rs727505158
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;C) | 6 | Brugada Syndrome |
(C;C) | 0 | common in clinvar |
Make rs727505158(-;-) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 38599005 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs727505158 |
dbSNP (classic) | rs727505158 |
ClinGen | rs727505158 |
ebi | rs727505158 |
HLI | rs727505158 |
Exac | rs727505158 |
Gnomad | rs727505158 |
Varsome | rs727505158 |
LitVar | rs727505158 |
Map | rs727505158 |
PheGenI | rs727505158 |
Biobank | rs727505158 |
1000 genomes | rs727505158 |
hgdp | rs727505158 |
ensembl | rs727505158 |
geneview | rs727505158 |
scholar | rs727505158 |
rs727505158 | |
pharmgkb | rs727505158 |
gwascentral | rs727505158 |
openSNP | rs727505158 |
23andMe | rs727505158 |
SNPshot | rs727505158 |
SNPdbe | rs727505158 |
MSV3d | rs727505158 |
GWAS Ctlg | rs727505158 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs727505158(-;-) |
Alt | rs727505158(-;-) |
Reference | Rs727505158(C;C) |
Significance | Pathogenic |
Disease | Brugada syndrome not provided |
Variation | info |
Gene | SCN5A |
CLNDBN | Brugada syndrome not provided |
Reversed | 1 |
HGVS | NC_000003.11:g.38640496delG |
CLNSRC | |
CLNACC | RCV000156628.4, RCV000183151.4, |