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rs2230641

From SNPedia

Orientationminus
Stabilizedminus
Make rs2230641(C;C)
Make rs2230641(C;T)
Make rs2230641(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position87399457
GeneCCNH
is asnp
is mentioned by
dbSNPrs2230641
dbSNP (classic)rs2230641
ClinGenrs2230641
ebirs2230641
HLIrs2230641
Exacrs2230641
Gnomadrs2230641
Varsomers2230641
LitVarrs2230641
Maprs2230641
PheGenIrs2230641
Biobankrs2230641
1000 genomesrs2230641
hgdprs2230641
ensemblrs2230641
geneviewrs2230641
scholarrs2230641
googlers2230641
pharmgkbrs2230641
gwascentralrs2230641
openSNPrs2230641
23andMers2230641
SNPshotrs2230641
SNPdbers2230641
MSV3drs2230641
GWAS Ctlgrs2230641
Merged fromRs2266690
GMAF0.1382
Max Magnitude0
? (C;C) (C;T) (T;T) 28


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[PMID 18854777OA-icon.png] Germline genetic variations in drug action pathways predict clinical outcomes in advanced lung cancer treated with platinum-based chemotherapy.


[PMID 19074885] Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic leukemia.


[PMID 19270000OA-icon.png] Genetic susceptibility to esophageal cancer: the role of the nucleotide excision repair pathway.


[PMID 20141440OA-icon.png] Acute myeloid leukemia outcome: role of nucleotide excision repair polymorphisms in intermediate risk patients.

[PMID 24351404] Pharmacogenetic predictors of severe peripheral neuropathy in colon cancer patients treated with oxaliplatin-based adjuvant chemotherapy: a GEMCAD group study

[PMID 31374908OA-icon.png] Thyroid Cancer: The Quest for Genetic Susceptibility Involving DNA Repair Genes.