Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908106
rs121908106
A 0.820 CausalMutation CLINVAR

dbSNP: rs121908103
rs121908103
C 0.800 CausalMutation CLINVAR

dbSNP: rs121908105
rs121908105
A 0.800 CausalMutation CLINVAR

dbSNP: rs1053713532
rs1053713532
0.700 GeneticVariation UNIPROT

dbSNP: rs121908104
rs121908104
T 0.700 CausalMutation CLINVAR

dbSNP: rs1283622290
rs1283622290
0.700 GeneticVariation UNIPROT

dbSNP: rs1324907355
rs1324907355
0.700 GeneticVariation UNIPROT

dbSNP: rs1555793103
rs1555793103
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555793199
rs1555793199
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1568049625
rs1568049625
C 0.700 CausalMutation CLINVAR

dbSNP: rs753558336
rs753558336
0.700 GeneticVariation UNIPROT

dbSNP: rs762039116
rs762039116
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121908106
rs121908106
0.820 GeneticVariation UNIPROT MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. 18724368

2008

dbSNP: rs121908106
rs121908106
0.820 GeneticVariation UNIPROT Navajo microvillous inclusion disease is due to a mutation in MYO5B. 19006234

2008

dbSNP: rs121908103
rs121908103
0.800 GeneticVariation UNIPROT MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. 18724368

2008

dbSNP: rs121908103
rs121908103
0.800 GeneticVariation UNIPROT Navajo microvillous inclusion disease is due to a mutation in MYO5B. 19006234

2008

dbSNP: rs121908105
rs121908105
0.800 GeneticVariation UNIPROT MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. 18724368

2008

dbSNP: rs121908105
rs121908105
0.800 GeneticVariation UNIPROT Navajo microvillous inclusion disease is due to a mutation in MYO5B. 19006234

2008

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

2008

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

2008

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

2008

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

2008

dbSNP: rs121908106
rs121908106
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

dbSNP: rs121908103
rs121908103
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
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