Have questions? Visit https://www.reddit.com/r/SNPedia

rs6687758

From SNPedia

Orientationplus
Stabilizedplus
Make rs6687758(A;A)
Make rs6687758(A;G)
Make rs6687758(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position221991606
is asnp
is mentioned by
dbSNPrs6687758
ebirs6687758
HLIrs6687758
Exacrs6687758
Varsomers6687758
Maprs6687758
PheGenIrs6687758
hapmaprs6687758
1000 genomesrs6687758
hgdprs6687758
ensemblrs6687758
gopubmedrs6687758
geneviewrs6687758
scholarrs6687758
googlers6687758
pharmgkbrs6687758
gwascentralrs6687758
openSNPrs6687758
23andMers6687758
23andMe allrs6687758
SNP Nexus

SNPshotrs6687758
SNPdbers6687758
MSV3drs6687758
GWAS Ctlgrs6687758
GMAF0.2153
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20972440]
Trait
Title Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
Risk Allele G
P-val 2E-9
Odds Ratio 1.0900 [1.06-1.12]
GWAS snp
PMID [PMID 21685912OA-icon.png]
Trait
Title Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
Risk Allele
P-val 6E-8
Odds Ratio 1.2700 [1.16-1.39]


[PMID 22076443OA-icon.png] Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13


[PMID 22999960OA-icon.png] Much of the genetic risk of colorectal cancer is likely to be mediated through susceptibility to adenomas.

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 G
P-val 9E-9
Odds Ratio 1.12 [1.08-1.17]


[PMID 26078566OA-icon.png] Association of colorectal cancer susceptibility variants with esophageal cancer in a Chinese population