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rs3135338

From SNPedia

Orientationminus
Stabilizedminus
Make rs3135338(A;A)
Make rs3135338(A;G)
Make rs3135338(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32433440
is asnp
is mentioned by
dbSNPrs3135338
ebirs3135338
HLIrs3135338
Exacrs3135338
Varsomers3135338
Maprs3135338
PheGenIrs3135338
hapmaprs3135338
1000 genomesrs3135338
hgdprs3135338
ensemblrs3135338
gopubmedrs3135338
geneviewrs3135338
scholarrs3135338
googlers3135338
pharmgkbrs3135338
gwascentralrs3135338
openSNPrs3135338
23andMers3135338
23andMe allrs3135338
SNP Nexus

SNPshotrs3135338
SNPdbers3135338
MSV3drs3135338
GWAS Ctlgrs3135338
GMAF0.3705
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20159113OA-icon.png]
Trait Multiple sclerosis
Title Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene
Risk Allele A
P-val 2E-25
Odds Ratio 3.43 [NR]


[PMID 19143815OA-icon.png] MHC fine mapping of human type 1 diabetes using the T1DGC data.