SH2D4B
SH2 domain containing 4B
Summary
Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs577059009 | 10:82,298,130 | C/G | — | uncertain significance |
| rs1021537180 | 10:82,298,148 | G/A | — | uncertain significance |
| rs532946393 | 10:82,298,181 | C/T | — | uncertain significance |
| rs780375316 | 10:82,298,212 | G/A | — | uncertain significance |
| rs768555525 | 10:82,298,227 | C/A | — | uncertain significance |
| rs770251464 | 10:82,298,247 | C/T | — | uncertain significance |
| rs147451124 | 10:82,330,036 | C/T | — | uncertain significance |
| rs755589540 | 10:82,331,224 | G/T | — | uncertain significance |
| rs140909202 | 10:82,348,395 | G/A | — | uncertain significance |
| rs144834825 | 10:82,348,516 | G/A | — | uncertain significance |
| rs753656530 | 10:82,363,341 | G/A | — | uncertain significance |
| rs370850128 | 10:82,363,349 | G/A | — | uncertain significance |
| rs778211117 | 10:82,363,395 | A/G | — | uncertain significance |
| rs1913762 | 10:82,363,405 | C/A | — | uncertain significance |
| rs776567930 | 10:82,363,416 | G/A | — | uncertain significance |
| rs374856801 | 10:82,363,421 | A/T | — | uncertain significance |
| rs573187550 | 10:82,363,434 | C/T | — | uncertain significance |
| rs775369326 | 10:82,363,460 | C/T | — | uncertain significance |
| rs548466013 | 10:82,363,464 | A/T | — | uncertain significance |
| rs61861597 | 10:82,363,518 | C/T | — | uncertain significance |
| rs147223384 | 10:82,369,224 | T/C | — | uncertain significance |
| rs144024335 | 10:82,369,225 | C/G | — | uncertain significance |
| rs774953296 | 10:82,369,270 | C/G | — | uncertain significance |
| rs191822402 | 10:82,374,209 | C/T | intron variant | — |
| rs563222478 | 10:82,374,293 | A/G | — | — |
| rs6586111 | 10:82,377,590 | T/C | intron variant | — |
| rs76298292 | 10:82,383,534 | A/G | intron variant | — |
| rs1461202750 | 10:82,403,752 | G/A | — | uncertain significance |
| rs759517871 | 10:82,403,763 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.