6E-05 29
rs757366142 0.657 0.500 3 46357714 missense variant G/A snp 4.0E-06 27
rs3212227 0.647 0.536 5 159315942 3 prime UTR variant T/G snp 0.25 27
rs11549465 0.662 0.357 14 61740839 missense variant C/T snp 8.8E-02 7.0E-02 27
rs104894228 0.662 0.500 11 534286 missense variant C/A,G,T snp 26
rs759728549 0.679 0.214 17 7676223 stop lost T/C snp 8.0E-06 26