Variant (rsID / SNP)

rs116840795

rs116840795 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAV3. Location: chromosome 3, position 8,787,266. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

CAV3Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 3:8787266
Cytoband: 3p25.3
HGVS: NM_033337.3(CAV3):c.169G>A (p.Val57Met)
Allele change: Missense_V57M

Associated conditions / phenotypes

Long QT syndrome|Cardiomyopathy

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.