rs3807031
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3807031(A;A) |
Make rs3807031(A;C) |
Make rs3807031(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 30066107 |
Gene | PPP1R11 |
is a | snp |
is | mentioned by |
dbSNP | rs3807031 |
dbSNP (classic) | rs3807031 |
ClinGen | rs3807031 |
ebi | rs3807031 |
HLI | rs3807031 |
Exac | rs3807031 |
Gnomad | rs3807031 |
Varsome | rs3807031 |
LitVar | rs3807031 |
Map | rs3807031 |
PheGenI | rs3807031 |
Biobank | rs3807031 |
1000 genomes | rs3807031 |
hgdp | rs3807031 |
ensembl | rs3807031 |
geneview | rs3807031 |
scholar | rs3807031 |
rs3807031 | |
pharmgkb | rs3807031 |
gwascentral | rs3807031 |
openSNP | rs3807031 |
23andMe | rs3807031 |
SNPshot | rs3807031 |
SNPdbe | rs3807031 |
MSV3d | rs3807031 |
GWAS Ctlg | rs3807031 |
GMAF | 0.1905 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 19010793] Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.