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rs113249837

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs113249837(C;T)
Make rs113249837(T;T)
ReferenceGRCh38 38.1/142
Chromosome15
Position48456691
GeneFBN1
is asnp
is mentioned by
dbSNPrs113249837
ebirs113249837
HLIrs113249837
Exacrs113249837
Varsomers113249837
Maprs113249837
PheGenIrs113249837
hapmaprs113249837
1000 genomesrs113249837
hgdprs113249837
ensemblrs113249837
gopubmedrs113249837
geneviewrs113249837
scholarrs113249837
googlers113249837
pharmgkbrs113249837
gwascentralrs113249837
openSNPrs113249837
23andMers113249837
23andMe allrs113249837
SNP Nexus

SNPshotrs113249837
SNPdbers113249837
MSV3drs113249837
GWAS Ctlgrs113249837
Max Magnitude0
ClinVar
Risk rs113249837(T;T)
Alt rs113249837(T;T)
Reference rs113249837(C;C)
Significance Pathogenic
Disease Marfan syndrome not provided
Variation info
Gene FBN1
CLNDBN Marfan syndrome not provided
Reversed 1
HGVS NC_000015.9:g.48748888G>A
CLNSRC ClinVar
CLNACC RCV000035224.2, RCV000181541.1,