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rs61749738(G;G)

From SNPedia

possible: Rett syndrome
Is agenotype
ofrs61749738
GeneMECP2
ChromosomeX
Position154,031,145
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(C;C) 0 common/normal
(C;G) 3 possible: carrier of a Rett syndrome allele
(G;G) 4 possible: Rett syndrome

possible but uncertain; see discussion at rs61749738