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
rs28934576 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 64
rs1042522 0.563 0.643 17 7676154 stop gained G/C,T snp 0.67 0.62 56
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
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
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
rs759728549 0.679 0.214 17 7676223 stop lost T/C snp 8.0E-06 26
rs28934574 0.667 0.393 17 7673776 missense variant G/A,C snp 4.0E-06 25
rs28934575 0.673 0.321 17 7674230 missense variant C/A,G,T snp 25
rs786201838 0.662 0.429 17 7674953 missense variant T/A,C,G snp 25
rs121912656 0.667 0.500 17 7674229 missense variant C/A,G,T snp 4.0E-06; 4.0E-06 24
rs573154688 0.652 0.357 17 7670711 missense variant C/T snp 4.4E-05 3.2E-05 24
rs587780070 0.667 0.286 17 7675077 missense variant G/A,C,T snp 4.0E-06 24
rs760043106 0.662 0.357 17 7674947 missense variant A/C,G,T snp 24
rs28934874 0.673 0.429 17 7675161 stop gained G/A,C,T snp 23
rs786201057 0.673 0.357 17 7675995 missense variant G/A,C,T snp 3.2E-05 23
rs121912657 0.679 0.464 17 7673806 missense variant C/A,T snp 4.0E-06 22
rs397514495 0.707 0.286 17 7675070 missense variant C/A,T snp 1.2E-05 3.2E-05 22