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

rs397515854

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515854(A;A)
Make rs397515854(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48421651
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515854
ebirs397515854
HLIrs397515854
Exacrs397515854
Varsomers397515854
Maprs397515854
PheGenIrs397515854
hapmaprs397515854
1000 genomesrs397515854
hgdprs397515854
ensemblrs397515854
gopubmedrs397515854
geneviewrs397515854
scholarrs397515854
googlers397515854
pharmgkbrs397515854
gwascentralrs397515854
openSNPrs397515854
23andMers397515854
23andMe allrs397515854
SNP Nexus

SNPshotrs397515854
SNPdbers397515854
MSV3drs397515854
GWAS Ctlgrs397515854
Max Magnitude0
ClinVar
Risk rs397515854(A;A)
Alt rs397515854(A;A)
Reference rs397515854(G;G)
Significance Pathogenic
Disease Marfan syndrome not provided
Variation info
Gene FBN1
CLNDBN Marfan syndrome not provided
Reversed 1
HGVS NC_000015.9:g.48713848C>T
CLNSRC ClinVar
CLNACC RCV000035274.2, RCV000181609.2,