ClinVar Miner

Submissions for variant NM_001256789.3(CACNA1F):c.5577C>T (p.Gly1859=)

gnomAD frequency: 0.00088  dbSNP: rs141521080
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) RCV000266133 SCV000332327 likely benign not specified 2015-06-24 criteria provided, single submitter clinical testing
Invitae RCV000978399 SCV001126328 benign not provided 2023-11-27 criteria provided, single submitter clinical testing

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