RS363847 FBN1
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Associated Conditions
Marfan syndrome
Geleophysic dysplasia
Stiff skin syndrome
Acromicric dysplasia
Weill-Marchesani syndrome
Familial thoracic aortic aneurysm and aortic dissection
Ectopia lentis 1
isolated
autosomal dominant
FBN1-related disorder
Marfan syndrome
Geleophysic dysplasia
Stiff skin syndrome
Acromicric dysplasia
Weill-Marchesani syndrome
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Height | — | OR: 0.14 | 5E-19 | PubMed |
Other Variants in FBN1