rs113882203
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs113882203(C;T) |
Make rs113882203(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 16148725 |
Gene | EPHA2 |
is a | snp |
is | mentioned by |
dbSNP | rs113882203 |
dbSNP (classic) | rs113882203 |
ClinGen | rs113882203 |
ebi | rs113882203 |
HLI | rs113882203 |
Exac | rs113882203 |
Gnomad | rs113882203 |
Varsome | rs113882203 |
LitVar | rs113882203 |
Map | rs113882203 |
PheGenI | rs113882203 |
Biobank | rs113882203 |
1000 genomes | rs113882203 |
hgdp | rs113882203 |
ensembl | rs113882203 |
geneview | rs113882203 |
scholar | rs113882203 |
rs113882203 | |
pharmgkb | rs113882203 |
gwascentral | rs113882203 |
openSNP | rs113882203 |
23andMe | rs113882203 |
SNPshot | rs113882203 |
SNPdbe | rs113882203 |
MSV3d | rs113882203 |
GWAS Ctlg | rs113882203 |
Max Magnitude | 0 |
[PMID 22829731] Screening and structural evaluation of deleterious Non-Synonymous SNPs of ePHA2 gene involved in susceptibility to cataract formation