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rs140537304

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs140537304(C;T)
Make rs140537304(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48427699
GeneFBN1
is asnp
is mentioned by
dbSNPrs140537304
ebirs140537304
HLIrs140537304
Exacrs140537304
Varsomers140537304
Maprs140537304
PheGenIrs140537304
hapmaprs140537304
1000 genomesrs140537304
hgdprs140537304
ensemblrs140537304
gopubmedrs140537304
geneviewrs140537304
scholarrs140537304
googlers140537304
pharmgkbrs140537304
gwascentralrs140537304
openSNPrs140537304
23andMers140537304
23andMe allrs140537304
SNP Nexus

SNPshotrs140537304
SNPdbers140537304
MSV3drs140537304
GWAS Ctlgrs140537304
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs140537304(T;T)
Alt rs140537304(T;T)
Reference rs140537304(C;C)
Significance Other
Disease Marfan syndrome not specified
Variation info
Gene FBN1
CLNDBN Marfan syndrome not specified
Reversed 0
HGVS NC_000015.9:g.48719896C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029773.2, RCV000181589.2,