Variant (rsID / SNP)

rs2281845

rs2281845 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CACNA1S. Location: chromosome 1, position 201,081,943. 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: 1:201081943
Cytoband: 1q32.1
HGVS: NM_000069.2(CACNA1S):c.-476G>A

Associated conditions / phenotypes

Thyrotoxic periodic paralysis, susceptibility to, 1

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.