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rs869025418

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025418(A;G)
Make rs869025418(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position48444662
GeneFBN1
is asnp
is mentioned by
dbSNPrs869025418
ebirs869025418
HLIrs869025418
Exacrs869025418
Varsomers869025418
Maprs869025418
PheGenIrs869025418
hapmaprs869025418
1000 genomesrs869025418
hgdprs869025418
ensemblrs869025418
gopubmedrs869025418
geneviewrs869025418
scholarrs869025418
googlers869025418
pharmgkbrs869025418
gwascentralrs869025418
openSNPrs869025418
23andMers869025418
23andMe allrs869025418
SNP Nexus

SNPshotrs869025418
SNPdbers869025418
MSV3drs869025418
GWAS Ctlgrs869025418
Max Magnitude0
ClinVar
Risk rs869025418(G;G)
Alt rs869025418(G;G)
Reference rs869025418(A;A)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48736859T>C
CLNSRC
CLNACC RCV000208432.1,