rs11547635
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs11547635(C;T) |
Make rs11547635(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 22 |
Position | 32857305 |
Gene | SYN3, TIMP3 |
is a | snp |
is | mentioned by |
dbSNP | rs11547635 |
dbSNP (classic) | rs11547635 |
ClinGen | rs11547635 |
ebi | rs11547635 |
HLI | rs11547635 |
Exac | rs11547635 |
Gnomad | rs11547635 |
Varsome | rs11547635 |
LitVar | rs11547635 |
Map | rs11547635 |
PheGenI | rs11547635 |
Biobank | rs11547635 |
1000 genomes | rs11547635 |
hgdp | rs11547635 |
ensembl | rs11547635 |
geneview | rs11547635 |
scholar | rs11547635 |
rs11547635 | |
pharmgkb | rs11547635 |
gwascentral | rs11547635 |
openSNP | rs11547635 |
23andMe | rs11547635 |
SNPshot | rs11547635 |
SNPdbe | rs11547635 |
MSV3d | rs11547635 |
GWAS Ctlg | rs11547635 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26579821] Polymorphisms and Plasma Levels of Tissue Inhibitor of Metalloproteinase-3: Impact on Genetic Susceptibility and Clinical Outcome of Oral Cancer
ClinVar | |
---|---|
Risk | rs11547635(T;T) |
Alt | rs11547635(T;T) |
Reference | Rs11547635(C;C) |
Significance | Non-pathogenic |
Disease | Pseudoinflammatory fundus dystrophy |
Variation | info |
Gene | SYN3 TIMP3 |
CLNDBN | Pseudoinflammatory fundus dystrophy |
Reversed | 0 |
HGVS | NC_000022.10:g.33253292C>T |
CLNSRC | |
CLNACC | RCV000270768.1, |