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Variant (rsID / SNP)

rs79129097

MYH11

rs79129097 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH11. Location: chromosome 16, position 15,808,856. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MYH11Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
16:15808856
Cytoband
16p13.11
HGVS
NM_002474.3(MYH11):c.5696A>G (p.Asn1899Ser)
Allele change
Silent

Associated conditions / phenotypes

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

Public references

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