rs60734921
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs60734921(C;T) |
Make rs60734921(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 1202303 |
Gene | CACNA1H |
is a | snp |
is | mentioned by |
dbSNP | rs60734921 |
dbSNP (classic) | rs60734921 |
ClinGen | rs60734921 |
ebi | rs60734921 |
HLI | rs60734921 |
Exac | rs60734921 |
Gnomad | rs60734921 |
Varsome | rs60734921 |
LitVar | rs60734921 |
Map | rs60734921 |
PheGenI | rs60734921 |
Biobank | rs60734921 |
1000 genomes | rs60734921 |
hgdp | rs60734921 |
ensembl | rs60734921 |
geneview | rs60734921 |
scholar | rs60734921 |
rs60734921 | |
pharmgkb | rs60734921 |
gwascentral | rs60734921 |
openSNP | rs60734921 |
23andMe | rs60734921 |
SNPshot | rs60734921 |
SNPdbe | rs60734921 |
MSV3d | rs60734921 |
GWAS Ctlg | rs60734921 |
GMAF | 0.0009183 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs60734921(T;T) |
Alt | rs60734921(T;T) |
Reference | Rs60734921(C;C) |
Significance | Other |
Disease | Epilepsy not specified |
Variation | info |
Gene | CACNA1H |
CLNDBN | Epilepsy, idiopathic generalized 6 not specified |
Reversed | 0 |
HGVS | NC_000016.9:g.1252303C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000002824.3, RCV000384435.1, |