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: rs2229616
rs2229616
11 0.801 0.107 18 60372043 missense variant C/T snp 1.6E-02 1.6E-02 0.010 1.000 1 2008 2008
dbSNP: rs4680
rs4680
155 0.484 0.821 22 19963748 missense variant G/A snp 0.46 0.45 0.010 < 0.001 1 2004 2004
dbSNP: rs800629
rs800629
1 1.000 0.036 2 37752757 intergenic variant snp 0.010 1.000 1 2010 2010