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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OSBPL2
(R50fs +1 more)
Deletion
(5 prime UTR variant +2 more)
Autosomal dominant nonsyndromic hearing loss 67
GPathogenic
OSBPL2
(Q41fs +1 more)
Microsatellite
(5 prime UTR variant +2 more)
Autosomal dominant nonsyndromic hearing loss 67
GPathogenic