GRAMD1A
GRAM domain containing 1A
Summary
Predicted to enable cholesterol binding activity and cholesterol transfer activity. Predicted to be involved in cellular response to cholesterol and intracellular sterol transport. Located in several cellular components, including cytosol; endoplasmic reticulum membrane; and organelle membrane contact site. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants56 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs67003112 | 19:35,487,933 | C/G | upstream gene variant | — |
| rs202243585 | 19:35,488,292 | C/A | — | — |
| rs62122148 | 19:35,492,575 | G/C | — | — |
| rs2514117059 | 19:35,500,039 | G/T | — | uncertain significance |
| rs538716547 | 19:35,500,040 | G/A | — | uncertain significance |
| rs780284522 | 19:35,500,067 | C/T | — | uncertain significance |
| rs2015039227 | 19:35,500,102 | C/T | — | uncertain significance |
| rs371587089 | 19:35,500,135 | G/A | — | uncertain significance |
| rs562417464 | 19:35,500,197 | G/C | — | uncertain significance |
| rs772065016 | 19:35,500,211 | G/A | — | uncertain significance |
| rs374494022 | 19:35,500,222 | C/T | — | uncertain significance |
| rs755034748 | 19:35,501,234 | C/T | — | uncertain significance |
| rs1045022070 | 19:35,501,247 | C/G | — | uncertain significance |
| rs765331104 | 19:35,502,408 | C/T | — | uncertain significance |
| rs771563151 | 19:35,504,172 | C/T | — | uncertain significance |
| rs773224886 | 19:35,504,205 | G/A | — | uncertain significance |
| rs770765265 | 19:35,504,254 | T/C | — | uncertain significance |
| rs907248598 | 19:35,504,266 | G/A | — | uncertain significance |
| rs372009504 | 19:35,504,447 | C/G | — | likely benign |
| rs201944800 | 19:35,504,495 | C/T | — | uncertain significance |
| rs182927749 | 19:35,504,510 | G/A | — | likely benign |
| rs372725667 | 19:35,504,561 | A/G | — | uncertain significance |
| rs199949479 | 19:35,504,573 | C/T | — | uncertain significance |
| rs371740352 | 19:35,504,581 | G/A | — | uncertain significance |
| rs781414377 | 19:35,505,160 | C/T | — | uncertain significance |
| rs2514155870 | 19:35,505,192 | C/G | — | uncertain significance |
| rs2514156310 | 19:35,505,226 | A/G | — | uncertain significance |
| rs375535357 | 19:35,506,732 | C/G | — | uncertain significance |
| rs368156191 | 19:35,506,753 | C/A | — | uncertain significance |
| rs780649596 | 19:35,506,802 | C/T | — | uncertain significance |
| rs200796879 | 19:35,506,824 | C/T | — | uncertain significance |
| rs1041857043 | 19:35,510,101 | C/T | — | uncertain significance |
| rs2514182588 | 19:35,510,155 | A/G | — | uncertain significance |
| rs2514183208 | 19:35,510,194 | C/T | — | uncertain significance |
| rs759830313 | 19:35,510,322 | G/A | — | uncertain significance |
| rs373185819 | 19:35,510,418 | C/T | — | uncertain significance |
| rs770491592 | 19:35,512,422 | C/T | — | uncertain significance |
| rs367650806 | 19:35,512,429 | G/A | — | uncertain significance |
| rs754266755 | 19:35,512,456 | C/T | — | uncertain significance |
| rs940309926 | 19:35,512,476 | T/G | — | uncertain significance |
| rs769675585 | 19:35,512,482 | G/A | — | uncertain significance |
| rs750130929 | 19:35,512,639 | G/A | — | uncertain significance |
| rs201039041 | 19:35,512,675 | C/T | — | uncertain significance |
| rs754452685 | 19:35,512,700 | G/A | — | uncertain significance |
| rs772403182 | 19:35,512,739 | C/A | — | uncertain significance |
| rs753446139 | 19:35,512,747 | C/T | — | uncertain significance |
| rs66528626 | 19:35,513,237 | T/C | intron variant | — |
| rs557724457 | 19:35,514,147 | A/G | — | likely benign |
| rs747901853 | 19:35,514,197 | A/C | — | uncertain significance |
| rs200311339 | 19:35,514,227 | C/G | — | uncertain significance |
| rs2151737159 | 19:35,514,234 | G/T | — | uncertain significance |
| rs2016219699 | 19:35,514,339 | C/T | — | uncertain significance |
| rs1048541704 | 19:35,514,395 | G/A | — | uncertain significance |
| rs370077465 | 19:35,514,434 | G/A | — | uncertain significance |
| rs756191681 | 19:35,516,953 | A/G | — | uncertain significance |
| rs765210680 | 19:35,517,022 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.