rs104894466

A SNP in the PABPN1 gene on chromosome 14. Its most notable genotype is C;G: Oculopharyngeal muscular dystrophy (OPMD)

Gene
PABPN1
Location
Chr 1423,321,504 (GRCh38)
Highest magnitude
5.0Very important
Tested on
AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;GMost notableBadOculopharyngeal muscular dystrophy (OPMD)Very important · 5.0
  2. G;GGoodcommon in clinvarTypical · 0.0

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

Other PABPN1 SNPs

All PABPN1 SNPs

Notes

From SNPedia

Notes

C;G

see links via main rs-page

Source and license

Adapted from rs104894466 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.