rs200223984
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs200223984(A;A) |
Make rs200223984(A;C) |
Make rs200223984(C;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 14 |
Position | 102139377 |
Gene | HSP90AA1, WDR20 |
is a | snp |
is | mentioned by |
dbSNP | rs200223984 |
dbSNP (classic) | rs200223984 |
ClinGen | rs200223984 |
ebi | rs200223984 |
HLI | rs200223984 |
Exac | rs200223984 |
Gnomad | rs200223984 |
Varsome | rs200223984 |
LitVar | rs200223984 |
Map | rs200223984 |
PheGenI | rs200223984 |
Biobank | rs200223984 |
1000 genomes | rs200223984 |
hgdp | rs200223984 |
ensembl | rs200223984 |
geneview | rs200223984 |
scholar | rs200223984 |
rs200223984 | |
pharmgkb | rs200223984 |
gwascentral | rs200223984 |
openSNP | rs200223984 |
23andMe | rs200223984 |
SNPshot | rs200223984 |
SNPdbe | rs200223984 |
MSV3d | rs200223984 |
GWAS Ctlg | rs200223984 |
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.