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rs121912663(A;T)

From SNPedia
pathogenic/causal mutation for Li-Fraumeni syndrome
Is agenotype
ofrs121912663
GeneTP53
Chromosome17
Position7,673,745
mentionedby
Magnitude6
ReputeBad
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 6 pathogenic/causal mutation for Li-Fraumeni syndrome

see Li-Fraumeni syndrome