Variant (rsID / SNP)

rs374359365

rs374359365 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CTF1. Location: chromosome 16, position 30,910,861. Clinical significance in the table: Likely benign.

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Reference-table entries

CTF1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 16:30910861
Cytoband: 16p11.2
HGVS: NM_001330.5(CTF1):c.144+7G>T
Allele change: Silent

Associated conditions / phenotypes

Dilated Cardiomyopathy, Dominant

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.