rs1057517886
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs1057517886(A;T) |
Make rs1057517886(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 12 |
Position | 88139174 |
Gene | CEP290 |
is a | snp |
is | mentioned by |
dbSNP | rs1057517886 |
dbSNP (classic) | rs1057517886 |
ClinGen | rs1057517886 |
ebi | rs1057517886 |
HLI | rs1057517886 |
Exac | rs1057517886 |
Gnomad | rs1057517886 |
Varsome | rs1057517886 |
LitVar | rs1057517886 |
Map | rs1057517886 |
PheGenI | rs1057517886 |
Biobank | rs1057517886 |
1000 genomes | rs1057517886 |
hgdp | rs1057517886 |
ensembl | rs1057517886 |
geneview | rs1057517886 |
scholar | rs1057517886 |
rs1057517886 | |
pharmgkb | rs1057517886 |
gwascentral | rs1057517886 |
openSNP | rs1057517886 |
23andMe | rs1057517886 |
SNPshot | rs1057517886 |
SNPdbe | rs1057517886 |
MSV3d | rs1057517886 |
GWAS Ctlg | rs1057517886 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057517886(T;T) |
Alt | rs1057517886(T;T) |
Reference | Rs1057517886(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CEP290 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000012.11:g.88532951T>A |
CLNSRC | |
CLNACC | RCV000413097.1, |