rs933151
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs933151(C;C) |
| Make rs933151(C;T) |
| Make rs933151(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 44416122 |
| Gene | TRPM2, TRPM2-AS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs933151 |
| dbSNP (classic) | rs933151 |
| ClinGen | rs933151 |
| ebi | rs933151 |
| HLI | rs933151 |
| Exac | rs933151 |
| Gnomad | rs933151 |
| Varsome | rs933151 |
| LitVar | rs933151 |
| Map | rs933151 |
| PheGenI | rs933151 |
| Biobank | rs933151 |
| 1000 genomes | rs933151 |
| hgdp | rs933151 |
| ensembl | rs933151 |
| geneview | rs933151 |
| scholar | rs933151 |
| rs933151 | |
| pharmgkb | rs933151 |
| gwascentral | rs933151 |
| openSNP | rs933151 |
| 23andMe | rs933151 |
| SNPshot | rs933151 |
| SNPdbe | rs933151 |
| MSV3d | rs933151 |
| GWAS Ctlg | rs933151 |
| GMAF | 0.2429 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[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 32046066
] One Single Nucleotide Polymorphism of the TRPM2 Channel Gene Identified as a Risk Factor in Bipolar Disorder Associates with Autism Spectrum Disorder in a Japanese Population.
[PMID 32100228] Associations Between Genomic Variants in lncRNA-TRPM2-AS and lncRNA-HNF1A-AS1 Genes and Risk of Multiple Sclerosis.
