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rs12144715

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs12144715(A;T)
Make rs12144715(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position84399547
GeneDNASE2B
is asnp
is mentioned by
dbSNPrs12144715
ebirs12144715
HLIrs12144715
Exacrs12144715
Varsomers12144715
Maprs12144715
PheGenIrs12144715
hapmaprs12144715
1000 genomesrs12144715
hgdprs12144715
ensemblrs12144715
gopubmedrs12144715
geneviewrs12144715
scholarrs12144715
googlers12144715
pharmgkbrs12144715
gwascentralrs12144715
openSNPrs12144715
23andMers12144715
23andMe allrs12144715
SNP Nexus

SNPshotrs12144715
SNPdbers12144715
MSV3drs12144715
GWAS Ctlgrs12144715
GMAF0.07622
Max Magnitude0
? (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 0.000007
Odds Ratio 0.6360 None