rs185803104
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs185803104(G;T) |
Make rs185803104(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 97600168 |
Gene | HOGA1 |
is a | snp |
is | mentioned by |
dbSNP | rs185803104 |
dbSNP (classic) | rs185803104 |
ClinGen | rs185803104 |
ebi | rs185803104 |
HLI | rs185803104 |
Exac | rs185803104 |
Gnomad | rs185803104 |
Varsome | rs185803104 |
LitVar | rs185803104 |
Map | rs185803104 |
PheGenI | rs185803104 |
Biobank | rs185803104 |
1000 genomes | rs185803104 |
hgdp | rs185803104 |
ensembl | rs185803104 |
geneview | rs185803104 |
scholar | rs185803104 |
rs185803104 | |
pharmgkb | rs185803104 |
gwascentral | rs185803104 |
openSNP | rs185803104 |
23andMe | rs185803104 |
SNPshot | rs185803104 |
SNPdbe | rs185803104 |
MSV3d | rs185803104 |
GWAS Ctlg | rs185803104 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs185803104(T;T) |
Alt | rs185803104(T;T) |
Reference | Rs185803104(G;G) |
Significance | Pathogenic |
Disease | Primary hyperoxaluria |
Variation | info |
Gene | HOGA1 |
CLNDBN | Primary hyperoxaluria, type III |
Reversed | 0 |
HGVS | NC_000010.10:g.99359925G>T |
CLNSRC | |
CLNACC | RCV000186492.2, |