rs1052823
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1052823(G;G) |
Make rs1052823(G;T) |
Make rs1052823(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 103137233 |
Gene | TNFAIP2 |
is a | snp |
is | mentioned by |
dbSNP | rs1052823 |
dbSNP (classic) | rs1052823 |
ClinGen | rs1052823 |
ebi | rs1052823 |
HLI | rs1052823 |
Exac | rs1052823 |
Gnomad | rs1052823 |
Varsome | rs1052823 |
LitVar | rs1052823 |
Map | rs1052823 |
PheGenI | rs1052823 |
Biobank | rs1052823 |
1000 genomes | rs1052823 |
hgdp | rs1052823 |
ensembl | rs1052823 |
geneview | rs1052823 |
scholar | rs1052823 |
rs1052823 | |
pharmgkb | rs1052823 |
gwascentral | rs1052823 |
openSNP | rs1052823 |
23andMe | rs1052823 |
SNPshot | rs1052823 |
SNPdbe | rs1052823 |
MSV3d | rs1052823 |
GWAS Ctlg | rs1052823 |
GMAF | 0.1175 |
Max Magnitude | 0 |
[PMID 21934093] A Functional Variant at the miR-184 Binding Site in TNFAIP2 and Risk of Squamous Cell Carcinoma of the Head and Neck
[PMID 23724109] The miR-184 Binding-Site rs8126 T>C Polymorphism in TNFAIP2 Is Associated with Risk of Gastric Cancer