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: rs3812762
rs3812762
1 1.000 0.120 11 8730093 missense variant G/C snv 0.32 0.27 0.700 1.000 1 2014 2014