rs2270031
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs2270031(C;G) |
Make rs2270031(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 1633343 |
Gene | WNT5B |
is a | snp |
is | mentioned by |
dbSNP | rs2270031 |
dbSNP (classic) | rs2270031 |
ClinGen | rs2270031 |
ebi | rs2270031 |
HLI | rs2270031 |
Exac | rs2270031 |
Gnomad | rs2270031 |
Varsome | rs2270031 |
LitVar | rs2270031 |
Map | rs2270031 |
PheGenI | rs2270031 |
Biobank | rs2270031 |
1000 genomes | rs2270031 |
hgdp | rs2270031 |
ensembl | rs2270031 |
geneview | rs2270031 |
scholar | rs2270031 |
rs2270031 | |
pharmgkb | rs2270031 |
gwascentral | rs2270031 |
openSNP | rs2270031 |
23andMe | rs2270031 |
SNPshot | rs2270031 |
SNPdbe | rs2270031 |
MSV3d | rs2270031 |
GWAS Ctlg | rs2270031 |
GMAF | 0.1295 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 18555673] IVS3C>G variant (rs2270031) may influence type-2 diabetes