rs587779413

A SNP in the TCIRG1 gene on chromosome 11. Its most notable genotype is A;C: Severe congenital neutropenia, type 1, autosomal dominant

Gene
TCIRG1
Location
Chr 1168,050,224 (GRCh38)
Highest magnitude
8.2Very important
Tested on
AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;CMost notableBadSevere congenital neutropenia, type 1, autosomal dominantVery important · 8.2
  2. C;CGoodcommon in clinvarTypical · 0.0

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

Notes

From SNPedia

Notes

c.2206C>A (p.Arg736Ser)

A;C

see links at rs587779413

Source and license

Adapted from rs587779413 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.