rs2234895
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2234895(C;C) |
Make rs2234895(C;T) |
Make rs2234895(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 16 |
Position | 27346606 |
Gene | IL4R |
is a | snp |
is | mentioned by |
dbSNP | rs2234895 |
dbSNP (classic) | rs2234895 |
ClinGen | rs2234895 |
ebi | rs2234895 |
HLI | rs2234895 |
Exac | rs2234895 |
Gnomad | rs2234895 |
Varsome | rs2234895 |
LitVar | rs2234895 |
Map | rs2234895 |
PheGenI | rs2234895 |
Biobank | rs2234895 |
1000 genomes | rs2234895 |
hgdp | rs2234895 |
ensembl | rs2234895 |
geneview | rs2234895 |
scholar | rs2234895 |
rs2234895 | |
pharmgkb | rs2234895 |
gwascentral | rs2234895 |
openSNP | rs2234895 |
23andMe | rs2234895 |
SNPshot | rs2234895 |
SNPdbe | rs2234895 |
MSV3d | rs2234895 |
GWAS Ctlg | rs2234895 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
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[PMID 26109524] Role of high-risk variants in the development of impaired glucose metabolism was modified by birth weight in Han Chinese