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: rs1799816
rs1799816
1 1.000 0.080 19 7125507 missense variant C/T snv 8.4E-03 5.3E-03 0.010 1.000 1 2016 2016