rs146980221
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs146980221(A;A) |
Make rs146980221(A;G) |
Make rs146980221(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 233354955 |
Gene | KIAA1804, MAP3K21 |
is a | snp |
is | mentioned by |
dbSNP | rs146980221 |
dbSNP (classic) | rs146980221 |
ClinGen | rs146980221 |
ebi | rs146980221 |
HLI | rs146980221 |
Exac | rs146980221 |
Gnomad | rs146980221 |
Varsome | rs146980221 |
LitVar | rs146980221 |
Map | rs146980221 |
PheGenI | rs146980221 |
Biobank | rs146980221 |
1000 genomes | rs146980221 |
hgdp | rs146980221 |
ensembl | rs146980221 |
geneview | rs146980221 |
scholar | rs146980221 |
rs146980221 | |
pharmgkb | rs146980221 |
gwascentral | rs146980221 |
openSNP | rs146980221 |
23andMe | rs146980221 |
SNPshot | rs146980221 |
SNPdbe | rs146980221 |
MSV3d | rs146980221 |
GWAS Ctlg | rs146980221 |
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.