rs398124282
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs398124282(C;C) |
Make rs398124282(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 144517276 |
Gene | ZEB2 |
is a | snp |
is | mentioned by |
dbSNP | rs398124282 |
dbSNP (classic) | rs398124282 |
ClinGen | rs398124282 |
ebi | rs398124282 |
HLI | rs398124282 |
Exac | rs398124282 |
Gnomad | rs398124282 |
Varsome | rs398124282 |
LitVar | rs398124282 |
Map | rs398124282 |
PheGenI | rs398124282 |
Biobank | rs398124282 |
1000 genomes | rs398124282 |
hgdp | rs398124282 |
ensembl | rs398124282 |
geneview | rs398124282 |
scholar | rs398124282 |
rs398124282 | |
pharmgkb | rs398124282 |
gwascentral | rs398124282 |
openSNP | rs398124282 |
23andMe | rs398124282 |
SNPshot | rs398124282 |
SNPdbe | rs398124282 |
MSV3d | rs398124282 |
GWAS Ctlg | rs398124282 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs398124282(C;C) |
Alt | rs398124282(C;C) |
Reference | Rs398124282(T;T) |
Significance | Pathogenic |
Disease | Mowat-Wilson syndrome |
Variation | info |
Gene | ZEB2 |
CLNDBN | Mowat-Wilson syndrome |
Reversed | 1 |
HGVS | NC_000002.11:g.145274843A>G |
CLNSRC | ClinVar |
CLNACC | RCV000081673.4, |