rs201845396
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs201845396(C;T) |
| Make rs201845396(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 18 |
| Position | 31545856 |
| Gene | DSG2, DSG2-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs201845396 |
| dbSNP (classic) | rs201845396 |
| ClinGen | rs201845396 |
| ebi | rs201845396 |
| HLI | rs201845396 |
| Exac | rs201845396 |
| Gnomad | rs201845396 |
| Varsome | rs201845396 |
| LitVar | rs201845396 |
| Map | rs201845396 |
| PheGenI | rs201845396 |
| Biobank | rs201845396 |
| 1000 genomes | rs201845396 |
| hgdp | rs201845396 |
| ensembl | rs201845396 |
| geneview | rs201845396 |
| scholar | rs201845396 |
| rs201845396 | |
| pharmgkb | rs201845396 |
| gwascentral | rs201845396 |
| openSNP | rs201845396 |
| 23andMe | rs201845396 |
| SNPshot | rs201845396 |
| SNPdbe | rs201845396 |
| MSV3d | rs201845396 |
| GWAS Ctlg | rs201845396 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs201845396(G;G) rs201845396(T;T) |
| Alt | rs201845396(G;G) rs201845396(T;T) |
| Reference | Rs201845396(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not specified not provided |
| Variation | info |
| Gene | DSG2-AS1 DSG2 |
| CLNDBN | not specified not provided |
| Reversed | 0 |
| HGVS | NC_000018.9:g.29125819C>T |
| CLNSRC | |
| CLNACC | RCV000219803.1, RCV000489296.1, |
