rs121909269
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs121909269(A;A) |
Make rs121909269(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 122284647 |
Gene | CASR |
is a | snp |
is | mentioned by |
dbSNP | rs121909269 |
dbSNP (classic) | rs121909269 |
ClinGen | rs121909269 |
ebi | rs121909269 |
HLI | rs121909269 |
Exac | rs121909269 |
Gnomad | rs121909269 |
Varsome | rs121909269 |
LitVar | rs121909269 |
Map | rs121909269 |
PheGenI | rs121909269 |
Biobank | rs121909269 |
1000 genomes | rs121909269 |
hgdp | rs121909269 |
ensembl | rs121909269 |
geneview | rs121909269 |
scholar | rs121909269 |
rs121909269 | |
pharmgkb | rs121909269 |
gwascentral | rs121909269 |
openSNP | rs121909269 |
23andMe | rs121909269 |
SNPshot | rs121909269 |
SNPdbe | rs121909269 |
MSV3d | rs121909269 |
GWAS Ctlg | rs121909269 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121909269(A;A) |
Alt | rs121909269(A;A) |
Reference | Rs121909269(G;G) |
Significance | Other |
Disease | Epilepsy |
Variation | info |
Gene | CASR |
CLNDBN | Epilepsy, idiopathic generalized 8 |
Reversed | 0 |
HGVS | NC_000003.11:g.122003494G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000008864.4, |