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rs12527818

From SNPedia

Orientationplus
Stabilizedplus
Make rs12527818(C;C)
Make rs12527818(C;T)
Make rs12527818(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position93201401
is asnp
is mentioned by
dbSNPrs12527818
ebirs12527818
HLIrs12527818
Exacrs12527818
Varsomers12527818
Maprs12527818
PheGenIrs12527818
hapmaprs12527818
1000 genomesrs12527818
hgdprs12527818
ensemblrs12527818
gopubmedrs12527818
geneviewrs12527818
scholarrs12527818
googlers12527818
pharmgkbrs12527818
gwascentralrs12527818
openSNPrs12527818
23andMers12527818
23andMe allrs12527818
SNP Nexus

SNPshotrs12527818
SNPdbers12527818
MSV3drs12527818
GWAS Ctlgrs12527818
GMAF0.2842
Max Magnitude
? (C;C) (C;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 0.000007
Odds Ratio 0.2740 None