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rs397515846

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs397515846(-;-)
Make rs397515846(-;CT)
ReferenceGRCh38 38.1/141
Chromosome15
Position48427603
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515846
ebirs397515846
HLIrs397515846
Exacrs397515846
Varsomers397515846
Maprs397515846
PheGenIrs397515846
hapmaprs397515846
1000 genomesrs397515846
hgdprs397515846
ensemblrs397515846
gopubmedrs397515846
geneviewrs397515846
scholarrs397515846
googlers397515846
pharmgkbrs397515846
gwascentralrs397515846
openSNPrs397515846
23andMers397515846
23andMe allrs397515846
SNP Nexus

SNPshotrs397515846
SNPdbers397515846
MSV3drs397515846
GWAS Ctlgrs397515846
Max Magnitude0
ClinVar
Risk rs397515846(;)
Alt rs397515846(;)
Reference rs397515846(CT;CT)
Significance Pathogenic
Disease Marfan syndrome not provided
Variation info
Gene FBN1
CLNDBN Marfan syndrome not provided
Reversed 1
HGVS NC_000015.9:g.48719800_48719801delAG
CLNSRC ClinVar
CLNACC RCV000035265.2, RCV000181675.1,