rs140002868
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs140002868(A;A) |
Make rs140002868(A;G) |
Make rs140002868(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 12 |
Position | 131840590 |
Gene | MMP17 |
is a | snp |
is | mentioned by |
dbSNP | rs140002868 |
dbSNP (classic) | rs140002868 |
ClinGen | rs140002868 |
ebi | rs140002868 |
HLI | rs140002868 |
Exac | rs140002868 |
Gnomad | rs140002868 |
Varsome | rs140002868 |
LitVar | rs140002868 |
Map | rs140002868 |
PheGenI | rs140002868 |
Biobank | rs140002868 |
1000 genomes | rs140002868 |
hgdp | rs140002868 |
ensembl | rs140002868 |
geneview | rs140002868 |
scholar | rs140002868 |
rs140002868 | |
pharmgkb | rs140002868 |
gwascentral | rs140002868 |
openSNP | rs140002868 |
23andMe | rs140002868 |
SNPshot | rs140002868 |
SNPdbe | rs140002868 |
MSV3d | rs140002868 |
GWAS Ctlg | rs140002868 |
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.