rs103612

A SNP in the NUP214 gene on chromosome 9. Its most notable genotype is C;T.

Gene
NUP214
Location
Chr 9131,144,705 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
33%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;TMost notableNot ratedNo summary available.Typical · 0.048% of people

On SNPedia: (C;T). 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.

  • AverageC;T 48%
  • European ancestry (Utah)C;T 50%
  • Han Chinese (Beijing)C;T 42%
  • Japanese (Tokyo)C;T 50%
  • Yoruba (Nigeria)C;T 50%
  • African ancestry (Southwest US)C;T 60%
  • Chinese (Denver)C;T 46%
  • Gujarati IndianC;T 50%
  • Luhya (Kenya)C;T 50%
  • Mexican ancestry (Los Angeles)C;T 36%
  • Maasai (Kenya)C;T 43%
  • TuscanC;T 48%

Source and license

Adapted from rs103612 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.