rs367823977
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs367823977(A;G) |
Make rs367823977(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 19 |
Position | 41422353 |
Gene | BCKDHA |
is a | snp |
is | mentioned by |
dbSNP | rs367823977 |
dbSNP (classic) | rs367823977 |
ClinGen | rs367823977 |
ebi | rs367823977 |
HLI | rs367823977 |
Exac | rs367823977 |
Gnomad | rs367823977 |
Varsome | rs367823977 |
LitVar | rs367823977 |
Map | rs367823977 |
PheGenI | rs367823977 |
Biobank | rs367823977 |
1000 genomes | rs367823977 |
hgdp | rs367823977 |
ensembl | rs367823977 |
geneview | rs367823977 |
scholar | rs367823977 |
rs367823977 | |
pharmgkb | rs367823977 |
gwascentral | rs367823977 |
openSNP | rs367823977 |
23andMe | rs367823977 |
SNPshot | rs367823977 |
SNPdbe | rs367823977 |
MSV3d | rs367823977 |
GWAS Ctlg | rs367823977 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs367823977(G;G) |
Alt | rs367823977(G;G) |
Reference | Rs367823977(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | BCKDHA |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.41928258A>G |
CLNSRC | |
CLNACC | RCV000224751.1, |