rs16901937
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16901937(A;A) |
Make rs16901937(A;G) |
Make rs16901937(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 44709039 |
is a | snp |
is | mentioned by |
dbSNP | rs16901937 |
dbSNP (classic) | rs16901937 |
ClinGen | rs16901937 |
ebi | rs16901937 |
HLI | rs16901937 |
Exac | rs16901937 |
Gnomad | rs16901937 |
Varsome | rs16901937 |
LitVar | rs16901937 |
Map | rs16901937 |
PheGenI | rs16901937 |
Biobank | rs16901937 |
1000 genomes | rs16901937 |
hgdp | rs16901937 |
ensembl | rs16901937 |
geneview | rs16901937 |
scholar | rs16901937 |
rs16901937 | |
pharmgkb | rs16901937 |
gwascentral | rs16901937 |
openSNP | rs16901937 |
23andMe | rs16901937 |
SNPshot | rs16901937 |
SNPdbe | rs16901937 |
MSV3d | rs16901937 |
GWAS Ctlg | rs16901937 |
GMAF | 0.4155 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20140701] Genetic variants on chromosome 5p12 are associated with risk of breast cancer in African American women: the Black Women's Health Study