rs112166594
From SNPedia
Merged into | rs9259013 |
Orientation | plus |
Make rs112166594(A;A) |
Make rs112166594(A;T) |
Make rs112166594(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 6 |
Position | 29874690 |
is a | snp |
is | mentioned by |
dbSNP | rs112166594 |
dbSNP (classic) | rs112166594 |
ClinGen | rs112166594 |
ebi | rs112166594 |
HLI | rs112166594 |
Exac | rs112166594 |
Gnomad | rs112166594 |
Varsome | rs112166594 |
LitVar | rs112166594 |
Map | rs112166594 |
PheGenI | rs112166594 |
Biobank | rs112166594 |
1000 genomes | rs112166594 |
hgdp | rs112166594 |
ensembl | rs112166594 |
geneview | rs112166594 |
scholar | rs112166594 |
rs112166594 | |
pharmgkb | rs112166594 |
gwascentral | rs112166594 |
openSNP | rs112166594 |
23andMe | rs112166594 |
SNPshot | rs112166594 |
SNPdbe | rs112166594 |
MSV3d | rs112166594 |
GWAS Ctlg | rs112166594 |
Status | Merged into rs9259013 |
Max Magnitude | 0 |
associated with Behçet's disease [PMID 24821759]