rs1061302

A SNP in the NBN gene on chromosome 8. Its most notable genotype is T;T: common in clinvar

Gene
NBN
Location
Chr 889,946,194 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommon in clinvarTypical · 0.047% of people

SNPedia records rs1061302 on the minus strand: (A;A). 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 47%
  • European ancestry (Utah)T;T 50%
  • Han Chinese (Beijing)T;T 30%
  • Japanese (Tokyo)T;T 34%
  • Yoruba (Nigeria)T;T 72%
  • African ancestry (Southwest US)T;T 63%
  • Chinese (Denver)T;T 37%
  • Gujarati IndianT;T 27%
  • Luhya (Kenya)T;T 63%
  • Mexican ancestry (Los Angeles)T;T 41%
  • Maasai (Kenya)T;T 51%
  • TuscanT;T 46%

Other NBN SNPs

All NBN SNPs

Source and license

Adapted from rs1061302 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.