Traits - Vitamin C Levels

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Vitamin C Levels

Vitamin Metabolism

Vitamin C (ascorbic acid) is a water-soluble antioxidant that supports collagen synthesis, immune function, and iron absorption.

Variants in SLC23A1 and SLC23A2 (vitamin C transporters) have been linked to differences in plasma ascorbate.

This result reflects research-level variation in vitamin C handling and is not a clinical test or a supplement recommendation.

Daily intake from fruits and vegetables, smoking, infections, and overall stress on the body strongly affect real vitamin C status.

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Report markers
11 SNP entries
Genes
0
Research
1 study
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Genetic tendency

Average genetic tendency

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Behind this report

Review the genes, tested markers and supporting research.

SNPs tested

These are the unique genetic markers analyzed for this trait. Genotypes showing "--" were not identified in your DNA file. Report marker totals can include repeated study entries; this table shows each SNP once.

Genotypes and reported variant frequencies
SNPChromosomeGenotypeVariant alleleFrequency
rs6693447GGG55.10%
rs10051765--C34.20%
rs10136000--A28.30%
rs117885456--A8.70%
rs13028225--C85.70%
rs174547--C32.80%
rs2559850--A59.80%
rs33972313--96.80%
rs56738967--C32.10%
rs7740812--59.40%
rs9895661--T81.70%

DNA Genics reports genotypes based on the 'positive' strand of the human genome reference sequence (build 37/HG19). Other companies may use the opposite strand, so genotypes may need conversion for comparison.

Research studies

The following peer-reviewed scientific studies support the genetic associations analyzed in this report.

2021 Jan Diabetes Care

Authors: Zheng JS, Luan J, Sofianopoulou E, Imamura F, Stewart ID, Day FR, Pietzner M, Wheeler E, Lotta LA, Gundersen TE, Amiano P, Ardanaz E, Chirlaque MD, Fagherazzi G, Franks PW, Kaaks R, Laouali N, Mancini FR, Nilsson PM, Onland-Moret NC, Olsen A, Overvad K, Panico S, Palli D, Ricceri F, Rolandsson O, Spijkerman AMW, Sánchez MJ, Schulze MB, Sala N, Sieri S, Tjønneland A, Tumino R, van der Schouw YT, Weiderpass E, Riboli E, Danesh J, Butterworth AS, Sharp SJ, Langenberg C, Forouhi NG, Wareham NJ

Study sample: 52,018 individuals (european ancestry)

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Coverage: 1/11 SNP entries detected (9%).

Reference: Human Genome Build 37 (HG19). Other testing companies may report using the opposite strand, requiring conversion for comparison.

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