rs1058372
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs1058372(C;C) |
Make rs1058372(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 16148904 |
Gene | EPHA2 |
is a | snp |
is | mentioned by |
dbSNP | rs1058372 |
dbSNP (classic) | rs1058372 |
ClinGen | rs1058372 |
ebi | rs1058372 |
HLI | rs1058372 |
Exac | rs1058372 |
Gnomad | rs1058372 |
Varsome | rs1058372 |
LitVar | rs1058372 |
Map | rs1058372 |
PheGenI | rs1058372 |
Biobank | rs1058372 |
1000 genomes | rs1058372 |
hgdp | rs1058372 |
ensembl | rs1058372 |
geneview | rs1058372 |
scholar | rs1058372 |
rs1058372 | |
pharmgkb | rs1058372 |
gwascentral | rs1058372 |
openSNP | rs1058372 |
23andMe | rs1058372 |
SNPshot | rs1058372 |
SNPdbe | rs1058372 |
MSV3d | rs1058372 |
GWAS Ctlg | rs1058372 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 22829731] Screening and structural evaluation of deleterious Non-Synonymous SNPs of ePHA2 gene involved in susceptibility to cataract formation