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: rs121434390
rs121434390
2 0.925 0.080 11 101504634 missense variant G/T snv 0.010 1.000 1 2010 2010
dbSNP: rs121434395
rs121434395
2 0.925 0.080 11 101453062 missense variant C/T snv 0.010 1.000 1 2010 2010
dbSNP: rs3802829
rs3802829
2 0.925 0.080 11 101583461 missense variant G/A snv 8.2E-02 7.0E-02 0.010 1.000 1 2012 2012
dbSNP: rs779430565
rs779430565
3 0.882 0.080 11 101504316 missense variant T/A snv 1.2E-05 1.4E-05 0.010 1.000 1 2011 2011