rs149150736
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs149150736(C;T) |
Make rs149150736(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 97611582 |
Gene | HOGA1 |
is a | snp |
is | mentioned by |
dbSNP | rs149150736 |
dbSNP (classic) | rs149150736 |
ClinGen | rs149150736 |
ebi | rs149150736 |
HLI | rs149150736 |
Exac | rs149150736 |
Gnomad | rs149150736 |
Varsome | rs149150736 |
LitVar | rs149150736 |
Map | rs149150736 |
PheGenI | rs149150736 |
Biobank | rs149150736 |
1000 genomes | rs149150736 |
hgdp | rs149150736 |
ensembl | rs149150736 |
geneview | rs149150736 |
scholar | rs149150736 |
rs149150736 | |
pharmgkb | rs149150736 |
gwascentral | rs149150736 |
openSNP | rs149150736 |
23andMe | rs149150736 |
SNPshot | rs149150736 |
SNPdbe | rs149150736 |
MSV3d | rs149150736 |
GWAS Ctlg | rs149150736 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs149150736(T;T) |
Alt | rs149150736(T;T) |
Reference | Rs149150736(C;C) |
Significance | Pathogenic |
Disease | Primary hyperoxaluria |
Variation | info |
Gene | HOGA1 |
CLNDBN | Primary hyperoxaluria, type III |
Reversed | 0 |
HGVS | NC_000010.10:g.99371339C>T |
CLNSRC | |
CLNACC | RCV000186486.1, |