rs141367015
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs141367015(C;G) |
Make rs141367015(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 89330081 |
Gene | POLG |
is a | snp |
is | mentioned by |
dbSNP | rs141367015 |
dbSNP (classic) | rs141367015 |
ClinGen | rs141367015 |
ebi | rs141367015 |
HLI | rs141367015 |
Exac | rs141367015 |
Gnomad | rs141367015 |
Varsome | rs141367015 |
LitVar | rs141367015 |
Map | rs141367015 |
PheGenI | rs141367015 |
Biobank | rs141367015 |
1000 genomes | rs141367015 |
hgdp | rs141367015 |
ensembl | rs141367015 |
geneview | rs141367015 |
scholar | rs141367015 |
rs141367015 | |
pharmgkb | rs141367015 |
gwascentral | rs141367015 |
openSNP | rs141367015 |
23andMe | rs141367015 |
SNPshot | rs141367015 |
SNPdbe | rs141367015 |
MSV3d | rs141367015 |
GWAS Ctlg | rs141367015 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs141367015(G;G) |
Alt | rs141367015(G;G) |
Reference | Rs141367015(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | POLG |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.89873312C>G |
CLNSRC | |
CLNACC | RCV000188644.2, |