Variant (rsID / SNP)

rs45544633

rs45544633 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH7. Location: chromosome 14, position 23,886,383. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

MYH7Pathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 14:23886383
Cytoband: 14q11.2
HGVS: NM_000257.4(MYH7):c.4498C>T (p.Arg1500Trp)
Allele change: Missense_R1500W

Associated conditions / phenotypes

Primary dilated cardiomyopathy|Hypertrophic cardiomyopathy|Cardiovascular phenotype|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.