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rs397515759

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515759(A;A)
Make rs397515759(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48510157
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515759
ebirs397515759
HLIrs397515759
Exacrs397515759
Varsomers397515759
Maprs397515759
PheGenIrs397515759
hapmaprs397515759
1000 genomesrs397515759
hgdprs397515759
ensemblrs397515759
gopubmedrs397515759
geneviewrs397515759
scholarrs397515759
googlers397515759
pharmgkbrs397515759
gwascentralrs397515759
openSNPrs397515759
23andMers397515759
23andMe allrs397515759
SNP Nexus

SNPshotrs397515759
SNPdbers397515759
MSV3drs397515759
GWAS Ctlgrs397515759
Max Magnitude0
ClinVar
Risk rs397515759(A;A)
Alt rs397515759(A;A)
Reference rs397515759(G;G)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48802354C>T
CLNSRC ClinVar
CLNACC RCV000035121.2,