rs1154233
A SNP in the LAMA3 gene on chromosome 18. Its most notable genotype is A;A: common in clinvar
- Gene
- LAMA3
- Location
- Chr 1823,931,125 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 0%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 7 HapMap populations.
- AverageA;A <1% G;G 98%
- European ancestry (Utah)A;A 0% G;G 100%
- Han Chinese (Beijing)A;A 0% G;G 100%
- Japanese (Tokyo)A;A <1% G;G 91%
- Yoruba (Nigeria)A;A 0% G;G 100%
- Gujarati IndianA;A 0% G;G 98%
- Maasai (Kenya)A;A 0% G;G 98%
- TuscanA;A 0% G;G 97%
Source and license
Adapted from rs1154233 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.