SH2D5
SH2 domain containing 5
Summary
Predicted to be located in synapse. Predicted to be active in postsynaptic density. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2545548512 | 1:21,048,289 | C/T | — | uncertain significance |
| rs761666159 | 1:21,048,311 | C/T | — | uncertain significance |
| rs746499995 | 1:21,048,362 | G/C | — | uncertain significance |
| rs749632362 | 1:21,048,440 | C/T | — | uncertain significance |
| rs1570500553 | 1:21,048,487 | T/C | — | uncertain significance |
| rs376876214 | 1:21,049,262 | C/T | — | uncertain significance |
| rs2054711795 | 1:21,049,284 | C/G | — | uncertain significance |
| rs752451134 | 1:21,049,293 | G/A | — | uncertain significance |
| rs200472543 | 1:21,049,313 | C/T | — | likely benign |
| rs763650474 | 1:21,049,367 | G/A | — | uncertain significance |
| rs184773097 | 1:21,050,201 | G/A | — | uncertain significance |
| rs746393113 | 1:21,050,216 | A/G | — | uncertain significance |
| rs765362118 | 1:21,050,590 | G/A | — | uncertain significance |
| rs1015162221 | 1:21,050,626 | T/C | — | uncertain significance |
| rs753269375 | 1:21,050,728 | G/A | — | uncertain significance |
| rs376777359 | 1:21,050,868 | C/T | intron variant | — |
| rs199520870 | 1:21,050,921 | G/A | — | uncertain significance |
| rs770826663 | 1:21,050,923 | C/T | — | uncertain significance |
| rs775575933 | 1:21,050,932 | A/G | — | uncertain significance |
| rs368343115 | 1:21,050,981 | G/A | — | uncertain significance |
| rs942014300 | 1:21,051,013 | A/G | — | uncertain significance |
| rs576868307 | 1:21,051,101 | G/A | — | uncertain significance |
| rs1478922719 | 1:21,051,107 | G/T | — | uncertain significance |
| rs994695707 | 1:21,052,462 | G/A | — | uncertain significance |
| rs767777430 | 1:21,052,472 | G/A | — | uncertain significance |
| rs749771908 | 1:21,052,489 | G/A | — | uncertain significance |
| rs376947239 | 1:21,052,502 | C/T | — | uncertain significance |
| rs752916913 | 1:21,052,544 | G/A | — | uncertain significance |
| rs967650232 | 1:21,053,568 | C/T | — | uncertain significance |
| rs199984518 | 1:21,054,041 | A/G | — | uncertain significance |
| rs776041908 | 1:21,054,080 | G/T | — | uncertain significance |
| rs200906509 | 1:21,054,480 | G/A | — | uncertain significance |
| rs10916855 | 1:21,056,382 | T/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.