rs26279
Orientation | plus |
Stabilized | plus |
Make rs26279(A;A) |
Make rs26279(A;G) |
Make rs26279(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 80873118 |
Gene | MSH3 |
is a | snp |
is | mentioned by |
dbSNP | rs26279 |
dbSNP (classic) | rs26279 |
ClinGen | rs26279 |
ebi | rs26279 |
HLI | rs26279 |
Exac | rs26279 |
Gnomad | rs26279 |
Varsome | rs26279 |
LitVar | rs26279 |
Map | rs26279 |
PheGenI | rs26279 |
Biobank | rs26279 |
1000 genomes | rs26279 |
hgdp | rs26279 |
ensembl | rs26279 |
geneview | rs26279 |
scholar | rs26279 |
rs26279 | |
pharmgkb | rs26279 |
gwascentral | rs26279 |
openSNP | rs26279 |
23andMe | rs26279 |
SNPshot | rs26279 |
SNPdbe | rs26279 |
MSV3d | rs26279 |
GWAS Ctlg | rs26279 |
GMAF | 0.3118 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22623965] The cumulative effects of polymorphisms in the DNA mismatch repair genes and tobacco smoking in oesophageal cancer risk
[PMID 18364438] Common variants in mismatch repair genes and risk of colorectal cancer.
[PMID 18701435] Polygenic model of DNA repair genetic polymorphisms in human breast cancer risk.
[PMID 19781088] Association of common variants in mismatch repair genes and breast cancer susceptibility: a multigene study.
[PMID 20386703] Association between DNA damage response and repair genes and risk of invasive serous ovarian cancer.
[PMID 26994442] A polymorphism in the MSH3 mismatch repair gene is associated with the levels of somatic instability of the expanded CTG repeat in the blood DNA of myotonic dystrophy type 1 patients.
[PMID 21974800] DNA repair gene polymorphisms and risk of early onset colorectal cancer in Lynch syndrome.
[PMID 26027715] Correlation between polymorphisms in DNA mismatch repair genes and the risk of primary hepatocellular carcinoma for the Han population in northern China
[PMID 29616133] Mismatch repair single nucleotide polymorphisms and thyroid cancer susceptibility.