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rs2291418

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2291418(C;T)
Make rs2291418(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position179798324
GeneMGAT4B, MIR1229
is asnp
is mentioned by
dbSNPrs2291418
dbSNP (classic)rs2291418
ClinGenrs2291418
ebirs2291418
HLIrs2291418
Exacrs2291418
Gnomadrs2291418
Varsomers2291418
LitVarrs2291418
Maprs2291418
PheGenIrs2291418
Biobankrs2291418
1000 genomesrs2291418
hgdprs2291418
ensemblrs2291418
geneviewrs2291418
scholarrs2291418
googlers2291418
pharmgkbrs2291418
gwascentralrs2291418
openSNPrs2291418
23andMers2291418
SNPshotrs2291418
SNPdbers2291418
MSV3drs2291418
GWAS Ctlgrs2291418
GMAF0.02893
Max Magnitude0
? (C;C) (C;T) (T;T) 28


snp near microRNA
ACC MI0006319
ID hsa-mir-1229
offset -12


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


[PMID 27328823OA-icon.png] Genome-wide identification of microRNA-related variants associated with risk of Alzheimer’s disease.