rs6051702
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6051702(A;A) |
Make rs6051702(A;C) |
Make rs6051702(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 3271278 |
Gene | C20orf194 |
is a | snp |
is | mentioned by |
dbSNP | rs6051702 |
dbSNP (classic) | rs6051702 |
ClinGen | rs6051702 |
ebi | rs6051702 |
HLI | rs6051702 |
Exac | rs6051702 |
Gnomad | rs6051702 |
Varsome | rs6051702 |
LitVar | rs6051702 |
Map | rs6051702 |
PheGenI | rs6051702 |
Biobank | rs6051702 |
1000 genomes | rs6051702 |
hgdp | rs6051702 |
ensembl | rs6051702 |
geneview | rs6051702 |
scholar | rs6051702 |
rs6051702 | |
pharmgkb | rs6051702 |
gwascentral | rs6051702 |
openSNP | rs6051702 |
23andMe | rs6051702 |
SNPshot | rs6051702 |
SNPdbe | rs6051702 |
MSV3d | rs6051702 |
GWAS Ctlg | rs6051702 |
GMAF | 0.1818 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
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[PMID 23933495] Association of ITPA polymorphisms rs6051702/rs1127354 instead of rs7270101/rs1127354 as predictor of ribavirin-associated anemia in chronic hepatitis C treated patients
[PMID 20977565] ITPA gene variant protects against anemia induced by pegylated interferon-alpha and ribavirin therapy for Japanese patients with chronic hepatitis C.
[PMID 26071337] Role of ITPA and SLC28A2 genes in the prediction of anaemia associated with protease inhibitor plus ribavirin and peginterferon in hepatitis C treatment
[PMID 25713999] VDR gene polymorphisms impact on anemia at 2 weeks of anti-HCV therapy: a possible mechanism for early RBV-induced anemia