Variant (rsID / SNP)

rs143584663

rs143584663 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEBL. Location: chromosome 10, position 21,097,546. Clinical significance in the table: Likely benign.

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Reference-table entries

NEBLLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 10:21097546
Cytoband: 10p12.31
HGVS: NM_006393.3(NEBL):c.2654C>T (p.Ser885Phe)
Allele change: Silent

Associated conditions / phenotypes

Primary dilated 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.