rs200190285
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs200190285(C;C) |
Make rs200190285(C;T) |
Make rs200190285(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 16 |
Position | 20964834 |
Gene | DNAH3 |
is a | snp |
is | mentioned by |
dbSNP | rs200190285 |
dbSNP (classic) | rs200190285 |
ClinGen | rs200190285 |
ebi | rs200190285 |
HLI | rs200190285 |
Exac | rs200190285 |
Gnomad | rs200190285 |
Varsome | rs200190285 |
LitVar | rs200190285 |
Map | rs200190285 |
PheGenI | rs200190285 |
Biobank | rs200190285 |
1000 genomes | rs200190285 |
hgdp | rs200190285 |
ensembl | rs200190285 |
geneview | rs200190285 |
scholar | rs200190285 |
rs200190285 | |
pharmgkb | rs200190285 |
gwascentral | rs200190285 |
openSNP | rs200190285 |
23andMe | rs200190285 |
SNPshot | rs200190285 |
SNPdbe | rs200190285 |
MSV3d | rs200190285 |
GWAS Ctlg | rs200190285 |
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.