rs12980275
Orientation | plus |
Stabilized | plus |
Make rs12980275(A;A) |
Make rs12980275(A;G) |
Make rs12980275(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 39241143 |
is a | snp |
is | mentioned by |
dbSNP | rs12980275 |
dbSNP (classic) | rs12980275 |
ClinGen | rs12980275 |
ebi | rs12980275 |
HLI | rs12980275 |
Exac | rs12980275 |
Gnomad | rs12980275 |
Varsome | rs12980275 |
LitVar | rs12980275 |
Map | rs12980275 |
PheGenI | rs12980275 |
Biobank | rs12980275 |
1000 genomes | rs12980275 |
hgdp | rs12980275 |
ensembl | rs12980275 |
geneview | rs12980275 |
scholar | rs12980275 |
rs12980275 | |
pharmgkb | rs12980275 |
gwascentral | rs12980275 |
openSNP | rs12980275 |
23andMe | rs12980275 |
SNPshot | rs12980275 |
SNPdbe | rs12980275 |
MSV3d | rs12980275 |
GWAS Ctlg | rs12980275 |
GMAF | 0.314 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
rs8099917(C) less likely to respond to Hepatitis C treatment.
rs12979860(C;C) better able to become naturally Hepatitis C virus-free. rs12980275(A) usually corresponds to the rs12979860(C)
[PMID 19749757] Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C
[PMID 21390311] Response prediction in chronic hepatitis C by assessment of IP-10 and IL28B-related single nucleotide polymorphisms
[PMID 21987611] IL28B polymorphisms associated with therapy response in Chilean chronic hepatitis C patients
[PMID 22118055] Single and combined IL28B, ITPA and SLC28A3 host genetic markers modulating response to anti-hepatitis C therapy
[PMID 22234924] Combined effects of different IL28B gene variants on the outcome of dual combination therapy in chronic HCV type 1 infection
[PMID 22253715] Impact of IL28B-Related Single Nucleotide Polymorphisms on Liver Histopathology in Chronic Hepatitis C Genotype 2 and 3
[PMID 22108195] Polymorphisms near IL28B and serologic response to peginterferon in HBeAg-positive patients with chronic hepatitis B
[PMID 22649509] IL28B Genetic Variation Is Associated with Spontaneous Clearance of Hepatitis C Virus, Treatment Response, Serum IL-28B Levels in Chinese Population
[PMID 22329371] IL28B genetic variants and gender are associated with spontaneous clearance of hepatitis C virus infection
GWAS snp | |
---|---|
PMID | [PMID 22497812] |
Trait | |
Title | Interleukin 28B polymorphisms are the only common genetic variants associated with low-density lipoprotein cholesterol (LDL-C) in genotype-1 chronic hepatitis C and determine the association between LDL-C and treatment response. |
Risk Allele | |
P-val | 5E-17 |
Odds Ratio | None None |
[PMID 20708617] Variants in IL28B in liver recipients and donors correlate with response to peg-interferon and ribavirin therapy for recurrent hepatitis C.
[PMID 21112657] Importance of IL28B gene polymorphisms in hepatitis C virus genotype 2 and 3 infected patients.
[PMID 21112660] Predictive value of the IL28B polymorphism on the effect of interferon therapy in chronic hepatitis C patients with genotypes 2a and 2b.
[PMID 21274371] Peginterferon and ribavirin treatment for hepatitis C virus infection.
[PMID 21354446] IL28B polymorphisms predict reduction of HCV RNA from the first day of therapy in chronic hepatitis C.
[PMID 21443535] IL28B polymorphisms, IP-10 and viral load predict virological response to therapy in chronic hepatitis C.
[PMID 22310928] Genetic variation in IL28B is associated with the development of hepatitis B-related hepatocellular carcinoma.
[PMID 23103287] IL28B polymorphisms are associated with severity of liver disease in human immunodeficiency virus (HIV) patients coinfected with hepatitis C virus.
[PMID 23135173] Analysis of IL28B alleles with virologic response patterns and plasma cytokine levels in HIV/HCV-coinfected patients.
[PMID 23314745] Impact of IL-28B polymorphisms on pegylated interferon plus ribavirin treatment response in children and adolescents infected with HCV genotypes 1 and 4.
[PMID 23565619] IL28RA polymorphism is associated with early hepatitis C virus (HCV) treatment failure in human immunodeficiency virus-/HCV-coinfected patients.
[PMID 24999753] Interleukin 28B Polymorphisms and Therapy Response in Egyptian Hepatitis C Genotype-4 Patients
[PMID 25032184] No association between the IL28B SNP and response to peginterferon plus ribavirin combination treatment in Korean chronic hepatitis C patients
[PMID 25652367] IL28B rs12980275 polymorphism shows association with response to treatment in Pakistani patients with Chronic Hepatitis C
[PMID 25769643] IL28B rs12980275 variant as a predictor of sustained virologic response to pegylated-interferon and ribavirin in chronic hepatitis C patients: A systematic review and meta-analysis
[PMID 24118788] Genetic variation in interleukin 28B and correlation with chronic hepatitis B virus infection in Saudi Arabian patients
[PMID 24924923] The relationship between IL-28B polymorphisms and the response to peginterferon alfa-2a monotherapy in anti-HBe-positive patients with chronic HBV infection
[PMID 25938745] IL28B polymorphisms of both recipient and donor cooperate to influence IFN treatment response in HCV recurrence after liver transplantation, but IL28B SNPs of the recipient play a major role in IFN-induced blocking of HCV replication
[PMID 25663241] Genetic Variants in Interleukin-28B Are Associated with Diabetes and Diabetes-Related Complications in Patients with Chronic Hepatitis C Virus Infection
[PMID 25661337] Role of pharmacogenetic in ribavirin outcome prediction and pharmacokinetics in an Italian cohort of HCV-1 and 4 patients
[PMID 24840315] Interleukin-28 gene polymorphisms may contribute to HBsAg persistence and the development of HBeAg-negative chronic hepatitis B
[PMID 26740868] Prevalence of Hepatitis C among Egyptian Children with Sickle Cell Disease and the Role of IL28b Gene Polymorphisms in Spontaneous Viral Clearance.
[PMID 32058988] IL-28B genotypes as predictors of long-term outcome in patients with hepatitis C-related severe liver injury.
[PMID 32478085] IFNL3 rs12980275 Polymorphism Predicts Septic Shock-Related Death in Patients Undergoing Major Surgery: A Retrospective Study.
- Is a snp
- In dbSNP
- SNPs on chromosome 19
- Has genotype
- Has population
- Uses omim
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip 23andMe v5
- On chip Affy GenomeWide 6
- On chip Ancestry v2c
- On chip Ancestry v2d
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M