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: rs121909525
rs121909525
2 1.000 0.080 1 229431994 missense variant C/A;G snv 0.700 1.000 6 2003 2015