rs1057519538
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AAA;AAA) | 0 | common in clinvar |
Make rs1057519538(-;-) |
Make rs1057519538(-;AAA) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 127651622 |
Gene | STXBP1 |
is a | snp |
is | mentioned by |
dbSNP | rs1057519538 |
dbSNP (classic) | rs1057519538 |
ClinGen | rs1057519538 |
ebi | rs1057519538 |
HLI | rs1057519538 |
Exac | rs1057519538 |
Gnomad | rs1057519538 |
Varsome | rs1057519538 |
LitVar | rs1057519538 |
Map | rs1057519538 |
PheGenI | rs1057519538 |
Biobank | rs1057519538 |
1000 genomes | rs1057519538 |
hgdp | rs1057519538 |
ensembl | rs1057519538 |
geneview | rs1057519538 |
scholar | rs1057519538 |
rs1057519538 | |
pharmgkb | rs1057519538 |
gwascentral | rs1057519538 |
openSNP | rs1057519538 |
23andMe | rs1057519538 |
SNPshot | rs1057519538 |
SNPdbe | rs1057519538 |
MSV3d | rs1057519538 |
GWAS Ctlg | rs1057519538 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057519538(-;-) |
Alt | rs1057519538(-;-) |
Reference | Rs1057519538(AAA;AAA) |
Significance | Pathogenic |
Disease | Epileptic encephalopathy |
Variation | info |
Gene | STXBP1 |
CLNDBN | Epileptic encephalopathy |
Reversed | 0 |
HGVS | NC_000009.11:g.130413901_130413903delAAA |
CLNSRC | |
CLNACC | RCV000417033.1, |