rs796052090
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs796052090(C;C) |
Make rs796052090(C;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 97599744 |
Gene | HOGA1 |
is a | snp |
is | mentioned by |
dbSNP | rs796052090 |
dbSNP (classic) | rs796052090 |
ClinGen | rs796052090 |
ebi | rs796052090 |
HLI | rs796052090 |
Exac | rs796052090 |
Gnomad | rs796052090 |
Varsome | rs796052090 |
LitVar | rs796052090 |
Map | rs796052090 |
PheGenI | rs796052090 |
Biobank | rs796052090 |
1000 genomes | rs796052090 |
hgdp | rs796052090 |
ensembl | rs796052090 |
geneview | rs796052090 |
scholar | rs796052090 |
rs796052090 | |
pharmgkb | rs796052090 |
gwascentral | rs796052090 |
openSNP | rs796052090 |
23andMe | rs796052090 |
SNPshot | rs796052090 |
SNPdbe | rs796052090 |
MSV3d | rs796052090 |
GWAS Ctlg | rs796052090 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796052090(C;C) |
Alt | rs796052090(C;C) |
Reference | Rs796052090(T;T) |
Significance | Pathogenic |
Disease | Primary hyperoxaluria |
Variation | info |
Gene | HOGA1 |
CLNDBN | Primary hyperoxaluria, type III |
Reversed | 0 |
HGVS | NC_000010.10:g.99359501T>C |
CLNSRC | |
CLNACC | RCV000186489.1, |