rs121434579
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs121434579(A;A) |
Make rs121434579(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 161895774 |
Gene | GABRA1 |
is a | snp |
is | mentioned by |
dbSNP | rs121434579 |
dbSNP (classic) | rs121434579 |
ClinGen | rs121434579 |
ebi | rs121434579 |
HLI | rs121434579 |
Exac | rs121434579 |
Gnomad | rs121434579 |
Varsome | rs121434579 |
LitVar | rs121434579 |
Map | rs121434579 |
PheGenI | rs121434579 |
Biobank | rs121434579 |
1000 genomes | rs121434579 |
hgdp | rs121434579 |
ensembl | rs121434579 |
geneview | rs121434579 |
scholar | rs121434579 |
rs121434579 | |
pharmgkb | rs121434579 |
gwascentral | rs121434579 |
openSNP | rs121434579 |
23andMe | rs121434579 |
SNPshot | rs121434579 |
SNPdbe | rs121434579 |
MSV3d | rs121434579 |
GWAS Ctlg | rs121434579 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121434579(A;A) |
Alt | rs121434579(A;A) |
Reference | Rs121434579(C;C) |
Significance | Other |
Disease | Epilepsy |
Variation | info |
Gene | GABRA1 |
CLNDBN | Epilepsy, juvenile myoclonic 5 |
Reversed | 0 |
HGVS | NC_000005.9:g.161322780C>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000017601.4, |