Variant (rsID / SNP)

rs200646285

rs200646285 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYPN. Location: chromosome 10, position 69,970,208. Clinical significance in the table: Uncertain significance.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MYPNUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 10:69970208
Cytoband: 10q21.3
HGVS: NM_032578.4(MYPN):c.3959T>C (p.Leu1320Pro)
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.