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Variant (rsID / SNP)

rs104894248

KCNJ11

rs104894248 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNJ11. Location: chromosome 11, position 17,408,863. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

KCNJ11Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:17408863
Cytoband
11p15.1
HGVS
NM_000525.4(KCNJ11):c.776A>G (p.His259Arg)
Allele change
Missense_H172R

Associated conditions / phenotypes

Hyperinsulinemic hypoglycemia, familial, 2|Type 2 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.