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rs536588176

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs536588176(C;T)
Make rs536588176(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48520715
GeneFBN1
is asnp
is mentioned by
dbSNPrs536588176
ebirs536588176
HLIrs536588176
Exacrs536588176
Varsomers536588176
Maprs536588176
PheGenIrs536588176
hapmaprs536588176
1000 genomesrs536588176
hgdprs536588176
ensemblrs536588176
gopubmedrs536588176
geneviewrs536588176
scholarrs536588176
googlers536588176
pharmgkbrs536588176
gwascentralrs536588176
openSNPrs536588176
23andMers536588176
23andMe allrs536588176
SNP Nexus

SNPshotrs536588176
SNPdbers536588176
MSV3drs536588176
GWAS Ctlgrs536588176
Max Magnitude0
ClinVar
Risk rs536588176(T;T)
Alt rs536588176(T;T)
Reference rs536588176(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.48812912C>G
CLNSRC
CLNACC RCV000181425.1,