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rs786204056(T;T)

From SNPedia
common in clinvar
Is agenotype
ofrs786204056
GenePTCH1
Chromosome9
Position95,458,011
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;T) 5.3 Basal cell nevus syndrome
(T;T) 0 common in clinvar