rs886037903
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(CT;CT) | 0 | common in clinvar |
Make rs886037903(-;-) |
Make rs886037903(-;CT) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 3 |
Position | 38551015 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs886037903 |
dbSNP (classic) | rs886037903 |
ClinGen | rs886037903 |
ebi | rs886037903 |
HLI | rs886037903 |
Exac | rs886037903 |
Gnomad | rs886037903 |
Varsome | rs886037903 |
LitVar | rs886037903 |
Map | rs886037903 |
PheGenI | rs886037903 |
Biobank | rs886037903 |
1000 genomes | rs886037903 |
hgdp | rs886037903 |
ensembl | rs886037903 |
geneview | rs886037903 |
scholar | rs886037903 |
rs886037903 | |
pharmgkb | rs886037903 |
gwascentral | rs886037903 |
openSNP | rs886037903 |
23andMe | rs886037903 |
SNPshot | rs886037903 |
SNPdbe | rs886037903 |
MSV3d | rs886037903 |
GWAS Ctlg | rs886037903 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886037903(-;-) |
Alt | rs886037903(-;-) |
Reference | Rs886037903(CT;CT) |
Significance | Probable-Pathogenic |
Disease | Brugada syndrome 1 |
Variation | info |
Gene | SCN5A |
CLNDBN | Brugada syndrome 1 |
Reversed | 1 |
HGVS | NC_000003.11:g.38592506_38592507delAG |
CLNSRC | |
CLNACC | RCV000240623.1, |