| Variant | Gene | Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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T | 0.800 | CausalMutation | CLINVAR | |||||||||
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A | 0.800 | CausalMutation | CLINVAR | |||||||||
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G | 0.700 | GeneticVariation | CLINVAR | |||||||||
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G | 0.700 | GeneticVariation | CLINVAR | |||||||||
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GT | 0.700 | CausalMutation | CLINVAR | |||||||||
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0.700 | GeneticVariation | UNIPROT | ||||||||||
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T | 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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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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0.700 | GeneticVariation | UNIPROT | ||||||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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0.700 | 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 | GeneticVariation | CLINVAR | |||||||||
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A | 0.700 | GeneticVariation | CLINVAR | |||||||||
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T | 0.700 | GeneticVariation | CLINVAR | |||||||||
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CGCCGCGCAGCA | 0.700 | CausalMutation | CLINVAR | The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules. | 1913827 | 1991 | ||||||
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CGCCGCGCAGCA | 0.700 | CausalMutation | CLINVAR | The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules. | 1913827 | 1991 | ||||||
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CGCCGCGCAGCA | 0.700 | CausalMutation | CLINVAR | A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules. | 1922361 | 1991 | ||||||
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CGCCGCGCAGCA | 0.700 | CausalMutation | CLINVAR | A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules. | 1922361 | 1991 | ||||||
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CGCCGCGCAGCA | 0.700 | CausalMutation | CLINVAR | Unilateral renal aplasia in X-linked Kallmann's syndrome. | 7820942 | 1994 | ||||||
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CGCCGCGCAGCA | 0.700 | CausalMutation | CLINVAR | Unilateral renal aplasia in X-linked Kallmann's syndrome. | 7820942 | 1994 | ||||||
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0.800 | GeneticVariation | UNIPROT | Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome. | 8504298 | 1993 |