rs6856616
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6856616(C;C) |
Make rs6856616(C;T) |
Make rs6856616(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 38323415 |
is a | snp |
is | mentioned by |
dbSNP | rs6856616 |
dbSNP (classic) | rs6856616 |
ClinGen | rs6856616 |
ebi | rs6856616 |
HLI | rs6856616 |
Exac | rs6856616 |
Gnomad | rs6856616 |
Varsome | rs6856616 |
LitVar | rs6856616 |
Map | rs6856616 |
PheGenI | rs6856616 |
Biobank | rs6856616 |
1000 genomes | rs6856616 |
hgdp | rs6856616 |
ensembl | rs6856616 |
geneview | rs6856616 |
scholar | rs6856616 |
rs6856616 | |
pharmgkb | rs6856616 |
gwascentral | rs6856616 |
openSNP | rs6856616 |
23andMe | rs6856616 |
SNPshot | rs6856616 |
SNPdbe | rs6856616 |
MSV3d | rs6856616 |
GWAS Ctlg | rs6856616 |
GMAF | 0.1795 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
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[PMID 23850713] Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations