Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs752746786 0.769 0.357 1 1806503 missense variant A/C,G,T snp 4.0E-06 27
rs113488022 0.407 0.786 7 140753336 missense variant snp 4.0E-06 21
rs377274761 0.801 0.179 14 87968393 missense variant C/T snp 8.0E-06 3.2E-05 19
rs121913500 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 19
rs1057518843 0.821 0.179 14 87988523 missense variant C/T snp 18
rs869312824 0.846 0.107 1 1804565 missense variant A/G snp 15
rs61749715 0.744 0.179 X 154031154 missense variant G/A,C snp 15
rs1064795760 0.878 0.143 9 92719007 inframe deletion CATT/C in-del 14
rs1006737 0.679 0.107 12 2236129 intron variant G/A snp 0.37 13
rs4647924 0.715 0.179 4 1801844 missense variant C/A,G,T snp 4.2E-06; 4.2E-06 3.2E-05; 3.2E-05 12
rs869312825 0.878 0.071 1 1804548 start lost T/C snp 11
rs886041116 0.846 0.143 20 50892526 stop gained G/A snp 10
rs6484218 0.801 0.036 11 10369034 intron variant G/A snp 0.21 10
rs1060503428 0.821 0.107 16 89546662 inframe deletion AGGCGGGAGA/A in-del 10
rs768823392 0.821 0.107 16 89546657 splice acceptor variant AGGAGAGGCG/A in-del 4.0E-06; 2.6E-04 4.1E-04 10
rs587783405 0.878 0.107 X 18588021 stop gained C/T snp 9
rs869312823 0.923 0.071 1 1806509 missense variant T/C snp 9
rs28934906 0.769 0.071 X 154031355 missense variant G/A snp 9
rs387907329 0.878 0.179 X 49075573 stop gained G/A,T snp 5.5E-06 8
rs869312702 0.923 0.036 9 128203609 missense variant G/A snp 7
rs1057519436 0.878 0.179 3 47846550 missense variant G/A snp 7
rs724159953 0.923 0.036 21 37505352 stop gained C/T snp 7
rs724159948 0.923 0.036 21 37490273 stop gained C/T snp 7
rs869312822 0.878 0.107 1 1806514 missense variant A/C snp 7
rs1057518921 X 71132465 missense variant G/A snp 7