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variant

C677T

· 7 retained evidence mentions

Supporting evidence

TypeEntitySource evidenceConfidenceExtractor
variantC677T“Prevalence of methylenetetrahydrofolate reductase gene polymorphisms (C677T, and A1298C) among Saudi children receiving dental treatment.”0.82literature_variant_regex_v2
variantC677T“Association of methylenetetrahydrofolate reductase C677T and reduced-f carrier-1 G80A gene polymorphism with preeclampsia in Sudanese women.”0.82literature_variant_regex_v2
variantC677T“Methylenetetrahydrofolate Reductase C677T Gene Polymorphism as Risk Factor for Psoriasis in Saudis.”0.82literature_variant_regex_v2
variantC677T“Results of this study suggest that theMTHFR C677T polymorphism may modify the association between dietary intake and breast cancer risk.”0.82literature_variant_regex_v2
variantC677T“OBJECTIVE: To study the frequency of Factor V Leiden (FVL), prothrombin gene mutation G20210A and methylenetetrahydrofolate reductase C677T in patients with acute pulmonary embolism (PE); and to investigate whether these factors are more frequent in patients who have no obvious risk factors for venous thrombo-embolism compared to those with obvious risk factors.”0.82literature_variant_regex_v2
variantC677T“Association of the methylenetetrahydrofolate reductase A1298C but not the C677T single nucleotide polymorphism with sickle cell disease in Bahrain.”0.82literature_variant_regex_v2
variantC677T“Frequency of methylenetetrahydrofolate reductase C677T polymorphism in patients with cardiovascular disease in Eastern Saudi Arabia.”0.82literature_variant_regex_v2