rs591323
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs591323(A;A) |
Make rs591323(A;G) |
Make rs591323(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 8 |
Position | 16839582 |
Gene | LOC105379297 |
is a | snp |
is | mentioned by |
dbSNP | rs591323 |
dbSNP (classic) | rs591323 |
ClinGen | rs591323 |
ebi | rs591323 |
HLI | rs591323 |
Exac | rs591323 |
Gnomad | rs591323 |
Varsome | rs591323 |
LitVar | rs591323 |
Map | rs591323 |
PheGenI | rs591323 |
Biobank | rs591323 |
1000 genomes | rs591323 |
hgdp | rs591323 |
ensembl | rs591323 |
geneview | rs591323 |
scholar | rs591323 |
rs591323 | |
pharmgkb | rs591323 |
gwascentral | rs591323 |
openSNP | rs591323 |
23andMe | rs591323 |
SNPshot | rs591323 |
SNPdbe | rs591323 |
MSV3d | rs591323 |
GWAS Ctlg | rs591323 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 26535683] Screening of polymorphisms located in the FGF20 and TMEM175 genes in North Chinese Parkinson's disease patients
[PMID 29774458] Effects of rs591323 on serotonin transporter availability in healthy male subjects.