rs375935084
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs375935084(A;A) |
Make rs375935084(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 89321217 |
Gene | POLG |
is a | snp |
is | mentioned by |
dbSNP | rs375935084 |
dbSNP (classic) | rs375935084 |
ClinGen | rs375935084 |
ebi | rs375935084 |
HLI | rs375935084 |
Exac | rs375935084 |
Gnomad | rs375935084 |
Varsome | rs375935084 |
LitVar | rs375935084 |
Map | rs375935084 |
PheGenI | rs375935084 |
Biobank | rs375935084 |
1000 genomes | rs375935084 |
hgdp | rs375935084 |
ensembl | rs375935084 |
geneview | rs375935084 |
scholar | rs375935084 |
rs375935084 | |
pharmgkb | rs375935084 |
gwascentral | rs375935084 |
openSNP | rs375935084 |
23andMe | rs375935084 |
SNPshot | rs375935084 |
SNPdbe | rs375935084 |
MSV3d | rs375935084 |
GWAS Ctlg | rs375935084 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs375935084(A;A) |
Alt | rs375935084(A;A) |
Reference | Rs375935084(G;G) |
Significance | Probable-Pathogenic |
Disease | not specified |
Variation | info |
Gene | POLG |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000015.9:g.89864448G>A |
CLNSRC | |
CLNACC | RCV000188677.2, |