rs12891047
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common/normal |
Make rs12891047(A;C) |
Make rs12891047(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 67776358 |
Gene | ZFYVE26 |
is a | snp |
is | mentioned by |
dbSNP | rs12891047 |
dbSNP (classic) | rs12891047 |
ClinGen | rs12891047 |
ebi | rs12891047 |
HLI | rs12891047 |
Exac | rs12891047 |
Gnomad | rs12891047 |
Varsome | rs12891047 |
LitVar | rs12891047 |
Map | rs12891047 |
PheGenI | rs12891047 |
Biobank | rs12891047 |
1000 genomes | rs12891047 |
hgdp | rs12891047 |
ensembl | rs12891047 |
geneview | rs12891047 |
scholar | rs12891047 |
rs12891047 | |
pharmgkb | rs12891047 |
gwascentral | rs12891047 |
openSNP | rs12891047 |
23andMe | rs12891047 |
SNPshot | rs12891047 |
SNPdbe | rs12891047 |
MSV3d | rs12891047 |
GWAS Ctlg | rs12891047 |
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 | 6E-7 |
Odds Ratio | NR NR |