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: rs1358566538
rs1358566538
1 1.000 0.120 16 2100552 missense variant C/T snv 8.1E-06 0.700 1.000 20 1996 2009