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rs121912656(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs121912656
GeneTP53
Chromosome17
Position7,674,229
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 6 pathogenic/causal mutation for Li-Fraumeni syndrome
(C;G) 7 Li-Fraumeni Syndrome (predicted)
(G;G) 0 common in clinvar
(G;T) 7 Li-Fraumeni Syndrome (predicted)