Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: rs1057519297
rs1057519297
Entrez Id: 51574;109864269
Gene Symbol: LARP7;MIR302CHG
LARP7;MIR302CHG
CUI: C3554439
Disease:
Microcephalic primordial dwarfism Alazami type
GAT 0.700 CausalMutation CLINVAR
dbSNP: rs1554011296
rs1554011296
Entrez Id: 51574;109864269
Gene Symbol: LARP7;MIR302CHG
LARP7;MIR302CHG
CUI: C3554439
Disease:
Microcephalic primordial dwarfism Alazami type
ATT 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: rs1560929898
rs1560929898
Entrez Id: 51574;109864269
Gene Symbol: LARP7;MIR302CHG
LARP7;MIR302CHG
CUI: C3554439
Disease:
Microcephalic primordial dwarfism Alazami type
G 0.700 GeneticVariation CLINVAR
dbSNP: rs756894838
rs756894838
Entrez Id: 51574;109864269
Gene Symbol: LARP7;MIR302CHG
LARP7;MIR302CHG
CUI: C3554439
Disease:
Microcephalic primordial dwarfism Alazami type
C 0.700 CausalMutation CLINVAR