rs776158594
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs776158594(A;G) |
Make rs776158594(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 22 |
Position | 50580356 |
Gene | CHKB, CHKB-CPT1B, CPT1B |
is a | snp |
is | mentioned by |
dbSNP | rs776158594 |
dbSNP (classic) | rs776158594 |
ClinGen | rs776158594 |
ebi | rs776158594 |
HLI | rs776158594 |
Exac | rs776158594 |
Gnomad | rs776158594 |
Varsome | rs776158594 |
LitVar | rs776158594 |
Map | rs776158594 |
PheGenI | rs776158594 |
Biobank | rs776158594 |
1000 genomes | rs776158594 |
hgdp | rs776158594 |
ensembl | rs776158594 |
geneview | rs776158594 |
scholar | rs776158594 |
rs776158594 | |
pharmgkb | rs776158594 |
gwascentral | rs776158594 |
openSNP | rs776158594 |
23andMe | rs776158594 |
SNPshot | rs776158594 |
SNPdbe | rs776158594 |
MSV3d | rs776158594 |
GWAS Ctlg | rs776158594 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs776158594(G;G) |
Alt | rs776158594(G;G) |
Reference | Rs776158594(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CHKB-CPT1B CHKB CPT1B |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000022.10:g.51018785A>G |
CLNSRC | |
CLNACC | RCV000494588.1, |