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rs41274239

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41274239(A;G)
Make rs41274239(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position129774734
GeneMIR183
is asnp
is mentioned by
dbSNPrs41274239
ebirs41274239
HLIrs41274239
Exacrs41274239
Varsomers41274239
Maprs41274239
PheGenIrs41274239
hapmaprs41274239
1000 genomesrs41274239
hgdprs41274239
ensemblrs41274239
gopubmedrs41274239
geneviewrs41274239
scholarrs41274239
googlers41274239
pharmgkbrs41274239
gwascentralrs41274239
openSNPrs41274239
23andMers41274239
23andMe allrs41274239
SNP Nexus

SNPshotrs41274239
SNPdbers41274239
MSV3drs41274239
GWAS Ctlgrs41274239
Max Magnitude0

[PMID 23828613OA-icon.png] A rare SNP in pre-miR-34a is associated with increased levels of miR-34a in pancreatic beta cells [PMID 19232555OA-icon.png] Signatures of purifying and local positive selection in human miRNAs.


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

ClinVar
Risk rs41274239(G;G)
Alt rs41274239(G;G)
Reference rs41274239(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene MIR183 MIR96
CLNDBN not specified
Reversed 0
HGVS NC_000007.13:g.129414574A>G
CLNSRC
CLNACC RCV000151023.1,