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

rs6772209

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs6772209(A;A)
Make rs6772209(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position175929377
is asnp
is mentioned by
dbSNPrs6772209
ebirs6772209
HLIrs6772209
Exacrs6772209
Varsomers6772209
Maprs6772209
PheGenIrs6772209
hapmaprs6772209
1000 genomesrs6772209
hgdprs6772209
ensemblrs6772209
gopubmedrs6772209
geneviewrs6772209
scholarrs6772209
googlers6772209
pharmgkbrs6772209
gwascentralrs6772209
openSNPrs6772209
23andMers6772209
23andMe allrs6772209
SNP Nexus

SNPshotrs6772209
SNPdbers6772209
MSV3drs6772209
GWAS Ctlgrs6772209
GMAF0.04867
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21642993]
Trait
Title Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations.
Risk Allele G
P-val 3E-7
Odds Ratio 1.4900 [1.28-1.75]