rs587777372

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

Gene
NR2F2
Location
Chr 1596,334,247 (GRCh38)
Highest magnitude
6.0Very important
Tested on
AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AGoodcommon in clinvarTypical · 0.0
  2. A;TMost notableBadpossible congenital heart defect mutationVery important · 6.0

On SNPedia: (A;A), (A;T). 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

A;T

see ClinVar links

Source and license

Adapted from rs587777372 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.