rs560020203
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs560020203(C;T) |
| Make rs560020203(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 10 |
| Position | 18538188 |
| Gene | CACNB2, NSUN6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs560020203 |
| dbSNP (classic) | rs560020203 |
| ClinGen | rs560020203 |
| ebi | rs560020203 |
| HLI | rs560020203 |
| Exac | rs560020203 |
| Gnomad | rs560020203 |
| Varsome | rs560020203 |
| LitVar | rs560020203 |
| Map | rs560020203 |
| PheGenI | rs560020203 |
| Biobank | rs560020203 |
| 1000 genomes | rs560020203 |
| hgdp | rs560020203 |
| ensembl | rs560020203 |
| geneview | rs560020203 |
| scholar | rs560020203 |
| rs560020203 | |
| pharmgkb | rs560020203 |
| gwascentral | rs560020203 |
| openSNP | rs560020203 |
| 23andMe | rs560020203 |
| SNPshot | rs560020203 |
| SNPdbe | rs560020203 |
| MSV3d | rs560020203 |
| GWAS Ctlg | rs560020203 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs560020203(A;A) rs560020203(T;T) |
| Alt | rs560020203(A;A) rs560020203(T;T) |
| Reference | Rs560020203(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | CACNB2 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000010.10:g.18827117C>A |
| CLNSRC | |
| CLNACC | RCV000170867.2, |
