rs756686919
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs756686919(C;C) |
Make rs756686919(C;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 144400207 |
Gene | ZEB2 |
is a | snp |
is | mentioned by |
dbSNP | rs756686919 |
dbSNP (classic) | rs756686919 |
ClinGen | rs756686919 |
ebi | rs756686919 |
HLI | rs756686919 |
Exac | rs756686919 |
Gnomad | rs756686919 |
Varsome | rs756686919 |
LitVar | rs756686919 |
Map | rs756686919 |
PheGenI | rs756686919 |
Biobank | rs756686919 |
1000 genomes | rs756686919 |
hgdp | rs756686919 |
ensembl | rs756686919 |
geneview | rs756686919 |
scholar | rs756686919 |
rs756686919 | |
pharmgkb | rs756686919 |
gwascentral | rs756686919 |
openSNP | rs756686919 |
23andMe | rs756686919 |
SNPshot | rs756686919 |
SNPdbe | rs756686919 |
MSV3d | rs756686919 |
GWAS Ctlg | rs756686919 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs756686919(C;C) rs756686919(T;T) |
Alt | rs756686919(C;C) rs756686919(T;T) |
Reference | Rs756686919(G;G) |
Significance | Pathogenic |
Disease | Mowat-Wilson syndrome |
Variation | info |
Gene | ZEB2 |
CLNDBN | Mowat-Wilson syndrome |
Reversed | 0 |
HGVS | NC_000002.11:g.145157774G>T |
CLNSRC | |
CLNACC | RCV000180324.1, |