rs61995958
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs61995958(A;A) |
Make rs61995958(A;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 1 |
Position | 226986598 |
Gene | ADCK3, COQ8A |
is a | snp |
is | mentioned by |
dbSNP | rs61995958 |
dbSNP (classic) | rs61995958 |
ClinGen | rs61995958 |
ebi | rs61995958 |
HLI | rs61995958 |
Exac | rs61995958 |
Gnomad | rs61995958 |
Varsome | rs61995958 |
LitVar | rs61995958 |
Map | rs61995958 |
PheGenI | rs61995958 |
Biobank | rs61995958 |
1000 genomes | rs61995958 |
hgdp | rs61995958 |
ensembl | rs61995958 |
geneview | rs61995958 |
scholar | rs61995958 |
rs61995958 | |
pharmgkb | rs61995958 |
gwascentral | rs61995958 |
openSNP | rs61995958 |
23andMe | rs61995958 |
SNPshot | rs61995958 |
SNPdbe | rs61995958 |
MSV3d | rs61995958 |
GWAS Ctlg | rs61995958 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs61995958(A;A) rs61995958(G;G) rs61995958(T;T) |
Alt | rs61995958(A;A) rs61995958(G;G) rs61995958(T;T) |
Reference | Rs61995958(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | COQ8A ADCK3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.227174299C>A |
CLNSRC | |
CLNACC | RCV000199828.2, |