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rs61751362(C;C)

From SNPedia

common in clinvar
Is agenotype
ofrs61751362
GeneMECP2
ChromosomeX
Position154,030,948
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 2 increased risk of Rett syndrome and Autism
(T;T) 2.5 increased risk of Rett syndrome and Autism