rs113690956
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs113690956(G;T) |
Make rs113690956(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 17 |
Position | 7223238 |
Gene | ACADVL, MIR324 |
is a | snp |
is | mentioned by |
dbSNP | rs113690956 |
dbSNP (classic) | rs113690956 |
ClinGen | rs113690956 |
ebi | rs113690956 |
HLI | rs113690956 |
Exac | rs113690956 |
Gnomad | rs113690956 |
Varsome | rs113690956 |
LitVar | rs113690956 |
Map | rs113690956 |
PheGenI | rs113690956 |
Biobank | rs113690956 |
1000 genomes | rs113690956 |
hgdp | rs113690956 |
ensembl | rs113690956 |
geneview | rs113690956 |
scholar | rs113690956 |
rs113690956 | |
pharmgkb | rs113690956 |
gwascentral | rs113690956 |
openSNP | rs113690956 |
23andMe | rs113690956 |
SNPshot | rs113690956 |
SNPdbe | rs113690956 |
MSV3d | rs113690956 |
GWAS Ctlg | rs113690956 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs113690956(A;A) rs113690956(T;T) |
Alt | rs113690956(A;A) rs113690956(T;T) |
Reference | Rs113690956(G;G) |
Significance | Other |
Disease | Very long chain acyl-CoA dehydrogenase deficiency |
Variation | info |
Gene | MIR324 ACADVL |
CLNDBN | Very long chain acyl-CoA dehydrogenase deficiency |
Reversed | 0 |
HGVS | NC_000017.10:g.7126557G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000001689.3, |