rs150061718
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs150061718(C;C) |
Make rs150061718(C;T) |
Make rs150061718(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 13 |
Position | 98385747 |
Gene | FARP1 |
is a | snp |
is | mentioned by |
dbSNP | rs150061718 |
dbSNP (classic) | rs150061718 |
ClinGen | rs150061718 |
ebi | rs150061718 |
HLI | rs150061718 |
Exac | rs150061718 |
Gnomad | rs150061718 |
Varsome | rs150061718 |
LitVar | rs150061718 |
Map | rs150061718 |
PheGenI | rs150061718 |
Biobank | rs150061718 |
1000 genomes | rs150061718 |
hgdp | rs150061718 |
ensembl | rs150061718 |
geneview | rs150061718 |
scholar | rs150061718 |
rs150061718 | |
pharmgkb | rs150061718 |
gwascentral | rs150061718 |
openSNP | rs150061718 |
23andMe | rs150061718 |
SNPshot | rs150061718 |
SNPdbe | rs150061718 |
MSV3d | rs150061718 |
GWAS Ctlg | rs150061718 |
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.