rs1801131
rs1801131 · SaudiVarKB evidence summary derived from retained literature mentions.
4Variant mentions
4Publications
6Associated gene records
3Associated phenotype records
Associated gene records
Co-mentioned in the same publicationsAssociated phenotype records
Co-mentioned in the same publications| Phenotype | Identifier / context | Articles | Mentions |
|---|---|---|---|
| autism spectrum disorder | HP:0000729 | 1 | 1 |
| coronary artery disease | — | 1 | 1 |
| breast cancer | — | 1 | 1 |
Associated population records
Co-mentioned in the same publications| Population | Identifier / context | Articles | Mentions |
|---|---|---|---|
| Saudi Arabia | Cohort 112 | 1 | 1 |
| Population record | Cohort 504 | 1 | 1 |
| Population record | Cohort 242 | 1 | 1 |
Supporting publications
4 records- 2026Development and validation of a tetra-primer ARMS-PCR assay for genotyping the MTHFR (rs1801131) c.1286 A > C (p.Glu429Ala) polymorphism: a comparative study with KASP.Molecular biology reports1 mentions
- 2025Genetic variants and breast carcinoma susceptibility: Unveiling the role of MTHFR (rs1801131, rs1801133) and TP53 (rs1042522).Gene1 mentions
- 2019Methylenetetrahydrofolate Reductase Gene Variants Confer Potential Vulnerability to Autism Spectrum Disorder in a Saudi Community.Neuropsychiatric disease and treatment1 mentions
- 2017The communal relation of MTHFR, MTR, ACE gene polymorphisms and hyperhomocysteinemia as conceivable risk of coronary artery disease.Applied physiology, nutrition, and metabolism = Physiologie appliquee, nutrition et metabolisme1 mentions