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rs786204841(G;G)

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common in clinvar

Is a	genotype
of	rs786204841
Gene	CLDN14, LOC105369301
Chromosome	21
Position	36,461,002
mentioned	by

0

Good

Geno	Mag	Summary
(A;A)	6	Deafness; early-onset (prelingual)
(A;G)	3	Carrier of a deafness mutation
(G;G)	0	common in clinvar

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Is a genotype