rs7558081
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7558081(C;C) |
Make rs7558081(C;T) |
Make rs7558081(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 227093753 |
Gene | COL4A4 |
is a | snp |
is | mentioned by |
dbSNP | rs7558081 |
dbSNP (classic) | rs7558081 |
ClinGen | rs7558081 |
ebi | rs7558081 |
HLI | rs7558081 |
Exac | rs7558081 |
Gnomad | rs7558081 |
Varsome | rs7558081 |
LitVar | rs7558081 |
Map | rs7558081 |
PheGenI | rs7558081 |
Biobank | rs7558081 |
1000 genomes | rs7558081 |
hgdp | rs7558081 |
ensembl | rs7558081 |
geneview | rs7558081 |
scholar | rs7558081 |
rs7558081 | |
pharmgkb | rs7558081 |
gwascentral | rs7558081 |
openSNP | rs7558081 |
23andMe | rs7558081 |
SNPshot | rs7558081 |
SNPdbe | rs7558081 |
MSV3d | rs7558081 |
GWAS Ctlg | rs7558081 |
GMAF | 0.4766 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22723992] Common variants in the COL4A4 gene confer susceptibility to lattice degeneration of the retina