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rs10052657

From SNPedia

Orientationplus
Stabilizedplus
Make rs10052657(A;A)
Make rs10052657(A;C)
Make rs10052657(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position59111944
GenePDE4D
is asnp
is mentioned by
dbSNPrs10052657
dbSNP (classic)rs10052657
ClinGenrs10052657
ebirs10052657
HLIrs10052657
Exacrs10052657
Gnomadrs10052657
Varsomers10052657
LitVarrs10052657
Maprs10052657
PheGenIrs10052657
Biobankrs10052657
1000 genomesrs10052657
hgdprs10052657
ensemblrs10052657
geneviewrs10052657
scholarrs10052657
googlers10052657
pharmgkbrs10052657
gwascentralrs10052657
openSNPrs10052657
23andMers10052657
SNPshotrs10052657
SNPdbers10052657
MSV3drs10052657
GWAS Ctlgrs10052657
GMAF0.1598
Max Magnitude0
? (A;A) (A;C) (C;C) 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 C
P-val 2E-19
Odds Ratio 1.4900 [1.37-1.61]