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rs800629

From SNPedia

Merged intors543852
Orientationminus
Make rs800629(C;C)
Make rs800629(C;T)
Make rs800629(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position37752757
is asnp
is mentioned by
dbSNPrs800629
dbSNP (classic)rs800629
ClinGenrs800629
ebirs800629
HLIrs800629
Exacrs800629
Gnomadrs800629
Varsomers800629
LitVarrs800629
Maprs800629
PheGenIrs800629
Biobankrs800629
1000 genomesrs800629
hgdprs800629
ensemblrs800629
geneviewrs800629
scholarrs800629
googlers800629
pharmgkbrs800629
gwascentralrs800629
openSNPrs800629
23andMers800629
SNPshotrs800629
SNPdbers800629
MSV3drs800629
GWAS Ctlgrs800629
StatusMerged into rs543852
Max Magnitude0

[PMID 27688118OA-icon.png] Single nucleotide polymorphisms as markers of genetic susceptibility for oral potentially malignant disorders risk: Review of evidence to date.

[PMID 30509964OA-icon.png] A Trial Sequential Meta-analysis of TNF- α -308G>A (rs800629) Gene Polymorphism and Susceptibility to Colorectal Cancer.