rs11652075
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs11652075(C;T) |
| Make rs11652075(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 80205094 |
| Gene | CARD14, SGSH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11652075 |
| dbSNP (classic) | rs11652075 |
| ClinGen | rs11652075 |
| ebi | rs11652075 |
| HLI | rs11652075 |
| Exac | rs11652075 |
| Gnomad | rs11652075 |
| Varsome | rs11652075 |
| LitVar | rs11652075 |
| Map | rs11652075 |
| PheGenI | rs11652075 |
| Biobank | rs11652075 |
| 1000 genomes | rs11652075 |
| hgdp | rs11652075 |
| ensembl | rs11652075 |
| geneview | rs11652075 |
| scholar | rs11652075 |
| rs11652075 | |
| pharmgkb | rs11652075 |
| gwascentral | rs11652075 |
| openSNP | rs11652075 |
| 23andMe | rs11652075 |
| SNPshot | rs11652075 |
| SNPdbe | rs11652075 |
| MSV3d | rs11652075 |
| GWAS Ctlg | rs11652075 |
| GMAF | 0.4229 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23905699] SNP rs11652075 in the CARD14 Gene as a Risk Factor for Psoriasis (PSORS2) in a Spanish Cohort
[PMID 22521419
] Rare and common variants in CARD14, encoding an epidermal regulator of NF-kappaB, in psoriasis.
| ClinVar | |
|---|---|
| Risk | rs11652075(T;T) |
| Alt | rs11652075(T;T) |
| Reference | Rs11652075(C;C) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | CARD14 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000017.10:g.78178893C>T |
| CLNSRC | |
| CLNACC | RCV000454417.1, |
