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rs104894401(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs104894401
GeneGJB2
Chromosome13
Position20,189,154
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 4 Deafness mutation (dominant)
(G;G) 0 common in clinvar