rs10067777
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10067777(A;A) |
Make rs10067777(A;G) |
Make rs10067777(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 110490595 |
Gene | TMEM232 |
is a | snp |
is | mentioned by |
dbSNP | rs10067777 |
dbSNP (classic) | rs10067777 |
ClinGen | rs10067777 |
ebi | rs10067777 |
HLI | rs10067777 |
Exac | rs10067777 |
Gnomad | rs10067777 |
Varsome | rs10067777 |
LitVar | rs10067777 |
Map | rs10067777 |
PheGenI | rs10067777 |
Biobank | rs10067777 |
1000 genomes | rs10067777 |
hgdp | rs10067777 |
ensembl | rs10067777 |
geneview | rs10067777 |
scholar | rs10067777 |
rs10067777 | |
pharmgkb | rs10067777 |
gwascentral | rs10067777 |
openSNP | rs10067777 |
23andMe | rs10067777 |
SNPshot | rs10067777 |
SNPdbe | rs10067777 |
MSV3d | rs10067777 |
GWAS Ctlg | rs10067777 |
GMAF | 0.08815 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22448455] Genetic variant rs4982958 at 14q11.2 is associated with allergic rhinitis in a Chinese Han population running title: 14q11.2 is a susceptibility locus for allergic rhinitis