Variant (rsID / SNP)
rs2070995
rs2070995 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNJ6. Location: chromosome 21, position 39,086,965. The table records no clinical significance for this variant.
Reference-table entries
KCNJ6Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 21:39086965
- HGVS
- NM_002240.5,c.495A>G,p.Pro165Pro
- Allele change
- Synonymous_P165P
Associated conditions / phenotypes
Pain Agnosia|Back Pain|Personality Disorder|Lung Cancer|Constipation|Avoidant Personality Disorder|Subacute Delirium|Chronic Pain
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.