ClinVar Miner

Submissions for variant NM_001110556.2(FLNA):c.3552C>A (p.Asp1184Glu)

dbSNP: rs80338837
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 RCV000020424 SCV000040825 not provided Melnick-Needles syndrome no assertion provided literature only

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