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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TMPRSS3
(A426T +2 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GPathogenic/Likely pathogenic
TMPRSS3
(D348N +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 8
+2 more
GConflicting classifications of pathogenicity
TMPRSS3
(Y112C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMPRSS3
(A138E +1 more)
Single nucleotide variant
(missense variant)
Nonsyndromic genetic hearing loss
+4 more
GPathogenic/Likely pathogenic
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