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rs397515789

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515789(A;A)
Make rs397515789(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48488112
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515789
ebirs397515789
HLIrs397515789
Exacrs397515789
Varsomers397515789
Maprs397515789
PheGenIrs397515789
hapmaprs397515789
1000 genomesrs397515789
hgdprs397515789
ensemblrs397515789
gopubmedrs397515789
geneviewrs397515789
scholarrs397515789
googlers397515789
pharmgkbrs397515789
gwascentralrs397515789
openSNPrs397515789
23andMers397515789
23andMe allrs397515789
SNP Nexus

SNPshotrs397515789
SNPdbers397515789
MSV3drs397515789
GWAS Ctlgrs397515789
Max Magnitude0
ClinVar
Risk rs397515789(A;A)
Alt rs397515789(A;A)
Reference rs397515789(G;G)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48780309C>T
CLNSRC ClinVar
CLNACC RCV000035167.2,