rs6599388
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6599388(C;C) |
Make rs6599388(C;T) |
Make rs6599388(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 945299 |
Gene | TMEM175 |
is a | snp |
is | mentioned by |
dbSNP | rs6599388 |
dbSNP (classic) | rs6599388 |
ClinGen | rs6599388 |
ebi | rs6599388 |
HLI | rs6599388 |
Exac | rs6599388 |
Gnomad | rs6599388 |
Varsome | rs6599388 |
LitVar | rs6599388 |
Map | rs6599388 |
PheGenI | rs6599388 |
Biobank | rs6599388 |
1000 genomes | rs6599388 |
hgdp | rs6599388 |
ensembl | rs6599388 |
geneview | rs6599388 |
scholar | rs6599388 |
rs6599388 | |
pharmgkb | rs6599388 |
gwascentral | rs6599388 |
openSNP | rs6599388 |
23andMe | rs6599388 |
SNPshot | rs6599388 |
SNPdbe | rs6599388 |
MSV3d | rs6599388 |
GWAS Ctlg | rs6599388 |
GMAF | 0.3044 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 21292315] |
Trait | |
Title | Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies |
Risk Allele | T |
P-val | 4E-12 |
Odds Ratio | 1.1600 [1.12-1.20] |
[PMID 26535683] Screening of polymorphisms located in the FGF20 and TMEM175 genes in North Chinese Parkinson's disease patients