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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MCM2
(E93K)
Single nucleotide variant
(missense variant +1 more)
Autosomal dominant nonsyndromic hearing loss 70
GUncertain significance
MCM2
(E411K)
Single nucleotide variant
(missense variant +1 more)
Autosomal dominant nonsyndromic hearing loss 70
GUncertain significance
MCM2
(P483S)
Single nucleotide variant
(missense variant +1 more)
Autosomal dominant nonsyndromic hearing loss 70
GUncertain significance
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