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: rs78311289
rs78311289
27 0.662 0.357 4 1806162 missense variant A/C,G snp 4.0E-06 0.040 1.000 4 1995 2014
dbSNP: rs28931614
rs28931614
11 0.744 0.179 4 1804392 missense variant G/A,C snp 0.010 1.000 1 2002 2002