rs886041261
A SNP in the PABPN1 gene on chromosome 14. Its most notable genotype is -;GGCGGC: Oculopharyngeal muscular dystrophy (OPMD)
- Gene
- PABPN1
- Location
- Chr 1423,321,492 (GRCh38)
- Highest magnitude
- 5.0Very important
- Tested on
- Not on consumer chips
Genotypes
As shown in 23andMe and AncestryDNA files.
- -;-Goodcommon in clinvar
- -;GGCGGCMost notableBadOculopharyngeal muscular dystrophy (OPMD)
- -;GGCGGCGGCBadOculopharyngeal muscular dystrophy (OPMD)
- T;TGoodcommon in clinvar
On SNPedia: (-;-), (-;GGCGGC), (-;GGCGGCGGC), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Notes
From SNPedia
Notes
-;GGCGGC
See links via main rs-page
-;GGCGGCGGC
See links via main rs-page
Source and license
Adapted from rs886041261 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.