Variant (rsID / SNP)
rs116347156
rs116347156 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CACNA1S. Location: chromosome 1, position 201,031,133. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
CACNA1SConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:201031133
- Cytoband
- 1q32.1
- HGVS
- NM_000069.3(CACNA1S):c.2992G>A (p.Asp998Asn)
- Allele change
- Missense_D998N
Associated conditions / phenotypes
Malignant hyperthermia of anesthesia|Hypokalemic periodic paralysis, type 1|Hypokalemic periodic paralysis, type 1|Malignant hyperthermia, susceptibility to, 5
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
