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rs113905529

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs113905529(C;T)
Make rs113905529(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48596328
GeneFBN1
is asnp
is mentioned by
dbSNPrs113905529
ebirs113905529
HLIrs113905529
Exacrs113905529
Varsomers113905529
Maprs113905529
PheGenIrs113905529
hapmaprs113905529
1000 genomesrs113905529
hgdprs113905529
ensemblrs113905529
gopubmedrs113905529
geneviewrs113905529
scholarrs113905529
googlers113905529
pharmgkbrs113905529
gwascentralrs113905529
openSNPrs113905529
23andMers113905529
23andMe allrs113905529
SNP Nexus

SNPshotrs113905529
SNPdbers113905529
MSV3drs113905529
GWAS Ctlgrs113905529
Max Magnitude0
ClinVar
Risk rs113905529(G,T;G,T)
Alt rs113905529(G,T;G,T)
Reference rs113905529(C;C)
Significance Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48888525G>A
CLNSRC ClinVar
CLNACC RCV000035214.2,