rs2834643
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2834643(A;A) |
Make rs2834643(A;G) |
Make rs2834643(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 34814099 |
Gene | RUNX1 |
is a | snp |
is | mentioned by |
dbSNP | rs2834643 |
dbSNP (classic) | rs2834643 |
ClinGen | rs2834643 |
ebi | rs2834643 |
HLI | rs2834643 |
Exac | rs2834643 |
Gnomad | rs2834643 |
Varsome | rs2834643 |
LitVar | rs2834643 |
Map | rs2834643 |
PheGenI | rs2834643 |
Biobank | rs2834643 |
1000 genomes | rs2834643 |
hgdp | rs2834643 |
ensembl | rs2834643 |
geneview | rs2834643 |
scholar | rs2834643 |
rs2834643 | |
pharmgkb | rs2834643 |
gwascentral | rs2834643 |
openSNP | rs2834643 |
23andMe | rs2834643 |
SNPshot | rs2834643 |
SNPdbe | rs2834643 |
MSV3d | rs2834643 |
GWAS Ctlg | rs2834643 |
GMAF | 0.4408 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23674219] Genetic variants in the JAK1 gene confer higher risk of Behcet's disease with ocular involvement in Han Chinese