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: rs376129674
rs376129674
HJV
1 1.000 0.080 1 146018204 missense variant C/T snv 2.8E-05 2.1E-05 0.010 1.000 1 2015 2015