rs7177008
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7177008(C;C) |
Make rs7177008(C;G) |
Make rs7177008(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 77672858 |
Gene | LINGO1 |
is a | snp |
is | mentioned by |
dbSNP | rs7177008 |
dbSNP (classic) | rs7177008 |
ClinGen | rs7177008 |
ebi | rs7177008 |
HLI | rs7177008 |
Exac | rs7177008 |
Gnomad | rs7177008 |
Varsome | rs7177008 |
LitVar | rs7177008 |
Map | rs7177008 |
PheGenI | rs7177008 |
Biobank | rs7177008 |
1000 genomes | rs7177008 |
hgdp | rs7177008 |
ensembl | rs7177008 |
geneview | rs7177008 |
scholar | rs7177008 |
rs7177008 | |
pharmgkb | rs7177008 |
gwascentral | rs7177008 |
openSNP | rs7177008 |
23andMe | rs7177008 |
SNPshot | rs7177008 |
SNPdbe | rs7177008 |
MSV3d | rs7177008 |
GWAS Ctlg | rs7177008 |
GMAF | 0.2764 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 19908305] Role of LINGO1 polymorphisms in Parkinson's disease