Variant (rsID / SNP)

rs372006344

rs372006344 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYOZ2. Location: chromosome 4, position 120,057,766. Clinical significance in the table: Likely benign.

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Reference-table entries

MYOZ2Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 4:120057766
Cytoband: 4q26
HGVS: NM_016599.5(MYOZ2):c.76+10A>G
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.