Have questions? Visit https://www.reddit.com/r/SNPedia

rs397515765

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515765(C;C)
Make rs397515765(C;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48497317
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515765
ebirs397515765
HLIrs397515765
Exacrs397515765
Varsomers397515765
Maprs397515765
PheGenIrs397515765
hapmaprs397515765
1000 genomesrs397515765
hgdprs397515765
ensemblrs397515765
gopubmedrs397515765
geneviewrs397515765
scholarrs397515765
googlers397515765
pharmgkbrs397515765
gwascentralrs397515765
openSNPrs397515765
23andMers397515765
23andMe allrs397515765
SNP Nexus

SNPshotrs397515765
SNPdbers397515765
MSV3drs397515765
GWAS Ctlgrs397515765
Max Magnitude0
ClinVar
Risk rs397515765(C;C)
Alt rs397515765(C;C)
Reference rs397515765(T;T)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48789514A>G
CLNSRC ClinVar
CLNACC RCV000035134.2,