rs161400
A SNP in the LOC105371492 gene on chromosome 17. Its most notable genotype is C;C: common in clinvar
- Gene
- LOC105371492
- Location
- Chr 173,658,102 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 16%
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 8% T;T 75%
- European ancestry (Utah)C;C 0% T;T 99%
- Han Chinese (Beijing)C;C 0% T;T 87%
- Japanese (Tokyo)C;C 0% T;T 89%
- Yoruba (Nigeria)C;C 31% T;T 27%
Related
Other LOC105371492 SNPs
- rs113994205A;GCarrier of a cystinosis mutationImportant
- rs113994208A;GCarrier of a cystinosis mutationImportant
- rs121908124G;TCarrier of a cystinosis mutationImportant
- rs121908126A;GCarrier of a cystinosis mutationImportant
- rs121908128C;GCarrier of a cystinosis mutationImportant
- rs121908129G;TCarrier of a cystinosis mutationImportant
- rs267606754C;TCarrier of a cystinosis mutationImportant
Source and license
Adapted from rs161400 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.