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: rs61712019
rs61712019 		1.000 0.040 2 77477763 intron variant C/A;G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 3 2015 2019
dbSNP: rs10170138
rs10170138 		2 76794802 intron variant C/T snv 0.16
CUI: C0038663
Disease: Suicide attempt
Suicide attempt 		Behavior and Behavior Mechanisms 0.700 1.000 1 2012 2012
dbSNP: rs10221841
rs10221841 		1.000 0.040 2 76795366 intron variant A/G snv 0.17
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs13389599
rs13389599 		2 76861472 intron variant T/C snv 2.6E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases 		Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs13428376
rs13428376 		1.000 0.040 2 76791825 intron variant C/T snv 0.13
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1400846
rs1400846 		1.000 0.040 2 76811415 intron variant G/A snv 0.13
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs143985312
rs143985312 		2 77072001 intron variant T/C snv 9.4E-03
CUI: C1285654
Disease: Memory performance
Memory performance 		0.700 1.000 1 2018 2018
dbSNP: rs1517782
rs1517782 		2 76794100 intron variant C/A snv 0.11
CUI: C0038663
Disease: Suicide attempt
Suicide attempt 		Behavior and Behavior Mechanisms 0.700 1.000 1 2012 2012
dbSNP: rs17013234
rs17013234 		1.000 0.040 2 76831385 intron variant A/T snv 0.25
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1914508
rs1914508 		1.000 0.040 2 76832073 intron variant G/A snv 0.63
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs4387822
rs4387822 		1.000 0.040 2 76809766 intron variant T/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs61354037
rs61354037 		2 77573273 intron variant T/C snv 0.41
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs6547100
rs6547100 		1.000 0.040 2 76811331 intron variant A/C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs977744
rs977744 		1.000 0.040 2 76810883 intron variant A/C snv 0.42
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs13388459
rs13388459 		1.000 0.040 2 76988371 intron variant C/T snv 0.21
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs2077823
rs2077823 		1.000 0.040 2 77021786 intron variant A/G snv 0.12
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs62170897
rs62170897 		1.000 0.040 2 77031414 intron variant A/G snv 0.12
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs62171995
rs62171995 		1.000 0.040 2 77001194 intron variant G/A snv 0.14
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		Mental Disorders 0.010 1.000 1 2019 2019