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: rs121434592
rs121434592
56 0.582 0.500 14 104780214 missense variant C/T snp 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs397514606
rs397514606
9 0.769 0.214 1 243695714 missense variant C/T snp 0.010 1.000 1 2016 2016