rs368435864
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs368435864(C;T) |
Make rs368435864(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 89318736 |
Gene | POLG |
is a | snp |
is | mentioned by |
dbSNP | rs368435864 |
dbSNP (classic) | rs368435864 |
ClinGen | rs368435864 |
ebi | rs368435864 |
HLI | rs368435864 |
Exac | rs368435864 |
Gnomad | rs368435864 |
Varsome | rs368435864 |
LitVar | rs368435864 |
Map | rs368435864 |
PheGenI | rs368435864 |
Biobank | rs368435864 |
1000 genomes | rs368435864 |
hgdp | rs368435864 |
ensembl | rs368435864 |
geneview | rs368435864 |
scholar | rs368435864 |
rs368435864 | |
pharmgkb | rs368435864 |
gwascentral | rs368435864 |
openSNP | rs368435864 |
23andMe | rs368435864 |
SNPshot | rs368435864 |
SNPdbe | rs368435864 |
MSV3d | rs368435864 |
GWAS Ctlg | rs368435864 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs368435864(A;A) rs368435864(T;T) |
Alt | rs368435864(A;A) rs368435864(T;T) |
Reference | Rs368435864(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | POLG |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.89861967C>A; NC_000015.9:g.89861967C>T |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000188616.3, RCV000188614.2, |