rs17503834

A SNP in the ENAH gene on chromosome 1. Its most notable genotype is C;C.

Gene
ENAH
Location
Chr 1225,648,975 (GRCh38)
Highest magnitude
1.0Minor
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
7%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableNot ratedNo summary available.Minor · 1.0<1% of people
  2. T;TGoodcommon in complete genomicsTypical · 0.088% of people

On SNPedia: (C;C), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 9 HapMap populations.

  • AverageC;C <1% T;T 88%
  • European ancestry (Utah)C;C 0% T;T 81%
  • Han Chinese (Beijing)C;C 0% T;T 93%
  • Japanese (Tokyo)C;C 0% T;T 97%
  • Yoruba (Nigeria)C;C 0% T;T 98%
  • Chinese (Denver)C;C 0% T;T 97%
  • Gujarati IndianC;C 0% T;T 87%
  • Mexican ancestry (Los Angeles)C;C 5% T;T 72%
  • Maasai (Kenya)C;C 0% T;T 91%
  • TuscanC;C 1% T;T 75%

Other ENAH SNPs

All ENAH SNPs

Source and license

Adapted from rs17503834 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.