Variant (rsID / SNP)

rs150911078

rs150911078 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYPN. Location: chromosome 10, position 69,926,240. 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: 10:69926240
Cytoband: 10q21.3
HGVS: NM_032578.4(MYPN):c.1790G>A (p.Arg597His)
Allele change: Silent

Associated conditions / phenotypes

Cardiovascular phenotype|Cardiomyopathy|Dilated cardiomyopathy 1KK

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.