ClinVar Miner

Submissions for variant NC_000020.11:g.7125642T>C

gnomAD frequency: 0.41043 dbSNP: rs1884302

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
OMIM	RCV000490626	SCV000579316	risk factor	Craniosynostosis 7	2021-02-15	no assertion criteria provided	literature only

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