ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001378183.1(PIEZO2):c.2305C>T (p.Leu769=) rs6505592 0.84626
NM_001378183.1(PIEZO2):c.4708+18C>T rs5024299 0.83716
NM_001378183.1(PIEZO2):c.3036A>G (p.Thr1012=) rs7227167 0.83322
NM_001378183.1(PIEZO2):c.3867C>T (p.Asn1289=) rs7407105 0.81713
NM_001378183.1(PIEZO2):c.3081C>T (p.Leu1027=) rs7241380 0.78175
NM_001378183.1(PIEZO2):c.4290T>A (p.Leu1430=) rs8096037 0.63926
NM_001378183.1(PIEZO2):c.7349+7C>T rs3748422 0.36363
NM_001378183.1(PIEZO2):c.4135G>A (p.Val1379Ile) rs7234309 0.30463
NM_001378183.1(PIEZO2):c.7035G>A (p.Pro2345=) rs2277860 0.29299
NM_001378183.1(PIEZO2):c.7215C>T (p.Ala2405=) rs3748421 0.27525
NM_001378183.1(PIEZO2):c.5589C>T (p.Ser1863=) rs7227022 0.26688
NM_001378183.1(PIEZO2):c.1527+10A>C rs7407224 0.22718
NM_001378183.1(PIEZO2):c.5006G>A (p.Arg1669Gln) rs2865121 0.20369
NM_001378183.1(PIEZO2):c.6031G>C (p.Glu2011Gln) rs4796901 0.20035
NM_001378183.1(PIEZO2):c.3518G>T (p.Cys1173Phe) rs35033671 0.15855
NM_001378183.1(PIEZO2):c.6488C>A (p.Ala2163Asp) rs113682091 0.11487
NM_001378183.1(PIEZO2):c.7726G>A (p.Val2576Ile) rs3748428 0.10248
NM_001378183.1(PIEZO2):c.5029+15G>C rs78691268 0.07088
NM_001378183.1(PIEZO2):c.1023G>A (p.Leu341=) rs61750910 0.05768
NM_001378183.1(PIEZO2):c.1201-19C>G rs7241307 0.05745
NM_001378183.1(PIEZO2):c.2226T>C (p.Ile742=) rs76488076 0.05629
NM_001378183.1(PIEZO2):c.1758+17C>T rs55646160 0.03921
NM_001378183.1(PIEZO2):c.6891C>T (p.Ser2297=) rs16975188 0.03894
NM_001378183.1(PIEZO2):c.7349+8G>A rs57838670 0.03315
NM_001378183.1(PIEZO2):c.717G>A (p.Pro239=) rs8085615 0.03052
NM_001378183.1(PIEZO2):c.6600C>T (p.Phe2200=) rs73945841 0.02239
NM_001378183.1(PIEZO2):c.1698T>C (p.Pro566=) rs11875564 0.01784
NM_001378183.1(PIEZO2):c.6012C>T (p.Asp2004=) rs16975235 0.01635
NM_001378183.1(PIEZO2):c.164A>C (p.His55Pro) rs145948919 0.01330
NM_001378183.1(PIEZO2):c.6530G>C (p.Arg2177Thr) rs79992793 0.00478
NM_001378183.1(PIEZO2):c.1239+13T>A rs142251928 0.00223
NM_001378183.1(PIEZO2):c.3907G>C (p.Asp1303His) rs371703803 0.00025
NM_001378183.1(PIEZO2):c.1882+10T>C
NM_001378183.1(PIEZO2):c.5598G>A (p.Thr1866=) rs78023192
NM_001378183.1(PIEZO2):c.5598G>T (p.Thr1866=) rs78023192

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.