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: rs1425166755
rs1425166755
1 1.000 17 72121722 missense variant G/A;C snv 0.700 1.000 11 1995 2018