rs3112612
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3112612(C;C) |
Make rs3112612(C;T) |
Make rs3112612(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 52601252 |
Gene | CASC16 |
is a | snp |
is | mentioned by |
dbSNP | rs3112612 |
dbSNP (classic) | rs3112612 |
ClinGen | rs3112612 |
ebi | rs3112612 |
HLI | rs3112612 |
Exac | rs3112612 |
Gnomad | rs3112612 |
Varsome | rs3112612 |
LitVar | rs3112612 |
Map | rs3112612 |
PheGenI | rs3112612 |
Biobank | rs3112612 |
1000 genomes | rs3112612 |
hgdp | rs3112612 |
ensembl | rs3112612 |
geneview | rs3112612 |
scholar | rs3112612 |
rs3112612 | |
pharmgkb | rs3112612 |
gwascentral | rs3112612 |
openSNP | rs3112612 |
23andMe | rs3112612 |
SNPshot | rs3112612 |
SNPdbe | rs3112612 |
MSV3d | rs3112612 |
GWAS Ctlg | rs3112612 |
GMAF | 0.4426 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21263130] |
Trait | |
Title | Novel Breast Cancer Susceptibility Locus at 9q31.2: Results of a Genome-Wide Association Study |
Risk Allele | T |
P-val | 4E-10 |
Odds Ratio | 1.1500 [1.10-1.21] |
[PMID 23354978] Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation.