rs752611838
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs752611838(A;A) |
| Make rs752611838(A;C) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 17 |
| Position | 63944804 |
| Gene | SCN4A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs752611838 |
| dbSNP (classic) | rs752611838 |
| ClinGen | rs752611838 |
| ebi | rs752611838 |
| HLI | rs752611838 |
| Exac | rs752611838 |
| Gnomad | rs752611838 |
| Varsome | rs752611838 |
| LitVar | rs752611838 |
| Map | rs752611838 |
| PheGenI | rs752611838 |
| Biobank | rs752611838 |
| 1000 genomes | rs752611838 |
| hgdp | rs752611838 |
| ensembl | rs752611838 |
| geneview | rs752611838 |
| scholar | rs752611838 |
| rs752611838 | |
| pharmgkb | rs752611838 |
| gwascentral | rs752611838 |
| openSNP | rs752611838 |
| 23andMe | rs752611838 |
| SNPshot | rs752611838 |
| SNPdbe | rs752611838 |
| MSV3d | rs752611838 |
| GWAS Ctlg | rs752611838 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs752611838(A;A) |
| Alt | rs752611838(A;A) |
| Reference | Rs752611838(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | SCN4A |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000017.10:g.62022164C>A |
| CLNSRC | |
| CLNACC | RCV000493171.1, |
