rs806606
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) |
Make rs806606(C;T) |
Make rs806606(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 85974061 |
Gene | LOC101928842 |
is a | snp |
is | mentioned by |
dbSNP | rs806606 |
dbSNP (classic) | rs806606 |
ClinGen | rs806606 |
ebi | rs806606 |
HLI | rs806606 |
Exac | rs806606 |
Gnomad | rs806606 |
Varsome | rs806606 |
LitVar | rs806606 |
Map | rs806606 |
PheGenI | rs806606 |
Biobank | rs806606 |
1000 genomes | rs806606 |
hgdp | rs806606 |
ensembl | rs806606 |
geneview | rs806606 |
scholar | rs806606 |
rs806606 | |
pharmgkb | rs806606 |
gwascentral | rs806606 |
openSNP | rs806606 |
23andMe | rs806606 |
SNPshot | rs806606 |
SNPdbe | rs806606 |
MSV3d | rs806606 |
GWAS Ctlg | rs806606 |
GMAF | 0.1579 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 17052657] Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.