rs369365976
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs369365976(A;A) |
Make rs369365976(A;G) |
Make rs369365976(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 7 |
Position | 112472842 |
Gene | IFRD1 |
is a | snp |
is | mentioned by |
dbSNP | rs369365976 |
dbSNP (classic) | rs369365976 |
ClinGen | rs369365976 |
ebi | rs369365976 |
HLI | rs369365976 |
Exac | rs369365976 |
Gnomad | rs369365976 |
Varsome | rs369365976 |
LitVar | rs369365976 |
Map | rs369365976 |
PheGenI | rs369365976 |
Biobank | rs369365976 |
1000 genomes | rs369365976 |
hgdp | rs369365976 |
ensembl | rs369365976 |
geneview | rs369365976 |
scholar | rs369365976 |
rs369365976 | |
pharmgkb | rs369365976 |
gwascentral | rs369365976 |
openSNP | rs369365976 |
23andMe | rs369365976 |
SNPshot | rs369365976 |
SNPdbe | rs369365976 |
MSV3d | rs369365976 |
GWAS Ctlg | rs369365976 |
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.