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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRH, LOC130000523
(P30R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
CRH
Single nucleotide variant
Autosomal dominant nocturnal frontal lobe epilepsy
Gnot provided
CRH
Single nucleotide variant
CRH-related condition
GLikely benign
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