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rs397515776

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515776(G;G)
Make rs397515776(G;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48495512
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515776
ebirs397515776
HLIrs397515776
Exacrs397515776
Varsomers397515776
Maprs397515776
PheGenIrs397515776
hapmaprs397515776
1000 genomesrs397515776
hgdprs397515776
ensemblrs397515776
gopubmedrs397515776
geneviewrs397515776
scholarrs397515776
googlers397515776
pharmgkbrs397515776
gwascentralrs397515776
openSNPrs397515776
23andMers397515776
23andMe allrs397515776
SNP Nexus

SNPshotrs397515776
SNPdbers397515776
MSV3drs397515776
GWAS Ctlgrs397515776
Max Magnitude0
ClinVar
Risk rs397515776(G;G)
Alt rs397515776(G;G)
Reference rs397515776(T;T)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48787709A>C
CLNSRC ClinVar
CLNACC RCV000035146.2,