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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRYL1, GJB2
+15 more
Deletion
Autosomal recessive nonsyndromic hearing loss 1A
+2 more
GPathogenic
GJB6
(A40V)
Single nucleotide variant
(missense variant)
not specified
+4 more
GUncertain significance
GJB6
(T5M)
Single nucleotide variant
(missense variant)
Autosomal dominant nonsyndromic hearing loss 3B
GPathogenic
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