rs886042807
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AA;AA) | 0 | common in clinvar |
Chromosome | 1 |
Position | 68446805 |
Gene | RPE65 |
is a | snp |
is | mentioned by |
dbSNP | rs886042807 |
dbSNP (classic) | rs886042807 |
ClinGen | rs886042807 |
ebi | rs886042807 |
HLI | rs886042807 |
Exac | rs886042807 |
Gnomad | rs886042807 |
Varsome | rs886042807 |
LitVar | rs886042807 |
Map | rs886042807 |
PheGenI | rs886042807 |
Biobank | rs886042807 |
1000 genomes | rs886042807 |
hgdp | rs886042807 |
ensembl | rs886042807 |
geneview | rs886042807 |
scholar | rs886042807 |
rs886042807 | |
pharmgkb | rs886042807 |
gwascentral | rs886042807 |
openSNP | rs886042807 |
23andMe | rs886042807 |
SNPshot | rs886042807 |
SNPdbe | rs886042807 |
MSV3d | rs886042807 |
GWAS Ctlg | rs886042807 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886042807(-;-) |
Alt | rs886042807(-;-) |
Reference | Rs886042807(AA;AA) |
Significance | Pathogenic |
Disease | Leber congenital amaurosis 2 |
Variation | info |
Gene | RPE65 |
CLNDBN | Leber congenital amaurosis 2 |
Reversed | 0 |
HGVS | NC_000001.10:g.68912488_68912489delAA |
CLNSRC | |
CLNACC | RCV000368059.1, |