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rs11090865(G;T)

From SNPedia
Carrier of a deafness-related modifier variant
Is agenotype
ofrs11090865
GeneTRMU
Chromosome22
Position46,335,792
mentionedby
Magnitude2.3
ReputeBad
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 2.3 Carrier of a deafness-related modifier variant
(T;T) 3 Modifier variant; some impact in rare cases

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