Gene entry
KCNJ6
potassium inwardly rectifying channel subfamily J member 6
- Chromosome
- 21
- Cytoband
- 21q22.13
- Variants (rsID)
- 88
KCNJ6 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 21 (region 21q22.13). Its official name is “potassium inwardly rectifying channel subfamily J member 6”. The reference table lists 88 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs2070995Not classifiedsynonymous_variantPain Agnosia|Back Pain|Personality Disorder|Lung Cancer|Constipation|Avoidant Personality Disorder|Subacute Delirium|Chronic Pain
Other listed variants
- rs702859
- rs702864
- rs762147
- rs857958
- rs857984
- rs858027
- rs858035
- rs858039
- rs858044
- rs1709806
- rs1709833
- rs1787406
- rs1892682
- rs2032090
- rs2835859
- rs2835862
- rs2835867
- rs2835872
- rs2835886
- rs2835893
- rs2835907
- rs2835931
- rs2835933
- rs2835951
- rs2835953
- rs2835987
- rs2835990
- rs2835998
- rs2836021
- rs2836028
- rs2836039
- rs2836048
- rs2898334
- rs3787835
- rs3787843
- rs3787867
- rs3827199
- rs4816585
- rs4817900
- rs4817901
- rs4817902
- rs7276020
- rs7278061
- rs7280538
- rs7282306
- rs7284047
- rs9983351
- rs10483039
- rs11701675
- rs11910276
- rs17229685
- rs17815177
- rs28828683
- rs57558558
- rs59350504
- rs73206048
- rs73206066
- rs73208109
- rs73208111
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
