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.
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%
Related
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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.