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rs786200885(T;T)

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common in clinvar

Is a	genotype
of	rs786200885
Gene	CLDN14, LOC105369301
Chromosome	21
Position	36,461,298
mentioned	by

0

Good

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

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Is a genotype