Variant (rsID / SNP)

rs559464457

rs559464457 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEXN. Location: chromosome 1, position 78,395,085. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

NEXNBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:78395085
Cytoband: 1p31.1
HGVS: NM_144573.4(NEXN):c.949A>C (p.Met317Leu)
Allele change: Missense_M317L

Associated conditions / phenotypes

Dilated cardiomyopathy 1CC|Hypertrophic cardiomyopathy 20|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.