rs2296336
A SNP in the ITPR3 gene on chromosome 6. Its most notable genotype is G;G: 2.9x risk of type-1 diabetes
- Gene
- ITPR3
- Location
- Chr 633,668,883 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 29%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs2296336 on the minus strand: (C;C), (C;G), (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 13% C;G 49% C;C 39%
- European ancestry (Utah)G;G 11% C;G 46% C;C 43%
- Han Chinese (Beijing)G;G 24% C;G 53% C;C 22%
- Japanese (Tokyo)G;G 14% C;G 59% C;C 27%
- Yoruba (Nigeria)G;G 2% C;G 36% C;C 63%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs2296336 has been reported in a Swedish study to be associated with type-1 diabetes. The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.3 (CI 1.00-1.69), and for homozygotes, 2.9 (CI 1.88-4.59). suggests this SNP does not play a direct role in type-1 diabetes, and was only seen in the previous study due to being in linkage disequilibrium with specific alleles of the HLA DQB1 gene.
Source and license
Adapted from rs2296336 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.