rs12416605
A SNP in the SVIL gene on chromosome 10. Its most notable genotype is C;C.
- Gene
- SVIL
- Location
- Chr 1029,602,331 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 15%
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 100% T;T 0%
- European ancestry (Utah)C;C 100% T;T 0%
- Han Chinese (Beijing)C;C 100% T;T 0%
- Japanese (Tokyo)C;C 100% T;T 0%
- Yoruba (Nigeria)C;C 100% T;T 0%
Related
Notes
From SNPedia
Notes
Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes.
T;T
rare in hapmap, but not uncommon in opensnp and https://www.23andme.com/you/community/thread/17209/
Source and license
Adapted from rs12416605 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.