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, |