rs6414624

A SNP in the EVC gene on chromosome 4. Its most notable genotype is C;C.

Gene
EVC
Location
Chr 45,741,785 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
23%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableNot ratedNo summary available.Typical · 0.055% of people
  2. T;TGoodcommon in clinvarTypical · 0.09% 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 11 HapMap populations.

  • AverageC;C 55% T;T 9%
  • European ancestry (Utah)C;C 62% T;T 4%
  • Han Chinese (Beijing)C;C 78% T;T 2%
  • Japanese (Tokyo)C;C 82% T;T <1%
  • Yoruba (Nigeria)C;C 25% T;T 27%
  • African ancestry (Southwest US)C;C 25% T;T 11%
  • Chinese (Denver)C;C 83% T;T <1%
  • Gujarati IndianC;C 63% T;T 4%
  • Luhya (Kenya)C;C 24% T;T 24%
  • Mexican ancestry (Los Angeles)C;C 74% T;T 3%
  • Maasai (Kenya)C;C 25% T;T 18%
  • TuscanC;C 60% T;T 5%

Other EVC SNPs

All EVC SNPs

Source and license

Adapted from rs6414624 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.