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rs2040639

From SNPedia

Orientationminus
Stabilizedminus
Make rs2040639(A;A)
Make rs2040639(A;G)
Make rs2040639(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position152678103
GeneXRCC2
is asnp
is mentioned by
dbSNPrs2040639
ebirs2040639
HLIrs2040639
Exacrs2040639
Varsomers2040639
Maprs2040639
PheGenIrs2040639
hapmaprs2040639
1000 genomesrs2040639
hgdprs2040639
ensemblrs2040639
gopubmedrs2040639
geneviewrs2040639
scholarrs2040639
googlers2040639
pharmgkbrs2040639
gwascentralrs2040639
openSNPrs2040639
23andMers2040639
23andMe allrs2040639
SNP Nexus

SNPshotrs2040639
SNPdbers2040639
MSV3drs2040639
GWAS Ctlgrs2040639
GMAF0.3705
Max Magnitude
? (A;A) (A;G) (G;G) 28

18067C>T possibly related to non-Hodgkin lymphoma

[PMID 18410587] rs2040639-AG, contribute to oral cancer risk.

pseudo-haplotype with AG-CC genotypes in


[PMID 22726897] Single nucleotide polymorphism barcoding to evaluate oral cancer risk using odds ratio-based genetic algorithms


[PMID 19690184OA-icon.png] Genetic variants in XRCC2: new insights into colorectal cancer tumorigenesis.