Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11540654 0.492 0.679 17 7676040 missense variant C/A,G,T snp 4.8E-05 3.2E-05 117
rs121913279 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 68
rs28934576 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 64
rs121434592 0.582 0.500 14 104780214 missense variant C/T snp 4.0E-06 56
rs104886003 0.580 0.393 3 179218303 missense variant G/A,C snp 4.0E-06 52
rs104894230 0.615 0.464 11 534288 missense variant C/A,G,T snp 42
rs121913500 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 42
rs121912651 0.618 0.464 17 7674221 missense variant G/A,C snp 4.0E-06 41
rs11540652 0.618 0.464 17 7674220 missense variant C/A,G,T snp 1.2E-05 40
rs56149945 0.626 0.643 5 143399752 missense variant T/A,C snp 2.0E-02 2.2E-02 35
rs121913499 0.630 0.464 2 208248389 missense variant G/A,C,T snp 34
rs121913274 0.626 0.286 3 179218304 missense variant A/C,G,T snp 33
rs104894229 0.634 0.500 11 534289 missense variant C/A,G,T snp 31
rs121912664 0.667 0.357 17 7670699 missense variant C/A,G,T snp 1.2E-05 31
rs121913343 0.638 0.464 17 7673803 missense variant G/A,T snp 1.2E-05 30
rs397516436 0.647 0.393 17 7674894 stop gained G/A,C snp 30
rs121913273 0.638 0.357 3 179218294 missense variant G/A,C snp 29
rs121912666 0.647 0.321 17 7674872 missense variant T/C,G snp 8.0E-06 29
rs587778720 0.647 0.321 17 7674893 missense variant C/A,G,T snp 4.0E-06 29
rs28934573 0.652 0.464 17 7674241 missense variant G/A,C,T snp 4.0E-06 28
rs138729528 0.657 0.464 17 7675089 missense variant G/A,C snp 1.6E-05 3.2E-05 27
rs28934578 0.647 0.357 17 7675088 missense variant snp 4.0E-06 27
rs104894228 0.662 0.500 11 534286 missense variant C/A,G,T snp 26
rs121913233 0.657 0.429 11 533874 missense variant T/A,C,G snp 25
rs28934574 0.667 0.393 17 7673776 missense variant G/A,C snp 4.0E-06 25