rs772685782
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs772685782(A;A) |
Make rs772685782(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 50591539 |
Gene | CACNA1G |
is a | snp |
is | mentioned by |
dbSNP | rs772685782 |
dbSNP (classic) | rs772685782 |
ClinGen | rs772685782 |
ebi | rs772685782 |
HLI | rs772685782 |
Exac | rs772685782 |
Gnomad | rs772685782 |
Varsome | rs772685782 |
LitVar | rs772685782 |
Map | rs772685782 |
PheGenI | rs772685782 |
Biobank | rs772685782 |
1000 genomes | rs772685782 |
hgdp | rs772685782 |
ensembl | rs772685782 |
geneview | rs772685782 |
scholar | rs772685782 |
rs772685782 | |
pharmgkb | rs772685782 |
gwascentral | rs772685782 |
openSNP | rs772685782 |
23andMe | rs772685782 |
SNPshot | rs772685782 |
SNPdbe | rs772685782 |
MSV3d | rs772685782 |
GWAS Ctlg | rs772685782 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs772685782(A;A) |
Alt | rs772685782(A;A) |
Reference | Rs772685782(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CACNA1G |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.48668900G>A |
CLNSRC | |
CLNACC | RCV000493653.1, |