rs539821357
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs539821357(A;A) |
| Make rs539821357(A;C) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 18 |
| Position | 31546425 |
| Gene | DSG2, DSG2-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs539821357 |
| dbSNP (classic) | rs539821357 |
| ClinGen | rs539821357 |
| ebi | rs539821357 |
| HLI | rs539821357 |
| Exac | rs539821357 |
| Gnomad | rs539821357 |
| Varsome | rs539821357 |
| LitVar | rs539821357 |
| Map | rs539821357 |
| PheGenI | rs539821357 |
| Biobank | rs539821357 |
| 1000 genomes | rs539821357 |
| hgdp | rs539821357 |
| ensembl | rs539821357 |
| geneview | rs539821357 |
| scholar | rs539821357 |
| rs539821357 | |
| pharmgkb | rs539821357 |
| gwascentral | rs539821357 |
| openSNP | rs539821357 |
| 23andMe | rs539821357 |
| SNPshot | rs539821357 |
| SNPdbe | rs539821357 |
| MSV3d | rs539821357 |
| GWAS Ctlg | rs539821357 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs539821357(A;A) rs539821357(T;T) |
| Alt | rs539821357(A;A) rs539821357(T;T) |
| Reference | Rs539821357(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | DSG2-AS1 DSG2 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000018.9:g.29126388C>A |
| CLNSRC | |
| CLNACC | RCV000431080.1, |
