rs368949613
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs368949613(C;T) |
Make rs368949613(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 128906220 |
Gene | ACAD9 |
is a | snp |
is | mentioned by |
dbSNP | rs368949613 |
dbSNP (classic) | rs368949613 |
ClinGen | rs368949613 |
ebi | rs368949613 |
HLI | rs368949613 |
Exac | rs368949613 |
Gnomad | rs368949613 |
Varsome | rs368949613 |
LitVar | rs368949613 |
Map | rs368949613 |
PheGenI | rs368949613 |
Biobank | rs368949613 |
1000 genomes | rs368949613 |
hgdp | rs368949613 |
ensembl | rs368949613 |
geneview | rs368949613 |
scholar | rs368949613 |
rs368949613 | |
pharmgkb | rs368949613 |
gwascentral | rs368949613 |
openSNP | rs368949613 |
23andMe | rs368949613 |
SNPshot | rs368949613 |
SNPdbe | rs368949613 |
MSV3d | rs368949613 |
GWAS Ctlg | rs368949613 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs368949613(T;T) |
Alt | rs368949613(T;T) |
Reference | Rs368949613(C;C) |
Significance | Pathogenic |
Disease | Acyl-CoA dehydrogenase family |
Variation | info |
Gene | ACAD9 |
CLNDBN | Acyl-CoA dehydrogenase family, member 9, deficiency of |
Reversed | 0 |
HGVS | NC_000003.11:g.128625063C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000023865.3, RCV000201722.1, |