rs886041888

A SNP in the PDCD10 gene on chromosome 3. Its most notable genotype is -;T: Cerebral cavernous angioma associated mutation; variable penetrance

Gene
PDCD10
Location
Chr 3167,687,621 (GRCh38)
Highest magnitude
5.2Very important
Tested on
Not on consumer chips

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. -;-Goodcommon in clinvarTypical · 0.0
  2. -;TMost notableBadCerebral cavernous angioma associated mutation; variable penetranceVery important · 5.2

SNPedia records rs886041888 on the minus strand: (-;-), (-;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Other PDCD10 SNPs

All PDCD10 SNPs

Notes

From SNPedia

Notes

aka c.467dupA (p.Asn156Lysfs)

-;T

see links via main rs-page

Source and license

Adapted from rs886041888 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.