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: rs121913482
rs121913482
30 0.685 0.393 4 1801837 missense variant C/T snp 0.800 9 1995 2008
dbSNP: rs121913279
rs121913279
68 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.800 6 2004 2012
dbSNP: rs104886003
rs104886003
52 0.580 0.393 3 179218303 missense variant G/A,C snp 4.0E-06 0.800 5 2004 2012
dbSNP: rs121913483
rs121913483
13 0.734 0.250 4 1801841 missense variant C/A,G,T snp 4.2E-06; 1.3E-05 3.2E-05 0.800 3 1996 2005
dbSNP: rs121913273
rs121913273
29 0.638 0.357 3 179218294 missense variant G/A,C snp 0.710 1.000 1 2007 2007
dbSNP: rs121913274
rs121913274
33 0.626 0.286 3 179218304 missense variant A/C,G,T snp 0.700 4 2004 2007
dbSNP: rs121913105
rs121913105
16 0.724 0.179 4 1806163 missense variant A/C,T snp 0.700 0
dbSNP: rs121913479
rs121913479
10 0.744 0.286 4 1804362 missense variant G/A,T snp 4.0E-06 3.2E-05 0.700 0
dbSNP: rs121913484
rs121913484
4 0.878 0.214 4 1804365 missense variant A/T snp 0.700 0
dbSNP: rs121913485
rs121913485
11 0.784 0.321 4 1804372 missense variant A/G snp 0.700 0
dbSNP: rs78311289
rs78311289
27 0.662 0.357 4 1806162 missense variant A/C,G snp 4.0E-06 0.700 0
dbSNP: rs28931615
rs28931615
13 0.756 0.214 4 1804426 missense variant C/A,T snp 3.2E-05 0.010 < 0.001 1 2007 2007