rs356221
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs356221(A;A) |
Make rs356221(A;T) |
Make rs356221(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 89721313 |
Gene | LOC105377329 |
is a | snp |
is | mentioned by |
dbSNP | rs356221 |
dbSNP (classic) | rs356221 |
ClinGen | rs356221 |
ebi | rs356221 |
HLI | rs356221 |
Exac | rs356221 |
Gnomad | rs356221 |
Varsome | rs356221 |
LitVar | rs356221 |
Map | rs356221 |
PheGenI | rs356221 |
Biobank | rs356221 |
1000 genomes | rs356221 |
hgdp | rs356221 |
ensembl | rs356221 |
geneview | rs356221 |
scholar | rs356221 |
rs356221 | |
pharmgkb | rs356221 |
gwascentral | rs356221 |
openSNP | rs356221 |
23andMe | rs356221 |
SNPshot | rs356221 |
SNPdbe | rs356221 |
MSV3d | rs356221 |
GWAS Ctlg | rs356221 |
GMAF | 0.4013 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 23182315] Genetic variants of SNCA and LRRK2 genes are associated with sporadic PD susceptibility: A replication study in a Taiwanese cohort
[PMID 19063963] Genetic susceptibility in Parkinson's disease.