rs786205418
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs786205418(-;GTGA) |
Make rs786205418(GTGA;GTGA) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 73343384 |
Gene | HCN4, LOC105370890 |
is a | snp |
is | mentioned by |
dbSNP | rs786205418 |
dbSNP (classic) | rs786205418 |
ClinGen | rs786205418 |
ebi | rs786205418 |
HLI | rs786205418 |
Exac | rs786205418 |
Gnomad | rs786205418 |
Varsome | rs786205418 |
LitVar | rs786205418 |
Map | rs786205418 |
PheGenI | rs786205418 |
Biobank | rs786205418 |
1000 genomes | rs786205418 |
hgdp | rs786205418 |
ensembl | rs786205418 |
geneview | rs786205418 |
scholar | rs786205418 |
rs786205418 | |
pharmgkb | rs786205418 |
gwascentral | rs786205418 |
openSNP | rs786205418 |
23andMe | rs786205418 |
SNPshot | rs786205418 |
SNPdbe | rs786205418 |
MSV3d | rs786205418 |
GWAS Ctlg | rs786205418 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786205418(GAGT;GAGT) |
Alt | rs786205418(GAGT;GAGT) |
Reference | Rs786205418(-;-) |
Significance | Pathogenic |
Disease | Brugada syndrome 8 Ventricular tachycardia |
Variation | info |
Gene | HCN4 |
CLNDBN | Brugada syndrome 8 Ventricular tachycardia |
Reversed | 1 |
HGVS | NC_000015.9:g.73635725_73635726insTCAC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000005485.4, RCV000171564.1, |