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rs104894408(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs104894408
GeneGJB2
Chromosome13
Position20,189,548
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 6 Deafness and keratitis; possible dominant or recessive
(C;G) 6 Deafness and keratitis; possible dominant or recessive
(G;G) 0 common in clinvar