SH2D6
SH2 domain containing 6
Summary
Predicted to be involved in cell surface receptor protein tyrosine kinase signaling pathway and intracellular signal transduction. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants22 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs72831579 | 2:85,649,757 | G/A | upstream gene variant | — |
| rs552411949 | 2:85,650,077 | C/T | — | — |
| rs148553793 | 2:85,655,208 | C/T | regulatory region variant | — |
| rs114006128 | 2:85,656,297 | G/C | intron variant | — |
| rs557040511 | 2:85,659,526 | T/G | — | — |
| rs55762624 | 2:85,659,527 | G/T | upstream gene variant | — |
| rs71411823 | 2:85,659,603 | G/A | — | — |
| rs745993889 | 2:85,662,101 | C/T | — | likely benign |
| rs1244559251 | 2:85,662,119 | C/T | — | uncertain significance |
| rs769042639 | 2:85,662,137 | C/T | — | likely benign |
| rs139067996 | 2:85,662,244 | G/A | — | uncertain significance |
| rs2529447312 | 2:85,662,536 | G/A | — | uncertain significance |
| rs747754782 | 2:85,662,808 | G/A | — | uncertain significance |
| rs1194498869 | 2:85,662,837 | C/T | — | uncertain significance |
| rs140818438 | 2:85,662,892 | G/A | — | likely benign |
| rs368611687 | 2:85,662,907 | G/A | — | likely benign |
| rs754404958 | 2:85,662,925 | G/A | — | uncertain significance |
| rs184075898 | 2:85,662,940 | G/A | — | likely benign |
| rs752259444 | 2:85,662,945 | G/A | — | uncertain significance |
| rs1044133644 | 2:85,663,611 | T/C | — | uncertain significance |
| rs765796378 | 2:85,663,627 | G/A | — | uncertain significance |
| rs201856380 | 2:85,663,661 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.