rs587777695

A SNP in the ZSWIM6 gene on chromosome 5. Its most notable genotype is C;T: acromelic frontonasal dysostosis possible

Gene
ZSWIM6
Location
Chr 561,544,156 (GRCh38)
Highest magnitude
5.0Very important
Tested on
23andMe, AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CGoodcommon in clinvarTypical · 0.0
  2. C;TMost notableBadacromelic frontonasal dysostosis possibleVery important · 5.0

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

Notes

From SNPedia

Notes

rs587777695, also known as R1163W, is a mutation in the ZSWIM6 gene on chromosome 5. See OMIM 615951.0001

C;T

see discussion at rs587777695

Source and license

Adapted from rs587777695 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.