rs515726215

A SNP in the SLC12A6 gene on chromosome 15. Its most notable genotype is -;-: ACCPN neurological disorder

Gene
SLC12A6
Location
Chr 1534,240,661 (GRCh38)
Highest magnitude
6.0Very important
Tested on
AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. -;-Most notableBadACCPN neurological disorderVery important · 6.0
  2. -;CBadcarrier of an ACCPN neurological mutationImportant · 3.0
  3. C;CGoodcommon/normalTypical · 0.0

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

Conditions, medicines and genes

Other SLC12A6 SNPs

All SLC12A6 SNPs

Notes

From SNPedia

Notes

Agenesis of the Corpus Callosum with Peripheral Neuropathy 23andMe name: i5012573

-;-

ACCPN = Agenesis of the Corpus Callosum with Peripheral Neuropathy

Source and license

Adapted from rs515726215 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.