rs1044009
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1044009(C;T) |
Make rs1044009(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 19 |
Position | 15160960 |
Gene | NOTCH3 |
is a | snp |
is | mentioned by |
dbSNP | rs1044009 |
dbSNP (classic) | rs1044009 |
ClinGen | rs1044009 |
ebi | rs1044009 |
HLI | rs1044009 |
Exac | rs1044009 |
Gnomad | rs1044009 |
Varsome | rs1044009 |
LitVar | rs1044009 |
Map | rs1044009 |
PheGenI | rs1044009 |
Biobank | rs1044009 |
1000 genomes | rs1044009 |
hgdp | rs1044009 |
ensembl | rs1044009 |
geneview | rs1044009 |
scholar | rs1044009 |
rs1044009 | |
pharmgkb | rs1044009 |
gwascentral | rs1044009 |
openSNP | rs1044009 |
23andMe | rs1044009 |
SNPshot | rs1044009 |
SNPdbe | rs1044009 |
MSV3d | rs1044009 |
GWAS Ctlg | rs1044009 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 25957329] Variations in genes involved in dormancy associated with outcome in patients with resected colorectal liver metastases
ClinVar | |
---|---|
Risk | rs1044009(T;T) |
Alt | rs1044009(T;T) |
Reference | Rs1044009(C;C) |
Significance | Non-pathogenic |
Disease | not specified Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy |
Variation | info |
Gene | NOTCH3 |
CLNDBN | not specified Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy |
Reversed | 1 |
HGVS | NC_000019.9:g.15271771G>A |
CLNSRC | |
CLNACC | RCV000249070.2, RCV000278901.1, |