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Variant (rsID / SNP)

rs145673861

ABCC8

rs145673861 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC8. Location: chromosome 11, position 17,415,927. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ABCC8Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:17415927
Cytoband
11p15.1
HGVS
NM_000352.6(ABCC8):c.4431C>T (p.Gly1477=)
Allele change
Synonymous_G1477G

Associated conditions / phenotypes

Hyperinsulinemic hypoglycemia, familial, 1|Permanent neonatal diabetes mellitus|Diabetes mellitus, transient neonatal, 2

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.