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rs2307424

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2307424(C;T)
Make rs2307424(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position161232815
GeneNR1I3
is asnp
is mentioned by
dbSNPrs2307424
dbSNP (classic)rs2307424
ClinGenrs2307424
ebirs2307424
HLIrs2307424
Exacrs2307424
Gnomadrs2307424
Varsomers2307424
LitVarrs2307424
Maprs2307424
PheGenIrs2307424
Biobankrs2307424
1000 genomesrs2307424
hgdprs2307424
ensemblrs2307424
geneviewrs2307424
scholarrs2307424
googlers2307424
pharmgkbrs2307424
gwascentralrs2307424
openSNPrs2307424
23andMers2307424
SNPshotrs2307424
SNPdbers2307424
MSV3drs2307424
GWAS Ctlgrs2307424
GMAF0.3444
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 20218903] Genetic polymorphisms of CYP1A2, CYP3A4, CYP3A5, pregnane/steroid X receptor and constitutive androstane receptor in 207 healthy Spanish volunteers


[PMID 21715435] Cytochrome P450 2B6 (CYP2B6) and constitutive androstane receptor (CAR) polymorphisms are associated with early discontinuation of efavirenz-containing regimens


[PMID 23172109] Correlates of Efavirenz Exposure in Chilean Patients Affected With Human Immunodeficiency Virus Reveals a Novel Association With a Polymorphism in the Constitutive Androstane Receptor


[PMID 24080498] Pharmacogenetic associations with plasma efavirenz concentrations and clinical correlates in a retrospective cohort of Ghanaian HIV-infected patients


[PMID 24232815] Influence of PPARA, RXRA, NR1I2 and NR1I3 gene polymorphisms on the lipid-lowering efficacy and safety of statin therapy


[PMID 22978668] The effect of fetal androgen metabolism-related gene variants on external genitalia virilization in congenital adrenal hyperplasia.


[PMID 23462807OA-icon.png] Single-nucleotide polymorphisms associated with outcome in metastatic renal cell carcinoma treated with sunitinib.


ClinVar
Risk rs2307424(T;T)
Alt rs2307424(T;T)
Reference Rs2307424(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene NR1I3
CLNDBN not specified
Reversed 1
HGVS NC_000001.10:g.161202605G>A
CLNSRC
CLNACC RCV000178902.1,