rs10241628
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10241628(A;A) |
Make rs10241628(A;G) |
Make rs10241628(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 7 |
Position | 55877867 |
is a | snp |
is | mentioned by |
dbSNP | rs10241628 |
dbSNP (classic) | rs10241628 |
ClinGen | rs10241628 |
ebi | rs10241628 |
HLI | rs10241628 |
Exac | rs10241628 |
Gnomad | rs10241628 |
Varsome | rs10241628 |
LitVar | rs10241628 |
Map | rs10241628 |
PheGenI | rs10241628 |
Biobank | rs10241628 |
1000 genomes | rs10241628 |
hgdp | rs10241628 |
ensembl | rs10241628 |
geneview | rs10241628 |
scholar | rs10241628 |
rs10241628 | |
pharmgkb | rs10241628 |
gwascentral | rs10241628 |
openSNP | rs10241628 |
23andMe | rs10241628 |
SNPshot | rs10241628 |
SNPdbe | rs10241628 |
MSV3d | rs10241628 |
GWAS Ctlg | rs10241628 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 27115672] SEPT14 Is Associated with a Reduced Risk for Parkinson's Disease and Expressed in Human Brain.