MIR618, microRNA 618, 693203

N. diseases: 35; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C0678222
Disease:
Breast Carcinoma
0.030 GeneticVariation BEFREE All in all, our meta-analysis had successfully chased down that miR-618 rs2682818</span> polymorphism is not linked with overall cancer risk, but in the dominant genotype of breast cancer. 31383788 2019
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.030 GeneticVariation BEFREE All in all, our meta-analysis had successfully chased down that miR-618 rs2682818</span> polymorphism is not linked with overall cancer risk, but in the dominant genotype of breast cancer. 31383788 2019
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C0678222
Disease:
Breast Carcinoma
0.030 GeneticVariation BEFREE Our findings support the following conclusions: a) rs6505162:C > A in pre-miR-423 increases risk of familial BC in families with a strong history of BC; b) the C/A genotype at rs2682818:C > A (pre-miR-618) increases BC risk in non-familial early-onset BC; and c) the G/G genotype at rs895819:A > G (miR-27a) reduces BC risk in families with a moderate history of BC. 27421647 2016
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.030 GeneticVariation BEFREE Our findings support the following conclusions: a) rs6505162:C > A in pre-miR-423 increases risk of familial BC in families with a strong history of BC; b) the C/A genotype at rs2682818:C > A (pre-miR-618) increases BC risk in non-familial early-onset BC; and c) the G/G genotype at rs895819:A > G (miR-27a) reduces BC risk in families with a moderate history of BC. 27421647 2016
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C0678222
Disease:
Breast Carcinoma
0.030 GeneticVariation BEFREE To explore the relevance of miRNA polymorphisms and female physiological characteristics to breast cancer risk, SNPs located within hsa-miR-605 (rs2043556), hsa-miR-149 (rs2292832), hsa-miR-27a (rs895819), hsa-miR-196a-2 (rs11614913) and hsa-miR-618 (rs2682818) were selected, and their associations with breast cancer risk were analysed. 22074121 2012
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.030 GeneticVariation BEFREE To explore the relevance of miRNA polymorphisms and female physiological characteristics to breast cancer risk, SNPs located within hsa-miR-605 (rs2043556), hsa-miR-149 (rs2292832), hsa-miR-27a (rs895819), hsa-miR-196a-2 (rs11614913) and hsa-miR-618 (rs2682818) were selected, and their associations with breast cancer risk were analysed. 22074121 2012
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C1306459
Disease:
Primary malignant neoplasm
0.010 GeneticVariation BEFREE All in all, our meta-analysis had successfully chased down that miR-618 rs2682818 polymorphism is not linked with overall cancer risk, but in the dominant genotype of breast cancer. 31383788 2019
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C0596263
Disease:
Carcinogenesis
0.010 GeneticVariation BEFREE Piles of evidence have supported the relationship between miR-618 rs2682818 polymorphism and tumorigenesis, but the conclusion remains inconsistent. 31383788 2019
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C0007847
Disease:
Malignant tumor of cervix
0.010 GeneticVariation BEFREE Because genetic variants in microRNAs (miRNAs) or their surrounding regions can alter miRNA processing, expression and final biological function, we investigated whether miRNA single-nucleotide polymorphisms (SNPs) are associated with cervical cancer (CC) susceptibility.Common miRNA SNPs (i.e. miR-146a rs2910164, miR-149 rs2292832, miR-196a2 rs11614913, miR-499 rs3746444, miR-605 rs2043556 and miR-618 rs2682818) were genotyped in the 954 patients and 1339 controls. 30852614 2019
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C4048328
Disease:
cervical cancer
0.010 GeneticVariation BEFREE Because genetic variants in microRNAs (miRNAs) or their surrounding regions can alter miRNA processing, expression and final biological function, we investigated whether miRNA single-nucleotide polymorphisms (SNPs) are associated with cervical cancer (CC) susceptibility.Common miRNA SNPs (i.e. miR-146a rs2910164, miR-149 rs2292832, miR-196a2 rs11614913, miR-499 rs3746444, miR-605 rs2043556 and miR-618 rs2682818) were genotyped in the 954 patients and 1339 controls. 30852614 2019
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C0006826
Disease:
Malignant Neoplasms
0.010 GeneticVariation BEFREE All in all, our meta-analysis had successfully chased down that miR-618 rs2682818 polymorphism is not linked with overall cancer risk, but in the dominant genotype of breast cancer. 31383788 2019
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C0302592
Disease:
Cervix carcinoma
0.010 GeneticVariation BEFREE Because genetic variants in microRNAs (miRNAs) or their surrounding regions can alter miRNA processing, expression and final biological function, we investigated whether miRNA single-nucleotide polymorphisms (SNPs) are associated with cervical cancer (CC) susceptibility.Common miRNA SNPs (i.e. miR-146a rs2910164, miR-149 rs2292832, miR-196a2 rs11614913, miR-499 rs3746444, miR-605 rs2043556 and miR-618 rs2682818) were genotyped in the 954 patients and 1339 controls. 30852614 2019
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE SNP rs2682818 in miR-618 has potential as a biomarker for individuals with high CRC susceptibility. 29533012 2018
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C4722085
Disease:
Malignant neoplasm of colon and/or rectum
0.010 GeneticVariation BEFREE Polymorphism rs2682818 in miR-618 is associated with colorectal cancer susceptibility in a Han Chinese population. 29533012 2018
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C0948008
Disease:
Ischemic stroke
0.010 GeneticVariation BEFREE Moreover, the variant genotypes (GT/TT) </span>of rs26</span>82818 were an independent prognostic factor for ischemic stroke in the multivariate Cox regression model. 27011381 2017
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C1611743
Disease:
Familial (FPAH)
0.010 GeneticVariation BEFREE Our study evaluated the association of the SNPs rs895819 in pre-miR27a, rs11614913 in pre-miR-196a2, rs6505162 in pre-miR-423, rs4919510 in miR-608, and rs2682818 in pre-mir-618 with familial BC and early-onset non-familial BC in non-carriers of BRCA1/2 mutations from a South American population. 27421647 2016
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C0024305
Disease:
Lymphoma, Non-Hodgkin
0.010 GeneticVariation BEFREE Findings were confirmed by genotyping a SNP (rs2682818) in the stem-loop sequence of miR-618 in a population-based case-control study of NHL (455 cases and 527 controls). 24503492 2014
dbSNP: rs2682818
rs2682818
Entrez Id: 8825;693203;105369869
Gene Symbol: LIN7A;MIR618;LOC105369869
LIN7A;MIR618;LOC105369869
CUI: C0024301
Disease:
Lymphoma, Follicular
0.010 GeneticVariation BEFREE This is consistent with our finding of a significant association between rs2682818 G>T in the miR-618 stem-loop and follicular lymphoma (FL) (OR: 1.65, 95% CI: 1.05-2.60). 24503492 2014