rs769637557
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs769637557(G;G) |
Make rs769637557(G;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 89327004 |
Gene | MIR6766, POLG |
is a | snp |
is | mentioned by |
dbSNP | rs769637557 |
dbSNP (classic) | rs769637557 |
ClinGen | rs769637557 |
ebi | rs769637557 |
HLI | rs769637557 |
Exac | rs769637557 |
Gnomad | rs769637557 |
Varsome | rs769637557 |
LitVar | rs769637557 |
Map | rs769637557 |
PheGenI | rs769637557 |
Biobank | rs769637557 |
1000 genomes | rs769637557 |
hgdp | rs769637557 |
ensembl | rs769637557 |
geneview | rs769637557 |
scholar | rs769637557 |
rs769637557 | |
pharmgkb | rs769637557 |
gwascentral | rs769637557 |
openSNP | rs769637557 |
23andMe | rs769637557 |
SNPshot | rs769637557 |
SNPdbe | rs769637557 |
MSV3d | rs769637557 |
GWAS Ctlg | rs769637557 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs769637557(G;G) |
Alt | rs769637557(G;G) |
Reference | Rs769637557(T;T) |
Significance | Probable-Pathogenic |
Disease | not specified |
Variation | info |
Gene | MIR6766 POLG |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000015.9:g.89870235T>G |
CLNSRC | |
CLNACC | RCV000188661.2, |