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rs6856616

From SNPedia

Orientationplus
Stabilizedplus
Make rs6856616(C;C)
Make rs6856616(C;T)
Make rs6856616(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position38323415
is asnp
is mentioned by
dbSNPrs6856616
ebirs6856616
HLIrs6856616
Exacrs6856616
Varsomers6856616
Maprs6856616
PheGenIrs6856616
hapmaprs6856616
1000 genomesrs6856616
hgdprs6856616
ensemblrs6856616
gopubmedrs6856616
geneviewrs6856616
scholarrs6856616
googlers6856616
pharmgkbrs6856616
gwascentralrs6856616
openSNPrs6856616
23andMers6856616
23andMe allrs6856616
SNP Nexus

SNPshotrs6856616
SNPdbers6856616
MSV3drs6856616
GWAS Ctlgrs6856616
GMAF0.1795
Max Magnitude
? (C;C) (C;T) (T;T) 28

[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