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rs111033299(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs111033299
GeneGJB2
Chromosome13
Position20,189,299
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 3 Carrier of a recessive deafness mutation
(G;G) 0 common in clinvar