rs199929403
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs199929403(A;A) |
Make rs199929403(A;G) |
Make rs199929403(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 208340070 |
Gene | PIKFYVE |
is a | snp |
is | mentioned by |
dbSNP | rs199929403 |
dbSNP (classic) | rs199929403 |
ClinGen | rs199929403 |
ebi | rs199929403 |
HLI | rs199929403 |
Exac | rs199929403 |
Gnomad | rs199929403 |
Varsome | rs199929403 |
LitVar | rs199929403 |
Map | rs199929403 |
PheGenI | rs199929403 |
Biobank | rs199929403 |
1000 genomes | rs199929403 |
hgdp | rs199929403 |
ensembl | rs199929403 |
geneview | rs199929403 |
scholar | rs199929403 |
rs199929403 | |
pharmgkb | rs199929403 |
gwascentral | rs199929403 |
openSNP | rs199929403 |
23andMe | rs199929403 |
SNPshot | rs199929403 |
SNPdbe | rs199929403 |
MSV3d | rs199929403 |
GWAS Ctlg | rs199929403 |
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.