rs1618355
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1618355(A;A) |
Make rs1618355(A;C) |
Make rs1618355(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 44406579 |
Gene | TRPM2 |
is a | snp |
is | mentioned by |
dbSNP | rs1618355 |
dbSNP (classic) | rs1618355 |
ClinGen | rs1618355 |
ebi | rs1618355 |
HLI | rs1618355 |
Exac | rs1618355 |
Gnomad | rs1618355 |
Varsome | rs1618355 |
LitVar | rs1618355 |
Map | rs1618355 |
PheGenI | rs1618355 |
Biobank | rs1618355 |
1000 genomes | rs1618355 |
hgdp | rs1618355 |
ensembl | rs1618355 |
geneview | rs1618355 |
scholar | rs1618355 |
rs1618355 | |
pharmgkb | rs1618355 |
gwascentral | rs1618355 |
openSNP | rs1618355 |
23andMe | rs1618355 |
SNPshot | rs1618355 |
SNPdbe | rs1618355 |
MSV3d | rs1618355 |
GWAS Ctlg | rs1618355 |
GMAF | 0.2911 |
Max Magnitude | 0 |
[PMID 19133961] rs1556314 associated with bipolar disorder type I
- C-T-A haplotype of SNPs rs1618355(C), rs933151(T), and rs749909(A) was significantly associated with early age at onset in BD-I families
[PMID 16252251] Association of the putative susceptibility gene, transient receptor potential protein melastatin type 2, with bipolar disorder.