Source: ALL
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: rs370443546
rs370443546
CTLA4
1 1.000 0.120 2 203870744 missense variant A/G snv 4.0E-06 2.8E-05 0.020 1.000 2 2006 2007