RS121434526 ACTA2

Health Risk Chr 10:88941793 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
Aortic aneurysm
familial thoracic 6
Familial thoracic aortic aneurysm and aortic dissection
familial thoracic 2
Cardiovascular phenotype
Aortic aneurysm
familial thoracic 6
Familial thoracic aortic aneurysm and aortic dissection
familial thoracic 2
Cardiovascular phenotype
Population Frequencies
gnomAD ALL
100%
Other Variants in ACTA2
rs121434527 rs121434528 rs387906592 rs397516683 rs397516685 rs112901682 rs397515325 rs727502878 rs794728031 rs794728029
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