rs13049286
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs13049286(G;G) |
Make rs13049286(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 41756639 |
Gene | RIPK4 |
is a | snp |
is | mentioned by |
dbSNP | rs13049286 |
dbSNP (classic) | rs13049286 |
ClinGen | rs13049286 |
ebi | rs13049286 |
HLI | rs13049286 |
Exac | rs13049286 |
Gnomad | rs13049286 |
Varsome | rs13049286 |
LitVar | rs13049286 |
Map | rs13049286 |
PheGenI | rs13049286 |
Biobank | rs13049286 |
1000 genomes | rs13049286 |
hgdp | rs13049286 |
ensembl | rs13049286 |
geneview | rs13049286 |
scholar | rs13049286 |
rs13049286 | |
pharmgkb | rs13049286 |
gwascentral | rs13049286 |
openSNP | rs13049286 |
23andMe | rs13049286 |
SNPshot | rs13049286 |
SNPdbe | rs13049286 |
MSV3d | rs13049286 |
GWAS Ctlg | rs13049286 |
GMAF | 0.1116 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 22479419] Genome-wide association study of treatment refractory schizophrenia in han chinese
ClinVar | |
---|---|
Risk | rs13049286(G;G) |
Alt | rs13049286(G;G) |
Reference | Rs13049286(T;T) |
Significance | Probable-non-pathogenic |
Disease | Popliteal pterygium syndrome |
Variation | info |
Gene | RIPK4 |
CLNDBN | Popliteal pterygium syndrome |
Reversed | 0 |
HGVS | NC_000021.8:g.43176799T>G |
CLNSRC | |
CLNACC | RCV000317325.1, |