rs2040639
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2040639(A;A) |
Make rs2040639(A;G) |
Make rs2040639(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 152678103 |
Gene | XRCC2 |
is a | snp |
is | mentioned by |
dbSNP | rs2040639 |
dbSNP (classic) | rs2040639 |
ClinGen | rs2040639 |
ebi | rs2040639 |
HLI | rs2040639 |
Exac | rs2040639 |
Gnomad | rs2040639 |
Varsome | rs2040639 |
LitVar | rs2040639 |
Map | rs2040639 |
PheGenI | rs2040639 |
Biobank | rs2040639 |
1000 genomes | rs2040639 |
hgdp | rs2040639 |
ensembl | rs2040639 |
geneview | rs2040639 |
scholar | rs2040639 |
rs2040639 | |
pharmgkb | rs2040639 |
gwascentral | rs2040639 |
openSNP | rs2040639 |
23andMe | rs2040639 |
SNPshot | rs2040639 |
SNPdbe | rs2040639 |
MSV3d | rs2040639 |
GWAS Ctlg | rs2040639 |
GMAF | 0.3705 |
Max Magnitude | 0 |
? | (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
- 2.45x risk rs2040639-rs861539
- 5.03x risk rs2040639-rs861539-rs2075685
- 10.10x risk rs2040639-rs861539-rs2075685-rs1799782
[PMID 22726897] Single nucleotide polymorphism barcoding to evaluate oral cancer risk using odds ratio-based genetic algorithms
[PMID 19690184] Genetic variants in XRCC2: new insights into colorectal cancer tumorigenesis.
[PMID 29038438] Haplotype analysis of XRCC2 gene polymorphisms and association with increased risk of head and neck cancer.