rs786203991
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs786203991(-;-) |
Make rs786203991(-;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 144389552 |
Gene | ZEB2 |
is a | snp |
is | mentioned by |
dbSNP | rs786203991 |
dbSNP (classic) | rs786203991 |
ClinGen | rs786203991 |
ebi | rs786203991 |
HLI | rs786203991 |
Exac | rs786203991 |
Gnomad | rs786203991 |
Varsome | rs786203991 |
LitVar | rs786203991 |
Map | rs786203991 |
PheGenI | rs786203991 |
Biobank | rs786203991 |
1000 genomes | rs786203991 |
hgdp | rs786203991 |
ensembl | rs786203991 |
geneview | rs786203991 |
scholar | rs786203991 |
rs786203991 | |
pharmgkb | rs786203991 |
gwascentral | rs786203991 |
openSNP | rs786203991 |
23andMe | rs786203991 |
SNPshot | rs786203991 |
SNPdbe | rs786203991 |
MSV3d | rs786203991 |
GWAS Ctlg | rs786203991 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786203991(-;-) |
Alt | rs786203991(-;-) |
Reference | Rs786203991(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ZEB2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000002.11:g.145147119delC |
CLNSRC | The Children's Hospital of Philadelphia |
CLNACC | RCV000167553.1, |