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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ANAPC15, LRTOMT
+1 more
(R208Q +2 more)
Single nucleotide variant
(missense variant +3 more)
Autosomal recessive nonsyndromic hearing loss 63
+2 more
GBenign
ANAPC15, LRTOMT
+1 more
(H268Y +3 more)
Single nucleotide variant
(missense variant +2 more)
not specified
+2 more
GUncertain significance