CRELD2
CRELD disulfide isomerase 2
Summary
Predicted to enable calcium ion binding activity and protein disulfide isomerase activity. Predicted to be located in Golgi apparatus; endoplasmic reticulum; and extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1004117296 | 22:50,312,430 | C/T | — | uncertain significance |
| rs1480913584 | 22:50,312,457 | C/T | — | uncertain significance |
| rs969485163 | 22:50,312,482 | C/T | — | uncertain significance |
| rs1272735690 | 22:50,312,514 | C/G | — | uncertain significance |
| rs867250364 | 22:50,312,515 | G/A | — | uncertain significance |
| rs1345023788 | 22:50,312,529 | G/C | — | uncertain significance |
| rs1375383540 | 22:50,313,379 | G/A | — | uncertain significance |
| rs2519299468 | 22:50,313,440 | A/G | — | uncertain significance |
| rs147653734 | 22:50,313,441 | G/C | — | uncertain significance |
| rs2060668325 | 22:50,313,834 | G/T | — | uncertain significance |
| rs114332575 | 22:50,313,880 | G/A | — | uncertain significance |
| rs1167175613 | 22:50,315,247 | T/C | — | uncertain significance |
| rs779886358 | 22:50,315,265 | G/A | — | uncertain significance |
| rs143858142 | 22:50,315,303 | C/T | — | benign |
| rs547369309 | 22:50,315,383 | G/A | — | uncertain significance |
| rs201818846 | 22:50,315,386 | A/G | — | uncertain significance |
| rs2519312468 | 22:50,315,399 | C/A | — | uncertain significance |
| rs562885075 | 22:50,315,966 | C/G | — | uncertain significance |
| rs200857048 | 22:50,316,016 | G/A | — | uncertain significance |
| rs779916602 | 22:50,316,019 | T/C | — | uncertain significance |
| rs186623329 | 22:50,316,038 | C/T | — | uncertain significance |
| rs372875064 | 22:50,316,052 | G/T | — | uncertain significance |
| rs758087960 | 22:50,316,079 | G/T | — | uncertain significance |
| rs868106914 | 22:50,316,287 | C/T | — | uncertain significance |
| rs138811682 | 22:50,316,288 | G/A | — | likely benign |
| rs1335713773 | 22:50,316,299 | A/G | — | uncertain significance |
| rs1243732892 | 22:50,316,319 | G/A | — | uncertain significance |
| rs371852940 | 22:50,316,346 | G/A | — | uncertain significance |
| rs2519323267 | 22:50,316,884 | G/A | — | uncertain significance |
| rs111557567 | 22:50,316,901 | C/T | — | benign |
| rs145684970 | 22:50,316,906 | C/T | missense variant | — |
| rs748258570 | 22:50,316,935 | A/G | — | likely benign |
| rs200705804 | 22:50,316,940 | C/T | — | likely benign |
| rs760466044 | 22:50,316,956 | A/G | — | uncertain significance |
| rs150525447 | 22:50,316,957 | C/T | — | uncertain significance |
| rs750166335 | 22:50,316,962 | G/A | — | uncertain significance |
| rs773937948 | 22:50,318,008 | A/C | — | uncertain significance |
| rs113168785 | 22:50,318,061 | G/C | missense variant | — |
| rs370768019 | 22:50,318,068 | T/C | — | uncertain significance |
| rs372396626 | 22:50,318,098 | G/A | — | uncertain significance |
| rs112352679 | 22:50,318,514 | T/C | regulatory region variant | — |
| rs12170411 | 22:50,318,741 | C/T | regulatory region variant | — |
| rs149127584 | 22:50,319,078 | C/T | — | likely benign |
| rs776108424 | 22:50,319,112 | G/A | — | uncertain significance |
| rs1223870064 | 22:50,319,140 | A/G | — | uncertain significance |
| rs200272727 | 22:50,320,912 | A/T | — | uncertain significance |
| rs151286715 | 22:50,320,921 | G/A | — | uncertain significance |
| rs777875561 | 22:50,320,949 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.