Variant carriers of the ''G'' allele had lower vitamin B12 levels when compared with individuals with the homozygous AA variant [R].

rs526934

Parent Gene: TCN1

Importance: 4
Less common allele: G = 20%
More common allele: A = 80%
My Genotype: Log In
Risk Allele: A

Disease/Trait: Vitamin B12 Measurement

rs526934 is associated with Vitamin B12 Measurement (R) . It is reported to have a 0.05 unit decrease on Folate pathway vitamin levels (Plasma Vitamin B12). No specific risk allele was identified in the study.

Disease/Trait: Vitamin B12 Measurement

The A allele of rs526934 is reported to be associated with Vitamin B12 Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Folate pathway vitamin levels (vitamin B12).