Variant (rsID / SNP)

rs9807556

rs9807556 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYOM1. Location: chromosome 18, position 3,151,736. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MYOM1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 18:3151736
Cytoband: 18p11.31
HGVS: NM_003803.4(MYOM1):c.1799A>T (p.Glu600Val)
Allele change: Missense_E600V

Associated conditions / phenotypes

Hypertrophic cardiomyopathy|Cardiovascular phenotype

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.