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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC26A5
(R689Q +1 more)
Single nucleotide variant
(missense variant +2 more)
Autosomal recessive nonsyndromic hearing loss 61
+1 more
GUncertain significance
SLC26A5
(T354N)
Single nucleotide variant
(missense variant +2 more)
Autosomal recessive nonsyndromic hearing loss 61
+1 more
GUncertain significance
SLC26A5
(N330S)
Single nucleotide variant
(missense variant +2 more)
Autosomal recessive nonsyndromic hearing loss 61
+2 more
GBenign
SLC26A5
Single nucleotide variant
(splice acceptor variant)
not specified
+2 more
GBenign/Likely benign
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