rs768653086
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs768653086(C;T) |
Make rs768653086(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 89320917 |
Gene | POLG |
is a | snp |
is | mentioned by |
dbSNP | rs768653086 |
dbSNP (classic) | rs768653086 |
ClinGen | rs768653086 |
ebi | rs768653086 |
HLI | rs768653086 |
Exac | rs768653086 |
Gnomad | rs768653086 |
Varsome | rs768653086 |
LitVar | rs768653086 |
Map | rs768653086 |
PheGenI | rs768653086 |
Biobank | rs768653086 |
1000 genomes | rs768653086 |
hgdp | rs768653086 |
ensembl | rs768653086 |
geneview | rs768653086 |
scholar | rs768653086 |
rs768653086 | |
pharmgkb | rs768653086 |
gwascentral | rs768653086 |
openSNP | rs768653086 |
23andMe | rs768653086 |
SNPshot | rs768653086 |
SNPdbe | rs768653086 |
MSV3d | rs768653086 |
GWAS Ctlg | rs768653086 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs768653086(T;T) |
Alt | rs768653086(T;T) |
Reference | Rs768653086(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | POLG |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.89864148C>T |
CLNSRC | |
CLNACC | RCV000188589.2, |