rs7899101
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7899101(C;C) |
Make rs7899101(C;T) |
Make rs7899101(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 5566239 |
Gene | LOC105376381 |
is a | snp |
is | mentioned by |
dbSNP | rs7899101 |
dbSNP (classic) | rs7899101 |
ClinGen | rs7899101 |
ebi | rs7899101 |
HLI | rs7899101 |
Exac | rs7899101 |
Gnomad | rs7899101 |
Varsome | rs7899101 |
LitVar | rs7899101 |
Map | rs7899101 |
PheGenI | rs7899101 |
Biobank | rs7899101 |
1000 genomes | rs7899101 |
hgdp | rs7899101 |
ensembl | rs7899101 |
geneview | rs7899101 |
scholar | rs7899101 |
rs7899101 | |
pharmgkb | rs7899101 |
gwascentral | rs7899101 |
openSNP | rs7899101 |
23andMe | rs7899101 |
SNPshot | rs7899101 |
SNPdbe | rs7899101 |
MSV3d | rs7899101 |
GWAS Ctlg | rs7899101 |
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 | 3E-6 |
Odds Ratio | NR NR |