SPARCL1
SPARC like 1
Summary
Predicted to enable calcium ion binding activity; collagen binding activity; and extracellular matrix binding activity. Predicted to be involved in regulation of synapse organization. Located in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs555798446 | 4:88,396,767 | C/T | — | — |
| rs4610302 | 4:88,400,110 | A/C | — | — |
| rs568252062 | 4:88,401,537 | G/A | — | uncertain significance |
| rs373530876 | 4:88,401,645 | T/C | — | uncertain significance |
| rs1723863668 | 4:88,403,617 | A/T | — | uncertain significance |
| rs955889606 | 4:88,403,668 | G/A | — | uncertain significance |
| rs2475900830 | 4:88,403,710 | T/C | — | uncertain significance |
| rs187843273 | 4:88,405,704 | T/A | intron variant | — |
| rs2475919700 | 4:88,411,487 | C/T | — | uncertain significance |
| rs41282397 | 4:88,411,494 | T/A | — | uncertain significance |
| rs2475919856 | 4:88,411,503 | G/T | — | uncertain significance |
| rs1210362383 | 4:88,411,529 | T/C | — | uncertain significance |
| rs764713722 | 4:88,414,747 | C/G | — | uncertain significance |
| rs139753398 | 4:88,414,754 | C/G | — | uncertain significance |
| rs765359802 | 4:88,414,822 | A/G | — | uncertain significance |
| rs2475931317 | 4:88,414,900 | T/G | — | uncertain significance |
| rs777300134 | 4:88,414,907 | C/T | — | uncertain significance |
| rs148930868 | 4:88,414,970 | C/T | — | uncertain significance |
| rs1292178655 | 4:88,414,981 | G/A | — | uncertain significance |
| rs1724478259 | 4:88,415,035 | C/G | — | uncertain significance |
| rs142254899 | 4:88,415,061 | C/A | — | uncertain significance |
| rs201942856 | 4:88,415,102 | C/T | — | likely benign |
| rs1396720882 | 4:88,415,137 | G/T | — | uncertain significance |
| rs1354721280 | 4:88,415,260 | C/T | — | uncertain significance |
| rs1724503244 | 4:88,415,327 | C/A | — | uncertain significance |
| rs1166529690 | 4:88,415,362 | A/G | — | uncertain significance |
| rs919995506 | 4:88,415,384 | T/C | — | uncertain significance |
| rs143076536 | 4:88,415,416 | C/G | — | uncertain significance |
| rs146144228 | 4:88,415,437 | T/C | — | uncertain significance |
| rs751106977 | 4:88,415,471 | C/T | — | uncertain significance |
| rs568621264 | 4:88,415,627 | C/T | — | uncertain significance |
| rs368372139 | 4:88,415,654 | G/T | — | uncertain significance |
| rs376909339 | 4:88,415,657 | C/T | — | uncertain significance |
| rs746532561 | 4:88,416,141 | G/A | — | uncertain significance |
| rs4693167 | 4:88,423,913 | T/C | regulatory region variant | — |
| rs181309496 | 4:88,426,634 | T/C | intron variant | — |
| rs4693170 | 4:88,445,567 | G/A | intron variant | — |
| rs62315966 | 4:88,446,413 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.