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rs2283873

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common genotype
Make rs2283873(A;A)
Make rs2283873(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position30617309
GeneTCN2
is asnp
is mentioned by
dbSNPrs2283873
dbSNP (classic)rs2283873
ClinGenrs2283873
ebirs2283873
HLIrs2283873
Exacrs2283873
Gnomadrs2283873
Varsomers2283873
LitVarrs2283873
Maprs2283873
PheGenIrs2283873
Biobankrs2283873
1000 genomesrs2283873
hgdprs2283873
ensemblrs2283873
geneviewrs2283873
scholarrs2283873
googlers2283873
pharmgkbrs2283873
gwascentralrs2283873
openSNPrs2283873
23andMers2283873
SNPshotrs2283873
SNPdbers2283873
MSV3drs2283873
GWAS Ctlgrs2283873
GMAF0.169
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 22544364OA-icon.png]
Trait
Title A genome-wide association study identifies susceptibility loci for Wilms tumor.
Risk Allele A
P-val 5E-12
Odds Ratio 2.0500 None