rs11651671
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11651671(A;A) |
Make rs11651671(A;G) |
Make rs11651671(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 17 |
Position | 42494785 |
Gene | ATP6V0A1, MIR548AT |
is a | snp |
is | mentioned by |
dbSNP | rs11651671 |
dbSNP (classic) | rs11651671 |
ClinGen | rs11651671 |
ebi | rs11651671 |
HLI | rs11651671 |
Exac | rs11651671 |
Gnomad | rs11651671 |
Varsome | rs11651671 |
LitVar | rs11651671 |
Map | rs11651671 |
PheGenI | rs11651671 |
Biobank | rs11651671 |
1000 genomes | rs11651671 |
hgdp | rs11651671 |
ensembl | rs11651671 |
geneview | rs11651671 |
scholar | rs11651671 |
rs11651671 | |
pharmgkb | rs11651671 |
gwascentral | rs11651671 |
openSNP | rs11651671 |
23andMe | rs11651671 |
SNPshot | rs11651671 |
SNPdbe | rs11651671 |
MSV3d | rs11651671 |
GWAS Ctlg | rs11651671 |
Max Magnitude | 0 |
[PMID 26670097] Genetic Variants in MicroRNAs and their Binding Sites are Associated with the Risk of Parkinson Disease