List of variants in gene PIEZO2 reported as uncertain significance by Breakthrough Genomics, Breakthrough Genomics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001378183.1(PIEZO2):c.5080G>A (p.Asp1694Asn)	rs114649884	0.00044
NM_001378183.1(PIEZO2):c.4250A>G (p.Lys1417Arg)	rs749257673	0.00031
NM_001378183.1(PIEZO2):c.8300A>G (p.Asn2767Ser)	rs376761944	0.00004

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