rs369569464

A SNP in the KEL gene on chromosome 7. Its most notable genotype is T;T: Kell null phenotype (predicted); no illness, but may produce anti-Ku antibodies

Gene
KEL
Location
Chr 7142,961,359 (GRCh38)
Highest magnitude
3.9Important
Tested on
Not on consumer chips

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CGoodcommon/normalTypical · 0.0
  2. C;TBadCarrier of a Kell antigen null alleleImportant · 3.0
  3. T;TMost notableBadKell null phenotype (predicted); no illness, but may produce anti-Ku antibodiesImportant · 3.9

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

Other KEL SNPs

All KEL SNPs

Notes

From SNPedia

Notes

The rs369569464(T) allele is reported to be an allele leading to the Kell null phenotype (when inherited in two copies or with another null allele). 23andMe name: i6025264

C;T

Unaffected in absence of a second KEL gene mutation

T;T

see links and text via main rs-page

Source and license

Adapted from rs369569464 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.