rs1136200
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs1136200(A;A) |
Make rs1136200(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 11810038 |
Gene | LINC00687 |
is a | snp |
is | mentioned by |
dbSNP | rs1136200 |
dbSNP (classic) | rs1136200 |
ClinGen | rs1136200 |
ebi | rs1136200 |
HLI | rs1136200 |
Exac | rs1136200 |
Gnomad | rs1136200 |
Varsome | rs1136200 |
LitVar | rs1136200 |
Map | rs1136200 |
PheGenI | rs1136200 |
Biobank | rs1136200 |
1000 genomes | rs1136200 |
hgdp | rs1136200 |
ensembl | rs1136200 |
geneview | rs1136200 |
scholar | rs1136200 |
rs1136200 | |
pharmgkb | rs1136200 |
gwascentral | rs1136200 |
openSNP | rs1136200 |
23andMe | rs1136200 |
SNPshot | rs1136200 |
SNPdbe | rs1136200 |
MSV3d | rs1136200 |
GWAS Ctlg | rs1136200 |
GMAF | 0.01653 |
Max Magnitude | 0 |
[PMID 18837888] and the risk of breast cancer