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rs397515756

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515756(A;G)
Make rs397515756(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48516364
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515756
ebirs397515756
HLIrs397515756
Exacrs397515756
Varsomers397515756
Maprs397515756
PheGenIrs397515756
hapmaprs397515756
1000 genomesrs397515756
hgdprs397515756
ensemblrs397515756
gopubmedrs397515756
geneviewrs397515756
scholarrs397515756
googlers397515756
pharmgkbrs397515756
gwascentralrs397515756
openSNPrs397515756
23andMers397515756
23andMe allrs397515756
SNP Nexus

SNPshotrs397515756
SNPdbers397515756
MSV3drs397515756
GWAS Ctlgrs397515756
Max Magnitude0
ClinVar
Risk rs397515756(G;G)
Alt rs397515756(G;G)
Reference rs397515756(A;A)
Significance Pathogenic
Disease Marfan syndrome not provided
Variation info
Gene FBN1
CLNDBN Marfan syndrome not provided
Reversed 1
HGVS NC_000015.9:g.48808561T>C; NC_000015.9:g.48808561T>G
CLNSRC ClinVar
CLNACC RCV000035116.2, RCV000181426.1,