rs201908721
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs201908721(C;T) |
Make rs201908721(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 226982719 |
Gene | ADCK3, COQ8A |
is a | snp |
is | mentioned by |
dbSNP | rs201908721 |
dbSNP (classic) | rs201908721 |
ClinGen | rs201908721 |
ebi | rs201908721 |
HLI | rs201908721 |
Exac | rs201908721 |
Gnomad | rs201908721 |
Varsome | rs201908721 |
LitVar | rs201908721 |
Map | rs201908721 |
PheGenI | rs201908721 |
Biobank | rs201908721 |
1000 genomes | rs201908721 |
hgdp | rs201908721 |
ensembl | rs201908721 |
geneview | rs201908721 |
scholar | rs201908721 |
rs201908721 | |
pharmgkb | rs201908721 |
gwascentral | rs201908721 |
openSNP | rs201908721 |
23andMe | rs201908721 |
SNPshot | rs201908721 |
SNPdbe | rs201908721 |
MSV3d | rs201908721 |
GWAS Ctlg | rs201908721 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201908721(T;T) |
Alt | rs201908721(T;T) |
Reference | Rs201908721(C;C) |
Significance | Pathogenic |
Disease | not provided Coenzyme Q10 deficiency |
Variation | info |
Gene | COQ8A ADCK3 |
CLNDBN | not provided Coenzyme Q10 deficiency, primary, 4 |
Reversed | 0 |
HGVS | NC_000001.10:g.227170420C>T |
CLNSRC | |
CLNACC | RCV000413531.1, RCV000416388.1, |