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: rs121913660
rs121913660
2 0.923 0.036 11 67611511 missense variant C/T snp 3.2E-05 3.2E-05 0.700 1 1999 1999
dbSNP: rs121913661
rs121913661
2 0.923 0.036 11 67610510 missense variant G/A snp 3.2E-05 0.700 1 2001 2001