rs786204814
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(CAGGC;CAGGC) | 0 | common in clinvar |
Make rs786204814(-;-) |
Make rs786204814(-;CAGGC) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 144399767 |
Gene | ZEB2 |
is a | snp |
is | mentioned by |
dbSNP | rs786204814 |
dbSNP (classic) | rs786204814 |
ClinGen | rs786204814 |
ebi | rs786204814 |
HLI | rs786204814 |
Exac | rs786204814 |
Gnomad | rs786204814 |
Varsome | rs786204814 |
LitVar | rs786204814 |
Map | rs786204814 |
PheGenI | rs786204814 |
Biobank | rs786204814 |
1000 genomes | rs786204814 |
hgdp | rs786204814 |
ensembl | rs786204814 |
geneview | rs786204814 |
scholar | rs786204814 |
rs786204814 | |
pharmgkb | rs786204814 |
gwascentral | rs786204814 |
openSNP | rs786204814 |
23andMe | rs786204814 |
SNPshot | rs786204814 |
SNPdbe | rs786204814 |
MSV3d | rs786204814 |
GWAS Ctlg | rs786204814 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786204814(-;-) |
Alt | rs786204814(-;-) |
Reference | Rs786204814(CAGGC;CAGGC) |
Significance | Pathogenic |
Disease | Mowat-Wilson syndrome |
Variation | info |
Gene | ZEB2 |
CLNDBN | Mowat-Wilson syndrome |
Reversed | 1 |
HGVS | NC_000002.11:g.145157334_145157338delGCCTG |
CLNSRC | |
CLNACC | RCV000169714.1, |