Source: CLINVAR ×
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: rs786201838
rs786201838
TP53
23 0.683 0.440 17 7674953 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016