rs112384084
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;T) | 0.1 | benign |
Make rs112384084(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 3 |
Position | 195867623 |
Gene | TNK2 |
is a | snp |
is | mentioned by |
dbSNP | rs112384084 |
dbSNP (classic) | rs112384084 |
ClinGen | rs112384084 |
ebi | rs112384084 |
HLI | rs112384084 |
Exac | rs112384084 |
Gnomad | rs112384084 |
Varsome | rs112384084 |
LitVar | rs112384084 |
Map | rs112384084 |
PheGenI | rs112384084 |
Biobank | rs112384084 |
1000 genomes | rs112384084 |
hgdp | rs112384084 |
ensembl | rs112384084 |
geneview | rs112384084 |
scholar | rs112384084 |
rs112384084 | |
pharmgkb | rs112384084 |
gwascentral | rs112384084 |
openSNP | rs112384084 |
23andMe | rs112384084 |
SNPshot | rs112384084 |
SNPdbe | rs112384084 |
MSV3d | rs112384084 |
GWAS Ctlg | rs112384084 |
Max Magnitude | 0.1 |
ClinVar | |
---|---|
Risk | rs112384084(T;T) |
Alt | rs112384084(T;T) |
Reference | Rs112384084(C;C) |
Significance | Probable-Pathogenic |
Disease | Parkinson disease not specified |
Variation | info |
Gene | TNK2 |
CLNDBN | Parkinson disease not specified |
Reversed | 0 |
HGVS | NC_000003.11:g.195594494C>T |
CLNSRC | |
CLNACC | RCV000210436.1, RCV000254280.1, |