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rs397515767

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515767(A;A)
Make rs397515767(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48613018
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515767
ebirs397515767
HLIrs397515767
Exacrs397515767
Varsomers397515767
Maprs397515767
PheGenIrs397515767
hapmaprs397515767
1000 genomesrs397515767
hgdprs397515767
ensemblrs397515767
gopubmedrs397515767
geneviewrs397515767
scholarrs397515767
googlers397515767
pharmgkbrs397515767
gwascentralrs397515767
openSNPrs397515767
23andMers397515767
23andMe allrs397515767
SNP Nexus

SNPshotrs397515767
SNPdbers397515767
MSV3drs397515767
GWAS Ctlgrs397515767
Max Magnitude0
ClinVar
Risk rs397515767(A;A)
Alt rs397515767(A;A)
Reference rs397515767(G;G)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48905215C>T
CLNSRC ClinVar
CLNACC RCV000035136.2,