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: rs121912609
rs121912609
1 1.000 0.107 9 14824929 missense variant G/A snp 0.800 1 2009 2009
dbSNP: rs121912610
rs121912610
1 1.000 0.107 9 14784494 missense variant C/T snp 2.4E-05 0.800 1 2009 2009