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rs2254135

From SNPedia

Orientationminus
Stabilizedminus
Make rs2254135(A;A)
Make rs2254135(A;G)
Make rs2254135(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position17508246
GeneLOC102723454
is asnp
is mentioned by
dbSNPrs2254135
ebirs2254135
HLIrs2254135
Exacrs2254135
Varsomers2254135
Maprs2254135
PheGenIrs2254135
hapmaprs2254135
1000 genomesrs2254135
hgdprs2254135
ensemblrs2254135
gopubmedrs2254135
geneviewrs2254135
scholarrs2254135
googlers2254135
pharmgkbrs2254135
gwascentralrs2254135
openSNPrs2254135
23andMers2254135
23andMe allrs2254135
SNP Nexus

SNPshotrs2254135
SNPdbers2254135
MSV3drs2254135
GWAS Ctlgrs2254135
GMAF0.3756
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 T
P-val 0.000003
Odds Ratio 0.2690 None