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: rs10772715
rs10772715
12 13885069 intron variant G/A snv 0.39
CUI: C0233565
Disease: Bradykinesia
Bradykinesia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs10772715
rs10772715
12 13885069 intron variant G/A snv 0.39
CUI: C0392156
Disease: Akathisia
Akathisia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms 0.010 1.000 1 2012 2012
dbSNP: rs10845779
rs10845779
1.000 0.040 12 13457576 intron variant T/C snv 0.53
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10845851
rs10845851
1.000 0.040 12 13871835 intron variant A/G snv 7.3E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs11055458
rs11055458
1.000 0.040 12 13463601 intron variant A/G snv 0.15
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11055460
rs11055460
1.000 0.040 12 13464778 intron variant C/T snv 7.5E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs117578877
rs117578877
1.000 0.040 12 13528544 intron variant C/T snv 3.1E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2015 2015
dbSNP: rs12228921
rs12228921
1.000 0.040 12 13452980 intron variant T/C snv 7.4E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12319804
rs12319804
1.000 0.040 12 13871204 intron variant T/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs12369358
rs12369358
1.000 0.040 12 13463323 intron variant C/T snv 0.10
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12582848
rs12582848
1.000 0.040 12 13878511 intron variant A/C snv 0.59
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs12820037
rs12820037
1.000 0.040 12 13963180 intron variant A/G snv 0.29
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs138009610
rs138009610
12 13711041 intron variant T/C snv 4.0E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs139593264
rs139593264
12 13819716 intron variant G/A snv 1.5E-02
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2017 2017
dbSNP: rs1457608
rs1457608
1.000 0.040 12 13463428 intron variant A/G snv 0.62
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1457610
rs1457610
1.000 0.040 12 13465368 intron variant A/T snv 0.42
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1477105
rs1477105
12 13474631 intron variant A/G snv 0.46
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs16909124
rs16909124
1.000 0.040 12 13465015 intron variant A/C snv 0.14
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs172677
rs172677
1.000 0.080 12 13944536 intron variant A/G snv 0.63
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs17821946
rs17821946
1.000 0.040 12 13455592 intron variant T/C snv 9.2E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs2098469
rs2098469
1.000 0.040 12 13918072 intron variant T/G snv 0.11
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs2163895
rs2163895
1.000 0.040 12 13455477 intron variant G/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs2192970
rs2192970
12 13683379 intron variant G/A snv 0.15
CUI: C0233565
Disease: Bradykinesia
Bradykinesia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs2192970
rs2192970
12 13683379 intron variant G/A snv 0.15
CUI: C0392156
Disease: Akathisia
Akathisia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms 0.010 1.000 1 2012 2012
dbSNP: rs220558
rs220558
12 13795131 intron variant G/A snv 0.42
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018