Variant (rsID / SNP)

rs121912999

rs121912999 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSP. Location: chromosome 6, position 7,585,996. Clinical significance in the table: Pathogenic.

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Reference-table entries

DSPPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 6:7585996
Cytoband: 6p24.3
HGVS: NM_004415.4(DSP):c.8501G>A (p.Arg2834His)
Allele change: Missense_R2391H

Associated conditions / phenotypes

Arrhythmogenic right ventricular dysplasia 8

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.