rs386134131

A SNP in the CP gene on chromosome 3. Its most notable genotype is T;T: Probably Aceruloplasminemia, aka Deficiency of Ferroxidase.

Gene
CP
Location
Chr 3149,178,618 (GRCh38)
Highest magnitude
4.0Very important
Tested on
AncestryDNA

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableBadProbably Aceruloplasminemia, aka Deficiency of Ferroxidase.Very important · 4.0
  2. C;CGoodcommon in clinvarTypical · 0.0

SNPedia records rs386134131 on the minus strand: (A;A), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Conditions, medicines and genes

Other CP SNPs

All CP SNPs

Notes

From SNPedia

Notes

T;T

This leads to iron accumulation in cells, damaged brain cells, dementia, damaged retina, and systemic hemosiderosis.

Source and license

Adapted from rs386134131 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.