rs114291795
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs114291795(C;C) |
Make rs114291795(C;G) |
Make rs114291795(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 6 |
Position | 31409863 |
Gene | MICA |
is a | snp |
is | mentioned by |
dbSNP | rs114291795 |
dbSNP (classic) | rs114291795 |
ClinGen | rs114291795 |
ebi | rs114291795 |
HLI | rs114291795 |
Exac | rs114291795 |
Gnomad | rs114291795 |
Varsome | rs114291795 |
LitVar | rs114291795 |
Map | rs114291795 |
PheGenI | rs114291795 |
Biobank | rs114291795 |
1000 genomes | rs114291795 |
hgdp | rs114291795 |
ensembl | rs114291795 |
geneview | rs114291795 |
scholar | rs114291795 |
rs114291795 | |
pharmgkb | rs114291795 |
gwascentral | rs114291795 |
openSNP | rs114291795 |
23andMe | rs114291795 |
SNPshot | rs114291795 |
SNPdbe | rs114291795 |
MSV3d | rs114291795 |
GWAS Ctlg | rs114291795 |
Max Magnitude | 0 |
[PMID 27157822] Genetic variants associated with antithyroid drug-induced agranulocytosis: a genome-wide association study in a European population.