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Variant (rsID / SNP)

rs765064661

KCNJ2

rs765064661 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNJ2. Location: chromosome 17, position 68,165,831. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

KCNJ2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
17:68165831
Cytoband
17q24.3
HGVS
NM_000891.3(KCNJ2):c.-228C>T
Allele change
Silent

Associated conditions / phenotypes

Atrial fibrillation, familial, 9|Andersen Tawil syndrome|Short QT syndrome type 3

Public references

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