Rs119485088
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs119485088 |
| PheGenI | rs119485088 |
| nextbio | rs119485088 |
| hapmap | rs119485088 |
| 1000 genomes | rs119485088 |
| hgdp | rs119485088 |
| ensembl | rs119485088 |
| gopubmed | rs119485088 |
| geneview | rs119485088 |
| scholar | rs119485088 |
| rs119485088 | |
| pharmgkb | rs119485088 |
| gwascentral | rs119485088 |
| openSNP | rs119485088 |
| 23andMe | rs119485088 |
| 23andMe all | rs119485088 |
| SNP Nexus | |
| SNPshot | rs119485088 |
| SNPdbe | rs119485088 |
| MSV3d | rs119485088 |
| Gene | GAN |
| Chromosome | 16 |
| Orientation | plus |
| Position | 81399037 |
| Reference | GRCh37 37.1/132 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs119485088(A;A) |
| Make rs119485088(A;G) |
| ClinVar | |
|---|---|
| Risk | rs119485088(A;A) |
| Normal | rs119485088(G;G) |
| Significance | 5 |
| Disease | Giant axonal neuropathy |
| ClinVar | info |
| Gene | GAN |
| CLNDBN | Giant axonal neuropathy |
| Reversed | 0 |
| CLNHGVS | NC_000016.9:g.81399037G>A |
| CLNSRC | OMIM Allelic Variant |
