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rs11047102

From SNPedia

Orientationplus
Stabilizedplus
Make rs11047102(C;C)
Make rs11047102(C;T)
Make rs11047102(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position23793212
GeneSOX5
is asnp
is mentioned by
dbSNPrs11047102
ebirs11047102
HLIrs11047102
Exacrs11047102
Varsomers11047102
Maprs11047102
PheGenIrs11047102
hapmaprs11047102
1000 genomesrs11047102
hgdprs11047102
ensemblrs11047102
gopubmedrs11047102
geneviewrs11047102
scholarrs11047102
googlers11047102
pharmgkbrs11047102
gwascentralrs11047102
openSNPrs11047102
23andMers11047102
23andMe allrs11047102
SNP Nexus

SNPshotrs11047102
SNPdbers11047102
MSV3drs11047102
GWAS Ctlgrs11047102
GMAF0.0753
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21779181OA-icon.png]
Trait
Title Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
Risk Allele
P-val 1E-7
Odds Ratio 1.3600 [1.21-1.52]

rs11047102 is associated with systemic sclerosis. [PMID 21779181]