RGSL1
regulator of G protein signaling like 1
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants62 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs750512973 | 1:182,419,308 | G/A | — | likely benign |
| rs771829309 | 1:182,423,108 | C/T | — | uncertain significance |
| rs74340015 | 1:182,423,581 | C/T | intron variant | — |
| rs191651831 | 1:182,426,359 | G/A | intron variant | — |
| rs199966529 | 1:182,429,146 | A/G | — | uncertain significance |
| rs551932979 | 1:182,429,155 | G/C | — | uncertain significance |
| rs745895536 | 1:182,429,182 | G/A | — | uncertain significance |
| rs1473837166 | 1:182,441,591 | A/G | — | uncertain significance |
| rs1394197253 | 1:182,441,641 | A/G | — | uncertain significance |
| rs1199207627 | 1:182,441,684 | T/C | — | uncertain significance |
| rs192789745 | 1:182,441,687 | A/G | — | uncertain significance |
| rs200412649 | 1:182,442,758 | G/A | — | uncertain significance |
| rs768739926 | 1:182,442,782 | A/G | — | uncertain significance |
| rs2525923204 | 1:182,442,810 | C/A | — | uncertain significance |
| rs1268081167 | 1:182,442,829 | T/C | — | uncertain significance |
| rs2525924364 | 1:182,442,868 | T/C | — | uncertain significance |
| rs200246535 | 1:182,442,981 | G/A | — | likely benign |
| rs1164958677 | 1:182,442,985 | T/G | — | uncertain significance |
| rs1412005081 | 1:182,443,093 | T/C | — | uncertain significance |
| rs2525930090 | 1:182,443,192 | A/C | — | uncertain significance |
| rs2525930459 | 1:182,443,210 | A/G | — | uncertain significance |
| rs372870777 | 1:182,443,239 | A/C | — | uncertain significance |
| rs147419839 | 1:182,443,308 | G/T | — | uncertain significance |
| rs796651047 | 1:182,443,393 | C/A | — | uncertain significance |
| rs770638378 | 1:182,443,400 | G/T | — | uncertain significance |
| rs927728231 | 1:182,443,466 | A/G | — | uncertain significance |
| rs1043211083 | 1:182,443,474 | C/T | — | uncertain significance |
| rs896098429 | 1:182,443,519 | C/T | — | uncertain significance |
| rs1327737019 | 1:182,443,546 | G/A | — | uncertain significance |
| rs555340145 | 1:182,443,568 | T/G | — | uncertain significance |
| rs370734373 | 1:182,443,618 | C/A | — | uncertain significance |
| rs761874156 | 1:182,443,633 | G/T | — | uncertain significance |
| rs1558294876 | 1:182,458,213 | G/C | — | uncertain significance |
| rs1377273280 | 1:182,458,328 | T/C | — | uncertain significance |
| rs551846717 | 1:182,462,172 | C/T | — | uncertain significance |
| rs2526412686 | 1:182,491,171 | A/T | — | uncertain significance |
| rs1382690005 | 1:182,491,214 | C/T | — | uncertain significance |
| rs200654801 | 1:182,496,739 | A/G | — | uncertain significance |
| rs367955469 | 1:182,496,778 | C/T | — | uncertain significance |
| rs1043272772 | 1:182,496,814 | G/A | — | likely benign |
| rs1658857194 | 1:182,496,851 | G/T | — | uncertain significance |
| rs376458323 | 1:182,499,420 | G/A | — | uncertain significance |
| rs146321650 | 1:182,499,429 | C/T | — | uncertain significance |
| rs1033024649 | 1:182,499,448 | C/T | — | uncertain significance |
| rs754464347 | 1:182,500,014 | A/G | — | uncertain significance |
| rs745901690 | 1:182,501,823 | C/A | — | uncertain significance |
| rs377205207 | 1:182,501,849 | G/A | — | uncertain significance |
| rs367804901 | 1:182,501,894 | A/G | — | uncertain significance |
| rs1310365459 | 1:182,509,402 | A/G | — | uncertain significance |
| rs999982008 | 1:182,509,403 | C/T | — | uncertain significance |
| rs769193141 | 1:182,509,511 | T/C | — | uncertain significance |
| rs192542146 | 1:182,517,495 | C/T | — | uncertain significance |
| rs1476567099 | 1:182,517,513 | G/T | — | uncertain significance |
| rs569358085 | 1:182,517,862 | G/A | — | uncertain significance |
| rs1348979141 | 1:182,517,934 | C/T | — | uncertain significance |
| rs1294901982 | 1:182,517,938 | T/A | — | uncertain significance |
| rs778131453 | 1:182,517,955 | A/G | — | uncertain significance |
| rs759688790 | 1:182,520,318 | C/T | — | uncertain significance |
| rs1660541268 | 1:182,520,336 | C/T | — | uncertain significance |
| rs369986568 | 1:182,523,762 | C/T | — | uncertain significance |
| rs756518318 | 1:182,523,794 | G/A | — | uncertain significance |
| rs769739061 | 1:182,525,177 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.