rs752130338
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs752130338(A;A) |
Make rs752130338(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 226986637 |
Gene | ADCK3, COQ8A |
is a | snp |
is | mentioned by |
dbSNP | rs752130338 |
dbSNP (classic) | rs752130338 |
ClinGen | rs752130338 |
ebi | rs752130338 |
HLI | rs752130338 |
Exac | rs752130338 |
Gnomad | rs752130338 |
Varsome | rs752130338 |
LitVar | rs752130338 |
Map | rs752130338 |
PheGenI | rs752130338 |
Biobank | rs752130338 |
1000 genomes | rs752130338 |
hgdp | rs752130338 |
ensembl | rs752130338 |
geneview | rs752130338 |
scholar | rs752130338 |
rs752130338 | |
pharmgkb | rs752130338 |
gwascentral | rs752130338 |
openSNP | rs752130338 |
23andMe | rs752130338 |
SNPshot | rs752130338 |
SNPdbe | rs752130338 |
MSV3d | rs752130338 |
GWAS Ctlg | rs752130338 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs752130338(A;A) rs752130338(C;C) |
Alt | rs752130338(A;A) rs752130338(C;C) |
Reference | Rs752130338(G;G) |
Significance | Pathogenic |
Disease | Coenzyme Q10 deficiency |
Variation | info |
Gene | COQ8A ADCK3 |
CLNDBN | Coenzyme Q10 deficiency, primary, 4 |
Reversed | 0 |
HGVS | NC_000001.10:g.227174338G>A |
CLNSRC | |
CLNACC | RCV000416410.1, |