rs4897475
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4897475(A;A) |
Make rs4897475(A;G) |
Make rs4897475(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 130911810 |
Gene | EPB41L2 |
is a | snp |
is | mentioned by |
dbSNP | rs4897475 |
dbSNP (classic) | rs4897475 |
ClinGen | rs4897475 |
ebi | rs4897475 |
HLI | rs4897475 |
Exac | rs4897475 |
Gnomad | rs4897475 |
Varsome | rs4897475 |
LitVar | rs4897475 |
Map | rs4897475 |
PheGenI | rs4897475 |
Biobank | rs4897475 |
1000 genomes | rs4897475 |
hgdp | rs4897475 |
ensembl | rs4897475 |
geneview | rs4897475 |
scholar | rs4897475 |
rs4897475 | |
pharmgkb | rs4897475 |
gwascentral | rs4897475 |
openSNP | rs4897475 |
23andMe | rs4897475 |
SNPshot | rs4897475 |
SNPdbe | rs4897475 |
MSV3d | rs4897475 |
GWAS Ctlg | rs4897475 |
GMAF | 0.1529 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 17903294] risk of cardiovascular disease rs4897475 in erythrocyte membrane protein band 4.1-like 2 (EPB41L2) associated with hematological phenotypes (GEE p < 10(-3))