rs1400816
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1400816(A;A) |
Make rs1400816(A;C) |
Make rs1400816(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 2 |
Position | 171824168 |
Gene | SLC25A12 |
is a | snp |
is | mentioned by |
dbSNP | rs1400816 |
dbSNP (classic) | rs1400816 |
ClinGen | rs1400816 |
ebi | rs1400816 |
HLI | rs1400816 |
Exac | rs1400816 |
Gnomad | rs1400816 |
Varsome | rs1400816 |
LitVar | rs1400816 |
Map | rs1400816 |
PheGenI | rs1400816 |
Biobank | rs1400816 |
1000 genomes | rs1400816 |
hgdp | rs1400816 |
ensembl | rs1400816 |
geneview | rs1400816 |
scholar | rs1400816 |
rs1400816 | |
pharmgkb | rs1400816 |
gwascentral | rs1400816 |
openSNP | rs1400816 |
23andMe | rs1400816 |
SNPshot | rs1400816 |
SNPdbe | rs1400816 |
MSV3d | rs1400816 |
GWAS Ctlg | rs1400816 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24529757] |
Trait | Amyotrophic lateral sclerosis (sporadic) |
Title | A genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. |
Risk Allele | |
P-val | 1E-6 |
Odds Ratio | NR NR |