Gene entry
SLC14A1
solute carrier family 14 member 1 (Kidd blood group)
- Chromosome
- 18
- Cytoband
- 18q12.3
- Variants (rsID)
- 51
SLC14A1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 18 (region 18q12.3). Its official name is “solute carrier family 14 member 1 (Kidd blood group)”. The reference table lists 51 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs1058396Benignsingle nucleotide variantKIDD BLOOD POLYMORPHISM Jk(a)/Jk(b)
- rs78242949Pathogenicsingle nucleotide variantJk-null variant, finnish type
Other listed variants
- rs577020
- rs900971
- rs2298718
- rs2298720
- rs3745006
- rs3819179
- rs4890588
- rs7237102
- rs7238033
- rs9948825
- rs10460032
- rs10460036
- rs10775480
- rs10853535
- rs11877062
- rs11877720
- rs17674580
- rs17675299
- rs28994270
- rs28994277
- rs28994278
- rs28994287
- rs62096937
- rs76015227
- rs78937798
- rs113029149
- rs113578396
- rs114362217
- rs116447192
- rs138222201
- rs138248117
- rs139053682
- rs142529927
- rs146079238
- rs146420195
- rs200153291
- rs201451018
- rs201612170
- rs201620887
- rs373247991
- rs374937387
- rs538368217
- rs563016158
- rs565898944
- rs749037771
- rs760253588
- rs760401643
- rs763262711
- rs868538651
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.