rs150516896
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs150516896(A;A) |
Make rs150516896(A;G) |
Make rs150516896(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 68561792 |
is a | snp |
is | mentioned by |
dbSNP | rs150516896 |
dbSNP (classic) | rs150516896 |
ClinGen | rs150516896 |
ebi | rs150516896 |
HLI | rs150516896 |
Exac | rs150516896 |
Gnomad | rs150516896 |
Varsome | rs150516896 |
LitVar | rs150516896 |
Map | rs150516896 |
PheGenI | rs150516896 |
Biobank | rs150516896 |
1000 genomes | rs150516896 |
hgdp | rs150516896 |
ensembl | rs150516896 |
geneview | rs150516896 |
scholar | rs150516896 |
rs150516896 | |
pharmgkb | rs150516896 |
gwascentral | rs150516896 |
openSNP | rs150516896 |
23andMe | rs150516896 |
SNPshot | rs150516896 |
SNPdbe | rs150516896 |
MSV3d | rs150516896 |
GWAS Ctlg | rs150516896 |
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 | 4E-6 |
Odds Ratio | NR NR |