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rs11242704

From SNPedia

Orientationplus
Stabilizedplus
Make rs11242704(A;A)
Make rs11242704(A;G)
Make rs11242704(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position1535763
GeneLOC102723958
is asnp
is mentioned by
dbSNPrs11242704
ebirs11242704
HLIrs11242704
Exacrs11242704
Varsomers11242704
Maprs11242704
PheGenIrs11242704
hapmaprs11242704
1000 genomesrs11242704
hgdprs11242704
ensemblrs11242704
gopubmedrs11242704
geneviewrs11242704
scholarrs11242704
googlers11242704
pharmgkbrs11242704
gwascentralrs11242704
openSNPrs11242704
23andMers11242704
23andMe allrs11242704
SNP Nexus

SNPshotrs11242704
SNPdbers11242704
MSV3drs11242704
GWAS Ctlgrs11242704
GMAF0.4454
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 0.000005
Odds Ratio 0.2570 None