rs2289030

minus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs2289030(C;G)

Make rs2289030(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

94834510

Gene	KRT19P2, MIR492

is a	snp
is	mentioned by
dbSNP	rs2289030
dbSNP (classic)	rs2289030
ClinGen	rs2289030
ebi	rs2289030
HLI	rs2289030
Exac	rs2289030
Gnomad	rs2289030
Varsome	rs2289030
LitVar	rs2289030
Map	rs2289030
PheGenI	rs2289030
Biobank	rs2289030
1000 genomes	rs2289030
hgdp	rs2289030
ensembl	rs2289030
geneview	rs2289030
scholar	rs2289030
google	rs2289030
pharmgkb	rs2289030
gwascentral	rs2289030
openSNP	rs2289030
23andMe	rs2289030
SNPshot	rs2289030
SNPdbe	rs2289030
MSV3d	rs2289030
GWAS Ctlg	rs2289030

GMAF

0.118

Max Magnitude

0

?

(C;C) (C;G) (G;G)

28

[PMID 20044760] Prognostic impact of microRNA-related gene polymorphisms on survival of patients with colorectal cancer

[PMID 19047128 ] Single nucleotide polymorphisms of microRNA machinery genes modify the risk of renal cell carcinoma.

[PMID 19138993 ] Genetic variations in microRNA-related genes are novel susceptibility loci for esophageal cancer risk.

[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.

[PMID 22818121] The prognostic impact of microRNA sequence polymorphisms on the recurrence of patients with completely resected non-small cell lung cancer

[PMID 26753964] miR-492G>C polymorphism (rs2289030) is associated with overall survival of hepatocellular carcinoma patients.