rs200967229
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 3 | Carrier of a mutation for Stargardt disease |
Make rs200967229(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 94030427 |
Gene | ABCA4 |
is a | snp |
is | mentioned by |
dbSNP | rs200967229 |
dbSNP (classic) | rs200967229 |
ClinGen | rs200967229 |
ebi | rs200967229 |
HLI | rs200967229 |
Exac | rs200967229 |
Gnomad | rs200967229 |
Varsome | rs200967229 |
LitVar | rs200967229 |
Map | rs200967229 |
PheGenI | rs200967229 |
Biobank | rs200967229 |
1000 genomes | rs200967229 |
hgdp | rs200967229 |
ensembl | rs200967229 |
geneview | rs200967229 |
scholar | rs200967229 |
rs200967229 | |
pharmgkb | rs200967229 |
gwascentral | rs200967229 |
openSNP | rs200967229 |
23andMe | rs200967229 |
SNPshot | rs200967229 |
SNPdbe | rs200967229 |
MSV3d | rs200967229 |
GWAS Ctlg | rs200967229 |
Max Magnitude | 3 |
ClinVar | |
---|---|
Risk | rs200967229(T;T) |
Alt | rs200967229(T;T) |
Reference | Rs200967229(C;C) |
Significance | Pathogenic |
Disease | Stargardt disease 1 |
Variation | info |
Gene | ABCA4 |
CLNDBN | Stargardt disease 1 |
Reversed | 0 |
HGVS | NC_000001.10:g.94495983C>T |
CLNSRC | |
CLNACC | RCV000408571.1, |