rs6711223
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs6711223(A;A) |
Make rs6711223(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 144400257 |
Gene | ZEB2 |
is a | snp |
is | mentioned by |
dbSNP | rs6711223 |
dbSNP (classic) | rs6711223 |
ClinGen | rs6711223 |
ebi | rs6711223 |
HLI | rs6711223 |
Exac | rs6711223 |
Gnomad | rs6711223 |
Varsome | rs6711223 |
LitVar | rs6711223 |
Map | rs6711223 |
PheGenI | rs6711223 |
Biobank | rs6711223 |
1000 genomes | rs6711223 |
hgdp | rs6711223 |
ensembl | rs6711223 |
geneview | rs6711223 |
scholar | rs6711223 |
rs6711223 | |
pharmgkb | rs6711223 |
gwascentral | rs6711223 |
openSNP | rs6711223 |
23andMe | rs6711223 |
SNPshot | rs6711223 |
SNPdbe | rs6711223 |
MSV3d | rs6711223 |
GWAS Ctlg | rs6711223 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs6711223(A;A) rs6711223(T;T) |
Alt | rs6711223(A;A) rs6711223(T;T) |
Reference | Rs6711223(G;G) |
Significance | Other |
Disease | not specified Mowat-Wilson syndrome not provided |
Variation | info |
Gene | ZEB2 |
CLNDBN | not specified Mowat-Wilson syndrome not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.145157824G>A; NC_000002.11:g.145157824G>T |
CLNSRC | HGMD |
CLNACC | RCV000081677.6, RCV000232228.3, RCV000418591.1, RCV000154157.3, |