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rs397515836

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515836(G;G)
Make rs397515836(G;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48432975
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515836
ebirs397515836
HLIrs397515836
Exacrs397515836
Varsomers397515836
Maprs397515836
PheGenIrs397515836
hapmaprs397515836
1000 genomesrs397515836
hgdprs397515836
ensemblrs397515836
gopubmedrs397515836
geneviewrs397515836
scholarrs397515836
googlers397515836
pharmgkbrs397515836
gwascentralrs397515836
openSNPrs397515836
23andMers397515836
23andMe allrs397515836
SNP Nexus

SNPshotrs397515836
SNPdbers397515836
MSV3drs397515836
GWAS Ctlgrs397515836
Max Magnitude0
ClinVar
Risk rs397515836(G;G)
Alt rs397515836(G;G)
Reference rs397515836(T;T)
Significance Pathogenic
Disease Marfan syndrome not provided
Variation info
Gene FBN1
CLNDBN Marfan syndrome not provided
Reversed 1
HGVS NC_000015.9:g.48725172A>C; NC_000015.9:g.48725172A>T
CLNSRC ClinVar
CLNACC RCV000035248.2, RCV000181560.1,