rs16889859
A SNP in the LOC105377865 gene on chromosome 6. Its most notable genotype is A;A: common in complete genomics
- Gene
- LOC105377865
- Location
- Chr 678,316,148 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 10%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 9 HapMap populations.
- AverageA;A 86%
- European ancestry (Utah)A;A 100%
- Han Chinese (Beijing)A;A 67%
- Japanese (Tokyo)A;A 58%
- Yoruba (Nigeria)A;A 100%
- African ancestry (Southwest US)A;A 93%
- Chinese (Denver)A;A 68%
- Gujarati IndianA;A 97%
- Maasai (Kenya)A;A 99%
- TuscanA;A 93%
Related
Genosets
Genosets combine several genotypes. Twofold checks them in your report.
Notes
From SNPedia
Notes
Here to enable genosets gs217 and gs218 which look for a CNV
Source and license
Adapted from rs16889859 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.