rs756489804
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs756489804(C;G) |
Make rs756489804(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 97611514 |
Gene | HOGA1 |
is a | snp |
is | mentioned by |
dbSNP | rs756489804 |
dbSNP (classic) | rs756489804 |
ClinGen | rs756489804 |
ebi | rs756489804 |
HLI | rs756489804 |
Exac | rs756489804 |
Gnomad | rs756489804 |
Varsome | rs756489804 |
LitVar | rs756489804 |
Map | rs756489804 |
PheGenI | rs756489804 |
Biobank | rs756489804 |
1000 genomes | rs756489804 |
hgdp | rs756489804 |
ensembl | rs756489804 |
geneview | rs756489804 |
scholar | rs756489804 |
rs756489804 | |
pharmgkb | rs756489804 |
gwascentral | rs756489804 |
openSNP | rs756489804 |
23andMe | rs756489804 |
SNPshot | rs756489804 |
SNPdbe | rs756489804 |
MSV3d | rs756489804 |
GWAS Ctlg | rs756489804 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs756489804(G;G) rs756489804(T;T) |
Alt | rs756489804(G;G) rs756489804(T;T) |
Reference | Rs756489804(C;C) |
Significance | Pathogenic |
Disease | Primary hyperoxaluria |
Variation | info |
Gene | HOGA1 |
CLNDBN | Primary hyperoxaluria, type III |
Reversed | 0 |
HGVS | NC_000010.10:g.99371271C>T |
CLNSRC | |
CLNACC | RCV000186484.1, |