rs1801133
rs1801133 · 11 retained evidence mentions
Source-grounded findings
Supporting evidence
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| variant | rs1801133 | “BACKGROUND: Studies have linked the methylenetetrahydrofolate reductase (MTHFR) c.665C > T (rs1801133) with hyperhomocysteinemia.” | 0.90 | hgvs_regex_v1 |
| variant | rs1801133 | “Genetic variants and breast carcinoma susceptibility: Unveiling the role of MTHFR (rs1801131, rs1801133) and TP53 (rs1042522).” | 0.90 | hgvs_regex_v1 |
| variant | rs1801133 | “A single nucleotide polymorphism (SNP) of MTHFR (rs1801133; C677T) is strongly associated with an increased risk of thrombophilia, heart attack, stroke, and dementia.” | 0.90 | hgvs_regex_v1 |
| variant | rs1801133 | “RESULTS: No association was identified between the targeted single-nucleotide polymorphism rs1801133 in MTHFR and TEEs in SCD (p = 0.79).” | 0.90 | hgvs_regex_v1 |
| variant | rs1801133 | “However, the genetic polymorphism of MTHFR C677T (rs1801133) and its association with MI in the presence of diabetes mellitus (DM) as a risk factor still needs to be investigated.” | 0.90 | hgvs_regex_v1 |
| variant | rs1801133 | “Role of metabolizing MTHFR gene polymorphism (rs1801133) and its mRNA expression among Type 2 Diabetes.” | 0.90 | hgvs_regex_v1 |
| variant | rs1801133 | “We evaluated the association between the clinical features and the methyl tetrahydrofolate (MTHFR) rs1801133 polymorphism and ASMs response among pediatric patients with epilepsy.” | 0.90 | hgvs_regex_v1 |
| variant | rs1801133 | “Genomic DNA from buccal cells was analyzed for 112 cases and 104 healthy controls using TaqMan genotyping assays of 677C>T rs1801133 and 1298A>C rs1801131 SNPs in the MTHFR gene.” | 0.90 | hgvs_regex_v1 |
| variant | rs1801133 | “Custom platform array was used to genotype the genetic polymorphisms within MTHFR (rs1801133) and ABCC2 (rs717620, rs3740066, rs2273697) genes.” | 0.90 | hgvs_regex_v1 |
| variant | rs1801133 | “METHODS: Two polymorphic sites of the MTHFR gene (c.677C>T, rs1801133 and c.1286A>C, rs1801131) were analyzed using RFLP and DNA sequencing in a group of vitamin B12 deficient individuals (45 males and 55 females).” | 0.90 | hgvs_regex_v1 |
| variant | rs1801133 | “Tetra primer allele refractory mutation system polymerase chain reaction (PCR) was used for resolving the genotypes of 5'10' methylenetetrahydrofolate reductase 'MTHFR' polymorphisms (rs1801133, rs1801131), 5' methyl tetrahydrofolate homocysteine methyltransferase 'MTR' polymorphism (rs1805087), paroxanse1 'PON1' polymorphism (rs662), and cystathionine beta synthase 'CBS' polymorphism (rs5742905).” | 0.90 | hgvs_regex_v1 |