rs11836796
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs11836796(C;C) |
Make rs11836796(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 88092734 |
Gene | CEP290 |
is a | snp |
is | mentioned by |
dbSNP | rs11836796 |
dbSNP (classic) | rs11836796 |
ClinGen | rs11836796 |
ebi | rs11836796 |
HLI | rs11836796 |
Exac | rs11836796 |
Gnomad | rs11836796 |
Varsome | rs11836796 |
LitVar | rs11836796 |
Map | rs11836796 |
PheGenI | rs11836796 |
Biobank | rs11836796 |
1000 genomes | rs11836796 |
hgdp | rs11836796 |
ensembl | rs11836796 |
geneview | rs11836796 |
scholar | rs11836796 |
rs11836796 | |
pharmgkb | rs11836796 |
gwascentral | rs11836796 |
openSNP | rs11836796 |
23andMe | rs11836796 |
SNPshot | rs11836796 |
SNPdbe | rs11836796 |
MSV3d | rs11836796 |
GWAS Ctlg | rs11836796 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs11836796(C;C) rs11836796(G;G) |
Alt | rs11836796(C;C) rs11836796(G;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, |