SESN2
sestrin 2
Summary
This gene encodes a member of the sestrin family of PA26-related proteins. The encoded protein may function in the regulation of cell growth and survival. This protein may be involved in cellular response to different stress conditions. [provided by RefSeq, Jul 2008]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1247721601 | 1:28,586,365 | G/T | — | uncertain significance |
| rs769060746 | 1:28,586,387 | C/T | — | uncertain significance |
| rs1237847095 | 1:28,586,396 | A/C | — | uncertain significance |
| rs774300976 | 1:28,586,419 | G/T | — | uncertain significance |
| rs770447335 | 1:28,586,434 | T/A | — | uncertain significance |
| rs146389695 | 1:28,595,709 | C/T | — | likely benign |
| rs367784435 | 1:28,595,715 | C/G | — | uncertain significance |
| rs144188948 | 1:28,595,716 | G/A | — | uncertain significance |
| rs996588734 | 1:28,595,731 | G/A | — | uncertain significance |
| rs151208219 | 1:28,598,229 | G/A | — | benign |
| rs1647782639 | 1:28,598,243 | C/T | — | uncertain significance |
| rs74896528 | 1:28,598,287 | C/T | — | benign |
| rs539873722 | 1:28,598,312 | G/C | — | uncertain significance |
| rs763209004 | 1:28,598,805 | G/A | — | uncertain significance |
| rs368963626 | 1:28,598,908 | G/A | — | likely benign |
| rs149809618 | 1:28,598,921 | G/A | — | uncertain significance |
| rs767095999 | 1:28,599,108 | G/C | — | uncertain significance |
| rs763645640 | 1:28,599,234 | C/T | — | uncertain significance |
| rs2524382392 | 1:28,599,299 | T/G | — | uncertain significance |
| rs145754239 | 1:28,599,897 | C/T | — | uncertain significance |
| rs117161934 | 1:28,599,898 | G/A | — | benign |
| rs1239081741 | 1:28,599,909 | G/A | — | uncertain significance |
| rs148305939 | 1:28,599,938 | C/T | — | uncertain significance |
| rs2524384280 | 1:28,599,945 | A/C | — | uncertain significance |
| rs77253003 | 1:28,599,952 | G/A | — | benign |
| rs61750960 | 1:28,599,961 | G/A | — | benign |
| rs193223062 | 1:28,600,024 | A/G | — | likely benign |
| rs373698755 | 1:28,600,027 | G/A | — | likely benign |
| rs114922467 | 1:28,600,574 | C/T | — | benign |
| rs777757853 | 1:28,600,592 | T/C | — | uncertain significance |
| rs2274848 | 1:28,600,607 | A/G | — | benign |
| rs549821005 | 1:28,600,613 | G/A | — | uncertain significance |
| rs146457553 | 1:28,600,644 | A/G | — | uncertain significance |
| rs2524385962 | 1:28,600,646 | G/C | — | uncertain significance |
| rs368191829 | 1:28,600,662 | G/A | — | uncertain significance |
| rs2524387821 | 1:28,601,336 | G/A | — | uncertain significance |
| rs35216750 | 1:28,601,407 | T/C | — | benign |
| rs757888911 | 1:28,601,459 | A/C | — | uncertain significance |
| rs375196432 | 1:28,601,463 | G/C | — | uncertain significance |
| rs1051382459 | 1:28,601,489 | G/T | — | uncertain significance |
| rs374917721 | 1:28,601,513 | G/A | — | uncertain significance |
| rs1467724038 | 1:28,605,718 | A/G | — | uncertain significance |
| rs1006193399 | 1:28,605,738 | C/T | — | uncertain significance |
| rs150802897 | 1:28,605,739 | G/A | — | uncertain significance |
| rs988053889 | 1:28,607,255 | C/T | — | uncertain significance |
| rs776133039 | 1:28,607,305 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.