rs61753022
From SNPedia
Merged into | rs61750566 |
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(AC;AC) | 0 | common in clinvar |
Make rs61753022(-;-) |
Make rs61753022(-;CA) |
Make rs61753022(CA;CA) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 94019617 |
Gene | ABCA4 |
is a | snp |
is | mentioned by |
dbSNP | rs61753022 |
dbSNP (classic) | rs61753022 |
ClinGen | rs61753022 |
ebi | rs61753022 |
HLI | rs61753022 |
Exac | rs61753022 |
Gnomad | rs61753022 |
Varsome | rs61753022 |
LitVar | rs61753022 |
Map | rs61753022 |
PheGenI | rs61753022 |
Biobank | rs61753022 |
1000 genomes | rs61753022 |
hgdp | rs61753022 |
ensembl | rs61753022 |
geneview | rs61753022 |
scholar | rs61753022 |
rs61753022 | |
pharmgkb | rs61753022 |
gwascentral | rs61753022 |
openSNP | rs61753022 |
23andMe | rs61753022 |
SNPshot | rs61753022 |
SNPdbe | rs61753022 |
MSV3d | rs61753022 |
GWAS Ctlg | rs61753022 |
Status | Merged into rs61750566 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs61753022(AC;AC) |
Significance | Pathogenic |
Disease | not provided Stargardt disease 1 |
Variation | info |
Gene | ABCA4 |
CLNDBN | not provided Stargardt disease 1 |
Reversed | 1 |
HGVS | NC_000001.10:g.94485172_94485173delGT |
CLNSRC | |
CLNACC | RCV000085702.2, RCV000301420.1, |