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rs2569788

From SNPedia

Orientationplus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2569788(C;G)
Make rs2569788(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position10403483
GeneCDC37, MIR1181
is asnp
is mentioned by
dbSNPrs2569788
ebirs2569788
HLIrs2569788
Exacrs2569788
Varsomers2569788
Maprs2569788
PheGenIrs2569788
hapmaprs2569788
1000 genomesrs2569788
hgdprs2569788
ensemblrs2569788
gopubmedrs2569788
geneviewrs2569788
scholarrs2569788
googlers2569788
pharmgkbrs2569788
gwascentralrs2569788
openSNPrs2569788
23andMers2569788
23andMe allrs2569788
SNP Nexus

SNPshotrs2569788
SNPdbers2569788
MSV3drs2569788
GWAS Ctlgrs2569788
Max Magnitude0
? (C;C) (C;G) (G;G) 28
snp near microRNA
ACC MI0006274
ID hsa-mir-1181
offset 15


[PMID 19458495OA-icon.png] Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes.