rs796052899
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs796052899(C;T) |
Make rs796052899(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 89333327 |
Gene | POLG |
is a | snp |
is | mentioned by |
dbSNP | rs796052899 |
dbSNP (classic) | rs796052899 |
ClinGen | rs796052899 |
ebi | rs796052899 |
HLI | rs796052899 |
Exac | rs796052899 |
Gnomad | rs796052899 |
Varsome | rs796052899 |
LitVar | rs796052899 |
Map | rs796052899 |
PheGenI | rs796052899 |
Biobank | rs796052899 |
1000 genomes | rs796052899 |
hgdp | rs796052899 |
ensembl | rs796052899 |
geneview | rs796052899 |
scholar | rs796052899 |
rs796052899 | |
pharmgkb | rs796052899 |
gwascentral | rs796052899 |
openSNP | rs796052899 |
23andMe | rs796052899 |
SNPshot | rs796052899 |
SNPdbe | rs796052899 |
MSV3d | rs796052899 |
GWAS Ctlg | rs796052899 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796052899(T;T) |
Alt | rs796052899(T;T) |
Reference | Rs796052899(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | POLG |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000015.9:g.89876558G>A |
CLNSRC | |
CLNACC | RCV000188634.1, |