rs242559
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs242559(A;A) |
Make rs242559(A;C) |
Make rs242559(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 45948522 |
Gene | MAPT |
is a | snp |
is | mentioned by |
dbSNP | rs242559 |
dbSNP (classic) | rs242559 |
ClinGen | rs242559 |
ebi | rs242559 |
HLI | rs242559 |
Exac | rs242559 |
Gnomad | rs242559 |
Varsome | rs242559 |
LitVar | rs242559 |
Map | rs242559 |
PheGenI | rs242559 |
Biobank | rs242559 |
1000 genomes | rs242559 |
hgdp | rs242559 |
ensembl | rs242559 |
geneview | rs242559 |
scholar | rs242559 |
rs242559 | |
pharmgkb | rs242559 |
gwascentral | rs242559 |
openSNP | rs242559 |
23andMe | rs242559 |
SNPshot | rs242559 |
SNPdbe | rs242559 |
MSV3d | rs242559 |
GWAS Ctlg | rs242559 |
GMAF | 0.2479 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 22451204] Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2
[PMID 18072964] No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease.
[PMID 18509094] Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study.