rs1060501114
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1060501114(A;A) |
Make rs1060501114(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 3 |
Position | 38585842 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs1060501114 |
dbSNP (classic) | rs1060501114 |
ClinGen | rs1060501114 |
ebi | rs1060501114 |
HLI | rs1060501114 |
Exac | rs1060501114 |
Gnomad | rs1060501114 |
Varsome | rs1060501114 |
LitVar | rs1060501114 |
Map | rs1060501114 |
PheGenI | rs1060501114 |
Biobank | rs1060501114 |
1000 genomes | rs1060501114 |
hgdp | rs1060501114 |
ensembl | rs1060501114 |
geneview | rs1060501114 |
scholar | rs1060501114 |
rs1060501114 | |
pharmgkb | rs1060501114 |
gwascentral | rs1060501114 |
openSNP | rs1060501114 |
23andMe | rs1060501114 |
SNPshot | rs1060501114 |
SNPdbe | rs1060501114 |
MSV3d | rs1060501114 |
GWAS Ctlg | rs1060501114 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1060501114(A;A) |
Alt | rs1060501114(A;A) |
Reference | Rs1060501114(G;G) |
Significance | Pathogenic |
Disease | Brugada syndrome |
Variation | info |
Gene | SCN5A |
CLNDBN | Brugada syndrome |
Reversed | 1 |
HGVS | NC_000003.11:g.38627333C>T |
CLNSRC | |
CLNACC | RCV000470092.1, |