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rs4460629

From SNPedia

Orientationplus
Stabilizedplus
Make rs4460629(C;C)
Make rs4460629(C;T)
Make rs4460629(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position155162859
is asnp
is mentioned by
dbSNPrs4460629
ebirs4460629
HLIrs4460629
Exacrs4460629
Varsomers4460629
Maprs4460629
PheGenIrs4460629
hapmaprs4460629
1000 genomesrs4460629
hgdprs4460629
ensemblrs4460629
gopubmedrs4460629
geneviewrs4460629
scholarrs4460629
googlers4460629
pharmgkbrs4460629
gwascentralrs4460629
openSNPrs4460629
23andMers4460629
23andMe allrs4460629
SNP Nexus

SNPshotrs4460629
SNPdbers4460629
MSV3drs4460629
GWAS Ctlgrs4460629
GMAF0.3554
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 22938415] Association of genetic polymorphisms at 1q22 but not 10q23 with gastric cancer in a southern Chinese population


[PMID 22740136] Association of 10q23 with colorectal cancer in a Chinese population.