rs4932194
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4932194(A;A) |
Make rs4932194(A;C) |
Make rs4932194(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 88702008 |
is a | snp |
is | mentioned by |
dbSNP | rs4932194 |
dbSNP (classic) | rs4932194 |
ClinGen | rs4932194 |
ebi | rs4932194 |
HLI | rs4932194 |
Exac | rs4932194 |
Gnomad | rs4932194 |
Varsome | rs4932194 |
LitVar | rs4932194 |
Map | rs4932194 |
PheGenI | rs4932194 |
Biobank | rs4932194 |
1000 genomes | rs4932194 |
hgdp | rs4932194 |
ensembl | rs4932194 |
geneview | rs4932194 |
scholar | rs4932194 |
rs4932194 | |
pharmgkb | rs4932194 |
gwascentral | rs4932194 |
openSNP | rs4932194 |
23andMe | rs4932194 |
SNPshot | rs4932194 |
SNPdbe | rs4932194 |
MSV3d | rs4932194 |
GWAS Ctlg | rs4932194 |
GMAF | 0.3398 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21732829] |
Trait | |
Title | Wnt signaling and Dupuytren's disease. |
Risk Allele | |
P-val | 8E-7 |
Odds Ratio | 1.2200 None |