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rs910049

From SNPedia

Orientationminus
Stabilizedminus
Make rs910049(A;A)
Make rs910049(A;G)
Make rs910049(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32347950
GeneC6orf10
is asnp
is mentioned by
dbSNPrs910049
ebirs910049
HLIrs910049
Exacrs910049
Varsomers910049
Maprs910049
PheGenIrs910049
hapmaprs910049
1000 genomesrs910049
hgdprs910049
ensemblrs910049
gopubmedrs910049
geneviewrs910049
scholarrs910049
googlers910049
pharmgkbrs910049
gwascentralrs910049
openSNPrs910049
23andMers910049
23andMe allrs910049
SNP Nexus

SNPshotrs910049
SNPdbers910049
MSV3drs910049
GWAS Ctlgrs910049
GMAF0.2163
Max Magnitude
? (A;A) (A;G) (G;G) 28
Repeatedly associated in genome association studies with type-2 diabetes, type-1 diabetes, multiple sclerosis, and coronary artery disease, according to [PMID 19161620OA-icon.png]

[PMID 17660530] Risk alleles for multiple sclerosis identified by a genomewide study.

[PMID 20546594OA-icon.png] An application of Random Forests to a genome-wide association dataset: methodological considerations & new findings.

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 9E-11
Odds Ratio 1.46 [1.28-1.62]