OFCC1
orofacial cleft 1 candidate 1 (pseudogene)
Summary
Predicted to be located in several cellular components, including endoplasmic reticulum; microtubule cytoskeleton; and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants15 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6939066 | 6:9,725,270 | C/G | — | — |
| rs1206968 | 6:9,836,699 | T/C | intron variant | — |
| rs4716055 | 6:9,853,919 | G/T | intron variant | — |
| rs569210477 | 6:9,868,036 | T/C | — | — |
| rs185958635 | 6:9,891,997 | G/A | intron variant | — |
| rs149747749 | 6:9,937,360 | G/A | intron variant | — |
| rs116201121 | 6:9,993,737 | G/A | intron variant | — |
| rs12214497 | 6:10,015,908 | G/T | intron variant | — |
| rs423119 | 6:10,025,880 | G/T | intron variant | — |
| rs67612840 | 6:10,028,826 | T/C | — | — |
| rs9477605 | 6:10,034,452 | G/A | intron variant | — |
| rs2327222 | 6:10,036,083 | T/C | intron variant | — |
| rs855394 | 6:10,049,717 | C/T | intron variant | — |
| rs13195786 | 6:10,163,968 | A/G | regulatory region variant | — |
| rs12210761 | 6:10,176,036 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.