rs71651682
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs71651682(C;T) |
Make rs71651682(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 26772759 |
Gene | GABRB3 |
is a | snp |
is | mentioned by |
dbSNP | rs71651682 |
dbSNP (classic) | rs71651682 |
ClinGen | rs71651682 |
ebi | rs71651682 |
HLI | rs71651682 |
Exac | rs71651682 |
Gnomad | rs71651682 |
Varsome | rs71651682 |
LitVar | rs71651682 |
Map | rs71651682 |
PheGenI | rs71651682 |
Biobank | rs71651682 |
1000 genomes | rs71651682 |
hgdp | rs71651682 |
ensembl | rs71651682 |
geneview | rs71651682 |
scholar | rs71651682 |
rs71651682 | |
pharmgkb | rs71651682 |
gwascentral | rs71651682 |
openSNP | rs71651682 |
23andMe | rs71651682 |
SNPshot | rs71651682 |
SNPdbe | rs71651682 |
MSV3d | rs71651682 |
GWAS Ctlg | rs71651682 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs71651682(T;T) |
Alt | rs71651682(T;T) |
Reference | Rs71651682(C;C) |
Significance | Other |
Disease | Epilepsy |
Variation | info |
Gene | GABRB3 |
CLNDBN | Epilepsy, childhood absence 5 |
Reversed | 0 |
HGVS | NC_000015.9:g.27017906C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000017577.3, |