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rs121912666(A;C)

From SNPedia

pathogenic/causal mutation for Li-Fraumeni syndrome
Is agenotype
ofrs121912666
GeneTP53
Chromosome17
Position7,674,872
mentionedby
Magnitude6
ReputeBad
Geno Mag Summary
(A;A) 0 common in clinvar
(A;C) 6 pathogenic/causal mutation for Li-Fraumeni syndrome

see Li-Fraumeni syndrome