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rs35887622(G;G)

From SNPedia

Variant of unclear significance wrt deafness
Is agenotype
ofrs35887622
GeneGJB2
Chromosome13
Position20,189,481
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;A) 0 normal hearing
(A;C) 3 Carrier of a recessive deafness mutation
(A;G) 3 Variant of unclear significance wrt deafness
(G;G) 3 Variant of unclear significance wrt deafness

see discussion at rs35887622