Variant (rsID / SNP)
rs111967655
rs111967655 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC8. Location: chromosome 11, position 17,432,147. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
ABCC8Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:17432147
- Cytoband
- 11p15.1
- HGVS
- NM_000352.6(ABCC8):c.2610C>T (p.Ala870=)
- Allele change
- Synonymous_A870A
Associated conditions / phenotypes
Diabetes mellitus, transient neonatal, 2|Permanent neonatal diabetes mellitus|Hyperinsulinemic hypoglycemia, familial, 1|Hereditary hyperinsulinism|Transitory neonatal diabetes mellitus|Maturity onset diabetes mellitus in young
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.