rs142347031
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs142347031(A;C) |
Make rs142347031(C;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 15 |
Position | 89320850 |
Gene | POLG |
is a | snp |
is | mentioned by |
dbSNP | rs142347031 |
dbSNP (classic) | rs142347031 |
ClinGen | rs142347031 |
ebi | rs142347031 |
HLI | rs142347031 |
Exac | rs142347031 |
Gnomad | rs142347031 |
Varsome | rs142347031 |
LitVar | rs142347031 |
Map | rs142347031 |
PheGenI | rs142347031 |
Biobank | rs142347031 |
1000 genomes | rs142347031 |
hgdp | rs142347031 |
ensembl | rs142347031 |
geneview | rs142347031 |
scholar | rs142347031 |
rs142347031 | |
pharmgkb | rs142347031 |
gwascentral | rs142347031 |
openSNP | rs142347031 |
23andMe | rs142347031 |
SNPshot | rs142347031 |
SNPdbe | rs142347031 |
MSV3d | rs142347031 |
GWAS Ctlg | rs142347031 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs142347031(C;C) |
Alt | rs142347031(C;C) |
Reference | Rs142347031(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | POLG |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.89864081A>C |
CLNSRC | |
CLNACC | RCV000413284.1, |