Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121908315
rs121908315 		1.000 0.120 19 3653454 missense variant C/T snv
CUI: C1969655
Disease: LETHAL CONGENITAL CONTRACTURAL SYNDROME 3
LETHAL CONGENITAL CONTRACTURAL SYNDROME 3 		Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases 0.800 1.000 1 2007 2007
dbSNP: rs10405681
rs10405681 		1.000 0.080 19 3634021 intron variant C/A;T snv
CUI: C0001956
Disease: Alcohol Use Disorder
Alcohol Use Disorder 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs10419980
rs10419980 		1.000 0.080 19 3685118 intron variant C/T snv 0.29
CUI: C0001956
Disease: Alcohol Use Disorder
Alcohol Use Disorder 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs10432303
rs10432303 		1.000 0.080 19 3656654 intron variant G/A snv 0.41
CUI: C0001956
Disease: Alcohol Use Disorder
Alcohol Use Disorder 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs1476592
rs1476592 		1.000 0.080 19 3679742 intron variant A/G;T snv
CUI: C0001956
Disease: Alcohol Use Disorder
Alcohol Use Disorder 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs2074957
rs2074957 		1.000 0.080 19 3653527 synonymous variant C/A;T snv 8.0E-06; 0.57
CUI: C0001956
Disease: Alcohol Use Disorder
Alcohol Use Disorder 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs4432372
rs4432372 		1.000 0.080 19 3698844 intron variant A/G;T snv
CUI: C0001956
Disease: Alcohol Use Disorder
Alcohol Use Disorder 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs4807493
rs4807493 		1.000 0.080 19 3631038 3 prime UTR variant A/G snv 0.84
CUI: C0001956
Disease: Alcohol Use Disorder
Alcohol Use Disorder 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs8109485
rs8109485 		1.000 0.080 19 3664096 intron variant A/G snv 0.21
CUI: C0001956
Disease: Alcohol Use Disorder
Alcohol Use Disorder 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2018 2018