Variant (rsID / SNP)

rs11596653

rs11596653 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYPN. Location: chromosome 10, position 69,908,157. Clinical significance in the table: Benign.

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Reference-table entries

MYPNBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:69908157
Cytoband: 10q21.3
HGVS: NM_032578.4(MYPN):c.1178T>C (p.Val393Ala)
Allele change: Silent

Associated conditions / phenotypes

Cardiovascular phenotype|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.