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rs11171747

From SNPedia

Orientationplus
Stabilizedplus
Make rs11171747(G;G)
Make rs11171747(G;T)
Make rs11171747(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position56124624
is asnp
is mentioned by
dbSNPrs11171747
ebirs11171747
HLIrs11171747
Exacrs11171747
Varsomers11171747
Maprs11171747
PheGenIrs11171747
hapmaprs11171747
1000 genomesrs11171747
hgdprs11171747
ensemblrs11171747
gopubmedrs11171747
geneviewrs11171747
scholarrs11171747
googlers11171747
pharmgkbrs11171747
gwascentralrs11171747
openSNPrs11171747
23andMers11171747
23andMe allrs11171747
SNP Nexus

SNPshotrs11171747
SNPdbers11171747
MSV3drs11171747
GWAS Ctlgrs11171747
GMAF0.3104
Max Magnitude
? (G;G) (G;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 6E-8
Odds Ratio 1.2300 [1.14-1.33]

[PMID 19956108OA-icon.png] Analysis of 55 autoimmune disease and type II diabetes loci: further confirmation of chromosomes 4q27, 12q13.2 and 12q24.13 as type I diabetes loci, and support for a new locus, 12q13.3-q14.1.