rs587783016
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs587783016(C;T) |
Make rs587783016(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 12 |
Position | 88089157 |
Gene | CEP290 |
is a | snp |
is | mentioned by |
dbSNP | rs587783016 |
dbSNP (classic) | rs587783016 |
ClinGen | rs587783016 |
ebi | rs587783016 |
HLI | rs587783016 |
Exac | rs587783016 |
Gnomad | rs587783016 |
Varsome | rs587783016 |
LitVar | rs587783016 |
Map | rs587783016 |
PheGenI | rs587783016 |
Biobank | rs587783016 |
1000 genomes | rs587783016 |
hgdp | rs587783016 |
ensembl | rs587783016 |
geneview | rs587783016 |
scholar | rs587783016 |
rs587783016 | |
pharmgkb | rs587783016 |
gwascentral | rs587783016 |
openSNP | rs587783016 |
23andMe | rs587783016 |
SNPshot | rs587783016 |
SNPdbe | rs587783016 |
MSV3d | rs587783016 |
GWAS Ctlg | rs587783016 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587783016(T;T) |
Alt | rs587783016(T;T) |
Reference | Rs587783016(C;C) |
Significance | Pathogenic |
Disease | Leber congenital amaurosis 10 Joubert syndrome 5 |
Variation | info |
Gene | CEP290 |
CLNDBN | Leber congenital amaurosis 10 Joubert syndrome 5 |
Reversed | 1 |
HGVS | NC_000012.11:g.88482934G>A |
CLNSRC | |
CLNACC | RCV000144467.1, RCV000201586.1, |