rs672601351
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common genotype |
(TG;TG) | 0 | common in clinvar |
Make rs672601351(-;-) |
Make rs672601351(-;TG) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 9 |
Position | 37425955 |
Gene | GRHPR |
is a | snp |
is | mentioned by |
dbSNP | rs672601351 |
dbSNP (classic) | rs672601351 |
ClinGen | rs672601351 |
ebi | rs672601351 |
HLI | rs672601351 |
Exac | rs672601351 |
Gnomad | rs672601351 |
Varsome | rs672601351 |
LitVar | rs672601351 |
Map | rs672601351 |
PheGenI | rs672601351 |
Biobank | rs672601351 |
1000 genomes | rs672601351 |
hgdp | rs672601351 |
ensembl | rs672601351 |
geneview | rs672601351 |
scholar | rs672601351 |
rs672601351 | |
pharmgkb | rs672601351 |
gwascentral | rs672601351 |
openSNP | rs672601351 |
23andMe | rs672601351 |
SNPshot | rs672601351 |
SNPdbe | rs672601351 |
MSV3d | rs672601351 |
GWAS Ctlg | rs672601351 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs672601351(-;-) |
Alt | rs672601351(-;-) |
Reference | Rs672601351(TG;TG) |
Significance | Pathogenic |
Disease | Primary hyperoxaluria |
Variation | info |
Gene | GRHPR |
CLNDBN | Primary hyperoxaluria, type II |
Reversed | 0 |
HGVS | NC_000009.11:g.37425952_37425953delTG |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000149442.5, |