Variant (rsID / SNP)

rs143574079

rs143574079 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYPN. Location: chromosome 10, position 69,881,929. Clinical significance in the table: Likely benign.

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Reference-table entries

MYPNLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 10:69881929
Cytoband: 10q21.3
HGVS: NM_032578.4(MYPN):c.734C>G (p.Ala245Gly)
Allele change: Silent

Associated conditions / phenotypes

Dilated cardiomyopathy 1KK|Cardiovascular phenotype

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.