rs1705236
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs1705236(A;A) |
Make rs1705236(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 71151778 |
Gene | TSPAN8 |
is a | snp |
is | mentioned by |
dbSNP | rs1705236 |
dbSNP (classic) | rs1705236 |
ClinGen | rs1705236 |
ebi | rs1705236 |
HLI | rs1705236 |
Exac | rs1705236 |
Gnomad | rs1705236 |
Varsome | rs1705236 |
LitVar | rs1705236 |
Map | rs1705236 |
PheGenI | rs1705236 |
Biobank | rs1705236 |
1000 genomes | rs1705236 |
hgdp | rs1705236 |
ensembl | rs1705236 |
geneview | rs1705236 |
scholar | rs1705236 |
rs1705236 | |
pharmgkb | rs1705236 |
gwascentral | rs1705236 |
openSNP | rs1705236 |
23andMe | rs1705236 |
SNPshot | rs1705236 |
SNPdbe | rs1705236 |
MSV3d | rs1705236 |
GWAS Ctlg | rs1705236 |
GMAF | 0.06612 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 20052686] Functional variants of TSPAN8 are associated with bipolar disorder and schizophrenia