ClinVar Miner

Submissions for variant NM_172107.4(KCNQ2):c.388-1_389del

dbSNP: rs118192196
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV000678080 SCV000041641 not provided Seizures, benign familial neonatal, 1 no assertion provided literature only BFNE (benign familial neonatal epilepsy)

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