Variant (rsID / SNP)

rs750903219

rs750903219 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYPN. Location: chromosome 10, position 69,959,338. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MYPNConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 10:69959338
Cytoband: 10q21.3
HGVS: NM_032578.4(MYPN):c.3493+6G>A
Allele change: Silent

Associated conditions / phenotypes

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.