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rs11652075

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs11652075(C;T)
Make rs11652075(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position80205094
GeneCARD14, SGSH
is asnp
is mentioned by
dbSNPrs11652075
dbSNP (classic)rs11652075
ClinGenrs11652075
ebirs11652075
HLIrs11652075
Exacrs11652075
Gnomadrs11652075
Varsomers11652075
LitVarrs11652075
Maprs11652075
PheGenIrs11652075
Biobankrs11652075
1000 genomesrs11652075
hgdprs11652075
ensemblrs11652075
geneviewrs11652075
scholarrs11652075
googlers11652075
pharmgkbrs11652075
gwascentralrs11652075
openSNPrs11652075
23andMers11652075
SNPshotrs11652075
SNPdbers11652075
MSV3drs11652075
GWAS Ctlgrs11652075
GMAF0.4229
Max Magnitude0
? (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 22521419OA-icon.png] 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,