rs733025
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs733025(C;C) |
Make rs733025(C;T) |
Make rs733025(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 62458475 |
is a | snp |
is | mentioned by |
dbSNP | rs733025 |
dbSNP (classic) | rs733025 |
ClinGen | rs733025 |
ebi | rs733025 |
HLI | rs733025 |
Exac | rs733025 |
Gnomad | rs733025 |
Varsome | rs733025 |
LitVar | rs733025 |
Map | rs733025 |
PheGenI | rs733025 |
Biobank | rs733025 |
1000 genomes | rs733025 |
hgdp | rs733025 |
ensembl | rs733025 |
geneview | rs733025 |
scholar | rs733025 |
rs733025 | |
pharmgkb | rs733025 |
gwascentral | rs733025 |
openSNP | rs733025 |
23andMe | rs733025 |
SNPshot | rs733025 |
SNPdbe | rs733025 |
MSV3d | rs733025 |
GWAS Ctlg | rs733025 |
GMAF | 0.2475 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19454617] Genetic variation in the chromosome 17q23 amplicon and breast cancer risk