rs202037973
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs202037973(A;G) |
Make rs202037973(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 89323423 |
Gene | POLG |
is a | snp |
is | mentioned by |
dbSNP | rs202037973 |
dbSNP (classic) | rs202037973 |
ClinGen | rs202037973 |
ebi | rs202037973 |
HLI | rs202037973 |
Exac | rs202037973 |
Gnomad | rs202037973 |
Varsome | rs202037973 |
LitVar | rs202037973 |
Map | rs202037973 |
PheGenI | rs202037973 |
Biobank | rs202037973 |
1000 genomes | rs202037973 |
hgdp | rs202037973 |
ensembl | rs202037973 |
geneview | rs202037973 |
scholar | rs202037973 |
rs202037973 | |
pharmgkb | rs202037973 |
gwascentral | rs202037973 |
openSNP | rs202037973 |
23andMe | rs202037973 |
SNPshot | rs202037973 |
SNPdbe | rs202037973 |
MSV3d | rs202037973 |
GWAS Ctlg | rs202037973 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs202037973(G;G) |
Alt | rs202037973(G;G) |
Reference | Rs202037973(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided not specified |
Variation | info |
Gene | POLG |
CLNDBN | not provided not specified |
Reversed | 0 |
HGVS | NC_000015.9:g.89866654A>G |
CLNSRC | |
CLNACC | RCV000188572.3, RCV000275508.1, |