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rs2617266

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2617266(C;T)
Make rs2617266(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position38075401
GeneCYP1B1
is asnp
is mentioned by
dbSNPrs2617266
ebirs2617266
HLIrs2617266
Exacrs2617266
Varsomers2617266
Maprs2617266
PheGenIrs2617266
hapmaprs2617266
1000 genomesrs2617266
hgdprs2617266
ensemblrs2617266
gopubmedrs2617266
geneviewrs2617266
scholarrs2617266
googlers2617266
pharmgkbrs2617266
gwascentralrs2617266
openSNPrs2617266
23andMers2617266
23andMe allrs2617266
SNP Nexus

SNPshotrs2617266
SNPdbers2617266
MSV3drs2617266
GWAS Ctlgrs2617266
GMAF0.2612
Max Magnitude0

[PMID 20057908OA-icon.png] Identification of four novel cytochrome P4501B1 mutations (p.I94X, p.H279D, p.Q340H, and p.K433K) in primary congenital glaucoma patients


[PMID 17615053OA-icon.png] Polymorphisms in the cytochrome P450 genes CYP1A2, CYP1B1, CYP3A4, CYP3A5, CYP11A1, CYP17A1, CYP19A1 and colorectal cancer risk.


[PMID 18268125OA-icon.png] Assessment of interactions between PAH exposure and genetic polymorphisms on PAH-DNA adducts in African American, Dominican, and Caucasian mothers and newborns.


[PMID 18544568OA-icon.png] CYP1B1 variants are associated with prostate cancer in non-Hispanic and Hispanic Caucasians.


[PMID 18989382OA-icon.png] Novel CYP1B1 mutations in consanguineous Pakistani families with primary congenital glaucoma.


[PMID 19597567OA-icon.png] Molecular analysis of CYP1B1 in Omani patients with primary congenital glaucoma: a pilot study.


ClinVar
Risk rs2617266(T;T)
Alt rs2617266(T;T)
Reference rs2617266(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene CYP1B1
CLNDBN not specified
Reversed 1
HGVS NC_000002.11:g.38302544G>A
CLNSRC
CLNACC RCV000153129.3,