rs587777232

A SNP in the EDN1 gene on chromosome 6. Its most notable genotype is A;C: Carrier for an auriculocondylar syndrome-3 mutation

Gene
EDN1
Location
Chr 612,292,506 (GRCh38)
Highest magnitude
3.0Important
Tested on
AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;CMost notableBadCarrier for an auriculocondylar syndrome-3 mutationImportant · 3.0
  2. C;CGoodcommon in clinvarTypical · 0.0

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

Other EDN1 SNPs

All EDN1 SNPs

Notes

From SNPedia

Notes

see OMIM 131240.0003

A;C

Unaffected in absence of a second EDN1 gene mutation

Source and license

Adapted from rs587777232 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.