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rs1880242

From SNPedia

Orientationplus
Stabilizedplus
Make rs1880242(G;G)
Make rs1880242(G;T)
Make rs1880242(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position22719988
is asnp
is mentioned by
dbSNPrs1880242
ebirs1880242
HLIrs1880242
Exacrs1880242
Varsomers1880242
Maprs1880242
PheGenIrs1880242
hapmaprs1880242
1000 genomesrs1880242
hgdprs1880242
ensemblrs1880242
gopubmedrs1880242
geneviewrs1880242
scholarrs1880242
googlers1880242
pharmgkbrs1880242
gwascentralrs1880242
openSNPrs1880242
23andMers1880242
23andMe allrs1880242
SNP Nexus

SNPshotrs1880242
SNPdbers1880242
MSV3drs1880242
GWAS Ctlgrs1880242
GMAF0.4784
Max Magnitude
? (G;G) (G;T) (T;T) 28
rs1880242 is a SNP well upstream of IL2 (Interleukin 2).

[PMID 19288024] among 151 patients with obstructive sleep apnea and 75 healthy controls from Southeast China, assoc. of reduced obstructive sleep apnea occurrence in minor allele rs1800796(G) carriers, haplotype rs1880242(T) + rs1800796(G) associated with sig. decreased risk of obstructive sleep apnea than the single rs1800796(G) allele


[PMID 17847004OA-icon.png] Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetrance.


[PMID 19387461OA-icon.png] Interleukin-6 haplotypes and the response to therapy of chronic hepatitis C virus infection.


[PMID 19401628OA-icon.png] Host genetics, steatosis and insulin resistance among African Americans and Caucasian Americans with hepatitis C virus genotype-1 infection.