rs369569464
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common/normal |
| (C;T) | 3 | Carrier of a Kell antigen null allele |
| (T;T) | 3.9 | Kell null phenotype (predicted); no illness, but may produce anti-Ku antibodies |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 7 |
| Position | 142961359 |
| Gene | KEL |
| is a | snp |
| is | mentioned by |
| dbSNP | rs369569464 |
| dbSNP (classic) | rs369569464 |
| ClinGen | rs369569464 |
| ebi | rs369569464 |
| HLI | rs369569464 |
| Exac | rs369569464 |
| Gnomad | rs369569464 |
| Varsome | rs369569464 |
| LitVar | rs369569464 |
| Map | rs369569464 |
| PheGenI | rs369569464 |
| Biobank | rs369569464 |
| 1000 genomes | rs369569464 |
| hgdp | rs369569464 |
| ensembl | rs369569464 |
| geneview | rs369569464 |
| scholar | rs369569464 |
| rs369569464 | |
| pharmgkb | rs369569464 |
| gwascentral | rs369569464 |
| openSNP | rs369569464 |
| 23andMe | rs369569464 |
| SNPshot | rs369569464 |
| SNPdbe | rs369569464 |
| MSV3d | rs369569464 |
| GWAS Ctlg | rs369569464 |
| Max Magnitude | 3.9 |
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
