ClinVar Miner

Submissions for variant NM_001256789.3(CACNA1F):c.3651C>T (p.Val1217=)

gnomAD frequency: 0.00216  dbSNP: rs150205903
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
Eurofins Ntd Llc (ga) RCV000730164 SCV000857879 likely benign not specified 2017-11-16 criteria provided, single submitter clinical testing
Invitae RCV000969874 SCV001117413 benign not provided 2024-01-16 criteria provided, single submitter clinical testing

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