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: rs652889
rs652889 		3 61808380 intron variant C/A;T snv
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 1 2009 2009
dbSNP: rs7609954
rs7609954 		1.000 0.080 3 61650482 intron variant G/T snv 0.17
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.710 1.000 1 2016 2016
dbSNP: rs10490775
rs10490775 		1.000 0.080 3 62051050 intron variant C/T snv 0.13
CUI: C0016781
Disease: Fuchs Endothelial Dystrophy
Fuchs Endothelial Dystrophy 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 1.000 1 2010 2010
dbSNP: rs13061878
rs13061878 		0.925 0.040 3 61634560 intron variant A/T snv 9.7E-02
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs13061878
rs13061878 		0.925 0.040 3 61634560 intron variant A/T snv 9.7E-02
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs13082242
rs13082242 		1.000 0.040 3 62132816 intron variant G/T snv 0.13
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17065527
rs17065527 		3 61864416 intron variant G/A snv 2.3E-02
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2012 2012
dbSNP: rs1713534
rs1713534 		3 61792590 intron variant T/G snv 8.7E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs1911746
rs1911746 		3 62115166 intron variant T/C snv 0.75
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2366684
rs2366684 		1.000 0.040 3 62138804 intron variant G/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs6445258
rs6445258 		3 62126524 intron variant T/C snv 0.79
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs666403
rs666403 		3 61790134 intron variant A/T snv 0.15
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs6764198
rs6764198 		1.000 0.040 3 62131511 intron variant T/G snv 0.44
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs704341
rs704341 		1.000 0.080 3 61963062 intron variant G/A snv 0.11
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2015 2015
dbSNP: rs704341
rs704341 		1.000 0.080 3 61963062 intron variant G/A snv 0.11
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2015 2015
dbSNP: rs73096591
rs73096591 		3 62160398 intron variant G/C snv 9.9E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7621604
rs7621604 		3 61572044 intron variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7621604
rs7621604 		3 61572044 intron variant A/G;T snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs7633054
rs7633054 		1.000 0.080 3 62153280 intron variant C/G snv 4.7E-02
CUI: C0004610
Disease: Bacteremia
Bacteremia 		Pathological Conditions, Signs and Symptoms; Infections 0.700 1.000 1 2016 2016
dbSNP: rs9825906
rs9825906 		3 62008030 intron variant G/T snv 0.39
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2292245
rs2292245 		0.925 0.080 3 62203515 missense variant G/A snv 0.19 0.16
CUI: C0010036
Disease: Corneal dystrophy
Corneal dystrophy 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2292245
rs2292245 		0.925 0.080 3 62203515 missense variant G/A snv 0.19 0.16
CUI: C4699184
Disease: Fuchs
Fuchs 		0.010 1.000 1 2014 2014
dbSNP: rs7640737
rs7640737 		0.925 0.080 3 62047679 intron variant C/T snv 0.12
CUI: C0010036
Disease: Corneal dystrophy
Corneal dystrophy 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.010 1.000 1 2014 2014
dbSNP: rs7640737
rs7640737 		0.925 0.080 3 62047679 intron variant C/T snv 0.12
CUI: C4699184
Disease: Fuchs
Fuchs 		0.010 1.000 1 2014 2014