rs730880059
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs730880059(A;A) |
Make rs730880059(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 10 |
Position | 18539383 |
Gene | CACNB2, NSUN6 |
is a | snp |
is | mentioned by |
dbSNP | rs730880059 |
dbSNP (classic) | rs730880059 |
ClinGen | rs730880059 |
ebi | rs730880059 |
HLI | rs730880059 |
Exac | rs730880059 |
Gnomad | rs730880059 |
Varsome | rs730880059 |
LitVar | rs730880059 |
Map | rs730880059 |
PheGenI | rs730880059 |
Biobank | rs730880059 |
1000 genomes | rs730880059 |
hgdp | rs730880059 |
ensembl | rs730880059 |
geneview | rs730880059 |
scholar | rs730880059 |
rs730880059 | |
pharmgkb | rs730880059 |
gwascentral | rs730880059 |
openSNP | rs730880059 |
23andMe | rs730880059 |
SNPshot | rs730880059 |
SNPdbe | rs730880059 |
MSV3d | rs730880059 |
GWAS Ctlg | rs730880059 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730880059(A;A) |
Alt | rs730880059(A;A) |
Reference | Rs730880059(G;G) |
Significance | Probable-Pathogenic |
Disease | Cardiac arrest not provided |
Variation | info |
Gene | CACNB2 |
CLNDBN | Cardiac arrest not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.18828312G>A |
CLNSRC | |
CLNACC | RCV000157131.1, RCV000170873.2, |