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: rs12721613
rs12721613
3 1.000 0.080 3 119807329 missense variant C/T snv 9.8E-03 3.8E-02 0.700 1.000 1 2012 2012