rs9869263
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs9869263(A;G) |
Make rs9869263(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 190312891 |
Gene | CLDN1, LOC107986170 |
is a | snp |
is | mentioned by |
dbSNP | rs9869263 |
dbSNP (classic) | rs9869263 |
ClinGen | rs9869263 |
ebi | rs9869263 |
HLI | rs9869263 |
Exac | rs9869263 |
Gnomad | rs9869263 |
Varsome | rs9869263 |
LitVar | rs9869263 |
Map | rs9869263 |
PheGenI | rs9869263 |
Biobank | rs9869263 |
1000 genomes | rs9869263 |
hgdp | rs9869263 |
ensembl | rs9869263 |
geneview | rs9869263 |
scholar | rs9869263 |
rs9869263 | |
pharmgkb | rs9869263 |
gwascentral | rs9869263 |
openSNP | rs9869263 |
23andMe | rs9869263 |
SNPshot | rs9869263 |
SNPdbe | rs9869263 |
MSV3d | rs9869263 |
GWAS Ctlg | rs9869263 |
GMAF | 0.1823 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24479816] Polymorphisms in the CLDN1 and CLDN7 genes are related to differentiation and tumor stage in colon carcinoma
ClinVar | |
---|---|
Risk | rs9869263(C;C) rs9869263(G;G) rs9869263(T;T) |
Alt | rs9869263(C;C) rs9869263(G;G) rs9869263(T;T) |
Reference | Rs9869263(A;A) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | CLDN1 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000003.11:g.190030680A>G |
CLNSRC | |
CLNACC | RCV000175932.2, |