rs146453758
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs146453758(C;T) |
Make rs146453758(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 128896520 |
Gene | ACAD9 |
is a | snp |
is | mentioned by |
dbSNP | rs146453758 |
dbSNP (classic) | rs146453758 |
ClinGen | rs146453758 |
ebi | rs146453758 |
HLI | rs146453758 |
Exac | rs146453758 |
Gnomad | rs146453758 |
Varsome | rs146453758 |
LitVar | rs146453758 |
Map | rs146453758 |
PheGenI | rs146453758 |
Biobank | rs146453758 |
1000 genomes | rs146453758 |
hgdp | rs146453758 |
ensembl | rs146453758 |
geneview | rs146453758 |
scholar | rs146453758 |
rs146453758 | |
pharmgkb | rs146453758 |
gwascentral | rs146453758 |
openSNP | rs146453758 |
23andMe | rs146453758 |
SNPshot | rs146453758 |
SNPdbe | rs146453758 |
MSV3d | rs146453758 |
GWAS Ctlg | rs146453758 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs146453758(T;T) |
Alt | rs146453758(T;T) |
Reference | Rs146453758(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACAD9 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.128615363C>T |
CLNSRC | |
CLNACC | RCV000200617.1, |