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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OTOGL
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
OTOGL
(M1189I +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 84B
GBenign
OTOGL
Single nucleotide variant
(synonymous variant)
Autosomal recessive nonsyndromic hearing loss 84B
GBenign
OTOGL
(R1941K +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 84B
GBenign
OTOGL
Single nucleotide variant
(synonymous variant)
Autosomal recessive nonsyndromic hearing loss 84B
GBenign
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