rs142554860
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs142554860(A;A) |
Make rs142554860(A;G) |
Make rs142554860(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 21730926 |
Gene | LOC107984214, MLLT10 |
is a | snp |
is | mentioned by |
dbSNP | rs142554860 |
dbSNP (classic) | rs142554860 |
ClinGen | rs142554860 |
ebi | rs142554860 |
HLI | rs142554860 |
Exac | rs142554860 |
Gnomad | rs142554860 |
Varsome | rs142554860 |
LitVar | rs142554860 |
Map | rs142554860 |
PheGenI | rs142554860 |
Biobank | rs142554860 |
1000 genomes | rs142554860 |
hgdp | rs142554860 |
ensembl | rs142554860 |
geneview | rs142554860 |
scholar | rs142554860 |
rs142554860 | |
pharmgkb | rs142554860 |
gwascentral | rs142554860 |
openSNP | rs142554860 |
23andMe | rs142554860 |
SNPshot | rs142554860 |
SNPdbe | rs142554860 |
MSV3d | rs142554860 |
GWAS Ctlg | rs142554860 |
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.