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rs141133182

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141133182(C;T)
Make rs141133182(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48415735
GeneFBN1
is asnp
is mentioned by
dbSNPrs141133182
ebirs141133182
HLIrs141133182
Exacrs141133182
Varsomers141133182
Maprs141133182
PheGenIrs141133182
hapmaprs141133182
1000 genomesrs141133182
hgdprs141133182
ensemblrs141133182
gopubmedrs141133182
geneviewrs141133182
scholarrs141133182
googlers141133182
pharmgkbrs141133182
gwascentralrs141133182
openSNPrs141133182
23andMers141133182
23andMe allrs141133182
SNP Nexus

SNPshotrs141133182
SNPdbers141133182
MSV3drs141133182
GWAS Ctlgrs141133182
Max Magnitude0
ClinVar
Risk rs141133182(T;T)
Alt rs141133182(T;T)
Reference rs141133182(C;C)
Significance Pathogenic
Disease Marfan syndrome not specified
Variation info
Gene FBN1
CLNDBN Marfan syndrome not specified
Reversed 0
HGVS NC_000015.9:g.48707932C>T
CLNSRC ClinVar University of Washington
CLNACC RCV000035279.3, RCV000154182.2,