ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.1968G>A (p.Gln656=)

dbSNP: rs797044487
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV000192015 SCV000196621 not provided Hutchinson-Gilford syndrome no assertion provided literature only
OMIM RCV000190822 SCV000245692 pathogenic Hutchinson-Gilford progeria syndrome, atypical 2015-08-01 no assertion criteria provided literature only

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