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rs10789491

From SNPedia

Orientationplus
Stabilizedplus
Make rs10789491(A;A)
Make rs10789491(A;G)
Make rs10789491(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position46713638
GeneKIAA0494
is asnp
is mentioned by
dbSNPrs10789491
ebirs10789491
HLIrs10789491
Exacrs10789491
Varsomers10789491
Maprs10789491
PheGenIrs10789491
hapmaprs10789491
1000 genomesrs10789491
hgdprs10789491
ensemblrs10789491
gopubmedrs10789491
geneviewrs10789491
scholarrs10789491
googlers10789491
pharmgkbrs10789491
gwascentralrs10789491
openSNPrs10789491
23andMers10789491
23andMe allrs10789491
SNP Nexus

SNPshotrs10789491
SNPdbers10789491
MSV3drs10789491
GWAS Ctlgrs10789491
GMAF0.1446
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 0.000001
Odds Ratio 0.3120 None