rs374726386
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs374726386(A;A) |
Make rs374726386(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 120738552 |
Gene | ACADS |
is a | snp |
is | mentioned by |
dbSNP | rs374726386 |
dbSNP (classic) | rs374726386 |
ClinGen | rs374726386 |
ebi | rs374726386 |
HLI | rs374726386 |
Exac | rs374726386 |
Gnomad | rs374726386 |
Varsome | rs374726386 |
LitVar | rs374726386 |
Map | rs374726386 |
PheGenI | rs374726386 |
Biobank | rs374726386 |
1000 genomes | rs374726386 |
hgdp | rs374726386 |
ensembl | rs374726386 |
geneview | rs374726386 |
scholar | rs374726386 |
rs374726386 | |
pharmgkb | rs374726386 |
gwascentral | rs374726386 |
openSNP | rs374726386 |
23andMe | rs374726386 |
SNPshot | rs374726386 |
SNPdbe | rs374726386 |
MSV3d | rs374726386 |
GWAS Ctlg | rs374726386 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs374726386(A;A) |
Alt | rs374726386(A;A) |
Reference | Rs374726386(G;G) |
Significance | Pathogenic |
Disease | not specified |
Variation | info |
Gene | ACADS |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000012.11:g.121176355G>A |
CLNSRC | |
CLNACC | RCV000185688.2, |