Variant (rsID / SNP)

rs77165728

rs77165728 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CTNNA3. Location: chromosome 10, position 67,862,992. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

CTNNA3Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 10:67862992
Cytoband: 10q21.3
HGVS: NM_013266.4(CTNNA3):c.1900G>A (p.Glu634Lys)
Allele change: Missense_E634K

Associated conditions / phenotypes

Arrhythmogenic right ventricular dysplasia 13

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.