rs532007026
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs532007026(C;G) |
Make rs532007026(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 3 |
Position | 25733983 |
Gene | NGLY1 |
is a | snp |
is | mentioned by |
dbSNP | rs532007026 |
dbSNP (classic) | rs532007026 |
ClinGen | rs532007026 |
ebi | rs532007026 |
HLI | rs532007026 |
Exac | rs532007026 |
Gnomad | rs532007026 |
Varsome | rs532007026 |
LitVar | rs532007026 |
Map | rs532007026 |
PheGenI | rs532007026 |
Biobank | rs532007026 |
1000 genomes | rs532007026 |
hgdp | rs532007026 |
ensembl | rs532007026 |
geneview | rs532007026 |
scholar | rs532007026 |
rs532007026 | |
pharmgkb | rs532007026 |
gwascentral | rs532007026 |
openSNP | rs532007026 |
23andMe | rs532007026 |
SNPshot | rs532007026 |
SNPdbe | rs532007026 |
MSV3d | rs532007026 |
GWAS Ctlg | rs532007026 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs532007026(G;G) |
Alt | rs532007026(G;G) |
Reference | Rs532007026(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | NGLY1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.25775474C>G |
CLNSRC | |
CLNACC | RCV000413780.1, |