rs7342847
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7342847(C;C) |
Make rs7342847(C;T) |
Make rs7342847(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 66806426 |
Gene | PRKCA |
is a | snp |
is | mentioned by |
dbSNP | rs7342847 |
dbSNP (classic) | rs7342847 |
ClinGen | rs7342847 |
ebi | rs7342847 |
HLI | rs7342847 |
Exac | rs7342847 |
Gnomad | rs7342847 |
Varsome | rs7342847 |
LitVar | rs7342847 |
Map | rs7342847 |
PheGenI | rs7342847 |
Biobank | rs7342847 |
1000 genomes | rs7342847 |
hgdp | rs7342847 |
ensembl | rs7342847 |
geneview | rs7342847 |
scholar | rs7342847 |
rs7342847 | |
pharmgkb | rs7342847 |
gwascentral | rs7342847 |
openSNP | rs7342847 |
23andMe | rs7342847 |
SNPshot | rs7342847 |
SNPdbe | rs7342847 |
MSV3d | rs7342847 |
GWAS Ctlg | rs7342847 |
GMAF | 0.4467 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19454617] Genetic variation in the chromosome 17q23 amplicon and breast cancer risk