rs794728914
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;TT) | 6 | Brugada Syndrome |
(TT;TT) | 0 | common in clinvar |
Make rs794728914(-;-) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 38585895 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs794728914 |
dbSNP (classic) | rs794728914 |
ClinGen | rs794728914 |
ebi | rs794728914 |
HLI | rs794728914 |
Exac | rs794728914 |
Gnomad | rs794728914 |
Varsome | rs794728914 |
LitVar | rs794728914 |
Map | rs794728914 |
PheGenI | rs794728914 |
Biobank | rs794728914 |
1000 genomes | rs794728914 |
hgdp | rs794728914 |
ensembl | rs794728914 |
geneview | rs794728914 |
scholar | rs794728914 |
rs794728914 | |
pharmgkb | rs794728914 |
gwascentral | rs794728914 |
openSNP | rs794728914 |
23andMe | rs794728914 |
SNPshot | rs794728914 |
SNPdbe | rs794728914 |
MSV3d | rs794728914 |
GWAS Ctlg | rs794728914 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs794728914(-;-) |
Alt | rs794728914(-;-) |
Reference | Rs794728914(TT;TT) |
Significance | Pathogenic |
Disease | not provided Brugada syndrome |
Variation | info |
Gene | SCN5A |
CLNDBN | not provided Brugada syndrome |
Reversed | 1 |
HGVS | NC_000003.11:g.38627386_38627387delAA |
CLNSRC | |
CLNACC | RCV000183155.1, RCV000201886.1, |