MIR938, microRNA 938, 100126327

N. diseases: 16; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2505901
rs2505901
Entrez Id: 6840;100126327
Gene Symbol: SVIL;MIR938
SVIL;MIR938
CUI: C0024623
Disease:
Malignant neoplasm of stomach 		0.020 GeneticVariation BEFREE Firstly, we have decided to perform a case-control study which included 897 GC patients and 992 controls to evaluate the association of miR-219-1 rs213210, miR-938 rs2505901, miR-34b/c rs4938723, and miR-218 rs11134527 polymorphisms with gastric cancer susceptibility. 28298809 2017
dbSNP: rs2505901
rs2505901
Entrez Id: 6840;100126327
Gene Symbol: SVIL;MIR938
SVIL;MIR938
CUI: C0699791
Disease:
Stomach Carcinoma 		0.020 GeneticVariation BEFREE Firstly, we have decided to perform a case-control study which included 897 GC patients and 992 controls to evaluate the association of miR-219-1 rs213210, miR-938 rs2505901, miR-34b/c rs4938723, and miR-218 rs11134527 polymorphisms with gastric cancer susceptibility. 28298809 2017
dbSNP: rs2505901
rs2505901
Entrez Id: 6840;100126327
Gene Symbol: SVIL;MIR938
SVIL;MIR938
CUI: C0699791
Disease:
Stomach Carcinoma 		0.020 GeneticVariation BEFREE The rs3748067 T polymorphism was associated with a decreased risk for intestinal GC (OR, 0.511; 95%CI, 0.272-0.962; p = 0.037), whereas rs2505901 C locus carried a decreased risk overall for GC (OR, 0.733; 95%CI, 0.545-0.985; p = 0.039). 22537748 2012
dbSNP: rs2505901
rs2505901
Entrez Id: 6840;100126327
Gene Symbol: SVIL;MIR938
SVIL;MIR938
CUI: C0024623
Disease:
Malignant neoplasm of stomach 		0.020 GeneticVariation BEFREE The rs3748067 T polymorphism was associated with a decreased risk for intestinal GC (OR, 0.511; 95%CI, 0.272-0.962; p = 0.037), whereas rs2505901 C locus carried a decreased risk overall for GC (OR, 0.733; 95%CI, 0.545-0.985; p = 0.039). 22537748 2012
dbSNP: rs12416605
rs12416605
Entrez Id: 6840;100126327
Gene Symbol: SVIL;MIR938
SVIL;MIR938
CUI: C0699791
Disease:
Stomach Carcinoma 		0.010 GeneticVariation BEFREE rs12416605:C>T in MIR938 associates with gastric cancer through affecting the regulation of the CXCL12 chemokine gene. 31273931 2019
dbSNP: rs12416605
rs12416605
Entrez Id: 6840;100126327
Gene Symbol: SVIL;MIR938
SVIL;MIR938
CUI: C0006826
Disease:
Malignant Neoplasms 		0.010 GeneticVariation BEFREE rs12416605 appears to be involved in gastric cancer by affecting the regulatory function of MIR938 on genes related to this cancer type, particularly on CXCL12 posttranscriptional regulation. 31273931 2019
dbSNP: rs12416605
rs12416605
Entrez Id: 6840;100126327
Gene Symbol: SVIL;MIR938
SVIL;MIR938
CUI: C0024623
Disease:
Malignant neoplasm of stomach 		0.010 GeneticVariation BEFREE rs12416605:C>T in MIR938 associates with gastric cancer through affecting the regulation of the CXCL12 chemokine gene. 31273931 2019