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: rs11466651
rs11466651
2 0.925 0.120 4 38774699 missense variant C/T snv 6.5E-02 4.6E-02 0.010 1.000 1 2010 2010