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rs10776934

From SNPedia

Orientationplus
Stabilizedplus
Make rs10776934(G;G)
Make rs10776934(G;T)
Make rs10776934(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position135137855
is asnp
is mentioned by
dbSNPrs10776934
ebirs10776934
HLIrs10776934
Exacrs10776934
Varsomers10776934
Maprs10776934
PheGenIrs10776934
hapmaprs10776934
1000 genomesrs10776934
hgdprs10776934
ensemblrs10776934
gopubmedrs10776934
geneviewrs10776934
scholarrs10776934
googlers10776934
pharmgkbrs10776934
gwascentralrs10776934
openSNPrs10776934
23andMers10776934
23andMe allrs10776934
SNP Nexus

SNPshotrs10776934
SNPdbers10776934
MSV3drs10776934
GWAS Ctlgrs10776934
GMAF0.3108
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 22095909]
Trait
Title Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy.
Risk Allele T
P-val 0.000001
Odds Ratio 0.2810 None