rs752197734
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common/normal |
Make rs752197734(A;T) |
Make rs752197734(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 12 |
Position | 88068657 |
Gene | CEP290 |
is a | snp |
is | mentioned by |
dbSNP | rs752197734 |
dbSNP (classic) | rs752197734 |
ClinGen | rs752197734 |
ebi | rs752197734 |
HLI | rs752197734 |
Exac | rs752197734 |
Gnomad | rs752197734 |
Varsome | rs752197734 |
LitVar | rs752197734 |
Map | rs752197734 |
PheGenI | rs752197734 |
Biobank | rs752197734 |
1000 genomes | rs752197734 |
hgdp | rs752197734 |
ensembl | rs752197734 |
geneview | rs752197734 |
scholar | rs752197734 |
rs752197734 | |
pharmgkb | rs752197734 |
gwascentral | rs752197734 |
openSNP | rs752197734 |
23andMe | rs752197734 |
SNPshot | rs752197734 |
SNPdbe | rs752197734 |
MSV3d | rs752197734 |
GWAS Ctlg | rs752197734 |
Max Magnitude | 0 |
Non-coding variant assessed as part of Blueprint Genetics Retinal dystrophy (266 gene) panel.