rs2435207
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2435207(A;A) |
Make rs2435207(A;G) |
Make rs2435207(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 45981562 |
Gene | MAPT |
is a | snp |
is | mentioned by |
dbSNP | rs2435207 |
dbSNP (classic) | rs2435207 |
ClinGen | rs2435207 |
ebi | rs2435207 |
HLI | rs2435207 |
Exac | rs2435207 |
Gnomad | rs2435207 |
Varsome | rs2435207 |
LitVar | rs2435207 |
Map | rs2435207 |
PheGenI | rs2435207 |
Biobank | rs2435207 |
1000 genomes | rs2435207 |
hgdp | rs2435207 |
ensembl | rs2435207 |
geneview | rs2435207 |
scholar | rs2435207 |
rs2435207 | |
pharmgkb | rs2435207 |
gwascentral | rs2435207 |
openSNP | rs2435207 |
23andMe | rs2435207 |
SNPshot | rs2435207 |
SNPdbe | rs2435207 |
MSV3d | rs2435207 |
GWAS Ctlg | rs2435207 |
GMAF | 0.2833 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19558713] Role of the H1 haplotype of microtubule-associated protein tau (MAPT) gene in Greek patients with Parkinson's disease
[PMID 15297935] Linkage disequilibrium and association of MAPT H1 in Parkinson disease.
[PMID 18509094] Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study.
[PMID 21898123] The age at motor symptoms onset in LRRK2-associated Parkinson's disease is affected by a variation in the MAPT locus: a possible interaction.