Variant (rsID / SNP)

rs9289231

rs9289231 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KALRN. Location: chromosome 3, position 123,774,078. Clinical significance in the table: Pathogenic.

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Reference-table entries

KALRNPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 3:123774078
Cytoband: 3q21.1
HGVS: NC_000003.11:g.123774078T>G

Associated conditions / phenotypes

Coronary heart disease, susceptibility to, 5

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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