rs10490113
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10490113(A;A) |
Make rs10490113(A;C) |
Make rs10490113(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 59272212 |
Gene | LINC01793, LOC105374754 |
is a | snp |
is | mentioned by |
dbSNP | rs10490113 |
dbSNP (classic) | rs10490113 |
ClinGen | rs10490113 |
ebi | rs10490113 |
HLI | rs10490113 |
Exac | rs10490113 |
Gnomad | rs10490113 |
Varsome | rs10490113 |
LitVar | rs10490113 |
Map | rs10490113 |
PheGenI | rs10490113 |
Biobank | rs10490113 |
1000 genomes | rs10490113 |
hgdp | rs10490113 |
ensembl | rs10490113 |
geneview | rs10490113 |
scholar | rs10490113 |
rs10490113 | |
pharmgkb | rs10490113 |
gwascentral | rs10490113 |
openSNP | rs10490113 |
23andMe | rs10490113 |
SNPshot | rs10490113 |
SNPdbe | rs10490113 |
MSV3d | rs10490113 |
GWAS Ctlg | rs10490113 |
GMAF | 0.09596 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 17903305] |
Trait | Breast cancer |
Title | A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study |
Risk Allele | |
P-val | 0.0000050000000000000004 |
Odds Ratio | NR NR |