C677T
C677T · SaudiVarKB evidence summary derived from retained literature mentions.
3Variant mentions
3Publications
1Associated gene records
2Associated phenotype records
Associated gene records
Co-mentioned in the same publications| Gene | Identifier / context | Articles | Mentions |
|---|---|---|---|
| MTHFR | HGNC:7436 | 3 | 3 |
Associated phenotype records
Co-mentioned in the same publications| Phenotype | Identifier / context | Articles | Mentions |
|---|---|---|---|
| sickle cell disease | HP:0001878 · 603903 | 1 | 1 |
| breast cancer | — | 1 | 1 |
Associated population records
Co-mentioned in the same publications| Population | Identifier / context | Articles | Mentions |
|---|---|---|---|
| Saudi Arabia | — | 1 | 1 |
| Population record | Cohort 100 | 1 | 1 |
| Population record | Cohort 106 | 1 | 1 |
Supporting publications
3 records- 2021Prevalence of methylenetetrahydrofolate reductase gene polymorphisms (C677T, and A1298C) among Saudi children receiving dental treatment.Annals of Saudi medicine1 mentions
- 2010Breast cancer risk, dietary intake, and methylenetetrahydrofolate reductase (MTHFR)single nucleotide polymorphisms.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association1 mentions
- 2006Association of the methylenetetrahydrofolate reductase A1298C but not the C677T single nucleotide polymorphism with sickle cell disease in Bahrain.Hemoglobin1 mentions