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: rs10873925
rs10873925
1 76996050 intron variant A/G snv 0.25
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs12065122
rs12065122
1.000 0.040 1 77007396 intron variant A/G snv 0.70
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs4949764
rs4949764
1.000 0.040 1 76996977 intron variant T/C snv 0.89
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs6603933
rs6603933
1.000 0.040 1 77006046 intron variant T/G snv 0.34
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs6663942
rs6663942
1.000 0.040 1 77007735 intron variant T/G snv 0.20
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1206787329
rs1206787329
1.000 0.040 1 77044237 missense variant G/A snv 4.0E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs17368584
rs17368584
1.000 0.120 1 76930481 intron variant T/A;C snv
Metastatic malignant neoplasm to brain
Pathological Conditions, Signs and Symptoms; Neoplasms; Nervous System Diseases 0.010 1.000 1 2017 2017