ClinVar Miner

List of variants in gene PIEZO2 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 28
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001378183.1(PIEZO2):c.8250A>T (p.Gly2750=) rs34134242 0.01209
NM_001378183.1(PIEZO2):c.8340C>T (p.Gly2780=) rs146400447 0.00192
NM_001378183.1(PIEZO2):c.6013G>A (p.Asp2005Asn) rs199842060 0.00170
NM_001378183.1(PIEZO2):c.3930C>T (p.Tyr1310=) rs146505222 0.00142
NM_001378183.1(PIEZO2):c.7969G>A (p.Ala2657Thr) rs147666072 0.00109
NM_001378183.1(PIEZO2):c.5030-15G>T rs527248198 0.00098
NM_001378183.1(PIEZO2):c.3000C>T (p.Tyr1000=) rs368969302 0.00079
NM_001378183.1(PIEZO2):c.6153C>T (p.Ala2051=) rs375812718 0.00072
NM_001378183.1(PIEZO2):c.6475G>C (p.Glu2159Gln) rs200276831 0.00072
NM_001378183.1(PIEZO2):c.4537C>G (p.Gln1513Glu) rs115526553 0.00067
NM_001378183.1(PIEZO2):c.5080G>A (p.Asp1694Asn) rs114649884 0.00044
NM_001378183.1(PIEZO2):c.8535A>G (p.Lys2845=) rs149395405 0.00042
NM_001378183.1(PIEZO2):c.6969C>A (p.Ala2323=) rs139705172 0.00027
NM_001378183.1(PIEZO2):c.5982C>T (p.Ser1994=) rs377649969 0.00026
NM_001378183.1(PIEZO2):c.2755G>A (p.Glu919Lys) rs564867814 0.00024
NM_001378183.1(PIEZO2):c.5877C>T (p.Asp1959=) rs539810112 0.00022
NM_001378183.1(PIEZO2):c.6694+9C>T rs181261032 0.00014
NM_001378183.1(PIEZO2):c.3123+9C>T rs184076139 0.00013
NM_001378183.1(PIEZO2):c.3840A>G (p.Ala1280=) rs199707250 0.00004
NM_001378183.1(PIEZO2):c.704-3T>C rs762788496 0.00004
NM_001378183.1(PIEZO2):c.7977G>A (p.Ser2659=) rs772882008 0.00004
NM_001378183.1(PIEZO2):c.6630G>A (p.Lys2210=) rs781075542 0.00003
NM_001378183.1(PIEZO2):c.5130C>T (p.Thr1710=) rs767427143 0.00002
NM_001378183.1(PIEZO2):c.6540C>T (p.Ser2180=) rs1386197549 0.00002
NM_001378183.1(PIEZO2):c.7002C>T (p.Thr2334=) rs770096177 0.00002
NM_001378183.1(PIEZO2):c.7092C>T (p.Tyr2364=) rs185544887 0.00001
NM_001378183.1(PIEZO2):c.1261G>C (p.Gly421Arg) rs202104395
NM_001378183.1(PIEZO2):c.7952+8C>T

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.