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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNQ4
(G222D)
Single nucleotide variant
(missense variant)
Autosomal dominant nonsyndromic hearing loss 2A
+2 more
GUncertain significance
KCNQ4
(G228C)
Single nucleotide variant
(missense variant)
Autosomal dominant nonsyndromic hearing loss 2A
+2 more
GUncertain significance
KCNQ4
(G277R)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
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