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rs1025689

From SNPedia

Orientationminus
Stabilizedplus
Make rs1025689(C;C)
Make rs1025689(C;G)
Make rs1025689(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position53849695
GeneIL17RB
is asnp
is mentioned by
dbSNPrs1025689
ebirs1025689
HLIrs1025689
Exacrs1025689
Varsomers1025689
Maprs1025689
PheGenIrs1025689
hapmaprs1025689
1000 genomesrs1025689
hgdprs1025689
ensemblrs1025689
gopubmedrs1025689
geneviewrs1025689
scholarrs1025689
googlers1025689
pharmgkbrs1025689
gwascentralrs1025689
openSNPrs1025689
23andMers1025689
23andMe allrs1025689
SNP Nexus

SNPshotrs1025689
SNPdbers1025689
MSV3drs1025689
GWAS Ctlgrs1025689
GMAF0.4564
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 22558321OA-icon.png] Choline Dehydrogenase Polymorphism rs12676 Is a Functional Variation and Is Associated with Changes in Human Sperm Cell Function

[PMID 22377791] Association of genetic polymorphisms of interleukins with new-onset diabetes after transplantation in renal transplantation[PMID 18454203OA-icon.png] Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.