rs78259398
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs78259398(C;C) |
Make rs78259398(C;T) |
Make rs78259398(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 13 |
Position | 41778035 |
Gene | VWA8 |
is a | snp |
is | mentioned by |
dbSNP | rs78259398 |
dbSNP (classic) | rs78259398 |
ClinGen | rs78259398 |
ebi | rs78259398 |
HLI | rs78259398 |
Exac | rs78259398 |
Gnomad | rs78259398 |
Varsome | rs78259398 |
LitVar | rs78259398 |
Map | rs78259398 |
PheGenI | rs78259398 |
Biobank | rs78259398 |
1000 genomes | rs78259398 |
hgdp | rs78259398 |
ensembl | rs78259398 |
geneview | rs78259398 |
scholar | rs78259398 |
rs78259398 | |
pharmgkb | rs78259398 |
gwascentral | rs78259398 |
openSNP | rs78259398 |
23andMe | rs78259398 |
SNPshot | rs78259398 |
SNPdbe | rs78259398 |
MSV3d | rs78259398 |
GWAS Ctlg | rs78259398 |
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.