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: rs10460716
rs10460716 		21 38084132 intron variant T/A snv 0.53
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs2211843
rs2211843 		21 37811882 intron variant G/C;T snv
CUI: C0030193
Disease: Pain
Pain 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2019 2019
dbSNP: rs3787823
rs3787823 		21 37739137 intron variant C/A;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs7283798
rs7283798 		21 38034828 intron variant A/T snv 0.18
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs786204795
rs786204795 		1.000 21 37714697 missense variant C/T snv
CUI: C3279800
Disease: KEPPEN-LUBINSKY SYNDROME
KEPPEN-LUBINSKY SYNDROME 		0.800 1.000 1 2015 2015
dbSNP: rs9976841
rs9976841 		21 38112229 intron variant G/A snv 0.45
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs1556023562
rs1556023562 		1.000 21 37714645 missense variant A/C snv
CUI: C3279800
Disease: KEPPEN-LUBINSKY SYNDROME
KEPPEN-LUBINSKY SYNDROME 		0.700 0
dbSNP: rs786204794
rs786204794 		1.000 21 37714700 inframe deletion GGT/- delins
CUI: C3279800
Disease: KEPPEN-LUBINSKY SYNDROME
KEPPEN-LUBINSKY SYNDROME 		0.700 0
dbSNP: rs2070995
rs2070995 		1.000 0.040 21 37714662 synonymous variant T/C snv 0.80 0.85
CUI: C0030193
Disease: Pain
Pain 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2019 2019
dbSNP: rs2070995
rs2070995 		1.000 0.040 21 37714662 synonymous variant T/C snv 0.80 0.85
CUI: C0457949
Disease: Chronic low back pain
Chronic low back pain 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2019 2019
dbSNP: rs7275707
rs7275707 		1.000 0.040 21 37916637 intron variant A/G snv 0.69
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs10483038
rs10483038 		1.000 0.080 21 37652469 intron variant T/C snv 0.26
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2012 2012
dbSNP: rs10483038
rs10483038 		1.000 0.080 21 37652469 intron variant T/C snv 0.26
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2012 2012
dbSNP: rs10483038
rs10483038 		1.000 0.080 21 37652469 intron variant T/C snv 0.26
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		Chemically-Induced Disorders 0.700 1.000 1 2012 2012
dbSNP: rs111372083
rs111372083 		1.000 0.080 21 37638374 intron variant C/A;T snv 0.27
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2012 2012
dbSNP: rs111372083
rs111372083 		1.000 0.080 21 37638374 intron variant C/A;T snv 0.27
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2012 2012
dbSNP: rs111372083
rs111372083 		1.000 0.080 21 37638374 intron variant C/A;T snv 0.27
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		Chemically-Induced Disorders 0.700 1.000 1 2012 2012
dbSNP: rs111576572
rs111576572 		1.000 0.080 21 37617262 3 prime UTR variant A/G snv 0.32
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2012 2012
dbSNP: rs111576572
rs111576572 		1.000 0.080 21 37617262 3 prime UTR variant A/G snv 0.32
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2012 2012
dbSNP: rs111576572
rs111576572 		1.000 0.080 21 37617262 3 prime UTR variant A/G snv 0.32
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		Chemically-Induced Disorders 0.700 1.000 1 2012 2012
dbSNP: rs12482570
rs12482570 		1.000 0.080 21 37705475 intron variant A/G snv 0.30
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2012 2012
dbSNP: rs12482570
rs12482570 		1.000 0.080 21 37705475 intron variant A/G snv 0.30
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		Chemically-Induced Disorders 0.700 1.000 1 2012 2012
dbSNP: rs12482570
rs12482570 		1.000 0.080 21 37705475 intron variant A/G snv 0.30
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2012 2012
dbSNP: rs1399590
rs1399590 		1.000 0.080 21 37681768 intron variant G/A snv 0.56
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2012 2012
dbSNP: rs1399590
rs1399590 		1.000 0.080 21 37681768 intron variant G/A snv 0.56
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2012 2012