rs369586696
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs369586696(A;G) |
Make rs369586696(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 101421877 |
Gene | ALDOB |
is a | snp |
is | mentioned by |
dbSNP | rs369586696 |
dbSNP (classic) | rs369586696 |
ClinGen | rs369586696 |
ebi | rs369586696 |
HLI | rs369586696 |
Exac | rs369586696 |
Gnomad | rs369586696 |
Varsome | rs369586696 |
LitVar | rs369586696 |
Map | rs369586696 |
PheGenI | rs369586696 |
Biobank | rs369586696 |
1000 genomes | rs369586696 |
hgdp | rs369586696 |
ensembl | rs369586696 |
geneview | rs369586696 |
scholar | rs369586696 |
rs369586696 | |
pharmgkb | rs369586696 |
gwascentral | rs369586696 |
openSNP | rs369586696 |
23andMe | rs369586696 |
SNPshot | rs369586696 |
SNPdbe | rs369586696 |
MSV3d | rs369586696 |
GWAS Ctlg | rs369586696 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs369586696(G;G) |
Alt | rs369586696(G;G) |
Reference | Rs369586696(A;A) |
Significance | Pathogenic |
Disease | Hereditary fructosuria |
Variation | info |
Gene | ALDOB |
CLNDBN | Hereditary fructosuria |
Reversed | 0 |
HGVS | NC_000009.11:g.104184159A>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000023971.3, |