rs564667614
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs564667614(C;T) |
Make rs564667614(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 22 |
Position | 31843170 |
Gene | DEPDC5 |
is a | snp |
is | mentioned by |
dbSNP | rs564667614 |
dbSNP (classic) | rs564667614 |
ClinGen | rs564667614 |
ebi | rs564667614 |
HLI | rs564667614 |
Exac | rs564667614 |
Gnomad | rs564667614 |
Varsome | rs564667614 |
LitVar | rs564667614 |
Map | rs564667614 |
PheGenI | rs564667614 |
Biobank | rs564667614 |
1000 genomes | rs564667614 |
hgdp | rs564667614 |
ensembl | rs564667614 |
geneview | rs564667614 |
scholar | rs564667614 |
rs564667614 | |
pharmgkb | rs564667614 |
gwascentral | rs564667614 |
openSNP | rs564667614 |
23andMe | rs564667614 |
SNPshot | rs564667614 |
SNPdbe | rs564667614 |
MSV3d | rs564667614 |
GWAS Ctlg | rs564667614 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs564667614(T;T) |
Alt | rs564667614(T;T) |
Reference | Rs564667614(C;C) |
Significance | Other |
Disease | Epilepsy |
Variation | info |
Gene | DEPDC5 |
CLNDBN | Epilepsy, familial focal, with variable foci 1 |
Reversed | 0 |
HGVS | NC_000022.10:g.32239156C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000157607.4, |