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: rs1420601296
rs1420601296
1 1.000 0.120 11 17442866 missense variant C/T snv 4.0E-06 3.5E-05 0.700 1.000 20 1996 2015