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rs397515757

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515757(A;A)
Make rs397515757(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48515382
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515757
ebirs397515757
HLIrs397515757
Exacrs397515757
Varsomers397515757
Maprs397515757
PheGenIrs397515757
hapmaprs397515757
1000 genomesrs397515757
hgdprs397515757
ensemblrs397515757
gopubmedrs397515757
geneviewrs397515757
scholarrs397515757
googlers397515757
pharmgkbrs397515757
gwascentralrs397515757
openSNPrs397515757
23andMers397515757
23andMe allrs397515757
SNP Nexus

SNPshotrs397515757
SNPdbers397515757
MSV3drs397515757
GWAS Ctlgrs397515757
Max Magnitude0
ClinVar
Risk rs397515757(A;A)
Alt rs397515757(A;A)
Reference rs397515757(G;G)
Significance Pathogenic
Disease Marfan syndrome not provided
Variation info
Gene FBN1
CLNDBN Marfan syndrome not provided
Reversed 1
HGVS NC_000015.9:g.48807579C>T
CLNSRC ClinVar
CLNACC RCV000035117.3, RCV000181432.2,