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rs869025403

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025403(C;G)
Make rs869025403(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position48610736
GeneFBN1
is asnp
is mentioned by
dbSNPrs869025403
ebirs869025403
HLIrs869025403
Exacrs869025403
Varsomers869025403
Maprs869025403
PheGenIrs869025403
hapmaprs869025403
1000 genomesrs869025403
hgdprs869025403
ensemblrs869025403
gopubmedrs869025403
geneviewrs869025403
scholarrs869025403
googlers869025403
pharmgkbrs869025403
gwascentralrs869025403
openSNPrs869025403
23andMers869025403
23andMe allrs869025403
SNP Nexus

SNPshotrs869025403
SNPdbers869025403
MSV3drs869025403
GWAS Ctlgrs869025403
Max Magnitude0
ClinVar
Risk rs869025403(G;G)
Alt rs869025403(G;G)
Reference rs869025403(C;C)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48902933G>C
CLNSRC
CLNACC RCV000208445.1,