RS387907306 SKI

Health Risk Chr 1:2228866
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Shprintzen-Goldberg syndrome
Inborn genetic diseases
Shprintzen-Goldberg syndrome
Inborn genetic diseases
Familial thoracic aortic aneurysm and aortic dissection
Shprintzen-Goldberg syndrome
Inborn genetic diseases
Shprintzen-Goldberg syndrome
Inborn genetic diseases
Familial thoracic aortic aneurysm and aortic dissection
Other Variants in SKI
rs387907303 rs387907304 rs387907305 rs398122889 rs398122914 rs397514589 rs397514590 rs149642284 rs756778048 rs773151547
Ask Dr. Hemsworth about this variant