rs4500567
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs4500567(C;C) |
Make rs4500567(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 71166082 |
is a | snp |
is | mentioned by |
dbSNP | rs4500567 |
dbSNP (classic) | rs4500567 |
ClinGen | rs4500567 |
ebi | rs4500567 |
HLI | rs4500567 |
Exac | rs4500567 |
Gnomad | rs4500567 |
Varsome | rs4500567 |
LitVar | rs4500567 |
Map | rs4500567 |
PheGenI | rs4500567 |
Biobank | rs4500567 |
1000 genomes | rs4500567 |
hgdp | rs4500567 |
ensembl | rs4500567 |
geneview | rs4500567 |
scholar | rs4500567 |
rs4500567 | |
pharmgkb | rs4500567 |
gwascentral | rs4500567 |
openSNP | rs4500567 |
23andMe | rs4500567 |
SNPshot | rs4500567 |
SNPdbe | rs4500567 |
MSV3d | rs4500567 |
GWAS Ctlg | rs4500567 |
GMAF | 0.1359 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 20052686] Functional variants of TSPAN8 are associated with bipolar disorder and schizophrenia