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rs121912651(C;T)

From SNPedia
pathogenic/causal mutation for Li-Fraumeni syndrome
Is agenotype
ofrs121912651
GeneTP53
Chromosome17
Position7,674,221
mentionedby
Magnitude6
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6 pathogenic/causal mutation for Li-Fraumeni syndrome

see Li-Fraumeni syndrome