rs10131300
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10131300(A;A) |
Make rs10131300(A;C) |
Make rs10131300(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 72472787 |
Gene | RGS6 |
is a | snp |
is | mentioned by |
dbSNP | rs10131300 |
dbSNP (classic) | rs10131300 |
ClinGen | rs10131300 |
ebi | rs10131300 |
HLI | rs10131300 |
Exac | rs10131300 |
Gnomad | rs10131300 |
Varsome | rs10131300 |
LitVar | rs10131300 |
Map | rs10131300 |
PheGenI | rs10131300 |
Biobank | rs10131300 |
1000 genomes | rs10131300 |
hgdp | rs10131300 |
ensembl | rs10131300 |
geneview | rs10131300 |
scholar | rs10131300 |
rs10131300 | |
pharmgkb | rs10131300 |
gwascentral | rs10131300 |
openSNP | rs10131300 |
23andMe | rs10131300 |
SNPshot | rs10131300 |
SNPdbe | rs10131300 |
MSV3d | rs10131300 |
GWAS Ctlg | rs10131300 |
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 | 5E-6 |
Odds Ratio | NR NR |