rs863224845
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs863224845(C;T) |
Make rs863224845(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 128912587 |
Gene | ACAD9, KIAA1257 |
is a | snp |
is | mentioned by |
dbSNP | rs863224845 |
dbSNP (classic) | rs863224845 |
ClinGen | rs863224845 |
ebi | rs863224845 |
HLI | rs863224845 |
Exac | rs863224845 |
Gnomad | rs863224845 |
Varsome | rs863224845 |
LitVar | rs863224845 |
Map | rs863224845 |
PheGenI | rs863224845 |
Biobank | rs863224845 |
1000 genomes | rs863224845 |
hgdp | rs863224845 |
ensembl | rs863224845 |
geneview | rs863224845 |
scholar | rs863224845 |
rs863224845 | |
pharmgkb | rs863224845 |
gwascentral | rs863224845 |
openSNP | rs863224845 |
23andMe | rs863224845 |
SNPshot | rs863224845 |
SNPdbe | rs863224845 |
MSV3d | rs863224845 |
GWAS Ctlg | rs863224845 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863224845(T;T) |
Alt | rs863224845(T;T) |
Reference | Rs863224845(C;C) |
Significance | Probable-Pathogenic |
Disease | Acyl-CoA dehydrogenase family |
Variation | info |
Gene | ACAD9 LOC100132731 |
CLNDBN | Acyl-CoA dehydrogenase family, member 9, deficiency of |
Reversed | 0 |
HGVS | NC_000003.11:g.128631430C>T |
CLNSRC | |
CLNACC | RCV000199949.1, |