rs8130963
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs8130963(A;A) |
Make rs8130963(A;G) |
Make rs8130963(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 21 |
Position | 34895121 |
Gene | RUNX1 |
is a | snp |
is | mentioned by |
dbSNP | rs8130963 |
dbSNP (classic) | rs8130963 |
ClinGen | rs8130963 |
ebi | rs8130963 |
HLI | rs8130963 |
Exac | rs8130963 |
Gnomad | rs8130963 |
Varsome | rs8130963 |
LitVar | rs8130963 |
Map | rs8130963 |
PheGenI | rs8130963 |
Biobank | rs8130963 |
1000 genomes | rs8130963 |
hgdp | rs8130963 |
ensembl | rs8130963 |
geneview | rs8130963 |
scholar | rs8130963 |
rs8130963 | |
pharmgkb | rs8130963 |
gwascentral | rs8130963 |
openSNP | rs8130963 |
23andMe | rs8130963 |
SNPshot | rs8130963 |
SNPdbe | rs8130963 |
MSV3d | rs8130963 |
GWAS Ctlg | rs8130963 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 26920143] Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population.