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

rs397515853

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515853(A;C)
Make rs397515853(C;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position48421677
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515853
ebirs397515853
HLIrs397515853
Exacrs397515853
Varsomers397515853
Maprs397515853
PheGenIrs397515853
hapmaprs397515853
1000 genomesrs397515853
hgdprs397515853
ensemblrs397515853
gopubmedrs397515853
geneviewrs397515853
scholarrs397515853
googlers397515853
pharmgkbrs397515853
gwascentralrs397515853
openSNPrs397515853
23andMers397515853
23andMe allrs397515853
SNP Nexus

SNPshotrs397515853
SNPdbers397515853
MSV3drs397515853
GWAS Ctlgrs397515853
Max Magnitude0
ClinVar
Risk rs397515853(C;C)
Alt rs397515853(C;C)
Reference rs397515853(A;A)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48713874T>G
CLNSRC ClinVar
CLNACC RCV000035273.3,