rs150702945
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs150702945(C;C) |
Make rs150702945(C;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 97598900 |
Gene | HOGA1 |
is a | snp |
is | mentioned by |
dbSNP | rs150702945 |
dbSNP (classic) | rs150702945 |
ClinGen | rs150702945 |
ebi | rs150702945 |
HLI | rs150702945 |
Exac | rs150702945 |
Gnomad | rs150702945 |
Varsome | rs150702945 |
LitVar | rs150702945 |
Map | rs150702945 |
PheGenI | rs150702945 |
Biobank | rs150702945 |
1000 genomes | rs150702945 |
hgdp | rs150702945 |
ensembl | rs150702945 |
geneview | rs150702945 |
scholar | rs150702945 |
rs150702945 | |
pharmgkb | rs150702945 |
gwascentral | rs150702945 |
openSNP | rs150702945 |
23andMe | rs150702945 |
SNPshot | rs150702945 |
SNPdbe | rs150702945 |
MSV3d | rs150702945 |
GWAS Ctlg | rs150702945 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs150702945(A;A) rs150702945(C;C) |
Alt | rs150702945(A;A) rs150702945(C;C) |
Reference | Rs150702945(G;G) |
Significance | Pathogenic |
Disease | Primary hyperoxaluria |
Variation | info |
Gene | HOGA1 |
CLNDBN | Primary hyperoxaluria, type III |
Reversed | 0 |
HGVS | NC_000010.10:g.99358657G>A |
CLNSRC | |
CLNACC | RCV000186477.1, |