rs138859323
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common genotype |
| Make rs138859323(A;A) |
| Make rs138859323(A;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 2 |
| Position | 144404939 |
| Gene | ZEB2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs138859323 |
| dbSNP (classic) | rs138859323 |
| ClinGen | rs138859323 |
| ebi | rs138859323 |
| HLI | rs138859323 |
| Exac | rs138859323 |
| Gnomad | rs138859323 |
| Varsome | rs138859323 |
| LitVar | rs138859323 |
| Map | rs138859323 |
| PheGenI | rs138859323 |
| Biobank | rs138859323 |
| 1000 genomes | rs138859323 |
| hgdp | rs138859323 |
| ensembl | rs138859323 |
| geneview | rs138859323 |
| scholar | rs138859323 |
| rs138859323 | |
| pharmgkb | rs138859323 |
| gwascentral | rs138859323 |
| openSNP | rs138859323 |
| 23andMe | rs138859323 |
| SNPshot | rs138859323 |
| SNPdbe | rs138859323 |
| MSV3d | rs138859323 |
| GWAS Ctlg | rs138859323 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs138859323(A;A) |
| Alt | rs138859323(A;A) |
| Reference | Rs138859323(G;G) |
| Significance | Other |
| Disease | not specified Mowat-Wilson syndrome |
| Variation | info |
| Gene | ZEB2 |
| CLNDBN | not specified Mowat-Wilson syndrome |
| Reversed | 0 |
| HGVS | NC_000002.11:g.145162506G>A |
| CLNSRC | |
| CLNACC | RCV000081671.8, RCV000353189.1, |
