rs17000647
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common genotype |
Make rs17000647(A;A) |
Make rs17000647(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 75556520 |
Gene | C4orf26 |
is a | snp |
is | mentioned by |
dbSNP | rs17000647 |
dbSNP (classic) | rs17000647 |
ClinGen | rs17000647 |
ebi | rs17000647 |
HLI | rs17000647 |
Exac | rs17000647 |
Gnomad | rs17000647 |
Varsome | rs17000647 |
LitVar | rs17000647 |
Map | rs17000647 |
PheGenI | rs17000647 |
Biobank | rs17000647 |
1000 genomes | rs17000647 |
hgdp | rs17000647 |
ensembl | rs17000647 |
geneview | rs17000647 |
scholar | rs17000647 |
rs17000647 | |
pharmgkb | rs17000647 |
gwascentral | rs17000647 |
openSNP | rs17000647 |
23andMe | rs17000647 |
SNPshot | rs17000647 |
SNPdbe | rs17000647 |
MSV3d | rs17000647 |
GWAS Ctlg | rs17000647 |
GMAF | 0.007805 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 22658654![]() |
Trait | |
Title | Genomic determinants of motor and cognitive outcomes in Parkinson's disease. |
Risk Allele | |
P-val | 0.000005 |
Odds Ratio | 5.5800 None |