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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC26A4
(A434D)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 4
+2 more
GUncertain significance
TG
(L850Q)
Single nucleotide variant
(missense variant)
Hypothyroidism
GUncertain significance