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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYO7A
(L16S +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 2
+4 more
GBenign
MYO7A
(T1566M +2 more)
Single nucleotide variant
(missense variant)
Usher syndrome type 1
+4 more
GBenign/Likely benign
MYO7A
(Y1719C +2 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GBenign/Likely benign
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