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rs3129860

From SNPedia

Orientationplus
Stabilizedplus
Make rs3129860(A;A)
Make rs3129860(A;G)
Make rs3129860(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32433302
is asnp
is mentioned by
dbSNPrs3129860
ebirs3129860
HLIrs3129860
Exacrs3129860
Varsomers3129860
Maprs3129860
PheGenIrs3129860
hapmaprs3129860
1000 genomesrs3129860
hgdprs3129860
ensemblrs3129860
gopubmedrs3129860
geneviewrs3129860
scholarrs3129860
googlers3129860
pharmgkbrs3129860
gwascentralrs3129860
openSNPrs3129860
23andMers3129860
23andMe allrs3129860
SNP Nexus

SNPshotrs3129860
SNPdbers3129860
MSV3drs3129860
GWAS Ctlgrs3129860
GMAF0.09734
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23321320]
Trait Hepatitis C induced liver cirrhosis
Title A genome-wide association study of HCV-induced liver cirrhosis in the Japanese population identifies novel susceptibility loci at the MHC region.
Risk Allele A
P-val 1E-9
Odds Ratio 1.36 [1.22-1.49]


[PMID 20405052OA-icon.png] The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.


[PMID 21379322OA-icon.png] Risk alleles for systemic lupus erythematosus in a large case-control collection and associations with clinical subphenotypes.