MYO5B, myosin VB, 4645

N. diseases: 60; N. variants: 21
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555793103
rs1555793103
Entrez Id: 4645;103091864
Gene Symbol: MYO5B;SNHG22
MYO5B;SNHG22
CUI: C0267557
Disease:
Secretory diarrhea
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555793199
rs1555793199
Entrez Id: 4645;103091864
Gene Symbol: MYO5B;SNHG22
MYO5B;SNHG22
CUI: C0267557
Disease:
Secretory diarrhea
T 0.700 GeneticVariation CLINVAR