rs132630265

A SNP in the CHM gene on chromosome X. Its most notable genotype is A;C: Choroideremia

Gene
CHM
Location
Chr X85,894,227 (GRCh38)
Highest magnitude
4.0Very important
Tested on
AncestryDNA

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;CGoodcommon in clinvarTypical · 0.0
  2. A;CMost notableBadChoroideremiaVery important · 4.0
  3. A;ABadrisk of ChoroideremiaVery important · 4.0

SNPedia records rs132630265 on the minus strand: (G;G), (G;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Conditions, medicines and genes

Other CHM SNPs

All CHM SNPs

Notes

From SNPedia

Notes

A;C

Choroideremia : Women would be a carrier, men would be affected

A;A

Choroideremia

Source and license

Adapted from rs132630265 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.