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rs397515863

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515863(A;G)
Make rs397515863(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48411228
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515863
ebirs397515863
HLIrs397515863
Exacrs397515863
Varsomers397515863
Maprs397515863
PheGenIrs397515863
hapmaprs397515863
1000 genomesrs397515863
hgdprs397515863
ensemblrs397515863
gopubmedrs397515863
geneviewrs397515863
scholarrs397515863
googlers397515863
pharmgkbrs397515863
gwascentralrs397515863
openSNPrs397515863
23andMers397515863
23andMe allrs397515863
SNP Nexus

SNPshotrs397515863
SNPdbers397515863
MSV3drs397515863
GWAS Ctlgrs397515863
Max Magnitude0
ClinVar
Risk rs397515863(G;G)
Alt rs397515863(G;G)
Reference rs397515863(A;A)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48703425T>C
CLNSRC ClinVar
CLNACC RCV000035289.2,