rs121912652(A;G)

pathogenic/causal mutation for Li-Fraumeni syndrome

Is a	genotype
of	rs121912652
Gene	TP53
Chromosome	17
Position	7,674,191
mentioned	by

Magnitude

6

Repute

Bad

Geno	Mag	Summary
(A;G)	6	pathogenic/causal mutation for Li-Fraumeni syndrome
(G;G)	0	common in clinvar
(G;T)	7	Li-Fraumeni Syndrome (predicted)

see Li-Fraumeni syndrome