Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs140148105

MYPN

rs140148105 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYPN. Location: chromosome 10, position 69,881,254. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

MYPNConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
10:69881254
Cytoband
10q21.3
HGVS
NM_032578.4(MYPN):c.59A>G (p.Tyr20Cys)
Allele change
Silent

Associated conditions / phenotypes

Familial hypertrophic cardiomyopathy 22|Dilated cardiomyopathy 1KK|Primary dilated cardiomyopathy|Cardiovascular phenotype

Public references

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