rs193922826
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common |
| (C;T) | 3 | susceptibility to malignant hyperthermia |
| Make rs193922826(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 38504319 |
| Gene | RYR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs193922826 |
| dbSNP (classic) | rs193922826 |
| ClinGen | rs193922826 |
| ebi | rs193922826 |
| HLI | rs193922826 |
| Exac | rs193922826 |
| Gnomad | rs193922826 |
| Varsome | rs193922826 |
| LitVar | rs193922826 |
| Map | rs193922826 |
| PheGenI | rs193922826 |
| Biobank | rs193922826 |
| 1000 genomes | rs193922826 |
| hgdp | rs193922826 |
| ensembl | rs193922826 |
| geneview | rs193922826 |
| scholar | rs193922826 |
| rs193922826 | |
| pharmgkb | rs193922826 |
| gwascentral | rs193922826 |
| openSNP | rs193922826 |
| 23andMe | rs193922826 |
| SNPshot | rs193922826 |
| SNPdbe | rs193922826 |
| MSV3d | rs193922826 |
| GWAS Ctlg | rs193922826 |
| Merged from | Rs28934001 |
| Max Magnitude | 3 |
| ClinVar | |
|---|---|
| Risk | rs193922826(T;T) |
| Alt | rs193922826(T;T) |
| Reference | Rs193922826(C;C) |
| Significance | Other |
| Disease | Malignant hyperthermia not provided |
| Variation | info |
| Gene | RYR1 |
| CLNDBN | Malignant hyperthermia, susceptibility to, 1 not provided |
| Reversed | 0 |
| HGVS | NC_000019.9:g.38994959C>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000013857.2, RCV000119737.2, |
[PMID 16163667] Correlations between genotype and pharmacological, histological, functional, and clinical phenotypes in malignant hyperthermia susceptibility.
[PMID 16917943] Mutations in RYR1 in malignant hyperthermia and central core disease.
