Source: ALL
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: rs7314976
rs7314976
HCAR2
3 0.925 0.040 12 122702353 missense variant G/A;C snv 3.9E-02; 4.5E-06 0.010 1.000 1 2017 2017