List of variants in gene PIEZO1 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001142864.4(PIEZO1):c.132C>T (p.Phe44=)	rs112488313	0.01303
NM_001142864.4(PIEZO1):c.4872A>G (p.Ala1624=)	rs35375982	0.01227
NM_001142864.4(PIEZO1):c.3363A>G (p.Thr1121=)	rs35100558	0.01077
NM_001142864.4(PIEZO1):c.6294C>T (p.Tyr2098=)	rs35015310	0.00960
NM_001142864.4(PIEZO1):c.5195C>T (p.Thr1732Met)	rs139051768	0.00749
NM_001142864.4(PIEZO1):c.5552C>T (p.Thr1851Met)	rs34370460	0.00731
NM_001142864.4(PIEZO1):c.4955+3G>A	rs569520386	0.00382
NM_001142864.4(PIEZO1):c.7495T>C (p.Leu2499=)	rs35736353	0.00265
NM_001142864.4(PIEZO1):c.7317-5C>T	rs150172633	0.00261
NM_001142864.4(PIEZO1):c.4992G>A (p.Leu1664=)	rs186462241	0.00001

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