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: rs11067815
rs11067815 		1.000 0.040 12 115876463 intron variant A/T snv 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.700 1.000 1 2013 2013
dbSNP: rs4767382
rs4767382 		1.000 0.040 12 115884185 intron variant A/G snv 0.32
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.700 1.000 1 2013 2013
dbSNP: rs7964653
rs7964653 		1.000 0.040 12 115875621 intron variant A/G snv 0.21
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.700 1.000 1 2013 2013
dbSNP: rs7967915
rs7967915 		1.000 0.040 12 115875910 intron variant T/C snv 0.23
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.700 1.000 1 2013 2013
dbSNP: rs7970014
rs7970014 		1.000 0.040 12 115840487 intron variant G/A snv 0.23
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7977515
rs7977515 		1.000 0.040 12 115838468 intron variant A/G snv 0.24
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs9989045
rs9989045 		1.000 0.040 12 115838611 intron variant A/G snv 0.26
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017