Gene entry
PIEZO2
piezo type mechanosensitive ion channel component 2
- Chromosome
- 18
- Cytoband
- 18p11.22-p11.21
- Variants (rsID)
- 163
PIEZO2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 18 (region 18p11.22-p11.21). Its official name is “piezo type mechanosensitive ion channel component 2”. The reference table lists 163 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs145948919Benignsingle nucleotide variant
- rs55646160Benignsingle nucleotide variant
- rs7227022Benignsingle nucleotide variantArthrogryposis- oculomotor limitation-electroretinal anomalies syndrome|Gordon syndrome|Marden-Walker syndrome|Arthrogryposis, distal, with impaired proprioception and touch
- rs7407224Benignsingle nucleotide variant
- rs192225494Uncertain significancesingle nucleotide variant
Other listed variants
- rs155325
- rs196956
- rs264212
- rs264251
- rs264264
- rs264266
- rs264272
- rs462166
- rs492137
- rs570852
- rs674698
- rs718509
- rs754968
- rs1039690
- rs1153767
- rs1189858
- rs1485777
- rs1567159
- rs1683378
- rs1918672
- rs1918674
- rs2016302
- rs2178100
- rs2298743
- rs2584732
- rs2584737
- rs2584739
- rs2625360
- rs2625372
- rs2625375
- rs2660258
- rs2660283
- rs3898148
- rs4519388
- rs4797487
- rs5022001
- rs6505593
- rs6505610
- rs6505615
- rs6505617
- rs7233628
- rs7234687
- rs7235865
- rs7236574
- rs7239893
- rs7241746
- rs7242015
- rs7243607
- rs7245148
- rs7504649
- rs8084083
- rs8086028
- rs8089791
- rs8090413
- rs8093366
- rs8093481
- rs8095476
- rs8095590
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.