rs755562733
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs755562733(G;T) |
Make rs755562733(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 97601889 |
Gene | HOGA1 |
is a | snp |
is | mentioned by |
dbSNP | rs755562733 |
dbSNP (classic) | rs755562733 |
ClinGen | rs755562733 |
ebi | rs755562733 |
HLI | rs755562733 |
Exac | rs755562733 |
Gnomad | rs755562733 |
Varsome | rs755562733 |
LitVar | rs755562733 |
Map | rs755562733 |
PheGenI | rs755562733 |
Biobank | rs755562733 |
1000 genomes | rs755562733 |
hgdp | rs755562733 |
ensembl | rs755562733 |
geneview | rs755562733 |
scholar | rs755562733 |
rs755562733 | |
pharmgkb | rs755562733 |
gwascentral | rs755562733 |
openSNP | rs755562733 |
23andMe | rs755562733 |
SNPshot | rs755562733 |
SNPdbe | rs755562733 |
MSV3d | rs755562733 |
GWAS Ctlg | rs755562733 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs755562733(A;A) rs755562733(T;T) |
Alt | rs755562733(A;A) rs755562733(T;T) |
Reference | Rs755562733(G;G) |
Significance | Pathogenic |
Disease | Primary hyperoxaluria |
Variation | info |
Gene | HOGA1 |
CLNDBN | Primary hyperoxaluria, type III |
Reversed | 0 |
HGVS | NC_000010.10:g.99361646G>A |
CLNSRC | |
CLNACC | RCV000186482.1, |