rs12150130
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12150130(C;C) |
Make rs12150130(C;T) |
Make rs12150130(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 17 |
Position | 14213965 |
is a | snp |
is | mentioned by |
dbSNP | rs12150130 |
dbSNP (classic) | rs12150130 |
ClinGen | rs12150130 |
ebi | rs12150130 |
HLI | rs12150130 |
Exac | rs12150130 |
Gnomad | rs12150130 |
Varsome | rs12150130 |
LitVar | rs12150130 |
Map | rs12150130 |
PheGenI | rs12150130 |
Biobank | rs12150130 |
1000 genomes | rs12150130 |
hgdp | rs12150130 |
ensembl | rs12150130 |
geneview | rs12150130 |
scholar | rs12150130 |
rs12150130 | |
pharmgkb | rs12150130 |
gwascentral | rs12150130 |
openSNP | rs12150130 |
23andMe | rs12150130 |
SNPshot | rs12150130 |
SNPdbe | rs12150130 |
MSV3d | rs12150130 |
GWAS Ctlg | rs12150130 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24800985] |
Trait | Conotruncal heart defects |
Title | Genome-wide association study of maternal and inherited loci for conotruncal heart defects. |
Risk Allele | |
P-val | 6E-6 |
Odds Ratio | 3.48 [1.96-6.21] |