rs485497
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs485497(A;A) |
Make rs485497(A;G) |
Make rs485497(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 160001345 |
Gene | IL12A-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs485497 |
dbSNP (classic) | rs485497 |
ClinGen | rs485497 |
ebi | rs485497 |
HLI | rs485497 |
Exac | rs485497 |
Gnomad | rs485497 |
Varsome | rs485497 |
LitVar | rs485497 |
Map | rs485497 |
PheGenI | rs485497 |
Biobank | rs485497 |
1000 genomes | rs485497 |
hgdp | rs485497 |
ensembl | rs485497 |
geneview | rs485497 |
scholar | rs485497 |
rs485497 | |
pharmgkb | rs485497 |
gwascentral | rs485497 |
openSNP | rs485497 |
23andMe | rs485497 |
SNPshot | rs485497 |
SNPdbe | rs485497 |
MSV3d | rs485497 |
GWAS Ctlg | rs485497 |
GMAF | 0.4761 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21418175] Genetic variation in Th1/Th2 pathway genes and risk of non-Hodgkin lymphoma: a pooled analysis of three population-based case-control studies
[PMID 19458352] Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.