rs846910
A SNP in the LOC101930114 gene on chromosome 1. Its most notable genotype is G;G: common in complete genomics
- Gene
- LOC101930114
- Location
- Chr 1209,701,909 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 11%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G). 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.
- AverageG;G 72%
- European ancestry (Utah)G;G 85%
- Han Chinese (Beijing)G;G 55%
- Japanese (Tokyo)G;G 48%
- Yoruba (Nigeria)G;G 100%
Notes
From SNPedia
Notes
{{PMID Auto |PMID=21622477 |Title=A combination of polymorphisms in HSD11B1 associates with in vivo 11{beta}-HSD1 activity and metabolic syndrome in women with and without polycystic ovary syndrome }}
Source and license
Adapted from rs846910 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.