rs4148941
A SNP in the CHST3 gene on chromosome 10. Its most notable genotype is A;C: Slightly higher (1.5) risk for lumbar disc disease (?)
- Gene
- CHST3
- Location
- Chr 1072,009,234 (GRCh38)
- Highest magnitude
- 1.5Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AGoodcommon/normal
- A;CMost notableBadSlightly higher (1.5) risk for lumbar disc disease (?)
- C;CBadSlightly higher (1.5) risk for lumbar disc disease (?)
On SNPedia: (A;A), (A;C), (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 10 HapMap populations.
- AverageA;A 42% A;C 41% C;C 17%
- European ancestry (Utah)A;A 43% A;C 45% C;C 13%
- Han Chinese (Beijing)A;A 18% A;C 54% C;C 28%
- Japanese (Tokyo)A;A 15% A;C 53% C;C 32%
- Yoruba (Nigeria)A;A 88% A;C 10% C;C 2%
- Chinese (Denver)A;A 18% A;C 48% C;C 34%
- Gujarati IndianA;A 26% A;C 52% C;C 23%
- Luhya (Kenya)A;A 86% A;C 14% C;C 0%
- Mexican ancestry (Los Angeles)A;A 34% A;C 54% C;C 13%
- Maasai (Kenya)A;A 54% A;C 42% C;C 4%
- TuscanA;A 35% A;C 43% C;C 22%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
aka c.*763C>A Possible risk factor for lumbar disc disease, based on a study of 4,000 patients; the AA and AC genotypes had an odds ratio of ~1.5 for developing the disorder. However, note that this variant is annotated as benign by the one submitter (Illumina) to ClinVar, whether for skeletal dysplasia or similar syndromes.
A;C
see discussion at main rs-page
C;C
see discussion at main rs-page
Source and license
Adapted from rs4148941 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.