DGCR8, DGCR8 microprocessor complex subunit, 54487

N. diseases: 101; N. variants: 8
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7364132
rs7364132
Entrez Id: 54487
Gene Symbol: DGCR8
DGCR8
CUI: C0202236
Disease:
Triglycerides measurement
A 0.700 GeneticVariation GWASCAT Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. 30926973 2019
dbSNP: rs112367533
rs112367533
Entrez Id: 54487
Gene Symbol: DGCR8
DGCR8
CUI: C0596887
Disease:
mathematical ability
G 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs417309
rs417309
Entrez Id: 54487
Gene Symbol: DGCR8
DGCR8
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.020 GeneticVariation BEFREE Moreover, associations of the rs417309 SNP could also be found in numerous subgroups including: Asian and Caucasian population subgroups; laryngeal and breast cancer subgroups; population-based (PB) and hospital-based (HB) subgroups. 29654164 2018
dbSNP: rs417309
rs417309
Entrez Id: 54487
Gene Symbol: DGCR8
DGCR8
CUI: C0678222
Disease:
Breast Carcinoma
0.020 GeneticVariation BEFREE Moreover, associations of the rs417309 SNP could also be found in numerous subgroups including: Asian and Caucasian population subgroups; laryngeal and breast cancer subgroups; population-based (PB) and hospital-based (HB) subgroups. 29654164 2018
dbSNP: rs417309
rs417309
Entrez Id: 54487
Gene Symbol: DGCR8
DGCR8
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.020 GeneticVariation BEFREE Our findings suggested that DGCR8 rs417309 G > A might affect breast cancer risk through the interruption of miRNA binding. 23629745 2013
dbSNP: rs417309
rs417309
Entrez Id: 54487
Gene Symbol: DGCR8
DGCR8
CUI: C0678222
Disease:
Breast Carcinoma
0.020 GeneticVariation BEFREE Our findings suggested that DGCR8 rs417309 G > A might affect breast cancer risk through the interruption of miRNA binding. 23629745 2013
dbSNP: rs417309
rs417309
Entrez Id: 54487
Gene Symbol: DGCR8
DGCR8
CUI: C0006826
Disease:
Malignant Neoplasms
0.010 GeneticVariation BEFREE In conclusion, the <i>DROSHA</i> rs10719, rs6877842 SNPs, and <i>DGCR8</i> rs417309 SNP play pivotal roles in cancerogenesis and may be potential biomarkers for cancer-forewarning. 29654164 2018
dbSNP: rs417309
rs417309
Entrez Id: 54487
Gene Symbol: DGCR8
DGCR8
CUI: C1306459
Disease:
Primary malignant neoplasm
0.010 GeneticVariation BEFREE In conclusion, the <i>DROSHA</i> rs10719, rs6877842 SNPs, and <i>DGCR8</i> rs417309 SNP play pivotal roles in cancerogenesis and may be potential biomarkers for cancer-forewarning. 29654164 2018
dbSNP: rs11089328
rs11089328
Entrez Id: 54487
Gene Symbol: DGCR8
DGCR8
CUI: C0006826
Disease:
Malignant Neoplasms
0.010 GeneticVariation BEFREE One SNP associated with cancer prior to adjustment for multiple comparisons, rs11089328 (DGCR8), was associated with altered levels of hsa-miR-645 in differential tissue under the dominant model. 27107574 2016
dbSNP: rs11089328
rs11089328
Entrez Id: 54487
Gene Symbol: DGCR8
DGCR8
CUI: C1306459
Disease:
Primary malignant neoplasm
0.010 GeneticVariation BEFREE One SNP associated with cancer prior to adjustment for multiple comparisons, rs11089328 (DGCR8), was associated with altered levels of hsa-miR-645 in differential tissue under the dominant model. 27107574 2016
dbSNP: rs3757
rs3757
Entrez Id: 27037;54487
Gene Symbol: TRMT2A;DGCR8
TRMT2A;DGCR8
CUI: C3714636
Disease:
Pneumonitis
0.010 GeneticVariation BEFREE After multiple comparison correction, RPS6KB2:rs10274, SMO:rs1061280, SMO:rs1061285 remained significantly associated with esophagitis, while processing gene DGCR8:rs720014, DGCR8:rs3757, DGCR8:rs1633445 remained significantly associated with pneumonitis. 26991123 2016
dbSNP: rs720014
rs720014
Entrez Id: 54487
Gene Symbol: DGCR8
DGCR8
CUI: C3714636
Disease:
Pneumonitis
0.010 GeneticVariation BEFREE After multiple comparison correction, RPS6KB2:rs10274, SMO:rs1061280, SMO:rs1061285 remained significantly associated with esophagitis, while processing gene DGCR8:rs720014, DGCR8:rs3757, DGCR8:rs1633445 remained significantly associated with pneumonitis. 26991123 2016
dbSNP: rs2073778
rs2073778
Entrez Id: 54487
Gene Symbol: DGCR8
DGCR8
CUI: C0178874
Disease:
Tumor Progression
0.010 GeneticVariation BEFREE Two linked SNPs (rs2073778 and rs720012) in DGCR8 showed significant association with tumor progression (HR = 4.00, 95% CI = 1.53-10.46, P = 0.005). 23322153 2013
dbSNP: rs720012
rs720012
Entrez Id: 54487
Gene Symbol: DGCR8
DGCR8
CUI: C0178874
Disease:
Tumor Progression
0.010 GeneticVariation BEFREE Two linked SNPs (rs2073778 and rs720012) in DGCR8 showed significant association with tumor progression (HR = 4.00, 95% CI = 1.53-10.46, P = 0.005). 23322153 2013
dbSNP: rs3757
rs3757
Entrez Id: 27037;54487
Gene Symbol: TRMT2A;DGCR8
TRMT2A;DGCR8
CUI: C0011581
Disease:
Depressive disorder
0.010 GeneticVariation BEFREE DGCR8 rs3757 and AGO1 rs636832 were found to have significant association with depression, and GEMIN4 rs7813 did not affect susceptibility to depression. 22694265 2012
dbSNP: rs3757
rs3757
Entrez Id: 27037;54487
Gene Symbol: TRMT2A;DGCR8
TRMT2A;DGCR8
CUI: C0344315
Disease:
Depressed mood
0.010 GeneticVariation BEFREE DGCR8 rs3757 and AGO1 rs636832 were found to have significant association with depression, and GEMIN4 rs7813 did not affect susceptibility to depression. 22694265 2012
dbSNP: rs3757
rs3757
Entrez Id: 27037;54487
Gene Symbol: TRMT2A;DGCR8
TRMT2A;DGCR8
CUI: C0011570
Disease:
Mental Depression
0.010 GeneticVariation BEFREE DGCR8 rs3757 and AGO1 rs636832 were found to have significant association with depression, and GEMIN4 rs7813 did not affect susceptibility to depression. 22694265 2012
dbSNP: rs3757
rs3757
Entrez Id: 27037;54487
Gene Symbol: TRMT2A;DGCR8
TRMT2A;DGCR8
CUI: C0438696
Disease:
Suicidal
0.010 GeneticVariation BEFREE Variant allele of DGCR8 rs3757 was associated with increased risk of suicidal tendency and improvement response to antidepressant treatment, whereas the variant of AGO1 rs636832 showed decreased risk of suicidal tendency, suicidal behavior, and recurrence. 22694265 2012