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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
ebirs800629
HLIrs800629
Exacrs800629
Varsomers800629
Maprs800629
PheGenIrs800629
hapmaprs800629
1000 genomesrs800629
hgdprs800629
ensemblrs800629
gopubmedrs800629
geneviewrs800629
scholarrs800629
googlers800629
pharmgkbrs800629
gwascentralrs800629
openSNPrs800629
23andMers800629
23andMe allrs800629
SNP Nexus

SNPshotrs800629
SNPdbers800629
MSV3drs800629
GWAS Ctlgrs800629
StatusMerged into rs543852
Max Magnitude

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