rs116075389
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs116075389(C;C) |
Make rs116075389(C;T) |
Make rs116075389(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 68563384 |
is a | snp |
is | mentioned by |
dbSNP | rs116075389 |
dbSNP (classic) | rs116075389 |
ClinGen | rs116075389 |
ebi | rs116075389 |
HLI | rs116075389 |
Exac | rs116075389 |
Gnomad | rs116075389 |
Varsome | rs116075389 |
LitVar | rs116075389 |
Map | rs116075389 |
PheGenI | rs116075389 |
Biobank | rs116075389 |
1000 genomes | rs116075389 |
hgdp | rs116075389 |
ensembl | rs116075389 |
geneview | rs116075389 |
scholar | rs116075389 |
rs116075389 | |
pharmgkb | rs116075389 |
gwascentral | rs116075389 |
openSNP | rs116075389 |
23andMe | rs116075389 |
SNPshot | rs116075389 |
SNPdbe | rs116075389 |
MSV3d | rs116075389 |
GWAS Ctlg | rs116075389 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 24322204] |
Trait | Bipolar disorder (body mass index interaction) |
Title | Genome-wide association study of bipolar disorder accounting for effect of body mass index identifies a new risk allele in TCF7L2. |
Risk Allele | |
P-val | 3E-6 |
Odds Ratio | NR NR |