Have questions? Visit https://www.reddit.com/r/SNPedia

rs111687884

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111687884(C;T)
Make rs111687884(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48537704
GeneFBN1
is asnp
is mentioned by
dbSNPrs111687884
ebirs111687884
HLIrs111687884
Exacrs111687884
Varsomers111687884
Maprs111687884
PheGenIrs111687884
hapmaprs111687884
1000 genomesrs111687884
hgdprs111687884
ensemblrs111687884
gopubmedrs111687884
geneviewrs111687884
scholarrs111687884
googlers111687884
pharmgkbrs111687884
gwascentralrs111687884
openSNPrs111687884
23andMers111687884
23andMe allrs111687884
SNP Nexus

SNPshotrs111687884
SNPdbers111687884
MSV3drs111687884
GWAS Ctlgrs111687884
Max Magnitude0
ClinVar
Risk rs111687884(G,T;G,T)
Alt rs111687884(G,T;G,T)
Reference rs111687884(C;C)
Significance Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48829901G>A
CLNSRC ClinVar
CLNACC RCV000035243.2,