rs121913126
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common genotype |
Make rs121913126(C;T) |
Make rs121913126(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 26773681 |
Gene | GABRB3 |
is a | snp |
is | mentioned by |
dbSNP | rs121913126 |
dbSNP (classic) | rs121913126 |
ClinGen | rs121913126 |
ebi | rs121913126 |
HLI | rs121913126 |
Exac | rs121913126 |
Gnomad | rs121913126 |
Varsome | rs121913126 |
LitVar | rs121913126 |
Map | rs121913126 |
PheGenI | rs121913126 |
Biobank | rs121913126 |
1000 genomes | rs121913126 |
hgdp | rs121913126 |
ensembl | rs121913126 |
geneview | rs121913126 |
scholar | rs121913126 |
rs121913126 | |
pharmgkb | rs121913126 |
gwascentral | rs121913126 |
openSNP | rs121913126 |
23andMe | rs121913126 |
SNPshot | rs121913126 |
SNPdbe | rs121913126 |
MSV3d | rs121913126 |
GWAS Ctlg | rs121913126 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121913126(T;T) |
Alt | rs121913126(T;T) |
Reference | Rs121913126(C;C) |
Significance | Other |
Disease | Epilepsy not specified |
Variation | info |
Gene | GABRB3 |
CLNDBN | Epilepsy, childhood absence 5 not specified |
Reversed | 1 |
HGVS | NC_000015.9:g.27018828G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000017576.3, RCV000414639.1, |