Gene: ASPM ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1189399471
rs1189399471
ASPM
C 0.700 CausalMutation CLINVAR A clinical and molecular genetic study of 112 Iranian families with primary microcephaly. 20978018

2010
dbSNP: rs1553227742
rs1553227742
ASPM
C 0.700 CausalMutation CLINVAR A clinical and molecular genetic study of 112 Iranian families with primary microcephaly. 20978018

2010
dbSNP: rs1553326645
rs1553326645
ASPM
G 0.700 GeneticVariation CLINVAR A clinical and molecular genetic study of 112 Iranian families with primary microcephaly. 20978018

2010
dbSNP: rs587783211
rs587783211
ASPM
A 0.700 CausalMutation CLINVAR A clinical and molecular genetic study of 112 Iranian families with primary microcephaly. 20978018

2010
dbSNP: rs1189399471
rs1189399471
ASPM
C 0.700 CausalMutation CLINVAR ASPM is a major determinant of cerebral cortical size. 12355089

2002
dbSNP: rs1553227742
rs1553227742
ASPM
C 0.700 CausalMutation CLINVAR ASPM is a major determinant of cerebral cortical size. 12355089

2002
dbSNP: rs1553326645
rs1553326645
ASPM
G 0.700 GeneticVariation CLINVAR ASPM is a major determinant of cerebral cortical size. 12355089

2002
dbSNP: rs587783211
rs587783211
ASPM
A 0.700 CausalMutation CLINVAR ASPM is a major determinant of cerebral cortical size. 12355089

2002
dbSNP: rs1189399471
rs1189399471
ASPM
C 0.700 CausalMutation CLINVAR ASPM mutations identified in patients with primary microcephaly and seizures. 16141009

2005
dbSNP: rs1553227742
rs1553227742
ASPM
C 0.700 CausalMutation CLINVAR ASPM mutations identified in patients with primary microcephaly and seizures. 16141009

2005
dbSNP: rs1553326645
rs1553326645
ASPM
G 0.700 GeneticVariation CLINVAR ASPM mutations identified in patients with primary microcephaly and seizures. 16141009

2005
dbSNP: rs587783211
rs587783211
ASPM
A 0.700 CausalMutation CLINVAR ASPM mutations identified in patients with primary microcephaly and seizures. 16141009

2005
dbSNP: rs1189399471
rs1189399471
ASPM
C 0.700 CausalMutation CLINVAR Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings. 15806441

2005
dbSNP: rs1553227742
rs1553227742
ASPM
C 0.700 CausalMutation CLINVAR Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings. 15806441

2005
dbSNP: rs1553326645
rs1553326645
ASPM
G 0.700 GeneticVariation CLINVAR Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings. 15806441

2005
dbSNP: rs587783211
rs587783211
ASPM
A 0.700 CausalMutation CLINVAR Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings. 15806441

2005
dbSNP: rs1189399471
rs1189399471
ASPM
C 0.700 CausalMutation CLINVAR Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family. 19332161

2009
dbSNP: rs1553227742
rs1553227742
ASPM
C 0.700 CausalMutation CLINVAR Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family. 19332161

2009
dbSNP: rs1553326645
rs1553326645
ASPM
G 0.700 GeneticVariation CLINVAR Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family. 19332161

2009
dbSNP: rs587783211
rs587783211
ASPM
A 0.700 CausalMutation CLINVAR Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family. 19332161

2009
dbSNP: rs1189399471
rs1189399471
ASPM
C 0.700 CausalMutation CLINVAR Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations. 19770472

2009
dbSNP: rs1553227742
rs1553227742
ASPM
C 0.700 CausalMutation CLINVAR Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations. 19770472

2009
dbSNP: rs1553326645
rs1553326645
ASPM
G 0.700 GeneticVariation CLINVAR Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations. 19770472

2009
dbSNP: rs587783211
rs587783211
ASPM
A 0.700 CausalMutation CLINVAR Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations. 19770472

2009
dbSNP: rs1189399471
rs1189399471
ASPM
C 0.700 CausalMutation CLINVAR Genetic heterogeneity in Pakistani microcephaly families. 22775483

2013