rs775538075
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs775538075(A;G) |
Make rs775538075(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 89327300 |
Gene | MIR6766, POLG |
is a | snp |
is | mentioned by |
dbSNP | rs775538075 |
dbSNP (classic) | rs775538075 |
ClinGen | rs775538075 |
ebi | rs775538075 |
HLI | rs775538075 |
Exac | rs775538075 |
Gnomad | rs775538075 |
Varsome | rs775538075 |
LitVar | rs775538075 |
Map | rs775538075 |
PheGenI | rs775538075 |
Biobank | rs775538075 |
1000 genomes | rs775538075 |
hgdp | rs775538075 |
ensembl | rs775538075 |
geneview | rs775538075 |
scholar | rs775538075 |
rs775538075 | |
pharmgkb | rs775538075 |
gwascentral | rs775538075 |
openSNP | rs775538075 |
23andMe | rs775538075 |
SNPshot | rs775538075 |
SNPdbe | rs775538075 |
MSV3d | rs775538075 |
GWAS Ctlg | rs775538075 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs775538075(G;G) |
Alt | rs775538075(G;G) |
Reference | Rs775538075(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MIR6766 POLG |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.89870531A>G |
CLNSRC | |
CLNACC | RCV000188654.1, |