rs139717885
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs139717885(A;A) |
Make rs139717885(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 15 |
Position | 89325610 |
Gene | POLG |
is a | snp |
is | mentioned by |
dbSNP | rs139717885 |
dbSNP (classic) | rs139717885 |
ClinGen | rs139717885 |
ebi | rs139717885 |
HLI | rs139717885 |
Exac | rs139717885 |
Gnomad | rs139717885 |
Varsome | rs139717885 |
LitVar | rs139717885 |
Map | rs139717885 |
PheGenI | rs139717885 |
Biobank | rs139717885 |
1000 genomes | rs139717885 |
hgdp | rs139717885 |
ensembl | rs139717885 |
geneview | rs139717885 |
scholar | rs139717885 |
rs139717885 | |
pharmgkb | rs139717885 |
gwascentral | rs139717885 |
openSNP | rs139717885 |
23andMe | rs139717885 |
SNPshot | rs139717885 |
SNPdbe | rs139717885 |
MSV3d | rs139717885 |
GWAS Ctlg | rs139717885 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs139717885(A;A) |
Alt | rs139717885(A;A) |
Reference | Rs139717885(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | POLG |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.89868841G>A |
CLNSRC | |
CLNACC | RCV000438492.1, |