Gene entry
KEL
Kell metallo-endopeptidase (Kell blood group)
- Chromosome
- 7
- Cytoband
- 7q34
- Variants (rsID)
- 51
KEL is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q34). Its official name is “Kell metallo-endopeptidase (Kell blood group)”. The reference table lists 51 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs8176058Benignsingle nucleotide variantKELL K/k BLOOD GROUP POLYMORPHISM
Other listed variants
- rs2293266
- rs7784417
- rs7797896
- rs7797908
- rs7799481
- rs7806742
- rs7807823
- rs7810229
- rs8175955
- rs8175963
- rs8175964
- rs8175974
- rs8175985
- rs8176003
- rs8176013
- rs8176018
- rs8176026
- rs8176031
- rs8176044
- rs8176059
- rs11980340
- rs61729032
- rs61729034
- rs61729035
- rs61729039
- rs61729047
- rs61729053
- rs141415549
- rs141741567
- rs143238294
- rs143332567
- rs144613404
- rs148753837
- rs149066842
- rs150259463
- rs190890637
- rs191311545
- rs191330570
- rs199509304
- rs200975047
- rs201473860
- rs369569464
- rs530961865
- rs751160465
- rs751207765
- rs751284993
- rs753948889
- rs762055174
- rs766427535
- rs868367052
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.