Gene: TP53 ×
Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1131691003
rs1131691003
TP53
A 0.700 CausalMutation CLINVAR

dbSNP: rs1131691039
rs1131691039
TP53
T 0.700 CausalMutation CLINVAR

dbSNP: rs1131691042
rs1131691042
TP53
T 0.700 CausalMutation CLINVAR

dbSNP: rs121912652
rs121912652
TP53
T 0.700 CausalMutation CLINVAR

dbSNP: rs121912653
rs121912653
TP53
G 0.700 CausalMutation CLINVAR

dbSNP: rs121912656
rs121912656
TP53
T 0.700 CausalMutation CLINVAR

dbSNP: rs121912657
rs121912657
TP53
A 0.700 CausalMutation CLINVAR

dbSNP: rs121912662
rs121912662
TP53
G 0.700 CausalMutation CLINVAR

dbSNP: rs121912663
rs121912663
TP53
A 0.700 CausalMutation CLINVAR

dbSNP: rs121912666
rs121912666
TP53
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555527002
rs1555527002
TP53
AG 0.700 GeneticVariation CLINVAR

dbSNP: rs17882252
rs17882252
TP53
A 0.700 CausalMutation CLINVAR

dbSNP: rs28934575
rs28934575
TP53
A 0.700 CausalMutation CLINVAR

dbSNP: rs28934873
rs28934873
TP53
G 0.700 CausalMutation CLINVAR

dbSNP: rs28934875
rs28934875
TP53
G 0.700 CausalMutation CLINVAR

dbSNP: rs55832599
rs55832599
TP53
A 0.700 GeneticVariation CLINVAR

dbSNP: rs587776768
rs587776768
TP53
G 0.700 CausalMutation CLINVAR

dbSNP: rs587782144
rs587782144
TP53
T 0.700 CausalMutation CLINVAR

dbSNP: rs587782705
rs587782705
TP53
A 0.700 CausalMutation CLINVAR

dbSNP: rs730882008
rs730882008
TP53
T 0.700 GeneticVariation CLINVAR

dbSNP: rs730882019
rs730882019
TP53
CG 0.700 CausalMutation CLINVAR

dbSNP: rs786202525
rs786202525
TP53
T 0.700 CausalMutation CLINVAR

dbSNP: rs28934576
rs28934576
TP53
T 0.700 GeneticVariation CLINVAR A child with Li-Fraumeni syndrome: Modes to inactivate the second allele of TP53 in three different malignancies. 25787918

2015
dbSNP: rs28934578
rs28934578
TP53
T 0.700 CausalMutation CLINVAR A common gain of function of p53 cancer mutants in inducing genetic instability. 19881536

2010
dbSNP: rs28934578
rs28934578
TP53
T 0.700 CausalMutation CLINVAR A common p53 mutation (R175H) activates c-Met receptor tyrosine kinase to enhance tumor cell invasion. 23792586

2013