GRAMD1C
GRAM domain containing 1C
Summary
Predicted to enable cholesterol binding activity and cholesterol transfer activity. Predicted to be involved in cellular response to cholesterol and intracellular sterol transport. Predicted to be located in endoplasmic reticulum; membrane; and organelle membrane contact site. Predicted to be active in endoplasmic reticulum membrane; endoplasmic reticulum-plasma membrane contact site; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs146532435 | 3:113,557,770 | C/G | — | uncertain significance |
| rs773648905 | 3:113,557,778 | C/A | — | uncertain significance |
| rs750349258 | 3:113,563,360 | A/G | — | uncertain significance |
| rs1298631649 | 3:113,563,413 | A/T | — | uncertain significance |
| rs761336771 | 3:113,563,450 | A/C | — | uncertain significance |
| rs552290581 | 3:113,563,468 | A/G | — | uncertain significance |
| rs1025398 | 3:113,585,633 | T/C | intron variant | — |
| rs755524312 | 3:113,594,373 | G/A | — | uncertain significance |
| rs746682121 | 3:113,594,422 | A/T | — | uncertain significance |
| rs199735566 | 3:113,595,066 | C/T | — | uncertain significance |
| rs1346652096 | 3:113,601,665 | G/A | — | uncertain significance |
| rs564438696 | 3:113,608,160 | C/T | — | — |
| rs181725618 | 3:113,619,952 | G/C | — | uncertain significance |
| rs1228330066 | 3:113,619,972 | C/T | — | uncertain significance |
| rs936946466 | 3:113,623,013 | A/T | — | uncertain significance |
| rs371194067 | 3:113,623,099 | G/A | — | uncertain significance |
| rs61077924 | 3:113,625,933 | C/G | intron variant | — |
| rs61634901 | 3:113,625,959 | G/A | intron variant | — |
| rs9843141 | 3:113,630,810 | G/A | intron variant | — |
| rs1936786707 | 3:113,634,566 | A/G | — | uncertain significance |
| rs984158465 | 3:113,634,567 | T/G | — | uncertain significance |
| rs550686355 | 3:113,634,593 | G/A | — | uncertain significance |
| rs78547874 | 3:113,634,682 | C/A | — | likely benign |
| rs770449892 | 3:113,652,427 | C/T | — | uncertain significance |
| rs376128249 | 3:113,652,470 | T/C | — | uncertain significance |
| rs149750566 | 3:113,655,151 | G/A | — | uncertain significance |
| rs895521964 | 3:113,655,199 | A/G | — | likely benign |
| rs148825583 | 3:113,655,214 | G/A | — | uncertain significance |
| rs1448116229 | 3:113,655,218 | A/G | — | uncertain significance |
| rs377757169 | 3:113,656,938 | A/G | — | uncertain significance |
| rs749133112 | 3:113,658,818 | C/T | — | uncertain significance |
| rs1222033161 | 3:113,659,101 | T/C | — | uncertain significance |
| rs138939818 | 3:113,659,148 | C/G | — | uncertain significance |
| rs373868249 | 3:113,659,149 | G/A | — | uncertain significance |
| rs149363738 | 3:113,664,291 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.