rs202039305
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs202039305(A;A) |
Make rs202039305(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 15 |
Position | 89333553 |
Gene | POLG |
is a | snp |
is | mentioned by |
dbSNP | rs202039305 |
dbSNP (classic) | rs202039305 |
ClinGen | rs202039305 |
ebi | rs202039305 |
HLI | rs202039305 |
Exac | rs202039305 |
Gnomad | rs202039305 |
Varsome | rs202039305 |
LitVar | rs202039305 |
Map | rs202039305 |
PheGenI | rs202039305 |
Biobank | rs202039305 |
1000 genomes | rs202039305 |
hgdp | rs202039305 |
ensembl | rs202039305 |
geneview | rs202039305 |
scholar | rs202039305 |
rs202039305 | |
pharmgkb | rs202039305 |
gwascentral | rs202039305 |
openSNP | rs202039305 |
23andMe | rs202039305 |
SNPshot | rs202039305 |
SNPdbe | rs202039305 |
MSV3d | rs202039305 |
GWAS Ctlg | rs202039305 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs202039305(A;A) |
Alt | rs202039305(A;A) |
Reference | Rs202039305(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | POLG |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.89876784G>A |
CLNSRC | |
CLNACC | RCV000296330.1, |