rs800629
From SNPedia
Merged into | rs543852 |
Orientation | minus |
Make rs800629(C;C) |
Make rs800629(C;T) |
Make rs800629(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 37752757 |
is a | snp |
is | mentioned by |
dbSNP | rs800629 |
dbSNP (classic) | rs800629 |
ClinGen | rs800629 |
ebi | rs800629 |
HLI | rs800629 |
Exac | rs800629 |
Gnomad | rs800629 |
Varsome | rs800629 |
LitVar | rs800629 |
Map | rs800629 |
PheGenI | rs800629 |
Biobank | rs800629 |
1000 genomes | rs800629 |
hgdp | rs800629 |
ensembl | rs800629 |
geneview | rs800629 |
scholar | rs800629 |
rs800629 | |
pharmgkb | rs800629 |
gwascentral | rs800629 |
openSNP | rs800629 |
23andMe | rs800629 |
SNPshot | rs800629 |
SNPdbe | rs800629 |
MSV3d | rs800629 |
GWAS Ctlg | rs800629 |
Status | Merged into rs543852 |
Max Magnitude | 0 |
[PMID 27688118] Single nucleotide polymorphisms as markers of genetic susceptibility for oral potentially malignant disorders risk: Review of evidence to date.
[PMID 30509964] A Trial Sequential Meta-analysis of TNF- α -308G>A (rs800629) Gene Polymorphism and Susceptibility to Colorectal Cancer.