rs4719220
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4719220(A;A) |
Make rs4719220(A;G) |
Make rs4719220(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 7 |
Position | 72215718 |
Gene | CALN1 |
is a | snp |
is | mentioned by |
dbSNP | rs4719220 |
dbSNP (classic) | rs4719220 |
ClinGen | rs4719220 |
ebi | rs4719220 |
HLI | rs4719220 |
Exac | rs4719220 |
Gnomad | rs4719220 |
Varsome | rs4719220 |
LitVar | rs4719220 |
Map | rs4719220 |
PheGenI | rs4719220 |
Biobank | rs4719220 |
1000 genomes | rs4719220 |
hgdp | rs4719220 |
ensembl | rs4719220 |
geneview | rs4719220 |
scholar | rs4719220 |
rs4719220 | |
pharmgkb | rs4719220 |
gwascentral | rs4719220 |
openSNP | rs4719220 |
23andMe | rs4719220 |
SNPshot | rs4719220 |
SNPdbe | rs4719220 |
MSV3d | rs4719220 |
GWAS Ctlg | rs4719220 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | 4E-6 |
Odds Ratio | NR NR |