rs111888148
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 3 | malignant hyperthermia |
(G;G) | 0 | common in clinvar |
Make rs111888148(A;A) |
Reference | GRCh38 38.1/142 |
Chromosome | 19 |
Position | 38455463 |
Gene | RYR1 |
is a | snp |
is | mentioned by |
dbSNP | rs111888148 |
dbSNP (classic) | rs111888148 |
ClinGen | rs111888148 |
ebi | rs111888148 |
HLI | rs111888148 |
Exac | rs111888148 |
Gnomad | rs111888148 |
Varsome | rs111888148 |
LitVar | rs111888148 |
Map | rs111888148 |
PheGenI | rs111888148 |
Biobank | rs111888148 |
1000 genomes | rs111888148 |
hgdp | rs111888148 |
ensembl | rs111888148 |
geneview | rs111888148 |
scholar | rs111888148 |
rs111888148 | |
pharmgkb | rs111888148 |
gwascentral | rs111888148 |
openSNP | rs111888148 |
23andMe | rs111888148 |
SNPshot | rs111888148 |
SNPdbe | rs111888148 |
MSV3d | rs111888148 |
GWAS Ctlg | rs111888148 |
Max Magnitude | 3 |
aka c.1589G>A (p.Arg530His or R530H)
23andMe name: i6017722
ClinVar | |
---|---|
Risk | rs111888148(A;A) rs111888148(T;T) |
Alt | rs111888148(A;A) rs111888148(T;T) |
Reference | Rs111888148(G;G) |
Significance | Pathogenic |
Disease | not provided Malignant hyperthermia not specified |
Variation | info |
Gene | RYR1 |
CLNDBN | not provided Malignant hyperthermia, susceptibility to, 1 not specified |
Reversed | 0 |
HGVS | NC_000019.9:g.38946103G>A; NC_000019.9:g.38946103G>T |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000119576.1, RCV000148805.1, RCV000194141.1, |