rs776776
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs776776(C;C) |
Make rs776776(C;T) |
Make rs776776(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 9 |
Position | 18657560 |
Gene | ADAMTSL1, LOC102724102 |
is a | snp |
is | mentioned by |
dbSNP | rs776776 |
dbSNP (classic) | rs776776 |
ClinGen | rs776776 |
ebi | rs776776 |
HLI | rs776776 |
Exac | rs776776 |
Gnomad | rs776776 |
Varsome | rs776776 |
LitVar | rs776776 |
Map | rs776776 |
PheGenI | rs776776 |
Biobank | rs776776 |
1000 genomes | rs776776 |
hgdp | rs776776 |
ensembl | rs776776 |
geneview | rs776776 |
scholar | rs776776 |
rs776776 | |
pharmgkb | rs776776 |
gwascentral | rs776776 |
openSNP | rs776776 |
23andMe | rs776776 |
SNPshot | rs776776 |
SNPdbe | rs776776 |
MSV3d | rs776776 |
GWAS Ctlg | rs776776 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | 2E-6 |
Odds Ratio | NR NR |