rs7753873
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7753873(A;A) |
Make rs7753873(A;C) |
Make rs7753873(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 137852285 |
Gene | LOC100130476, LOC107986649 |
is a | snp |
is | mentioned by |
dbSNP | rs7753873 |
dbSNP (classic) | rs7753873 |
ClinGen | rs7753873 |
ebi | rs7753873 |
HLI | rs7753873 |
Exac | rs7753873 |
Gnomad | rs7753873 |
Varsome | rs7753873 |
LitVar | rs7753873 |
Map | rs7753873 |
PheGenI | rs7753873 |
Biobank | rs7753873 |
1000 genomes | rs7753873 |
hgdp | rs7753873 |
ensembl | rs7753873 |
geneview | rs7753873 |
scholar | rs7753873 |
rs7753873 | |
pharmgkb | rs7753873 |
gwascentral | rs7753873 |
openSNP | rs7753873 |
23andMe | rs7753873 |
SNPshot | rs7753873 |
SNPdbe | rs7753873 |
MSV3d | rs7753873 |
GWAS Ctlg | rs7753873 |
GMAF | 0.1708 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 23161053] TNFAIP3 gene polymorphisms confer risk for Behcet's disease in a Chinese Han population