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Variant (rsID / SNP)

rs372702466

CACNA1C

rs372702466 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CACNA1C. Location: chromosome 12, position 2,775,936. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

CACNA1CConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
12:2775936
Cytoband
12p13.33
HGVS
NM_000719.7(CACNA1C):c.4611C>T (p.Arg1537=)
Allele change
Synonymous_R1557R

Associated conditions / phenotypes

History of neurodevelopmental disorder|Long QT syndrome

Public references

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