rs587783010
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(TT;TT) | 0 | common in clinvar |
Make rs587783010(-;-) |
Make rs587783010(-;TT) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 12 |
Position | 88111320 |
Gene | CEP290 |
is a | snp |
is | mentioned by |
dbSNP | rs587783010 |
dbSNP (classic) | rs587783010 |
ClinGen | rs587783010 |
ebi | rs587783010 |
HLI | rs587783010 |
Exac | rs587783010 |
Gnomad | rs587783010 |
Varsome | rs587783010 |
LitVar | rs587783010 |
Map | rs587783010 |
PheGenI | rs587783010 |
Biobank | rs587783010 |
1000 genomes | rs587783010 |
hgdp | rs587783010 |
ensembl | rs587783010 |
geneview | rs587783010 |
scholar | rs587783010 |
rs587783010 | |
pharmgkb | rs587783010 |
gwascentral | rs587783010 |
openSNP | rs587783010 |
23andMe | rs587783010 |
SNPshot | rs587783010 |
SNPdbe | rs587783010 |
MSV3d | rs587783010 |
GWAS Ctlg | rs587783010 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587783010(-;-) |
Alt | rs587783010(-;-) |
Reference | Rs587783010(TT;TT) |
Significance | Pathogenic |
Disease | Leber congenital amaurosis 10 |
Variation | info |
Gene | CEP290 |
CLNDBN | Leber congenital amaurosis 10 |
Reversed | 1 |
HGVS | NC_000012.11:g.88505097_88505098delAA |
CLNSRC | |
CLNACC | RCV000144460.1, |