rs147737574
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs147737574(A;A) |
Make rs147737574(A;G) |
Make rs147737574(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 17 |
Position | 4810930 |
Gene | PLD2 |
is a | snp |
is | mentioned by |
dbSNP | rs147737574 |
dbSNP (classic) | rs147737574 |
ClinGen | rs147737574 |
ebi | rs147737574 |
HLI | rs147737574 |
Exac | rs147737574 |
Gnomad | rs147737574 |
Varsome | rs147737574 |
LitVar | rs147737574 |
Map | rs147737574 |
PheGenI | rs147737574 |
Biobank | rs147737574 |
1000 genomes | rs147737574 |
hgdp | rs147737574 |
ensembl | rs147737574 |
geneview | rs147737574 |
scholar | rs147737574 |
rs147737574 | |
pharmgkb | rs147737574 |
gwascentral | rs147737574 |
openSNP | rs147737574 |
23andMe | rs147737574 |
SNPshot | rs147737574 |
SNPdbe | rs147737574 |
MSV3d | rs147737574 |
GWAS Ctlg | rs147737574 |
Max Magnitude | 0 |
[PMID 27120077] Exome Sequencing of Familial Bipolar Disorder. The minor allele of this SNP is one of 84 rare variants speculated to have an impact (positive or negative; see publication for specific SNP details) on risk for bipolar disorder. The analysis of many more patients is likely to be required to confirm or refute this association.