rs760011764
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs760011764(A;G) |
Make rs760011764(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 38613766 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs760011764 |
dbSNP (classic) | rs760011764 |
ClinGen | rs760011764 |
ebi | rs760011764 |
HLI | rs760011764 |
Exac | rs760011764 |
Gnomad | rs760011764 |
Varsome | rs760011764 |
LitVar | rs760011764 |
Map | rs760011764 |
PheGenI | rs760011764 |
Biobank | rs760011764 |
1000 genomes | rs760011764 |
hgdp | rs760011764 |
ensembl | rs760011764 |
geneview | rs760011764 |
scholar | rs760011764 |
rs760011764 | |
pharmgkb | rs760011764 |
gwascentral | rs760011764 |
openSNP | rs760011764 |
23andMe | rs760011764 |
SNPshot | rs760011764 |
SNPdbe | rs760011764 |
MSV3d | rs760011764 |
GWAS Ctlg | rs760011764 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs760011764(G;G) |
Alt | rs760011764(G;G) |
Reference | Rs760011764(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided not specified Brugada syndrome |
Variation | info |
Gene | SCN5A |
CLNDBN | not provided not specified Brugada syndrome |
Reversed | 0 |
HGVS | NC_000003.11:g.38655257A>G |
CLNSRC | |
CLNACC | RCV000182943.2, RCV000223856.1, RCV000229800.1, |