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rs786204841(G;G)

From SNPedia

common in clinvar
Is agenotype
ofrs786204841
GeneLOC105369301, CLDN14
Chromosome21
Position36,461,002
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 6 Deafness; early-onset (prelingual)
(A;G) 3 Carrier of a deafness mutation
(G;G) 0 common in clinvar