Have questions? Visit https://www.reddit.com/r/SNPedia

rs11836796

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs11836796(C;C)
Make rs11836796(C;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position88092734
GeneCEP290
is asnp
is mentioned by
dbSNPrs11836796
ebirs11836796
HLIrs11836796
Exacrs11836796
Varsomers11836796
Maprs11836796
PheGenIrs11836796
hapmaprs11836796
1000 genomesrs11836796
hgdprs11836796
ensemblrs11836796
gopubmedrs11836796
geneviewrs11836796
scholarrs11836796
googlers11836796
pharmgkbrs11836796
gwascentralrs11836796
openSNPrs11836796
23andMers11836796
23andMe allrs11836796
SNP Nexus

SNPshotrs11836796
SNPdbers11836796
MSV3drs11836796
GWAS Ctlgrs11836796
Max Magnitude0
? (C;C) (C;T) (T;T) 28


Venter snp
Source plos
Gene CEP290
allele C
frequency 0
sift TOLERATED
HuRef 1103649501611
Disease Association Antibodies against Cep290 are present in sera from patients with cutaneous T-cell lymphomas, but not in the healthy control population.



ClinVar
Risk rs11836796(C,G;C,G)
Alt rs11836796(C,G;C,G)
Reference rs11836796(T;T)
Significance Unknown
Disease not specified
Variation info
Gene CEP290
CLNDBN not specified
Reversed 0
HGVS NC_000012.11:g.88486511T>C
CLNSRC
CLNACC RCV000193317.1,