rs3092904
A SNP in the RB1 gene on chromosome 13. Its most notable genotype is T;T: common in clinvar
- Gene
- RB1
- Location
- Chr 1348,477,345 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (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.
- AverageT;T 61%
- European ancestry (Utah)T;T 56%
- Han Chinese (Beijing)T;T 58%
- Japanese (Tokyo)T;T 47%
- Yoruba (Nigeria)T;T 83%
Related
Other RB1 SNPs
- rs3092891C;TRetinoblastoma (predicted)Very important
- rs121913296G;TRetinoblastoma (predicted)Very important
- rs121913300C;TRetinoblastoma (predicted)Very important
- rs121913301C;TRetinoblastoma (predicted)Very important
- rs121913302C;TRetinoblastoma (predicted)Very important
- rs121913303C;TRetinoblastoma (predicted)Very important
- rs121913304C;TRetinoblastoma (predicted)Very important
- rs121913305C;TRetinoblastoma (predicted)Very important
Source and license
Adapted from rs3092904 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.