rs138859323
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common genotype |
Make rs138859323(A;A) |
Make rs138859323(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 144404939 |
Gene | ZEB2 |
is a | snp |
is | mentioned by |
dbSNP | rs138859323 |
dbSNP (classic) | rs138859323 |
ClinGen | rs138859323 |
ebi | rs138859323 |
HLI | rs138859323 |
Exac | rs138859323 |
Gnomad | rs138859323 |
Varsome | rs138859323 |
LitVar | rs138859323 |
Map | rs138859323 |
PheGenI | rs138859323 |
Biobank | rs138859323 |
1000 genomes | rs138859323 |
hgdp | rs138859323 |
ensembl | rs138859323 |
geneview | rs138859323 |
scholar | rs138859323 |
rs138859323 | |
pharmgkb | rs138859323 |
gwascentral | rs138859323 |
openSNP | rs138859323 |
23andMe | rs138859323 |
SNPshot | rs138859323 |
SNPdbe | rs138859323 |
MSV3d | rs138859323 |
GWAS Ctlg | rs138859323 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs138859323(A;A) |
Alt | rs138859323(A;A) |
Reference | Rs138859323(G;G) |
Significance | Other |
Disease | not specified Mowat-Wilson syndrome |
Variation | info |
Gene | ZEB2 |
CLNDBN | not specified Mowat-Wilson syndrome |
Reversed | 0 |
HGVS | NC_000002.11:g.145162506G>A |
CLNSRC | |
CLNACC | RCV000081671.8, RCV000353189.1, |