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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EPS8
(T726I)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 102
+3 more
GUncertain significance
EPS8
Single nucleotide variant
(synonymous variant)
Autosomal recessive nonsyndromic hearing loss 102
+1 more
GBenign/Likely benign
EPS8
(A150V)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 102
+1 more
GUncertain significance
EPS8
(H35R)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 102
+2 more
GBenign/Likely benign
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