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rs397515829

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515829(C;T)
Make rs397515829(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48445424
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515829
ebirs397515829
HLIrs397515829
Exacrs397515829
Varsomers397515829
Maprs397515829
PheGenIrs397515829
hapmaprs397515829
1000 genomesrs397515829
hgdprs397515829
ensemblrs397515829
gopubmedrs397515829
geneviewrs397515829
scholarrs397515829
googlers397515829
pharmgkbrs397515829
gwascentralrs397515829
openSNPrs397515829
23andMers397515829
23andMe allrs397515829
SNP Nexus

SNPshotrs397515829
SNPdbers397515829
MSV3drs397515829
GWAS Ctlgrs397515829
Max Magnitude0
ClinVar
Risk rs397515829(T;T)
Alt rs397515829(T;T)
Reference rs397515829(C;C)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48737621G>A
CLNSRC ClinVar
CLNACC RCV000035238.2,