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variant

A1298C

· 6 retained evidence mentions

Supporting evidence

TypeEntitySource evidenceConfidenceExtractor
variantA1298C“Methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms are associated with major depressive disorder in the Saudi patients attending Erada complex for mental health and Erada services - Jeddah, Saudi Arabia.”0.82literature_variant_regex_v2
variantA1298C“Genotype distributions of the 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T variant for patients were (χ2 = 22.43) and for controls were (χ2 = 0.07); for the MTHFR A1298C variant, they were (χ2 = 54.44) for patients and (χ2 = 4.58) for controls.”0.82literature_variant_regex_v2
variantA1298C“The genetic workup for thrombophilia risk identified several genetic thrombophilia mutations: the homozygous factor XIII V34L and MTHFR A1298C mutations and heterozygous factor V Leiden mutation.”0.82literature_variant_regex_v2
variantA1298C“Association of MTHFR C677T and A1298C gene polymorphisms with hypertension.”0.82literature_variant_regex_v2
variantA1298C“The association of factor V-Leiden and methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C mutations with stroke was investigated in 118 patients with stroke and 120 control subjects.”0.82literature_variant_regex_v2
variantA1298C“Two common variants in the MTHFR gene (C677T and A1298C) have been associated with reduced enzyme activity, thereby making MTHFR polymorphisms a potential candidate as a cancer-predisposing factor.”0.82literature_variant_regex_v2