rs796052086
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs796052086(C;T) |
Make rs796052086(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 97601919 |
Gene | HOGA1 |
is a | snp |
is | mentioned by |
dbSNP | rs796052086 |
dbSNP (classic) | rs796052086 |
ClinGen | rs796052086 |
ebi | rs796052086 |
HLI | rs796052086 |
Exac | rs796052086 |
Gnomad | rs796052086 |
Varsome | rs796052086 |
LitVar | rs796052086 |
Map | rs796052086 |
PheGenI | rs796052086 |
Biobank | rs796052086 |
1000 genomes | rs796052086 |
hgdp | rs796052086 |
ensembl | rs796052086 |
geneview | rs796052086 |
scholar | rs796052086 |
rs796052086 | |
pharmgkb | rs796052086 |
gwascentral | rs796052086 |
openSNP | rs796052086 |
23andMe | rs796052086 |
SNPshot | rs796052086 |
SNPdbe | rs796052086 |
MSV3d | rs796052086 |
GWAS Ctlg | rs796052086 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796052086(T;T) |
Alt | rs796052086(T;T) |
Reference | Rs796052086(C;C) |
Significance | Pathogenic |
Disease | Primary hyperoxaluria |
Variation | info |
Gene | HOGA1 |
CLNDBN | Primary hyperoxaluria, type III |
Reversed | 0 |
HGVS | NC_000010.10:g.99361676C>T |
CLNSRC | |
CLNACC | RCV000186483.1, |