rs2159100
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common/normal |
(C;T) | ||
(T;T) | 2.36 increased odds of bipolar disorder |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 2237227 |
Gene | CACNA1C |
is a | snp |
is | mentioned by |
dbSNP | rs2159100 |
dbSNP (classic) | rs2159100 |
ClinGen | rs2159100 |
ebi | rs2159100 |
HLI | rs2159100 |
Exac | rs2159100 |
Gnomad | rs2159100 |
Varsome | rs2159100 |
LitVar | rs2159100 |
Map | rs2159100 |
PheGenI | rs2159100 |
Biobank | rs2159100 |
1000 genomes | rs2159100 |
hgdp | rs2159100 |
ensembl | rs2159100 |
geneview | rs2159100 |
scholar | rs2159100 |
rs2159100 | |
pharmgkb | rs2159100 |
gwascentral | rs2159100 |
openSNP | rs2159100 |
23andMe | rs2159100 |
SNPshot | rs2159100 |
SNPdbe | rs2159100 |
MSV3d | rs2159100 |
GWAS Ctlg | rs2159100 |
GMAF | 0.3053 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
23andMe blog ([PMID 18711365]) rs1006737 or (rs2159100) Each T at this SNP increased the odds of bipolar disorder by 1.18 times compared to having two CC copies
[PMID 25453756] A role for noncoding variation in schizophrenia. This study finds evidence for rs2159100 allele T as a factor in schizophrenia.