rs147815528
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs147815528(C;C) |
Make rs147815528(C;G) |
Make rs147815528(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 184795047 |
Gene | FAM129A |
is a | snp |
is | mentioned by |
dbSNP | rs147815528 |
dbSNP (classic) | rs147815528 |
ClinGen | rs147815528 |
ebi | rs147815528 |
HLI | rs147815528 |
Exac | rs147815528 |
Gnomad | rs147815528 |
Varsome | rs147815528 |
LitVar | rs147815528 |
Map | rs147815528 |
PheGenI | rs147815528 |
Biobank | rs147815528 |
1000 genomes | rs147815528 |
hgdp | rs147815528 |
ensembl | rs147815528 |
geneview | rs147815528 |
scholar | rs147815528 |
rs147815528 | |
pharmgkb | rs147815528 |
gwascentral | rs147815528 |
openSNP | rs147815528 |
23andMe | rs147815528 |
SNPshot | rs147815528 |
SNPdbe | rs147815528 |
MSV3d | rs147815528 |
GWAS Ctlg | rs147815528 |
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.