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: rs10009145
rs10009145
1.000 0.080 4 99126778 intron variant G/A snv 0.39 0.34
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs1800759
rs1800759
0.925 0.120 4 99144358 intron variant T/G snv 0.49
CUI: C0009088
Disease: Cluster Headache
Cluster Headache
Nervous System Diseases 0.020 0.500 2 2018 2020
dbSNP: rs1800759
rs1800759
0.925 0.120 4 99144358 intron variant T/G snv 0.49
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
Chemically-Induced Disorders; Mental Disorders 0.020 1.000 2 2006 2011
dbSNP: rs1800759
rs1800759
0.925 0.120 4 99144358 intron variant T/G snv 0.49
CUI: C1510472
Disease: Drug Dependence
Drug Dependence
Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2006 2006
dbSNP: rs1800759
rs1800759
0.925 0.120 4 99144358 intron variant T/G snv 0.49
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs4699720
rs4699720
4 99152104 intron variant C/T snv 0.74
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs1126671
rs1126671
0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75
CUI: C0009088
Disease: Cluster Headache
Cluster Headache
Nervous System Diseases 0.020 1.000 2 2010 2018
dbSNP: rs1126671
rs1126671
0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75
CUI: C0600427
Disease: Cocaine Dependence
Cocaine Dependence
Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2005 2005
dbSNP: rs1126671
rs1126671
0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75
CUI: C0524662
Disease: Opiate Addiction
Opiate Addiction
Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2005 2005
dbSNP: rs1126671
rs1126671
0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75
CUI: C1510472
Disease: Drug Dependence
Drug Dependence
Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2005 2005
dbSNP: rs1126671
rs1126671
0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2005 2005
dbSNP: rs2851246
rs2851246
1.000 0.040 4 99124953 intron variant T/C snv 0.79
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1042365
rs1042365
1.000 0.040 4 99124349 3 prime UTR variant T/G snv 0.79
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs2602896
rs2602896
1.000 0.040 4 99125056 intron variant A/G snv 0.79
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs6855482
rs6855482
1.000 0.040 4 99135808 intron variant C/T snv 0.96
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017