rs1986734
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1986734(C;C) |
Make rs1986734(C;T) |
Make rs1986734(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 76499631 |
Gene | SHROOM3 |
is a | snp |
is | mentioned by |
dbSNP | rs1986734 |
dbSNP (classic) | rs1986734 |
ClinGen | rs1986734 |
ebi | rs1986734 |
HLI | rs1986734 |
Exac | rs1986734 |
Gnomad | rs1986734 |
Varsome | rs1986734 |
LitVar | rs1986734 |
Map | rs1986734 |
PheGenI | rs1986734 |
Biobank | rs1986734 |
1000 genomes | rs1986734 |
hgdp | rs1986734 |
ensembl | rs1986734 |
geneview | rs1986734 |
scholar | rs1986734 |
rs1986734 | |
pharmgkb | rs1986734 |
gwascentral | rs1986734 |
openSNP | rs1986734 |
23andMe | rs1986734 |
SNPshot | rs1986734 |
SNPdbe | rs1986734 |
MSV3d | rs1986734 |
GWAS Ctlg | rs1986734 |
GMAF | 0.4371 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20208534] |
Trait | Eosinophilic esophagitis (pediatric) |
Title | Common variants at 5q22 associate with pediatric eosinophilic esophagitis |
Risk Allele | |
P-val | 0.000001 |
Odds Ratio | 1.54 [1.22-1.89] |