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rs397515852

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs397515852(-;-)
Make rs397515852(-;AT)
ReferenceGRCh38 38.1/141
Chromosome15
Position48422024
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515852
ebirs397515852
HLIrs397515852
Exacrs397515852
Varsomers397515852
Maprs397515852
PheGenIrs397515852
hapmaprs397515852
1000 genomesrs397515852
hgdprs397515852
ensemblrs397515852
gopubmedrs397515852
geneviewrs397515852
scholarrs397515852
googlers397515852
pharmgkbrs397515852
gwascentralrs397515852
openSNPrs397515852
23andMers397515852
23andMe allrs397515852
SNP Nexus

SNPshotrs397515852
SNPdbers397515852
MSV3drs397515852
GWAS Ctlgrs397515852
Max Magnitude0
ClinVar
Risk rs397515852(;)
Alt rs397515852(;)
Reference rs397515852(AT;AT)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48714221_48714222delAT
CLNSRC ClinVar
CLNACC RCV000035272.2,