rs116159732
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs116159732(C;C) |
Make rs116159732(C;T) |
Make rs116159732(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 3 |
Position | 129272193 |
Gene | COPG1, MIR6826 |
is a | snp |
is | mentioned by |
dbSNP | rs116159732 |
dbSNP (classic) | rs116159732 |
ClinGen | rs116159732 |
ebi | rs116159732 |
HLI | rs116159732 |
Exac | rs116159732 |
Gnomad | rs116159732 |
Varsome | rs116159732 |
LitVar | rs116159732 |
Map | rs116159732 |
PheGenI | rs116159732 |
Biobank | rs116159732 |
1000 genomes | rs116159732 |
hgdp | rs116159732 |
ensembl | rs116159732 |
geneview | rs116159732 |
scholar | rs116159732 |
rs116159732 | |
pharmgkb | rs116159732 |
gwascentral | rs116159732 |
openSNP | rs116159732 |
23andMe | rs116159732 |
SNPshot | rs116159732 |
SNPdbe | rs116159732 |
MSV3d | rs116159732 |
GWAS Ctlg | rs116159732 |
Max Magnitude | 0 |
[PMID 27380242] Genetic variants in microRNA and microRNA biogenesis pathway genes and breast cancer risk among women of African ancestry.