ClinVar Miner

Submissions for variant NM_000504.4(F10):c.814del (p.Ile271_Leu272insTer)

dbSNP: rs387906506
Minimum review status: Collection method:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000012834 SCV000033074 pathogenic Factor X deficiency 1989-10-01 no assertion criteria provided literature only

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