Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
---|---|---|---|---|---|---|---|---|---|---|
|
A | 0.820 | CausalMutation | CLINVAR | ||||||
|
C | 0.800 | CausalMutation | CLINVAR | ||||||
|
A | 0.800 | CausalMutation | CLINVAR | ||||||
|
0.700 | GeneticVariation | UNIPROT | |||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
0.700 | GeneticVariation | UNIPROT | |||||||
|
0.700 | GeneticVariation | UNIPROT | |||||||
|
G | 0.700 | GeneticVariation | CLINVAR | ||||||
|
T | 0.700 | GeneticVariation | CLINVAR | ||||||
|
C | 0.700 | CausalMutation | CLINVAR | ||||||
|
0.700 | GeneticVariation | UNIPROT | |||||||
|
A | 0.700 | GeneticVariation | CLINVAR | ||||||
|
0.820 | GeneticVariation | UNIPROT | MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. | 18724368 | 2008 |
||||
|
0.820 | GeneticVariation | UNIPROT | Navajo microvillous inclusion disease is due to a mutation in MYO5B. | 19006234 | 2008 |
||||
|
0.800 | GeneticVariation | UNIPROT | MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. | 18724368 | 2008 |
||||
|
0.800 | GeneticVariation | UNIPROT | Navajo microvillous inclusion disease is due to a mutation in MYO5B. | 19006234 | 2008 |
||||
|
0.800 | GeneticVariation | UNIPROT | MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. | 18724368 | 2008 |
||||
|
0.800 | GeneticVariation | UNIPROT | Navajo microvillous inclusion disease is due to a mutation in MYO5B. | 19006234 | 2008 |
||||
|
0.700 | GeneticVariation | UNIPROT | MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. | 18724368 | 2008 |
||||
|
0.700 | GeneticVariation | UNIPROT | Navajo microvillous inclusion disease is due to a mutation in MYO5B. | 19006234 | 2008 |
||||
|
T | 0.700 | CausalMutation | CLINVAR | MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. | 18724368 | 2008 |
|||
|
T | 0.700 | GeneticVariation | CLINVAR | MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. | 18724368 | 2008 |
|||
|
0.820 | GeneticVariation | UNIPROT | Loss-of-function of MYO5B is the main cause of microvillus inclusion disease: 15 novel mutations and a CaCo-2 RNAi cell model. | 20186687 | 2010 |
||||
|
0.800 | GeneticVariation | UNIPROT | Loss-of-function of MYO5B is the main cause of microvillus inclusion disease: 15 novel mutations and a CaCo-2 RNAi cell model. | 20186687 | 2010 |
||||
|
0.800 | GeneticVariation | UNIPROT | Loss-of-function of MYO5B is the main cause of microvillus inclusion disease: 15 novel mutations and a CaCo-2 RNAi cell model. | 20186687 | 2010 |