SEMA4G, semaphorin 4G, 57715

N. diseases: 8; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C0678222
Disease:
Breast Carcinoma
0.050 GeneticVariation BEFREE In the first set, although rs4919510:C>G was unrelated to breast cancer in general patients, variant genotypes (CG/GG) were specifically associated with increased risk of HER2-positive subtype (Adjusted OR = 1.97, 95% CI, 1.34-2.90 in the recessive model). 22586447 2012
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.050 GeneticVariation BEFREE In the first set, although rs4919510:C>G was unrelated to breast cancer in general patients, variant genotypes (CG/GG) were specifically associated with increased risk of HER2-positive subtype (Adjusted OR = 1.97, 95% CI, 1.34-2.90 in the recessive model). 22586447 2012
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C1960398
Disease:
HER2-positive carcinoma of breast
0.010 GeneticVariation BEFREE Polymorphism rs4919510:C>G in mature sequence of human microRNA-608 contributes to the risk of HER2-positive breast cancer but not other subtypes. 22586447 2012
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C0009402
Disease:
Colorectal Carcinoma
0.050 GeneticVariation BEFREE There was no significant association between rs4919510 and colorectal cancer risk (African American: OR(GG vs. CC) 0.89 [95% CI, 0.41-1.80]) (Caucasian: OR(GG vs. CC) 1.76, ([95% CI, 0.48-6.39]). 22606253 2012
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C4722085
Disease:
Malignant neoplasm of colon and/or rectum
0.030 GeneticVariation BEFREE There was no significant association between rs4919510 and colorectal cancer risk (African American: OR(GG vs. CC) 0.89 [95% CI, 0.41-1.80]) (Caucasian: OR(GG vs. CC) 1.76, ([95% CI, 0.48-6.39]). 22606253 2012
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C2931822
Disease:
Nasopharyngeal carcinoma
0.020 GeneticVariation BEFREE Our findings reveal rs4919510C > G in miR-608 as a simple marker to predict LRR in patients with radiotherapy-treated nasopharyngeal carcinoma. 23796562 2013
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C2986682
Disease:
Locally Recurrent Malignant Neoplasm
0.010 GeneticVariation BEFREE Our findings reveal rs4919510C > G in miR-608 as a simple marker to predict LRR</span> in patients with radiotherapy-treated nasopharyngeal carcinoma. 23796562 2013
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C0036690
Disease:
Septicemia
0.010 GeneticVariation BEFREE Our results indicate that the rs4919510G/C SNP in hsa-mir-608 may be a prognostic biomarker for sepsis in patients with major trauma. 24743625 2015
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C0243026
Disease:
Sepsis
0.010 GeneticVariation BEFREE Our results indicate that the rs4919510G/C SNP in hsa-mir-608 may be a prognostic biomarker for sepsis in patients with major trauma. 24743625 2015
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C0036690
Disease:
Septicemia
0.010 GeneticVariation BEFREE Among the 9 selected SNPs with potential functional significance, only 1 (miR-608 rs4919510) was found to be strongly associated with a higher risk of developing sepsis and multiple organ dysfunction in all 3 independent study cohorts. 24743625 2015
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C0243026
Disease:
Sepsis
0.010 GeneticVariation BEFREE Among the 9 selected SNPs with potential functional significance, only 1 (miR-608 rs4919510) was found to be strongly associated with a higher risk of developing sepsis and multiple organ dysfunction in all 3 independent study cohorts. 24743625 2015
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C2239176
Disease:
Liver carcinoma
0.020 GeneticVariation BEFREE However, no significant association between miRNA‑608 rs4919510 and the risk of HCC/HBV‑associated HCC was found. 25190221 2014
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C0085215
Disease:
Ovarian Failure, Premature
0.010 GeneticVariation BEFREE Four breast cancer-related microRNA polymorphisms (miR-27aA > G [rs895819], miR-135bC > T [rs74141216], miR-423C > A [rs6505162], and miR-608G > C [rs4919510]) were genotyped in 136 women with idiopathic POI and 224 controls of Korean ethnicity using polymerase chain reaction-restriction fragment length polymorphism analysis. 25203895 2015
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C0027651
Disease:
Neoplasms
0.020 GeneticVariation BEFREE After further stratification for tumor grading, stage III patients carrying the G allele of rs4919510 and undergoing adjuvant chemotherapy were at decreased risk of relapse (HR = 0.44; 95% CI: 0.20-0.94; adjusted P = 0.03). 25368035 2015
