rs3733242
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3733242(A;A) |
Make rs3733242(A;G) |
Make rs3733242(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 76754352 |
Gene | LOC105377289, SHROOM3 |
is a | snp |
is | mentioned by |
dbSNP | rs3733242 |
dbSNP (classic) | rs3733242 |
ClinGen | rs3733242 |
ebi | rs3733242 |
HLI | rs3733242 |
Exac | rs3733242 |
Gnomad | rs3733242 |
Varsome | rs3733242 |
LitVar | rs3733242 |
Map | rs3733242 |
PheGenI | rs3733242 |
Biobank | rs3733242 |
1000 genomes | rs3733242 |
hgdp | rs3733242 |
ensembl | rs3733242 |
geneview | rs3733242 |
scholar | rs3733242 |
rs3733242 | |
pharmgkb | rs3733242 |
gwascentral | rs3733242 |
openSNP | rs3733242 |
23andMe | rs3733242 |
SNPshot | rs3733242 |
SNPdbe | rs3733242 |
MSV3d | rs3733242 |
GWAS Ctlg | rs3733242 |
GMAF | 0.4876 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19740415] Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis
[PMID 17362836] Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data.