rs587784563
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs587784563(C;T) |
Make rs587784563(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 144399231 |
Gene | ZEB2 |
is a | snp |
is | mentioned by |
dbSNP | rs587784563 |
dbSNP (classic) | rs587784563 |
ClinGen | rs587784563 |
ebi | rs587784563 |
HLI | rs587784563 |
Exac | rs587784563 |
Gnomad | rs587784563 |
Varsome | rs587784563 |
LitVar | rs587784563 |
Map | rs587784563 |
PheGenI | rs587784563 |
Biobank | rs587784563 |
1000 genomes | rs587784563 |
hgdp | rs587784563 |
ensembl | rs587784563 |
geneview | rs587784563 |
scholar | rs587784563 |
rs587784563 | |
pharmgkb | rs587784563 |
gwascentral | rs587784563 |
openSNP | rs587784563 |
23andMe | rs587784563 |
SNPshot | rs587784563 |
SNPdbe | rs587784563 |
MSV3d | rs587784563 |
GWAS Ctlg | rs587784563 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587784563(T;T) |
Alt | rs587784563(T;T) |
Reference | Rs587784563(C;C) |
Significance | Pathogenic |
Disease | Mowat-Wilson syndrome |
Variation | info |
Gene | ZEB2 |
CLNDBN | Mowat-Wilson syndrome |
Reversed | 1 |
HGVS | NC_000002.11:g.145156798G>A |
CLNSRC | |
CLNACC | RCV000147993.1, |