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rs397515769

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs397515769(-;-)
Make rs397515769(-;AT)
ReferenceGRCh38 38.1/141
Chromosome15
Position48496106
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515769
ebirs397515769
HLIrs397515769
Exacrs397515769
Varsomers397515769
Maprs397515769
PheGenIrs397515769
hapmaprs397515769
1000 genomesrs397515769
hgdprs397515769
ensemblrs397515769
gopubmedrs397515769
geneviewrs397515769
scholarrs397515769
googlers397515769
pharmgkbrs397515769
gwascentralrs397515769
openSNPrs397515769
23andMers397515769
23andMe allrs397515769
SNP Nexus

SNPshotrs397515769
SNPdbers397515769
MSV3drs397515769
GWAS Ctlgrs397515769
Max Magnitude0
ClinVar
Risk rs397515769(;)
Alt rs397515769(;)
Reference rs397515769(AT;AT)
Significance Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48788303_48788304delAT
CLNSRC ClinVar
CLNACC RCV000035138.2,