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rs16864968

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs16864968(A;G)
Make rs16864968(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position223594965
GeneSCG2
is asnp
is mentioned by
dbSNPrs16864968
ebirs16864968
HLIrs16864968
Exacrs16864968
Varsomers16864968
Maprs16864968
PheGenIrs16864968
hapmaprs16864968
1000 genomesrs16864968
hgdprs16864968
ensemblrs16864968
gopubmedrs16864968
geneviewrs16864968
scholarrs16864968
googlers16864968
pharmgkbrs16864968
gwascentralrs16864968
openSNPrs16864968
23andMers16864968
23andMe allrs16864968
SNP Nexus

SNPshotrs16864968
SNPdbers16864968
MSV3drs16864968
GWAS Ctlgrs16864968
GMAF0.1428
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 0.000003
Odds Ratio 0.8260 None