rs773926353
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs773926353(C;G) |
Make rs773926353(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 19 |
Position | 38467667 |
Gene | RYR1 |
is a | snp |
is | mentioned by |
dbSNP | rs773926353 |
dbSNP (classic) | rs773926353 |
ClinGen | rs773926353 |
ebi | rs773926353 |
HLI | rs773926353 |
Exac | rs773926353 |
Gnomad | rs773926353 |
Varsome | rs773926353 |
LitVar | rs773926353 |
Map | rs773926353 |
PheGenI | rs773926353 |
Biobank | rs773926353 |
1000 genomes | rs773926353 |
hgdp | rs773926353 |
ensembl | rs773926353 |
geneview | rs773926353 |
scholar | rs773926353 |
rs773926353 | |
pharmgkb | rs773926353 |
gwascentral | rs773926353 |
openSNP | rs773926353 |
23andMe | rs773926353 |
SNPshot | rs773926353 |
SNPdbe | rs773926353 |
MSV3d | rs773926353 |
GWAS Ctlg | rs773926353 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs773926353(G;G) rs773926353(T;T) |
Alt | rs773926353(G;G) rs773926353(T;T) |
Reference | Rs773926353(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | RYR1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.38958307C>G |
CLNSRC | |
CLNACC | RCV000182604.1, |