ZFYVE26, zinc finger FYVE-type containing 26, 23503
N. diseases: 79; N. variants: 59
Source: ALL
Variant | Gene | Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||
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A | 0.700 | CausalMutation | CLINVAR | Spastizin mutation in hereditary spastic paraplegia with thin corpus callosum. | 27544497 | 2016 | ||||||
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C | 0.700 | GeneticVariation | CLINVAR | SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum. | 19805727 | 2009 | ||||||
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C | 0.700 | GeneticVariation | CLINVAR | SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum. | 19805727 | 2009 | ||||||
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C | 0.700 | GeneticVariation | CLINVAR | Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome. | 18394578 | 2008 | ||||||
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C | 0.700 | GeneticVariation | CLINVAR | Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome. | 18394578 | 2008 | ||||||
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T | 0.700 | CausalMutation | CLINVAR | [Koryak of Kamchatka. The genetic differentiation of the population]. | 6944241 | 1981 | ||||||
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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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T | 0.700 | CausalMutation | CLINVAR | |||||||||
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A | 0.700 | GeneticVariation | CLINVAR | |||||||||
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GGCCCTTC | 0.700 | CausalMutation | CLINVAR |