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rs397515820

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515820(C;T)
Make rs397515820(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48460291
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515820
ebirs397515820
HLIrs397515820
Exacrs397515820
Varsomers397515820
Maprs397515820
PheGenIrs397515820
hapmaprs397515820
1000 genomesrs397515820
hgdprs397515820
ensemblrs397515820
gopubmedrs397515820
geneviewrs397515820
scholarrs397515820
googlers397515820
pharmgkbrs397515820
gwascentralrs397515820
openSNPrs397515820
23andMers397515820
23andMe allrs397515820
SNP Nexus

SNPshotrs397515820
SNPdbers397515820
MSV3drs397515820
GWAS Ctlgrs397515820
Max Magnitude0
ClinVar
Risk rs397515820(T;T)
Alt rs397515820(T;T)
Reference rs397515820(C;C)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48752488G>A
CLNSRC ClinVar
CLNACC RCV000035221.2,