rs863225273
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 6 | Brugada Syndrome |
(G;G) | 0 | common in clinvar |
Make rs863225273(A;A) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 38554320 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs863225273 |
dbSNP (classic) | rs863225273 |
ClinGen | rs863225273 |
ebi | rs863225273 |
HLI | rs863225273 |
Exac | rs863225273 |
Gnomad | rs863225273 |
Varsome | rs863225273 |
LitVar | rs863225273 |
Map | rs863225273 |
PheGenI | rs863225273 |
Biobank | rs863225273 |
1000 genomes | rs863225273 |
hgdp | rs863225273 |
ensembl | rs863225273 |
geneview | rs863225273 |
scholar | rs863225273 |
rs863225273 | |
pharmgkb | rs863225273 |
gwascentral | rs863225273 |
openSNP | rs863225273 |
23andMe | rs863225273 |
SNPshot | rs863225273 |
SNPdbe | rs863225273 |
MSV3d | rs863225273 |
GWAS Ctlg | rs863225273 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs863225273(A;A) |
Alt | rs863225273(A;A) |
Reference | Rs863225273(G;G) |
Significance | Pathogenic |
Disease | Brugada syndrome |
Variation | info |
Gene | SCN5A |
CLNDBN | Brugada syndrome |
Reversed | 1 |
HGVS | NC_000003.11:g.38595811C>T |
CLNSRC | |
CLNACC | RCV000201896.1, |