Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4236167
rs4236167
DTNBP1 ; LOC105374947
6 15533720 intron variant C/T snv 0.44
CUI: C0233765
Disease: Hallucinations, Olfactory
Hallucinations, Olfactory 		0.010 1.000 1 2015 2015
dbSNP: rs4236167
rs4236167
DTNBP1 ; LOC105374947
6 15533720 intron variant C/T snv 0.44
CUI: C0233762
Disease: Hallucinations, Auditory
Hallucinations, Auditory 		0.010 1.000 1 2015 2015