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rs2504916

From SNPedia

Orientationminus
Stabilizedminus
Make rs2504916(A;A)
Make rs2504916(A;T)
Make rs2504916(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position160402996
GeneSLC22A3
is asnp
is mentioned by
dbSNPrs2504916
ebirs2504916
HLIrs2504916
Exacrs2504916
Varsomers2504916
Maprs2504916
PheGenIrs2504916
hapmaprs2504916
1000 genomesrs2504916
hgdprs2504916
ensemblrs2504916
gopubmedrs2504916
geneviewrs2504916
scholarrs2504916
googlers2504916
pharmgkbrs2504916
gwascentralrs2504916
openSNPrs2504916
23andMers2504916
23andMe allrs2504916
SNP Nexus

SNPshotrs2504916
SNPdbers2504916
MSV3drs2504916
GWAS Ctlgrs2504916
GMAF0.1515
Max Magnitude
? (A;A) (A;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 0.000002
Odds Ratio 0.3060 None