rs121908217
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs121908217(A;A) |
| Make rs121908217(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 13308452 |
| Gene | CACNA1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs121908217 |
| dbSNP (classic) | rs121908217 |
| ClinGen | rs121908217 |
| ebi | rs121908217 |
| HLI | rs121908217 |
| Exac | rs121908217 |
| Gnomad | rs121908217 |
| Varsome | rs121908217 |
| LitVar | rs121908217 |
| Map | rs121908217 |
| PheGenI | rs121908217 |
| Biobank | rs121908217 |
| 1000 genomes | rs121908217 |
| hgdp | rs121908217 |
| ensembl | rs121908217 |
| geneview | rs121908217 |
| scholar | rs121908217 |
| rs121908217 | |
| pharmgkb | rs121908217 |
| gwascentral | rs121908217 |
| openSNP | rs121908217 |
| 23andMe | rs121908217 |
| SNPshot | rs121908217 |
| SNPdbe | rs121908217 |
| MSV3d | rs121908217 |
| GWAS Ctlg | rs121908217 |
| Merged from | Rs121909321 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs121908217(A;A) |
| Alt | rs121908217(A;A) |
| Reference | Rs121908217(G;G) |
| Significance | Pathogenic |
| Disease | Familial hemiplegic migraine type 1 Migraine Spinocerebellar ataxia 6 |
| Variation | info |
| Gene | CACNA1A |
| CLNDBN | Familial hemiplegic migraine type 1 Migraine, sporadic hemiplegic Spinocerebellar ataxia 6 |
| Reversed | 1 |
| HGVS | NC_000019.9:g.13419266C>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (variants) |
| CLNACC | RCV000009028.8, RCV000009029.6, RCV000009030.5, |
[PMID 11439943] The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
