rs796052908
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(CT;CT) | 0 | common in clinvar |
Make rs796052908(-;-) |
Make rs796052908(-;CT) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 89327329 |
Gene | MIR6766, POLG |
is a | snp |
is | mentioned by |
dbSNP | rs796052908 |
dbSNP (classic) | rs796052908 |
ClinGen | rs796052908 |
ebi | rs796052908 |
HLI | rs796052908 |
Exac | rs796052908 |
Gnomad | rs796052908 |
Varsome | rs796052908 |
LitVar | rs796052908 |
Map | rs796052908 |
PheGenI | rs796052908 |
Biobank | rs796052908 |
1000 genomes | rs796052908 |
hgdp | rs796052908 |
ensembl | rs796052908 |
geneview | rs796052908 |
scholar | rs796052908 |
rs796052908 | |
pharmgkb | rs796052908 |
gwascentral | rs796052908 |
openSNP | rs796052908 |
23andMe | rs796052908 |
SNPshot | rs796052908 |
SNPdbe | rs796052908 |
MSV3d | rs796052908 |
GWAS Ctlg | rs796052908 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796052908(-;-) |
Alt | rs796052908(-;-) |
Reference | Rs796052908(CT;CT) |
Significance | Pathogenic |
Disease | not provided Generalized epilepsy Global developmental delay Obesity |
Variation | info |
Gene | MIR6766 POLG |
CLNDBN | not provided Generalized epilepsy Global developmental delay Obesity |
Reversed | 1 |
HGVS | NC_000015.9:g.89870560_89870561delAG |
CLNSRC | |
CLNACC | RCV000188674.2, RCV000449589.1, |