rs768711283
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs768711283(A;A) |
Make rs768711283(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 237770827 |
Gene | RYR2 |
is a | snp |
is | mentioned by |
dbSNP | rs768711283 |
dbSNP (classic) | rs768711283 |
ClinGen | rs768711283 |
ebi | rs768711283 |
HLI | rs768711283 |
Exac | rs768711283 |
Gnomad | rs768711283 |
Varsome | rs768711283 |
LitVar | rs768711283 |
Map | rs768711283 |
PheGenI | rs768711283 |
Biobank | rs768711283 |
1000 genomes | rs768711283 |
hgdp | rs768711283 |
ensembl | rs768711283 |
geneview | rs768711283 |
scholar | rs768711283 |
rs768711283 | |
pharmgkb | rs768711283 |
gwascentral | rs768711283 |
openSNP | rs768711283 |
23andMe | rs768711283 |
SNPshot | rs768711283 |
SNPdbe | rs768711283 |
MSV3d | rs768711283 |
GWAS Ctlg | rs768711283 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs768711283(A;A) |
Alt | rs768711283(A;A) |
Reference | Rs768711283(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | RYR2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.237934127G>A |
CLNSRC | |
CLNACC | RCV000182796.2, |