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rs397515781

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515781(-;-)
Make rs397515781(-;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48492482
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515781
ebirs397515781
HLIrs397515781
Exacrs397515781
Varsomers397515781
Maprs397515781
PheGenIrs397515781
hapmaprs397515781
1000 genomesrs397515781
hgdprs397515781
ensemblrs397515781
gopubmedrs397515781
geneviewrs397515781
scholarrs397515781
googlers397515781
pharmgkbrs397515781
gwascentralrs397515781
openSNPrs397515781
23andMers397515781
23andMe allrs397515781
SNP Nexus

SNPshotrs397515781
SNPdbers397515781
MSV3drs397515781
GWAS Ctlgrs397515781
Max Magnitude0
ClinVar
Risk rs397515781(;)
Alt rs397515781(;)
Reference rs397515781(G;G)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48784679delC
CLNSRC ClinVar
CLNACC RCV000035151.2,