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Variant (rsID / SNP)

rs149887823

MYPN

rs149887823 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYPN. Location: chromosome 10, position 69,948,821. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

MYPNConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
10:69948821
Cytoband
10q21.3
HGVS
NM_032578.4(MYPN):c.2863C>T (p.Arg955Trp)
Allele change
Silent

Associated conditions / phenotypes

Dilated cardiomyopathy 1KK|Cardiovascular phenotype

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.