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Variant (rsID / SNP)

rs115276158

CTNNA3

rs115276158 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CTNNA3. Location: chromosome 10, position 68,526,108. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CTNNA3Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
10:68526108
Cytoband
10q21.3
HGVS
NM_013266.4(CTNNA3):c.1195C>A (p.Leu399Ile)
Allele change
Missense_L399I

Associated conditions / phenotypes

Arrhythmogenic right ventricular dysplasia 13

Public references

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