rs1064792926
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(TGCATTGCCACCC;TGCATTGCCACCC) | 0 | common in clinvar |
Chromosome | 3 |
Position | 38581137 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs1064792926 |
dbSNP (classic) | rs1064792926 |
ClinGen | rs1064792926 |
ebi | rs1064792926 |
HLI | rs1064792926 |
Exac | rs1064792926 |
Gnomad | rs1064792926 |
Varsome | rs1064792926 |
LitVar | rs1064792926 |
Map | rs1064792926 |
PheGenI | rs1064792926 |
Biobank | rs1064792926 |
1000 genomes | rs1064792926 |
hgdp | rs1064792926 |
ensembl | rs1064792926 |
geneview | rs1064792926 |
scholar | rs1064792926 |
rs1064792926 | |
pharmgkb | rs1064792926 |
gwascentral | rs1064792926 |
openSNP | rs1064792926 |
23andMe | rs1064792926 |
SNPshot | rs1064792926 |
SNPdbe | rs1064792926 |
MSV3d | rs1064792926 |
GWAS Ctlg | rs1064792926 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064792926(-;-) |
Alt | rs1064792926(-;-) |
Reference | Rs1064792926(TGCATTGCCACCC;TGCATTGCCACCC) |
Significance | Pathogenic |
Disease | Brugada syndrome not provided |
Variation | info |
Gene | SCN5A |
CLNDBN | Brugada syndrome not provided |
Reversed | 1 |
HGVS | NC_000003.11:g.38622628_38622640delGGGTGGCAATGCA |
CLNSRC | |
CLNACC | RCV000476373.1, RCV000482498.1, |