rs796051958
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs796051958(A;G) |
Make rs796051958(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 4 |
Position | 158697656 |
Gene | ETFDH |
is a | snp |
is | mentioned by |
dbSNP | rs796051958 |
dbSNP (classic) | rs796051958 |
ClinGen | rs796051958 |
ebi | rs796051958 |
HLI | rs796051958 |
Exac | rs796051958 |
Gnomad | rs796051958 |
Varsome | rs796051958 |
LitVar | rs796051958 |
Map | rs796051958 |
PheGenI | rs796051958 |
Biobank | rs796051958 |
1000 genomes | rs796051958 |
hgdp | rs796051958 |
ensembl | rs796051958 |
geneview | rs796051958 |
scholar | rs796051958 |
rs796051958 | |
pharmgkb | rs796051958 |
gwascentral | rs796051958 |
openSNP | rs796051958 |
23andMe | rs796051958 |
SNPshot | rs796051958 |
SNPdbe | rs796051958 |
MSV3d | rs796051958 |
GWAS Ctlg | rs796051958 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796051958(G;G) |
Alt | rs796051958(G;G) |
Reference | Rs796051958(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ETFDH |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.159618808A>G |
CLNSRC | |
CLNACC | RCV000185895.2, |