rs7041

A SNP in the GC gene on chromosome 4. Its most notable genotype is A;A: ex-smokers at 2x higher risk for COPD; supplement with Vitamin D?

Gene
GC
Location
Chr 471,752,617 (GRCh38)
Highest magnitude
1.5Minor
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
39%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. A;AMost notableNot ratedex-smokers at 2x higher risk for COPD; supplement with Vitamin D?Minor · 1.549% of people

SNPedia records rs7041 on the minus strand: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 11 HapMap populations.

  • AverageA;A 49%
  • European ancestry (Utah)A;A 19%
  • Han Chinese (Beijing)A;A 50%
  • Japanese (Tokyo)A;A 59%
  • Yoruba (Nigeria)A;A 84%
  • African ancestry (Southwest US)A;A 68%
  • Chinese (Denver)A;A 43%
  • Gujarati IndianA;A 26%
  • Luhya (Kenya)A;A 86%
  • Mexican ancestry (Los Angeles)A;A 26%
  • Maasai (Kenya)A;A 58%
  • TuscanA;A 18%

Conditions, medicines and genes

Notes

From SNPedia

Show notes, about 160 words

rs7041(T), the more common allele in many non-Caucasian or Hispanic populations, encodes an aspartic acid (Asp) at position 432 in the vitamin D binding protein (VDBP); in older literature, this is numbered as position 416. rs7041(G), the rarer allele, encodes a glutamic acid (Glu) at this position. see discussion at the GC gene for how rs4588 and rs7041 together define three forms of the VDB protein A study of 414 (ex)-smokers older than 50 years concluded that vitamin D levels were reduced by 25% in [[rs7041](T;T) homozygotes (p<0.0001), and even after correction for age, gender and smoking history, they were also at increased risk for chronic obstructive pulmonary disease (COPD; odds ratio 2.11, CI: 1.20-3.71, p=0.009). They conclude that since vitamin D deficiency occurs frequently in COPD and correlates with its severity, vitamin D supplementation may be warranted in patients with severe COPD, and especially in those carrying rs7041(T) alleles.

Source and license

Adapted from rs7041 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.

SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.