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rs11725957

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs11725957(A;A)
Make rs11725957(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position49060875
GeneCWH43
is asnp
is mentioned by
dbSNPrs11725957
ebirs11725957
HLIrs11725957
Exacrs11725957
Varsomers11725957
Maprs11725957
PheGenIrs11725957
hapmaprs11725957
1000 genomesrs11725957
hgdprs11725957
ensemblrs11725957
gopubmedrs11725957
geneviewrs11725957
scholarrs11725957
googlers11725957
pharmgkbrs11725957
gwascentralrs11725957
openSNPrs11725957
23andMers11725957
23andMe allrs11725957
SNP Nexus

SNPshotrs11725957
SNPdbers11725957
MSV3drs11725957
GWAS Ctlgrs11725957
GMAF0.01561
Max Magnitude0
? (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 0.000008
Odds Ratio 0.7270 None