ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.2707C>T (p.His903Tyr)

gnomAD frequency: 0.00001 dbSNP: rs765300713

Minimum review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Athena Diagnostics	RCV000710940	SCV000841252	uncertain significance	not provided	2017-12-27	criteria provided, single submitter	clinical testing

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