rs869025222
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs869025222(C;C) |
Make rs869025222(C;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 3 |
Position | 25580574 |
Gene | RARB |
is a | snp |
is | mentioned by |
dbSNP | rs869025222 |
dbSNP (classic) | rs869025222 |
ClinGen | rs869025222 |
ebi | rs869025222 |
HLI | rs869025222 |
Exac | rs869025222 |
Gnomad | rs869025222 |
Varsome | rs869025222 |
LitVar | rs869025222 |
Map | rs869025222 |
PheGenI | rs869025222 |
Biobank | rs869025222 |
1000 genomes | rs869025222 |
hgdp | rs869025222 |
ensembl | rs869025222 |
geneview | rs869025222 |
scholar | rs869025222 |
rs869025222 | |
pharmgkb | rs869025222 |
gwascentral | rs869025222 |
openSNP | rs869025222 |
23andMe | rs869025222 |
SNPshot | rs869025222 |
SNPdbe | rs869025222 |
MSV3d | rs869025222 |
GWAS Ctlg | rs869025222 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs869025222(C;C) |
Alt | rs869025222(C;C) |
Reference | Rs869025222(T;T) |
Significance | Probable-Pathogenic |
Disease | Microphthalmia |
Variation | info |
Gene | RARB |
CLNDBN | Microphthalmia, syndromic 12 |
Reversed | 0 |
HGVS | NC_000003.11:g.25622065T>C |
CLNSRC | |
CLNACC | RCV000207485.1, |