rs786205652
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs786205652(-;-) |
Make rs786205652(-;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 65495232 |
Gene | EYS |
is a | snp |
is | mentioned by |
dbSNP | rs786205652 |
dbSNP (classic) | rs786205652 |
ClinGen | rs786205652 |
ebi | rs786205652 |
HLI | rs786205652 |
Exac | rs786205652 |
Gnomad | rs786205652 |
Varsome | rs786205652 |
LitVar | rs786205652 |
Map | rs786205652 |
PheGenI | rs786205652 |
Biobank | rs786205652 |
1000 genomes | rs786205652 |
hgdp | rs786205652 |
ensembl | rs786205652 |
geneview | rs786205652 |
scholar | rs786205652 |
rs786205652 | |
pharmgkb | rs786205652 |
gwascentral | rs786205652 |
openSNP | rs786205652 |
23andMe | rs786205652 |
SNPshot | rs786205652 |
SNPdbe | rs786205652 |
MSV3d | rs786205652 |
GWAS Ctlg | rs786205652 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786205652(-;-) |
Alt | rs786205652(-;-) |
Reference | Rs786205652(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | EYS |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000006.11:g.66205125delA |
CLNSRC | |
CLNACC | RCV000171525.1, |