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rs8030672

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs8030672(A;A)
Make rs8030672(A;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position68766745
is asnp
is mentioned by
dbSNPrs8030672
ebirs8030672
HLIrs8030672
Exacrs8030672
Varsomers8030672
Maprs8030672
PheGenIrs8030672
hapmaprs8030672
1000 genomesrs8030672
hgdprs8030672
ensemblrs8030672
gopubmedrs8030672
geneviewrs8030672
scholarrs8030672
googlers8030672
pharmgkbrs8030672
gwascentralrs8030672
openSNPrs8030672
23andMers8030672
23andMe allrs8030672
SNP Nexus

SNPshotrs8030672
SNPdbers8030672
MSV3drs8030672
GWAS Ctlgrs8030672
GMAF0.05188
Max Magnitude0
? (A;A) (A;T) (T;T) 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 A
P-val 1E-11
Odds Ratio 1.5600 [1.37-1.78]