rs764328696
A SNP in the TBX20 gene on chromosome 7. Its most notable genotype is A;A: Atrial septal defect, type 4
- Gene
- TBX20
- Location
- Chr 735,248,696 (GRCh38)
- Highest magnitude
- 5.0Very important
- Tested on
- Not on consumer chips
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableBadAtrial septal defect, type 4
- A;GBadAtrial septal defect, type 4
- C;CGoodcommon/normal
On SNPedia: (A;A), (A;G), (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Notes
From SNPedia
Notes
rs764328696, also known as c.526G>A, p.Asp176Asn and D176N, represents a mutation in the TBX20 gene on chromosome 7. The rare (A) allele was identified based on whole exome sequencing of a Chinese family as causative for familial atrial septal defect, type 4.
A;A
see rs764328696
A;G
see rs764328696
Source and license
Adapted from rs764328696 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.