rs11231379
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11231379(C;C) |
Make rs11231379(C;G) |
Make rs11231379(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 63137463 |
Gene | SLC22A24 |
is a | snp |
is | mentioned by |
dbSNP | rs11231379 |
dbSNP (classic) | rs11231379 |
ClinGen | rs11231379 |
ebi | rs11231379 |
HLI | rs11231379 |
Exac | rs11231379 |
Gnomad | rs11231379 |
Varsome | rs11231379 |
LitVar | rs11231379 |
Map | rs11231379 |
PheGenI | rs11231379 |
Biobank | rs11231379 |
1000 genomes | rs11231379 |
hgdp | rs11231379 |
ensembl | rs11231379 |
geneview | rs11231379 |
scholar | rs11231379 |
rs11231379 | |
pharmgkb | rs11231379 |
gwascentral | rs11231379 |
openSNP | rs11231379 |
23andMe | rs11231379 |
SNPshot | rs11231379 |
SNPdbe | rs11231379 |
MSV3d | rs11231379 |
GWAS Ctlg | rs11231379 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 24800985] Genome-wide association study of maternal and inherited Loci for conotruncal heart defects