MIR302D, microRNA 302d, 442896

N. diseases: 29; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4513633
rs4513633
Entrez Id: 51574;407028;442894;442895;442896;442912;109864269
Gene Symbol: LARP7;MIR302A;MIR302B;MIR302C;MIR302D;MIR367;MIR302CHG
LARP7;MIR302A;MIR302B;MIR302C;MIR302D;MIR367;MIR302CHG
CUI: C2697764
Disease:
Interleukin 16 Measurement
C 0.700 GeneticVariation GWASCAT Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. 27989323 2017
dbSNP: rs1057519017
rs1057519017
Entrez Id: 51574;407028;442896;442912;109864269
Gene Symbol: LARP7;MIR302A;MIR302D;MIR367;MIR302CHG
LARP7;MIR302A;MIR302D;MIR367;MIR302CHG
CUI: C3554439
Disease:
Microcephalic primordial dwarfism Alazami type
AAAAGGAT 0.700 CausalMutation CLINVAR
dbSNP: rs1554011754
rs1554011754
Entrez Id: 51574;407028;442894;442895;442896;442912;109864269
Gene Symbol: LARP7;MIR302A;MIR302B;MIR302C;MIR302D;MIR367;MIR302CHG
LARP7;MIR302A;MIR302B;MIR302C;MIR302D;MIR367;MIR302CHG
CUI: C3554439
Disease:
Microcephalic primordial dwarfism Alazami type
G 0.700 CausalMutation CLINVAR
dbSNP: rs199971565
rs199971565
Entrez Id: 51574;407028;442894;442895;442896;442912;109864269
Gene Symbol: LARP7;MIR302A;MIR302B;MIR302C;MIR302D;MIR367;MIR302CHG
LARP7;MIR302A;MIR302B;MIR302C;MIR302D;MIR367;MIR302CHG
CUI: C0699791
Disease:
Stomach Carcinoma
0.010 GeneticVariation BEFREE In conclusion, for the first time, this study indicated the association and in silico investigations of rs199971565 and suggested it as a novel INDEL biomarker located in the seed site of miR-302c, which may have crucial roles in the susceptibility to GC and its incidence risk. 31219213 2019
dbSNP: rs199971565
rs199971565
Entrez Id: 51574;407028;442894;442895;442896;442912;109864269
Gene Symbol: LARP7;MIR302A;MIR302B;MIR302C;MIR302D;MIR367;MIR302CHG
LARP7;MIR302A;MIR302B;MIR302C;MIR302D;MIR367;MIR302CHG
CUI: C0006826
Disease:
Malignant Neoplasms
0.010 GeneticVariation BEFREE Gastric cancer (GC) is the fifth most prevalent malignant tumor and the third most frequent cause of cancer mortality worldwide. rs199971565 is an insertion/deletion (INDEL) located in microRNA-302c (miR-302c) seed site, which may affect its function and biogenesis. 31219213 2019
dbSNP: rs199971565
rs199971565
Entrez Id: 51574;407028;442894;442895;442896;442912;109864269
Gene Symbol: LARP7;MIR302A;MIR302B;MIR302C;MIR302D;MIR367;MIR302CHG
LARP7;MIR302A;MIR302B;MIR302C;MIR302D;MIR367;MIR302CHG
CUI: C0024623
Disease:
Malignant neoplasm of stomach
0.010 GeneticVariation BEFREE In conclusion, for the first time, this study indicated the association and in silico investigations of rs199971565 and suggested it as a novel INDEL biomarker located in the seed site of miR-302c, which may have crucial roles in the susceptibility to GC and its incidence risk. 31219213 2019