rs199962136
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs199962136(A;A) |
Make rs199962136(A;G) |
Make rs199962136(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 119052704 |
Gene | HYOU1 |
is a | snp |
is | mentioned by |
dbSNP | rs199962136 |
dbSNP (classic) | rs199962136 |
ClinGen | rs199962136 |
ebi | rs199962136 |
HLI | rs199962136 |
Exac | rs199962136 |
Gnomad | rs199962136 |
Varsome | rs199962136 |
LitVar | rs199962136 |
Map | rs199962136 |
PheGenI | rs199962136 |
Biobank | rs199962136 |
1000 genomes | rs199962136 |
hgdp | rs199962136 |
ensembl | rs199962136 |
geneview | rs199962136 |
scholar | rs199962136 |
rs199962136 | |
pharmgkb | rs199962136 |
gwascentral | rs199962136 |
openSNP | rs199962136 |
23andMe | rs199962136 |
SNPshot | rs199962136 |
SNPdbe | rs199962136 |
MSV3d | rs199962136 |
GWAS Ctlg | rs199962136 |
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.