rs2970332
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2970332(A;A) |
Make rs2970332(A;G) |
Make rs2970332(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 14338889 |
Gene | RRAS2 |
is a | snp |
is | mentioned by |
dbSNP | rs2970332 |
dbSNP (classic) | rs2970332 |
ClinGen | rs2970332 |
ebi | rs2970332 |
HLI | rs2970332 |
Exac | rs2970332 |
Gnomad | rs2970332 |
Varsome | rs2970332 |
LitVar | rs2970332 |
Map | rs2970332 |
PheGenI | rs2970332 |
Biobank | rs2970332 |
1000 genomes | rs2970332 |
hgdp | rs2970332 |
ensembl | rs2970332 |
geneview | rs2970332 |
scholar | rs2970332 |
rs2970332 | |
pharmgkb | rs2970332 |
gwascentral | rs2970332 |
openSNP | rs2970332 |
23andMe | rs2970332 |
SNPshot | rs2970332 |
SNPdbe | rs2970332 |
MSV3d | rs2970332 |
GWAS Ctlg | rs2970332 |
GMAF | 0.3623 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21085126] SNPs in axon guidance pathway genes and susceptibility for Parkinson's disease in the Korean population
[PMID 18628988] Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease.