Variant (rsID / SNP)

rs149883381

rs149883381 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM43. Location: chromosome 3, position 14,172,438. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TMEM43Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:14172438
Cytoband: 3p25.1
HGVS: NM_024334.3(TMEM43):c.279C>T (p.Gly93=)
Allele change: Synonymous_G93G

Associated conditions / phenotypes

Arrhythmogenic right ventricular dysplasia 5|Cardiovascular phenotype|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.