Variant | Gene | Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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C | 0.890 | GeneticVariation | CLINVAR | |||||||||
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G | 0.860 | CausalMutation | CLINVAR | |||||||||
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A | 0.830 | CausalMutation | CLINVAR | |||||||||
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C | 0.830 | CausalMutation | CLINVAR | |||||||||
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|
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T | 0.820 | CausalMutation | CLINVAR | |||||||||
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C | 0.800 | CausalMutation | CLINVAR | |||||||||
|
|
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0.800 | GeneticVariation | UNIPROT | ||||||||||
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|
|
0.730 | GeneticVariation | UNIPROT | ||||||||||
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|
|
A | 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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|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
|
|
|
T | 0.700 | GeneticVariation | CLINVAR | |||||||||
|
|
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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|
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0.700 | GeneticVariation | UNIPROT | ||||||||||
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|
|
G | 0.700 | CausalMutation | CLINVAR | |||||||||
|
|
|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
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|
|
C | 0.700 | CausalMutation | CLINVAR | |||||||||
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|
|
G | 0.700 | CausalMutation | CLINVAR | |||||||||
|
|
|
T | 0.700 | SusceptibilityMutation | CLINVAR | |||||||||
|
|
|
G | 0.700 | CausalMutation | CLINVAR | |||||||||
|
|
|
0.700 | GeneticVariation | UNIPROT | ||||||||||
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|
|
0.760 | GeneticVariation | BEFREE | Heterozygosity for apolipoprotein E-4Philadelphia(Glu13----Lys, Arg145----Cys) is associated with incomplete dominance of type III hyperlipoproteinemia. | 1352296 | 1992 | |||||||
|
|
|
0.720 | GeneticVariation | BEFREE | Heterozygosity for apolipoprotein E-4Philadelphia(Glu13----Lys, Arg145----Cys) is associated with incomplete dominance of type III hyperlipoproteinemia. | 1352296 | 1992 | |||||||
|
|
|
0.100 | GeneticVariation | BEFREE | Heterozygosity for apolipoprotein E-4Philadelphia(Glu13----Lys, Arg145----Cys) is associated with incomplete dominance of type III hyperlipoproteinemia. | 1352296 | 1992 |