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Links from MedGen

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLIC5
(N134S +2 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 103
GUncertain significance
Autosomal recessive nonsyndromic hearing loss 103
GPathogenic
CLIC5
(N112D +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
CLIC5
(R79S)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GBenign/Likely benign
CLIC5
(C32* +1 more)
Single nucleotide variant
(nonsense +1 more)
Autosomal recessive nonsyndromic hearing loss 103
GPathogenic
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