ClinVar Miner

List of variants in gene PIEZO2 reported by Department of Pathology and Laboratory Medicine, Sinai Health System

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001378183.1(PIEZO2):c.1006G>A (p.Ala336Thr) rs368601054 0.00021
NM_001378183.1(PIEZO2):c.172C>T (p.Arg58Trp) rs142351929 0.00009
NM_001378183.1(PIEZO2):c.6622C>T (p.Arg2208Trp) rs541120113 0.00009
NM_001378183.1(PIEZO2):c.6623G>A (p.Arg2208Gln) rs745694128 0.00007
NM_001378183.1(PIEZO2):c.86G>T (p.Gly29Val) rs772178114 0.00004
NM_001378183.1(PIEZO2):c.716C>T (p.Pro239Leu) rs776926434 0.00001
NM_001378183.1(PIEZO2):c.8179A>T (p.Ile2727Phe) rs952699419 0.00001
NM_001378183.1(PIEZO2):c.147A>C (p.Lys49Asn)
NM_001378183.1(PIEZO2):c.149C>T (p.Thr50Met)
NM_001378183.1(PIEZO2):c.2021T>A (p.Val674Asp)
NM_001378183.1(PIEZO2):c.2449G>C (p.Asp817His) rs375966918
NM_001378183.1(PIEZO2):c.3568A>G (p.Ile1190Val)
NM_001378183.1(PIEZO2):c.3956T>G (p.Phe1319Cys) rs2143770600
NM_001378183.1(PIEZO2):c.4588C>T (p.Pro1530Ser)
NM_001378183.1(PIEZO2):c.4801A>G (p.Arg1601Gly)
NM_001378183.1(PIEZO2):c.5219G>T (p.Arg1740Ile)
NM_001378183.1(PIEZO2):c.5365T>G (p.Ser1789Ala)
NM_001378183.1(PIEZO2):c.5975C>T (p.Thr1992Met)
NM_001378183.1(PIEZO2):c.6445C>T (p.His2149Tyr)

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.