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: rs1309566180
rs1309566180
1 1.000 0.080 9 21971170 missense variant C/T snv 0.010 1.000 1 1998 1998