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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PTPRQ
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
PTPRQ
(Y1203H)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 84A
+2 more
GLikely benign
PTPRQ
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
PTPRQ
(M2196V)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
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