rs6964587
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs6964587(G;T) |
Make rs6964587(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 7 |
Position | 92001306 |
Gene | AKAP9 |
is a | snp |
is | mentioned by |
dbSNP | rs6964587 |
dbSNP (classic) | rs6964587 |
ClinGen | rs6964587 |
ebi | rs6964587 |
HLI | rs6964587 |
Exac | rs6964587 |
Gnomad | rs6964587 |
Varsome | rs6964587 |
LitVar | rs6964587 |
Map | rs6964587 |
PheGenI | rs6964587 |
Biobank | rs6964587 |
1000 genomes | rs6964587 |
hgdp | rs6964587 |
ensembl | rs6964587 |
geneview | rs6964587 |
scholar | rs6964587 |
rs6964587 | |
pharmgkb | rs6964587 |
gwascentral | rs6964587 |
openSNP | rs6964587 |
23andMe | rs6964587 |
SNPshot | rs6964587 |
SNPdbe | rs6964587 |
MSV3d | rs6964587 |
GWAS Ctlg | rs6964587 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 26510858] Patients with a high polygenic risk of breast cancer do not have an increased risk of radiotherapy toxicity
ClinVar | |
---|---|
Risk | rs6964587(T;T) |
Alt | rs6964587(T;T) |
Reference | Rs6964587(G;G) |
Significance | Probable-non-pathogenic |
Disease | not specified Colorectal cancer Cardiovascular phenotype Long QT syndrome |
Variation | info |
Gene | AKAP9 |
CLNDBN | not specified Colorectal cancer Cardiovascular phenotype Long QT syndrome |
Reversed | 0 |
HGVS | NC_000007.13:g.91630620G>T |
CLNSRC | |
CLNACC | RCV000123592.6, RCV000171778.2, RCV000244317.1, RCV000350947.1, |