rs104893937
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs104893937(A;A) |
| Make rs104893937(A;C) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 5 |
| Position | 176621218 |
| Gene | SNCB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs104893937 |
| dbSNP (classic) | rs104893937 |
| ClinGen | rs104893937 |
| ebi | rs104893937 |
| HLI | rs104893937 |
| Exac | rs104893937 |
| Gnomad | rs104893937 |
| Varsome | rs104893937 |
| LitVar | rs104893937 |
| Map | rs104893937 |
| PheGenI | rs104893937 |
| Biobank | rs104893937 |
| 1000 genomes | rs104893937 |
| hgdp | rs104893937 |
| ensembl | rs104893937 |
| geneview | rs104893937 |
| scholar | rs104893937 |
| rs104893937 | |
| pharmgkb | rs104893937 |
| gwascentral | rs104893937 |
| openSNP | rs104893937 |
| 23andMe | rs104893937 |
| SNPshot | rs104893937 |
| SNPdbe | rs104893937 |
| MSV3d | rs104893937 |
| GWAS Ctlg | rs104893937 |
| GMAF | 0.0009183 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs104893937(A;A) |
| Alt | rs104893937(A;A) |
| Reference | Rs104893937(C;C) |
| Significance | Pathogenic |
| Disease | Lewy body dementia |
| Variation | info |
| Gene | SNCB |
| CLNDBN | Lewy body dementia |
| Reversed | 1 |
| HGVS | NC_000005.9:g.176048219G>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000007441.2, |
