rs77231105
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs77231105(A;A) |
Make rs77231105(A;G) |
Make rs77231105(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 7 |
Position | 55863084 |
Gene | SEPT14 |
is a | snp |
is | mentioned by |
dbSNP | rs77231105 |
dbSNP (classic) | rs77231105 |
ClinGen | rs77231105 |
ebi | rs77231105 |
HLI | rs77231105 |
Exac | rs77231105 |
Gnomad | rs77231105 |
Varsome | rs77231105 |
LitVar | rs77231105 |
Map | rs77231105 |
PheGenI | rs77231105 |
Biobank | rs77231105 |
1000 genomes | rs77231105 |
hgdp | rs77231105 |
ensembl | rs77231105 |
geneview | rs77231105 |
scholar | rs77231105 |
rs77231105 | |
pharmgkb | rs77231105 |
gwascentral | rs77231105 |
openSNP | rs77231105 |
23andMe | rs77231105 |
SNPshot | rs77231105 |
SNPdbe | rs77231105 |
MSV3d | rs77231105 |
GWAS Ctlg | rs77231105 |
Max Magnitude | 0 |
[PMID 27115672] SEPT14 Is Associated with a Reduced Risk for Parkinson's Disease and Expressed in Human Brain.