rs188509769
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs188509769(A;A) |
Make rs188509769(A;G) |
Make rs188509769(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 20 |
Position | 45940563 |
Gene | PCIF1 |
is a | snp |
is | mentioned by |
dbSNP | rs188509769 |
dbSNP (classic) | rs188509769 |
ClinGen | rs188509769 |
ebi | rs188509769 |
HLI | rs188509769 |
Exac | rs188509769 |
Gnomad | rs188509769 |
Varsome | rs188509769 |
LitVar | rs188509769 |
Map | rs188509769 |
PheGenI | rs188509769 |
Biobank | rs188509769 |
1000 genomes | rs188509769 |
hgdp | rs188509769 |
ensembl | rs188509769 |
geneview | rs188509769 |
scholar | rs188509769 |
rs188509769 | |
pharmgkb | rs188509769 |
gwascentral | rs188509769 |
openSNP | rs188509769 |
23andMe | rs188509769 |
SNPshot | rs188509769 |
SNPdbe | rs188509769 |
MSV3d | rs188509769 |
GWAS Ctlg | rs188509769 |
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.