rs796051917
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CT;CT) | 0 | common in clinvar |
Make rs796051917(-;-) |
Make rs796051917(-;CT) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 7224863 |
Gene | ACADVL, DVL2, MIR324 |
is a | snp |
is | mentioned by |
dbSNP | rs796051917 |
dbSNP (classic) | rs796051917 |
ClinGen | rs796051917 |
ebi | rs796051917 |
HLI | rs796051917 |
Exac | rs796051917 |
Gnomad | rs796051917 |
Varsome | rs796051917 |
LitVar | rs796051917 |
Map | rs796051917 |
PheGenI | rs796051917 |
Biobank | rs796051917 |
1000 genomes | rs796051917 |
hgdp | rs796051917 |
ensembl | rs796051917 |
geneview | rs796051917 |
scholar | rs796051917 |
rs796051917 | |
pharmgkb | rs796051917 |
gwascentral | rs796051917 |
openSNP | rs796051917 |
23andMe | rs796051917 |
SNPshot | rs796051917 |
SNPdbe | rs796051917 |
MSV3d | rs796051917 |
GWAS Ctlg | rs796051917 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796051917(-;-) |
Alt | rs796051917(-;-) |
Reference | Rs796051917(CT;CT) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MIR324 ACADVL DVL2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.7128182_7128183delCT |
CLNSRC | |
CLNACC | RCV000185740.1, |