rs587780455
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common genotype |
| Make rs587780455(A;G) |
| Make rs587780455(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 12 |
| Position | 51807116 |
| Gene | SCN8A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs587780455 |
| dbSNP (classic) | rs587780455 |
| ClinGen | rs587780455 |
| ebi | rs587780455 |
| HLI | rs587780455 |
| Exac | rs587780455 |
| Gnomad | rs587780455 |
| Varsome | rs587780455 |
| LitVar | rs587780455 |
| Map | rs587780455 |
| PheGenI | rs587780455 |
| Biobank | rs587780455 |
| 1000 genomes | rs587780455 |
| hgdp | rs587780455 |
| ensembl | rs587780455 |
| geneview | rs587780455 |
| scholar | rs587780455 |
| rs587780455 | |
| pharmgkb | rs587780455 |
| gwascentral | rs587780455 |
| openSNP | rs587780455 |
| 23andMe | rs587780455 |
| SNPshot | rs587780455 |
| SNPdbe | rs587780455 |
| MSV3d | rs587780455 |
| GWAS Ctlg | rs587780455 |
| Max Magnitude | 0 |
aka NM_014191.3(SCN8A):c.5630A>G or (p.Asn1877Ser)
OMIM pathogenic variant
