rs796051915
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs796051915(-;G) |
Make rs796051915(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 7223859 |
Gene | ACADVL, MIR324 |
is a | snp |
is | mentioned by |
dbSNP | rs796051915 |
dbSNP (classic) | rs796051915 |
ClinGen | rs796051915 |
ebi | rs796051915 |
HLI | rs796051915 |
Exac | rs796051915 |
Gnomad | rs796051915 |
Varsome | rs796051915 |
LitVar | rs796051915 |
Map | rs796051915 |
PheGenI | rs796051915 |
Biobank | rs796051915 |
1000 genomes | rs796051915 |
hgdp | rs796051915 |
ensembl | rs796051915 |
geneview | rs796051915 |
scholar | rs796051915 |
rs796051915 | |
pharmgkb | rs796051915 |
gwascentral | rs796051915 |
openSNP | rs796051915 |
23andMe | rs796051915 |
SNPshot | rs796051915 |
SNPdbe | rs796051915 |
MSV3d | rs796051915 |
GWAS Ctlg | rs796051915 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796051915(G;G) |
Alt | rs796051915(G;G) |
Reference | Rs796051915(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACADVL MIR324 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.7127178dupG |
CLNSRC | |
CLNACC | RCV000185738.1, |