MIR18A, microRNA 18a, 406953

N. diseases: 154; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4284505
rs4284505
Entrez Id: 406952;406953;406979;406980;406982;407975
Gene Symbol: MIR17;MIR18A;MIR19A;MIR19B1;MIR20A;MIR17HG
MIR17;MIR18A;MIR19A;MIR19B1;MIR20A;MIR17HG
CUI: C0026764
Disease:
Multiple Myeloma
0.010 GeneticVariation BEFREE Haplotype AC (rs4284505</span>-rs1428) and CA (rs7336610-rs4284505) evidently reduce MM risk, whereas haplotype GC (rs4284505-rs1428) significantly elevated MM risk (all P < .05). 31029648 2019
dbSNP: rs770419845
rs770419845
Entrez Id: 406952;406953;406979;406980;406982;407048;407975
Gene Symbol: MIR17;MIR18A;MIR19A;MIR19B1;MIR20A;MIR92A1;MIR17HG
MIR17;MIR18A;MIR19A;MIR19B1;MIR20A;MIR92A1;MIR17HG
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE The deletion was screened in 458 high-risk <i>BRCA1/2</i>-negative Chilean families and 480 controls. rs770419845 was not detected in any control but identified in a single family with two cases of BC and other cancers. 29361751 2018
dbSNP: rs770419845
rs770419845
Entrez Id: 406952;406953;406979;406980;406982;407048;407975
Gene Symbol: MIR17;MIR18A;MIR19A;MIR19B1;MIR20A;MIR92A1;MIR17HG
MIR17;MIR18A;MIR19A;MIR19B1;MIR20A;MIR92A1;MIR17HG
CUI: C1611743
Disease:
Familial (FPAH)
0.010 GeneticVariation BEFREE Here, we report the identification of rs770419845, a rare 6 bp deletion located within the polycistronic miR-17-92 cluster, in two first-degree relatives from a Chilean family with familial BC and negative for point mutations in <i>BRCA 1/2</i> genes. 29361751 2018
dbSNP: rs770419845
rs770419845
Entrez Id: 406952;406953;406979;406980;406982;407048;407975
Gene Symbol: MIR17;MIR18A;MIR19A;MIR19B1;MIR20A;MIR92A1;MIR17HG
MIR17;MIR18A;MIR19A;MIR19B1;MIR20A;MIR92A1;MIR17HG
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE The deletion was screened in 458 high-risk <i>BRCA1/2</i>-negative Chilean families and 480 controls. rs770419845 was not detected in any control but identified in a single family with two cases of BC and other cancers. 29361751 2018