ClinVar Miner

Submissions for variant NM_001113491.2(SEPTIN9):c.332C>T (p.Ser111Phe)

dbSNP: rs80338762
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
OMIM RCV000006222 SCV000026404 pathogenic Amyotrophic neuralgia 2009-05-19 no assertion criteria provided literature only
GeneReviews RCV000006222 SCV000041184 not provided Amyotrophic neuralgia no assertion provided literature only

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