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: rs80338941
rs80338941
2 1.000 0.120 13 20189526 missense variant C/A;G snv 2.8E-05; 1.2E-05 0.710 1.000 1 2005 2005