Variant (rsID / SNP)

rs786205457

rs786205457 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYPN. Location: chromosome 10, position 69,902,729. Clinical significance in the table: Uncertain significance.

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Reference-table entries

MYPNUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 10:69902729
Cytoband: 10q21.3
HGVS: NM_032578.4(MYPN):c.935C>T (p.Ser312Phe)
Allele change: Silent

Associated conditions / phenotypes

Hypertrophic cardiomyopathy

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.