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: rs3805322
rs3805322
1.000 0.080 4 99135847 intron variant A/G snv 1.1E-02
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
Digestive System Diseases; Neoplasms 0.800 1.000 2 2010 2012
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: rs13110176
rs13110176
1.000 0.040 4 99141279 intron variant A/G snv 0.21
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs13110764
rs13110764
1.000 0.040 4 99141315 intron variant G/A snv 0.21
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17028615
rs17028615
1.000 0.080 4 99150767 intron variant A/C;G snv
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs17028615
rs17028615
1.000 0.080 4 99150767 intron variant A/C;G snv
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders
Chemically-Induced Disorders 0.700 1.000 1 2014 2014
dbSNP: rs17028615
rs17028615
1.000 0.080 4 99150767 intron variant A/C;G snv
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders
Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs17028615
rs17028615
1.000 0.080 4 99150767 intron variant A/C;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2014 2014
dbSNP: rs17218560
rs17218560
1.000 0.040 4 99139643 intron variant A/G snv 0.21
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17817958
rs17817958
1.000 0.040 4 99140094 intron variant G/T snv 0.21
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
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: 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: 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: rs2851247
rs2851247
1.000 0.040 4 99124940 intron variant G/C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs2851248
rs2851248
1.000 0.040 4 99124823 intron variant T/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs29001203
rs29001203
1.000 0.040 4 99131940 intron variant T/C snv 0.21
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs34936974
rs34936974
1.000 0.040 4 99131233 intron variant G/A snv 0.21
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
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: rs5860563
rs5860563
1.000 0.080 4 99126006 intron variant -/A delins
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders
Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs5860563
rs5860563
1.000 0.080 4 99126006 intron variant -/A delins
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs5860563
rs5860563
1.000 0.080 4 99126006 intron variant -/A delins
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders
Chemically-Induced Disorders 0.700 1.000 1 2019 2019
dbSNP: rs6532800
rs6532800
1.000 0.040 4 99137733 intron variant T/C;G snv
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
dbSNP: rs7694844
rs7694844
1.000 0.040 4 99138675 intron variant T/A;C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1042364
rs1042364
1.000 0.080 4 99124423 stop gained T/A;C snv 0.78
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
Chemically-Induced Disorders; Mental Disorders 0.020 1.000 2 2011 2016