ClinVar Miner

Submissions for variant NM_030777.4(SLC2A10):c.961del (p.Val321fs)

dbSNP: rs587776599
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 RCV000004848 SCV000025024 pathogenic Arterial tortuosity syndrome 2006-04-01 no assertion criteria provided literature only
GeneReviews RCV000004848 SCV000195664 not provided Arterial tortuosity syndrome no assertion provided literature only

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