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: rs16938372
rs16938372 		1.000 0.040 8 72795902 intron variant C/T snv 0.30
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs16938508
rs16938508 		1.000 0.040 8 72938577 downstream gene variant A/G snv 0.12
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1866737
rs1866737 		1.000 0.040 8 72799079 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: rs2128158
rs2128158 		8 72917865 intron variant G/A snv 0.12
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2013 2013
dbSNP: rs2247572
rs2247572 		8 72720793 intron variant C/T snv 0.21
CUI: C0027902
Disease: Neuropsychological Tests
Neuropsychological Tests 		0.700 1.000 1 2010 2010
dbSNP: rs2251898
rs2251898 		1.000 0.040 8 72779886 intron variant G/A snv 0.68
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs2251899
rs2251899 		1.000 0.040 8 72779869 intron variant A/T snv 0.35
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs349356
rs349356 		8 72541711 intron variant G/T snv 0.74
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs4738296
rs4738296 		1.000 0.040 8 72945304 upstream gene variant A/C snv 7.9E-02
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata 		Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs7845090
rs7845090 		8 72537705 5 prime UTR variant G/A snv 0.67
CUI: C0518026
Disease: body fat percentage (physical finding)
body fat percentage (physical finding) 		0.700 1.000 1 2019 2019
dbSNP: rs7845090
rs7845090 		8 72537705 5 prime UTR variant G/A snv 0.67
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs877521
rs877521 		1.000 0.040 8 72796734 intron variant T/C snv 9.6E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs770305852
rs770305852 		1.000 0.080 8 72936703 missense variant G/A;C snv 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs17187449
rs17187449 		8 72830736 intron variant G/A snv
CUI: C0027794
Disease: Neural Tube Defects
Neural Tube Defects 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs349358
rs349358 		8 72539240 intron variant C/T snv 0.88
CUI: C0027497
Disease: Nausea
Nausea 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2020 2020
dbSNP: rs349358
rs349358 		8 72539240 intron variant C/T snv 0.88
CUI: C0232602
Disease: Retching
Retching 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2020 2020
dbSNP: rs349358
rs349358 		8 72539240 intron variant C/T snv 0.88
CUI: C0520909
Disease: Postoperative Nausea and Vomiting
Postoperative Nausea and Vomiting 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2020 2020