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rs61749721(C;C)

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common in clinvar

Is a	genotype
of	rs61749721
Gene	MECP2
Chromosome	X
Position	154,031,065
mentioned	by

0

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	8.2	Rett Syndrome (predicted)

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Is a genotype