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rs397515754

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515754(A;T)
Make rs397515754(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48516318
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515754
ebirs397515754
HLIrs397515754
Exacrs397515754
Varsomers397515754
Maprs397515754
PheGenIrs397515754
hapmaprs397515754
1000 genomesrs397515754
hgdprs397515754
ensemblrs397515754
gopubmedrs397515754
geneviewrs397515754
scholarrs397515754
googlers397515754
pharmgkbrs397515754
gwascentralrs397515754
openSNPrs397515754
23andMers397515754
23andMe allrs397515754
SNP Nexus

SNPshotrs397515754
SNPdbers397515754
MSV3drs397515754
GWAS Ctlgrs397515754
Max Magnitude0
ClinVar
Risk rs397515754(T;T)
Alt rs397515754(T;T)
Reference rs397515754(A;A)
Significance Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48808515T>A
CLNSRC ClinVar
CLNACC RCV000035114.2,