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rs9275390

From SNPedia

Orientationplus
Stabilizedplus
Make rs9275390(C;C)
Make rs9275390(C;T)
Make rs9275390(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32701379
is asnp
is mentioned by
dbSNPrs9275390
ebirs9275390
HLIrs9275390
Exacrs9275390
Varsomers9275390
Maprs9275390
PheGenIrs9275390
hapmaprs9275390
1000 genomesrs9275390
hgdprs9275390
ensemblrs9275390
gopubmedrs9275390
geneviewrs9275390
scholarrs9275390
googlers9275390
pharmgkbrs9275390
gwascentralrs9275390
openSNPrs9275390
23andMers9275390
23andMe allrs9275390
SNP Nexus

SNPshotrs9275390
SNPdbers9275390
MSV3drs9275390
GWAS Ctlgrs9275390
GMAF0.3136
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 1.6100 [1.35-1.92]

[PMID 19458352OA-icon.png] Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.