Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72549321
rs72549321
FMO3 ; MIR1295A
CUI: C0342739
Disease: Trimethylaminuria
Trimethylaminuria 		0.800 GeneticVariation UNIPROT Clinical utility gene card for: trimethylaminuria. 22126753

2012
dbSNP: rs72549321
rs72549321
FMO3 ; MIR1295A
CUI: C0342739
Disease: Trimethylaminuria
Trimethylaminuria 		A 0.800 CausalMutation CLINVAR