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 0.923 0.071 11 101504634 missense variant G/T snp 0.010 1.000 1 2011 2011
dbSNP: rs121434395
rs121434395
2 0.923 0.071 11 101453062 missense variant C/T snp 0.010 1.000 1 2011 2011
dbSNP: rs779430565
rs779430565
3 0.878 0.071 11 101504316 missense variant T/A snp 1.2E-05 0.010 1.000 1 2011 2011