rs2267386
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2267386(A;A) |
Make rs2267386(A;G) |
Make rs2267386(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 38436107 |
Gene | KCNJ4, LOC105373029 |
is a | snp |
is | mentioned by |
dbSNP | rs2267386 |
dbSNP (classic) | rs2267386 |
ClinGen | rs2267386 |
ebi | rs2267386 |
HLI | rs2267386 |
Exac | rs2267386 |
Gnomad | rs2267386 |
Varsome | rs2267386 |
LitVar | rs2267386 |
Map | rs2267386 |
PheGenI | rs2267386 |
Biobank | rs2267386 |
1000 genomes | rs2267386 |
hgdp | rs2267386 |
ensembl | rs2267386 |
geneview | rs2267386 |
scholar | rs2267386 |
rs2267386 | |
pharmgkb | rs2267386 |
gwascentral | rs2267386 |
openSNP | rs2267386 |
23andMe | rs2267386 |
SNPshot | rs2267386 |
SNPdbe | rs2267386 |
MSV3d | rs2267386 |
GWAS Ctlg | rs2267386 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24800985] Genome-wide association study of maternal and inherited Loci for conotruncal heart defects