rs61736969
A SNP in the TBC1D4 gene on chromosome 13. Its most notable genotype is G;G: common in clinvar
- Gene
- TBC1D4
- Location
- Chr 1375,324,385 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Notes
From SNPedia
Show notes, about 190 words
Study "A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes" found association with higher 2 hour plasma glucose (β = 3.8 mmol l−1, P = 2.5 × 10−35 homozygous) and serum insulin (β = 165 pmol l−1, P = 1.5 × 10−20 homozygous) and subset of diabetes that features deterioration of postprandial glucose homeostasis among Greenlandic population. Each minor allele of resulting p.Arg684Ter (Triallelic, stop gained allele A, MAF 17% in study) conferred increasingly lower levels of messenger RNA and protein levels of the long isoform of TBC1D4 needed in skeletal muscle, and lower muscle protein levels of the glucose transporter GLUT4. rs7330796, rs1062087, rs2297206 are in close linkage disequilibrium with this SNPnature.com, however they're much more common than this causal variant, which has so far been only found in those of Greenlandic descent. A genotyping panel with rs7330796 was used for discovery of this variant.
Source and license
Adapted from rs61736969 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.