GLCCI1
glucocorticoid induced 1
Summary
This gene encodes a protein of unknown function. Expression of this gene is induced by glucocorticoids and may be an early marker for glucocorticoid-induced apoptosis. Single nucleotide polymorphisms in this gene are associated with a decreased response to inhaled glucocorticoids in asthmatic patients. [provided by RefSeq, Feb 2012]
Known Variants66 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs37972 | 7:8,007,509 | T/C | coding sequence variant | — |
| rs37973 | 7:8,007,876 | G/C | — | drug response |
| rs7786263 | 7:8,008,970 | C/A | — | — |
| rs776980379 | 7:8,008,994 | T/G | — | uncertain significance |
| rs1208812413 | 7:8,009,082 | T/G | — | uncertain significance |
| rs1200649830 | 7:8,009,093 | G/C | — | uncertain significance |
| rs2483102151 | 7:8,009,097 | G/C | — | uncertain significance |
| rs1021717468 | 7:8,009,105 | G/A | — | uncertain significance |
| rs2483102180 | 7:8,009,106 | G/C | — | uncertain significance |
| rs1780290471 | 7:8,009,108 | G/C | — | uncertain significance |
| rs541216640 | 7:8,009,111 | G/A | — | uncertain significance |
| rs1780291557 | 7:8,009,132 | T/G | — | uncertain significance |
| rs2483102280 | 7:8,009,134 | C/G | — | uncertain significance |
| rs965965715 | 7:8,009,135 | G/T | — | uncertain significance |
| rs976419070 | 7:8,009,148 | G/C | — | uncertain significance |
| rs545986371 | 7:8,009,280 | C/T | — | likely benign |
| rs1278060681 | 7:8,009,286 | G/T | — | uncertain significance |
| rs1780298041 | 7:8,009,294 | A/C | — | uncertain significance |
| rs2483102768 | 7:8,009,295 | G/C | — | uncertain significance |
| rs1780298392 | 7:8,009,300 | T/G | — | uncertain significance |
| rs2115396835 | 7:8,009,303 | A/C | — | uncertain significance |
| rs1430857493 | 7:8,009,312 | C/G | — | uncertain significance |
| rs564447167 | 7:8,009,331 | C/T | — | uncertain significance |
| rs1445325120 | 7:8,009,336 | G/A | — | uncertain significance |
| rs753549912 | 7:8,009,352 | C/T | — | uncertain significance |
| rs2483103209 | 7:8,009,424 | C/T | — | uncertain significance |
| rs73049252 | 7:8,016,602 | G/T | — | — |
| rs7804306 | 7:8,018,180 | G/A | upstream gene variant | — |
| rs73049256 | 7:8,018,489 | A/T | regulatory region variant | — |
| rs56073406 | 7:8,020,656 | A/G | coding sequence variant | — |
| rs37983 | 7:8,021,213 | C/T | — | — |
| rs73049270 | 7:8,021,646 | C/T | coding sequence variant | — |
| rs73049276 | 7:8,022,016 | G/A | downstream gene variant | — |
| rs145044782 | 7:8,035,497 | G/A | intron variant | — |
| rs142269087 | 7:8,037,507 | G/A | intron variant | — |
| rs73049300 | 7:8,041,946 | C/G | intron variant | — |
| rs38008 | 7:8,042,197 | C/G | — | — |
| rs38010 | 7:8,042,389 | C/T | intron variant | — |
| rs116960194 | 7:8,043,538 | C/T | — | likely benign |
| rs1309483245 | 7:8,043,579 | A/G | — | uncertain significance |
| rs756641981 | 7:8,043,639 | C/T | — | uncertain significance |
| rs139383513 | 7:8,043,669 | A/C | — | uncertain significance |
| rs73050915 | 7:8,050,244 | G/C | — | — |
| rs2483216833 | 7:8,062,122 | T/A | — | uncertain significance |
| rs73050940 | 7:8,067,512 | A/G | intron variant | — |
| rs73050959 | 7:8,076,699 | G/A | intron variant | — |
| rs79643401 | 7:8,094,011 | T/C | intron variant | — |
| rs765273461 | 7:8,095,159 | A/G | — | uncertain significance |
| rs2483279634 | 7:8,095,161 | A/G | — | uncertain significance |
| rs2483279670 | 7:8,095,172 | A/T | — | uncertain significance |
| rs111677347 | 7:8,095,483 | C/T | intron variant | — |
| rs912783546 | 7:8,099,792 | C/T | — | uncertain significance |
| rs12702693 | 7:8,101,039 | C/T | intron variant | — |
| rs117620902 | 7:8,101,148 | A/T | — | — |
| rs56195338 | 7:8,107,922 | G/A | intron variant | — |
| rs747666296 | 7:8,110,651 | G/A | — | uncertain significance |
| rs1444258171 | 7:8,110,683 | G/C | — | uncertain significance |
| rs537920233 | 7:8,110,702 | C/T | — | uncertain significance |
| rs766857328 | 7:8,110,729 | C/T | — | uncertain significance |
| rs116973462 | 7:8,120,471 | G/T | — | — |
| rs17142814 | 7:8,122,876 | C/G | intron variant | — |
| rs2483331675 | 7:8,124,575 | C/G | — | uncertain significance |
| rs1431676809 | 7:8,125,837 | T/C | — | uncertain significance |
| rs201269303 | 7:8,125,906 | G/C | — | uncertain significance |
| rs1306083229 | 7:8,126,065 | G/A | — | uncertain significance |
| rs1235469187 | 7:8,126,070 | A/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.