rs758304537
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs758304537(C;T) |
Make rs758304537(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 97584911 |
Gene | HOGA1 |
is a | snp |
is | mentioned by |
dbSNP | rs758304537 |
dbSNP (classic) | rs758304537 |
ClinGen | rs758304537 |
ebi | rs758304537 |
HLI | rs758304537 |
Exac | rs758304537 |
Gnomad | rs758304537 |
Varsome | rs758304537 |
LitVar | rs758304537 |
Map | rs758304537 |
PheGenI | rs758304537 |
Biobank | rs758304537 |
1000 genomes | rs758304537 |
hgdp | rs758304537 |
ensembl | rs758304537 |
geneview | rs758304537 |
scholar | rs758304537 |
rs758304537 | |
pharmgkb | rs758304537 |
gwascentral | rs758304537 |
openSNP | rs758304537 |
23andMe | rs758304537 |
SNPshot | rs758304537 |
SNPdbe | rs758304537 |
MSV3d | rs758304537 |
GWAS Ctlg | rs758304537 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs758304537(T;T) |
Alt | rs758304537(T;T) |
Reference | Rs758304537(C;C) |
Significance | Pathogenic |
Disease | Primary hyperoxaluria |
Variation | info |
Gene | HOGA1 |
CLNDBN | Primary hyperoxaluria, type III |
Reversed | 0 |
HGVS | NC_000010.10:g.99344668C>T |
CLNSRC | |
CLNACC | RCV000186476.1, |