Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137854467
rs137854467
FBN1
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome 		A 0.810 CausalMutation CLINVAR

dbSNP: rs137854467
rs137854467
FBN1
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome 		A 0.810 GeneticVariation CLINVAR