rs141679163
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs141679163(G;G) |
Make rs141679163(G;T) |
Make rs141679163(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 183240079 |
Gene | LAMC2 |
is a | snp |
is | mentioned by |
dbSNP | rs141679163 |
dbSNP (classic) | rs141679163 |
ClinGen | rs141679163 |
ebi | rs141679163 |
HLI | rs141679163 |
Exac | rs141679163 |
Gnomad | rs141679163 |
Varsome | rs141679163 |
LitVar | rs141679163 |
Map | rs141679163 |
PheGenI | rs141679163 |
Biobank | rs141679163 |
1000 genomes | rs141679163 |
hgdp | rs141679163 |
ensembl | rs141679163 |
geneview | rs141679163 |
scholar | rs141679163 |
rs141679163 | |
pharmgkb | rs141679163 |
gwascentral | rs141679163 |
openSNP | rs141679163 |
23andMe | rs141679163 |
SNPshot | rs141679163 |
SNPdbe | rs141679163 |
MSV3d | rs141679163 |
GWAS Ctlg | rs141679163 |
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.