rs201786064
From SNPedia
Merged into | rs111200466 |
Orientation | minus |
Make rs201786064(-;-) |
Make rs201786064(-;AGAGAACGCCGAGCAGCCGCCTG) |
Make rs201786064(AGAGAACGCCGAGCAGCCGCCTG;AGAGAACGCCGAGCAGCCGCCTG) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 4 |
Position | 153684312 |
Gene | TLR2 |
is a | snp |
is | mentioned by |
dbSNP | rs201786064 |
dbSNP (classic) | rs201786064 |
ClinGen | rs201786064 |
ebi | rs201786064 |
HLI | rs201786064 |
Exac | rs201786064 |
Gnomad | rs201786064 |
Varsome | rs201786064 |
LitVar | rs201786064 |
Map | rs201786064 |
PheGenI | rs201786064 |
Biobank | rs201786064 |
1000 genomes | rs201786064 |
hgdp | rs201786064 |
ensembl | rs201786064 |
geneview | rs201786064 |
scholar | rs201786064 |
rs201786064 | |
pharmgkb | rs201786064 |
gwascentral | rs201786064 |
openSNP | rs201786064 |
23andMe | rs201786064 |
SNPshot | rs201786064 |
SNPdbe | rs201786064 |
MSV3d | rs201786064 |
GWAS Ctlg | rs201786064 |
Status | Merged into rs111200466 |
Max Magnitude | 0 |
[PMID 26919710] Variations in genes involved in regulation of the nuclear factor - κB pathway and the risk of acute myeloid leukaemia.