rs760431841
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs760431841(G;G) |
Make rs760431841(G;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 89320944 |
Gene | POLG |
is a | snp |
is | mentioned by |
dbSNP | rs760431841 |
dbSNP (classic) | rs760431841 |
ClinGen | rs760431841 |
ebi | rs760431841 |
HLI | rs760431841 |
Exac | rs760431841 |
Gnomad | rs760431841 |
Varsome | rs760431841 |
LitVar | rs760431841 |
Map | rs760431841 |
PheGenI | rs760431841 |
Biobank | rs760431841 |
1000 genomes | rs760431841 |
hgdp | rs760431841 |
ensembl | rs760431841 |
geneview | rs760431841 |
scholar | rs760431841 |
rs760431841 | |
pharmgkb | rs760431841 |
gwascentral | rs760431841 |
openSNP | rs760431841 |
23andMe | rs760431841 |
SNPshot | rs760431841 |
SNPdbe | rs760431841 |
MSV3d | rs760431841 |
GWAS Ctlg | rs760431841 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs760431841(G;G) |
Alt | rs760431841(G;G) |
Reference | Rs760431841(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | POLG |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.89864175T>A |
CLNSRC | |
CLNACC | RCV000188588.1, |