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: rs11887534
rs11887534
29 0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 0.020 1.000 2 2004 2008
dbSNP: rs4148211
rs4148211
3 0.882 0.080 2 43844604 missense variant A/G snv 0.43 0.35 0.010 1.000 1 2008 2008