rs796051906
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CGC;CGC) | 0 | common in clinvar |
Make rs796051906(CGC;TGT) |
Make rs796051906(TGT;TGT) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 120738874 |
Gene | ACADS |
is a | snp |
is | mentioned by |
dbSNP | rs796051906 |
dbSNP (classic) | rs796051906 |
ClinGen | rs796051906 |
ebi | rs796051906 |
HLI | rs796051906 |
Exac | rs796051906 |
Gnomad | rs796051906 |
Varsome | rs796051906 |
LitVar | rs796051906 |
Map | rs796051906 |
PheGenI | rs796051906 |
Biobank | rs796051906 |
1000 genomes | rs796051906 |
hgdp | rs796051906 |
ensembl | rs796051906 |
geneview | rs796051906 |
scholar | rs796051906 |
rs796051906 | |
pharmgkb | rs796051906 |
gwascentral | rs796051906 |
openSNP | rs796051906 |
23andMe | rs796051906 |
SNPshot | rs796051906 |
SNPdbe | rs796051906 |
MSV3d | rs796051906 |
GWAS Ctlg | rs796051906 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796051906(TGT;TGT) |
Alt | rs796051906(TGT;TGT) |
Reference | Rs796051906(CGC;CGC) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACADS |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.121176677_121176679delCGCinsTGT |
CLNSRC | |
CLNACC | RCV000185708.3, |