ClinVar Miner

Submissions for variant NM_001142864.4(PIEZO1):c.2329+11C>T

gnomAD frequency: 0.00004 dbSNP: rs1313856152

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
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	RCV001001109	SCV001158246	benign	not specified	2019-03-06	criteria provided, single submitter	clinical testing

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