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rs1803965

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1803965(C;T)
Make rs1803965(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position129707928
GeneMGMT
is asnp
is mentioned by
dbSNPrs1803965
ebirs1803965
HLIrs1803965
Exacrs1803965
Varsomers1803965
Maprs1803965
PheGenIrs1803965
hapmaprs1803965
1000 genomesrs1803965
hgdprs1803965
ensemblrs1803965
gopubmedrs1803965
geneviewrs1803965
scholarrs1803965
googlers1803965
pharmgkbrs1803965
gwascentralrs1803965
openSNPrs1803965
23andMers1803965
23andMe allrs1803965
SNP Nexus

SNPshotrs1803965
SNPdbers1803965
MSV3drs1803965
GWAS Ctlgrs1803965
GMAF0.1469
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 20938339] Temozolomide-induced severe myelosuppression: analysis of clinically associated polymorphisms in two patients


[PMID 17267408OA-icon.png] Allelic imbalance in gene expression as a guide to cis-acting regulatory single nucleotide polymorphisms in cancer cells.


[PMID 17482892OA-icon.png] Human variants of O6-alkylguanine-DNA alkyltransferase.


[PMID 18454203OA-icon.png] Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.


[PMID 19536092OA-icon.png] Explorative study to identify novel candidate genes related to oxaliplatin efficacy and toxicity using a DNA repair array.