rs786203993
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs786203993(G;T) |
Make rs786203993(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 144401308 |
Gene | ZEB2 |
is a | snp |
is | mentioned by |
dbSNP | rs786203993 |
dbSNP (classic) | rs786203993 |
ClinGen | rs786203993 |
ebi | rs786203993 |
HLI | rs786203993 |
Exac | rs786203993 |
Gnomad | rs786203993 |
Varsome | rs786203993 |
LitVar | rs786203993 |
Map | rs786203993 |
PheGenI | rs786203993 |
Biobank | rs786203993 |
1000 genomes | rs786203993 |
hgdp | rs786203993 |
ensembl | rs786203993 |
geneview | rs786203993 |
scholar | rs786203993 |
rs786203993 | |
pharmgkb | rs786203993 |
gwascentral | rs786203993 |
openSNP | rs786203993 |
23andMe | rs786203993 |
SNPshot | rs786203993 |
SNPdbe | rs786203993 |
MSV3d | rs786203993 |
GWAS Ctlg | rs786203993 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786203993(T;T) |
Alt | rs786203993(T;T) |
Reference | Rs786203993(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ZEB2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000002.11:g.145158875C>A |
CLNSRC | The Children's Hospital of Philadelphia |
CLNACC | RCV000167556.1, |