rs796051974
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs796051974(-;-) |
Make rs796051974(-;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 26283049 |
Gene | HADHB |
is a | snp |
is | mentioned by |
dbSNP | rs796051974 |
dbSNP (classic) | rs796051974 |
ClinGen | rs796051974 |
ebi | rs796051974 |
HLI | rs796051974 |
Exac | rs796051974 |
Gnomad | rs796051974 |
Varsome | rs796051974 |
LitVar | rs796051974 |
Map | rs796051974 |
PheGenI | rs796051974 |
Biobank | rs796051974 |
1000 genomes | rs796051974 |
hgdp | rs796051974 |
ensembl | rs796051974 |
geneview | rs796051974 |
scholar | rs796051974 |
rs796051974 | |
pharmgkb | rs796051974 |
gwascentral | rs796051974 |
openSNP | rs796051974 |
23andMe | rs796051974 |
SNPshot | rs796051974 |
SNPdbe | rs796051974 |
MSV3d | rs796051974 |
GWAS Ctlg | rs796051974 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796051974(-;-) |
Alt | rs796051974(-;-) |
Reference | Rs796051974(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | HADHB |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.26505917delT |
CLNSRC | |
CLNACC | RCV000185943.1, |