rs1027615
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1027615(A;A) |
Make rs1027615(A;G) |
Make rs1027615(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 43318486 |
is a | snp |
is | mentioned by |
dbSNP | rs1027615 |
dbSNP (classic) | rs1027615 |
ClinGen | rs1027615 |
ebi | rs1027615 |
HLI | rs1027615 |
Exac | rs1027615 |
Gnomad | rs1027615 |
Varsome | rs1027615 |
LitVar | rs1027615 |
Map | rs1027615 |
PheGenI | rs1027615 |
Biobank | rs1027615 |
1000 genomes | rs1027615 |
hgdp | rs1027615 |
ensembl | rs1027615 |
geneview | rs1027615 |
scholar | rs1027615 |
rs1027615 | |
pharmgkb | rs1027615 |
gwascentral | rs1027615 |
openSNP | rs1027615 |
23andMe | rs1027615 |
SNPshot | rs1027615 |
SNPdbe | rs1027615 |
MSV3d | rs1027615 |
GWAS Ctlg | rs1027615 |
GMAF | 0.168 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
This SNP was associated with amyotrophic lateral sclerosis (ALS) based on a study of 1,152 patients.[PMID 17671248]