rs2987763
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2987763(A;A) |
Make rs2987763(A;T) |
Make rs2987763(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 153313558 |
Gene | PGLYRP3 |
is a | snp |
is | mentioned by |
dbSNP | rs2987763 |
dbSNP (classic) | rs2987763 |
ClinGen | rs2987763 |
ebi | rs2987763 |
HLI | rs2987763 |
Exac | rs2987763 |
Gnomad | rs2987763 |
Varsome | rs2987763 |
LitVar | rs2987763 |
Map | rs2987763 |
PheGenI | rs2987763 |
Biobank | rs2987763 |
1000 genomes | rs2987763 |
hgdp | rs2987763 |
ensembl | rs2987763 |
geneview | rs2987763 |
scholar | rs2987763 |
rs2987763 | |
pharmgkb | rs2987763 |
gwascentral | rs2987763 |
openSNP | rs2987763 |
23andMe | rs2987763 |
SNPshot | rs2987763 |
SNPdbe | rs2987763 |
MSV3d | rs2987763 |
GWAS Ctlg | rs2987763 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 24838182] Peptidoglycan recognition protein genes and risk of Parkinson's disease