CLGN
calmegin
Summary
Calmegin is a testis-specific endoplasmic reticulum chaperone protein. CLGN may play a role in spermatogeneisis and infertility. [provided by RefSeq, Jul 2008]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1205610318 | 4:141,310,388 | C/T | — | uncertain significance |
| rs374544072 | 4:141,310,403 | C/T | — | uncertain significance |
| rs533174138 | 4:141,311,816 | C/T | — | uncertain significance |
| rs145828622 | 4:141,311,874 | T/C | — | likely benign |
| rs1728786322 | 4:141,313,387 | T/G | — | uncertain significance |
| rs745319283 | 4:141,313,421 | C/A | — | uncertain significance |
| rs1280798583 | 4:141,313,439 | C/T | — | uncertain significance |
| rs1728790336 | 4:141,313,504 | T/G | — | uncertain significance |
| rs2546252274 | 4:141,315,017 | C/T | — | uncertain significance |
| rs200652126 | 4:141,315,036 | C/A | — | uncertain significance |
| rs139581390 | 4:141,315,053 | G/A | — | uncertain significance |
| rs369401077 | 4:141,315,111 | C/A | — | uncertain significance |
| rs139813038 | 4:141,315,185 | C/T | — | uncertain significance |
| rs377332621 | 4:141,317,003 | T/A | — | uncertain significance |
| rs757530731 | 4:141,317,037 | A/T | — | uncertain significance |
| rs142360750 | 4:141,317,112 | G/A | missense variant | — |
| rs1728868813 | 4:141,317,253 | C/T | — | uncertain significance |
| rs868506790 | 4:141,317,274 | C/G | — | uncertain significance |
| rs1560739587 | 4:141,317,285 | T/C | — | likely pathogenic |
| rs141471500 | 4:141,320,141 | T/C | — | uncertain significance |
| rs201306926 | 4:141,320,158 | T/C | — | uncertain significance |
| rs1475083337 | 4:141,321,577 | C/T | — | uncertain significance |
| rs2546258399 | 4:141,321,619 | T/C | — | uncertain significance |
| rs112605307 | 4:141,321,650 | A/G | — | benign |
| rs555545813 | 4:141,323,142 | A/C | — | uncertain significance |
| rs751694520 | 4:141,323,197 | C/A | — | uncertain significance |
| rs1560743601 | 4:141,327,129 | G/T | — | uncertain significance |
| rs200441670 | 4:141,327,142 | C/T | — | uncertain significance |
| rs150607652 | 4:141,327,206 | G/T | — | uncertain significance |
| rs377056189 | 4:141,330,994 | C/T | — | uncertain significance |
| rs779997811 | 4:141,334,104 | A/T | — | uncertain significance |
| rs140230014 | 4:141,334,150 | G/A | — | likely benign |
| rs923059232 | 4:141,334,152 | C/G | — | uncertain significance |
| rs773224523 | 4:141,334,157 | C/T | — | uncertain significance |
| rs2546268401 | 4:141,334,182 | A/C | — | uncertain significance |
| rs2546268448 | 4:141,334,226 | A/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.