rs767898276
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs767898276(A;A) |
Make rs767898276(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 12 |
Position | 64486018 |
Gene | TBK1 |
is a | snp |
is | mentioned by |
dbSNP | rs767898276 |
dbSNP (classic) | rs767898276 |
ClinGen | rs767898276 |
ebi | rs767898276 |
HLI | rs767898276 |
Exac | rs767898276 |
Gnomad | rs767898276 |
Varsome | rs767898276 |
LitVar | rs767898276 |
Map | rs767898276 |
PheGenI | rs767898276 |
Biobank | rs767898276 |
1000 genomes | rs767898276 |
hgdp | rs767898276 |
ensembl | rs767898276 |
geneview | rs767898276 |
scholar | rs767898276 |
rs767898276 | |
pharmgkb | rs767898276 |
gwascentral | rs767898276 |
openSNP | rs767898276 |
23andMe | rs767898276 |
SNPshot | rs767898276 |
SNPdbe | rs767898276 |
MSV3d | rs767898276 |
GWAS Ctlg | rs767898276 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs767898276(A;A) |
Alt | rs767898276(A;A) |
Reference | Rs767898276(G;G) |
Significance | Pathogenic |
Disease | Frontotemporal dementia and/or amyotrophic lateral sclerosis 4 |
Variation | info |
Gene | TBK1 |
CLNDBN | Frontotemporal dementia and/or amyotrophic lateral sclerosis 4 |
Reversed | 0 |
HGVS | NC_000012.11:g.64879798G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000185599.2, |