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rs34861192

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs34861192(A;A)
Make rs34861192(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position7668689
GeneRETN
is asnp
is mentioned by
dbSNPrs34861192
ebirs34861192
HLIrs34861192
Exacrs34861192
Varsomers34861192
Maprs34861192
PheGenIrs34861192
hapmaprs34861192
1000 genomesrs34861192
hgdprs34861192
ensemblrs34861192
gopubmedrs34861192
geneviewrs34861192
scholarrs34861192
googlers34861192
pharmgkbrs34861192
gwascentralrs34861192
openSNPrs34861192
23andMers34861192
23andMe allrs34861192
SNP Nexus

SNPshotrs34861192
SNPdbers34861192
MSV3drs34861192
GWAS Ctlgrs34861192
GMAF0.06612
Max Magnitude0

[PMID 20300528OA-icon.png] A at single nucleotide polymorphism-358 is required for g at -420 to confer the highest plasma resistin in the general Japanese population[PMID 19727657] Plasma resistin concentration determined by common variants in the resistin gene and associated with metabolic traits in an aged Japanese population.

[PMID 20131043OA-icon.png] Is rs34861192 or rs1862513 a more promising variant for determining plasma resistin in an aged Japanese population?

[PMID 26404063] Epigenome-wide association study suggests that SNPs in the promoter region of RETN influence plasma resistin level via effects on DNA methylation at neighbouring sites

[PMID 27699082] Relevance Study on Cerebral Infarction and Resistin Gene Polymorphism in Chinese Han Population.