rs199564443
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(I;I) | 0 | common genotype |
(TTTT;TTTT) | 0 | common/normal |
Make rs199564443(-;-) |
Make rs199564443(-;TTTT) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 6 |
Position | 1388744 |
Gene | FOXF2, LOC105374880 |
is a | snp |
is | mentioned by |
dbSNP | rs199564443 |
dbSNP (classic) | rs199564443 |
ClinGen | rs199564443 |
ebi | rs199564443 |
HLI | rs199564443 |
Exac | rs199564443 |
Gnomad | rs199564443 |
Varsome | rs199564443 |
LitVar | rs199564443 |
Map | rs199564443 |
PheGenI | rs199564443 |
Biobank | rs199564443 |
1000 genomes | rs199564443 |
hgdp | rs199564443 |
ensembl | rs199564443 |
geneview | rs199564443 |
scholar | rs199564443 |
rs199564443 | |
pharmgkb | rs199564443 |
gwascentral | rs199564443 |
openSNP | rs199564443 |
23andMe | rs199564443 |
SNPshot | rs199564443 |
SNPdbe | rs199564443 |
MSV3d | rs199564443 |
GWAS Ctlg | rs199564443 |
Max Magnitude | 0 |
[PMID 27157822] Genetic variants associated with antithyroid drug-induced agranulocytosis: a genome-wide association study in a European population.