rs9259013
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9259013(A;A) |
Make rs9259013(A;T) |
Make rs9259013(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 6 |
Position | 29874690 |
is a | snp |
is | mentioned by |
dbSNP | rs9259013 |
dbSNP (classic) | rs9259013 |
ClinGen | rs9259013 |
ebi | rs9259013 |
HLI | rs9259013 |
Exac | rs9259013 |
Gnomad | rs9259013 |
Varsome | rs9259013 |
LitVar | rs9259013 |
Map | rs9259013 |
PheGenI | rs9259013 |
Biobank | rs9259013 |
1000 genomes | rs9259013 |
hgdp | rs9259013 |
ensembl | rs9259013 |
geneview | rs9259013 |
scholar | rs9259013 |
rs9259013 | |
pharmgkb | rs9259013 |
gwascentral | rs9259013 |
openSNP | rs9259013 |
23andMe | rs9259013 |
SNPshot | rs9259013 |
SNPdbe | rs9259013 |
MSV3d | rs9259013 |
GWAS Ctlg | rs9259013 |
Merged from | Rs112166594 |
Max Magnitude | 0 |
Formerly known as rs112166594 and associated with Behçet's disease [PMID 24821759]