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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EYA1
(A68G +1 more)
Single nucleotide variant
(missense variant +1 more)
Otofaciocervical syndrome 1
GUncertain significance
EYA1
(R41H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GConflicting classifications of pathogenicity
EYA1
(M32I +1 more)
Single nucleotide variant
(missense variant +1 more)
Otofaciocervical syndrome 1
GUncertain significance
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