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rs9868873

From SNPedia

Orientationplus
Stabilizedplus
Make rs9868873(A;A)
Make rs9868873(A;G)
Make rs9868873(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position123012063
GeneSEMA5B
is asnp
is mentioned by
dbSNPrs9868873
dbSNP (classic)rs9868873
ClinGenrs9868873
ebirs9868873
HLIrs9868873
Exacrs9868873
Gnomadrs9868873
Varsomers9868873
LitVarrs9868873
Maprs9868873
PheGenIrs9868873
Biobankrs9868873
1000 genomesrs9868873
hgdprs9868873
ensemblrs9868873
geneviewrs9868873
scholarrs9868873
googlers9868873
pharmgkbrs9868873
gwascentralrs9868873
openSNPrs9868873
23andMers9868873
SNPshotrs9868873
SNPdbers9868873
MSV3drs9868873
GWAS Ctlgrs9868873
GMAF0.2925
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 1E-7
Odds Ratio 1.1900 [1.11-1.27]