rs863224532
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;G) | 6 | Brugada Syndrome |
Make rs863224532(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 38560210 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs863224532 |
dbSNP (classic) | rs863224532 |
ClinGen | rs863224532 |
ebi | rs863224532 |
HLI | rs863224532 |
Exac | rs863224532 |
Gnomad | rs863224532 |
Varsome | rs863224532 |
LitVar | rs863224532 |
Map | rs863224532 |
PheGenI | rs863224532 |
Biobank | rs863224532 |
1000 genomes | rs863224532 |
hgdp | rs863224532 |
ensembl | rs863224532 |
geneview | rs863224532 |
scholar | rs863224532 |
rs863224532 | |
pharmgkb | rs863224532 |
gwascentral | rs863224532 |
openSNP | rs863224532 |
23andMe | rs863224532 |
SNPshot | rs863224532 |
SNPdbe | rs863224532 |
MSV3d | rs863224532 |
GWAS Ctlg | rs863224532 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863224532(G;G) |
Alt | rs863224532(G;G) |
Reference | Rs863224532(C;C) |
Significance | Pathogenic |
Disease | Brugada syndrome |
Variation | info |
Gene | SCN5A |
CLNDBN | Brugada syndrome |
Reversed | 1 |
HGVS | NC_000003.11:g.38601701G>C |
CLNSRC | |
CLNACC | RCV000199303.1, |