rs28933368
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs28933368(A;A) |
| Make rs28933368(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 39725721 |
| Gene | ERBB2, MIR4728 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs28933368 |
| dbSNP (classic) | rs28933368 |
| ClinGen | rs28933368 |
| ebi | rs28933368 |
| HLI | rs28933368 |
| Exac | rs28933368 |
| Gnomad | rs28933368 |
| Varsome | rs28933368 |
| LitVar | rs28933368 |
| Map | rs28933368 |
| PheGenI | rs28933368 |
| Biobank | rs28933368 |
| 1000 genomes | rs28933368 |
| hgdp | rs28933368 |
| ensembl | rs28933368 |
| geneview | rs28933368 |
| scholar | rs28933368 |
| rs28933368 | |
| pharmgkb | rs28933368 |
| gwascentral | rs28933368 |
| openSNP | rs28933368 |
| 23andMe | rs28933368 |
| SNPshot | rs28933368 |
| SNPdbe | rs28933368 |
| MSV3d | rs28933368 |
| GWAS Ctlg | rs28933368 |
| Max Magnitude | 0 |
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
| ClinVar | |
|---|---|
| Risk | rs28933368(A;A) |
| Alt | rs28933368(A;A) |
| Reference | Rs28933368(G;G) |
| Significance | Pathogenic |
| Disease | Glioma susceptibility 1 |
| Variation | info |
| Gene | MIR4728 ERBB2 |
| CLNDBN | Glioma susceptibility 1 |
| Reversed | 0 |
| HGVS | NC_000017.10:g.37881974G>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000014892.5, |
