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rs2276466

From SNPedia

Orientationplus
Stabilizedplus
Make rs2276466(C;C)
Make rs2276466(C;G)
Make rs2276466(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position13949318
GeneERCC4
is asnp
is mentioned by
dbSNPrs2276466
ebirs2276466
HLIrs2276466
Exacrs2276466
Varsomers2276466
Maprs2276466
PheGenIrs2276466
hapmaprs2276466
1000 genomesrs2276466
hgdprs2276466
ensemblrs2276466
gopubmedrs2276466
geneviewrs2276466
scholarrs2276466
googlers2276466
pharmgkbrs2276466
gwascentralrs2276466
openSNPrs2276466
23andMers2276466
23andMe allrs2276466
SNP Nexus

SNPshotrs2276466
SNPdbers2276466
MSV3drs2276466
GWAS Ctlgrs2276466
GMAF0.2245
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 23166636OA-icon.png] Polymorphisms in ERCC1 and XPF Genes and Risk of Gastric Cancer in an Eastern Chinese Population


[PMID 23909490OA-icon.png] Polymorphisms in the ERCC1 and XPF Genes and Risk of Breast Cancer in a Chinese Population


[PMID 24353636OA-icon.png] Effect of Xeroderma pigmentosum complementation group F polymorphisms and H.pylori infection on the risk of gastric cancer


[PMID 22848636OA-icon.png] Association between single nucleotide polymorphisms in ERCC4 and risk of squamous cell carcinoma of the head and neck.


[PMID 24861646] Association of single nucleotide polymorphisms of ERCC1 and XPF with colorectal cancer risk and interaction with tobacco use


[PMID 24938470] Association of polymorphisms of the xeroderma pigmentosum complementation group F gene with increased glioma risk