Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934576 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 38
rs121913279 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 33
rs104886003 0.580 0.393 3 179218303 missense variant G/A,C snp 4.0E-06 32
rs11540652 0.618 0.464 17 7674220 missense variant C/A,G,T snp 1.2E-05 32
rs104894230 0.615 0.464 11 534288 missense variant C/A,G,T snp 30
rs121912651 0.618 0.464 17 7674221 missense variant G/A,C snp 4.0E-06 30
rs66527965 0.801 0.179 17 50193038 missense variant C/A,T snp 29
rs104894229 0.634 0.500 11 534289 missense variant C/A,G,T snp 28
rs752746786 0.769 0.357 1 1806503 missense variant A/C,G,T snp 4.0E-06 27
rs121913274 0.626 0.286 3 179218304 missense variant A/C,G,T snp 27
rs587778720 0.647 0.321 17 7674893 missense variant C/A,G,T snp 4.0E-06 25
rs397516436 0.647 0.393 17 7674894 stop gained G/A,C snp 25
rs121913343 0.638 0.464 17 7673803 missense variant G/A,T snp 1.2E-05 25
rs121913281 0.662 0.429 3 179234296 missense variant C/T snp 24
rs28934575 0.673 0.321 17 7674230 missense variant C/A,G,T snp 24
rs138729528 0.657 0.464 17 7675089 missense variant G/A,C snp 1.6E-05 3.2E-05 24
rs121912666 0.647 0.321 17 7674872 missense variant T/C,G snp 8.0E-06 24
rs121918494 0.878 0.107 10 121517363 missense variant G/C snp 23
rs121913482 0.685 0.393 4 1801837 missense variant C/T snp 23
rs11554290 0.618 0.464 1 114713908 missense variant T/A,C,G snp 23
rs121913275 0.673 0.286 3 179218305 missense variant G/A,C,T snp 4.0E-06 23
rs28934574 0.667 0.393 17 7673776 missense variant G/A,C snp 4.0E-06 23
rs786201057 0.673 0.357 17 7675995 missense variant G/A,C,T snp 3.2E-05 23
rs28934573 0.652 0.464 17 7674241 missense variant G/A,C,T snp 4.0E-06 23
rs201893408 0.707 0.429 8 93795970 missense variant T/A,C snp 8.0E-06; 1.5E-04 9.6E-05 22