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rs397515790

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515790(A;G)
Make rs397515790(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48487383
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515790
ebirs397515790
HLIrs397515790
Exacrs397515790
Varsomers397515790
Maprs397515790
PheGenIrs397515790
hapmaprs397515790
1000 genomesrs397515790
hgdprs397515790
ensemblrs397515790
gopubmedrs397515790
geneviewrs397515790
scholarrs397515790
googlers397515790
pharmgkbrs397515790
gwascentralrs397515790
openSNPrs397515790
23andMers397515790
23andMe allrs397515790
SNP Nexus

SNPshotrs397515790
SNPdbers397515790
MSV3drs397515790
GWAS Ctlgrs397515790
Max Magnitude0
ClinVar
Risk rs397515790(G;G)
Alt rs397515790(G;G)
Reference rs397515790(A;A)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48779580T>C
CLNSRC ClinVar
CLNACC RCV000035168.2,