rs2306677
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 |
| Make rs2306677(C;T) |
| Make rs2306677(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 26483453 |
| Gene | ITPR2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2306677 |
| dbSNP (classic) | rs2306677 |
| ClinGen | rs2306677 |
| ebi | rs2306677 |
| HLI | rs2306677 |
| Exac | rs2306677 |
| Gnomad | rs2306677 |
| Varsome | rs2306677 |
| LitVar | rs2306677 |
| Map | rs2306677 |
| PheGenI | rs2306677 |
| Biobank | rs2306677 |
| 1000 genomes | rs2306677 |
| hgdp | rs2306677 |
| ensembl | rs2306677 |
| geneview | rs2306677 |
| scholar | rs2306677 |
| rs2306677 | |
| pharmgkb | rs2306677 |
| gwascentral | rs2306677 |
| openSNP | rs2306677 |
| 23andMe | rs2306677 |
| SNPshot | rs2306677 |
| SNPdbe | rs2306677 |
| MSV3d | rs2306677 |
| GWAS Ctlg | rs2306677 |
| GMAF | 0.1901 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS | |
|---|---|
| SNP | rs2306677 |
| PubMedID | [PMID 17827064] |
| Condition | Amyotrophic lateral sclerosis |
| Gene | ITPR2 |
| Risk Allele | |
| pValue | 3.00E-006 |
| OR | 1.58 |
| 95% CI | 1.30-1.91 |
[PMID 19193627
] A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis.
[PMID 22795786] No association of five candidate genetic variants with amyotrophic lateral sclerosis in a Chinese population
