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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GIPC3
(R107P)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 15
GUncertain significance
GIPC3
(A134T)
Single nucleotide variant
(missense variant)
Sensorineural hearing loss disorder
GLikely pathogenic