Rs2306677
From SNPedia
| Orientation | minus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2306677 |
| PheGenI | rs2306677 |
| nextbio | rs2306677 |
| hapmap | rs2306677 |
| 1000 genomes | rs2306677 |
| hgdp | rs2306677 |
| ensembl | rs2306677 |
| gopubmed | rs2306677 |
| geneview | rs2306677 |
| scholar | rs2306677 |
| rs2306677 | |
| pharmgkb | rs2306677 |
| gwascentral | rs2306677 |
| openSNP | rs2306677 |
| 23andMe | rs2306677 |
| 23andMe all | rs2306677 |
| SNP Nexus | |
| SNPshot | rs2306677 |
| SNPdbe | rs2306677 |
| MSV3d | rs2306677 |
| Gene | ITPR2 |
| Chromosome | 12 |
| Orientation | minus |
| GMAF | 0.19 |
| Position | 26636386 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 |
| Make rs2306677(C;T) |
| Make rs2306677(T;T) |
| ? | (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.
| GET Evidence | |
|---|---|
| rs2306677 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.773438 |
| summary | |
[PMID 22795786] No association of five candidate genetic variants with amyotrophic lateral sclerosis in a Chinese population
