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rs7229639

From SNPedia

Orientationplus
Stabilizedplus
Make rs7229639(A;A)
Make rs7229639(A;G)
Make rs7229639(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position48924606
GeneSMAD7
is asnp
is mentioned by
dbSNPrs7229639
ebirs7229639
HLIrs7229639
Exacrs7229639
Varsomers7229639
Maprs7229639
PheGenIrs7229639
hapmaprs7229639
1000 genomesrs7229639
hgdprs7229639
ensemblrs7229639
gopubmedrs7229639
geneviewrs7229639
scholarrs7229639
googlers7229639
pharmgkbrs7229639
gwascentralrs7229639
openSNPrs7229639
23andMers7229639
23andMe allrs7229639
SNP Nexus

SNPshotrs7229639
SNPdbers7229639
MSV3drs7229639
GWAS Ctlgrs7229639
GMAF0.1419
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 24448986OA-icon.png] Genome-wide association study identifies a new SMAD7 risk variant associated with colorectal cancer risk in East Asians
GWAS snp
PMID [PMID 24836286OA-icon.png]
Trait Colorectal cancer
Title Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk.
Risk Allele A
P-val 2E-8
Odds Ratio 1.20 [1.16-1.25]


[PMID 26989026] SMAD7 loci contribute to risk of hepatocellular carcinoma and clinicopathologic development among Chinese Han population.


[PMID 27769063] Risk of eighteen genome-wide association study-identified genetic variants for colorectal cancer and colorectal adenoma in Han Chinese.