rs767983680
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs767983680(C;G) |
Make rs767983680(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 1204058 |
Gene | CACNA1H |
is a | snp |
is | mentioned by |
dbSNP | rs767983680 |
dbSNP (classic) | rs767983680 |
ClinGen | rs767983680 |
ebi | rs767983680 |
HLI | rs767983680 |
Exac | rs767983680 |
Gnomad | rs767983680 |
Varsome | rs767983680 |
LitVar | rs767983680 |
Map | rs767983680 |
PheGenI | rs767983680 |
Biobank | rs767983680 |
1000 genomes | rs767983680 |
hgdp | rs767983680 |
ensembl | rs767983680 |
geneview | rs767983680 |
scholar | rs767983680 |
rs767983680 | |
pharmgkb | rs767983680 |
gwascentral | rs767983680 |
openSNP | rs767983680 |
23andMe | rs767983680 |
SNPshot | rs767983680 |
SNPdbe | rs767983680 |
MSV3d | rs767983680 |
GWAS Ctlg | rs767983680 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs767983680(A;A) rs767983680(G;G) |
Alt | rs767983680(A;A) rs767983680(G;G) |
Reference | Rs767983680(C;C) |
Significance | Probable-Pathogenic |
Disease | Abnormality of brain morphology |
Variation | info |
Gene | CACNA1H |
CLNDBN | Abnormality of brain morphology |
Reversed | 0 |
HGVS | NC_000016.9:g.1254058C>A |
CLNSRC | |
CLNACC | RCV000454200.1, |