Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908188
rs121908188
SELENON
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1565679039
rs1565679039
COL2A1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1568019012
rs1568019012
LAMA1
A 0.700 CausalMutation CLINVAR

dbSNP: rs199564797
rs199564797
SELENON
A 0.700 GeneticVariation CLINVAR

dbSNP: rs745886248
rs745886248
SELENON
A 0.700 GeneticVariation CLINVAR

dbSNP: rs4680
rs4680
COMT ; MIR4761
0.010 GeneticVariation BEFREE There was no significant effect of catechol-O-methyltransferase Val(158)Met genotype or presence of velopharyngeal insufficiency on olfactory functioning. 30007867

2018