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Variant (rsID / SNP)

rs201960644

MYH11

rs201960644 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH11. Location: chromosome 16, position 15,811,165. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

MYH11Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
16:15811165
Cytoband
16p13.11
HGVS
NM_002474.3(MYH11):c.5336C>T (p.Thr1779Met)
Allele change
Silent

Associated conditions / phenotypes

Aortic aneurysm, familial thoracic 4|Familial thoracic aortic aneurysm and aortic dissection|Cardiovascular phenotype

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.