rs796051909
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs796051909(G;T) |
Make rs796051909(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 7221595 |
Gene | ACADVL, DLG4 |
is a | snp |
is | mentioned by |
dbSNP | rs796051909 |
dbSNP (classic) | rs796051909 |
ClinGen | rs796051909 |
ebi | rs796051909 |
HLI | rs796051909 |
Exac | rs796051909 |
Gnomad | rs796051909 |
Varsome | rs796051909 |
LitVar | rs796051909 |
Map | rs796051909 |
PheGenI | rs796051909 |
Biobank | rs796051909 |
1000 genomes | rs796051909 |
hgdp | rs796051909 |
ensembl | rs796051909 |
geneview | rs796051909 |
scholar | rs796051909 |
rs796051909 | |
pharmgkb | rs796051909 |
gwascentral | rs796051909 |
openSNP | rs796051909 |
23andMe | rs796051909 |
SNPshot | rs796051909 |
SNPdbe | rs796051909 |
MSV3d | rs796051909 |
GWAS Ctlg | rs796051909 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796051909(T;T) |
Alt | rs796051909(T;T) |
Reference | Rs796051909(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | DLG4 ACADVL |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.7124914G>T |
CLNSRC | |
CLNACC | RCV000185712.1, |