rs12590667
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12590667(C;C) |
Make rs12590667(C;T) |
Make rs12590667(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 106779223 |
Gene | IGH@ |
is a | snp |
is | mentioned by |
dbSNP | rs12590667 |
dbSNP (classic) | rs12590667 |
ClinGen | rs12590667 |
ebi | rs12590667 |
HLI | rs12590667 |
Exac | rs12590667 |
Gnomad | rs12590667 |
Varsome | rs12590667 |
LitVar | rs12590667 |
Map | rs12590667 |
PheGenI | rs12590667 |
Biobank | rs12590667 |
1000 genomes | rs12590667 |
hgdp | rs12590667 |
ensembl | rs12590667 |
geneview | rs12590667 |
scholar | rs12590667 |
rs12590667 | |
pharmgkb | rs12590667 |
gwascentral | rs12590667 |
openSNP | rs12590667 |
23andMe | rs12590667 |
SNPshot | rs12590667 |
SNPdbe | rs12590667 |
MSV3d | rs12590667 |
GWAS Ctlg | rs12590667 |
GMAF | 0.32 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
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[PMID 21326860] Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study