Variant (rsID / SNP)

rs187262922

rs187262922 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM43. Location: chromosome 3, position 14,183,153. Clinical significance in the table: Likely benign.

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Reference-table entries

TMEM43Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:14183153
Cytoband: 3p25.1
HGVS: NM_024334.3(TMEM43):c.1061G>C (p.Cys354Ser)
Allele change: Missense_C354S

Associated conditions / phenotypes

Cardiovascular phenotype|Arrhythmogenic right ventricular dysplasia 5|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.