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rs397515801

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515801(A;G)
Make rs397515801(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48474305
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515801
ebirs397515801
HLIrs397515801
Exacrs397515801
Varsomers397515801
Maprs397515801
PheGenIrs397515801
hapmaprs397515801
1000 genomesrs397515801
hgdprs397515801
ensemblrs397515801
gopubmedrs397515801
geneviewrs397515801
scholarrs397515801
googlers397515801
pharmgkbrs397515801
gwascentralrs397515801
openSNPrs397515801
23andMers397515801
23andMe allrs397515801
SNP Nexus

SNPshotrs397515801
SNPdbers397515801
MSV3drs397515801
GWAS Ctlgrs397515801
Max Magnitude0
ClinVar
Risk rs397515801(G;G)
Alt rs397515801(G;G)
Reference rs397515801(A;A)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48766502T>C
CLNSRC ClinVar
CLNACC RCV000035189.2,