Variant (rsID / SNP)

rs12406479

rs12406479 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CACNA1S. Location: chromosome 1, position 201,079,344. Clinical significance in the table: Benign.

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Reference-table entries

CACNA1SBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:201079344
Cytoband: 1q32.1
HGVS: NM_000069.3(CACNA1S):c.206C>G (p.Ala69Gly)
Allele change: Missense_A69G

Associated conditions / phenotypes

Hypokalemic periodic paralysis, type 1|Hypokalemic periodic paralysis, type 1|Malignant hyperthermia, 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.