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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRXCR1
(P38L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GRXCR1
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
GRXCR1
(Y111H)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 25
+2 more
GUncertain significance
GRXCR1
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
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