rs61752909
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs61752909(C;C) |
Make rs61752909(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 68438293 |
Gene | RPE65 |
is a | snp |
is | mentioned by |
dbSNP | rs61752909 |
dbSNP (classic) | rs61752909 |
ClinGen | rs61752909 |
ebi | rs61752909 |
HLI | rs61752909 |
Exac | rs61752909 |
Gnomad | rs61752909 |
Varsome | rs61752909 |
LitVar | rs61752909 |
Map | rs61752909 |
PheGenI | rs61752909 |
Biobank | rs61752909 |
1000 genomes | rs61752909 |
hgdp | rs61752909 |
ensembl | rs61752909 |
geneview | rs61752909 |
scholar | rs61752909 |
rs61752909 | |
pharmgkb | rs61752909 |
gwascentral | rs61752909 |
openSNP | rs61752909 |
23andMe | rs61752909 |
SNPshot | rs61752909 |
SNPdbe | rs61752909 |
MSV3d | rs61752909 |
GWAS Ctlg | rs61752909 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs61752909(C;C) |
Alt | rs61752909(C;C) |
Reference | Rs61752909(T;T) |
Significance | Pathogenic |
Disease | Retinitis pigmentosa 20 not provided |
Variation | info |
Gene | RPE65 |
CLNDBN | Retinitis pigmentosa 20 not provided |
Reversed | 1 |
HGVS | NC_000001.10:g.68903976A>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000013997.24, RCV000085141.1, |