rs117356004
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs117356004(A;A) |
Make rs117356004(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 12 |
Position | 120737097 |
Gene | ACADS |
is a | snp |
is | mentioned by |
dbSNP | rs117356004 |
dbSNP (classic) | rs117356004 |
ClinGen | rs117356004 |
ebi | rs117356004 |
HLI | rs117356004 |
Exac | rs117356004 |
Gnomad | rs117356004 |
Varsome | rs117356004 |
LitVar | rs117356004 |
Map | rs117356004 |
PheGenI | rs117356004 |
Biobank | rs117356004 |
1000 genomes | rs117356004 |
hgdp | rs117356004 |
ensembl | rs117356004 |
geneview | rs117356004 |
scholar | rs117356004 |
rs117356004 | |
pharmgkb | rs117356004 |
gwascentral | rs117356004 |
openSNP | rs117356004 |
23andMe | rs117356004 |
SNPshot | rs117356004 |
SNPdbe | rs117356004 |
MSV3d | rs117356004 |
GWAS Ctlg | rs117356004 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs117356004(A;A) |
Alt | rs117356004(A;A) |
Reference | Rs117356004(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACADS |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.121174900G>A |
CLNSRC | |
CLNACC | RCV000442937.1, |