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: rs9001
rs9001
2 0.925 0.080 3 53823890 missense variant T/G snv 0.15 0.17 0.010 1.000 1 2009 2009