rs41274239
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs41274239(A;G) |
Make rs41274239(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 129774734 |
Gene | MIR183, MIR96 |
is a | snp |
is | mentioned by |
dbSNP | rs41274239 |
dbSNP (classic) | rs41274239 |
ClinGen | rs41274239 |
ebi | rs41274239 |
HLI | rs41274239 |
Exac | rs41274239 |
Gnomad | rs41274239 |
Varsome | rs41274239 |
LitVar | rs41274239 |
Map | rs41274239 |
PheGenI | rs41274239 |
Biobank | rs41274239 |
1000 genomes | rs41274239 |
hgdp | rs41274239 |
ensembl | rs41274239 |
geneview | rs41274239 |
scholar | rs41274239 |
rs41274239 | |
pharmgkb | rs41274239 |
gwascentral | rs41274239 |
openSNP | rs41274239 |
23andMe | rs41274239 |
SNPshot | rs41274239 |
SNPdbe | rs41274239 |
MSV3d | rs41274239 |
GWAS Ctlg | rs41274239 |
Max Magnitude | 0 |
[PMID 23828613] A rare SNP in pre-miR-34a is associated with increased levels of miR-34a in pancreatic beta cells [PMID 19232555] Signatures of purifying and local positive selection in human miRNAs.
[PMID 19458495] 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, |