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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TBC1D24
(D70Y)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 86
GPathogenic
TBC1D24
(S178L)
Single nucleotide variant
(missense variant)
not provided
+3 more
GPathogenic
TBC1D24
(R293P)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 86
GPathogenic
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