rs201641342
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs201641342(A;A) |
Make rs201641342(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 38603950 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs201641342 |
dbSNP (classic) | rs201641342 |
ClinGen | rs201641342 |
ebi | rs201641342 |
HLI | rs201641342 |
Exac | rs201641342 |
Gnomad | rs201641342 |
Varsome | rs201641342 |
LitVar | rs201641342 |
Map | rs201641342 |
PheGenI | rs201641342 |
Biobank | rs201641342 |
1000 genomes | rs201641342 |
hgdp | rs201641342 |
ensembl | rs201641342 |
geneview | rs201641342 |
scholar | rs201641342 |
rs201641342 | |
pharmgkb | rs201641342 |
gwascentral | rs201641342 |
openSNP | rs201641342 |
23andMe | rs201641342 |
SNPshot | rs201641342 |
SNPdbe | rs201641342 |
MSV3d | rs201641342 |
GWAS Ctlg | rs201641342 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201641342(A;A) |
Alt | rs201641342(A;A) |
Reference | Rs201641342(G;G) |
Significance | Probable-Pathogenic |
Disease | Brugada syndrome |
Variation | info |
Gene | SCN5A |
CLNDBN | Brugada syndrome |
Reversed | 0 |
HGVS | NC_000003.11:g.38645441G>A |
CLNSRC | |
CLNACC | RCV000171573.1, |