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rs371100799(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs371100799
GeneCLDN14, LOC105369301
Chromosome21
Position36,461,529
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Carrier of a deafness mutation
(T;T) 6 Deafness; early-onset (prelingual)