Variant (rsID / SNP)

rs143682596

rs143682596 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CTNNA3. Location: chromosome 10, position 68,526,170. Clinical significance in the table: Benign.

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Reference-table entries

CTNNA3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:68526170
Cytoband: 10q21.3
HGVS: NM_013266.4(CTNNA3):c.1133G>A (p.Arg378His)
Allele change: Missense_R378H

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.