Gene: MYO5B ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555648414
rs1555648414
MYO5B
0.700 GeneticVariation UNIPROT Microvillus inclusion disease: loss of Myosin vb disrupts intracellular traffic and cell polarity. 24138727

2014
dbSNP: rs1555648414
rs1555648414
MYO5B
0.700 GeneticVariation UNIPROT Myosin Vb uncoupling from RAB8A and RAB11A elicits microvillus inclusion disease. 24892806

2014
dbSNP: rs1555648414
rs1555648414
MYO5B
0.700 GeneticVariation UNIPROT Functional characterization of mutations in the myosin Vb gene associated with microvillus inclusion disease. 21206382

2011
dbSNP: rs1555648414
rs1555648414
MYO5B
0.700 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
dbSNP: rs1555648414
rs1555648414
MYO5B
0.700 GeneticVariation UNIPROT MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. 18724368

2008
dbSNP: rs1555648414
rs1555648414
MYO5B
0.700 GeneticVariation UNIPROT Navajo microvillous inclusion disease is due to a mutation in MYO5B. 19006234

2008
dbSNP: rs727505394
rs727505394
MYO5B
T 0.700 CausalMutation CLINVAR MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. 18724368

2008
dbSNP: rs727505395
rs727505395
MYO5B
T 0.700 GeneticVariation CLINVAR MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. 18724368

2008
dbSNP: rs1053713532
rs1053713532
MYO5B
0.700 GeneticVariation UNIPROT

dbSNP: rs121908104
rs121908104
MYO5B
T 0.700 CausalMutation CLINVAR

dbSNP: rs1283622290
rs1283622290
MYO5B
0.700 GeneticVariation UNIPROT

dbSNP: rs1324907355
rs1324907355
MYO5B
0.700 GeneticVariation UNIPROT

dbSNP: rs1555793103
rs1555793103
MYO5B ; SNHG22
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555793199
rs1555793199
MYO5B ; SNHG22
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1568049625
rs1568049625
MYO5B
C 0.700 CausalMutation CLINVAR

dbSNP: rs753558336
rs753558336
MYO5B
0.700 GeneticVariation UNIPROT

dbSNP: rs762039116
rs762039116
MYO5B ; SNHG22
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121908103
rs121908103
MYO5B
0.800 GeneticVariation UNIPROT Microvillus inclusion disease: loss of Myosin vb disrupts intracellular traffic and cell polarity. 24138727

2014
dbSNP: rs121908103
rs121908103
MYO5B
0.800 GeneticVariation UNIPROT Myosin Vb uncoupling from RAB8A and RAB11A elicits microvillus inclusion disease. 24892806

2014
dbSNP: rs121908105
rs121908105
MYO5B
0.800 GeneticVariation UNIPROT Microvillus inclusion disease: loss of Myosin vb disrupts intracellular traffic and cell polarity. 24138727

2014
dbSNP: rs121908105
rs121908105
MYO5B
0.800 GeneticVariation UNIPROT Myosin Vb uncoupling from RAB8A and RAB11A elicits microvillus inclusion disease. 24892806

2014
dbSNP: rs121908103
rs121908103
MYO5B
0.800 GeneticVariation UNIPROT Functional characterization of mutations in the myosin Vb gene associated with microvillus inclusion disease. 21206382

2011
dbSNP: rs121908105
rs121908105
MYO5B
0.800 GeneticVariation UNIPROT Functional characterization of mutations in the myosin Vb gene associated with microvillus inclusion disease. 21206382

2011
dbSNP: rs121908103
rs121908103
MYO5B
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
dbSNP: rs121908105
rs121908105
MYO5B
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