| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
A | 0.830 | CausalMutation | CLINVAR | ||||||
|
G | 0.830 | CausalMutation | CLINVAR | ||||||
|
T | 0.830 | CausalMutation | CLINVAR | ||||||
|
T | 0.830 | CausalMutation | CLINVAR | ||||||
|
A | 0.810 | CausalMutation | CLINVAR | ||||||
|
T | 0.810 | CausalMutation | CLINVAR | ||||||
|
C | 0.800 | CausalMutation | CLINVAR | ||||||
|
A | 0.800 | CausalMutation | CLINVAR | ||||||
|
A | 0.800 | CausalMutation | CLINVAR | ||||||
|
A | 0.800 | CausalMutation | CLINVAR | ||||||
|
A | 0.800 | CausalMutation | CLINVAR | ||||||
|
A | 0.730 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
0.830 | GeneticVariation | UNIPROT | Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. | 10973259 | 2000 |
||||
|
0.830 | GeneticVariation | UNIPROT | Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly. | 10973260 | 2000 |
||||
|
0.830 | GeneticVariation | UNIPROT | Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly. | 10973260 | 2000 |
||||
|
0.830 | GeneticVariation | UNIPROT | Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. | 10973259 | 2000 |
||||
|
0.810 | GeneticVariation | UNIPROT | Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly. | 10973260 | 2000 |
||||
|
0.810 | GeneticVariation | UNIPROT | Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. | 10973259 | 2000 |
||||
|
0.810 | GeneticVariation | UNIPROT | Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. | 10973259 | 2000 |
||||
|
0.810 | GeneticVariation | UNIPROT | Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly. | 10973260 | 2000 |
||||
|
0.800 | GeneticVariation | UNIPROT | Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. | 10973259 | 2000 |
||||
|
0.800 | GeneticVariation | UNIPROT | Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly. | 10973260 | 2000 |