rs797044881
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs797044881(C;C) |
Make rs797044881(C;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 2608651 |
Gene | CACNA1C |
is a | snp |
is | mentioned by |
dbSNP | rs797044881 |
dbSNP (classic) | rs797044881 |
ClinGen | rs797044881 |
ebi | rs797044881 |
HLI | rs797044881 |
Exac | rs797044881 |
Gnomad | rs797044881 |
Varsome | rs797044881 |
LitVar | rs797044881 |
Map | rs797044881 |
PheGenI | rs797044881 |
Biobank | rs797044881 |
1000 genomes | rs797044881 |
hgdp | rs797044881 |
ensembl | rs797044881 |
geneview | rs797044881 |
scholar | rs797044881 |
rs797044881 | |
pharmgkb | rs797044881 |
gwascentral | rs797044881 |
openSNP | rs797044881 |
23andMe | rs797044881 |
SNPshot | rs797044881 |
SNPdbe | rs797044881 |
MSV3d | rs797044881 |
GWAS Ctlg | rs797044881 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs797044881(C;C) |
Alt | rs797044881(C;C) |
Reference | Rs797044881(T;T) |
Significance | Pathogenic |
Disease | Inborn genetic diseases |
Variation | info |
Gene | CACNA1C |
CLNDBN | Inborn genetic diseases |
Reversed | 0 |
HGVS | NC_000012.11:g.2717817T>C |
CLNSRC | |
CLNACC | RCV000190696.1, |