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rs397515825

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515825(-;-)
Make rs397515825(-;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48537786
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515825
ebirs397515825
HLIrs397515825
Exacrs397515825
Varsomers397515825
Maprs397515825
PheGenIrs397515825
hapmaprs397515825
1000 genomesrs397515825
hgdprs397515825
ensemblrs397515825
gopubmedrs397515825
geneviewrs397515825
scholarrs397515825
googlers397515825
pharmgkbrs397515825
gwascentralrs397515825
openSNPrs397515825
23andMers397515825
23andMe allrs397515825
SNP Nexus

SNPshotrs397515825
SNPdbers397515825
MSV3drs397515825
GWAS Ctlgrs397515825
Max Magnitude0
ClinVar
Risk rs397515825(;)
Alt rs397515825(;)
Reference rs397515825(T;T)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48829983delA
CLNSRC ClinVar
CLNACC RCV000035231.2,