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rs4374642

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs4374642(C;C)
Make rs4374642(C;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position122179956
GeneKIAA1109
is asnp
is mentioned by
dbSNPrs4374642
ebirs4374642
HLIrs4374642
Exacrs4374642
Varsomers4374642
Maprs4374642
PheGenIrs4374642
hapmaprs4374642
1000 genomesrs4374642
hgdprs4374642
ensemblrs4374642
gopubmedrs4374642
geneviewrs4374642
scholarrs4374642
googlers4374642
pharmgkbrs4374642
gwascentralrs4374642
openSNPrs4374642
23andMers4374642
23andMe allrs4374642
SNP Nexus

SNPshotrs4374642
SNPdbers4374642
MSV3drs4374642
GWAS Ctlgrs4374642
GMAF0.1006
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 21760890OA-icon.png] Potential celiac patients: a model of celiac disease pathogenesis


[PMID 17558408OA-icon.png] A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.