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rs7041 GC

GC Asp432Glu homozygous. Lower vitamin D binding protein affinity; may need higher vitamin D intake.

Curated · human-reviewed Nutrition · Risk / effect allele: T · dbSNP

What is rs7041?

rs7041 is a single-nucleotide polymorphism (SNP) in the GC gene (GC vitamin D binding protein). Each person carries two copies, one from each parent, so a result is reported as a pair of letters such as TT. The table below describes what studies associate with each genotype; the association is statistical, across populations, and is not a diagnosis.

What does each rs7041 genotype mean?

GenotypeAssociationWhat the evidence saysConfidence
TTincreasedGC Asp432Glu homozygous. Lower vitamin D binding protein affinity; may need higher vitamin D intake.82%
GT / TGtypicalIntermediate vitamin D binding capacity.78%
GGtypicalNormal vitamin D binding protein function.82%

How common is the T allele of rs7041?

Minor-allele frequency by population (gnomAD / 1000 Genomes):

European43.0%
East Asian20.0%
African85.0%
South Asian35.0%
Admixed American45.0%
Global45.0%

Which drugs have annotations for rs7041?

PharmGKB clinical annotations (level 1A is the strongest evidence, 4 the weakest):

DrugAnnotation typeEvidence level
deferasiroxEfficacy3

Is rs7041 on 23andMe and AncestryDNA chips?

Yes — it is genotyped directly on 23andMe V3, 23andMe V4, 23andMe V5, AncestryDNA V1, AncestryDNA V2. Orviva reads it from a raw-data export without imputation.

Sources

Genetic associations describe risk across populations, not a diagnosis for any one person. Most variants shift risk modestly and act alongside lifestyle, environment and other genes. Consumer DNA chips do not read every position and can be wrong at any single one. For general education only; talk to a clinician or genetic counsellor before acting on anything here, and never change a prescribed medicine without your prescriber.