rs200995432
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs200995432(G;G) |
Make rs200995432(G;T) |
Make rs200995432(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 65872330 |
Gene | EFEMP2 |
is a | snp |
is | mentioned by |
dbSNP | rs200995432 |
dbSNP (classic) | rs200995432 |
ClinGen | rs200995432 |
ebi | rs200995432 |
HLI | rs200995432 |
Exac | rs200995432 |
Gnomad | rs200995432 |
Varsome | rs200995432 |
LitVar | rs200995432 |
Map | rs200995432 |
PheGenI | rs200995432 |
Biobank | rs200995432 |
1000 genomes | rs200995432 |
hgdp | rs200995432 |
ensembl | rs200995432 |
geneview | rs200995432 |
scholar | rs200995432 |
rs200995432 | |
pharmgkb | rs200995432 |
gwascentral | rs200995432 |
openSNP | rs200995432 |
23andMe | rs200995432 |
SNPshot | rs200995432 |
SNPdbe | rs200995432 |
MSV3d | rs200995432 |
GWAS Ctlg | rs200995432 |
GMAF | 0.0009183 |
Max Magnitude | 0 |
[PMID 24470074] Rare coding variants and breast cancer risk: Evaluation of susceptibility loci identified in genome-wide association studies