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: rs376862893
rs376862893
1 1.000 0.036 22 50683352 missense variant C/T snp 1.1E-04 3.2E-05 0.010 1.000 1 2012 2012
dbSNP: rs76224556
rs76224556
1 1.000 0.036 22 50695096 intron variant C/A,T snp 2.0E-02 2.4E-02 0.010 < 0.001 1 2013 2013