rs2523605

A SNP in the MIR6891 gene on chromosome 6. Its most notable genotype is T;T: common in clinvar

Gene
MIR6891
Location
Chr 631,355,632 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
15%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommon in clinvarTypical · 0.02% of people
  2. C;CGoodcommon in complete genomicsTypical · 0.077% of people

SNPedia records rs2523605 on the minus strand: (A;A), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 11 HapMap populations.

  • AverageT;T 2% C;C 77%
  • European ancestry (Utah)T;T 4% C;C 60%
  • Han Chinese (Beijing)T;T 2% C;C 71%
  • Japanese (Tokyo)T;T <1% C;C 75%
  • Yoruba (Nigeria)T;T 1% C;C 88%
  • African ancestry (Southwest US)T;T 2% C;C 75%
  • Chinese (Denver)T;T 3% C;C 69%
  • Gujarati IndianT;T 1% C;C 85%
  • Luhya (Kenya)T;T 2% C;C 82%
  • Mexican ancestry (Los Angeles)T;T 2% C;C 83%
  • Maasai (Kenya)T;T <1% C;C 85%
  • TuscanT;T 2% C;C 78%

Other MIR6891 SNPs

All MIR6891 SNPs

Source and license

Adapted from rs2523605 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.