Variant | Gene | Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||
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0.700 | GeneticVariation | GWASCAT | Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. | 29844566 | 2018 | |||||||
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T | 0.700 | GeneticVariation | GWASCAT | Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. | 29942086 | 2018 | ||||||
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A | 0.700 | GeneticVariation | GWASCAT | Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. | 30038396 | 2018 | ||||||
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0.700 | GeneticVariation | UNIPROT | The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes. | 20531442 | 2010 | |||||||
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0.700 | GeneticVariation | UNIPROT | The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes. | 20531442 | 2010 | |||||||
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0.700 | GeneticVariation | UNIPROT | Mutations in the human SIX3 gene in holoprosencephaly are loss of function. | 18791198 | 2008 | |||||||
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0.700 | GeneticVariation | UNIPROT | Mutations in the human SIX3 gene in holoprosencephaly are loss of function. | 18791198 | 2008 | |||||||
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0.700 | GeneticVariation | UNIPROT | SIX3 mutations with holoprosencephaly. | 17001667 | 2006 | |||||||
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0.700 | GeneticVariation | UNIPROT | SIX3 mutations with holoprosencephaly. | 17001667 | 2006 | |||||||
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0.700 | GeneticVariation | UNIPROT | Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations. | 15221788 | 2004 | |||||||
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0.700 | GeneticVariation | UNIPROT | Functional characterization of SIX3 homeodomain mutations in holoprosencephaly: interaction with the nuclear receptor NR4A3/NOR1. | 15523651 | 2004 | |||||||
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0.700 | GeneticVariation | UNIPROT | Functional characterization of SIX3 homeodomain mutations in holoprosencephaly: interaction with the nuclear receptor NR4A3/NOR1. | 15523651 | 2004 | |||||||
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0.700 | GeneticVariation | UNIPROT | Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations. | 15221788 | 2004 | |||||||
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0.700 | GeneticVariation | UNIPROT | Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly. | 10369266 | 1999 | |||||||
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0.700 | GeneticVariation | UNIPROT | Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly. | 10369266 | 1999 | |||||||
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G | 0.700 | CausalMutation | CLINVAR | |||||||||
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C | 0.700 | CausalMutation | CLINVAR | |||||||||
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C | 0.700 | CausalMutation | CLINVAR | |||||||||
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G | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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T | 0.700 | CausalMutation | CLINVAR | |||||||||
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T | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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0.700 | GeneticVariation | UNIPROT | ||||||||||
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0.800 | GeneticVariation | UNIPROT | The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes. | 20531442 | 2010 |