Variant | Gene | Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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|
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C | 0.700 | GeneticVariation | GWASCAT | Cancer risk susceptibility loci in a Swedish population. | 29299148 | 2017 | ||||||
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|
|
T | 0.700 | CausalMutation | CLINVAR | Kohlschütter-Tönz syndrome: mutations in ROGDI and evidence of genetic heterogeneity. | 23086778 | 2013 | ||||||
|
|
|
C | 0.700 | GeneticVariation | CLINVAR | Mutations in ROGDI Cause Kohlschütter-Tönz Syndrome. | 22424600 | 2012 | ||||||
|
|
|
T | 0.700 | CausalMutation | CLINVAR | Mutations in ROGDI Cause Kohlschütter-Tönz Syndrome. | 22424600 | 2012 | ||||||
|
|
|
GC | 0.700 | CausalMutation | CLINVAR | |||||||||
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|
|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
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|
|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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|
A | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | CausalMutation | CLINVAR |