rs151344523

A SNP in the LOC107985154 gene on chromosome 18. Its most notable genotype is C;T: Spinocerebellar ataxia-28 (predicted)

Gene
LOC107985154
Location
Chr 1812,337,411 (GRCh38)
Highest magnitude
6.8Very important
Tested on
AncestryDNA

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;TMost notableBadSpinocerebellar ataxia-28 (predicted)Very important · 6.8
  2. C;CGoodcommon in clinvarTypical · 0.0

SNPedia records rs151344523 on the minus strand: (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Notes

From SNPedia

Notes

aka c.2105G>A (p.Arg702Gln or R702Q) Considered in ClinVar to be a dominant mutation leading to spinocerebellar ataxia-28.

C;T

see links via main rs-page

Source and license

Adapted from rs151344523 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.