rs587777373

A SNP in the NR2F2 gene on chromosome 15. Its most notable genotype is -;GCA: possible causal congenital heart defect mutation

Gene
NR2F2
Location
Chr 1596,332,329 (GRCh38)
Highest magnitude
6.0Very important
Tested on
Not on consumer chips

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. -;-Goodcommon in clinvarTypical · 0.0
  2. -;GCAMost notableBadpossible causal congenital heart defect mutationVery important · 6.0

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

Other NR2F2 SNPs

All NR2F2 SNPs

Notes

From SNPedia

Notes

-;GCA

see ClinVar links

Source and license

Adapted from rs587777373 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.