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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PCDH15
(R245* +3 more)
Single nucleotide variant
(nonsense)
Autosomal recessive nonsyndromic hearing loss 23
+5 more
GPathogenic
USH1G
(R135fs +1 more)
Deletion
(frameshift variant)
Usher syndrome type 1G
GPathogenic