rs78098482
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs78098482(A;A) |
| Make rs78098482(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 10 |
| Position | 43109146 |
| Gene | RET |
| is a | snp |
| is | mentioned by |
| dbSNP | rs78098482 |
| dbSNP (classic) | rs78098482 |
| ClinGen | rs78098482 |
| ebi | rs78098482 |
| HLI | rs78098482 |
| Exac | rs78098482 |
| Gnomad | rs78098482 |
| Varsome | rs78098482 |
| LitVar | rs78098482 |
| Map | rs78098482 |
| PheGenI | rs78098482 |
| Biobank | rs78098482 |
| 1000 genomes | rs78098482 |
| hgdp | rs78098482 |
| ensembl | rs78098482 |
| geneview | rs78098482 |
| scholar | rs78098482 |
| rs78098482 | |
| pharmgkb | rs78098482 |
| gwascentral | rs78098482 |
| openSNP | rs78098482 |
| 23andMe | rs78098482 |
| SNPshot | rs78098482 |
| SNPdbe | rs78098482 |
| MSV3d | rs78098482 |
| GWAS Ctlg | rs78098482 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs78098482(A;A) |
| Alt | rs78098482(A;A) |
| Reference | Rs78098482(C;C) |
| Significance | Other |
| Disease | Hirschsprung disease 1 |
| Variation | info |
| Gene | RET |
| CLNDBN | Hirschsprung disease 1 |
| Reversed | 0 |
| HGVS | NC_000010.10:g.43604594C>A |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000014952.2, |
