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rs2234895

From SNPedia

Orientationplus
Stabilizedplus
Make rs2234895(C;C)
Make rs2234895(C;T)
Make rs2234895(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position27346606
GeneIL4R
is asnp
is mentioned by
dbSNPrs2234895
ebirs2234895
HLIrs2234895
Exacrs2234895
Varsomers2234895
Maprs2234895
PheGenIrs2234895
hapmaprs2234895
1000 genomesrs2234895
hgdprs2234895
ensemblrs2234895
gopubmedrs2234895
geneviewrs2234895
scholarrs2234895
googlers2234895
pharmgkbrs2234895
gwascentralrs2234895
openSNPrs2234895
23andMers2234895
23andMe allrs2234895
SNP Nexus

SNPshotrs2234895
SNPdbers2234895
MSV3drs2234895
GWAS Ctlgrs2234895
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 26109524] Role of high-risk variants in the development of impaired glucose metabolism was modified by birth weight in Han Chinese