rs6678616
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs6678616(C;T) |
Make rs6678616(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 16148628 |
Gene | EPHA2 |
is a | snp |
is | mentioned by |
dbSNP | rs6678616 |
dbSNP (classic) | rs6678616 |
ClinGen | rs6678616 |
ebi | rs6678616 |
HLI | rs6678616 |
Exac | rs6678616 |
Gnomad | rs6678616 |
Varsome | rs6678616 |
LitVar | rs6678616 |
Map | rs6678616 |
PheGenI | rs6678616 |
Biobank | rs6678616 |
1000 genomes | rs6678616 |
hgdp | rs6678616 |
ensembl | rs6678616 |
geneview | rs6678616 |
scholar | rs6678616 |
rs6678616 | |
pharmgkb | rs6678616 |
gwascentral | rs6678616 |
openSNP | rs6678616 |
23andMe | rs6678616 |
SNPshot | rs6678616 |
SNPdbe | rs6678616 |
MSV3d | rs6678616 |
GWAS Ctlg | rs6678616 |
GMAF | 0.2296 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19649315] EPHA2 is associated with age-related cortical cataract in mice and humans
ClinVar | |
---|---|
Risk | rs6678616(T;T) |
Alt | rs6678616(T;T) |
Reference | Rs6678616(C;C) |
Significance | Non-pathogenic |
Disease | not specified Age-related cortical cataract |
Variation | info |
Gene | EPHA2 |
CLNDBN | not specified Age-related cortical cataract |
Reversed | 0 |
HGVS | NC_000001.10:g.16475123C>T |
CLNSRC | |
CLNACC | RCV000253199.1, RCV000309096.1, |