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C0238463
Disease:
Papillary thyroid carcinoma
0.030 GeneticVariation BEFREE Three SNPs (rs67106263 in mir-3144, GA versus GG, OR = 1.35, 1.09-1.68; rs4919510 in mir-608, CC versus GG/GC, OR = 0.76, 0.60-0.97; and rs79402775 in mir-933, AA versus GG/GA, OR = 1.76, 1.00-3.12) were associated with PTC risk. 25381599 2015
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C0154038
Disease:
Benign neoplasm of thyroid gland
0.010 GeneticVariation BEFREE In addition, three SNPs (rs10061133 in mir-449b, rs79402775 in mir-933 and rs4919510 in mir-608) showed at least borderline correlations with the risk of BN. 25381599 2015
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C2931822
Disease:
Nasopharyngeal carcinoma
0.020 GeneticVariation BEFREE Moreover, the rs4919510C>G adverse genotypes significantly interacted with Epstein-Barr virus (EBV) infection on increasing NPC risk (P=0.001). 25861865 2015
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C0149678
Disease:
Epstein-Barr Virus Infections
0.010 GeneticVariation BEFREE Moreover, the rs4919510C>G adverse genotypes significantly interacted with Epstein-Barr virus (EBV) infection on increasing NPC risk (P=0.001). 25861865 2015
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C0684249
Disease:
Carcinoma of lung
0.050 GeneticVariation BEFREE The individuals with both risk genotypes of miRNA SNPs and exposure to risk factor (cooking oil fumes) were in a higher risk of lung cancer than persons with only one of the two risk factors (ORs were 1.91, 1.05 and 1.41 for miR-146a rs2910164, ORs were 1.94, 1.23 and 1.34 for miR-196a2 rs11614913, ORs were 2.06, 1.41 and 1.68 for miR-608 rs4919510, ORs were 1.76, 0.82 and 1.07 for miR-27a rs895819, and ORs were 2.13, 1.15 and 1.02 for miR-423 rs6505162, respectively). 26083623 2015
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.050 GeneticVariation BEFREE The individuals with both risk genotypes of miRNA SNPs and exposure to risk factor (cooking oil fumes) were in a higher risk of lung cancer than persons with only one of the two risk factors (ORs were 1.91, 1.05 and 1.41 for miR-146a rs2910164, ORs were 1.94, 1.23 and 1.34 for miR-196a2 rs11614913, ORs were 2.06, 1.41 and 1.68 for miR-608 rs4919510, ORs were 1.76, 0.82 and 1.07 for miR-27a rs895819, and ORs were 2.13, 1.15 and 1.02 for miR-423 rs6505162, respectively). 26083623 2015
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C0242379
Disease:
Malignant neoplasm of lung
0.050 GeneticVariation BEFREE The individuals with both risk genotypes of miRNA SNPs and exposure to risk factor (cooking oil fumes) were in a higher risk of lung cancer than persons with only one of the two risk factors (ORs were 1.91, 1.05 and 1.41 for miR-146a rs2910164, ORs were 1.94, 1.23 and 1.34 for miR-196a2 rs11614913, ORs were 2.06, 1.41 and 1.68 for miR-608 rs4919510, ORs were 1.76, 0.82 and 1.07 for miR-27a rs895819, and ORs were 2.13, 1.15 and 1.02 for miR-423 rs6505162, respectively). 26083623 2015
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C2239176
Disease:
Liver carcinoma
0.020 GeneticVariation BEFREE In conclusion, our results illustrated the potential role of miR-608 rs4919510 as a prognostic marker for HCC patients undergoing surgical resection of the tumor. 26815502 2016
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C0027651
Disease:
Neoplasms
0.020 GeneticVariation BEFREE Further stratification analysis indicated that rs4919510 was significantly associated with OS in patients who were satisfied with one of the following criteria: male gender, HbsAg-positive, α-fetoprotein (AFP)-positive, tumor size >5 cm, cirrhosis, solitary tumor, I + II pTNM stage, or no tumor capsule. 26815502 2016
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C0023890
Disease:
Liver Cirrhosis
0.010 GeneticVariation BEFREE Finally, a significantly higher frequency of rs4919510 CC genotype was observed in patients with cirrhosis (22.9 %, 55/240) than those without cirrhosis (14.0 %, 17/121) (P = 0.047). 26815502 2016
dbSNP: rs4919510
rs4919510
Entrez Id: 57715;84545;693193
Gene Symbol: SEMA4G;MRPL43;MIR608
SEMA4G;MRPL43;MIR608
CUI: C1623038
Disease:
Cirrhosis
0.010 GeneticVariation BEFREE Finally, a significantly higher frequency of rs4919510 CC genotype was observed in patients with cirrhosis (22.9 %, 55/240) than those without cirrhosis (14.0 %, 17/121) (P = 0.047). 26815502 2016