Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554333853
rs1554333853
G 0.700 GeneticVariation CLINVAR Phenotypic and molecular characterisation of CDK13-related congenital heart defects, dysmorphic facial features and intellectual developmental disorders. 28807008

2017

dbSNP: rs587777893
rs587777893
A 0.700 CausalMutation CLINVAR Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism. 27159400

2016

dbSNP: rs1009298200
rs1009298200
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057520063
rs1057520063
CA 0.700 CausalMutation CLINVAR

dbSNP: rs1064795760
rs1064795760
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1085307993
rs1085307993
T 0.700 GeneticVariation CLINVAR

dbSNP: rs114925667
rs114925667
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553621496
rs1553621496
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1553770577
rs1553770577
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554208945
rs1554208945
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554846212
rs1554846212
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555452127
rs1555452127
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555939456
rs1555939456
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1561273261
rs1561273261
A 0.700 GeneticVariation CLINVAR

dbSNP: rs369160589
rs369160589
G 0.700 GeneticVariation CLINVAR

dbSNP: rs770374710
rs770374710
TG 0.700 CausalMutation CLINVAR

dbSNP: rs794727774
rs794727774
T 0.700 CausalMutation CLINVAR

dbSNP: rs796052243
rs796052243
T 0.700 GeneticVariation CLINVAR

dbSNP: rs797045412
rs797045412
A 0.700 GeneticVariation CLINVAR