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rs31564

From SNPedia

Orientationminus
Stabilizedminus
Make rs31564(A;A)
Make rs31564(A;C)
Make rs31564(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position135894564
GeneIL9
is asnp
is mentioned by
dbSNPrs31564
ebirs31564
HLIrs31564
Exacrs31564
Varsomers31564
Maprs31564
PheGenIrs31564
hapmaprs31564
1000 genomesrs31564
hgdprs31564
ensemblrs31564
gopubmedrs31564
geneviewrs31564
scholarrs31564
googlers31564
pharmgkbrs31564
gwascentralrs31564
openSNPrs31564
23andMers31564
23andMe allrs31564
SNP Nexus

SNPshotrs31564
SNPdbers31564
MSV3drs31564
GWAS Ctlgrs31564
GMAF0.3728
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 23886125] Interleukin 10 rs1800872 T>G Polymorphism was Associated with an Increased Risk of Esophageal Cancer in a Chinese Population


[PMID 17713557OA-icon.png] Genes at human chromosome 5q31.1 regulate delayed-type hypersensitivity responses associated with Leishmania chagasi infection.


[PMID 17903295OA-icon.png] Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.


[PMID 18404645OA-icon.png] FBXL21 association with schizophrenia in Irish family and case-control samples.


[PMID 18520591OA-icon.png] Sequence variants in host cell factor C1 are associated with Meniere's disease.