rs10911193
A SNP in the LAMC1 gene on chromosome 1. Its most notable genotype is T;T.
- Gene
- LAMC1
- Location
- Chr 1183,021,513 (GRCh38)
- Highest magnitude
- 1.9Minor
- Tested on
- 23andMe
- Minor allele frequency
- 12%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageC;C 76% T;T 2%
- European ancestry (Utah)C;C 79% T;T 0%
- Han Chinese (Beijing)C;C 87% T;T 2%
- Japanese (Tokyo)C;C 64% T;T 7%
- Yoruba (Nigeria)C;C 76% T;T 0%
Notes
From SNPedia
Notes
T;T
some papers suggest an increased risk of pelvic organ prolapse, but the most recent analysis does not replicate that result.
Source and license
Adapted from rs10911193 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.