MIR30A, microRNA 30a, 407029

N. diseases: 218; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2222722
rs2222722
Entrez Id: 79940;407029
Gene Symbol: LINC00472;MIR30A
LINC00472;MIR30A
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE The frequency of the miR-30a rs2222722 T allele was significantly associated with increased CRC risk in the studied population ( P = 0.0019; OR = 1.47; 95% CI, 1.15-1.89). 30387187 2018
dbSNP: rs2222722
rs2222722
Entrez Id: 79940;407029
Gene Symbol: LINC00472;MIR30A
LINC00472;MIR30A
CUI: C0027726
Disease:
Nephrotic Syndrome
0.010 GeneticVariation BEFREE The SNPs of miR-30a [i.e., rs2222722 (C>T)], Notch1 [i.e., rs3124599 (G>A), rs3124591 (C>T), and rs139994842 (G>A)], Snail1 [i.e., rs6020178 (T>C)], p53 [i.e., rs1042522 (C>G)], and CD73 [i.e., rs9444348 (G>A) and rs4431401 (T>C)] were significantly correlated with both differed NS risk and altered hormone sensitivity to NS (all p < 0.05). 29356585 2018
dbSNP: rs1358379
rs1358379
Entrez Id: 79940;407029
Gene Symbol: LINC00472;MIR30A
LINC00472;MIR30A
CUI: C2239176
Disease:
Liver carcinoma
0.010 GeneticVariation BEFREE We found that rs1358379 was associated with susceptibility to HBV infection, HBV clearance, persistent chronic HBV infection and liver cirrhosis+HCC. 28685993 2017
dbSNP: rs1358379
rs1358379
Entrez Id: 79940;407029
Gene Symbol: LINC00472;MIR30A
LINC00472;MIR30A
CUI: C0023890
Disease:
Liver Cirrhosis
0.010 GeneticVariation BEFREE We found that rs1358379 was associated with susceptibility to HBV infection, HBV clearance, persistent chronic HBV infection and liver cirrhosis+HCC. 28685993 2017
dbSNP: rs1358379
rs1358379
Entrez Id: 79940;407029
Gene Symbol: LINC00472;MIR30A
LINC00472;MIR30A
CUI: C0019163
Disease:
Hepatitis B
0.010 GeneticVariation BEFREE We found that rs1358379 was associated with susceptibility to HBV infection, HBV clearance, persistent chronic HBV infection and liver cirrhosis+HCC. 28685993 2017