rs201732356
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs201732356(A;A) |
Make rs201732356(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 89318737 |
Gene | POLG |
is a | snp |
is | mentioned by |
dbSNP | rs201732356 |
dbSNP (classic) | rs201732356 |
ClinGen | rs201732356 |
ebi | rs201732356 |
HLI | rs201732356 |
Exac | rs201732356 |
Gnomad | rs201732356 |
Varsome | rs201732356 |
LitVar | rs201732356 |
Map | rs201732356 |
PheGenI | rs201732356 |
Biobank | rs201732356 |
1000 genomes | rs201732356 |
hgdp | rs201732356 |
ensembl | rs201732356 |
geneview | rs201732356 |
scholar | rs201732356 |
rs201732356 | |
pharmgkb | rs201732356 |
gwascentral | rs201732356 |
openSNP | rs201732356 |
23andMe | rs201732356 |
SNPshot | rs201732356 |
SNPdbe | rs201732356 |
MSV3d | rs201732356 |
GWAS Ctlg | rs201732356 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201732356(A;A) rs201732356(C;C) |
Alt | rs201732356(A;A) rs201732356(C;C) |
Reference | Rs201732356(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | POLG |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.89861968G>A; NC_000015.9:g.89861968G>C |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000188613.3, RCV000188612.1, |