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rs397515866

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs397515866(-;-)
Make rs397515866(-;TT)
ReferenceGRCh38 38.1/141
Chromosome15
Position48411000
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515866
ebirs397515866
HLIrs397515866
Exacrs397515866
Varsomers397515866
Maprs397515866
PheGenIrs397515866
hapmaprs397515866
1000 genomesrs397515866
hgdprs397515866
ensemblrs397515866
gopubmedrs397515866
geneviewrs397515866
scholarrs397515866
googlers397515866
pharmgkbrs397515866
gwascentralrs397515866
openSNPrs397515866
23andMers397515866
23andMe allrs397515866
SNP Nexus

SNPshotrs397515866
SNPdbers397515866
MSV3drs397515866
GWAS Ctlgrs397515866
Max Magnitude0
ClinVar
Risk rs397515866(;)
Alt rs397515866(;)
Reference rs397515866(TT;TT)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48703197_48703198delAA
CLNSRC ClinVar
CLNACC RCV000035293.2,