List of variants in gene PIEZO1 reported as benign for not specified

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: 18

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001142864.4(PIEZO1):c.4956-3T>C	rs9935872	0.87681
NM_001142864.4(PIEZO1):c.7500C>T (p.Tyr2500=)	rs1061228	0.10667
NM_001142864.4(PIEZO1):c.3456-11C>T	rs77276858	0.03009
NM_001142864.4(PIEZO1):c.6390G>A (p.Thr2130=)	rs34679131	0.02567
NM_001142864.4(PIEZO1):c.4385G>A (p.Arg1462Gln)	rs188337046	0.01884
NM_001142864.4(PIEZO1):c.6678C>T (p.Ser2226=)	rs34655152	0.01329
NM_001142864.4(PIEZO1):c.6963C>T (p.Asn2321=)	rs35917730	0.01098
NM_001142864.4(PIEZO1):c.5195C>T (p.Thr1732Met)	rs139051768	0.00749
NM_001142864.4(PIEZO1):c.7529C>T (p.Pro2510Leu)	rs61745086	0.00748
NM_001142864.4(PIEZO1):c.7505A>G (p.Lys2502Arg)	rs34830861	0.00599
NM_001142864.4(PIEZO1):c.6891C>T (p.Ala2297=)	rs34325377	0.00562
NM_001142864.4(PIEZO1):c.4580G>A (p.Arg1527His)	rs148870219	0.00229
NM_001142864.4(PIEZO1):c.6804G>A (p.Ala2268=)	rs371847339	0.00045
NM_001142864.4(PIEZO1):c.5627G>A (p.Arg1876Lys)	rs201967733	0.00025
NM_001142864.4(PIEZO1):c.5121G>C (p.Ser1707=)	rs34346312
NM_001142864.4(PIEZO1):c.5743C>A (p.Arg1915Ser)	rs13338527
NM_001142864.4(PIEZO1):c.64+12G>T	rs1207737714
NM_001142864.4(PIEZO1):c.6651C>A (p.Gly2217=)	rs117669855

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.