Variant (rsID / SNP)

rs73373171

rs73373171 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYOM1. Location: chromosome 18, position 3,134,644. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MYOM1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 18:3134644
Cytoband: 18p11.31
HGVS: NM_003803.4(MYOM1):c.2384+4A>T
Allele change: Silent

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.