rs112563513
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 3 | malignant hyperthermia |
(G;G) | 0 | common in clinvar |
Make rs112563513(A;A) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 19 |
Position | 38499223 |
Gene | RYR1 |
is a | snp |
is | mentioned by |
dbSNP | rs112563513 |
dbSNP (classic) | rs112563513 |
ClinGen | rs112563513 |
ebi | rs112563513 |
HLI | rs112563513 |
Exac | rs112563513 |
Gnomad | rs112563513 |
Varsome | rs112563513 |
LitVar | rs112563513 |
Map | rs112563513 |
PheGenI | rs112563513 |
Biobank | rs112563513 |
1000 genomes | rs112563513 |
hgdp | rs112563513 |
ensembl | rs112563513 |
geneview | rs112563513 |
scholar | rs112563513 |
rs112563513 | |
pharmgkb | rs112563513 |
gwascentral | rs112563513 |
openSNP | rs112563513 |
23andMe | rs112563513 |
SNPshot | rs112563513 |
SNPdbe | rs112563513 |
MSV3d | rs112563513 |
GWAS Ctlg | rs112563513 |
Max Magnitude | 3 |
aka c.7007G>A (p.Arg2336His or R2336H)
23andMe name: i6017686
ClinVar | |
---|---|
Risk | rs112563513(A;A) |
Alt | rs112563513(A;A) |
Reference | Rs112563513(G;G) |
Significance | Untested |
Disease | not provided |
Variation | info |
Gene | RYR1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.38989863G>A |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000119673.1, |