Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4647924
rs4647924
20 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 0.740 1.000 11 1997 2017
dbSNP: rs28933068
rs28933068
11 0.784 0.107 4 1805644 stop gained C/A,G,T snp 1.6E-05 0.700 9 1995 2017
dbSNP: rs28931615
rs28931615
13 0.756 0.214 4 1804426 missense variant C/A,T snp 3.2E-05 0.700 7 1996 2017
dbSNP: rs28931614
rs28931614
11 0.744 0.179 4 1804392 missense variant G/A,C snp 0.700 6 1996 2017
dbSNP: rs78311289
rs78311289
27 0.662 0.357 4 1806162 missense variant A/C,G snp 4.0E-06 0.700 5 2001 2017
dbSNP: rs28928868
rs28928868
3 0.923 0.107 4 1806164 missense variant G/C,T snp 4.0E-06 0.700 4 2001 2017
dbSNP: rs121913105
rs121913105
16 0.724 0.179 4 1806163 missense variant A/C,T snp 0.700 1 2017 2017
dbSNP: rs397515514
rs397515514
3 0.923 0.071 4 1807261 stop lost G/T snp 0.700 1 2017 2017