Variant (rsID / SNP)

rs786204291

rs786204291 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSG2. Location: chromosome 18, position 29,102,115. Clinical significance in the table: Uncertain significance.

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Reference-table entries

DSG2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 18:29102115
Cytoband: 18q12.1
HGVS: NM_001943.5(DSG2):c.593A>G (p.Tyr198Cys)
Allele change: Missense_Y198C

Associated conditions / phenotypes

Hypertrophic cardiomyopathy|Arrhythmogenic right ventricular dysplasia 10|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.