rs6519955
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6519955(G;G) |
Make rs6519955(G;T) |
Make rs6519955(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 46025962 |
is a | snp |
is | mentioned by |
dbSNP | rs6519955 |
dbSNP (classic) | rs6519955 |
ClinGen | rs6519955 |
ebi | rs6519955 |
HLI | rs6519955 |
Exac | rs6519955 |
Gnomad | rs6519955 |
Varsome | rs6519955 |
LitVar | rs6519955 |
Map | rs6519955 |
PheGenI | rs6519955 |
Biobank | rs6519955 |
1000 genomes | rs6519955 |
hgdp | rs6519955 |
ensembl | rs6519955 |
geneview | rs6519955 |
scholar | rs6519955 |
rs6519955 | |
pharmgkb | rs6519955 |
gwascentral | rs6519955 |
openSNP | rs6519955 |
23andMe | rs6519955 |
SNPshot | rs6519955 |
SNPdbe | rs6519955 |
MSV3d | rs6519955 |
GWAS Ctlg | rs6519955 |
GMAF | 0.4376 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21732829] |
Trait | |
Title | Wnt signaling and Dupuytren's disease. |
Risk Allele | A |
P-val | 3E-33 |
Odds Ratio | 1.5400 None |